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Formulation and Physical Characterization of Bio-Degradable Chitosan-Poloxamer Gel Base for Local Drug Delivery

机译:生物降解壳聚糖 - 泊洛沙姆凝胶基碱基局部药物递送的配制和物理特征

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Objective: Thermo-modulated in-situ hydrogel (TSHG) are formulated routinely utilizing poloxamer for extended drug release. However physical properties of such formulations may have some flaws, which can be rectified using a combination of polymers with better physical properties such as chitosan. The purpose of the present study was to fabricate biodegradable chitosan-poloxamer-based in-situ drug delivery systems and assessment of their physical properties. Methods: The present chitosan-poloxamer gel base was formulated using a two-stage method. Initially, chitosan gel was prepared by dissolving 1% w/w chitosan in glacial acetic acid. The poloxamer gel was prepared using “cold method”. The final chitosan-poloxamer gel base was prepared by mixing equal amounts of both solutions and evaluated for physical and mechanical properties. Result and Discussion: The DSC thermogram demonstrated no obvious interactions among ingredients or micellization temperature. The gelation temperature of the gel was between 27 and 33sup0/supC. The pH was 7 with slight clarity. The viscosity of the gel ranged from 15.14 to 41.19 pa.s. The gel was syringable between 4-30sup0/supC and biodegradable under physiological conditions. The mean particle size of the gel under SEM was found in the range of 300-554 nm. Conclusion: After the evaluation of the formulation, it can be concluded that all the ingredients in the gel showed good compatibility with each other, which could form a stable and homogeneous gel with favorable mechanical and physical properties.
机译:目的:经常使用热调制的原位水凝胶(TSHG)用于延长药物释放泊洛沙姆。然而,这种制剂的物理性质可能具有一些缺陷,其可以使用具有更好的物理性质如壳聚糖的聚合物组合整流。本研究的目的是制造基于生物降解的壳聚糖 - 泊洛沙姆的原位药物递送系统和对其物理性质的评估。方法:使用两阶段法配制本发明的壳聚糖 - 泊洛沙姆凝胶碱。最初,通过将1%w / w壳聚糖溶解在冰醋酸中来制备壳聚糖凝胶。使用“冷法”制备泊洛沙姆凝胶。通过混合两种溶液并评价物理和机械性能来制备最终的壳聚糖 - 泊洛氧基凝胶碱。结果和讨论:DSC热图在成分或胶束化温度下显示出明显的相互作用。凝胶的凝胶化温度在27至33 0℃之间。 pH值为7,轻微清晰。凝胶的粘度范围为15.14至41.19Pa。凝胶在4-30 0 c之间的注射和在生理条件下可生物降解。 SEM下凝胶的平均粒度在300-554nm的范围内。结论:评价制剂后,可以得出结论,凝胶中的所有成分均显示彼此良好的相容性,其可以形成具有有利机械和物理性质的稳定和均匀的凝胶。

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