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of SeNPs and other selenium drugs with the same dose of selenium.

      It was proposed that the inclusion of SeNPs in liposomes was a highly effective form of treatment for streptozotocin‐induced experimental diabetes. Liposomal forms of SeNPs made it possible to preserve the integrity of β‐cells of the pancreas followed by an increase in insulin secretion and, thus, led to reduction of blood glucose levels, suppression of oxidative stress, increase of antioxidant defense system, and inhibiting of pancreatic inflammation (Ahmed et al. 2017). Selenium nanocomposites loaded with mulberry leaf and Pueraria lobata extracts showed a slow phytomedicines release and good physiological stability in the simulated digestive fluid. These nanocomposites exert pronounced hypoglycemic effects in both normal and diabetic rats after oral administration. Ex vivo intestinal visualization showed that the nanocomposite had good permeability into the intestinal wall and the ability of transepithelial transport. It was also found that the composite improved the function of the pancreas and promoted glucose utilization by adipocytes (Deng et al. 2019).

      In recent years, SeNPs have commonly been used for the delivery of proteins and peptides. Proteins, being a kind of stabilizer, are often involved in the synthesis of SeNPs (Zhang et al. 2018). SeNPs was used for oral delivery of insulin. In this case insulin acts as a therapeutic agent and stabilizer of SeNPs and acquires the ability to avoid degradation by digestive enzymes in the gastrointestinal tract. The composite had intestinal permeability, and after oral administration it exerts significant hypoglycemic effect in both normal rats and rats with type 2 diabetes. The relative pharmacological bioavailability was up to 9.15% compared to subcutaneously injected insulin (Deng et al. 2017). SeNPs loaded with pituitary adenylate cyclase‐activating peptide resulted in increased insulin secretion and sustained hypoglycemic effect with an injection dose of 20 nmol l−1 in mice with type 2 diabetes. Repeated administration for 12 weeks significantly improved glucose and lipids profile, insulin sensitivity, and histomorphology of pancreatic and adipose tissues (Zhao et al. 2017b). Therefore, diabetes treatment can be one of the potential applications for the use of selenium nanocomposites.

      Ren et al. (2019) in a rat model of rheumatoid arthritis induced by Freund's adjuvant showed that SeNPs loaded with p‐Сoumaric acid are an effective therapeutic agent for inflammatory diseases. The data were confirmed by histological examination, the level of antioxidant enzyme activity, and inflammatory cytokines (TNF‐α, IL‐1β, IL‐6, and MCP‐1) (Ren et al. 2019). El‐Ghazaly et al. (2017) showed that nano‐Se has potential anti‐inflammatory activity against radiation‐induced inflammation in rats.

Photos depict the regenerative process during fracture (a) The control group. Bone regenerate in the upper third of the perforated fracture of the tibia. Hematoxylin and eosin. (b) Experimental group. Lack of bone regenerate in perforated fracture. Hematoxylin and eosin. (c) Experimental group. Osteoclast activation in the area of the fracture. Hematoxylin and eosin. Photos depict the effect of the nanocomposite of elemental selenium and arabinogalactan on the repair of muscle tissue when administered locally for 35 days. (a) Experimental group: Loss of cross-striations, disorientation of individual muscle fibers in the fracture zone. Hematoxylin and eosin. (b) Experimental group: Death of individual muscle fibers, infiltration of lymphocytes and macrophages in the area of the fracture. Hematoxylin and eosin.

      The electron microscope study of the muscular tissue from damaged area in animals after introduction of the selenium nanocomposite has shown that the muscular tissue is considerably changed compared to the control group. Areas of abnormal orientation of muscular fibers were revealed, Z‐lines were considerably curved, I‐bands were expanded, and contractile proteins were degradable. Nuclei of myocyte were of irregular shape with clearing zones. The biotesting data indicate that local application of the nanobiocomposite of elemental selenium in the reparation area at injury of bone and muscular tissue leads to a considerably impaired reparative process of both bone and muscular tissue. Impairments of osteoreparation are expressed in osteoresorption, and slowing of bone regeneration was also observed. In our opinion, significant damage to muscle fibers of a toxic nature is observed: loss of transverse striation of muscle fibers, death of some fibers, and infiltration by lymphocytes and macrophages.

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