\r\n\t2) Human sexual disorders in males and females. \r\n\t3) Psychological aspects of the human sexual response cycle and its disorders. \r\n\t4) The therapeutic aspects.
\r\n
\r\n\tThe human sexual response cycle and human sexual behavior are interrelated. How this inter-relationship and its association to normal sexual health need to be delineated. In a world torn between sex and sexually transmitted disease, clear-cut scientific information in the form of a monograph is required to educate.
\r\n
\r\n\tHuman sexuality, gender identity, and sexuo-erotic orientation play great roles in human health and disease. Sex education is the need of the hour and a reflection will be timely.
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\n
1. Introduction
\n
Since its beginning, robotics has been a research field strongly influenced by nature. For robotic platforms where wheels to displace themselves are not used, researchers have taken inspiration not only in the physical form of living beings as archetypes of their designs (e.g., legged, finned or winged robotic platforms), but also in the mechanisms to allow their locomotion (e.g., walking, swimming or flying), mainly known as central pattern generators (CPGs) [1]. In biology, the basis of CPGs was settled down in Brown’s studies about how the rhythmic movements of locomotion in living beings are created [2]. In [3], Brown experimentally discovered that neurons, which inhibiting each other, generate periodically rhythmic activities that control bending and tension of muscles involved in locomotion. Moreover, GPGs have been linked to other unconscious activities besides locomotion such as swallowing, digestion, heart beating and breathing [4, 5].
\n
Furthermore, CPGs have become a suitable alternative to nonbiologically inspired methods for locomotion systems of nonwheeled robotic platforms [6]; this is due to several and interesting features of CPGs such as adaptability, rhythmicity, stability and variety [7]. The CPG-based locomotion systems have been successfully designed and implemented at software and/or hardware levels for different nonwheeled robotic platforms [8] such as walking robots (biped [9], quadruped [10], hexapod [11] and octopod [12]), swimming robots [13], flying robots [14]), among others (i.e., snake robots [15] and salamander robots [16]). Although vast amount of works made and reported in the state of the art about CPG-based locomotion systems, there is not a general and standard methodology to build CPGs [6]; however, working with CPGs commonly involves the following three phases [7]: (1) choosing the processing unit model, the coupling type and the connectivity topology (modeling and analysis), (2) dealing with parameter tuning, usually solved by optimization methods and gait transition, to handle variation on gaits as type or frequency (modulation) and (3) executing the designed CPG at the software and/or hardware level (implementation).
\n
In this chapter, we focus on locomotion systems for legged robots, which are based on spiking central pattern generators (SCPGs) and reverse engineering methods for automatically design them. The study and implementation of SCPGs as locomotion systems have been barely explored and compared with other CPGs, which are built with oscillators or low-plausible neuron models (see [6, 7, 17] as reference). The SCPGs are built with plausible neuron models known as spiking neurons, models that define the third generation of artificial neural networks [18]; these neuron models naturally receive and send spatio-temporal information as generating rhythmic patterns are required for CPGs. The SCPGs have been designed and implemented as locomotion systems for robotic platforms such as bipeds [19–21, 25], quadrupeds [23, 25] and hexapods [22, 24, 25, 26, 27], where the design methodologies used in [19, 20, 21, 27] tend to follow the phases proposed in [7], while in [22, 23, 24, 25, 26] reverse engineering methods are used. Basically, a reverse engineering method to design SCPG-based locomotion systems for robotic platforms uses either deterministic or stochastic optimization methods, which, given an input set of discretized rhythmic signals and a fixed spiking neuron model, are capable of defining a spiking neural network (SNN), including both synaptic connections and weights, that endogenously and periodically replicates the input set of discretized rhythmic signals, which contribute to locomotion of a robotic platform. Herein, we present a generalization of reverse engineering methods to design SCPG-based locomotion systems for robotic platforms based on details of implementations of reviewed works.
\n
\n
\n
2. Robotic platforms and controllers
\n
Nowadays, there are a variety of robotic platforms, and each of them has particular technical specifications in design, displacement ways and so on. In reviewed works, for real implementations of SCPG-based locomotion systems, three types of legged robotic platforms have been particularly used such as hexapod, quadruped and biped robots. Particularly, the used robotic platforms have 3 degrees of freedom (DOFs) or servomotors per leg, that is, the hexapod has 18 DOFs, the quadruped has 12 DOFs and the biped has 6 DOFs. Although for the hexapod and the quadruped, just two DOFs per leg were used; the two are closer to the body of robots and directly related to the movement of the robot. Figure 1 shows the robotic platforms with a specific label for identifying the position of their respective servomotors.
\n
Figure 1.
Robotic platforms from Lynxmotion company. (a) Phoenix hexapod robot model, (b) symmetric quadruped robot model and (c) Brat biped robot model. In ovals are marked and labeled the servomotors used in their locomotion where letters C, F and a stand for Coxa, femur and ankle, respectively, letters L and R represent left and right sides, and numbers mark the number according to their position (taken from [25]).
\n
Servomotors in the robotic platforms are handled by a processing unit, which in reviewed works, a SCPG is embedded into them to provide a locomotion mechanism to the robots. In Figure 2, we present the electronic boards, which have been used as processing units such as Arduino (Figure 2a), Field Programmable Gate Array (FPGA) (Figure 2b) and a Raspberry Pi 3 Model B (Figure 2c) boards. Also, a servo controller board (Figure 2d) is required to send the output of the processing units to the servomotors of the robotic platforms.
\n
Figure 2.
Boards for robot control. Processing units: (a) Arduino board, BotBoarduino for Lynxmotion robots, (b) FPGA Spartan 6 XEM6310-LX45 board from OpalKelly, and (c) Raspberry Pi 3 Model B board. Servo controller: (d) SSC-32 board.
\n
Basically, the integration of the processing boards and platforms works as follows: an embedded SCPG into a processing board generates rhythmic signals, which are sent to the legs through a servo controller. This converts the spiking activity generated by the SCPGs into a control signal (voltage). The transmission process is carried out by using the RS-232 communication protocol. Figure 3 shows a block diagram of this integration.
\n
Figure 3.
System block diagram of robotic controller coupled with servomotors of robotic platforms through a servo controller.
\n
Thus, an important aspect to achieve locomotion in robotic platforms is to design a SCPG according to the capabilities of the processing board, which, for reviewed works, must exactly replicate and periodically generate specific rhythmic patterns. In Section 3, we describe in detail the functionality of SCPGs and methods used for designing them.
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\n
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3. SCPG-based locomotion system
\n
The SCPGs, reviewed in this chapter, can generate endogenously discrete rhythmic signals; in other words, each periodical signal of a locomotion gait is represented by means of a spike train with spike times occurring periodically. This idea was firstly presented by Rostro-Gonzalez et al. in [22], where SCPGs built with discrete spiking neurons (Section 3.2.1) were automatically designed by using a deterministic reverse engineering method (Section 4.1) to imitate walking forms of a stick insect; based on steps sketches of walking forms of stick insect reported in [28], Rostro proposed three sets of discrete rhythmic signals as locomotion gaits (Section 3.1) to achieve hexapod robot locomotion by means of designing one SCPG for each of them.
\n
In Figure 4, Rostro-Gonzalez’s approach to achieve locomotion for six-legged robots through discrete events over time by means of SNNs is schematized. In Figure 4a, a walking form of stick insect reported in [28] is presented; black rectangles represent a leg on ground, while white ones represent a leg in the air. The L1 row is marked with dotted rectangle to exemplify how a step of real hexapod insect is interpreted and extended to a step of robot hexapod. Notice in Figure 4b that leg sketch coincides with a black rectangle in Figure 4a as leg is on the ground, and at this point the leg displacement that contributes to whole walking action occurs. Figure 4c shows the rhythmic signals over time to move a leg according to locomotion gait in Figure 4a; the coxa moves to front with spike events and to back without spike events, while the femur moves to down with spike events and to up in the absence of spike events. Finally, the combination of such movements according to the presence and absence of spikes of all legs provokes locomotion of legged robot.
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Figure 4.
Representation of extrapolation of steps observed of hexapod insect into discrete rhythmic signals for SCPG-based locomotion design. (a) Walking form of stick insect reported in [28], (b) extrapolation of a step into position of a leg over time and (c) proposal of a step (femur row) with additional information (coxa row) represented as spike trains, in each row, darker rectangles represent a spike and lighter ones indicate the absence of spike.
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Later, Espinal et al. generated SCPG-based locomotion systems for quadruped and hexapod robots based on Rostro-Gonzalez’s idea by using the same discrete spiking neuron model (Section 3.2.1) and a stochastic reverse engineering (Section 4.2) for designing them. There were designed and implemented SCPG-based locomotion systems for quadruped robots in [23] and hexapod robots in [24]; the difference with the Rostro’s work is that more compact SNN topologies were achieved, and it was achieved to design a single SCPG capable of generating the three original locomotion gaits for hexapod robots and was extended for quadruped ones as well.
\n
Lately, SCPG-based locomotion systems for hexapods, quadrupeds and bipeds were designed by Guerra-Hernandez et al. in [25]. In his work, there was proposed a locomotion gait for biped robots following the Rostro’s idea, and SNNs were designed by using the discrete spiking neuron model and a variant of stochastic reverse engineering (Section 4.2) proposed by Espinal et al.
\n
Lately, in [26], Perez-Trujillo et al. designed SCPG-based locomotion systems for hexapod robots based on Rostro-Gonzalez’s, Espinal’s and Guerra-Hernandez’s works. The contribution of Perez-Trujillo’s work was to create SCPG-based locomotion systems built with a nondiscrete spiking neuron model (Section 3.2.2), and the reverse engineering method was a variant stochastic one (Section 4.2).
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The reviewed works are summarized in Table 1, including robotic platforms and processing boards as well as reverse engineering method and spiking neuron model used.
Summary of Legged Robot Locomotion System Configurations and reverse engineering methods.
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Following subsections complement the description of SCPG-based locomotion systems. In Section 3.1, the different rhythmic signal sets reported for each locomotion gait to robotic platforms are shown. Section 3.2 describes the spiking neuron models that have been used to define SNN as SCPGs on robot locomotion.
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3.1. Locomotion patterns
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The locomotion patterns contain the discrete rhythmic signals for each servomotor of a robotic platform. Each of them serves to define a specific locomotion gait that a SCPG must replicate endogenously and periodically. Besides, they are used for engineering reverse methods (Section 4) to design SCPGs. In Figures 5–7, show the different designed discrete rhythmic signals for hexapod, quadruped and biped robots, respectively; for each row corresponds a servomotor with the same label according to the robotic platform.
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Figure 5.
Hexapod robot locomotion gaits proposed in [22] (figures taken from [26]). (a) Walk gait, (b) jog gait and (c) run gait.
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Figure 6.
Quadruped robot locomotion gaits proposed in [23] (figures taken from [26]). (a) Walk gait, (b) jog gait and (c) run gait.
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Figure 7.
Biped walking locomotion gait proposed in [26].
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3.2. Spiking neuron models
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3.2.1. Beslon-Mazet-Soula neuron model
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The Belson-Mazet-Soula (BMS) neuron [29] is a discrete-time model derived from a well-known spiking neuron, that is, the integrate-and-fire [30] model. The BMS neuron model is defined by Eqs. (1) and (2), and they describe the behavior of the \n\ni\n\n-th neuron over time\n\n\nk\n\n; former equation models its membrane potential \n\n\nV\ni\n\n\n, and the last equation defines its firing state \n\n\nZ\ni\n\n\n.
In Eq. (1), \n\nγ\n∈\n\n0\n1\n\n\n represents the leaky factor. The number of spiking neurons into the neural network is given by \n\nN\n\n. The synaptic strength weights are given by \n\n\n\nW\nij\n\n\n. The \n\n\nI\ni\next\n\n\n is either a varying or constant external stimuli; due to that, CPGs endogenously produce periodic patterns \n\n\nI\ni\next\n\n=\n0\n.\n\n
For Eq. (2), the fixed firing threshold is given by \n\nθ\n\n. Eq. (2) is used in Eq. (1) for tracking spike occurrence (\n\n\nZ\ni\n\n\nk\n\n)\n\n and resetting the membrane potential of \n\ni\n\n-th neuron \n\n\n\n1\n−\n\nZ\ni\n\n\nk\n\n\n\n\n.
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\n
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3.2.2. Integrate-and-fire neuron model
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The integrate-and-fire (I&F) neuron [30], basically, models the evolution of its membrane potential’s state over time as a resistor-capacitor (RC) circuit. In particular, the current-based leaky integrate-and-fire (LIF) model, or “if_curr_exp” model in the PyNN library [31], is a LIF neuron with a fixed firing threshold and exponentially decaying postsynaptic conductance given in Eq. (3); besides, the model requires of \n\ntau\n_\nrefrac\n\n to define the refractory value and \n\nv\n_\nthresh\n\n to set the fixed firing threshold.
In Eq. (3), the membrane potential is represented with \n\nv\n\n. The excitatory and inhibitory current injections \n\nie\n\n and \n\nii\n\n are modelled by differential equations in Eqs. (4) and (5), respectively. The \n\ni\n_\noffset\n\n stands for a base input current, and \n\ni\n_\ninj\n\n is an external current injection; both added each timestep, but \n\ni\n_\ninj\n=\n0\n\n due to the nature of CPGs.
Finally, \n\ntau\n_\nsyn\n_\nE\n\n and \n\ntau\n_\nsyn\n_\nI\n\n, in Eqs. (5) and (6), are excitatory and inhibitory input current decay time constant.
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4. Reverse engineering methods for designing SCPGs
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In this section, we describe reverse engineering methods for automatically design SNNs by defining both their topology and synaptic weights. The reviewed methods can be generalized in diagram shown in Figure 8.
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Figure 8.
Diagram of reverse engineering method for designing SCPG.
