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Formulation and evaluation of liposomes in carbopol gels for mixed vaginalinfections

机译:卡波姆凝胶中用于混合性阴道感染的脂质体的配制和评估

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Objective: The aim of our study was to formulate and evaluate the liposomal carrier system for the local treatment for mixed vaginal infections. The combination of voriconazole and metronidazole were selected as model drugs for mixed vaginal infections.Methods:Multi lamellar liposomescomposed phosphatidylcholine and cholesterol along with combination of drugs was prepared by the thin film hydration method. The prepared liposome were characterized for fourier transform infrared, size distribution, entrapment efficiency, in vitrorelease study in simulated vaginal fluid and stability studies.The liposomes were loaded to carbopol gel. The liposomes loaded carbopol gels were evaluated for in vitrodrugs release study and compared with control gel. Results: FTIR study indicated that there is no significant chemical interaction between the components.The cumulative percent releasefrom liposomal gels FL1 was found to be 69.90% for metronidazole and 56.02 % for voriconazole.In vitro release studies of liposomes incorporated in the carbopol gel have shown a prolonged release of entrapped metronidazole and voriconazole compared to control gel. Stability studies showed that the vesicles were stable inrefrigerated temperature (4 °C) for 60 days without significant differences in drug entrapment.Conclusion:From the results it was evident that the liposomes are capable to efficiently deliver entrapped drug for the extended period of time within a bioadhesive gel. The bioadhesive gel in combination of these two drugs is effective in more than one type of vaginal infections.
机译:目的:我们的研究目的是制定和评估脂质体载体系统,用于混合阴道感染的局部治疗。方法:用伏立康唑和甲硝唑组合作为混合型阴道感染的模型药物。方法:采用薄膜水化法制备磷脂酰胆碱和胆固醇组成的多层脂质体。对制备的脂质体进行傅立叶变换红外光谱,尺寸分布,包封率,在模拟阴道液中的体外释放研究和稳定性研究。该脂质体被加载到卡波姆凝胶中。评估脂质体载有卡波姆凝胶的体外药物释放研究,并与对照凝胶进行比较。结果:FTIR研究表明各组分之间无明显的化学相互作用,甲硝唑从脂质体凝胶FL1的累积释放百分比为69.90%,伏立康唑为56.02%。卡波普凝胶中掺入脂质体的体外释放研究表明与对照凝胶相比,捕获的甲硝唑和伏立康唑的释放时间更长。稳定性研究表明,该囊泡在60°C的稳定冷藏温度下保持60天没有明显的药物截留差异。结论:从结果可以明显看出,脂质体能够在一段较长的时间内有效地释放被包裹的药物生物粘附凝胶。将这两种药物结合使用的生物粘附凝胶对一种以上类型的阴道感染有效。

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