Deoxycholate-TPGS mixed nanomicelles for encapsulation of methotrexate with enhanced in vitro cytotoxicity on breast cancer cell lines

被引:21
作者
Bernabeu, Ezequiel [1 ,3 ]
Gonzalez, Lorena [2 ]
Cagel, Maximiliano [1 ,3 ]
Moretton, Marcela A. [1 ,3 ]
Chiappetta, Diego A. [1 ,3 ]
机构
[1] Univ Buenos Aires, Fac Farm & Bioquim, Catedra Tecnol Farmaceut 1, Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Fac Farm & Bioquim, Catedra Quim Biol, Buenos Aires, DF, Argentina
[3] Natl Sci Res Council CONICET, Buenos Aires, DF, Argentina
关键词
Methotrexate; Pralatrexate; Mixed micelles; TPGS; In vitro anti-tumoral activity; Breast cancer cell lines; CRITICAL MICELLE CONCENTRATION; DRUG-DELIVERY; MULTIDRUG-RESISTANCE; COPOLYMER MICELLES; ANTITUMOR-ACTIVITY; NANOPARTICLES; BIOAVAILABILITY; PACLITAXEL; CHITOSAN; DESIGN;
D O I
10.1016/j.jddst.2019.01.041
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Biocompatible mixed nanomicelles consisting of sodium deoxycholate and D-alpha-tocopheryl polyethylene glycol 1000 succinate have been prepared in different molar ratios (100:0, 75:25, 50:50, 25:75 and 0:100) in order to improve the aqueous solubility and in vitro anti-tumor activity of methotrexate. The nanomicelles loaded with methotrexate were prepared without using any organic solvents and characterized in terms of critical micellar concentration, particle size and drug solubilization capacity of the micellar dispersion. The optimized formulation (ratio 25:75) exhibited a spherical shape and a particle size of about 8 nm. The results of the in vitro release assay showed that the micellar system presented a sustained release behaviour compared to the solution of methotrexate. Cell viability studies in MCF-7 and MDA-MB-231 cells revealed that mixed micelles achieved lower IC50 values, in comparison to methotrexate and pralatrexate solutions. The formulated system showed a significant increase in the methotrexate cellular uptake, when compared to the free drug in both cell lines. Furthermore, hemolytic assay confirmed that methotrexate-loaded mixed micelles are compatible with red blood cells. Therefore, the mixed micelles developed in this study might be a potential nano-drug delivery system capable of overcoming in vitro resistance to methotrexate in breast cancer cells.
引用
收藏
页码:293 / 304
页数:12
相关论文
共 60 条
[21]   Functionalized Lipid-Polymer Hybrid Nanoparticles Mediated Codelivery of Methotrexate and Aceclofenac: A Synergistic Effect in Breast Cancer with Improved Pharmacokinetics Attributes [J].
Garg, Neeraj K. ;
Tyagi, Rajeev K. ;
Sharma, Gajanand ;
Jain, Ashay ;
Singh, Bhupinder ;
Jain, Sanyog ;
Kataret, O. P. .
MOLECULAR PHARMACEUTICS, 2017, 14 (06) :1883-1897
[22]   The ligand (s) anchored lipobrid nanoconstruct mediated delivery of methotrexate: an effective approach in breast cancer therapeutics [J].
Garg, Neeraj K. ;
Singh, Bhupinder ;
Kushwah, Varun ;
Tyagi, Rajeev K. ;
Sharma, Rajeev ;
Jain, Sanyog ;
Katare, Om Prakash .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2016, 12 (07) :2043-2060
[23]   Antifolates in cancer therapy: Structure, activity and mechanisms of drug resistance [J].
Gonen, Nitzan ;
Assaraf, Yehuda G. .
DRUG RESISTANCE UPDATES, 2012, 15 (04) :183-210
[24]   Poly(aspartic-acid) derivatives as polymeric micelle drug delivery systems [J].
Jiang, Tong-ying ;
Wang, Zhong-yan ;
Chen, Chuang ;
Mo, Feng-kui ;
Xu, Yan-li ;
Tang, Lin-xi ;
Liang, Ji-jun .
JOURNAL OF APPLIED POLYMER SCIENCE, 2006, 101 (05) :2871-2878
[25]   Methotrexate: a detailed review on drug delivery and clinical aspects [J].
Khan, Zulfequar Ahamad ;
Tripathi, Rahul ;
Mishra, Brahmeshwar .
EXPERT OPINION ON DRUG DELIVERY, 2012, 9 (02) :151-169
[26]   Hemocompatibility of liposomes loaded with lipophilic prodrugs of methotrexate and melphalan in the lipid bilayer [J].
Kuznetsova, Natalia R. ;
Sevrin, Chantal ;
Lespineux, David ;
Bovin, Nicolai V. ;
Vodovozova, Elena L. ;
Meszaros, Tamas ;
Szebeni, Janos ;
Grandfils, Christian .
JOURNAL OF CONTROLLED RELEASE, 2012, 160 (02) :394-400
[27]   Intrathecal chemotherapy for hematologic malignancies: drugs and toxicities [J].
Kwong, Yok-Lam ;
Yeung, Dominic Y. M. ;
Chan, Joyce C. W. .
ANNALS OF HEMATOLOGY, 2009, 88 (03) :193-201
[28]   Overcoming methotrexate resistance in breast cancer tumour cells by the use of a new cell-penetrating peptide [J].
Lindgren, M ;
Rosenthal-Aizman, K ;
Saar, K ;
Eiríksdóttir, E ;
Jiang, Y ;
Sassian, M ;
Östlund, P ;
Hällbrink, M ;
Langel, Ü .
BIOCHEMICAL PHARMACOLOGY, 2006, 71 (04) :416-425
[29]  
Lungu M., 2015, Nanoparticles' Promises and Risks, P1, DOI [DOI 10.1007/978-3-319-11728-7, 10.1007/978-3-319-11728-7]
[30]   Self-assembly in aqueous bile salt solutions [J].
Madenci, D. ;
Egelhaaf, S. U. .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2010, 15 (1-2) :109-115