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Potential Application of Poly(N-isopropylacrylamide) Gel Containing Polymeric Micelles to Drug Delivery Systems

机译:含聚合物胶束的聚(N-异丙基丙烯酰胺)凝胶在药物输送系统中的潜在应用

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摘要

We have investigated rapidly thermo-responsive NIPA gel containing polymer surfactant PMDP(NIPA-PMDP gel) as a potential drug carrier using (+)-L-ascorbic acid as a model drug. In theNIPA-PMDP gel system micelles of polymer surfactant PMDP are trapped by the entanglement ofpolymer chains inside the gel networks. Therefore, in principle the gel system tightly stores targeted drugin the micelles and rapidly releases controlled amount of the drug by switching on-off of external stimulisuch as temperature or infrared laser beam. In our investigation on release profile, the NIPA-PMDP gelsystem showed completely different releasing behavior from that of the conventional NIPA gel. TheNIPA-PMDP gel released rapidly all loaded (+)-L-ascorbic acid above the phase transition temperature(ca. 34 ℃), while slowly released the corresponding amount of the drug below the temperature. Incontrast, the conventional NIPA gel released more slowly limited amount of the drug above the phasetransition temperature while similarly did to the NIPA-PMDP gel below the temperature. The releaseprofile of the NIPA-PMDP gel seems to be governed by only kinetics of volume phase transition of thegel network but not by the hydrophobic domains of the micelles probably because of too hydrophilicnature of (+)-L-ascorbic acid.
机译:我们已经使用(+)-L-抗坏血酸作为模型药物,对包含聚合物表面活性剂PMDP(NIPA-PMDP凝胶)作为潜在药物载体的快速热响应NIPA凝胶进行了研究。在NIPA-PMDP凝胶体系中,聚合物表面活性剂PMDP的胶束被凝胶网络内部的聚合物链缠结捕获。因此,原则上,凝胶系统将目标药物紧密地存储在胶束中,并通过打开或关闭诸如温度或红外激光束之类的外部刺激来迅速释放受控量的药物。在我们对释放曲线的研究中,NIPA-PMDP凝胶系统显示出与常规NIPA凝胶完全不同的释放行为。 NIPA-PMDP凝胶在相变温度(约34℃)以上快速释放所有负载的(+)-L-抗坏血酸,而在该温度以下缓慢释放相应量的药物。相比之下,常规的NIPA凝胶在相变温度以上释放的药物数量有限,而在温度低于此温度下与NIPA-PMDP凝胶相似。 NIPA-PMDP凝胶的释放曲线似乎仅受凝胶网络的体积相变动力学控制,而不受胶束的疏水域控制,这可能是因为(+)-L-抗坏血酸的亲水性太强。

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  • 作者

    Yan, Hu; Tsujii, Kaoru;

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  • 年度 2005
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  • 原文格式 PDF
  • 正文语种 en
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