用于阴道局部和持续给药的原位凝胶聚合物复合材料的研制

Q2 Pharmacology, Toxicology and Pharmaceutics Drug Delivery Letters Pub Date : 2019-08-20 DOI:10.2174/2210303109666190226152857
S. S. Boregowda, Sadanand R. Maggidi, Rajamma A. Jayaramu, Nethravathi Puttegowda, Nikhat Parbin
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引用次数: 2

摘要

目前的研究工作旨在开发一种原位凝胶聚合物复合物,以在阴道中提供局部和持续的治疗剂递送。将药物凝胶注入阴道非常复杂、不方便,需要专家协助。液体制剂有可能从应用部位排出,导致疗效不佳。用于阴道腔的有效药物递送系统应该是用于应用的液体和驻留在腔中的凝胶。开发了由壳聚糖(0.8%)与β-甘油磷酸酯(15%)交联和戊二醛处理的瓜尔胶(0.2%)组成的原位凝胶。对凝胶的原位胶凝性能进行了表征。在含有衰减E的营养琼脂培养基上测试凝胶的体外药物释放模式。大肠杆菌和枯草芽孢杆菌。采用KC扩散池,以pH4.2的模拟阴道液(SVF)为扩散介质,对凝胶的体外扩散模式进行了测试。原位凝胶在35±2°C、pH 5.4和62±1.31秒内表现出最明显的溶胶-凝胶转变。聚合物复合材料的粘度在20±2°C.为51.25±3.68 CPs,在35±2中为328.56±4.16 CPs。随着交联剂β-GP浓度的增加,凝胶的凝胶化时间逐渐缩短。制剂表现出剪切稀化特性。发现这种聚合物复合物的药物释放是高度线性的,并遵循非菲克扩散机制。这种先进的热敏原位凝胶易于涂抹并在阴道腔中长时间停留。该凝胶具有粘性,可生物降解,适合在腔内进行药物控释。
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Development of an In situ Gel Polymer Composite for Local and Sustained Delivery of Drugs in Vaginal Cavity
The present research work is aimed at the development of an in situ gel polymer composite to provide local and sustained delivery of therapeutic agents in the vaginal cavity. Administration of medicated gel into a vaginal cavity is very complicated, inconvenient and needs expert assistance. There is a chance of expulsion of liquid formulation from site of application, leads to poor therapeutic efficacy. The effective drug delivery system for the vaginal cavity should be of liquid for application and gel to reside in the cavity. In situ gel composed of chitosan (0.8%) cross-linked with β-glycerol phosphate (15%) and glutaraldehyde treated guar gum (0.2%) was developed. Gel was characterized for in situ gelling properties. In vitro drug release pattern of the gel was tested on a nutrient agar medium containing attenuated E. coli and B. Subtilis. In vitro diffusion pattern of gel was tested using KC-diffusion cell with Simulated Vaginal Fluid (SVF) (pH 4.2) as the diffusion medium. In situ gel exhibited sharpest sol-gel transition at 35±2°C, at pH 5.4 in 62±1.31sec. The viscosity of polymer composite is 51.25±3.68 CPs at 20±2°C and 328.56±4.16 CPs at 35±2°C. The gelation time of gel was found to be decreasing as the concentration of cross-linking agent β-GP increased. Formulations exhibited a shear thinning property. Drug release from this polymeric composite was found to be highly linear and follows non-fickian diffusion mechanism. This advanced thermosensitive in situ gel is convenient to apply and reside in the vaginal cavity for a prolonged period of time. The gel is mucoadhesive, biodegradable and suitable for controlled drug delivery in the cavity.
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来源期刊
Drug Delivery Letters
Drug Delivery Letters Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.70
自引率
0.00%
发文量
30
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