Folate receptor targeted delivery of paclitaxel to breast cancer cells via folic acid conjugated graphene oxide grafted methyl acrylate nanocarrier

被引:80
|
作者
Vinothini, Kandasamy [1 ]
Rajendran, Naresh Kumar [2 ]
Ramu, Andy [1 ]
Elumalai, Nandhakumar [3 ]
Rajan, Mariappan [1 ]
机构
[1] Madurai Kamaraj Univ, Biomat Med Chem Lab, Dept Nat Prod Chem, Sch Chem, Madurai 625021, Tamil Nadu, India
[2] Madurai Kamaraj Univ, Sch Chem, Dept Inorgan Chem, Madurai 625021, Tamil Nadu, India
[3] Univ Johannesburg, Fac Hlth Sci, Laser Res Ctr, ZA-2028 Johannesburg, South Africa
关键词
Breast cancer rats; Caspases; Cytotoxicity; Drug delivery; Folic acid; Graphene oxide; Nanocarrier; Paclitaxel; LACTATE-DEHYDROGENASE; CONTROLLED-RELEASE; MAMMARY-CARCINOMA; DRUG-DELIVERY; NANOPARTICLES; COMBINATION; APOPTOSIS; AGENTS; RATS;
D O I
10.1016/j.biopha.2018.12.008
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The adaptability, joint with a large surface area, electronic flexibility, high intrinsic mobility, high mechanical strength and supreme thermal conductivity have condensed graphene family materials attractive as technological tools of the drug delivery system. In this present study, investigate a modified graphene oxide-methyl acrylate (GO-g-MA) nanocarrier for targeted anti-cancer drug delivery in breast cancer cells and the GO-g-MA fascinated with folic acidas a targeting ligand to target the cancer cells. Paclitaxel (PTX) was assembled through pi-pi stacking, hydrophophic interaction on the surface of the GO-g-MA/FA carrier. Structural modification of GO-g-MA, functionalization of targeting ligands GO-g-MA/FA and drug loaded GO-g-MA/FA-PTX was characterized and confirmed through FTIR, XRD, SEM, TEM and AFM analysis. The in-vitro drug release pattern of PTX from the GO-g-MA/FA was examined in different pH ranges. An MTT assay was performed to evaluate the cytotoxicity behaviour of the carrier and PTX loaded nanocarrier in the human breast cancer cell line (MDA-MB-231). GO-g-MA/FA-PTX carrier showed that 39% of cytotoxic effect Furthermore, the in-vivo (DMBA induced breast cancer rats) studies were carried out and treatment with PTX-loaded GO-g-MA/FA nanocarrier attenuates the levels of mitochondrial citric acids enzymes to near normal.
引用
收藏
页码:906 / 917
页数:12
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