Several Dosage Forms Containing Vitamin B and Their Use in Therapy

Vitamin B plays a critical role in the synthesis of DNA and maintaining the normal functioning of tissues. Therefore, its deficiency may lead to mental problems such as depression, schizophrenia, dementia, and systemic problems such as megaloblastic anemia and peripheral neuropathy. Vitamin B deficiency may be based on nutrition, as well as the use of some drugs such as metformin and omeprazole suppress the absorption of B vitamins, which may lead to deficiency. Since B vitamin is water soluble, it cannot be stored in the body. For this reason, it should be taken continuously with food. However, in cases where the vitamin B taken with food is not sufficient for the body, it should be reinforced with drugs or dietary supplements from outside. Studies have shown that the absorption of Vitamin B is 50% higher in food supplements than in foods. It can also be used as a targeting agent in tumor therapy, due to its overexpression in some tumor cells. Due to these properties of Vitamin B, various dosage forms are being developed. In this chapter, vitamin B-containing dosage forms, their production techniques, and their use in therapy will be mentioned.

B vitamins act as coenzymes for enzymes essential for cell function. Thanks to this their function, they take place in several physiological events including glucose, various clinical symptoms such as memory impairment, dementia, delirium, peripheral neuropathy, sub-acute combined degeneration of the spinal cord, megaloblastic anemia and pancytopenia are observed [13].
However, vitamin deficiency should not be attributed only to insufficient dietary intake of vitamins. For example, cobalamin deficiency can occur due to gastric atrophy, which causes absorption problems, and the use of gastric reflux medications, which lower acid levels in the stomach [7,14].
As mentioned above, vitamin B has a protective effect in mental disorders such as schizophrenia, depression, neurological disorders such as Alzheimer's and Parkinson's, and metabolic disorders such as cardiovascular and diabetes. However, there is also the problem of absorption and stability of vitamin B. For this reason, these parameters should be taken into account when developing a formulation. In this section, the properties of various dosage forms containing vitamins belonging to the vitamin B family and the methods used during their preparation will be discussed.

Several dosage forms containing vitamin B and their use in therapy
Thiamine (vitamin B1) can improve immune system function and reduce the risk of type-2 diabetes, cardiovascular and kidney diseases, age-related, mental and neurodegenerative disorders and cancer. Therefore, its deficiency may affect the cardiovascular system, develop neuroinflammation, increase inflammation and cause atypical antibody responses [15]. Thiamine also acts as a carbonic anhydrase isoenzyme inhibitor [16,17].
Riboflavin (vitamin B2) is the precursor of flavin adenine dinucleotide (FAD+) and makes folate coenzymes stabilize the C677T variant of 5,10-methylenetetrahydrofolate reductase (C677T MTHFR) by preventing the polymorphic enzyme from displacing the flavin cofactor [18]. In combination with UV light, riboflavin causes irreversible damage to nucleic acids such as DNA and RNA, rendering microbial pathogens unable to reproduce, and in this way may be effective against MERS-CoV virus as well as SARS-CoV-2 [19].
Niacin (vitamin B3, nicotinamide) serves as the building block of NAD and nicotinamide adenine dinucleotide phosphate (NADP), which are vital in chronic systemic inflammation [20]. In this respect, it serves as the sole substrate for poly (ADP-ribose) polymerase-1 (PARP), which is required for cell differentiation, DNA repair and expression, and apoptosis [18]. Since NAD+ acts as a coenzyme in various metabolic pathways, its high levels are required to treat a variety of pathophysiological conditions. For example, NAD+ has immunomodulatory properties, is released in the early stages of inflammation, and reduces serum levels of the proinflammatory cytokines IL-1β, IL-6, and TNF-α [7,21,22]. In addition, niacin reduces neutrophil infiltration and exerts anti-inflammatory effects in patients with ventilator-induced lung injury. It has been observed that niacin and nicotinamide prevent lung tissue damage in hamsters [23]. In addition, nicotinamide reduces viral replication and strengthens the body's defense mechanisms [24,25].
Pantothenic acid (vitamin B5) has cholesterol and triglyceride lowering properties. It also speeds up wound healing, reduces inflammation and improves mental health [15]. However, there are limited studies showing its effects on the immune system [17].
