首页> 外文期刊>Journal of Materials Science. Materials in Medicine >Effect of gelatin on the drug release behaviors for the organic hybrid gels based on N-isopropylacrylamide and gelatin
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Effect of gelatin on the drug release behaviors for the organic hybrid gels based on N-isopropylacrylamide and gelatin

机译:明胶对基于N-异丙基丙烯酰胺和明胶的有机杂化凝胶的释药行为的影响

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摘要

A series of organic hybrid gels were prepared based on poly(N-isopropylacrylamide), poly (NIPAAm), and gelatin. The hybrid gels were cross-linked through a two-step process with genipin or glutaraldehyde. The swelling behavior and physical properties of the gels were investigated in the previous report. In this study, we loaded sulfanilamide, caffeine, vitamin B12, phenol red, and neutral red in the hybrid gels. The effects of gelatin on the drug release profile were demonstrated. The ionicity of hybrid gels strongly influenced the release of phenol red (anionic) and neutral red (cationic). However, the releases of sulfanilamide, caffeine and vitamin B12 were not influenced by the ionicity of hybrid gel. The drug released from the gels crosslinked with genipin was significantly smaller than that released from the gels crosslinked with glutaraldehyde.
机译:基于聚(N-异丙基丙烯酰胺),聚(NIPAAm)和明胶,制备了一系列有机杂化凝胶。杂化凝胶通过二步法与Genipin或戊二醛交联。在先前的报告中研究了凝胶的溶胀行为和物理性质。在这项研究中,我们在杂化凝胶中加入了磺胺,咖啡因,维生素B12,酚红和中性红。证明了明胶对药物释放曲线的影响。杂化凝胶的离子性​​强烈影响酚红(阴离子)和中性红(阳离子)的释放。但是,杂合凝胶的离子性​​不会影响磺胺,咖啡因和维生素B12的释放。从与Genipin交联的凝胶中释放的药物明显小于从与戊二醛交联的凝胶中释放的药物。

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