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聚乙烯亚胺修饰的负载姜黄素的介孔二氧化硅纳米颗粒(MCM-41)诱导MCF-7细胞系细胞死亡。

Polyethylenimine-modified curcumin-loaded mesoporus silica nanoparticle (MCM-41) induces cell death in MCF-7 cell line.

作者信息

Harini Lakshminarasimhan, Karthikeyan Bose, Srivastava Sweta, Suresh Srinag Bangalore, Ross Cecil, Gnanakumar Georgepeter, Rajagopal Srinivasan, Sundar Krishnan, Kathiresan Thandavarayan

机构信息

Department of Biotechnology, Kalasalingam University, Krishnankoil - 626 126, Tamil Nadu, India.

Department of Translation Medicine, St. Johns National Academy of Health Sciences, Bangalore - 560 034, Karnataka, India.

出版信息

IET Nanobiotechnol. 2017 Feb;11(1):57-61. doi: 10.1049/iet-nbt.2016.0075.

Abstract

Breast cancer accounts for the first highest mortality rate in India and second in world. Though current treatment strategies are effectively killing cancer cells, they also end in causing severe side effects and drug resistance. Curcumin is a nutraceutical with multipotent activity but its insolubility in water limits its therapeutic potential as an anti-cancer drug. The hydrophilicity of curcumin could be increased by nanoformulation or changing its functional groups. In this study, curcumin is loaded on mesoporous silica nanoparticle and its anti-cancer activity is elucidated with MCF-7 cell death. Structural characteristics of Mobil Composition of Matter - 41(MCM-41) as determined by high-resolution transmission electron microscopy (HR-TEM) shows that MCM-41 size ranges from 100 to 200 nm diameters with pore size 2-10 nm for drug adsorption. The authors found 80-90% of curcumin is loaded on MCM-41 and curcumin is released efficiently at pH 3.0. The 50 µM curcumin-loaded MCM-41 induced 50% mortality of MCF-7 cells. Altogether, their results suggested that increased curcumin loading and sustained release from MCM-41 effectively decreased cell survival of MCF-7 cells in vitro.

摘要

乳腺癌在印度的死亡率位居第一,在全球位居第二。尽管目前的治疗策略能有效杀死癌细胞,但也会导致严重的副作用和耐药性。姜黄素是一种具有多种活性的营养保健品,但其在水中的不溶性限制了其作为抗癌药物的治疗潜力。可以通过纳米制剂或改变其官能团来提高姜黄素的亲水性。在本研究中,姜黄素被负载在介孔二氧化硅纳米颗粒上,并通过MCF-7细胞死亡来阐明其抗癌活性。通过高分辨率透射电子显微镜(HR-TEM)测定的Mobil Composition of Matter - 41(MCM-41)的结构特征表明,MCM-41的直径范围为100至200 nm,孔径为2至10 nm,用于药物吸附。作者发现80-90%的姜黄素被负载在MCM-41上,并且姜黄素在pH 3.0时能有效释放。负载50 μM姜黄素的MCM-41诱导了MCF-7细胞50%的死亡率。总之,他们的结果表明,增加姜黄素负载量并从MCM-41中持续释放,能有效降低体外MCF-7细胞的存活率。

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