Pyridoxine (vitamin B6, Pyridoxal 5 0 -phosphate) is required for the transsulfuration of vasculotoxic homocysteine and the activity of serine hydroxymethyl transferase (SHMT), which is the main entry point of one-carbon units into folatedependent one-carbon metabolism [18]. Pyridoxal 5 0 -phosphate (PLP), the active form of pyridoxine, is an essential cofactor in various inflammatory pathways and its deficiency leads to immune dysregulation. Also, thirty years ago, PLP levels were shown to reduce abnormalities in platelet aggregation and blood clot formation. During inflammation, the use of PLP increases and accordingly, its amount in the body decreases. PLP levels are low in patients with type-2 diabetes and cardiovascular disease, and the elderly [26][27][28][29]. Recently, researchers at the University of Victoria reported that pyridoxine (as well as riboflavin and folic acid) is a potent anti-inflammatory that can deactivate macrophages and monocytes, inhibit antigen-presenting cells and T cells, and upregulate the immunosuppressive cytokine IL-10 [30].
Biotin (vitamin B7) acts as a coenzyme for three important carboxylation reactions involving the conversion of pyruvate to oxalacetate, acetyl-CoA to malonyl-CoA, and propionyl-CoA to methylmalonyl-CoA in humans. These enzymes are vital in numerous metabolic processes. For example, these conversions break down food into glucose, the primary source of carbohydrates for the brain and body. Recently, the roles of biotin in cell signaling and epigenetic regulation have been recognized [31].
Folic acid (vitamin B9, folate) is an essential vitamin for DNA and protein synthesis and adaptive immune response [32]. It plays several essential and direct roles in the synthesis, repair, and expression of DNA [18]. Furin is an enzyme associated with bacterial and viral infections and is a promising target for the treatment of infections. Recently, it has been noted that folic acid can inhibit furin and thus preventing SARS-CoV-2 spike protein binding, cell entry and virus transformation [32].
Cobalamin (vitamin B12) is essential for red blood cell synthesis, nervous system health, myelin synthesis, cellular growth and rapid synthesis of DNA. Its active forms are hydroxo-, adenosyl-and methylcobalamin. Cobalamin acts as a modulator of the gut microbiota and its low levels elevate methylmalonic acid and homocysteine, resulting in increased inflammation, reactive oxygen species (ROS) and oxidative stress [22]. Hyperhomocysteinemia causes endothelial dysfunction, activation of platelet and coagulation cascades, megaloblastic anemia, disruption of myelin sheath integrity and decreased immune responses. In addition, cobalamin deficiency can cause disorders in the respiratory, gastrointestinal, and central nervous systems [17].

Preparation and characterization of the dosage forms containing vitamin B
In this title, particular attention has been given to drug delivery systems in nano/ micro size, from formulations prepared to contain various vitamins from the vitamin B family alone or in combination. Various nano/microsystems containing vitamin B are summarized in Table 1 in terms of preparation methods and characterization results. Apart from this, alternative dosage forms were also evaluated since nano/micro drug carrier systems were not encountered or rarely encountered in some vitamins.