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Basically, the generalization defines an input-process-output system where its inputs are a fixed spiking neuron model (Section 3.2) and one or more sets of discrete rhythmic signals (Section 3.1), and the process is defined according to an optimization method, which can be deterministic (Section 4.1) or stochastic (Section 4.2). Finally, the output is generally a partially connected, directed and weighted graph that defines all aspects of a SNN to behave as a SCPG.
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Next, the optimization is briefly described, and their strengths and weaknesses are pointed out.
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\n
4.1. Deterministic method: Simplex method
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This method, originally proposed by Rostro in [34], was created to build SNNs to replicate recorded biological neural dynamics. It was developed to work with the BMS spiking neuron model (Section 3.2.1). It is described in [22] as follows:
\n
First, Eq. (1) must be rewritten in form expressed in Eq. (6).
where \n\n\nI\nikτ\n\n=\n\n∑\n\nτ\n=\n0\n\n\nτ\nik\n\n\n\nγ\nτ\n\n\nI\ni\n\next\n\n\n\n\nk\n−\nτ\n\n\n\n with: \n\n\nτ\nik\n\n=\nk\n−\n\n arg \n\n\nmin\n\nl\n>\n0\n\n\n\n\n\nZ\ni\n\n\n\nl\n−\n1\n\n\n=\n1\n\n\n\n; see [34] for derivation details. With Eqs. (1) and (2), a linear programming system can be formulated to determine the synaptic connections and weights of SNNs, which replicates locomotion gaits represented as rhythmic spiking dynamics through the evolution of all \n\n\nV\ni\n\n\nk\n\n\n (the membrane potential of each spiking neuron into the network), which are not known. Now, we define the expression: \n\n\nZ\ni\n\n\nk\n\n=\n0\n⇔\n\nV\ni\n\n\nk\n\n<\nθ\n\n and \n\n\nZ\ni\n\n\nk\n\n=\n1\n⇔\n\nV\ni\n\n\nk\n\n≥\nθ\n\n; where \n\nθ\n=\n1\n\n for simplification. Last expression can be written as next inequality: \n\n\nZ\ni\n\n\nk\n\n=\n0\n⇔\n\nV\ni\n\n\nk\n\n<\nθ\n\n.
\n
By substituting Eq. (6) in the last expression, we can get a linear programming system [35], given the expression in Eq. (7).
Solving the aforementioned formulated linear programming problem in Eq. (7), by using a simple method (or any existing linear programming solver), we obtain the synaptic weights of all neurons and, indirectly, a SNN topology.
\n
Next, the features of this method are listed as follows:
Strengths:
The definition of whole SNN is made by executing the method once.
It has been successfully used as a reverse engineering method for designing SNNs, which replicate recorded biological neural dynamics.
Weaknesses:
It can design SNN by using only BMS spiking neuron models.
It generates one SNN for replicating just one neural dynamic pattern.
For stochastic reverse engineering methods, evolutionary algorithms have been used; particularly, a variant of well-known genetic programming [36] called grammatical evolution (GE) [37]. Practically, GE is an optimization tool that searches approximated optimal solutions by representing them indirectly for a given problem; thus, working with GE to solve a specific problem requires four components: problem instance(s), representation of solutions, a fitness function to evaluate solution’s quality and a search engine.
\n
For the SCPG design problem, two types of representations have been proposed: one as a Context-Free Grammar (CFG) in Backus-Naur Form (BNF) and another as a Christiansen Grammar (CG) to use GE (in [25, 26]) and a variant called Christiansen Grammar Evolution (CGE) [38] (in [23, 24]), respectively. In general, both representations describe languages that define the presynaptic connectivity (including weights) of a specific spiking neuron; the common structure of expected words of two grammars is as follows: \n\n\n\n\n\n\nid\n1\n\n,\n\nweight\n1\n\n\n︷\n\n\n1\nst\n\nconfigured synapse\n\n\n\n∣\n⋯\n∣\n\n\n\n\nid\nn\n\n,\n\nweight\nn\n\n\n︷\n\n\nn\n−\nth\n\nconfigur\ned\n\nsynapse\n\n\n\n. The connectivity defined by a word has at least one connection and a maximum of connections according to number of neurons into the SNNs. The main difference between both representations is that words of CG representation are syntactically and semantically correct, this means that any generated word is valid and there are not repeated indexes, while words of CFG BNF are just syntactically correct or any generated word is just valid.
\n
The fitness function is usually defined by the problem; to solve this, three fitness functions based on SPIKE [39] (used in [23, 24, 26]) and Victor-Purpura distances [40] (used in [25]) to compare similarity between generated spike train and target spike train to guide the search process have been proposed. Basically, first and second distance-based fitness functions are for generating one SCPG per locomotion gait; the difference is that the second one looks for minimal presynaptic connectivity and the first one does not care about number of presynaptic connections. The third distance-based fitness function allows to generate a single SCPG, which can replicate different locomotion gaits.
\n
The search engine in GE is usually a metaheuristic algorithm, which tries to improve the quality of solutions. For reviewed works, three different algorithms have been used: Univariate Marginal Distribution Algorithm [40] (used in 23), (1 + 1)-Evolution Strategy [41] (used in [24]) and Differential Evolution [42] (used in [25, 26]).
\n
For implementation details, see [23, 24, 25]. Next, the features of this method are listed:
Strengths:
It can design SNNs which use either BMS spiking neuron model or LIF neuron model.
It can handle design criteria to design compact SNN topologies or SNN, which can replicate different neural dynamics or locomotion gaits.
Weaknesses:
The process must be executed several times to build a single SNN; due to that, it defines synaptic connection and weights one neuron at time.
It has not been tested on other design problems than design SCPGs.
\n
\n
\n
\n
5. Discussion and conclusion
\n
Nowadays, autonomous robot locomotion is still a valid problem that has been partially solved in robotics. Particularly, locomotion of nonwheeled robotic platforms is a problem highly susceptible for trying to be solved by means of bioinspired algorithms known as CPGs. However, sometimes working with CPGs may represent a problem itself since its design; this is due to the different choices that must be made before implement the CPG according to [7]. In this chapter, we have explored researches made on SCPG field, a particular type of CPGs, which have been barely explored to date. The SCPGs are built with spiking neurons, a plausible neuron model, which handle similar information as such observed in biological neural systems. We specifically focus on SCPG designed by approaches that allow to dispense with human experts for explicitly define each CPG design phase. These kinds of works use reverse engineering methods to solve de SCPG design problem as an optimization one. By means of these methods, there are generated weighted and directed graphs as SNNs, which endogenously generate rhythmic discrete signals to allow locomotion of legged robots.
\n
Biological CPGs do not work in isolation; they depend on the information interaction with other parts of the central nervous system [32]; even, external afferent inputs are used to shape their outputs [33]. Based on the aforementioned, the next step of SCPG-based locomotion systems could be their integration in navigation systems to endow them with sensors and can build more robust and plausible bioinspired algorithms.
\n
Finally, there are other reasons to keep studying and implementing SCPGs, which go far beyond the locomotion of nonwheeled robots, their possible application in other areas, like medicine in developing prosthetic robotic devices for patients with spinal damage or amputated limbs [20].
\n
\n
Acknowledgments
\n
The authors wish to thank the Consejo Nacional de Ciencia y Tecnología (CONACyT) for the support through the Computational Neuroscience: Theory of Neuromorphic Systems Development project, N. 1961, the University of Guanajuato and National Technology of Mexico. Horacio Rostro-Gonzalez wishes to thank the University of Guanajuato for the support provided through a sabbatical year.
\n
\n',keywords:"central pattern generators, spiking neural networks, reverse engineering, metaheuristic, locomotion patterns",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/58334.pdf",chapterXML:"https://mts.intechopen.com/source/xml/58334.xml",downloadPdfUrl:"/chapter/pdf-download/58334",previewPdfUrl:"/chapter/pdf-preview/58334",totalDownloads:1067,totalViews:190,totalCrossrefCites:1,totalDimensionsCites:1,totalAltmetricsMentions:0,impactScore:0,impactScorePercentile:8,impactScoreQuartile:1,hasAltmetrics:0,dateSubmitted:"September 9th 2017",dateReviewed:"November 9th 2017",datePrePublished:null,datePublished:"May 30th 2018",dateFinished:"December 21st 2017",readingETA:"0",abstract:"In robotics, there have been proposed methods for locomotion of nonwheeled robots based on artificial neural networks; those built with plausible neurons are called spiking central pattern generators (SCPGs). In this chapter, we present a generalization of reported deterministic and stochastic reverse engineering methods for automatically designing SCPG for legged robots locomotion systems; such methods create a spiking neural network capable of endogenously and periodically replicating one or several rhythmic signal sets, when a spiking neuron model and one or more locomotion gaits are given as inputs. Designed SCPGs have been implemented in different robotic controllers for a variety of robotic platforms. Finally, some aspects to improve and/or complement these SCPG-based locomotion systems are pointed out.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/58334",risUrl:"/chapter/ris/58334",book:{id:"6167",slug:"cognitive-and-computational-neuroscience-principles-algorithms-and-applications"},signatures:"Andrés Espinal, Marco Sotelo-Figueroa, Héctor J. Estrada-García,\nManuel Ornelas-Rodríguez and Horacio Rostro-Gonzalez",authors:[{id:"184956",title:"Dr.",name:"Horacio",middleName:null,surname:"Rostro-Gonzalez",fullName:"Horacio Rostro-Gonzalez",slug:"horacio-rostro-gonzalez",email:"hrostrog@ugto.mx",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null},{id:"221405",title:"Dr.",name:"Andrés",middleName:null,surname:"Espinal",fullName:"Andrés Espinal",slug:"andres-espinal",email:"aespinal@ugto.mx",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null},{id:"223976",title:"Dr.",name:"Marco",middleName:null,surname:"Sotelo-Figueroa",fullName:"Marco Sotelo-Figueroa",slug:"marco-sotelo-figueroa",email:"masotelo@ugto.mx",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null},{id:"230875",title:"Dr.",name:"Héctor Javier",middleName:null,surname:"Estrada-García",fullName:"Héctor Javier Estrada-García",slug:"hector-javier-estrada-garcia",email:"hestrada@ugto.mx",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null},{id:"230876",title:"Dr.",name:"Manuel",middleName:null,surname:"Ornelas-Rodríguez",fullName:"Manuel Ornelas-Rodríguez",slug:"manuel-ornelas-rodriguez",email:"manuel.ornelas@itleon.edu.mx",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:null}],sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. Robotic platforms and controllers",level:"1"},{id:"sec_3",title:"3. SCPG-based locomotion system",level:"1"},{id:"sec_3_2",title:"3.1. Locomotion patterns",level:"2"},{id:"sec_4_2",title:"3.2. Spiking neuron models",level:"2"},{id:"sec_4_3",title:"3.2.1. Beslon-Mazet-Soula neuron model",level:"3"},{id:"sec_5_3",title:"3.2.2. Integrate-and-fire neuron model",level:"3"},{id:"sec_8",title:"4. Reverse engineering methods for designing SCPGs",level:"1"},{id:"sec_8_2",title:"4.1. Deterministic method: Simplex method",level:"2"},{id:"sec_9_2",title:"4.2. Stochastic method: Grammar-based genetic programming",level:"2"},{id:"sec_11",title:"5. Discussion and conclusion",level:"1"},{id:"sec_12",title:"Acknowledgments",level:"1"}],chapterReferences:[{id:"B1",body:'Floreano D, Ijspeert AJ, Schaal S. Robotics and neuroscience. Current Biology. 2014;24(18):R910-R920. DOI: 10.1016/j.cub.2014.07.058\n'},{id:"B2",body:'Brown TG. 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New York: Springer; 2006. 195 p\n'}],footnotes:[],contributors:[{corresp:"yes",contributorFullName:"Andrés Espinal",address:"aespinal@ugto.mx",affiliation:'
Department of Organizational Studies, DCEA-University of Guanajuato, Mexico
Department of Electronic Engineering, DICIS-University of Guanajuato, Mexico
Neuroscientific System Theory, Department of Electrical and Computer Engineering, Technical University of Munich, Germany
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1. Introduction
Every country develops studies for their main fruit chains to determine main losses and provide solutions for reducing them. When fruit shelf life cannot be increased, processing will avoid fruit spoilage. Food losses and waste are estimated globally in 1.3 billion tons annually. Commercialization loss was estimated in 9.5 tons/week in Salvador, Brazil, in highly perishable fruits such as banana, papaya, and tomato [1]. The annual loss of fruits during postharvest operation represents in Sri Lanka about 210,000 metric tons of fruit, which corresponds to 30–40% of the harvest, representing a loss of US$90 million [2]. Mexico is the leading producer of prickly pear plants with 230,000 hectares, being 67,000 for fruit production [3]. Mexico is also the world leader in exporting fresh mangoes in 2019 [4]. Postharvest losses of fresh mango fruits in Pakistan were reported to average 69% [5] but sometimes reach 100% under disease-favorable environments. In the 2014 season, an increase in mango stem end rot (SER) at Israel caused a 30–40% loss of the harvested fruit [6]. This disease occurs in mango, avocado, and citrus fruit [7].
The rind or exocarp includes the hard cases of nuts or the shell of watermelon. The peel forms the pericarp, meanwhile the pulp or edible portion of the fruit is the endocarp [8]. Fruit or vegetable peel or rind appears as its outer protective layer. Watermelon, a round fruit, has a firm outer rind that surrounds a white inner rind layer. The interior edible pulp of red or yellow color is the endocarp. The outer walls of the epidermal cells of all plant organs are coated with a cuticular membrane [9]. Physical properties and chemical composition of the fruit cuticle change markedly during its development [10]. During early fruit development, maximum cuticle deposition rates per unit area appear increasing cuticle thickness. Cuticle composition changes after depositions of wax, phenolic compounds, and polysaccharides [11].
