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Synthesis and Drug Release from a PH/Temperature Sensitive Bead of Poly(N-Acryloylglycinate) and Alginate

机译:来自聚(N-丙烯酰基丙烯酸盐)和藻酸盐的pH /温度敏感珠粒合成和药物释放

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In this paper, a new pH/temperature sensitive beads with core-shelled structure, composed of sodium alginate and poly(N-acryloylglycinate), were prepared using as drug delivery carrier. Selecting indomethacin as a model drug, in vitro drug release behaviors were investigated at different temperatures, phosphate buffer solutions (PBS) and polymer content. At pH=2.1, the release amount of indomethacin loaded in the beads was only 2.46% while this value approached to 95.23% in pH=7.4 PBS. In addition, the release rate of indomethacin at 37°C is much higher than at 18°C.
机译:本文使用藻酸钠和聚(N-丙烯酰基丙烯酸盐组成的具有核壳结构的新型pH /温度敏感珠粒,用作药物递送载体制备。选择吲哚美辛作为模型药物,在不同温度下进行体外药物释放行为,磷酸盐缓冲溶液(PBS)和聚合物含量。在pH = 2.1时,珠子中装载的吲哚美辛的释放量仅为2.46%,而该值在pH = 7.4 PBS中接近95.23%。此外,在37℃下的吲哚美辛的释放速率远高于18℃。

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