Edible hydrogels containing thiamine were prepared by hot extrusion-based three-dimensional (3D) printing and casting method. In the 3D printing method, products are produced as three-dimensional sized on special printers by the layering of the models created in the digital environment. First of all, hydrogels containing thiamine based on agar or kappa-carrageenan were prepared at 70°C and 80°C, respectively. In the preparation of these gels, 1 M NaOH was added to the medium to protect agar, kappa-carrageenan and thiamine from degradation, and the pH was maintained at 5.5. The prepared hydrogels were filled into the syringe of the printer while they were hot, the temperature of the environment where the plate was located was adjusted to 20°C, and various formulations were prepared by changing the parameters in terms of % filling, printing speed, flow percentage and layer height. Cast samples, on the other hand, were obtained by pouring the hydrogel solutions into the mold and leaving them to gel for 2 minutes (close to the printing time) at ambient temperature. When these two preparation methods were compared in terms of hardness, Young's modulus and release rate, it was observed that cast samples were harder and had higher Young's modulus than 3D ones, while their release rate was lower. Since it is based on layering, the microstructure of 3D products differs from cast samples. Printed gels are less resistant to external damage as they are a discontinuous network with several semi-fused small meshes, while cast gels can resist greater amounts of force since they are a single continuous mesh [53]. Thiamine-containing microparticles were prepared by the self-emulsion polymerization method. According to this method, first of all, empty polycitric acid (CA), polymaleic acid (MA) or polycitric acid-co-maleic acid (CA-MA) microparticles were synthesized at 25°C using a mechanical stirrer. For this, CA or MA, or CA/MA and 20 mL of deionized water were added to the reaction vessel, and then 10% mol of N,N 0 -methylenebisacrylamide (MBA), 0.08 mL of N,N,N 0 ,N 0tetramethylethylenediamine (TEMED) and finally 3 mol% of ammonium persulfate (APS) aqueous solution were added to the reaction vessel, respectively, and finally mixed. The prepared poly(MA) or poly(CA) microparticles were washed with water and acetone and centrifuged for 20 minutes to remove the remaining chemicals without reacting. Thiamine was adsorbed to these prepared microparticles and loaded [33]. Finally, liposomes containing thiamine were prepared using lecithin, L-α-phosphatidylcholine and high-speed homogenization. Phosphatidylcholine was dissolved in chloroform and chloroform was removed with a fast evaporator to form a phosphatidylcholine layer. Thiamine solution was added to the layer and hydrated, and this mixture was homogenized at room temperature using a highspeed homogenizer. The nanoliposome solution was passed through a 0.2 μm syringe filter to collect small particles [34]. Studies as systems containing riboflavin include microparticles prepared using pea protein as carrier and transglutaminase as cross-linker. Emulsion-enzymatic gelation was preferred as the method. In this method, riboflavin was dissolved in the solution of pea proteins in phosphate buffer saline (PBS). Transglutaminase was added to this solution. The water phase thus formed was added to the preheated oil phase consisting of Mgliol under stirring. This mixture was left to incubate for a few more hours under stirring to allow gelation to occur. Microparticles formed over time were separated from the oil phase by centrifugation, washing with 2% Tween 80 solution, and filtration, respectively, and were lyophilized [35]. In addition, liposome formulations of riboflavin were prepared by the thin-film method using phosphatidylcholine and cholesterol. During the preparation, phosphatidylcholine and cholesterol were dissolved in methanol: chloroform mixture and the organic phase was removed in a rotary evaporator. The solution of riboflavin in PBS was added to the thin film and hydrated by rotation at $40°C. The centrifugally formed liposomes were removed from the dispersion medium and extruded to reduce their size [37].
Microspheres were prepared by Water/Oil/Oil (W/O/O) double emulsion solvent diffusion method using ethyl cellulose for niacin. For this, niacin and ethyl cellulose were dissolved in an acetonitrile-dichloromethane mixture and deionized water was added to this mixture under a stirrer to prepare a Water/Oil (W/O) primer emulsion. Afterwards, this emulsion was added into liquid paraffin containing Span 80 under stirring. Pet ether was then added to the double emulsion to harden the microspheres. To obtain the resulting microspheres, filtration, washing with pet ether (to remove liquid paraffin) and then drying were performed, respectively. Size, encapsulation efficiency and release studies were performed on the obtained microspheres. As the polymer-drug ratio increased up to a certain value, the encapsulation efficiency increased but decreased after a certain value. The reason for this may be that the viscosity of the solution increases due to the increase in the polymer ratio, and accordingly the formation of large polymer/ solvent droplets, in this case, the curing of the microspheres is delayed and drug diffusion occurs during [39]. Niacin microemulsions were prepared by dilution method using the triangular phase diagram. Labrasol was used as a surfactant, Peceol as cosurfactant, isopropyl myristate as oil phase and water as water phase. Dimethylformamide (DMF), propylene glycol and lauric acid were preferred as penetration enhancers. In this method, the oil phase and the surfactant: cosurfactant mixture were mixed first and then titrated with water to form microemulsions. Particle size, rheological properties, conductivity and pH, refractive index, physical stability and in vitro skin penetration studies were performed on the formulations. In these studies, the highest permeation values were obtained with DMF in pH values ranging between 4.32 and 5.09 [41].