Fleshy fruit cuticles and vegetative organs have similar compounds, but fruit cuticles are thicker [12, 13]. The hydrophobic nature of fruit cuticle makes it an effective barrier to reduce water loss. Cuticle permeance differs between mango fruits receiving sunshine and those growing under the canopy shade [14]. In addition, intracuticular waxes limit movement of surface water into the fruit and reduce transpiration. Cuticular wax load increases during fruit development leading to a thicker mango cuticle at maturity [15].
The fruit cuticle provides an important physical barrier against pathogens [16] avoiding fungal colonization on sweet oranges [17]. Industrial food wastes such as peels from juice production provide raw material for obtaining wax compounds [18]. The cuticle also provides protection against environmental conditions, where excessive solar radiation produces physiological disorders such as sunscald [19]. Cuticle strength and rigidity decrease as it becomes warmer [20]. The cuticle inner surface is fully hydrated, meanwhile the cuticle outer surface in contact with the atmosphere is less hydrated. Although waxes are present in both sides of the cuticle, water absorption takes place [10]. Cuticle swelling and softening alter its mechanical properties. Fruit cracking is triggered by cuticle breaking, linked to rainwater and high humidity [21, 22].
Handling fruits up to 15 days after harvest has a profound effect on its final quality because fruits are still alive and vulnerable to adverse conditions [23]. Throughout fruit ripening, softening results from the modification of polymers within the primary cell wall [24]. Cuticle and wax deposition increased during the first 15 days of postharvest shelf life in mango fruits of cultivars “Kent,” “Tommy Atkins,” and “Ataúlfo” [25]. Mango fruits with higher wax deposition in their cuticle were more resistant to fruit fly attack [26]; also fruits presented lower transpiration and deterioration. Pectin solubilization during fruit ripening is directly related with the ripe fruit texture [27]. Fruits showing a melting texture, such as avocado, kiwifruit, tomato, and peach, soften in a short time [28]. Fruits having a crispy texture during maturation, such as apple or watermelon, present low pectin solubilization [29]. The simplest postharvest procedure to increase fruits shelf life consists of storing them under controlled temperature and humidity conditions. However, rheological and mechanical properties of fruit cuticles are affected [20]. Peach firmness dropped after being stored at low temperatures. It was associated to a reduction of covalently bound pectins [30]. Apricot controlled-atmosphere treatments showed also pectin degradation [31].
Mango fruit pedicel (Figure 1a) presents an internal network of resin ducts, and the latex is kept under plant turgor pressure [32]. When the pedicel is broken or cut, a secretion of milky-viscous sap leaves the fruit [33]. This latex contains oily antifungal resorcinol [34]. The contact of the fruit surface with the sap exudate (Figure 1c) can lead to skin injury (sap burn) and develop under-skin browning [32]. This injury decreases mango quality after damaging seriously its skin, and if the fruit contacts the soil, it can be easily infected. These fruits are rejected at the entrance of fresh fruit packinghouses [35]. Lenticels also appear after sap exudation showing symptoms of early sap burn injury [36]. A delay in the appearance of stem end rot was noted by keeping a short pedicel at harvest [6, 34]. Mango fruits harvested with stems have more sap and less incidence of anthracnose [37].
Figure 1.
Mango fruit (a) pedicel, (b) washing, and (c) showing latex in the peel.
Opuntia species present fleshy edible fruits (tunas) with thick rinds and relatively large round seeds. Prickly pear fruits are consumed in the local Mexican market and exported to the United States, Canada, Japan, and Europe [38, 39]. Edible prickly pear fruits and cladodes are used as food for livestock [40]. Fruit pulp and peel present a high quantity of carotenoids, betalain content, polyphenolic content, and ascorbic acid [41, 42]. Those pigments have revalorized prickly pear production for agro industries and pharmaceutical use [3, 43]. The fruit is perishable, and after being stored for nine days at room temperature, it starts rotting [44]. Ready-to-eat (RTE) fruit storage includes controlled atmosphere storage of minimally processed cactus pear fruits at 2°C reducing browning content [45]. Cactus pear peeled and stored within passive-modified atmosphere at low temperature limited fruit decay [46].
Heat transfer within fruits stored at a cold storage warehouse after harvesting has been studied before long-term shipping [47, 48, 49]. Harvested fruits are treated with different technologies to delay ripening, preventing physiological and pathological disorders [49]. Producers sometimes target distant markets, so they must harvest their tomatoes in a mature green state to allow longer ripening and senescence periods [50]. Excessive field heat increases fruit metabolic activity, so immediate cooling after harvest is recommended [51]. Low and high temperatures lead to the denaturation of enzymes, modifying fruit’s respiration rate [52]. Stone fruits such as plums and mangoes have a seed inside and present different thermophysical parameters within the pulp [53, 54]. The contact surface between the seed and the pulp is the deepest point that can be reached in the fruit and becomes a thermal center. The finite element method can simulate heat transfer within food products that present irregular geometries [55].
Hot water immersion and hot air treatments at temperatures between 40 and 60°C from seconds to several hours control pathogens in apples, pears, citrus, and melons [56]. Postharvest quality of apples improved after being heated with air during one day at 40°C [57]. Heat treatment caused important changes in epicuticular wax altering microcrack structure. Mandarins were immersed in hydrothermal treatments, maintaining the fruit surface temperature at 50°C for 2.5 min [58]. Once the mandarin peel heats up, thermal energy transfers by conduction to subsequent layers toward the center. Heat transfer stops after reaching an equilibrium condition [59]. Thermally treated mandarins present higher TSS (total soluble solids), lower maturity index, and similar citric acid content.
Mango fruit must be treated to ensure that it is free of fruit flies, so that importing markets allow their acceptance [60]. Small mango fruits weighing less than 375 g require 65 min of immersion in hot water at 46.1°C [61]. A thermocouple was inserted at the surface of the endocarp and another in the center of the mango fruit to record temperature changes during hot water immersion. The temperature at the center of the fruit continued increasing for 10 min after removing the fruit from the hot water bath [61]. Although the hot water treatment reduces fruit firmness, it influences positively in oxidative processes, cell wall changes, and steady-state levels of protein [62].
2. Mango treatment
Thermal treatment application maintains mango fruit quality and produces higher economic returns. Cauterization is a very useful technique that can close any tissue after applying heat. After harvesting, all the wounds of the fruit that were cauterized and sealed hermetically avoiding transpiration and increasing shelf life.
2.1 Mango after farm harvest
Postharvest mango quality depends on proper harvesting and even better production practices. Mangoes are generally handpicked or retrieved with poles adapted with a cutting blade and a bag [63]. The blade end breaks the pedicel and latex covers the fruit peel (Figure 1c). Although de-sapping after harvest avoids peel sap burn, it reduces fruit protection against anthracnose and stem end rot. The main cause of mango sap burn is attributed to a deposit of volatile compounds such as terpinolene and car-3-ene through the lenticels [64]. Stem trim cutting results in latex stains deposited on the fruit surface. The sap stored in the fruit ducts under high pressure falls on the peel of mango fruit [65]. Delatexing can be done by inverting freshly de-stemmed fruits on plastic or steel mesh racks for 30 min. Another technique is to dip freshly de-stemmed fruits in 1% alum solution (one-half kg powdered alum per 50 L of water) for 1 min; fruits should dry before packing [65]. The contact of latex with mango skin induces lenticel discoloration, resulting in red spots caused by the synthesis of anthocyanins [66]; these spots can also be induced by chilling injury [64]. Resorcinols and gallotannins are inhibitory to major postharvest pathogens including anthracnose [67].
If a 1 cm long pedicel remains attached to the fruit after harvest, latex will not leave the fruit avoiding sap burn. More than 80% of sap flow was observed within the first minute of stalk removal [37]. Sap pH varies between 4.43 and 4.6, and the ratio of nonaqueous fluid (oil) to aqueous fluid is of 1:6.5 [37]. The best hour for harvesting mango fruits was just after midday [68]. Early morning harvesting causes a rapid flow of sap from the pedicel end. High solar radiation and vapor pressure deficit increased stem water flow within mature fruit during the morning and decreased after midday [69]. Pedicel cutting place does not affect sap output flow. If stem is cut at the abscission zone, delayed ripening of mango fruit results [68].
2.2 Mango diseases
Two of the main diseases of mango fruits are anthracnose and stem end rot. Anthracnose caused by the Colletotrichum gloeosporioides at the green stage cannot be perceived, and the infection is noted when the mango ripens. Anthracnose produces the enzymes polygalacturonase and pectolyase, which degrade the cell wall [70]. If mango fruit is healthy, the polyphenol oxidase (PPO) enzyme is found within chloroplasts and the phenolic compounds in vacuoles, both being separated, avoiding any reaction.
Stem end rot (SER) is a disease caused by Lasiodiplodia theobromae. At the beginning, it appears as a small dark-brown area in the peel around the base of the fruit stem end, progressing into soft decay at the stem end [6]. Ethylene, a phytohormone, controls most of the ripening events linked with climacteric fruits. Small amounts of ethylene maintain fruit resistance to pathogens [71].
2.3 Mango pedicel treatment
If latex is retained within the fruit at harvest, it reduces anthracnose and stem end rot (SER) development during ripening. Fruit ripening parameters are not affected by pedicel length, and substantially less number of diseases appear compared with fruits harvested without stems. Anthracnose lesions decrease when mango fruit is harvested with a long stem [33]. SER onset in fruits with short pedicel was later than in fruit without stems [6]. Latex aqueous phase having chitinase contributes to fruit resistance against SER [67]. Two systems were developed to minimize latex de-sapping:
Cut stems 0.5 cm long and cauterize them with a hot knife implement.
If harvest brings fruits without stems, fruits are washed, dried and a wax is applied at the stem end.
Automatic fruit harvesting follows different picking patterns including bending, lifting, twisting, and pulling [72]. Modern soft grippers employ soft and flexible materials for holding the fruits [73]. Mechanical cutting devices for fruits consist of knifes [74, 75], scissors [76], and hot wires [77]. Knives used to cut stems have to be continuously immersed in skimmed milk. This action avoids virus invasion and should take place before contacting each plant. Therefore, it is not practical for automated processes [74]. A scissor employed to cut tomato stalks was articulated by a finger phalanx, but could also be fixed to the gripper palm [76].
Nichrome wire electrodes were mounted at a thermal cutting end effector. A high voltage of 300 V cuts 1 mm sweet pepper stems in 2 s [77]. As the diameter doubled, the cutting period increased to 5 s after applying the same voltage between electrodes [77]. Thermal stem cut ceased fungal or bacterial infestation, increasing pepper shelf life over 15 days. Peppers harvested by normal scissors showed physical changes after the fifth day and perished after nine days. Mechanical cutting is suitable for cucumbers where peduncle direction is uniform [74]. Laser cutting of variable-diameter tomato peduncles (1.5–5 mm) was studied [78]. It became impossible to cut off a peduncle directly by focusing a laser beam on it, as the focusing spot is smaller than the peduncle size. After tomato peduncle drilling, laser cut a 5 mm diameter stem in 15.2 s [78].
A harvesting robot requires a transmission system to drive the end effector [79]. A robot gripper with four pneumatic fingers has been used with mango fruits. The gripper can handle various shapes and sizes and has been used to determine fruit firmness [79]. A gripper was also developed to handle mango fruits and estimate their ripeness. This robot integrated accelerometers and optical sensors and worked without contacting the fruit [80]. Two robots were used for tomato grafting, cutting 240 plants per hour. The graft is accomplished when both plants are placed in intimate contact between them, and a clip is pressed against them [81].
Mango fruits collected at the Mexican Pacific coast were green, firm, and starting to ripe. The developed gripper to hold the fruit presented integrated soft cushions (Figure 3(a and b)) to protect the fruit and move it for cutting the stem. Two linear knifes were used by the trimmer equipment. One knife was fixed, meanwhile the other was ejected by a 24 VDC (direct current voltage) linear actuator. Preliminary tests show successful results in stem cutting with only one movement. The mango enters the transporting system, but not all the fruits have attached pedicels. Those having the pedicel were cut by a warm knife having a temperature of 35°C. An image of the mango peduncle or abscission zone was obtained with a X800 digital microscope. The effect of anthracnose infestation was analyzed after fruit matured.
Wax was applied to mango fruits without the stem end. Paraffin was warmed up in the interior of a conventional gun (Figure 3a) and applied to the mango abscission orifice to avoid fungal or bacteria infestation. The manual gun uses paraffin sticks that melt after being heated by an electric resistance. When the trigger is squeezed, liquid wax leaves the gun through an output nozzle. Better results are obtained after applying pressure with a conical stamp over the liquid wax placed at the fruit peduncle orifice (Figures 1a and 2b). An industrial wax application gun pressurizes the hot fluid with a pneumatic system (Figure 3b). A camera at the top provides information of whether the fruit has a 1 cm long stem and would only apply wax when there is no pedicel.
Figure 2.
Robotic gripper (a) with mango pedicel, (b) without mango pedicel and having wounds, (c) cauterizer knife machine.
Figure 3.
Robotic arms handling a mango fruit for (a) manual, and (b) industrial wax application.
2.4 Mango pedicel and abscission microscope images
Large latex channel openings were seen at and below the abscission zone close to the fruit. High volume of latex spurts out through these channels after detaching the pedicel from the fruit [82]. Latex canals are seen as large perforations in the fruit peel reaching the outer pulp [34, 82]. After cutting the Keitt mango pedicel 2 cm away from the abscission zone, it was cauterized at 35°C, showing latex channels (Figure 4a). Cauterization at 35°C does not heat mango peel tissue (Figure 4b). If the stalk was cauterized at 45°C, the cells surrounding the channels were burnt and reduced in size (Figure 4c). Latex channels are clearly observed within red circles in the green tissue just after removing the pedicel (Figure 5a). If the stem gets cauterized, latex channels are still present after cutting the pedicel with a razor blade, 0.5 cm toward the fruit abscission end (Figure 5b). If honey covers the green tissue, it will enclose the latex channels (Figure 5c).
Figure 4.
