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首页> 外文期刊>Indian Journal of Pharmaceutical Education & Research >Formulation and Evaluation of Chitosan Based Transdermal Patches of Lornoxicam for Prolonged Drug Release and to Study the Effect of Permeation Enhancer
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Formulation and Evaluation of Chitosan Based Transdermal Patches of Lornoxicam for Prolonged Drug Release and to Study the Effect of Permeation Enhancer

机译:基于壳聚糖的氯诺昔康透皮贴剂的配制和评估,以延长药物释放时间,并研究渗透增强剂的作用

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摘要

Objective: The objectives of present investigation were to develop transdermal system for Lornoxicam using chitosan as rate controlling polymer and Tween 20 as permeation enhancer. Then evaluate the effect of Tween 20 on the physico-chemical properties of the patches and on drug permeation across the membrane. Methods: Transdermal patches of Lornoxicam were prepared by solvent casting method. The prepared patches were evaluated for physicochemical characteristics such as in vitro drug release, skin irritation studies. The interaction between drug and polymer were investigated by FTIR, DSC, XRPD methods. Results: The in vitro release studies revealed Formulation L4 containing higher concentration of Tween 20 showed 74.6 diffusion in 12 h and follows Korsmeyer-Peppas drug release kinetics. Respective formulation did not showed any sign of erythema or edema in skin irritation test. FTIR study reveals good compatibility between drug and polymer. Conclusion: The prepared transdermal drug delivery system of Lornoxicam using Chitosan had shown good promising results for sustained release matrix transdermal patch formulation.
机译:目的:本研究的目的是开发以壳聚糖为控速率聚合物,吐温20为渗透增强剂的氯诺昔康透皮系统。然后评估吐温 20 对贴片的理化性质和药物跨膜渗透的影响。方法:采用溶剂灌型法制备氯诺昔康透皮贴剂。对制备的贴剂进行物理化学特性评估,如体外药物释放、皮肤刺激研究。采用FTIR、DSC、XRPD等方法研究了药物与聚合物的相互作用。结果:体外释放研究表明,含有较高浓度吐温20的制剂L4在12 h内扩散率为74.6%,并遵循Korsmeyer-Peppas药物释放动力学。在皮肤刺激试验中,各制剂均未显示任何红斑或水肿迹象。FTIR研究揭示了药物与聚合物之间的良好相容性。结论:壳聚糖制备的氯诺昔康透皮给药系统在缓释基质透皮贴剂制剂方面显示出良好的效果。

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