To protect pantothenic acid from environmental factors and improve its stability, liposomes, and alginate and alginate-pectin microparticles loaded liposomes have been developed. Liposomal formulations were prepared by the proliposome method. After dissolving Phospholipon 90 G (phosphatidylcholine) in ethanol, the vitamin was added to this solution. This mixture was raised to 60°C for a few minutes and then cooled to room temperature. Liposomes were obtained by adding citric acid solution dropwise to this mixture under stirring. Microparticles were prepared using an encapsulator with a 120 mm nozzle. For liposome-loaded microparticles, the pantothenic acid-loaded liposome suspension was mixed with 3% alginate or alginate-pectin mixture at a ratio of 1:1 (v/v), then these mixtures were passed through the encapsulator and sent to a solution containing 1.5% CaCl 2 (w/v) for hardening. The formulations prepared were evaluated in terms of morphology, encapsulation efficiency and release rate. Liposomes containing encapsulated pantothenic acid showed higher stability at moderate-acidic pH (4.0). However, microencapsulation of pantothenic acid-loaded liposomes using alginate or alginate pectin mixtures did not increase the encapsulation efficiency and retention of pantothenic acid [42]. Since pantothenic acid can be used in wound healing due to its fibroblast migration and proliferation effect, silk nanofibers containing pantothenic acid have been produced. Pantothenic acid and silk fibroin were dissolved in ultrapure water and nanofibers were produced by spraying this solution in an electrospinning device at a distance of 20 cm from the collector and a rate of 0.3 mL/h. The produced nanofibers were then exposed to 75% ethanol vapor. Morphological analyzes, cell viability and antioxidant activity were examined as characterization studies [43].
Unilamellar liposomes containing pyridoxine were prepared using ethanol injection, thin film, modified thin film and reverse phase evaporation methods. In the ethanol injection method, Lipoid S 100 was dissolved in ethanol and injected dropwise into an aqueous medium containing pyridoxine under stirring. In the thin film method, Lipoid S 100 was dissolved in chloroform and the organic solvent was evaporated in a rotary evaporator at low pressure at a temperature above the phase transition temperature of the lipid. The resulting dry lipid film was hydrated with an aqueous solution of pyridoxine. In the modified thin film method, a small amount of ethanol was used to dissolve the pyridoxine. Lipoid S 100 was dissolved in this ethanolic solution and the ethanol was evaporated at reduced pressure. The resulting lipid film was hydrated with deionized water. And finally, in the reverse phase evaporation method, Lipoid S 100 was dissolved in chloroform and pyridoxine was dissolved in 10% distilled water. Then, these solutions were mixed in a bath sonicator for 5 minutes to obtain an emulsion. The organic solvent was evaporated at reduced pressure and the remainder of the aqueous phase was added. Deionized water was used instead of buffer in all methods as the dispersion medium because when the buffer is used, the electrostatic interaction between pyridoxine and liposome decreases and accordingly the encapsulation efficiency decreases [44]. Within the scope of personalized treatment, the tablet formulation containing 4 different substances (thiamine, niacin, pyridoxine and caffeine) together and in which vitamins are released rapidly and caffeine is released in a sustained was prepared using a semi-solid pneumatic activated paste extrusion 3D printer at room temperature. Weight variation, moisture content, hardness, in vitro dissolution and active ingredient content analyzes were performed on 3D tablets [54].
