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Solid Dispersions of Chitosan Glutamate for the Local Delivery of Miconazole: Characterization and In Vitro Activity

机译:壳聚糖谷氨酸盐固体分散体用于咪康唑的局部递送:表征和体外活性

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The incorporation of miconazole nitrate (MCN) in mucoadhesive microparticles made of a water-soluble chitosansalt, chitosan glutamate (CHG) was studied. These solid systems may be proposed for buccal or vaginal applicationsagainst mycotic infections, taking advantage of the muco-adhesive and permeation enhancing properties of this polymer.Two series of solid dispersions were obtained by either spray-drying and lyophilization, under different formulation variables.The in vitro release of MCN from both the series of microparticles was analyzed at pH simulating the mouth orvaginal environments. A high amount (60 to 85%) of the loaded MCN was released quickly within the first 30 min both atpH 5.0 and 6.6 from all the systems, while the release did not further increase in the following 4 h. These results suggestthat the released drug was the fraction of drug desorbed from the CHG particle surface, while a residual amount of drugremained associated or entrapped within them.An in vitro microbiological assay was carried out against different strains of Candida. MCN- CHG lyophilized solid dispersionsgave enhanced inhibitory activity on yeast growth compared to the free drug, whereas the inclusion of MCN inspray-dried microparticles generally did not improve the activity of the drug. The different physical properties of the twokinds of dispersions seemed to be at the basis of the observed different in vitro antimycotic activity.
机译:研究了硝酸咪康唑(MCN)在水溶性壳聚糖盐,壳聚糖谷氨酸盐(CHG)制成的粘膜粘附微粒中的掺入。可以利用这些聚合物的粘膜黏附和渗透增强特性,针对霉菌感染建议将这些固体体系用于颊或阴道应用。通过不同的配方变量,通过喷雾干燥和冻干获得了两种系列的固体分散体。在模拟口腔或阴道环境的pH值下,分析了这两种微粒在体外释放MCN的情况。在最初的30分钟内,pH值为5.0和6.6时,所有系统中大量(60%到85%)的MCN迅速释放,而随后的4 h释放没有进一步增加。这些结果表明释放的药物是从CHG颗粒表面解吸的药物的一部分,而残留的药物仍保留在其中或残留在其中。针对不同的念珠菌菌株进行了体外微生物学检测。与游离药物相比,MCN-CHG冻干的固体分散体对酵母的生长具有增强的抑制活性,而包含MCN喷雾干燥的微粒通常不会改善药物的活性。两种分散体的不同物理性质似乎是所观察到的不同的体外抗真菌活性的基础。

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