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新型盐酸二甲双胍粘膜粘附微丸的研制

Development of novel mucoadhesive pellets of metformin hydrochloride.

作者信息

Piao Jingshu, Lee Ji-Eun, Weon Kwon-Yeon, Kim Dong-Wook, Lee Jung Suk, Park James D S, Nishiyama Yuichi, Fukui Ikuo, Kim Jin-Seok

机构信息

Sookmyung Women's University, Seoul, 140-742, Korea.

出版信息

Arch Pharm Res. 2009 Mar;32(3):391-7. doi: 10.1007/s12272-009-1312-0. Epub 2009 Apr 23.

Abstract

Mucoadhesive polymer-coated pellets containing metformin hydrochloride were prepared by the powder-layering technique using a centrifugal fluidizing (CF)-granulator. Four high-viscosity polymers were applied to make the pellets: 1) hydroxymethylcellulose (HPMC), 2) sodium alginate (Na-Alg), 3) HPMC/Carbopol, and 4) sodium carboxylmethylcellulose (Na-CMC). The physical crushing test, mucoadhesive test, zeta-potential test, in vitro release study and observation of gastroretention state of the dosage form were performed to investigate the pellets. The strong adhesive interaction between the Na-CMC-coated pellets and the mucin disc was obtained by mucoadhesive test. Na-Alg was most effective among the polymers used in changing the value of zeta potential of the mucin solution by the interaction between a polymer and a mucin particle. Results from drug dissolution study showed that over 95% of the drug from all the four pellets was released before 2 h, while Na-CMC- and Na-Alg-coated pellets showed a moderate sustained-release in SGF (simulated gastric fluid) and SIF (simulated intestine fluid), respectively. In conclusion, Na-CMC and Na-Alg seem to be promising candidates for mucoadhesive formulation and further studies to improve the sustained-release property are underway for achieving the ultimate goal of once-a-day formulation of metformin hydrochloride.

摘要

采用离心流化(CF)制粒机通过粉末分层技术制备了含盐酸二甲双胍的黏膜黏附聚合物包衣微丸。应用了四种高粘度聚合物来制备微丸:1)羟丙基甲基纤维素(HPMC)、2)海藻酸钠(Na-Alg)、3)HPMC/卡波姆,以及4)羧甲基纤维素钠(Na-CMC)。对微丸进行了物理压碎试验、黏膜黏附试验、ζ电位试验、体外释放研究以及剂型胃内滞留状态观察。通过黏膜黏附试验发现,Na-CMC包衣微丸与黏蛋白盘之间存在强烈的黏附相互作用。在通过聚合物与黏蛋白颗粒之间的相互作用改变黏蛋白溶液ζ电位值方面,Na-Alg在所使用的聚合物中最为有效。药物溶出研究结果表明,所有四种微丸中超过95%的药物在2小时前释放,而Na-CMC包衣微丸和Na-Alg包衣微丸分别在模拟胃液(SGF)和模拟肠液(SIF)中表现出适度的缓释效果。总之,Na-CMC和Na-Alg似乎是黏膜黏附制剂的有前景的候选材料,并且正在进行进一步研究以改善缓释性能,以实现盐酸二甲双胍每日一次给药剂型的最终目标。

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