The tablet dosage form in the form of a combination of biotin with various vitamins and minerals, although not alone, was prepared by the researchers. Prepared as a bilayer, this tablet contains biotin (with A, D, E, C and various B vitamins) in one layer and minerals in another layer. Since the active ingredients can be included in the form of premixes, the direct tableting method was used in the preparation of bilayer tablets. For this formulation, powder blends were evaluated in terms of angle of repose, bulk density, tapped density, Hausner ratio and Carr Index, while tablets were evaluated in terms of weight uniformity, diameterthickness, friability, hardness, disintegration time and dissolution [55]. Unfortunately, no studies have been found on biotin loaded nano/microsystem formulations. However, there are studies on nano/microsystems where biotin is used as a ligand for active targeting. As an example of these; is the design of biotinconjugated sunitinib-loaded nanostructures for use in lung cancer therapy. The reason why biotin is conjugated to the surface of the nanocarrier is that it is overexpressed by various cancer cells such as lung cancer [56]. Thus, it is envisaged that the nanosystem can only be delivered to tumor cells. In this study, after the preparation of biotin-sterylamine conjugate, nanostructured lipid carriers were prepared by emulsification-solvent evaporation method. In the conjugation process, the amine group of stearylamine and the activated carboxyl group of biotin were reacted in the medium of dicyclohexylcarbodiimide (DCC) and 4-Nhydroxysuccinimide (NHS) [56]. To increase oral penetration of insulin by targeting it to enterocytes, biotin-conjugated muco-inert nanocomplexes were prepared by Cui and coworkers. Although there are many ligands such as biotin, transferrin, and folic acid in enterocytes, the reason for choosing biotin in this study is that biotin receptors are widely located on the surface of enterocytes and that it has specific intracellular traffic and basal exocytosis through the transport of sodium-dependent multivitamins. In this study, after the chitosan-biotin copolymer was synthesized, insulin-loaded and hyaluronic acid (HA) coated chitosan-biotin nanocomplexes were prepared by self-assembly method (HA was used to increase mucus penetration) [57]. Apart from these studies, there are several studies in which biotin is used in surface modification; photoactive gold nanoparticles for improving the photothermal therapy of brain cancer, liposomes for use in targeted breast cancer treatment, and polymeric micelles to release paclitaxel [58][59][60].
Folic acid-containing nanoemulsion was prepared by Assadpour and coworkers by double emulsion method to protect folic acid from environmental and production conditions. According to this method, first of all, the W/O primary microemulsion was obtained. For this, the aqueous phase consisting of folic acid solution and Span 80 was added dropwise to the oil phase consisting of canola oil at 1 000 rpm under magnetic stirring. This primer emulsion was then added to the aqueous solution containing maltodextrin-whey protein, and the Water/Oil/Water (W/O/W) double emulsion was obtained mixing with a homogenizer at 12 000 rpm-10°C for 5 min, and then in the same homogenizer at 15 000 rpm-10°C for 8 min. In this way, nanoemulsions in which folic acid is encapsulated have been obtained [47]. Pamunuwa et al., on the other hand, encapsulated folic acid into alginate-pectin nanoparticles using the ionic gelation method to provide controlled release of folic acid. Accordingly, a small amount of Span 80 and then folic acid was added to the aqueous solution of the polymer adjusted to pH 5, and the mixture was stirred at 1 500 rpm for 30 min. CaCl 2 solution was added dropwise to this solution to ensure nanoparticle formation by gelation [48]. Apart from these, various nanosystems have been developed in which folic acid is conjugated to the surface, as in biotin. The general reason for using folic acid in these studies is the widespread presence of folic acid receptors in cancer cells. Examples of these studies are doxorubicin-loaded chitosan nanospheres for use in nuclear targeted cancer therapy, spiropyran and imidazole-loaded photoactive gold nanoparticles to increase the radiosensitivity of prostate cancer cells, and chitosan-coated trans-resveratrolferulic acid-loaded solid lipid nanoparticles to act on colon cancer cells [61][62][63].
Cobalamin loaded zein microstructures were prepared by Coelho et al. using electrospinning and spray drying methods. In the electrospinning method, 3 different microstructures were obtained as film, bead and fiber, while only microparticles were obtained in spray drying. A solution of zein in ethanol was used for both methods. However, while absolute ethanol is used in spray drying, aqueous alcohol is preferred in electrospinning. The formulation solutions were prepared by adding cobalamin to the solutions of zein in alcohol [50]. As a non-invasive supporting approach in cobalamin deficiency, cobalamin-loaded buccoadhesive films were prepared using solvent casting as a method, and poly(vinyl alcohol) (PVA) and chitosan as polymers. For this, glycerin or poly(ethylene glycol) 400 (PEG 400) as a plastisizer, propylene glycol as a penetration enhancer and maleic acid for chemical polymerization were added to the PVA: chitosan solution in various proportions in addition to cobalamin. After the prepared mixture was poured into the mold, it was kept at ambient temperature for 24-48 hours to form a film. Thickness, weight variation, drug content, moisture uptake and moisture content percentage, surface pH, mechanical properties, in vitro release and mucoadhesion tests were performed on the prepared formulations. In addition, in vivo pharmacokinetic studies on rabbits showed that the AUC value of bucoadhesive films was approximately 1.5 times higher than the market preparation administered intramuscularly [64]. As with other B vitamins, cobalamin has been used in the functionalization of various nanosystems. For example, calcium phosphate nanoparticles coated with cobalamin-chitosan conjugate and sodium alginate were prepared to increase receptor-mediated endocytosis and thus absorption of insulin from epithelial cells. For this, first of all, insulin-loaded calcium phosphate nanoparticles were prepared by microemulsion method, and then layer-by-layer coating process was performed [65]. In addition, solid lipid nanoparticles loaded with amphotericin B and coated with cobalamin-stearic acid conjugate were prepared to evaluate the antileishmanial effect of amphotericin B in vitro [66].

