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含克霉唑的口腔念珠菌病原位凝胶的制剂与评价

Formulation and Evaluation of in situ Gels Containing Clotrimazole for Oral Candidiasis.

作者信息

Harish N M, Prabhu P, Charyulu R N, Gulzar M A, Subrahmanyam E V S

机构信息

NGSM Institute of Pharmaceutical Sciences, Paneer, Deralakatte Post, Mangalore-574 160, India.

出版信息

Indian J Pharm Sci. 2009 Jul;71(4):421-7. doi: 10.4103/0250-474X.57291.

Abstract

Gel dosage forms are successfully used as drug delivery systems to control drug release and protect the medicaments from a hostile environment. The main objective is to formulate and evaluate in situ oral topical gels of clotrimazole based on the concept of pH triggered and ion activated systems. The system utilizes polymers that exhibit sol-to-gel phase transition due to change in specific physico-chemical parameters. A pH triggered system consisting of carbopol 934P (0.2-1.4% w/v) and ion triggered system using gellan gum (0.1-0.75% w/v) along with hydroxylpropylmethylcelluose E50LV was used to prolong the release of clotrimazole (0.1% w/v). Formulations were evaluated for gelling capacity, viscosity, gel strength, bioadhesive force, spreadability, microbiological studies and in vitro release. The use of carbopol as in situ gel forming system was substantiated by the property to transform into stiff gels when the pH was raised, whereas in gellan gum this transformation occurred in the presence of monovalent/divalent cations. Effect of calcium carbonate and other process parameters optimized and found that increase in calcium ions produced stronger gels. The drug content, clarity, and pH of the formulation were found to be satisfactory. The viscosity was found to be in the range 5 to 85 centipoise for the sol, whereas for the gels it was up to 16000 centipoise. The formulation showed pseudoplastic flow with thixotrophy. The maximum gel strength (using texture analyzer) and bioadhesion was found to be up to 6.5 g and 4 g, respectively. The optimized formulations were able to release the drug up to 6 h. The formulation containing gellan gum showed better sustained release compared to carbopol based gels.

摘要

凝胶剂型作为药物递送系统已成功用于控制药物释放,并保护药物免受恶劣环境的影响。主要目的是基于pH触发和离子激活系统的概念,制备并评估克霉唑的原位口服局部用凝胶。该系统利用由于特定物理化学参数变化而呈现溶胶-凝胶相变的聚合物。使用由卡波姆934P(0.2 - 1.4% w/v)组成的pH触发系统和使用结冷胶(0.1 - 0.75% w/v)以及羟丙基甲基纤维素E50LV的离子触发系统来延长克霉唑(0.1% w/v)的释放。对制剂的胶凝能力、粘度、凝胶强度、生物粘附力、铺展性、微生物学研究和体外释放进行了评估。当pH升高时,卡波姆作为原位凝胶形成系统会转变为硬凝胶,这证实了其用途,而对于结冷胶,这种转变发生在单价/二价阳离子存在的情况下。优化了碳酸钙和其他工艺参数的影响,发现钙离子增加会产生更强的凝胶。制剂的药物含量、澄清度和pH值均令人满意。溶胶的粘度范围为5至85厘泊,而凝胶的粘度高达16000厘泊。该制剂表现出具有触变性的假塑性流动。使用质构分析仪测得的最大凝胶强度和生物粘附力分别高达6.5 g和4 g。优化后的制剂能够在长达6小时内释放药物。与基于卡波姆的凝胶相比,含有结冷胶的制剂显示出更好的缓释效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dd8/2865814/9bc9277b57b4/IJPhS-71-421-g001.jpg

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