A. A. Makeeva, A. S. Shumilkin, A. S. Ryzhkova, O. I. Vernaya, A. V. Shabatin, A. M. Semenov, T. I. Shabatina
{"title":"基于水解胶原蛋白的生物聚合物控释系统:冷冻成型、结构和特性","authors":"A. A. Makeeva, A. S. Shumilkin, A. S. Ryzhkova, O. I. Vernaya, A. V. Shabatin, A. M. Semenov, T. I. Shabatina","doi":"10.3103/S0027131424700147","DOIUrl":null,"url":null,"abstract":"<p>Biopolymer materials based on natural collagen (gelatin, hydrolyzed collagen) are widely used in the food, pharmaceutical, and cosmetic industries due to their low toxicity, high biocompatibility, low antigenicity, and unique mechanical and technological properties. Hydrolyzed collagen, unlike gelatin, is formed by peptides with a lower molecular weight. Its advantages are higher bioavailability and biodegradability in comparison with gelatin. In this study, biopolymer matrices containing a dioxidine antibacterial drug are obtained based on hydrolyzed collagen using low-temperature technologies. It is shown that, varying synthesis parameters such as the concentration of hydrolyzed collagen in the precursor solution (from 1 to 10%), matrix crosslinking time (0.1–24 h), and cryoforming temperature (–30 and –196°C), it is possible to change the morphology and structure of the matrix, its degradation time, and drug release time. The composition and structure of dioxidine/hydrolyzed collagen systems are characterized by SEM and IR and UV spectroscopy. The antibacterial activity of the resulting dioxidine/hydrolyzed collagen systems against <i>E. coli</i> and <i>S. aureus</i> is characterized by the disk diffusion method.</p>","PeriodicalId":709,"journal":{"name":"Moscow University Chemistry Bulletin","volume":"79 3","pages":"175 - 181"},"PeriodicalIF":0.7000,"publicationDate":"2024-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Biopolymer Controlled Release Systems Based on Hydrolyzed Collagen: Cryoforming, Structure, and Properties\",\"authors\":\"A. A. Makeeva, A. S. Shumilkin, A. S. Ryzhkova, O. I. Vernaya, A. V. Shabatin, A. M. Semenov, T. I. Shabatina\",\"doi\":\"10.3103/S0027131424700147\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Biopolymer materials based on natural collagen (gelatin, hydrolyzed collagen) are widely used in the food, pharmaceutical, and cosmetic industries due to their low toxicity, high biocompatibility, low antigenicity, and unique mechanical and technological properties. Hydrolyzed collagen, unlike gelatin, is formed by peptides with a lower molecular weight. Its advantages are higher bioavailability and biodegradability in comparison with gelatin. In this study, biopolymer matrices containing a dioxidine antibacterial drug are obtained based on hydrolyzed collagen using low-temperature technologies. It is shown that, varying synthesis parameters such as the concentration of hydrolyzed collagen in the precursor solution (from 1 to 10%), matrix crosslinking time (0.1–24 h), and cryoforming temperature (–30 and –196°C), it is possible to change the morphology and structure of the matrix, its degradation time, and drug release time. The composition and structure of dioxidine/hydrolyzed collagen systems are characterized by SEM and IR and UV spectroscopy. The antibacterial activity of the resulting dioxidine/hydrolyzed collagen systems against <i>E. coli</i> and <i>S. aureus</i> is characterized by the disk diffusion method.</p>\",\"PeriodicalId\":709,\"journal\":{\"name\":\"Moscow University Chemistry Bulletin\",\"volume\":\"79 3\",\"pages\":\"175 - 181\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2024-07-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Moscow University Chemistry Bulletin\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://link.springer.com/article/10.3103/S0027131424700147\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Moscow University Chemistry Bulletin","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.3103/S0027131424700147","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Biopolymer Controlled Release Systems Based on Hydrolyzed Collagen: Cryoforming, Structure, and Properties
Biopolymer materials based on natural collagen (gelatin, hydrolyzed collagen) are widely used in the food, pharmaceutical, and cosmetic industries due to their low toxicity, high biocompatibility, low antigenicity, and unique mechanical and technological properties. Hydrolyzed collagen, unlike gelatin, is formed by peptides with a lower molecular weight. Its advantages are higher bioavailability and biodegradability in comparison with gelatin. In this study, biopolymer matrices containing a dioxidine antibacterial drug are obtained based on hydrolyzed collagen using low-temperature technologies. It is shown that, varying synthesis parameters such as the concentration of hydrolyzed collagen in the precursor solution (from 1 to 10%), matrix crosslinking time (0.1–24 h), and cryoforming temperature (–30 and –196°C), it is possible to change the morphology and structure of the matrix, its degradation time, and drug release time. The composition and structure of dioxidine/hydrolyzed collagen systems are characterized by SEM and IR and UV spectroscopy. The antibacterial activity of the resulting dioxidine/hydrolyzed collagen systems against E. coli and S. aureus is characterized by the disk diffusion method.
期刊介绍:
Moscow University Chemistry Bulletin is a journal that publishes review articles, original research articles, and short communications on various areas of basic and applied research in chemistry, including medical chemistry and pharmacology.