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pH-sensitive polyelectrolyte complex gel microspheres composed of chitosan/sodium tripolyphosphate/dextran sulfate: swelling kinetics and drug delivery properties

机译:由壳聚糖/三聚磷酸钠/葡聚糖硫酸盐组成的pH敏感的聚电解质复合物凝胶微球:溶胀动力学和药物传递特性

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Porous chitosan (CS) polyelectrolyte complex (PEC) hydrogel microspheres were prepared via either wet phase-inversion or ionotropic crosslinking with sodium tripolyphosphate (Na+-TPP) and dextran sulfate (DS). The resulting microspheres were characterized using scanning electron microscopy (SEM) and elemental analysis (EA). The controlled release behavior of ibuprofen (IBU) from these microspheres was investigated. The PEC microspheres were about 700-950 mu m in diameter with large pores and open porous structure. The CS/TPP/DS microspheres resisted hydrolysis in strong acid and,biodegradation in enzymatic surroundings. The swelling kinetics for CS microspheres was close to Fickian diffusion, whereas those for CS/TPP and CS/TPP/DS were non-Fickian. Furthermore, the equilibrium water content (EWC) and water diffusion coefficient (D) increased with the pH of the media. The release profiles of IBU from CS/TPP/DS microspheres were slow in simulated gastric fluid (SGF, pH 1.4) over 3 h, but nearly all of the initial drug content was released in simulated intestinal fluid (SIF, pH 6.8) within 6 h after changing media. Overall the results demonstrated that CS/TPP/DS microspheres could successfully deliver a hydrophobic drug to the intestine without losing the drug in the stomach, and hence could be potential candidates as an orally administered drug delivery system. (c) 2005 Elsevier B.V. All rights reserved.
机译:多孔壳聚糖(CS)聚电解质复合物(PEC)水凝胶微球是通过湿相转化或与三聚磷酸钠(Na + -TPP)和葡聚糖硫酸盐(DS)的离子交联制备的。使用扫描电子显微镜(SEM)和元素分析(EA)对所得微球进行表征。研究了布洛芬(IBU)从这些微球的控释行为。 PEC微球的直径约为700-950μm,具有大孔和开放的多孔结构。 CS / TPP / DS微球可抵抗强酸中的水解和酶环境中的生物降解。 CS微球的溶胀动力学接近Fickian扩散,而CS / TPP和CS / TPP / DS的溶胀动力学则非Fickian。此外,平衡水含量(EWC)和水扩散系数(D)随着介质pH的增加而增加。 IBU从CS / TPP / DS微球的释放曲线在模拟胃液(SGF,pH 1.4)中持续3 h较慢,但几乎所有初始药物含量在6天内在模拟肠液(SIF,pH 6.8)中均释放h更换媒体后。总体而言,结果表明CS / TPP / DS微球可以成功地将疏水性药物输送至肠道,而不会在胃中损失药物,因此,它可能是口服给药的潜在药物。 (c)2005 Elsevier B.V.保留所有权利。

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