壳聚糖-pluronic纳米颗粒的开发和表征及其对MCF-7细胞的细胞毒性

Rajath Othayoth, V. Karthik, K. Santhosh Kumar
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引用次数: 3

摘要

本研究采用离子凝胶(IG)法制备了负载他莫昔芬的壳聚糖pluronic纳米颗粒。采用粒度分析、扫描电镜(SEM)、Zeta电位测量、傅里叶变换红外光谱(FT-IR)和差示扫描量热法(DSC)对纳米颗粒进行表征。在MCF-7细胞系中测定了纳米颗粒的细胞毒性。优化后的负载他莫昔芬的纳米颗粒呈球形,带正电荷,平均直径为150 ~ 300 nm。FT-IR和DSC研究发现,由于药物与纳米颗粒基质的有效相互作用,药物以无定形分散。他莫昔芬在8mg/ml时包封率最高。负载他莫昔芬的壳聚糖pluronic纳米颗粒具有良好的血液相容性,对MCF-7细胞系无毒。所有的研究结果表明,纳米颗粒可以作为一种有效的药物递送载体用于乳腺癌的治疗。
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Development and characterization of chitosan-pluronic nanoparticles for tamoxifen delivery and cytotoxicity to MCF-7 cells
In this study, tamoxifen-loaded chitosan-pluronic nanoparticles have been prepared by an ionic gelation (IG) method. Particle size analysis, Scanning electron microscopy (SEM), Zeta potential measurements, Fourier transform infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC) were used for nanoparticle characterization. The cytotoxicity of the nanoparticles was assayed in the MCF-7 cell line. The optimized tamoxifen loaded nanoparticles had a spherical shape with positive charge and mean diameter 150 to 300 nm. The FT-IR and DSC studies found that the drug was dispersed in amorphous form due to its potent interaction with nanoparticles matrix. The maximum encapsulation efficiency was obtained at 8mg/ml tamoxifen. The tamoxifen loaded chitosan-pluronic nanoparticles had good blood compatibility and the particles were nontoxic to the MCF-7 cell line. All study results suggest that the nanoparticles could be used as an effective drug delivery carrier for the breast cancer treatment.
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