Size of PEGylated Au NPs (in nm; with relative error) determined by TEM and DLS methods. Polydispersity index (PDI) of colloidal systems was determined by DLS analysis .
Cathode sputtering is a well-established technique for preparation of metal nanostructures. However, the substrate properties are very important in this process. On glass substrates, there is a difficulty with poor adhesion of the metal layers, but thanks to this, metal nanostructures can be produced using solid state dewetting process. Thin metal films on polymer substrates are strongly influenced by the surface properties of the polymers, which originate in the method of their preparation. A recent focus is direct sputtering of metal nanoparticles (NPs) into liquid substrates and their characterizations and applications. Polyethylene glycol (PEG) is one of the most commonly used liquid, which provides “stealth” character to nanostructures. Recent results in this area are reviewed in this chapter. PEGylated NPs could find application in drug delivery systems, therapy, imaging, biosensing, and tissue regeneration.
- noble metal
- thin film
- polyethylene glycol
- colloidal stability
Cathode sputtering as a method of thin noble metal film preparation has been recently extended to a much wider variety of applications not only in electronics industry, but also in, for example, medicine or biotechnology. It has become an important technology for material processing for technologies such as multifunctional materials or nanoelectromechanical systems. A special attention in the process must be paid to the underlying substrate, which is the key factor in determining properties of the material. The material types used for substrates can be basically divided into metals, glass and ceramics, and polymers. While metals as substrates for noble metal films possess some advantageous properties (such as good adhesion), the real potential of thin film structures on substrates stems from the different properties of each component of the material. In many cases, an insulating material is needed for the material to be functional. Of the insulating substrates, the most significant are glass and polymer substrates, which will be discussed further in this chapter.
Completely new possibilities have opened up with sputtering of noble metals onto liquid substrates. Under appropriate conditions, the use of liquid capture media leads to direct preparation of metal nanoparticles, which show some unique possibilities compared to those prepared by other methods. Ionic liquids (ILs) are one of the most commonly used capturing media for direct metal sputtering. Their significantly less toxic alternatives are vegetable oils. The main condition for selecting a suitable liquid substrate is sufficiently low vapor pressure in vacuum. Polyethylene glycol is one of the most used NP stabilizing polymers. Therefore, the use of liquid substrates for sputtering deposition has recently become a highly studied topic.
2. Cathode sputtering
When high-energy ions impact on a solid surface, the atoms of the surface material are ejected from the surface and spread into the vicinity. The phenomenon is called sputtering and is a widespread method used for deposition of thin films and ion etching.
Three main types of sputtering systems in practical use are: direct current (DC) sputtering, radio-frequency (RF) sputtering, and magnetron sputtering. Among these, the simplest is the DC sputtering system. It consists of two planar electrodes placed in a vacuum chamber. A sheet of the material to be deposited (target) is placed on one of the electrodes (cathode). Substrates to be covered with the target material are positioned on the anode. After a sufficient vacuum is established, an inert work gas (usually Ar at pressure of about 1–5 Pa) is introduced and high voltage is brought to the electrodes. The working gas is then ionized due to collisions with electrons and plasma is formed in the chamber. The generated Ar ions then collide with the cathode resulting in deposition of the target material on the substrates.
Two major drawbacks of the basic direct current are slow deposition rate and overheating and structural damage of the substrate due to extensive electron bombardment. Therefore, magnetic field is often introduced in magnetron sputtering systems in such a way it forces electrons to follow spiral trajectories, which lead to more ionizing collisions. This allows use of lower sputtering pressure and leads to higher sputtering yield. Furthermore, only electrically conductive materials can be deposited by DC sputtering. For deposition of insulating materials, the RF sputtering technique was introduced.
To control the sputtering rate, energy of the sputtered atoms and, in turn, the characteristics of the prepared films, discharge voltage, current, distance between the target and the substrate, and the work gas pressure can be manipulated. Another important parameter is the vacuum and work gas purity. Residual oxygen remaining in the sputtering chamber leads to oxidation of the deposited material. Noble metals—great electrical conductors resistant to oxidation and other chemical reactions—are ideal materials to be used for thin film preparation by the DC diode sputtering method. More in-depth studies on the topic of cathode sputtering can be found in the literature [1, 2, 3, 4, 5].
