PEG functionalized selenium nanoparticles as a carrier of crocin to achieve anticancer synergism

被引:60
作者
Mary, Thottumugathu Ancil [2 ]
Shanthi, Krishnamurthy [2 ]
Vimala, Karuppaiya [1 ]
Soundarapandian, Kannan [1 ]
机构
[1] Periyar Univ, Dept Zool, Prote & Mol Cell Physiol Lab, Salem 636011, Tamil Nadu, India
[2] Bharathiar Univ, Dept Zool, Coimbatore 641046, Tamil Nadu, India
关键词
DRUG-DELIVERY; SATIVUS L; ISCHEMIA-REPERFUSION; ACTIVE CONSTITUENTS; ELEMENTAL SELENIUM; SAFFRON EXTRACT; CANCER-CELLS; HEPG2; CELLS; IN-VITRO; APOPTOSIS;
D O I
10.1039/c5ra25109e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Selenium nanoparticles (SeNPs) have garnered a great deal of attention as potential cancer therapeutic payloads. However, the in vivo targeting drug delivery has been challenging. Herein, we describe the synthesis of PEG functionalized SeNPs (PEG-SeNPs) and its use as a cancer-targeted delivery vehicle to achieve enhanced anticancer efficacy. Crocin, a major active product of saffron (dried stigmas of Crocus sativus), having many therapeutic properties was conjugated to PEG-SeNPs. PEG-SeNPs showed pH-mediated crocin release for potential cancer therapy. Crocin conjugated PEG-SeNPs exhibits unprecedented enhanced cytotoxicity toward lung cancer cells through induction of apoptosis. Furthermore, crocin conjugated PEG-SeNPs significantly inhibited in vivo tumor growth in nude mice model. This cancer-targeted design of SeNPs opens a new path for synergistic treating of cancer with higher efficacy and decreased side effects.
引用
收藏
页码:22936 / 22949
页数:14
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