Transverse section of Keitt mango fruit stem, showing the latex canals after cauterization at (a) 35°C on the abscission zone, (b) 35°C on the pedicel, and (c) 45°C on the pedicel.
Figure 5.
Transverse section of Keitt mango showing the latex canals after (a) removing the pedicel, (b) cauterizing, and (c) removing the stem and adding honey.
3. Prickly pear treatments and measurements
Cactus pear (Opuntia ficus-indica L.) is an important fruit, but its consumption is limited by the presence of spines and glochids on its surface. Fresh-cut, ready-to-eat (RTE) cactus pears have higher preference than the whole fruits [83]. Actually, cactus pear at the green-yellow ripening stage is processed as a ready-to-eat fruit and stored for nine days in modified atmosphere packaging at 4°C [84]. Green yellow fruits present intermediate peel thickness and pulp softness, which is suited for peeling and for RTE fruits [85].
Cauterization prototypes were developed to increase prickly pear shelf life and decrease fruit diseases. A review on cauterization techniques including high-temperature contact and cryo-cauterization was presented [38]; both of these systems are patented [86, 87]. A cauterizer for harvested fruits applied 100 kPa of pressure at 200°C during 30 s [88]. Cactus pears subjected to a cauterization treatment were cut at the top-peduncle section, leaving a sealing area of 13 cm2. The system is efficient in controlling postharvest diseases, but its excessive heat application results in expensive energy consumption [88]. Pulp temperature increased to 86°C after heating the fruit at 200°C for 45 s [88].
Prickly pear and their cladodes have natural polymers, and several eco-friendly materials are under development [89]. Cactus mucilage can be used as gelling, stabilizing, or encapsulating agent. The use of this bio-polymer material opens new opportunities in the food packaging. It is also used as a flocculating agent for heavy metals in water [90]. All these properties open new economic opportunities for cactus produce.
3.1 Prickly pear automatic cold cauterization
Several mechanisms have been developed for detaching the fruit from the cladode [91] and for fruit cold cauterization [92]. A harvesting arm with four degrees of freedom is used as hydraulic piston to collect prickly pears [91]. Cryo-cauterization results from pressing the fruit sliced area against a dry ice wall. The thermal shock maintained cactus pear over 120 days without further cooling [44]. Energy consumption of cryo-cauterization was minimum as no resistance was used; meanwhile the cauterizer working at 200°C employed 13 W per fruit [88]. The first automatic fruit cauterizer uses sensors and mechanisms to detect when the prickly pear is present within the metal container, rotate it 90° counterclockwise, displace it against the dry ice wall and deposit it again into the original band. The processing of 1000 fruits took a little more than 500 min [92]. Further development to simplify the system used a two-finger gripper that picks the fruit (Figure 6a). The most significant features to select a gripper include its opening range, its maximum applied force, its type of movement (angular, parallel or self-centered), and the grasp strategy (external or internal grasp). The robotic end effector uses two fingers to press the thick fruit peel without damaging it. The mechanism rotates the fruit by180° until it touches the ice pad (Figure 6b). However, dry ice melts in 5 h and has to be replaced in both systems. The last prototype has a gripper that grasps the fruit more efficiently with six fingers (Figure 6c). The gripper moves horizontally toward the dry ice chamber by sliding on pneumatic actuators. In the slider actuators, the gripper is mounted to the carriage. Precise slicing of the top-peduncle section is done by means of a circular blade. Once the fruit is sliced, it moves further to the left until it presses the dry ice chamber. With additional volume of dry ice within the chamber, it can last more than one day.
Figure 6.
Rotating gripper (a) picking the fruit, (b) contacting the heating surface, and (c) over a linear mechanism sliding toward the dry ice chamber.
3.2 Prickly pear temperature measurements
Thermocouple sensors are being used for monitoring temperature within the fruit. Sensors were added below mesocarp and in the center of the fruit to study fruit changes during hot water treatments [58]. Three thermocouples of type J were inserted in the flat prickly pear surface to study variations during cauterization. As well after keeping the fruits for nine and 15 days at ambient storage, 10 prickly pears were cut nearby the sealed surface and in the middle of the fruit to measure TSS changes. Fruits stored for nine and 15 days at ambient storage were cut nearby the sealed surface and in the middle of the fruit to measure TSS and acidity changes.
4. Mango physicochemical analyses
Mango cuticle is thin and does not resist the high thermal gradient required by cauterization operations. Therefore, thermal treatments have to be applied carefully, mainly in the mango fruit abscission-pedicel interface.
Average biochemical maturity properties of fruits at early harvest for Haden, Kent, and Keitt were analyzed. These properties include pH, total soluble solids (TSS, °Brix), ascorbic acid (mg.100 g−1), moisture content (%), and dry matter content DM (%). Kent and Keitt late varieties were harvested 137 and 148 days after fruit set, respectively. These results are similar with those obtained at Ghana plantations [93]. Mango trees with higher fertilization delayed fruit firmness decay. At the moment of harvest, fruits were green and firm for all varieties and fertilization regimes. After nine days of storage at 25°C, firmness decreased to 16.93 N for Kent fruits and remained firmer for Keitt mangoes. Chemical composition changes result from physiological and biochemical events controlled during fruit ripening [94]. Pectins are responsible for fruit texture and rise in the fifth week of mango fruit setting until the stone is formed. Pectins are responsible for fruit texture and rise five weeks after mango fruit setting until the stone is formed. Afterward, pectin content decreases, and fruit starts softening due to enzymatic degradation [64].
Fruits were harvested at a very green stage showing low TSS, acidity, and pH values (Table 1). As fruits mature nine days after, firmness decreased to 25.73, 16.93, and 32.91 N for Haden, Kent, and Keitt fruit, respectively (Table 2). After mango harvest, quality losses occur, affecting the content of nutritional components at different points during the handling chain [65].
Variety
Pulp pH
TSS (°Brix)
TA (% citric acid)
DM (%)
Firmness N
Haden
3.81
9.72
2.11
16.27
113.27
Kent
3.98
6.42
1.45
17.84
122.42
Keitt
3.66
7.63
2.43
17.85
121.05
Table 1.
Physicochemical analyses of different mango varieties considering pulp pH, TSS (total soluble solids), TA (Titratable acidity), DM (dry matter), and firmness of just harvested fruit.
Physicochemical analyses of different mango varieties considering pulp pH, TSS (total soluble solids), TA (Titratable acidity), DM (dry matter), and firmness in the market place.
Measurements of fruits without latex removal.
Kent mangoes show a rapid decrease in firmness during ripening [95]. Kent mango trees with normal fertilization level produce fruits with high respiratory activity, lower ascorbic acid concentration, and fruit firmness drop [95]. Lower content of potassium within tissues is related to higher acidity, while lower pulp pH responds to the fertilization regime [96]. Keitt mangoes showed the lower quantity of total soluble solids (15.72°Brix) and a low acidity of 0.18 (Table 2). On the other hand, Ca applications increased citric acid content in “Haden” mango fruits [97]; meanwhile pulp pH jumped to 5.12. Keitt mango showed higher vitamin C content than Kent and Haden fruits in their ripe phases, because of the inhibition of polyphenol oxidase (PPO). This mango variety provides better color and flavor retention during processing [98]. Mango refrigerated at 4°C tends to maintain the same TSS and TA during nine days of storage (Figure 7a and b). If the pedicel gets cauterized, mango TSS drops. Titratable acidity (Figure 7b) was significantly affected by fruit respiration, consuming organic acid.
Figure 7.
Keitt mango (a) total soluble solid (TSS) concentration, and (b) Titratable acidity (TA) during the nine days of storage at 4 and 20°C with and without pedicel cauterization.
4.1 Mango latex and diseases
Fruit fly control and removal of surface fungal diseases can be carried out by hot water immersion [99] and by hot air application. Hot water immersion is relatively easy to use, economic, and can provide accurate monitoring of fruit and water temperature. Mango fruits immersed in hot water at 52°C for 5 min eliminated anthracnose fungal infection [60]. Anthracnose infestation was not present after storing the fruit for 15 days at ambient temperature [100]. The effect of hot water treatment on pulp TSS was insignificant and mango visual quality remained outstanding. If green mature fruits are dipped for 20 min in water heated to 53°C, it will control both anthracnose and SER. If water is heated below 52°C, it is not effective to control anthracnose, and at 5 degrees warmer, it will scald the peel [101]. Hot water immersion without waxing affects the natural wax layer of the fruit surface, enhancing its senescence. Fruits coated with wax delay the ripening and extend their shelf life [102]. Keitt and Tommy Atkins mango fruits develop yellow pigments in the skin after hot water immersion [60]. TSS content of fruits immersed in hot water increased to 20°Brix, meanwhile untreated fruits remained at 17° Brix. In mangoes infected with SER, immersed in hot water and stored for 13 days, TSS content reached 19°Brix; fruits remained in 14°Brix if they were untreated [103].
At immature stage, anthracnose is not perceived, and the infection appears when mango ripens. Mango latex contains antifungal resorcinols and chitinase, so its retention during harvest will protect fruits against anthracnose and stem end rot [67]. Stem trimming deposits latex stains on the fruit surface, as pressurized sap stored in mango ducts falls on the fruit peel [65, 104]. Keitt mango fruit that preserved latex at harvest developed slightly smaller anthracnose lesions than fruits in which latex was drained (Figure 8). Keitt mango lesion area increases to 200 mm2 after 10 days when fruits do not have latex (Figure 8a). Mango lesion corresponds to the black spot area growing on the fruit peel. When latex is present, the lesion only increases to 50 mm2. The size of the remaining stem is correlated to the lesion area (Figure 8a). As it is longer and cauterized, less sap leaves the fruit, and it is more protected against pathogen infections. Higher anthracnose infection was noted in Keitt trees when more nitrogen was applied during fruit development [105]. This result was also found after analyzing “Willard” mango fruits [34].
Figure 8.
Keitt mango anthracnose lesion area after several days of harvest (a) with and without latex, and (b) after petiole trimming.
When Keitt mango fruit stems were cauterized or their peduncle orifice covered with wax just after harvest, latex fluid remained within the fruit. Average anthracnose lesion was 38 and 54% smaller for wax and cauterization treatments, respectively, with respect to the control treatment after 11 days (Figure 9); no stem, wax, and latex were present on control fruits.
Figure 9.
Anthracnose lesion area several days of harvest for fruits cauterized and for mangoes after wax application.
5. Prickly pear grippers and deformation experiments
Gripper suction cups grasp products by means of pressure difference [106, 107]. These grippers can be joined with other mechanisms easily, but are impractical for high-temperature grasping [108]. Modern granular-material grippers align themselves in malleable shapes to grasp the end product [108, 109, 110]. The prickly pear gripper used a grasping force of 40 N with a holding time of 30 s. The cauterizer robot (Figure 6a) presents a gripper moved by a mechanism containing two DC motors. One of the gripper fingers´ remains static during grasping, meanwhile the opposite finger presses the fruit; this finger moves using a DC motor. The second prototype used a pneumatic actuator. The slide actuator (Figure 6b) transports the six-finger gripper until a sensor detects its contact against the dry ice wall. A timer ensures that the fruit surface contacts the dry ice block during the right period. The pneumatic slider returns the fruit back to the pick and place area; this process takes 25 s. The end effector damaged the prickly pear during grasping and cauterization, when the fingers did not allow fruit movement. Fruit compression plotted in the vertical axis of Figure 10 corresponds to the prickly pear deflection caused by finger pressing.
Figure 10.
Fruit firmness vs. compression for prickly pears having different slice diameter.
Prickly pears were sliced and cauterized by the robotic systems. Large prickly pears present an average diameter of 15 mm at the sliced section; smaller pears present a larger slice diameter ranging between 30 and 35 mm. Two clusters appear after plotting fruit firmness against pear compression (Figure 10). The black marks within the red circle show big fruits having firmness within 13 and 16 Ncm−2. Fruit damage during processing decreased for pears compressed less than 3 mm. Orange markers show fruits with higher firmness (17.5–21.5 Ncm−2), where the slicing area rises.
Prickly pear is a desert fruit with a thick peel. Pear firmness decreases once it is sliced (Table 3), and the fruit is destroyed when compression overpasses 5.2 mm. Red data in Table 3 shows prickly pear values suffering some kind of damage. As the cauterizing diameter (ϱ) increases, fruit firmness drops and a lower pressure should be applied to avoid its destruction. Yellow fruits are softer and their tissue compresses easily. Therefore, yellow fruits are unable to withstand the cauterizing force (Table 3). As the prickly pear sliced area receives an orthogonal force, the airspaces within the pulp fill up. Pulp deformation takes place, growing sideways until the peel cannot withstand the pressure and explodes.
Diameter (mm)
Color
Firmness (Ncm−2)
Compression (mm)
Damage (%)
Min
Max
Min
Max
<15
green
16.12
16.82
2.5
3.2
0
15 < ϱ < 25
green
15.28
15.94
2.8
4.1
0
25 < ϱ < 35
green
14.47
15.35
4.2
5.5
50
<15
yellow
14.21
14.72
4.9
5.5
100
15 < ϱ < 25
yellow
13.73
14.15
5.1
5.5
100
25 < ϱ < 35
yellow
13.04
13.57
5.3
5.5
100
Table 3.
Green and yellow prickly pear firmness and compression having different slice diameters.
5.1 Prickly pear physicochemical analyses and measurements
Temperature measurements 2 mm within the pulp sliced area and at the middle of the prickly pear differ (Figure 11). The thermocouple placed 2 mm away from the sliced area reached only −4°C after 50 s, being hotter than the temperature of the dry ice block (−78°C). For the rotating robot (Figure 6a), fruit temperature decays after 50 s once the gripper contacts the dry ice surface, reaching its minimum temperature 10 s later. The green area in Figure 11 shows negative pear temperature values in the sliced area during fruit cauterization contact. The complete temperature signal within the prickly pear during the cauterization cycle is shown in Figure 11. Fruit cauterization ended 125 s later, arriving to 17.4°C 145 s after; At this moment the slide system returned the pear back. Pulp temperature measurements acquired 15 mm below the sliced area were almost constant during the 6 min (Figure 11, dot line). Tissue temperature returns quicker to its natural thermal state (17.4°C) with the sliding system as shown by the red line, Figure 11. Cell walls have a more rigid contact when touching the dry ice chamber surface. Similar results were achieved by prickly pears that contacted the dry ice for 25 s.