3. Sputtering of noble metals onto solid insulating substrates
3.1. Glass substrates
Glass is an often-used substrate for preparation of thin metal films for electronics and optics. Its surface can be prepared with a very low roughness, is therefore able to support films with thickness as low as several nanometers and enables preparation of very delicate nanostructures. A downside of a glass substrate for sputtering of Au films is a poor adhesion of the films to the substrate. Due to surface morphology and chemical properties of the glass, the surface free energy between Au, and the glass is too high. The as-sputtered continuous films are therefore metastable. A lot of effort is therefore made to improve the adhesion between the substrates and the metal films, but the metastable nature of the films also enables advantageous preparation of isolated island nanostructure. While continuous Au films are necessary for preparation of reliable and durable metallization in electronics, the nanostructures can be used in construction of sensor devices due to their specific optical properties.
3.1.1. Adhesion of Au layers
The adhesion is defined as the energy required to create free surfaces from the bonded materials. In a practical arrangement, the interfacial toughness involves prevention of initiation and propagation of cracks, plastic deformation, and friction in the thin film-substrate system . To achieve good adhesion, a strong bond between the film and the substrate must be established and parameters such as crystal orientation, contact area and, chemical affinity play very important roles. Typical methods to improve adhesion between noble metal film and glass substrate include preparation of interlayers of more reactive metals (e.g., Cr or Ti) [7, 8, 9, 10], irradiation by energetic ion beams [11, 12, 13], thermal conditioning , or chemical modification of the substrate surface [15, 16], though each method has certain limitations. The metal interlayers create alloys with the thin film, changing its optical properties . Ion irradiation leads to contamination of the substrate with material of the vacuum chamber and implantation of the ions in the substrate. Thermal processes lead to compromising homogeneity of very thin films. The chemical modifications of the substrate lead to introduction of more substances in the system worsening reproducibility of the production of the material.
The most common approaches to measure adhesion of a film to the substrate involve peeling of the films with adhesive tapes and various arrangements of a solid point penetrating the thin film . The solid point methods include indentation measurements, which can be used to evaluate adhesion of brittle and weakly bonded layers, and scratch. The adhesion of the thin film is determined by critical loads at which some type of failure of the film-substrate system begins. The adhesion is usually evaluated in optical microscope or by acoustic emission or friction force . Quantitative evaluation of the interfacial toughness from the scratch test is difficult though, but it is still very useful when comparing adhesion of films deposited under different conditions [19, 20].
3.1.2. Solid state dewetting
Thin metal films on glass substrates undergo a morphology transformation upon annealing. The sputtering deposition is accomplished at relatively low substrate temperatures and the films grow too fast for the atoms to occupy spots with the lowest energy. Therefore, the as-deposited metal layers are in a metastable state. Annealing then leads to transformation of thin film structure from continuous layers to island-like structure. This process is called solid state dewetting. The cleavage of the metal layer then often manifests in the absorption spectrum of the material, where bands connected to localized surface plasmon resonance arise. This phenomenon can be observed as a change of color of the metal film (Figure 1).
The dewetting is then realized at elevated temperature by diffusion of the metal atoms over the substrate in solid state, without actual phase transformation. The driving force of the process is reaching the equilibrium state with the minimum surface free energy of the metal-glass interface. The equilibrium state is defined by the interfacial energies between the metal, substrate, and the surrounding atmosphere, and it is described by the Young equation (Figure 2). If the surface energy of the gas-substrate interface is higher than the sum of the surface energies of substrate-metal and metal-gas interfaces, then the equilibrium state is a planar film of metal over the substrate. In most cases, however, when the substrate is of a very different nature from the film, the surface energy of the gas-substrate interface is lower than the sum and the dewetting takes place during the annealing [21, 22, 23].
On glass substrates, the dewetting of Au thin films occurs at temperatures as low as about 300°C, well below the melting temperature. Evolution of island-like structure was observed after annealing for 1 h duration, with optical and electrical properties of the material dramatically changing due to the alteration of the nanostructure [24, 25]. Later, it was found that the process is gradual and longer annealing times lead to further evolution of the structure at the same temperature . The dependence of the process on the surrounding atmosphere was proven by annealing of the layers in vacuum. The vacuum annealed layers tend to be more stable and the surface diffusion of the Au is somewhat slower . The forming Au nanostructures were used as sensitive material for detection of vapors of organic solvents due to their specific optical properties. This is possible due to the isolated island nanostructure supporting localized surface plasmon resonance, which is strongly dependent on the refractive index of the surrounding atmosphere .
