A TPGS-incorporating nanoemulsion of paclitaxel circumvents drug resistance in breast cancer

被引:95
作者
Bu, Huihui [1 ]
He, Xinyu [1 ]
Zhang, Zhiwen [1 ]
Yin, Qi [1 ]
Yu, Haijun [1 ]
Li, Yaping [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, Ctr Pharmaceut, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
Paclitaxel; Self-assembly; TPGS; Nanoemulsion; Multidrug resistance; Breast cancer; OVERCOME MULTIDRUG-RESISTANCE; IN-VITRO; ANTITUMOR-ACTIVITY; TARGETED DELIVERY; P-GLYCOPROTEIN; NANOPARTICLES; MITOCHONDRIA; LIPOSOMES; BIOAVAILABILITY; DOXORUBICIN;
D O I
10.1016/j.ijpharm.2014.05.039
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Paclitaxel resistance is usually developed in clinical chemotherapy, which remains a major obstacle for successful cancer treatment. Herein, we attempted to develop a TPGS incorporating nanoemulsion of paclitaxel (NE-PTX) to circumvent the drug resistance in breast cancer. NE-PTX was prepared by a self-assembly technique and the physicochemical properties were characterized. The efficacy of NE-PTX on overcoming paclitaxel resistance was measured by in vitro and in vivo evaluation. The measured results indicated that NE-PTX was nanometer-sized droplets with the mean diameter of 24.93 +/- 3.45 nm. The IC50 value of paclitaxel in resistant MCF-7/ADR cells was greatly reduced from 101.45 mg/mL to 5.39 mg/mL, which indicated that the paclitaxel resistance was effectively reduced by NE-PTX. The reversal of paclitaxel resistance could mainly ascribe to the significant inhibition of P-gp activity and enhancement of anti-cancer activity. Moreover, the tumor volume in resistant tumor xenograft model treated with NE-PTX was only 10.06% of that of paclitaxel solution group, and the tumor inhibitory rate of NE-PTX reached 93.84%, which effectively verified the efficacy of NE-PTX on treating paclitaxel resistance. Thereby, NE-PTX could provide an effective strategy for circumventing paclitaxel resistance in breast cancer. (C) 2014 Elsevier B. V. All rights reserved.
引用
收藏
页码:206 / 213
页数:8
相关论文
共 40 条
[1]
Polyethylene glycol-phosphatidylethanolamine (PEG-PE)/vitamin E micelles for co-delivery of paclitaxel and curcumin to overcome multi-drug resistance in ovarian cancer [J].
Abouzeid, Abraham H. ;
Patel, Niravkumar R. ;
Torchilin, Vladimir P. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2014, 464 (1-2) :178-184
[2]
Design and development of paclitaxel-loaded bovine serum albumin nanoparticles for brain targeting [J].
Bansal, Amit ;
Kapoor, Deepak N. ;
Kapil, Rishi ;
Chhabra, Neha ;
Dhawan, Sanju .
ACTA PHARMACEUTICA, 2011, 61 (02) :141-156
[3]
Novel formulation approaches for optimising delivery of anticancer drugs based on P-glycoprotein modulation [J].
Bansal, Tripta ;
Akhtar, Naseem ;
Jaggi, Manu ;
Khar, Roop K. ;
Talegaonkar, Sushama .
DRUG DISCOVERY TODAY, 2009, 14 (21-22) :1067-1074
[4]
Liposomes loaded with paclitaxel and modified with novel triphenylphosphonium-PEG-PE conjugate possess low toxicity, target mitochondria and demonstrate enhanced antitumor effects in vitro and in vivo [J].
Biswas, Swati ;
Dodwadkar, Namita S. ;
Deshpande, Pranali P. ;
Torchilin, Vladimir P. .
JOURNAL OF CONTROLLED RELEASE, 2012, 159 (03) :393-402
[5]
Role of specific apoptotic pathways in the restoration of paclitaxel-induced apoptosis by valspodar in doxorubicin-resistant MCF-7 breast cancer cells [J].
Chadderton, A ;
Villeneuve, DJ ;
Gluck, S ;
Kirwan-Rhude, AF ;
Gannon, BR ;
Blais, DE ;
Parissenti, AM .
BREAST CANCER RESEARCH AND TREATMENT, 2000, 59 (03) :231-244
[6]
Improvement of cellular uptake, in vitro antitumor activity and sustained release profile with increased bioavailability from a nanoemulsion platform [J].
Choudhury, Hira ;
Gorain, Bapi ;
Karmakar, Sanmoy ;
Biswas, Easha ;
Dey, Goutam ;
Barik, Rajib ;
Mandal, Mahitosh ;
Pal, Tapan Kumar .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2014, 460 (1-2) :131-143
[7]
To exploit the tumor microenvironment: Passive and active tumor targeting of nanocarriers for anti-cancer drug delivery [J].
Danhier, Fabienne ;
Feron, Olivier ;
Preat, Veronique .
JOURNAL OF CONTROLLED RELEASE, 2010, 148 (02) :135-146
[8]
Doxorubicin and Paclitaxel-Loaded Lipid-Based Nanoparticles Overcome Multidrug Resistance by Inhibiting P-Glycoprotein and Depleting ATP [J].
Dong, Xiaowei ;
Mattingly, Cynthia A. ;
Tseng, Michael T. ;
Cho, Moo J. ;
Liu, Yang ;
Adams, Val R. ;
Mumper, Russell J. .
CANCER RESEARCH, 2009, 69 (09) :3918-3926
[9]
Targeting mitochondria for cancer therapy [J].
Fulda, Simone ;
Galluzzi, Lorenzo ;
Kroemer, Guido .
NATURE REVIEWS DRUG DISCOVERY, 2010, 9 (06) :447-464
[10]
Coadministration of Paclitaxel and Curcumin in Nanoemulsion Formulations To Overcome Multidrug Resistance in Tumor Cells [J].
Ganta, Srinivas ;
Amiji, Mansoor .
MOLECULAR PHARMACEUTICS, 2009, 6 (03) :928-939