Figure 11.
Prickly pear pulp temperature monitored 2 mm and 15 mm away from the sliced surface during cauterization.
TTS and total acidity (TA) were measured every 15 days after cutting three fruits at the center. TSS and TA monitoring was repeated in fruits stored for three months. Total soluble solids (TSS) concentration estimates the sugar content in the fruit and determines its degree of sweetness [111]. TSS concentration of prickly pears of cultivar “Blanca Cristalina” just after cryo-cauterization remained in 13.5°Brix. Measurements taken one, two, and three months later showed values of 13.4, 13.3, and 13.2°Brix, respectively. TSS minimum variations show that cryo-cauterization preserves fruit quality. Blanca Cristalina and Esmeralda fruits present 13.6 and 14°Brix at harvest, respectively [112]. Twenty-eight days later, TSS concentration was of 11.4 and 12° Brix for Blanca Cristalina and Esmeralda pears [112]. Cactus pears from the “Orito” cultivar presented 14.9°Brix after harvest and 14°Brix after 28 days later [111]. Blanca Cristalina TA values remained constant at 0.25% during the three months, so fruits remain acid and fruit acceptance high [111]. Blanca Cristalina and Esmeralda presented 0.27 and 0.29% of citric acid at harvest, respectively. After four weeks, it decreased to 0.18% in Blanca Cristalina [112]. For all the varieties, pulp citric acid decreased during ripening [113]. Although in these experiments cuticle thickness was not measured after heat treatments. Cuticle thickness reduction on some varieties was due to the effect of heat treatments [114]. The resistance provided by the cuticle against mechanical damage depends on the cuticle structure [115].
6. Conclusions
An increase in the quality and shelf life of mango fruit and prickly pear will increase their marketing worldwide. The first step to increase mango quality is to reduce fungal diseases such as anthracnose and stem end rot that appear due to environmental changes. Thermal treatments on mango fruits preserve their quality and reduce postharvest fruit disease infestation. Mango fruits must be harvested with care as mechanical damage of the stem end can start rotting in the fruit. Latex de-sapping after field harvest will reduce fruit sap burn.
Mango latex that contains antifungal resorcinols and chitinase should remain within the fruit to decrease anthracnose and stem end rot infestation. Stem channel thickness where latex flows can decrease after cauterization or by applying liquid paraffin. Two systems were developed to maintain latex after harvesting.
In the first system, a gripper grabbed the mango fruit and proceeded to cut the stem by means of two hot knifes maintained at 45°C. The cauterized pedicel presented burnt cells at the surface and reduced in size toward the stem end. This technique decreased anthracnose infestation by 50% after 11 days of storage when compared with de-sapped mango fruits. TSS concentration drops after pedicel cauterization. In the second equipment, warm paraffin wax was applied by a conventional gun to mango fruits without the stem end. Average anthracnose lesion was 38% smaller for paraffin application after 11 storage days than in untreated infested mangoes.
Prickly pears are native fruits from Mexico that grow in arid zones and have very important nutritional properties. Cauterization increased prickly pear fruits’ shelf life over two months. Hot and cold cauterizer equipment extended shelf life without pathogen damage as the treatment seals the fruit and avoids dehydration. Two grippers were developed to cryo-cauterize prickly pears as this system is more energy-efficient than hot cauterization. The first gripper uses two fingers to press the thick fruit peel without damaging it. In this robotic system, the biggest disadvantage is the reduced dry ice pad duration. Warm air moves around the dry ice pad and melts in 5 h, so it has to be replaced. The second robotic system was more efficient as the dry ice block was within a chamber isolated from the air. Dry ice lasted for more than one day. This system used a six-finger gripper that moved over a pneumatic actuator, cryo-cauterizing a pear every 25 s. When the gripper contacted the dry ice wall, the temperature inside the fruit 2 mm away from the fruit sliced area was of −4°C. The temperature was measured with a thermocouple inserted in the fruit. Another temperature measurement was taken inside the pear 15 mm away from the sliced zone and the colder temperature was of 16°C. Gripper grasping damaged yellow fruits and its compression should be limited to 3 mm in green fruits. TSS and TA remained constant in cryo-cauterized fruit during the three months of fruit storage.
Acknowledgments
This work was supported by mango and prickly pear producers in Mexico by providing fruits for analysis. Also I would like to thank the DGIP, who funded the cauterizer project 21013-DTT. I appreciate the assistance of MI Angel Hernandez Facundo in the preparation of the drawings and the Language Department of the Universidad Autonoma Chapingo for reviewing this manuscript. As well I acknowledge the help from Biol and Ruth Perez in the analysis of data.
Conflict of interest
The authors declare no conflict of interest.
\n',keywords:"mango fruits, anthracnose, grippers, prickly pear, paraffin wax, cryo-cauterization, total soluble solid concentration, stem end rot",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/79678.pdf",chapterXML:"https://mts.intechopen.com/source/xml/79678.xml",downloadPdfUrl:"/chapter/pdf-download/79678",previewPdfUrl:"/chapter/pdf-preview/79678",totalDownloads:133,totalViews:0,totalCrossrefCites:0,dateSubmitted:"October 22nd 2021",dateReviewed:"November 9th 2021",datePrePublished:"December 21st 2021",datePublished:"April 28th 2022",dateFinished:"December 16th 2021",readingETA:"0",abstract:"Mexico is the main exporter of mango fruits and prickly pears, so new postharvest techniques to increase shelf life are studied. Thermal treatments on both fruits can affect their cuticle so it was reviewed. When mango latex remains within the fruits, it avoids sap burn and decreases anthracnose and stem end rot infestation, so two systems were developed to minimize latex de-sapping. A gripper cuts stems 0.5 cm long and cauterizes them with a hot knife implement. A heating gun applied paraffin wax to mangoes without the stem end and protected them better against anthracnose lesions. Physicochemical analysis of several mango varieties was carried out after harvesting, at market place and after pedicel cutting and cauterizing. Keitt mangoes showed the lower quantity of total soluble solids (TSSs) and total acidity (TA). When the pedicel was cauterized, TSS dropped. Two grippers were developed to cryo-cauterize prickly pears as this system is more energy-efficient than hot cauterization. A six-finger gripper moved over a pneumatic actuator toward a dry ice chamber to optimize pear cryo-cauterization. Gripper’s strong grasping damaged the fruits due to excessive compression. TSS and TA of cryo-cauterized fruit remained constant during the three months of fruit storage.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/79678",risUrl:"/chapter/ris/79678",signatures:"Federico Félix Hahn Schlam",book:{id:"10899",type:"book",title:"Postharvest Technology",subtitle:"Recent Advances, New Perspectives and Applications",fullTitle:"Postharvest Technology - Recent Advances, New Perspectives and Applications",slug:"postharvest-technology-recent-advances-new-perspectives-and-applications",publishedDate:"April 28th 2022",bookSignature:"Md Ahiduzzaman",coverURL:"https://cdn.intechopen.com/books/images_new/10899.jpg",licenceType:"CC BY 3.0",editedByType:"Edited by",isbn:"978-1-83969-924-5",printIsbn:"978-1-83969-923-8",pdfIsbn:"978-1-83969-925-2",isAvailableForWebshopOrdering:!0,editors:[{id:"321606",title:"Dr.",name:"Md",middleName:null,surname:"Ahiduzzaman",slug:"md-ahiduzzaman",fullName:"Md Ahiduzzaman"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:[{id:"203571",title:"Dr.",name:"Federico",middleName:null,surname:"Félix Hahn Schlam",fullName:"Federico Félix Hahn Schlam",slug:"federico-felix-hahn-schlam",email:"fhahn@correo.chapingo.mx",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:{name:"Chapingo Autonomous University",institutionURL:null,country:{name:"Mexico"}}}],sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. Mango treatment",level:"1"},{id:"sec_2_2",title:"2.1 Mango after farm harvest",level:"2"},{id:"sec_3_2",title:"2.2 Mango diseases",level:"2"},{id:"sec_4_2",title:"2.3 Mango pedicel treatment",level:"2"},{id:"sec_5_2",title:"2.4 Mango pedicel and abscission microscope images",level:"2"},{id:"sec_7",title:"3. Prickly pear treatments and measurements",level:"1"},{id:"sec_7_2",title:"3.1 Prickly pear automatic cold cauterization",level:"2"},{id:"sec_8_2",title:"3.2 Prickly pear temperature measurements",level:"2"},{id:"sec_10",title:"4. Mango physicochemical analyses",level:"1"},{id:"sec_10_2",title:"4.1 Mango latex and diseases",level:"2"},{id:"sec_12",title:"5. Prickly pear grippers and deformation experiments",level:"1"},{id:"sec_12_2",title:"5.1 Prickly pear physicochemical analyses and measurements",level:"2"},{id:"sec_14",title:"6. Conclusions",level:"1"},{id:"sec_15",title:"Acknowledgments",level:"1"},{id:"sec_18",title:"Conflict of interest",level:"1"}],chapterReferences:[{id:"B1",body:'Santos SF, Cardoso R, Borges ÍM, Almeida AC, Andrade ES, Ferreira IO, et al. Post-harvest losses of fruits and vegetables in supply centers in Salvador, Brazil: Analysis of determinants, volumes and reduction strategies. Waste Management. 2019;101:161-170. DOI: 10.1016/j.wasman.2019.10.007'},{id:"B2",body:'Rajapaksha L, Gunathilake DM, Pathirana SM, Fernando TN. Reducing post-harvest losses in fruits and vegetables for ensuring food security—Case of Sri Lanka. MOJ Food Processing and Technology. 2021;9(1):7-16. DOI: 10.15406/mojfpt.2021.09.00255'},{id:"B3",body:'Losada HR, Vieyra JE, Luna L, Cortés J, Vargas JM. Economic indicators, capacity of the ecosystem of prickly pear cactus (opuntia megacantha) and environmental services in Teotihuacan, México to Supply Urban Consumption. 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\r\n\tTransforming our World: the 2030 Agenda for Sustainable Development endorsed by United Nations and 193 Member States, came into effect on Jan 1, 2016, to guide decision making and actions to the year 2030 and beyond. Central to this Agenda are 17 Goals, 169 associated targets and over 230 indicators that are reviewed annually. The vision envisaged in the implementation of the SDGs is centered on the five Ps: People, Planet, Prosperity, Peace and Partnership. This call for renewed focused efforts ensure we have a safe and healthy planet for current and future generations.
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\r\n\t
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\r\n\tThis Series focuses on covering research and applied research involving the five Ps through the following topics:
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\r\n\t
\r\n
\r\n\t1. Sustainable Economy and Fair Society that relates to SDG 1 on No Poverty, SDG 2 on Zero Hunger, SDG 8 on Decent Work and Economic Growth, SDG 10 on Reduced Inequalities, SDG 12 on Responsible Consumption and Production, and SDG 17 Partnership for the Goals
\r\n
\r\n\t
\r\n
\r\n\t2. Health and Wellbeing focusing on SDG 3 on Good Health and Wellbeing and SDG 6 on Clean Water and Sanitation
\r\n
\r\n\t
\r\n
\r\n\t3. Inclusivity and Social Equality involving SDG 4 on Quality Education, SDG 5 on Gender Equality, and SDG 16 on Peace, Justice and Strong Institutions
\r\n
\r\n\t
\r\n
\r\n\t4. Climate Change and Environmental Sustainability comprising SDG 13 on Climate Action, SDG 14 on Life Below Water, and SDG 15 on Life on Land
\r\n
\r\n\t
\r\n
\r\n\t5. Urban Planning and Environmental Management embracing SDG 7 on Affordable Clean Energy, SDG 9 on Industry, Innovation and Infrastructure, and SDG 11 on Sustainable Cities and Communities.
\r\n
\r\n\t
\r\n
\r\n\tThe series also seeks to support the use of cross cutting SDGs, as many of the goals listed above, targets and indicators are all interconnected to impact our lives and the decisions we make on a daily basis, making them impossible to tie to a single topic.