3.2. Polymer substrates
Due to the demand for elastic electronics for displays , flexible solar cells,  and electronic textiles , materials consisting of thin metal films on polymer substrates have become a highly studied subject recently. In a practical application, it is necessary to assemble stable components so the devices have the required endurance.
Compared to glass, the surface of polymers has usually higher roughness, but depending on the specific polymer, the roughness can vary a lot. Due to this fact, the morphology of film sputtered on polymers is very dependent on the surface structure of the polymer. Surface structure of substrates is formed during the preparation of the polymer foil (e.g., extrusion, casting of a solution or melted polymer, rolling, and blowing). Chemical and physical properties often govern the method that can be used to prepare a sheet the polymer—for example, sheets of polytetrafluoroethylene are prepared by cutting a block of the polymer, because it cannot be mechanically formed after its polymerization . The character of functional groups on the polymer chain can also have a significant impact on the surface morphology, since it determines the polymer crystallinity . This effect can be observed during annealing of the polymer. When exceeding temperatures of secondary phase transitions of the surface morphology can be significantly altered—at temperatures over the glass transition point (
An example of polymer substrates with very different surface morphologies are polyimide (PI) and polyetheretherketone (PEEK). The polymers were used as substrates for thin Au layer deposition and subsequently annealed. In the case of the PEEK substrate, the
The PI substrate is more thermally stable and preserves its surface structure during annealing at 300°C (Figure 4). Compared to the abovementioned case of glass substrate, the solid state dewetting was not observed on the polymer substrate, probably due to much better adhesion of the Au film . Another thermally stable polymer substrate is polytetrafluoroethylene, which has a very rough surface structure. However, its surface structure can be manipulated, for example, by ion exposition in plasma discharge . An intriguing substrate to support Au layers is poly-l-lactic acid. Samples with thin films show evolution of an interesting lamellar nanostructure during annealing at 60°C, which is caused by exposing of the polymer crystallites .
4. Sputtering of noble metals onto liquid substrates
In this part of the chapter, synthesis, properties, stability, and applications of noble metals sputtered directly into liquid substrates will be discussed. Metal nanoparticles (MNPs) have broad spectrum of applications, from electronics and catalysis to drug carriers and bio-imaging. Gold NPs (Au NPs), in particular, are widely used because of their unique properties such as size, shape, optical properties, and low toxicity . NPs can be prepared by either chemical (Mie, Turkevich, Brust-Schiffrin, etc., methods) [38, 39, 40] or physical route (physical vapor deposition, laser ablation, and γ irradiation) [3, 41, 42]. The size, shape, and geometry of the NPs are strongly dependent on the employed method. Chemical synthesis offers advantages in simplicity of NP size and shape control, which enables preparation of NPs with required properties for specific application. Downside of this method is generation of harmful products and NPs with limited purity. On the other hand, the physical methods are very clean and the purity of the NPs synthesized is the same as the bulk material. In 1996 radiofrequency, sputtering of Ag NPs into a liquid substrate (silicone oil) was performed for the first time [3, 43]. However, silicone oil proved to be a suboptimal capping agent and thus the synthesized NPs were not sufficiently stable. After 10 years of experiments, in 2006, researchers started to use ionic liquids (ILs) as liquid substrates for preparation of noble metal nanoparticles. Apart from the ILs, there are other liquid substrates, which are suitable for preparation of NPs by physical vapor deposition (i.e., sputtering). The main condition for selecting a suitable liquid substrate is sufficiently low vapor pressure in vacuum . Vegetable oils , liquid polyethylene glycol [46, 47], molten 6-mercaptohexyltrimethylammonium bromide , and glycerol were used for preparation of MNPs . For example, Siegel et al. demonstrated that by sputtering of various noble metals spherical NPs of different sizes can be prepared: 6.1 ± 1.0 nm for Au, 4.2 ± 0.9 nm for Ag, 2.5 ± 0.6 nm for Pd, and 1.8 ± 0.4 nm for Pt . Polyethylene glycol (PEG) is one of the most commonly used stabilizing agents. It is a neutral amphiphilic polymer that gives “stealth” character to nanostructures. PEGylation of NPs is a process that introduces PEG ligands onto NPs surface. This method was introduced by Ballou et al. for the first time . PEGylation generally increases circulation of NPs in blood, decreases immunity response, and slows the cleansing by the reticuloendothelial system . PEG is versatile, inexpensive, and it has been approved by Food and Drug Administration (FDA) . Properties of PEGylated MNPs also depend on molecular weight of the liquid PEG. Slepicka et al. prepared Au and Ag NPs by sputtering into PEG with molecular weight of 200, 400, and 600 g mol−1. Since PEG-200 and PEG-600 showed lower stability during aging, only PEG-400 was used for further experiments. The prepared Au and Ag NPs were spherical with size of 7.97 ± 2.92 nm and 30–50 nm, respectively. Localized surface plasmon resonance absorption bands lied between 513 and 560 nm for Au NPs and 401–421 nm for Ag NPs .
