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首页> 外文期刊>Bulletin of the Korean Chemical Society >Controlled Ondansetron Release Based on Hydroxyethyl Starch Hydroxyethyl Methacrylate
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Controlled Ondansetron Release Based on Hydroxyethyl Starch Hydroxyethyl Methacrylate

机译:基于羟乙基淀粉羟乙基甲基丙烯酸酯的恩丹西酮控释

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Presented study describes the synthesis of photo cross-linkable and water soluble hydroxyethyl starch hydroxyethyl methacrylate (HESHEMA) samples with different degree of substitution (DS) by functionalization of hydroxyethyl starch (HES) with hydroxyethyl methacrylate (HEMA) or hydroxyethyl methacrylate carbonylimidazole (HEMACI) in DMSO using two different routes. It was revealed that the reaction time for HESHEMA synthesis can be reduced from 5 days to 24 h by conducting the reaction at 80 oC instead of at room temperature. Solubility of HESHEMA was found to be dependent on DS which in turn was dependent on ratio between HES and HEMA or HEMACI. HESHEMA samples with DS 0.24 depicted insoluble in water, whereas the samples with DS 0.05 did not form appreciable gel. HESHEMA samples with appropriate DS were converted into hydrogels by cross-linking polymer chains under UV radiations and resulting HESHEMA hydrogels showed swelling up to 1200%. Application of HESHEMA in controlled drug delivery was investigated by diffusion based encapsulation of Ondansetron, a serotonin 5-HT3 receptor antagonist drug, mainly used for nausea and vomiting treatment.
机译:本研究描述了通过用甲基丙烯酸羟乙酯(HEMA)或甲基丙烯酸羟乙酯羰基咪唑(HEMACI)官能化羟乙基淀粉(HES)来合成具有不同取代度(DS)的光可交联和水溶性羟乙基淀粉羟甲基丙烯酸甲酯(HESHEMA)样品的方法在DMSO中使用两种不同的路线。结果表明,通过在80 oC而不是室温下进行反应,可以将HESHEMA合成的反应时间从5天减少到24 h。发现HESHEMA的溶解度取决于DS,而DS又取决于HES与HEMA或HEMACI之间的比例。 DS> 0.24的HESHEMA样品显示不溶于水,而DS <0.05的样品未形成明显的凝胶。通过在紫外线辐射下交联聚合物链,将具有适当DS的HESHEMA水凝胶转化为水凝胶,所得HESHEMA水凝胶的溶胀率高达1200%。通过色散5-羟色胺5-HT3受体拮抗剂药物Ondansetron的扩散包封研究了HESHEMA在受控药物递送中的应用,该药物主要用于恶心和呕吐治疗。

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