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His research interests include optimization, computer graphics, computer vision, image processing, machine learning, pattern recognition, soft computing, data science, and intelligent systems. Prof. Sarfraz has been a keynote/invited speaker at various platforms around the globe. He has advised/supervised more than 110 students for their MSc and Ph.D. theses. He has published more than 400 publications as books, journal articles, and conference papers. He has authored and/or edited around seventy books. Prof. Sarfraz is a member of various professional societies. He is a chair and member of international advisory committees and organizing committees of numerous international conferences. He is also an editor and editor in chief for various international journals.",institutionString:"Kuwait University",institution:{name:"Kuwait University",country:{name:"Kuwait"}}},{id:"32650",title:"Prof.",name:"Lukas",middleName:"Willem",surname:"Snyman",slug:"lukas-snyman",fullName:"Lukas Snyman",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/32650/images/4136_n.jpg",biography:"Lukas Willem Snyman received his basic education at primary and high schools in South Africa, Eastern Cape. He enrolled at today's Nelson Metropolitan University and graduated from this university with a BSc in Physics and Mathematics, B.Sc Honors in Physics, MSc in Semiconductor Physics, and a Ph.D. in Semiconductor Physics in 1987. After his studies, he chose an academic career and devoted his energy to the teaching of physics to first, second, and third-year students. After positions as a lecturer at the University of Port Elizabeth, he accepted a position as Associate Professor at the University of Pretoria, South Africa.\r\n\r\nIn 1992, he motivates the concept of 'television and computer-based education” as means to reach large student numbers with only the best of teaching expertise and publishes an article on the concept in the SA Journal of Higher Education of 1993 (and later in 2003). The University of Pretoria subsequently approved a series of test projects on the concept with outreach to Mamelodi and Eerste Rust in 1993. In 1994, the University established a 'Unit for Telematic Education ' as a support section for multiple faculties at the University of Pretoria. In subsequent years, the concept of 'telematic education” subsequently becomes well established in academic circles in South Africa, grew in popularity, and is adopted by many universities and colleges throughout South Africa as a medium of enhancing education and training, as a method to reaching out to far out communities, and as a means to enhance study from the home environment.\r\n\r\nProfessor Snyman in subsequent years pursued research in semiconductor physics, semiconductor devices, microelectronics, and optoelectronics.\r\n\r\nIn 2000 he joined the TUT as a full professor. Here served for a period as head of the Department of Electronic Engineering. Here he makes contributions to solar energy development, microwave and optoelectronic device development, silicon photonics, as well as contributions to new mobile telecommunication systems and network planning in SA.\r\n\r\nCurrently, he teaches electronics and telecommunications at the TUT to audiences ranging from first-year students to Ph.D. level.\r\n\r\nFor his research in the field of 'Silicon Photonics” since 1990, he has published (as author and co-author) about thirty internationally reviewed articles in scientific journals, contributed to more than forty international conferences, about 25 South African provisional patents (as inventor and co-inventor), 8 PCT international patent applications until now. Of these, two USA patents applications, two European Patents, two Korean patents, and ten SA patents have been granted. A further 4 USA patents, 5 European patents, 3 Korean patents, 3 Chinese patents, and 3 Japanese patents are currently under consideration.\r\n\r\nRecently he has also published an extensive scholarly chapter in an internet open access book on 'Integrating Microphotonic Systems and MOEMS into standard Silicon CMOS Integrated circuitry”.\r\n\r\nFurthermore, Professor Snyman recently steered a new initiative at the TUT by introducing a 'Laboratory for Innovative Electronic Systems ' at the Department of Electrical Engineering. The model of this laboratory or center is to primarily combine outputs as achieved by high-level research with lower-level system development and entrepreneurship in a technical university environment. Students are allocated to projects at different levels with PhDs and Master students allocated to the generation of new knowledge and new technologies, while students at the diploma and Baccalaureus level are allocated to electronic systems development with a direct and a near application for application in industry or the commercial and public sectors in South Africa.\r\n\r\nProfessor Snyman received the WIRSAM Award of 1983 and the WIRSAM Award in 1985 in South Africa for best research papers by a young scientist at two international conferences on electron microscopy in South Africa. He subsequently received the SA Microelectronics Award for the best dissertation emanating from studies executed at a South African university in the field of Physics and Microelectronics in South Africa in 1987. In October of 2011, Professor Snyman received the prestigious Institutional Award for 'Innovator of the Year” for 2010 at the Tshwane University of Technology, South Africa. This award was based on the number of patents recognized and granted by local and international institutions as well as for his contributions concerning innovation at the TUT.",institutionString:null,institution:{name:"University of South Africa",country:{name:"South Africa"}}},{id:"317279",title:"Mr.",name:"Ali",middleName:"Usama",surname:"Syed",slug:"ali-syed",fullName:"Ali Syed",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/317279/images/16024_n.png",biography:"A creative, talented, and innovative young professional who is dedicated, well organized, and capable research fellow with two years of experience in graduate-level research, published in engineering journals and book, with related expertise in Bio-robotics, equally passionate about the aesthetics of the mechanical and electronic system, obtained expertise in the use of MS Office, MATLAB, SolidWorks, LabVIEW, Proteus, Fusion 360, having a grasp on python, C++ and assembly language, possess proven ability in acquiring research grants, previous appointments with social and educational societies with experience in administration, current affiliations with IEEE and Web of Science, a confident presenter at conferences and teacher in classrooms, able to explain complex information to audiences of all levels.",institutionString:null,institution:{name:"Air University",country:{name:"Pakistan"}}},{id:"75526",title:"Ph.D.",name:"Zihni Onur",middleName:null,surname:"Uygun",slug:"zihni-onur-uygun",fullName:"Zihni Onur Uygun",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/75526/images/12_n.jpg",biography:"My undergraduate education and my Master of Science educations at Ege University and at Çanakkale Onsekiz Mart University have given me a firm foundation in Biochemistry, Analytical Chemistry, Biosensors, Bioelectronics, Physical Chemistry and Medicine. After obtaining my degree as a MSc in analytical chemistry, I started working as a research assistant in Ege University Medical Faculty in 2014. In parallel, I enrolled to the MSc program at the Department of Medical Biochemistry at Ege University to gain deeper knowledge on medical and biochemical sciences as well as clinical chemistry in 2014. In my PhD I deeply researched on biosensors and bioelectronics and finished in 2020. Now I have eleven SCI-Expanded Index published papers, 6 international book chapters, referee assignments for different SCIE journals, one international patent pending, several international awards, projects and bursaries. In parallel to my research assistant position at Ege University Medical Faculty, Department of Medical Biochemistry, in April 2016, I also founded a Start-Up Company (Denosens Biotechnology LTD) by the support of The Scientific and Technological Research Council of Turkey. Currently, I am also working as a CEO in Denosens Biotechnology. The main purposes of the company, which carries out R&D as a research center, are to develop new generation biosensors and sensors for both point-of-care diagnostics; such as glucose, lactate, cholesterol and cancer biomarker detections. My specific experimental and instrumental skills are Biochemistry, Biosensor, Analytical Chemistry, Electrochemistry, Mobile phone based point-of-care diagnostic device, POCTs and Patient interface designs, HPLC, Tandem Mass Spectrometry, Spectrophotometry, ELISA.",institutionString:null,institution:{name:"Ege University",country:{name:"Turkey"}}},{id:"246502",title:"Dr.",name:"Jaya T.",middleName:"T",surname:"Varkey",slug:"jaya-t.-varkey",fullName:"Jaya T. Varkey",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/246502/images/11160_n.jpg",biography:"Jaya T. Varkey, PhD, graduated with a degree in Chemistry from Cochin University of Science and Technology, Kerala, India. She obtained a PhD in Chemistry from the School of Chemical Sciences, Mahatma Gandhi University, Kerala, India, and completed a post-doctoral fellowship at the University of Minnesota, USA. She is a research guide at Mahatma Gandhi University and Associate Professor in Chemistry, St. Teresa’s College, Kochi, Kerala, India.\nDr. Varkey received a National Young Scientist award from the Indian Science Congress (1995), a UGC Research award (2016–2018), an Indian National Science Academy (INSA) Visiting Scientist award (2018–2019), and a Best Innovative Faculty award from the All India Association for Christian Higher Education (AIACHE) (2019). She Hashas received the Sr. Mary Cecil prize for best research paper three times. She was also awarded a start-up to develop a tea bag water filter. \nDr. Varkey has published two international books and twenty-seven international journal publications. She is an editorial board member for five international journals.",institutionString:"St. Teresa’s College",institution:null},{id:"250668",title:"Dr.",name:"Ali",middleName:null,surname:"Nabipour Chakoli",slug:"ali-nabipour-chakoli",fullName:"Ali Nabipour Chakoli",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/250668/images/system/250668.jpg",biography:"Academic Qualification:\r\n•\tPhD in Materials Physics and Chemistry, From: Sep. 2006, to: Sep. 2010, School of Materials Science and Engineering, Harbin Institute of Technology, Thesis: Structure and Shape Memory Effect of Functionalized MWCNTs/poly (L-lactide-co-ε-caprolactone) Nanocomposites. Supervisor: Prof. Wei Cai,\r\n•\tM.Sc in Applied Physics, From: 1996, to: 1998, Faculty of Physics & Nuclear Science, Amirkabir Uni. of Technology, Tehran, Iran, Thesis: Determination of Boron in Micro alloy Steels with solid state nuclear track detectors by neutron induced auto radiography, Supervisors: Dr. M. Hosseini Ashrafi and Dr. A. Hosseini.\r\n•\tB.Sc. in Applied Physics, From: 1991, to: 1996, Faculty of Physics & Nuclear Science, Amirkabir Uni. of Technology, Tehran, Iran, Thesis: Design of shielding for Am-Be neutron sources for In Vivo neutron activation analysis, Supervisor: Dr. M. Hosseini Ashrafi.\r\n\r\nResearch Experiences:\r\n1.\tNanomaterials, Carbon Nanotubes, Graphene: Synthesis, Functionalization and Characterization,\r\n2.\tMWCNTs/Polymer Composites: Fabrication and Characterization, \r\n3.\tShape Memory Polymers, Biodegradable Polymers, ORC, Collagen,\r\n4.\tMaterials Analysis and Characterizations: TEM, SEM, XPS, FT-IR, Raman, DSC, DMA, TGA, XRD, GPC, Fluoroscopy, \r\n5.\tInteraction of Radiation with Mater, Nuclear Safety and Security, NDT(RT),\r\n6.\tRadiation Detectors, Calibration (SSDL),\r\n7.\tCompleted IAEA e-learning Courses:\r\nNuclear Security (15 Modules),\r\nNuclear Safety:\r\nTSA 2: Regulatory Protection in Occupational Exposure,\r\nTips & Tricks: Radiation Protection in Radiography,\r\nSafety and Quality in Radiotherapy,\r\nCourse on Sealed Radioactive Sources,\r\nCourse on Fundamentals of Environmental Remediation,\r\nCourse on Planning for Environmental Remediation,\r\nKnowledge Management Orientation Course,\r\nFood Irradiation - Technology, Applications and Good Practices,\r\nEmployment:\r\nFrom 2010 to now: Academic staff, Nuclear Science and Technology Research Institute, Kargar Shomali, Tehran, Iran, P.O. Box: 14395-836.