4.1. Synthesis and properties of PEGylated gold nanoparticles
In this segment, results of our research for the preparation, properties, and examination of temperature and aging stability of gold nanoparticles (Au NPs) are presented. In many research papers, NPs synthesis is a multistep process consisting of many purification processes. In the first step, NPs are synthesized using a surfactant (e.g., citrate) as a stabilizing agent and, in the next step, the capping agent is exchanged with PEG molecules [54, 55, 56]. We present a simple, reproducible, environmentally friendly, low cost, and easily applicable approach of Au NPs preparation by direct sputtering of Au into a mixture of polyethylene glycol (PEG) and thiolated PEG (see Figure 5A). NPs consist of two components: the core and the corona, which interacts with the surrounding media (Figure 5B). The ─OH groups of PEG create hydrogen bridges with water, which leads to formation of a solvation shell and stabilization of the NPs, preventing aggregation during dissolution. A stronger stabilization is achieved with thiol groups that have good affinity to Au. In the case of thiolated PEGs, the bond between Au and the thiol group is very strong (197.4 kJ/mol) and minimizes desorption of PEG from NP surface (Figure 5C) .
Our research group prepared Au NPs by direct sputtering for 300, 900, and 1800 s into PEG (300 s—A; 900 s—B), PEG: PEG-SH (1800 s—C), PEG: PEG-S2H2 (900 s—D; 300 s—E), PEG admixed with PEG-SH (300 s—F; 900 s—G) and PEG admixed with PEG-S2H2 (300 s—H; 900 s—I). Immediately after sputtering, the PEG with Au NPs was mixed with distilled water in the volume ratio of 1:9 (PEG: water). Molecular weights of selected polyethylene glycols were: 400 g mol−1 for PEG, 800 g mol−1 for PEG-SH, and 1500 g mol−1 for PEG-S2H2, respectively. The TEM images in Figure 6 show that Au NPs were successfully prepared in all types of the capturing media. Despite the fact that the shape of Au NPs was spherical in all cases, an apparent difference in size, distribution, and concentration was detected.
The size and size distribution of individual PEGylated Au NP solutions are summarized in Table 1 and in insets in Figure 6. The direct sputtering of Au atoms into pure PEG for 300 s and 900 s led to spherical NPs with an average diameter of 5.6 and 5.9 nm. TEM images show that the nanoparticles prepared under such conditions have the worst size distribution with inclination to create agglomerates (see Figure 6A and B). The Au NPs prepared in the solution of PEG-SH had average diameter of 2.9 nm. The small size of the nanoparticles can be caused by low interfacial tension of PEG-SH and high nucleation rates or by PEG-SH slowing down the growth of the Au NPs (Figure 6C) due to high stabilization effect of thiolated PEG [3, 58]. On top of that, these NPs have a narrower size distribution and a lower tendency to aggregate. During the stabilization of Au NPs in PEG-S2H2 solution, disulfide bridges are created. Due to interaction of thiol groups, the nanoparticles have higher tendency to agglomerate (Figure 6D). In the case of Au sputtering into PEG-S2H2 for 300 s, the tendency to aggregate was less apparent and the size distribution was narrower (i.e., 3.6 ± 0.6 nm, Figure 6E). Post-deposition addition of PEG-SH improves the homogeneity of the nanoparticles in terms of size, shape, and aggregation (Figure 6F and G) and leads to a small decrease of average NP size too (see Table 1). In the case of the post-deposition PEG-S2H2 addition (Figure 6H, I and Table 1) the AuNPs size decreased as well, but the agglomeration was more noticable (Figure 6I). This behavior might be connected to the decrease of energy of the system after post-deposition addition of PEG-S2H2 compared to the energy of the system after addition of PEG-SH, and thus, the growth slowdown is more pronounced . Another reason could be the different molecule weights of the used PEG-S2H2 and PEG-SH. Sputtering of Au into thiolated PEG or its addition leads to change of the color of the solution from dark/light red to dark/light brown (depending on concentration of the Au NPs in the solution) .
