Simple surface functionalization of magnetic nanoparticles with methotrexate-conjugated bovine serum albumin as a biocompatible drug delivery vehicle

被引:10
作者
Azizi, Sedigheh [1 ]
Nosrati, Hamed [1 ,2 ]
Danafar, Hossein [1 ,2 ]
机构
[1] Zanjan Univ Med Sci, Zanjan Pharmaceut Nanotechnol Res Ctr, Zanjan, Iran
[2] Zanjan Univ Med Sci, Sch Pharm, Dept Pharmaceut Biomat, Zanjan, Iran
关键词
bovine serum albumin (BSA); enzyme-dependent release; magnetic nanoparticles; methotrexate (MTX); protein-based vehicle; IRON-OXIDE NANOPARTICLES; SUPERPARAMAGNETIC NANOPARTICLES; CANCER; MICELLES; RELEASE; COMBINATION; THERAPY; ENHANCE;
D O I
10.1002/aoc.5479
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Magnetic nanoparticles (MNPs) functionalized with methotrexate (MTX)-conjugated bovine serum albumin (BSA) as a biocompatible drug delivery vehicle were synthesized using a facile method. Characterization of the functionalized MNPs (Fe3O4@BSA-MTX NPs) was performed using various techniques including UV-visible spectroscopy, dynamic light scattering, vibrating sample magnetometry and X-ray diffraction. The particle size and zeta potential of Fe3O4@BSA-MTX NPs were 105.7 +/- 3.81 nm (mean +/- SD) and -18.2 mV, respectively. MTX release from Fe3O4@BSA-MTX NPs showed an enzyme-dependent release pattern. Hemo-biocompatibility of Fe3O4@BSA-MTX NPs was confirmed using hemolysis test. In addition, the cytotoxicity of functionalized MNPs and free MTX against MCF-7 cell line was investigated using MTT assay. The results of experiments revealed that the Fe3O4@BSA-MTX NPs as a biocompatible carrier could improve the therapeutic effect of MTX.
引用
收藏
页数:9
相关论文
共 42 条
[1]   Strategies for Preparing Albumin-based Nanoparticles for Multifunctional Bioimaging and Drug Delivery [J].
An, Fei-Fei ;
Zhang, Xiao-Hong .
THERANOSTICS, 2017, 7 (15) :3667-3689
[2]  
Bertino JR, 1996, ONCOLOGIST, V1, P223, DOI [DOI 10.1634/THEONCOLOGIST.1-4-223, DOI 10.1002/STEM.140005]
[3]   Phase II study of MTX-HSA in combination with Cisplatin as first line treatment in patients with advanced or metastatic transitional cell carcinoma [J].
Bolling, C. ;
Graefe, T. ;
Luebbing, C. ;
Jankevicius, F. ;
Uktveris, S. ;
Cesas, A. ;
Meyer-Moldenhauer, W. -H. ;
Starkmann, H. ;
Weigel, M. ;
Burk, K. ;
Hanauske, A. -R. .
INVESTIGATIONAL NEW DRUGS, 2006, 24 (06) :521-527
[4]   An Imagable and Photothermal "Abraxane-Like" Nanodrug for Combination Cancer Therapy to Treat Subcutaneous and Metastatic Breast Tumors [J].
Chen, Qian ;
Liang, Chao ;
Wang, Chao ;
Liu, Zhuang .
ADVANCED MATERIALS, 2015, 27 (05) :903-910
[5]   Multifunctional Nanoparticles: Cost Versus Benefit of Adding Targeting and Imaging Capabilities [J].
Cheng, Zhiliang ;
Al Zaki, Ajlan ;
Hui, James Z. ;
Muzykantov, Vladimir R. ;
Tsourkas, Andrew .
SCIENCE, 2012, 338 (6109) :903-910
[6]   Magnetic nanoparticles and targeted drug delivering [J].
Chomoucka, Jana ;
Drbohlavova, Jana ;
Huska, Dalibor ;
Adam, Vojtech ;
Kizek, Rene ;
Hubalek, Jaromir .
PHARMACOLOGICAL RESEARCH, 2010, 62 (02) :144-149
[7]   Albumin-based nanoparticles as potential controlled release drug delivery systems [J].
Elzoghby, Ahmed O. ;
Samy, Wael M. ;
Elgindy, Nazik A. .
JOURNAL OF CONTROLLED RELEASE, 2012, 157 (02) :168-182
[8]   Glycyrrhetinic acid-modified PEG-PCL copolymeric micelles for the delivery of curcumin [J].
Feng, Runliang ;
Deng, Peizong ;
Song, Zhimei ;
Chu, Wei ;
Zhu, Wenxia ;
Teng, Fangfang ;
Zhou, Feilong .
REACTIVE & FUNCTIONAL POLYMERS, 2017, 111 :30-37
[9]   Polymeric micelles drug delivery system in oncology [J].
Gong, Jian ;
Chen, Meiwan ;
Zheng, Ying ;
Wang, Shengpeng ;
Wang, Yitao .
JOURNAL OF CONTROLLED RELEASE, 2012, 159 (03) :312-323
[10]  
Hajshafii P., 2014, Iran. J. Biotechnol, V12, P63