\r\nFrom 1997 to 2006: Expert of Materials Analysis and Characterization. Research Center of Agriculture and Medicine. Rajaeeshahr, Karaj, Iran, P. O. Box: 31585-498.",institutionString:"Atomic Energy Organization of Iran",institution:{name:"Atomic Energy Organization of Iran",country:{name:"Iran"}}},{id:"248279",title:"Dr.",name:"Monika",middleName:"Elzbieta",surname:"Machoy",slug:"monika-machoy",fullName:"Monika Machoy",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/248279/images/system/248279.jpeg",biography:"Monika Elżbieta Machoy, MD, graduated with distinction from the Faculty of Medicine and Dentistry at the Pomeranian Medical University in 2009, defended her PhD thesis with summa cum laude in 2016 and is currently employed as a researcher at the Department of Orthodontics of the Pomeranian Medical University. She expanded her professional knowledge during a one-year scholarship program at the Ernst Moritz Arndt University in Greifswald, Germany and during a three-year internship at the Technical University in Dresden, Germany. She has been a speaker at numerous orthodontic conferences, among others, American Association of Orthodontics, European Orthodontic Symposium and numerous conferences of the Polish Orthodontic Society. She conducts research focusing on the effect of orthodontic treatment on dental and periodontal tissues and the causes of pain in orthodontic patients.",institutionString:"Pomeranian Medical University",institution:{name:"Pomeranian Medical University",country:{name:"Poland"}}},{id:"252743",title:"Prof.",name:"Aswini",middleName:"Kumar",surname:"Kar",slug:"aswini-kar",fullName:"Aswini Kar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/252743/images/10381_n.jpg",biography:"uploaded in cv",institutionString:null,institution:{name:"KIIT University",country:{name:"India"}}},{id:"204256",title:"Dr.",name:"Anil",middleName:"Kumar",surname:"Kumar Sahu",slug:"anil-kumar-sahu",fullName:"Anil Kumar Sahu",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/204256/images/14201_n.jpg",biography:"I have nearly 11 years of research and teaching experience. I have done my master degree from University Institute of Pharmacy, Pt. Ravi Shankar Shukla University, Raipur, Chhattisgarh India. I have published 16 review and research articles in international and national journals and published 4 chapters in IntechOpen, the world’s leading publisher of Open access books. I have presented many papers at national and international conferences. I have received research award from Indian Drug Manufacturers Association in year 2015. My research interest extends from novel lymphatic drug delivery systems, oral delivery system for herbal bioactive to formulation optimization.",institutionString:null,institution:{name:"Chhattisgarh Swami Vivekanand Technical University",country:{name:"India"}}},{id:"253468",title:"Dr.",name:"Mariusz",middleName:null,surname:"Marzec",slug:"mariusz-marzec",fullName:"Mariusz Marzec",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/253468/images/system/253468.png",biography:"An assistant professor at Department of Biomedical Computer Systems, at Institute of Computer Science, Silesian University in Katowice. Scientific interests: computer analysis and processing of images, biomedical images, databases and programming languages. He is an author and co-author of scientific publications covering analysis and processing of biomedical images and development of database systems.",institutionString:"University of Silesia",institution:null},{id:"212432",title:"Prof.",name:"Hadi",middleName:null,surname:"Mohammadi",slug:"hadi-mohammadi",fullName:"Hadi Mohammadi",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/212432/images/system/212432.jpeg",biography:"Dr. Hadi Mohammadi is a biomedical engineer with hands-on experience in the design and development of many engineering structures and medical devices through various projects that he has been involved in over the past twenty years. Dr. Mohammadi received his BSc. and MSc. degrees in Mechanical Engineering from Sharif University of Technology, Tehran, Iran, and his PhD. degree in Biomedical Engineering (biomaterials) from the University of Western Ontario. He was a postdoctoral trainee for almost four years at University of Calgary and Harvard Medical School. He is an industry innovator having created the technology to produce lifelike synthetic platforms that can be used for the simulation of almost all cardiovascular reconstructive surgeries. He’s been heavily involved in the design and development of cardiovascular devices and technology for the past 10 years. He is currently an Assistant Professor with the University of British Colombia, Canada.",institutionString:"University of British Columbia",institution:{name:"University of British Columbia",country:{name:"Canada"}}},{id:"254463",title:"Prof.",name:"Haisheng",middleName:null,surname:"Yang",slug:"haisheng-yang",fullName:"Haisheng Yang",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/254463/images/system/254463.jpeg",biography:"Haisheng Yang, Ph.D., Professor and Director of the Department of Biomedical Engineering, College of Life Science and Bioengineering, Beijing University of Technology. He received his Ph.D. degree in Mechanics/Biomechanics from Harbin Institute of Technology (jointly with University of California, Berkeley). Afterwards, he worked as a Postdoctoral Research Associate in the Purdue Musculoskeletal Biology and Mechanics Lab at the Department of Basic Medical Sciences, Purdue University, USA. He also conducted research in the Research Centre of Shriners Hospitals for Children-Canada at McGill University, Canada. Dr. Yang has over 10 years research experience in orthopaedic biomechanics and mechanobiology of bone adaptation and regeneration. He earned an award from Beijing Overseas Talents Aggregation program in 2017 and serves as Beijing Distinguished Professor.",institutionString:"Beijing University of Technology",institution:null},{id:"255757",title:"Dr.",name:"Igor",middleName:"Victorovich",surname:"Lakhno",slug:"igor-lakhno",fullName:"Igor Lakhno",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/255757/images/system/255757.jpg",biography:"Lakhno Igor Victorovich was born in 1971 in Kharkiv (Ukraine). \nMD – 1994, Kharkiv National Medical Univesity.\nOb&Gyn; – 1997, master courses in Kharkiv Medical Academy of Postgraduate Education.\nPhD – 1999, Kharkiv National Medical Univesity.\nDSc – 2019, PL Shupik National Academy of Postgraduate Education \nLakhno Igor has been graduated from an international training courses on reproductive medicine and family planning held in Debrecen University (Hungary) in 1997. Since 1998 Lakhno Igor has worked as an associate professor of the department of obstetrics and gynecology of VN Karazin National University and an associate professor of the perinatology, obstetrics and gynecology department of Kharkiv Medical Academy of Postgraduate Education. Since June 2019 he’s a professor of the department of obstetrics and gynecology of VN Karazin National University and a professor of the perinatology, obstetrics and gynecology department of Kharkiv Medical Academy of Postgraduate Education . He’s an author of about 200 printed works and there are 17 of them in Scopus or Web of Science databases. Lakhno Igor is a rewiever of Journal of Obstetrics and Gynaecology (Taylor and Francis), Informatics in Medicine Unlocked (Elsevier), The Journal of Obstetrics and Gynecology Research (Wiley), Endocrine, Metabolic & Immune Disorders-Drug Targets (Bentham Open), The Open Biomedical Engineering Journal (Bentham Open), etc. He’s defended a dissertation for DSc degree \\'Pre-eclampsia: prediction, prevention and treatment”. Lakhno Igor has participated as a speaker in several international conferences and congresses (International Conference on Biological Oscillations April 10th-14th 2016, Lancaster, UK, The 9th conference of the European Study Group on Cardiovascular Oscillations). His main scientific interests: obstetrics, women’s health, fetal medicine, cardiovascular medicine.",institutionString:"V.N. Karazin Kharkiv National University",institution:{name:"Kharkiv Medical Academy of Postgraduate Education",country:{name:"Ukraine"}}},{id:"89721",title:"Dr.",name:"Mehmet",middleName:"Cuneyt",surname:"Ozmen",slug:"mehmet-ozmen",fullName:"Mehmet Ozmen",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/89721/images/7289_n.jpg",biography:null,institutionString:null,institution:{name:"Gazi University",country:{name:"Turkey"}}},{id:"243698",title:"M.D.",name:"Xiaogang",middleName:null,surname:"Wang",slug:"xiaogang-wang",fullName:"Xiaogang Wang",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/243698/images/system/243698.png",biography:"Dr. Xiaogang Wang, a faculty member of Shanxi Eye Hospital specializing in the treatment of cataract and retinal disease and a tutor for postgraduate students of Shanxi Medical University, worked in the COOL Lab as an international visiting scholar under the supervision of Dr. David Huang and Yali Jia from October 2012 through November 2013. Dr. Wang earned an MD from Shanxi Medical University and a Ph.D. from Shanghai Jiao Tong University. Dr. Wang was awarded two research project grants focused on multimodal optical coherence tomography imaging and deep learning in cataract and retinal disease, from the National Natural Science Foundation of China. He has published around 30 peer-reviewed journal papers and four book chapters and co-edited one book.",institutionString:"Shanxi Eye Hospital",institution:{name:"Shanxi Eye Hospital",country:{name:"China"}}},{id:"242893",title:"Ph.D. Student",name:"Joaquim",middleName:null,surname:"De Moura",slug:"joaquim-de-moura",fullName:"Joaquim De Moura",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/242893/images/7133_n.jpg",biography:"Joaquim de Moura received his degree in Computer Engineering in 2014 from the University of A Coruña (Spain). In 2016, he received his M.Sc degree in Computer Engineering from the same university. He is currently pursuing his Ph.D degree in Computer Science in a collaborative project between ophthalmology centers in Galicia and the University of A Coruña. His research interests include computer vision, machine learning algorithms and analysis and medical imaging processing of various kinds.",institutionString:null,institution:{name:"University of A Coruña",country:{name:"Spain"}}},{id:"267434",title:"Dr.",name:"Rohit",middleName:null,surname:"Raja",slug:"rohit-raja",fullName:"Rohit Raja",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRZkkQAG/Profile_Picture_2022-05-09T12:55:18.jpg",biography:null,institutionString:null,institution:null},{id:"294334",title:"B.Sc.",name:"Marc",middleName:null,surname:"Bruggeman",slug:"marc-bruggeman",fullName:"Marc Bruggeman",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/294334/images/8242_n.jpg",biography:"Chemical engineer graduate, with a passion for material science and specific interest in polymers - their near infinite applications intrigue me. \n\nI plan to continue my scientific career in the field of polymeric biomaterials as I am fascinated by intelligent, bioactive and biomimetic materials for use in both consumer and medical applications.",institutionString:null,institution:null},{id:"244950",title:"Dr.",name:"Salvatore",middleName:null,surname:"Di Lauro",slug:"salvatore-di-lauro",fullName:"Salvatore Di Lauro",position:null,profilePictureURL:"https://intech-files.s3.amazonaws.com/0030O00002bSF1HQAW/ProfilePicture%202021-12-20%2014%3A54%3A14.482",biography:"Name:\n\tSALVATORE DI LAURO\nAddress:\n\tHospital Clínico Universitario Valladolid\nAvda Ramón y Cajal 3\n47005, Valladolid\nSpain\nPhone number: \nFax\nE-mail:\n\t+34 983420000 ext 292\n+34 983420084\nsadilauro@live.it\nDate and place of Birth:\nID Number\nMedical Licence \nLanguages\t09-05-1985. Villaricca (Italy)\n\nY1281863H\n474707061\nItalian (native language)\nSpanish (read, written, spoken)\nEnglish (read, written, spoken)\nPortuguese (read, spoken)\nFrench (read)\n\t\t\nCurrent position (title and company)\tDate (Year)\nVitreo-Retinal consultant in ophthalmology. Hospital Clinico Universitario Valladolid. Sacyl. National Health System.\nVitreo-Retinal consultant in ophthalmology. Instituto Oftalmologico Recoletas. Red Hospitalaria Recoletas. Private practise.\t2017-today\n\n2019-today\n\t\n\t\nEducation (High school, university and postgraduate training > 3 months)\tDate (Year)\nDegree in Medicine and Surgery. University of Neaples 'Federico II”\nResident in Opthalmology. Hospital Clinico Universitario Valladolid\nMaster in Vitreo-Retina. IOBA. University of Valladolid\nFellow of the European Board of Ophthalmology. Paris\nMaster in Research in Ophthalmology. University of Valladolid\t2003-2009\n2012-2016\n2016-2017\n2016\n2012-2013\n\t\nEmployments (company and positions)\tDate (Year)\nResident in Ophthalmology. Hospital Clinico Universitario Valladolid. Sacyl.\nFellow in Vitreo-Retina. IOBA. University of Valladolid\nVitreo-Retinal consultant in ophthalmology. Hospital Clinico Universitario Valladolid. Sacyl. National Health System.\nVitreo-Retinal consultant in ophthalmology. Instituto Oftalmologico Recoletas. Red Hospitalaria Recoletas. \n\t2012-2016\n2016-2017\n2017-today\n\n2019-Today\n\n\n\t\nClinical Research Experience (tasks and role)\tDate (Year)\nAssociated investigator\n\n' FIS PI20/00740: DESARROLLO DE UNA CALCULADORA DE RIESGO DE\nAPARICION DE RETINOPATIA DIABETICA BASADA EN TECNICAS DE IMAGEN MULTIMODAL EN PACIENTES DIABETICOS TIPO 1. Grant by: Ministerio de Ciencia e Innovacion \n\n' (BIO/VA23/14) Estudio clínico multicéntrico y prospectivo para validar dos\nbiomarcadores ubicados en los genes p53 y MDM2 en la predicción de los resultados funcionales de la cirugía del desprendimiento de retina regmatógeno. Grant by: Gerencia Regional de Salud de la Junta de Castilla y León.\n' Estudio multicéntrico, aleatorizado, con enmascaramiento doble, en 2 grupos\nparalelos y de 52 semanas de duración para comparar la eficacia, seguridad e inmunogenicidad de SOK583A1 respecto a Eylea® en pacientes con degeneración macular neovascular asociada a la edad' (CSOK583A12301; N.EUDRA: 2019-004838-41; FASE III). Grant by Hexal AG\n\n' Estudio de fase III, aleatorizado, doble ciego, con grupos paralelos, multicéntrico para comparar la eficacia y la seguridad de QL1205 frente a Lucentis® en pacientes con degeneración macular neovascular asociada a la edad. (EUDRACT: 2018-004486-13). Grant by Qilu Pharmaceutical Co\n\n' Estudio NEUTON: Ensayo clinico en fase IV para evaluar la eficacia de aflibercept en pacientes Naive con Edema MacUlar secundario a Oclusion de Vena CenTral de la Retina (OVCR) en regimen de tratamientO iNdividualizado Treat and Extend (TAE)”, (2014-000975-21). Grant by Fundacion Retinaplus\n\n' Evaluación de la seguridad y bioactividad de anillos de tensión capsular en conejo. Proyecto Procusens. Grant by AJL, S.A.\n\n'Estudio epidemiológico, prospectivo, multicéntrico y abierto\\npara valorar la frecuencia de la conjuntivitis adenovírica diagnosticada mediante el test AdenoPlus®\\nTest en pacientes enfermos de conjuntivitis aguda”\\n. National, multicenter study. Grant by: NICOX.\n\nEuropean multicentric trial: 'Evaluation of clinical outcomes following the use of Systane Hydration in patients with dry eye”. Study Phase 4. Grant by: Alcon Labs'\n\nVLPs Injection and Activation in a Rabbit Model of Uveal Melanoma. Grant by Aura Bioscience\n\nUpdating and characterization of a rabbit model of uveal melanoma. Grant by Aura Bioscience\n\nEnsayo clínico en fase IV para evaluar las variantes genéticas de la vía del VEGF como biomarcadores de eficacia del tratamiento con aflibercept en pacientes con degeneración macular asociada a la edad (DMAE) neovascular. Estudio BIOIMAGE. IMO-AFLI-2013-01\n\nEstudio In-Eye:Ensayo clínico en fase IV, abierto, aleatorizado, de 2 brazos,\nmulticçentrico y de 12 meses de duración, para evaluar la eficacia y seguridad de un régimen de PRN flexible individualizado de 'esperar y extender' versus un régimen PRN según criterios de estabilización mediante evaluaciones mensuales de inyecciones intravítreas de ranibizumab 0,5 mg en pacientes naive con neovascularización coriodea secunaria a la degeneración macular relacionada con la edad. CP: CRFB002AES03T\n\nTREND: Estudio Fase IIIb multicéntrico, randomizado, de 12 meses de\nseguimiento con evaluador de la agudeza visual enmascarado, para evaluar la eficacia y la seguridad de ranibizumab 0.5mg en un régimen de tratar y extender comparado con un régimen mensual, en pacientes con degeneración macular neovascular asociada a la edad. CP: CRFB002A2411 Código Eudra CT:\n2013-002626-23\n\n\n\nPublications\t\n\n2021\n\n\n\n\n2015\n\n\n\n\n2021\n\n\n\n\n\n2021\n\n\n\n\n2015\n\n\n\n\n2015\n\n\n2014\n\n\n\n\n2015-16\n\n\n\n2015\n\n\n2014\n\n\n2014\n\n\n\n\n2014\n\n\n\n\n\n\n\n2014\n\nJose Carlos Pastor; Jimena Rojas; Salvador Pastor-Idoate; Salvatore Di Lauro; Lucia Gonzalez-Buendia; Santiago Delgado-Tirado. Proliferative vitreoretinopathy: A new concept of disease pathogenesis and practical\nconsequences. Progress in Retinal and Eye Research. 