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Ellagic acid encapsulated chitosan nanoparticles for drug delivery system in human oral cancer cell line (KB)

机译:鞣花酸包封的壳聚糖纳米粒用于人类口腔癌细胞系(KB)的药物递送系统

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摘要

Ellagic acid (EA), a naturally occurring polyphenolic compound is well documented for its anticancer property in numerous pre-clinical models. The properties like poor water solubility and limited oral bio-availability of ellagic acid has hampered its clinical applications. The present study, reports the preparation of ellagic acid encapsulated chitosan nanoparticles (EA@CS-NP) by ionic gelation method as an effective drug delivery for oral cancer treatment. The synthesized ellagic acid nanoparticle is spherical shaped with an average particle size of 176nm. The drug-encapsulation and loading-efficiency of the nanoparticles were 94±1.03% and 33±2.15% respectively. The in vitro drug release profile in the PBS medium shows sustained release of EA from EA@CS-NP. Further, this study evaluates the therapeutic efficacy of EA@CS-NP in human oral cancer cell line (KB) using MTT and DNA fragmentation analysis. EA@CS-NP exhibit significant cytotoxicity in KB cells in a dose-dependent manner with a very low IC_(50) value compared to the free EA. The results of the present study strengthen our hypothesis and hope that this novel formulation could possibly overcome the current limitations of ellagic acid and can open a new avenue for oral cancer therapy.
机译:鞣花酸(EA)是一种天然存在的多酚化合物,在许多临床前模型中均已被证明具有抗癌特性。鞣花酸的水溶性差和口服生物利用度有限等特性阻碍了其临床应用。本研究报道了通过离子凝胶法制备鞣花酸包封的壳聚糖纳米粒子(EA @ CS-NP)作为有效的药物治疗口腔癌的方法。合成的鞣花酸纳米颗粒为球形,平均粒径为176nm。纳米颗粒的药物包封率和载药率分别为94±1.03%和33±2.15%。 PBS介质中的体外药物释放曲线表明EA从EA @ CS-NP持续释放。此外,这项研究使用MTT和DNA片段分析评估了EA @ CS-NP在人口腔癌细胞系(KB)中的治疗效果。与游离EA相比,EA @ CS-NP在KB细胞中以剂量依赖性方式表现出显着的细胞毒性,其IC_(50)值非常低。本研究的结果加强了我们的假设,并希望这种新颖的制剂可以克服鞣花酸的当前局限性,并可以为口腔癌治疗开辟新的途径。

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