外用姜黄素壳聚糖纳米颗粒:配方设计、体外评价、动力学和稳定性研究

J. Nesalin, N PreethiRajM
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引用次数: 0

摘要

本研究的主要目的是评估一种制备生物黏附纳米颗粒的新方法,并设计一种创新的姜黄素局部给药系统,以提高药物的抗癌活性。采用离子凝胶法制备了姜黄素包封纳米颗粒。发现纳米颗粒是离散的,球形的,具有自由流动的特性,并对粒径分析,形状(扫描电子显微镜),药物包封效率,FTIR, DSC研究和体外释放性能进行了评估。选择最佳的纳米颗粒配方(FS5,含药与聚合物比1:5)与生物黏附聚合物结合成凝胶。对纳米胶囊外用凝胶的pH、铺展性、挤压性、黏度、体外释药、释药动力学、生物黏附试验、加速稳定性等进行了评价。选择的纳米胶囊生物黏附外用凝胶(FS3凝胶,含有1% w/w的载药纳米颗粒和0.6% w/w的卡波波尔934)的体外药物释放率可控制姜黄素的释放12小时。然后对结果进行统计比较,得到满意的相关性。综上所述,纳米胶囊外用凝胶研究的制备方案可用于姜黄素外用的成功递送。
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CURCUMIN LOADED CHITOSAN NANOPARTICLES FOR TOPICAL DELIVERY: FORMULATION DESIGN, IN VITRO EVALUATION, KINETICS AND STABILITY STUDIES
The main objective of this research is to evaluate a new approach for the preparation of bio adhesive nanoparticles and to design an innovative topical delivery system for curcumin which is able to enhance the drug anticancer activity. Curcumin encapsulated nanoparticles were prepared by ionic gelation method. The nanoparticles were found to be discrete, spherical with free-flowing properties and evaluated for particle size analysis, shape (scanning electron microscopy), drug encapsulation efficiency, FTIR, DSC studies and in vitro release performance. The best selected nanoparticles formulation (FS5, containing drug: polymer ratio 1:5) was incorporated into gels with a bio adhesive polymer. The Nanoencapsulated topical gels were evaluated for pH, spreadability, extrudability, viscosity, in vitro drug release, drug release kinetics, bio adhesion test, accelerated stability of selected gel formulation. In vitro drug release rate for selected Nanoencapsulated bio adhesive topical gel (FS3 gel, containing 1 % w/w of drug loaded nanoparticles and 0.6 % w/w of Carbopol 934) was found to control curcumin release over 12h. The results were then compared statistically and obtained a satisfactory correlation. Thus, in conclusion preparation protocol of Nanoencapsulated topical gel study may be adopted for a successful delivery of Curcumin for topical use.
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