51, pp. 125 - 155. 03/2016. DOI: 10.1016/j.preteyeres.2015.07.005\n\n\nLabrador-Velandia S; Alonso-Alonso ML; Di Lauro S; García-Gutierrez MT; Srivastava GK; Pastor JC; Fernandez-Bueno I. Mesenchymal stem cells provide paracrine neuroprotective resources that delay degeneration of co-cultured organotypic neuroretinal cultures.Experimental Eye Research. 185, 17/05/2019. DOI: 10.1016/j.exer.2019.05.011\n\nSalvatore Di Lauro; Maria Teresa Garcia Gutierrez; Ivan Fernandez Bueno. Quantification of pigment epithelium-derived factor (PEDF) in an ex vivo coculture of retinal pigment epithelium cells and neuroretina.\nJournal of Allbiosolution. 2019. ISSN 2605-3535\n\nSonia Labrador Velandia; Salvatore Di Lauro; Alonso-Alonso ML; Tabera Bartolomé S; Srivastava GK; Pastor JC; Fernandez-Bueno I. Biocompatibility of intravitreal injection of human mesenchymal stem cells in immunocompetent rabbits. Graefe's archive for clinical and experimental ophthalmology. 256 - 1, pp. 125 - 134. 01/2018. DOI: 10.1007/s00417-017-3842-3\n\n\nSalvatore Di Lauro, David Rodriguez-Crespo, Manuel J Gayoso, Maria T Garcia-Gutierrez, J Carlos Pastor, Girish K Srivastava, Ivan Fernandez-Bueno. A novel coculture model of porcine central neuroretina explants and retinal pigment epithelium cells. Molecular Vision. 2016 - 22, pp. 243 - 253. 01/2016.\n\nSalvatore Di Lauro. Classifications for Proliferative Vitreoretinopathy ({PVR}): An Analysis of Their Use in Publications over the Last 15 Years. Journal of Ophthalmology. 2016, pp. 1 - 6. 01/2016. DOI: 10.1155/2016/7807596\n\nSalvatore Di Lauro; Rosa Maria Coco; Rosa Maria Sanabria; Enrique Rodriguez de la Rua; Jose Carlos Pastor. Loss of Visual Acuity after Successful Surgery for Macula-On Rhegmatogenous Retinal Detachment in a Prospective Multicentre Study. Journal of Ophthalmology. 2015:821864, 2015. DOI: 10.1155/2015/821864\n\nIvan Fernandez-Bueno; Salvatore Di Lauro; Ivan Alvarez; Jose Carlos Lopez; Maria Teresa Garcia-Gutierrez; Itziar Fernandez; Eva Larra; Jose Carlos Pastor. Safety and Biocompatibility of a New High-Density Polyethylene-Based\nSpherical Integrated Porous Orbital Implant: An Experimental Study in Rabbits. Journal of Ophthalmology. 2015:904096, 2015. DOI: 10.1155/2015/904096\n\nPastor JC; Pastor-Idoate S; Rodríguez-Hernandez I; Rojas J; Fernandez I; Gonzalez-Buendia L; Di Lauro S; Gonzalez-Sarmiento R. Genetics of PVR and RD. Ophthalmologica. 232 - Suppl 1, pp. 28 - 29. 2014\n\nRodriguez-Crespo D; Di Lauro S; Singh AK; Garcia-Gutierrez MT; Garrosa M; Pastor JC; Fernandez-Bueno I; Srivastava GK. Triple-layered mixed co-culture model of RPE cells with neuroretina for evaluating the neuroprotective effects of adipose-MSCs. Cell Tissue Res. 358 - 3, pp. 705 - 716. 2014.\nDOI: 10.1007/s00441-014-1987-5\n\nCarlo De Werra; Salvatore Condurro; Salvatore Tramontano; Mario Perone; Ivana Donzelli; Salvatore Di Lauro; Massimo Di Giuseppe; Rosa Di Micco; Annalisa Pascariello; Antonio Pastore; Giorgio Diamantis; Giuseppe Galloro. Hydatid disease of the liver: thirty years of surgical experience.Chirurgia italiana. 59 - 5, pp. 611 - 636.\n(Italia): 2007. ISSN 0009-4773\n\nChapters in books\n\t\n' Salvador Pastor Idoate; Salvatore Di Lauro; Jose Carlos Pastor Jimeno. PVR: Pathogenesis, Histopathology and Classification. Proliferative Vitreoretinopathy with Small Gauge Vitrectomy. Springer, 2018. ISBN 978-3-319-78445-8\nDOI: 10.1007/978-3-319-78446-5_2. \n\n' Salvatore Di Lauro; Maria Isabel Lopez Galvez. Quistes vítreos en una mujer joven. Problemas diagnósticos en patología retinocoroidea. Sociedad Española de Retina-Vitreo. 2018.\n\n' Salvatore Di Lauro; Salvador Pastor Idoate; Jose Carlos Pastor Jimeno. iOCT in PVR management. OCT Applications in Opthalmology. pp. 1 - 8. INTECH, 2018. DOI: 10.5772/intechopen.78774.\n\n' Rosa Coco Martin; Salvatore Di Lauro; Salvador Pastor Idoate; Jose Carlos Pastor. amponadores, manipuladores y tinciones en la cirugía del traumatismo ocular.Trauma Ocular. Ponencia de la SEO 2018..\n\n' LOPEZ GALVEZ; DI LAURO; CRESPO. OCT angiografia y complicaciones retinianas de la diabetes. PONENCIA SEO 2021, CAPITULO 20. (España): 2021.\n\n' Múltiples desprendimientos neurosensoriales bilaterales en paciente joven. Enfermedades Degenerativas De Retina Y Coroides. SERV 04/2016. \n' González-Buendía L; Di Lauro S; Pastor-Idoate S; Pastor Jimeno JC. Vitreorretinopatía proliferante (VRP) e inflamación: LA INFLAMACIÓN in «INMUNOMODULADORES Y ANTIINFLAMATORIOS: MÁS ALLÁ DE LOS CORTICOIDES. RELACION DE PONENCIAS DE LA SOCIEDAD ESPAÑOLA DE OFTALMOLOGIA. 10/2014.",institutionString:null,institution:null},{id:"265335",title:"Mr.",name:"Stefan",middleName:"Radnev",surname:"Stefanov",slug:"stefan-stefanov",fullName:"Stefan Stefanov",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/265335/images/7562_n.jpg",biography:null,institutionString:null,institution:null},{id:"318905",title:"Prof.",name:"Elvis",middleName:"Kwason",surname:"Tiburu",slug:"elvis-tiburu",fullName:"Elvis Tiburu",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Ghana",country:{name:"Ghana"}}},{id:"336193",title:"Dr.",name:"Abdullah",middleName:null,surname:"Alamoudi",slug:"abdullah-alamoudi",fullName:"Abdullah Alamoudi",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Majmaah University",country:{name:"Saudi Arabia"}}},{id:"318657",title:"MSc.",name:"Isabell",middleName:null,surname:"Steuding",slug:"isabell-steuding",fullName:"Isabell Steuding",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Harz University of Applied Sciences",country:{name:"Germany"}}},{id:"318656",title:"BSc.",name:"Peter",middleName:null,surname:"Kußmann",slug:"peter-kussmann",fullName:"Peter Kußmann",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Harz University of Applied Sciences",country:{name:"Germany"}}},{id:"338222",title:"Mrs.",name:"María José",middleName:null,surname:"Lucía Mudas",slug:"maria-jose-lucia-mudas",fullName:"María José Lucía Mudas",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Carlos III University of Madrid",country:{name:"Spain"}}},{id:"147824",title:"Mr.",name:"Pablo",middleName:null,surname:"Revuelta Sanz",slug:"pablo-revuelta-sanz",fullName:"Pablo Revuelta Sanz",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Carlos III University of Madrid",country:{name:"Spain"}}}]}},subseries:{item:{id:"18",type:"subseries",title:"Proteomics",keywords:"Mono- and Two-Dimensional Gel Electrophoresis (1-and 2-DE), Liquid Chromatography (LC), Mass Spectrometry/Tandem Mass Spectrometry (MS; MS/MS), Proteins",scope:"With the recognition that the human genome cannot provide answers to the etiology of a disorder, changes in the proteins expressed by a genome became a focus in research. Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. The Proteomics topic aims to attract contributions on all aspects of MS-based proteomics that, by pushing the boundaries of MS capabilities, may address biological problems that have not been resolved yet.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",hasOnlineFirst:!0,hasPublishedBooks:!0,annualVolume:11414,editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",slug:"paolo-iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",biography:"Paolo Iadarola graduated with a degree in Chemistry from the University of Pavia (Italy) in July 1972. He then worked as an Assistant Professor at the Faculty of Science of the same University until 1984. In 1985, Prof. Iadarola became Associate Professor at the Department of Biology and Biotechnologies of the University of Pavia and retired in October 2017. Since then, he has been working as an Adjunct Professor in the same Department at the University of Pavia. His research activity during the first years was primarily focused on the purification and structural characterization of enzymes from animal and plant sources. During this period, Prof. Iadarola familiarized himself with the conventional techniques used in column chromatography, spectrophotometry, manual Edman degradation, and electrophoresis). Since 1995, he has been working on: i) the determination in biological fluids (serum, urine, bronchoalveolar lavage, sputum) of proteolytic activities involved in the degradation processes of connective tissue matrix, and ii) on the identification of biological markers of lung diseases. In this context, he has developed and validated new methodologies (e.g., Capillary Electrophoresis coupled to Laser-Induced Fluorescence, CE-LIF) whose application enabled him to determine both the amounts of biochemical markers (Desmosines) in urine/serum of patients affected by Chronic Obstructive Pulmonary Disease (COPD) and the activity of proteolytic enzymes (Human Neutrophil Elastase, Cathepsin G, Pseudomonas aeruginosa elastase) in sputa of these patients. More recently, Prof. Iadarola was involved in developing techniques such as two-dimensional electrophoresis coupled to liquid chromatography/mass spectrometry (2DE-LC/MS) for the proteomic analysis of biological fluids aimed at the identification of potential biomarkers of different lung diseases. He is the author of about 150 publications (According to Scopus: H-Index: 23; Total citations: 1568- According to WOS: H-Index: 20; Total Citations: 1296) of peer-reviewed international journals. He is a Consultant Reviewer for several journals, including the Journal of Chromatography A, Journal of Chromatography B, Plos ONE, Proteomes, International Journal of Molecular Science, Biotech, Electrophoresis, and others. He is also Associate Editor of Biotech.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",slug:"simona-viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",biography:"Simona Viglio is an Associate Professor of Biochemistry at the Department of Molecular Medicine at the University of Pavia. She has been working since 1995 on the determination of proteolytic enzymes involved in the degradation process of connective tissue matrix and on the identification of biological markers of lung diseases. She gained considerable experience in developing and validating new methodologies whose applications allowed her to determine both the amount of biomarkers (Desmosine and Isodesmosine) in the urine of patients affected by COPD, and the activity of proteolytic enzymes (HNE, Cathepsin G, Pseudomonas aeruginosa elastase) in the sputa of these patients. Simona Viglio was also involved in research dealing with the supplementation of amino acids in patients with brain injury and chronic heart failure. She is presently engaged in the development of 2-DE and LC-MS techniques for the study of proteomics in biological fluids. The aim of this research is the identification of potential biomarkers of lung diseases. She is an author of about 90 publications (According to Scopus: H-Index: 23; According to WOS: H-Index: 20) on peer-reviewed journals, a member of the “Società Italiana di Biochimica e Biologia Molecolare,“ and a Consultant Reviewer for International Journal of Molecular Science, Journal of Chromatography A, COPD, Plos ONE and Nutritional Neuroscience.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,series:{id:"11",title:"Biochemistry",doi:"10.5772/intechopen.72877",issn:"2632-0983"},editorialBoard:[{id:"72288",title:"Dr.",name:"Arli Aditya",middleName:null,surname:"Parikesit",slug:"arli-aditya-parikesit",fullName:"Arli Aditya Parikesit",profilePictureURL:"https://mts.intechopen.com/storage/users/72288/images/system/72288.jpg",institutionString:null,institution:{name:"Indonesia International Institute for Life Sciences",institutionURL:null,country:{name:"Indonesia"}}},{id:"40928",title:"Dr.",name:"Cesar",middleName:null,surname:"Lopez-Camarillo",slug:"cesar-lopez-camarillo",fullName:"Cesar Lopez-Camarillo",profilePictureURL:"https://mts.intechopen.com/storage/users/40928/images/3884_n.png",institutionString:null,institution:{name:"Universidad Autónoma de la Ciudad de México",institutionURL:null,country:{name:"Mexico"}}},{id:"81926",title:"Dr.",name:"Shymaa",middleName:null,surname:"Enany",slug:"shymaa-enany",fullName:"Shymaa Enany",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRqB9QAK/Profile_Picture_1626163237970",institutionString:null,institution:{name:"Suez Canal University",institutionURL:null,country:{name:"Egypt"}}}]},onlineFirstChapters:{paginationCount:3,paginationItems:[{id:"81756",title:"Alteration of Cytokines Level and Oxidative Stress Parameters in COVID-19",doi:"10.5772/intechopen.104950",signatures:"Marija Petrusevska, Emilija Atanasovska, Dragica Zendelovska, Aleksandar Eftimov and Katerina Spasovska",slug:"alteration-of-cytokines-level-and-oxidative-stress-parameters-in-covid-19",totalDownloads:9,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Chemokines Updates",coverURL:"https://cdn.intechopen.com/books/images_new/11672.jpg",subseries:{id:"18",title:"Proteomics"}}},{id:"81188",title:"Structure- and Design-Based Difficulties in Recombinant Protein Purification in Bacterial Expression",doi:"10.5772/intechopen.103958",signatures:"Kubra Acikalin Coskun, Nazlıcan Yurekli, Elif Cansu Abay, Merve Tutar, Mervenur Al and Yusuf Tutar",slug:"structure-and-design-based-difficulties-in-recombinant-protein-purification-in-bacterial-expression",totalDownloads:24,totalCrossrefCites:0,totalDimensionsCites:0,authors:[{name:"Yusuf",surname:"Tutar"},{name:"Nazlican",surname:"Yurekli"},{name:"Merve",surname:"Tutar"},{name:"Mervenur",surname:"Al"},{name:"Elif Cansu",surname:"Abay"},{name:"Kubra",surname:"Acikalin Coskun"}],book:{title:"Protein Detection",coverURL:"https://cdn.intechopen.com/books/images_new/10839.jpg",subseries:{id:"18",title:"Proteomics"}}},{id:"79353",title:"Protein Detection in Clinical Diagnosis and Management of Prevalent Neurodegenerative Diseases and Metabolic Disorders",doi:"10.5772/intechopen.101051",signatures:"Ohanube A.K. 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