罗望子胶制备的伊曲康唑微乳生物胶粘剂:体外和离体评价

K. Mali, S. Dhawale, R. Dias
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引用次数: 16

摘要

本研究旨在制备和评价含伊曲康唑(itraconazole, ITZ)微乳液(microemulsion, ME)的生物胶粘剂,并尝试考察罗罗子胶(rotind gum, TG)作为胶凝剂的适宜性。考察了ITZ在油脂、表面活性剂和助表面活性剂中的溶解度,选择了合适的组分。通过构建拟三元相图,优化了表面活性剂与助表面活性剂的配比。以肉豆肉酸异丙酯(IPM)和油酸(OA)为油相,吐温80为表面活性剂,异丙醇(IPA)为共表面活性剂,构建三元相图,得到ME区。通过定性和定量测试对优化后的酶解酶进行了表征,并将其掺入卡波醇(CBP)、黄原胶(XG)和TG的聚合物凝胶中。对ME基ITZ凝胶的pH、药物含量、黏度、体外生物黏附性、铺展性和体外药物释放度进行了评价。此外,利用琼脂杯扩散技术对白色念珠菌培养物进行了抗真菌活性测定。在IPM与OA(1:1)的混合物中,ITZ的溶解度最大。以IPM和OA为油相,Tween 80为表面活性剂,异丙醇(IPA)为助表面活性剂,质量比为10:45:45,得到稳定的ME。优化后的ME基凝胶的pH值为6.11 ~ 6.48,涂胶性能为4.1 ~ 7.1gm。Cm /秒,离体生物粘附在65 ~ 84gm范围内。粘度研究表明了所有基于ME的凝胶配方的假塑性行为。在所研究的ME凝胶中,含TG的凝胶在24h结束时表现出快速和完全的药物释放。含TG的配方F7具有广域抑制作用,3个月稳定。这些结果表明,含TG的ME凝胶可以作为药物局部递送的载体。
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Microemulsion based bioadhesive gel of itraconazole using tamarind gum: in-vitro and ex-vivo evaluation
The current study was aimed to formulate and evaluate bioadhesive gel containing microemulsion (ME) of itraconazole (ITZ) and an attempt was made to investigate suitability of tamarind gum (TG) as a gelling agent. The solubility of ITZ in oils, surfactants and co-surfactant was evaluated for the selection of appropriate component. The ratio of surfactant and co-surfactant was optimized by constructing pseudoternary phase diagram. Ternary phase diagram was constructed using isopropyl myristate (IPM) and oleic acid (OA) as oil phase, tween 80 as surfactant and isopropyl alcohol (IPA) as cosurfactant in order to obtain ME region. The optimized ME of ITZ was characterized by its qualitative and quantitative tests and incorporated into polymeric gels of carbopol (CBP), xanthan gum (XG) and TG. The ME based ITZ gels were evaluated for pH, drug content, viscosity, ex-vivo bioadhesion, spreadability and in vitro drug release. Furthermore, antifungal activity of the gels was performed by agar cup diffusion technique using cultures of Candida albicans. ITZ showed maximum solubility in mixture of IPM and OA (1:1). Stable ME was obtained when IPM and OA was taken in the ratio of 1:1 as oil phase, Tween 80 as surfactant and isopropyl alcohol (IPA) as cosurfactant at the weight ratio of 10:45:45. The optimized ME based gels showed pH in the range of 6.11 to 6.48, spreadability in the range of 4.1 to 7.1gm.cm/sec and ex vivo bioadhesion in the range of 65 to 84gm. The viscosity study indicated pseudoplastic behaviour of all ME based gel formulations. Amongst the studied ME gels, TG containing gels exhibited fast and complete drug release at the end of 24h. Formulation F7 containing TG showed wide zone of inhibition and found to be stable for three months. These results indicate that the TG containing ME gel may be a used as vehicle for topical delivery of drugs.
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