|Sample||Au NP size (nm)||PDI|
|A||5.6 ± 1.8||9.2 ± 1.5||0.429|
|B||5.9 ± 0.8||8.8 ± 2.2||0.201|
|C||2.9 ± 0.4||3.0 ± 0.6||0.026|
|D||4.0 ± 1.2||4.9 ± 1.0||0.066|
|E||3.6 ± 0.6||4.3 ± 1.2||0.107|
|F||4.2 ± 0.8||5.2 ± 1.5||0.517|
|G||5.7 ± 1.3||7.0 ± 1.9||0.311|
|H||2.1 ± 0.7||4.3 ± 1.1||0.112|
|I||4.1 ± 1.3||6.5 ± 1.3||0.214|
To confirm measured dimensions of NPs obtained from TEM, dynamic light scattering (DLS) analysis was conducted. The values of nanoparticle sizes together with polydispersity index (quantifying the degree of the size dispersion) are listed in Table 1. In the case of DLS, the statistical significance of designated values of particle size is much higher because all particles in a particular sample are used for the calculation (determination). The prepared colloidal solutions have mono-nodal distribution of sizes (see Table 1), that means, they do not contain nanoparticle aggregates, which are in good agreement with TEM results (Figure 6). We believe that this discrepancy is caused by the coalescence of NPs during preparation of TEM sample for the analysis. The phenomenon probably occurs during evaporation of solution on the copper grid. To assess the monodispersity of the prepared PEGylated Au NPs, we present the results of DLS analysis in the form of intensity-esteemed distribution curve of the sizes. This curve is most sensitive to presence of agglomerates, which would not be visible in the case of transformation to other types of distribution curve (volume-esteemed or number-esteemed). Another reason for discrepancy between the DLS and the TEM results is that the DLS method is not based only on hydrodynamic average of the particles themselves, but also includes the solvation shel.l . Since the nanoparticles are stabilized with relatively long macromolecular chains, the detected NP sizes may be influenced by PEG corona. This is the reason for not using number-esteemed averages for DLS, because the calculation for this type of results may alter the output significantly. Despite some weaknesses mentioned above, the results presented on the basis of DLS correspond well with published studies .
Figure 7 shows UV-Vis spectra of Au NPs sputtered into solutions of different polyethylene glycols. Comparing absorbance of each sample, significant differences in the spectra of the PEGylated Au NPs are observed. The occurrence of a singular SPR absorption peak confirms that spherical NPs are present in all colloidal PEG solutions with size ranging between 4 and 50 nm. PEGylated Au NPs prepared by sputtering for 300 s into pure PEG exhibit a narrow SPR band (at 519 nm) with the highest UV-Vis absorption. With increasing sputtering time, the SPR band tends to get wider, which is caused by the poor size distribution of NPs. The absorption also decreases, which suggests formation of sedimentation aggregates (see Figure 6B). In contrast, SPR bands are not observed in the spectra of Au NPs sputtered for 1800 s into PEG-SH (Figure 7—line C). According to literature, the peak position and absorption of the plasmon band depend on Au NPs’ size and shape . When the diameter of spherical Au NPs is lower than 3 nm, the plasmon band disappears . Weak and broad SPR band observed for NPs stabilized with PEG-S2H2 (Figure 7—line D) might be connected to the creation of disulfide bridges, aggregation of the nanoparticles, their sedimentation and the subsequent decrease of metal concentration in the colloidal solution. The disappearance of SPR band was noticed for Au NPs obtained by sputtering for 300 s into PEG-S2H2 as well as for sample C, because their size was close to 3 nm (see Table 1). Admixing thiolated PEG in both cases of 300 s and 900 s sputtering time leads to the disappearance of SPR bands. In the literature, the SPR absorption decrease is associated with binding of stabilizing agents containing thiol groups onto NP surface [54, 63]. Higher UV-Vis absorption of sample G is caused by the higher concentration of metal in the colloid solution. If the gold is sputtered for 300 s into PEG and the PEG-S2H2 is added subsequently, the prepared nanoparticles are 2.1 nm in diameter which induce the loss of the SPR band. Another possible cause is the connection of thiol groups to the Au NPs surface . In the case of the gold sputtered for 900 s into pure PEG and subsequently mixed with PEG-S2H2, bigger nanoparticles were observed. Sputtering time of 900 s seems to be sufficient for the growth of bigger nanoparticles and, thus, the SPR band is visible in the spectrum.
