An in vitro cytotoxicity of a novel pH-Sensitive lectin loaded-cockle shell-derived calcium carbonate nanoparticles against MCF-7 breast tumour cell

被引:16
作者
Mahmood, Rana, I [1 ,2 ]
Abbass, Amal Kh [1 ]
Al-Saffar, Ali Z. [3 ]
Al-Obaidi, Jameel R. [4 ]
机构
[1] Baghdad Univ, Coll Sci, Dept Biol, Baghdad, Iraq
[2] Al Nahrain Univ, Coll Engn, Dept Biomed Engn, Baghdad, Iraq
[3] Al Nahrain Univ, Coll Biotechnol, Dept Mol & Med Biotechnol, Baghdad, Iraq
[4] Univ Pendidikan Sultan Idris, Fac Sci & Math, Dept Biol, Tanjong Malim 35900, Perak, Malaysia
关键词
Agaricus bisporus; Lectin; ACC; Cytotoxicity; MCF-7;
D O I
10.1016/j.jddst.2020.102230
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The acidic microenvironment of tumour cells requires a pH-sensitive delivery mechanism for improving drug release. In this study, we investigated the feasibility of using pH-sensitive ACC nanoparticles with sustained-release performance and slow degradability as carriers for lectins isolated from edible mushroom Agaricus bisporus (ABL) that exhibited anti-proliferating effects on tumour cells. ABL was purified and characterized using ion-exchange, gel filtration chromatography, sodium dodecyl sulfate-polyacrylamide gel electrophoresis and mass spectrometry. ABL-ACC nanoparticles were synthesized through a simple precipitation process coupled with mechanical grinding. The conjugated ABL-ACC-NPs were characterized using Fourier-transform infrared spectroscopy, X-ray powder diffraction, scanning electron microscope, transmission electron microscope and zeta potential. Cytotoxicity of ABL-ACC-NPs was analyzed using methylthiazol tetrazolium assay against MCF-7 cells compared with ABL and ACC-NPs. The results indicated biostability of ACC-NPs and low toxicity toward MCF-7 cells, and induced increased reduction in MCF-7 viability compared with ABL. ABL-ACC-NPs-FITC showed fully internalization and accumulation inside the nucleus comparing with ABL-FITC which showed only accumulation around the nuclear envelope. Inclusively, conjugation of ABL with ACC-NPs has improved its cytotoxicity, enhanced its bioavailability, internalization into the tumour cells, accumulation in cell organelles which may promote cell responses and subsequently triggered cell death.
引用
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页数:14
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