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    P(γ-PGA-co-NIPAAm)水凝胶对5-氟尿嘧啶药物分子的释放行为

    Release Behavior of 5-Fluorouracil Drug Molecules from P(γPGA-co-NIPAAm) Hydrogels

    • 摘要: 以γ-聚谷氨酸(γ-PGA)、N-异丙基丙烯酰胺(NIPAAm)为单体,通过自由基共聚法制备一种水凝胶缓释材料。采用扫描电镜观察水凝胶的多孔断面形貌,并研究不同温度(25 ℃和37 ℃)下水凝胶表面的亲疏水性和不同pH(2.0~10.0)时的溶胀率变化。将该共聚水凝胶用作药物缓释载体,通过紫外分光光度计法研究其对5 氟尿嘧啶(5-FU)药物分子的缓释行为。结果表明:该凝胶在酸性条件下释药速率最快,碱性条件下次之,中性条件下释放最慢,25 ℃下释放量与γ-PGA含量呈正相关,37 ℃下结果相反;该凝胶具有温度、pH双敏感性,在弱碱性条件下释放缓慢、释药量小,具有一定的靶向释药能力。

       

      Abstract: A novel hydrogel was prepared via free radical copolymerization of γ-polyglutamic acid (γ-PGA) and N isopropyl acrylamide (NIPAAm). The cross section morphology of the hydrogel was observed by Scanning Electron Microscopy (SEM). The hydrophilic hydrophobic properties at different temperature (25、37 ℃) and the swelling change in various pH ranging from 2.0 to 10.0 were studied. The hydrogels were used as the controlled release carrier for the anticancer drug 5- Fluorouracil (5-FU), of which the release behavior was studied by the UV spectrophotometric method. Results showed that the drug release rate was lower at neutral pH (7.4) than at acidic and alkaline pH. At 25 ℃, drug release rate was positively correlated with the content of γ-PGA, while at 37 ℃ the result was different. With the noticeable pH-temperature sensitivity and slower drug release rate in weakly alkaline condition, the hydrogels were proposed to be a promising material in the fields of targeted drug delivery.

       

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