Table 2 summarizes Au concentration in the solution measured by atomic absorption spectroscopy (AAS). Obtained data are in good agreement with results published by Slepicka et al.; in that, Au concentration linearly increases with the increasing sputtering time . AAS confirmed results (see above) that dithiol-stabilized Au NPs are less stable aggregates and thus lower Au concentration is observed. Since these results were examined in the case of post-deposition addition of dithiols as well, we can infer that the lower concentration of Au is not connected to different liquid substrates used in the Au sputtering. With this knowledge, we are able to prepare colloids of desired NPs’ size and concentration by managing the preparation conditions. Gold concentration in colloid solutions influences optical properties of the solutions such as color and UV-Vis absorption (see Figures 6 and 7).
|Sample||cAu (mg l−1)|
4.2. Aging and temperature stability of PEGylated gold nanoparticles
For aging and temperature stability study, we have chosen samples C and D as representatives of direct Au sputtering into PEG-SH and PEG-S2H2, respectively. Aging and temperature stability of Au colloids was studied by UV-Vis spectroscopy (see Figures 8 and 9). Aging stability was examined in the period of 0–14 days (see Figure 8). Figure 8 shows a decrease of UV-Vis absorption, which means the PEGylated Au NPs tend to slightly aggregate with aging time. Au NPs protected by PEG-SH appear to be more stable than the NPs protected by PEG-S2H2, since there are no significant changes in the UV-Vis absorption spectrum of those after 14 days of aging.
The progress in temperature stability of samples C and D is well documented by spectra in Figure 9. Immediately after the preparation of Au NPs, the samples were heated for one hour at 35, 60, 75–100°C, respectively. UV-Vis spectra measured at room temperature (RT) were used as reference. Figure 9 shows that the post-deposition heating of colloidal solution C (Au NPs stabilized by PEG-SH) at temperature 35°C induces only a mild decrease of UV-Vis absorption, which did not change with further temperature increase. The post-sputtering heating of sample D (Au NPs protected by PEG-S2H2) caused a gradual decrease of UV-Vis absorption with increasing temperature. The sample D turns out to have lower temperature stability with the tendency for aggregation compared to the sample C. The results of aging and temperature stability of Au NPs with core shielded by PEG-SH molecules (sample C) are in good agreement with data published by Hatakeyama et al. .
Hatakeyama et al. investigated the effect of temperature on the structure and growth of Au NPs prepared by sputtering method by small-angle X-ray scattering. Ionic liquid 1-buthyl-3-methylimidazolium tetrafluoroborate was used as the liquid substrate. The liquid was heated from 20 to 80°C before sputtering. It was found that the Au NP sizes (i) are uniform at constant temperature, (ii) increase as the temperature rises, and (iii) values of
4.3. Applications of PEGylated nanoparticles
Polyethylene glycol is one of the most used NP stabilizing polymer and the gold standard for “stealth” polymers in the emerging area of polymer-based drug carriers, gene vectors, imaging, therapeutic agents, bio-sensing, and tissue regeneration [65, 66].
Localized surface plasmon resonance (LSPR) is specific property of Au NPs that depends on particle size and distance between the particles. In the case of Au NPs, the absorption maximum connected to LSPR is between 500 and 550 nm. LSPR phenomenon is associated with oscillation of the electron gas due to excitation by incident light beam. This property puts the Au NPs to the forefront of interest in the area of biosensors technology. Creation of Au NPs aggregates invokes interparticle surface plasmon coupling, which leads to a dramatic change of color of the colloidal solution from red to blue. It also causes broadening of the surface plasmon resonance peak. Significant color change of colloids can be easily seen by the naked eye, without usage of any analytical method. Aggregation of Au NPs is extensively used in colorimetric detection of DNA, metal ions, proteins, toxins, and enzyme activity too [67, 68]. Kim et al. have found a simple procedure that can identify differences between normal and increased calcium ion (Ca2+) levels in serum using calsequestrin (CSQ)-immobilized Au NPs [69, 70]. Zhang et al. successfully grafted PEG-SH onto CTAB shielded gold nanorods (Au NR) and prepared uniform monolayer of Au NRs on silicon by gradual evaporation of the residual water. This approach brings a new opportunity to prepare uniform plasmonic sensing platforms due to stability of PEGylated Au NRs in the serum .