Vitamin B use in therapy
When cobalamin is metabolically significantly deficient, the methylation process, which is also essential in the conversion of dietary folate (methyltetrahydrofolate) to its active metabolic form (tetrahydrofolate), will be disrupted and the amount of intracellular and serum homocysteine will increase. The state of hyperhomocysteinemia has a potentially toxic effect on neuron and vascular endothelium. Also, as a cofactor, cobalamin helps convert methylmalonyl CoA to succinyl-CoA. Therefore, in its deficiency, this conversion decreases and an increase in serum methylmalonic acid (MMA) occurs. As a result, a defect develops in fatty acid synthesis in neuronal membranes [13]. Because cobalamin plays a vital role in the metabolism of fatty acids, which are necessary for the protection of nerve myelin [67]. Cobalamin is essential in the synthesis of monoamines or neurotransmitters such as serotonin and dopamine, and its deficiency disrupts this synthesis [13]. Similarly, pyridoxine plays a role in the production of serotonin and norepinephrine, chemicals that transmit signals in the brain, and in the formation of myelin [67].
Diabetes mellitus is one of the most common and serious metabolic disorders characterized by hyperglycemia, altered lipid, carbohydrate and protein metabolism, leading to oxidative stress and cell death in the brain, resulting in cognitive and behavioral disorders. The disease is associated with peripheral neuropathy and dysfunctions in the central nervous system. Patients have moderate changes in memory and cognitive functions, poor motor coordination and reduced motor activity. It is also associated with progressive end-organ damage in "diabetic encephalopathy" in the central nervous system. When the role of vitamin B complex in the prevention of neuronal death is examined, it has been observed that thiamine supplementation can improve and usually completely resolve the symptoms associated with Wernicke's encephalopathy (ophthalmoplegia, ataxia and confusion triad), folic acid improves memory in the elderly, and vitamin B complex protects Purkinje neurons, which is the main relay neurons of the cerebellum and play a very important role in motor coordination and learning, from degeneration and loss in diabetes [67][68][69].
There is substantial evidence to suggest that one-carbon metabolism is associated with cardiovascular disease, and particularly stroke. A one-carbon metabolism requires adequate folate along with cobalamin, pyridoxine, and riboflavin. The suboptimal state of any of these B vitamins and/or genetic polymorphisms on Bvitamin-dependent enzymes in one-carbon metabolism may cause disruption of one-carbon metabolic pathways that can lead to adverse phenotypes even if dietary folate and vitamin B intake are adequate. However, riboflavin supplementation may offer an effective personalized approach to managing hypertension in genetically at risk individuals. In fact, according to the findings from the 5-year Chinese Stroke Primary Prevention Study (CSPPT), which included 20 702 hypertensive patients, it was observed that intervention with folic acid did not reduce blood pressure but reduced the incidence of first stroke by 21% [70].
Because neuropathic pain that develops after nerve injury is severe and persistent, current drugs and non-drug treatments cannot provide significant pain relief in most patients. In a study investigating the analgesic effects of B vitamins (thiamine, pyridoxine and cobalamin) in rats with neuropathic pain due to spinal ganglion compression (CCD) or loose ligation of the sciatic nerve (CCI), the results showed that intraperitoneal injection of thiamine/pyridoxine or cobalamin significantly reduced thermal hyperalgesia; when used in combination synergistically inhibited thermal hyperalgesia; when administered repeatedly, it provided prolonged inhibition of thermal hyperalgesia and did not affect mechanical hyperalgesia or normal pain sensation, but showed similar effects on CCD and CCIinduced hyperalgesia. In conclusion, the effects of B vitamins on pain and hyperalgesia following primary sensory neuron injury have been demonstrated, and the possible clinical use of B vitamins has been suggested in the treatment of neuropathic pain conditions following injury, inflammation, degeneration or other disorders in the nervous system for humans [11].
