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Formulation and evaluation of chitosan solid lipid nanoparticles of carbamazepine

机译:卡马西平壳聚糖固体脂质纳米粒的制备与评价

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摘要

The present work aims at preparing aqueous suspension of Solid lipid Nanoparticles containing Chitosan (CT) which is a biopolymer that exhibits a number of interesting properties which include controlled drug delivery. Carbamezapine (CBZ) is a lipophilic drug which shows it antiepileptic activity by inactivating sodium channels. The solid lipid Nanoparticles (SLN) of Chitosan-CBZ were prepared by using solvent injection method using ethanol as organic solvent. The prepared SLN formulations exhibited high encapsulation efficiency, high physical stability. The drug incorporated SLNs have demonstrated that the controlled release patterns of the drug for prolonged period. The prepared SLNs were characterized for surface morphology by SEM analysis, entrapment efficiency, zeta potential, FTIR, DSC and In-vitro diffusion studies. The hydrodynamic mean diameter and zeta potential were 168.7 ±1.8?nm and ?28.9 ±2.0?mV for SLN-chitosan-CBZ respectively. Therefore chitosan-SLN can be good candidates to encapsulate CBZ and to increase its therapeutic efficacy in the treatment of Epilepsy.
机译:本工作旨在制备含有壳聚糖(CT)的固体脂质纳米颗粒的水性悬浮液,该壳聚糖是一种生物聚合物,具有许多令人关注的特性,包括受控的药物传递。卡巴氮平(CBZ)是一种亲脂性药物,可通过灭活钠通道而表现出抗癫痫活性。以乙醇为有机溶剂,采用溶剂注入法制备了壳聚糖-CBZ固体脂质纳米粒。所制备的SLN制剂表现出高封装效率,高物理稳定性。掺入药物的SLNs已证明药物的控制释放模式延长了。通过SEM分析,包封率,ζ电势,FTIR,DSC和体外扩散研究表征了制备的SLN的表面形态。 SLN-壳聚糖-CBZ的流体力学平均直径和Zeta电位分别为168.7±1.8?nm和?28.9±2.0?mV。因此,壳聚糖-SLN可能是封装CBZ并提高其在癫痫治疗中的疗效的良好候选者。

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