Molecular imaging is associated with processes ongoing in living organisms at cellular and molecular levels. Diseases in early stage can be identified and monitored by specific molecular-imaging agents, which are very powerful method enabling a rapid and targeted treatment. Nowadays, MRI, CT, ultrasound, optical imaging, single-photon emission computed tomography (SPECT), and positron-emission tomography (PET) are the most commonly used imaging methods . In contrast to other imaging agents, Au NPs offer better optical imaging properties because: (i) their light scattering effect is very strong, (ii) they are much brighter than chemical fluorophores, (iii) they resist photo-bleaching, and (iv) they can be easily spotted at low concentrations (10−16 M). For Au NPs-based contrast agents, the most promising imaging technique is Raman spectroscopy. Au NPs immobilized with thiolated PEG and conjugated with antibody specifically bind to the epidermal growth factor. These SERS nanoparticles for active targeting of both cancer cells and tumor xenografts were more than 200 times brighter than near-infrared-emitting quantum dots, and allowed spectroscopic detection of small tumors at a penetration depth of 1–2 cm . Silvestri et al. have synthesized Au NPs stabilized by PEG-SH and used them as CT contrast agents for
LSPR band of Au NPs leads to strong light absorption and efficient conversion of the energy into localized heat, which can be used for selective ablation of cancer cells . This procedure is called plasmonic photothermal therapy (PPT). Liu et al. have shown that the multidentate PEG ligand functionalized Au NRs can be used as an effective NIR photothermal agent for tumor ablation
Besides the PPT, PEGylated gold nanoparticles are very promising material for photodynamic therapy (PDT) drug delivery [78, 79]. NPs can be stabilized by steric repulsion to inhibit colloid aggregation in physiological conditions by using water-soluble PEG . PEGylated Au NPs show remarkable resistance in protein adsorption due to the high degree of hydration of the randomly coiled PEG molecules . According to this property, drugs carried by NPs could be shielded from being cleared/removed by the reticuloendothelial system (RES) . Therefore, the blood circulation time of NPs can be prolonged. Drug distribution
Cathode sputtering is a well-established technique for the preparation of metal nanostructures. The manipulation of the deposition parameters enable formation of precisely controlled material. For the properties of the resulting material, the proper selection of substrate is necessary. For the traditional application of the thin metal films in electronics, insulating substrates are usually necessary, of which the glass and polymer substrates are the most important. In this chapter, we have discussed the problems of glass substrates in adhesion of the metal layers and possibilities of dewetting. The polymer substrates on the other hand provide better adhesion to the metals, but surface morphology effects are more pronounced. A new and perspective branch of substrates for sputtering deposition are liquids. Therefore, this chapter provides a deeper insight into the problems of direct sputtering of noble metals into liquid substrate, i.e., preparation of NPs. Basic characteristics, technology of preparation, and applications of those materials are explained. The results of the authors’ team support the general overview. Direct sputtering of Au atoms onto PEG and thiol terminated PEG has led to successful formation of spherical NPs. The diameters of the prepared Au NPs ranged from 2.1 to 5.9 nm depending on the capturing medium. NPs smaller than 3 nm in diameter exhibited loss of SPR band because of the small NP size and/or attachment of thiolated PEG on the Au NPs’ surface. Solution of Au NPs stabilized by PEG-SH (sample C) exhibited higher time and temperature stability compared to the solution where Au NPs were stabilized by PEG-S2H2 (sample D). This colloidal solution showed the best time and temperature stability with the size of Au NPs of 2.9 nm, which can have a positive effect in biomedical use and for catalysis of chemical reactions. PEGylated NPs have huge potential in biomedical applications (drug delivery, therapy, imaging, and biosensing).
Financial support of this work under the GACR projects 17-00939S and P108/12/G108 is gratefully acknowledged.
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