Because vitamin B plays a crucial role in cell function, energy metabolism and immune function, it helps activate both the hereditary and adaptive immune response, reduces proinflammatory cytokine levels, improves respiratory function, maintains endothelial integrity and prevents hypercoagulability. Because of these effects, it can be used in the prevention or reduction of COVID 19 symptoms, or in the treatment of SARS-CoV-2 infection. For this reason, the vitamin B status of COVID-19 patients can be evaluated and their existing treatments can be supplemented [17].
It is known that behavioral symptoms mimicking schizophrenia and long-term changes in brain function are observed in animals exposed to maternal deprivation (MD) during early development, and the positive effect of vitamin B complex on schizophrenia. In an experiment in Wistar rats, a decrease in long and short-term memory was observed in addition to anxiety-like behaviors in subjects exposed to maternal deprivation. However, it was determined that rats receiving vitamin B complex showed a decrease in behavioral decline, histomorphological deterioration and oxidative stress caused by MD due to the enhancement of endogenous antioxidant defense, and thus nootropic behavior and reduced anxiety. In conclusion, it has been confirmed that the vitamin B complex is neuroprotective against neuropathological changes caused by maternal deprivation [71].
Vitamin B has effects not only on humans but also on animal and plant health. For example, B vitamins mainly have an indirect effect on the immune function of the gut and their interaction with the bacterial cells and network in the gut. However, impaired redox balance and uncontrolled inflammation can often occur in pigs, especially due to rapid genetic improvement and intensive production methods. Therefore, antioxidant vitamins, such as vitamin B, can be used for the control of reactive oxygen species and peroxides and, accordingly, improved enteric immunity and inflammation control [72]. As in humans, pigs have a decrease in plasma homocysteine due to folic acid and/or cobalamin supplements (although not as much as in humans) [73,74]. To evaluate the effect of high homocysteinemia on piglets (birth to 8 weeks of age), two piglet populations with high or low homocysteinemia were used in one study. The low homocysteine group was formed by giving sows folate and cobalamin during pregnancy and lactation, and by intramuscular injection of cobalamin into piglets during lactation. As an indicator of cellmediated immunity, the proliferative response of lymphocyte to mitogen activation was investigated. However, as a positive correlation between growth rate and feed conversion (gain:feed) and plasma homocysteine was observed in piglets, young "high performance" piglets producing high levels of plasma homocysteine may appear immunologically suppressed [75] and are may be less prone to develop an optimal adaptive immune response to antigenic challenges. However, the disease resistance of high-performing piglets is also high in the clinic. This may be due to homocysteine being an important metabolite that plays a central role in the interface between transsulfuration and trans-and re-methylation, linking dietary intake of at least three B vitamins and regulation of endogenous antioxidation activity, innate and adaptive immune responses [72]. Although ultraviolet-B radiation is essential for plant growth at low doses, it can have serious adverse effects on plants at high doses. Reactive oxygen species (ROS) can form in some plants in response to UV-B, and pyridoxine is known to be a quencher of ROS [76].

Conclusions
Vitamin B is a family of vitamins that are water-soluble and cannot be accumulated and synthesized in the body, is essential for vital functions in the body, therefore it must be taken with food. It mostly functions as a coenzyme and is also responsible for DNA repair. It has antioxidant activity. It has various activities in metabolic disease, inflammatory conditions, and mental disorders such as schizophrenia, dementia, Alzheimer's. In this respect, its deficiency may trigger these conditions in people with a genetic predisposition. Also, although it can be taken with food, some gastrointestinal conditions and medications can reduce its absorption. Therefore, external reinforcement is recommended. However, effective formulations are needed due to their low in vitro stability and limited in vivo bioavailability. In this respect, it is aimed to develop nano/microsystems that are known to be more effective rather than conventional dosage forms such as tablets and capsules. However, when we look at the literature, there are not enough studies on these drug delivery systems containing vitamin B. Therefore, researchers can be advised to develop dosage forms containing vitamin B with high bioavailability and in vitro stability.