In situ synthesized BSA capped gold nanoparticles: Effective carrier of anticancer drug Methotrexate to MCF-7 breast cancer cells

被引:93
作者
Murawala, Priyanka [1 ]
Tirmale, Amruta [1 ,2 ]
Shiras, Anjali [2 ]
Prasad, B. L. V. [1 ]
机构
[1] Natl Chem Lab, Phys & Mat Chem Div, Pune 411008, Maharashtra, India
[2] NCCS, Natl Ctr Cell Sci, Pune 411007, Maharashtra, India
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2014年 / 34卷
关键词
Gold nanoparticles; Dual active agents; Bovine serum albumin; Cancer therapy; Cytotoxicity; Apoptosis; ALBUMIN-BOUND PACLITAXEL; PHASE-II TRIAL; SERUM-ALBUMIN; DESIGNING DENDRIMERS; MTX-HSA; DELIVERY; APOPTOSIS; PHARMACOKINETICS; DOXORUBICIN; LIPOSOMES;
D O I
10.1016/j.msec.2013.09.004
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The proficiency of MTX loaded BSA capped gold nanoparticles (Au-BSA-MTX) in inhibiting the proliferation of breast cancer cells MCF-7 as compared to the free drug Methotrexate (MTX) is demonstrated based on MTT and Ki-67 proliferation assays. In addition, DNA ladder gel electrophoresis studies, flow cytometry and TUNEL assay confirmed the induction of apoptosis by MTX and Au-BSA-MTX in MCF-7 cells. Notably, Au-BSA-MTX: was found to have higher cytotoxicity on MCF-7 cells compared with an equivalent dose of free MTX. The enhanced activity is attributed to the preferential uptake of Au-BSA-MTX particles by MCF-7 cells due to the presence of BSA that acts as a source of nutrient and energy to the rapidly proliferating MCF-7 cells. Moreover, the targeting ability of the drug MTX to the over expressed folate receptors on MCF-7 cells also contributes to the enhanced uptake and activity. Taken together, these results unveil that Au-BSA-MTX could be more effective than free drug for cancer treatment. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:158 / 167
页数:10
相关论文
共 63 条
[1]   Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[2]  
[Anonymous], 2008, CANC INCIDENCE MORTA
[3]  
ARENDS MJ, 1990, AM J PATHOL, V136, P593
[4]  
Baker James R Jr, 2009, Hematology Am Soc Hematol Educ Program, P708, DOI 10.1182/asheducation-2009.1.708
[5]  
BLEYER WA, 1978, CANCER-AM CANCER SOC, V41, P36, DOI 10.1002/1097-0142(197801)41:1<36::AID-CNCR2820410108>3.0.CO
[6]  
2-I
[7]   Gold nanoparticles in nanomedicine: preparations, imaging, diagnostics, therapies and toxicity [J].
Boisselier, Elodie ;
Astruc, Didier .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (06) :1759-1782
[8]   Apoptosis, cancer and cancer therapy [J].
Bold, RJ ;
Termuhlen, PM ;
McConkey, DJ .
SURGICAL ONCOLOGY-OXFORD, 1997, 6 (03) :133-142
[9]   Methotrexate-induced apoptosis is enhanced by altered expression of methylenetetrahydrofolate reductase [J].
Celtikci, Basak ;
Lawrance, Andrea K. ;
Wu, Qing ;
Rozen, Rima .
ANTI-CANCER DRUGS, 2009, 20 (09) :787-793
[10]  
Chemmanur AT, 2006, CURR OPIN INVEST DR, V7, P750