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

R. Mangiafico, V. Pantó, G. Puglisi, P. Furneri
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引用次数: 8

Abstract

The incorporation of miconazole nitrate (MCN) in mucoadhesive microparticles made of a water-soluble chito- san salt, chitosan glutamate (CHG) was studied. These solid systems may be proposed for buccal or vaginal applications against 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 vari- ables. The in vitro release of MCN from both the series of microparticles was analyzed at pH simulating the mouth or vaginal environments. A high amount (60 to 85%) of the loaded MCN was released quickly within the first 30 min both at pH 5.0 and 6.6 from all the systems, while the release did not further increase in the following 4 h. These results suggest that the released drug was the fraction of drug desorbed from the CHG particle surface, while a residual amount of drug remained associated or entrapped within them. An in vitro microbiological assay was carried out against different strains of Candida. MCN- CHG lyophilized solid dis- persions gave enhanced inhibitory activity on yeast growth compared to the free drug, whereas the inclusion of MCN in spray-dried microparticles generally did not improve the activity of the drug. The different physical properties of the two kinds of dispersions seemed to be at the basis of the observed different in vitro antimycotic activity.
谷氨酸壳聚糖局部递送咪康唑的固体分散体:表征和体外活性
研究了硝酸咪康唑(MCN)在水溶性甲壳素盐壳聚糖谷氨酸(CHG)粘接微粒中的掺入。这些固体系统可用于口腔或阴道应用,以对抗真菌感染,利用该聚合物的黏附性和渗透性增强特性。在不同的配方变量下,通过喷雾干燥和冻干得到了两种系列的固体分散体。在模拟口腔或阴道环境的pH下,分析了这两种微颗粒的体外释放。在pH为5.0和6.6的条件下,负载的MCN在前30分钟内迅速释放出大量(60 - 85%),而在随后的4小时内释放量没有进一步增加。这些结果表明,释放的药物是从CHG颗粒表面解吸的药物部分,而剩余的药物仍与CHG颗粒相关或被包裹在其中。对不同念珠菌进行了体外微生物学测定。与游离药物相比,MCN- CHG冻干固体分散体对酵母生长的抑制活性增强,而在喷雾干燥微颗粒中包含MCN通常不会提高药物的活性。这两种分散体的不同物理性质似乎是观察到的不同体外抗真菌活性的基础。
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