Nanoformulated water-soluble paclitaxel to enhance drug efficacy and reduce hemolysis side effect

被引:14
作者
Gu, Weiting [1 ]
Chen, Jie [2 ]
Patra, Prabir [3 ]
Yang, Xiaoyan [2 ]
Gu, Quanrong [2 ]
Wei, Lingxuan [1 ]
Acker, Jason P. [4 ,5 ]
Kong, Beihua [1 ]
机构
[1] Shandong Univ, Qilu Hosp, Jinan, Peoples R China
[2] Univ Alberta, Dept Biomed Engn, Edmonton, AB, Canada
[3] Univ Bridgeport, Dept Biomed Engn, Bridgeport, CT 06601 USA
[4] Canadian Blood Serv, Ctr Innovat, Edmonton, AB, Canada
[5] Univ Alberta, Dept Lab Med & Pathol, Edmonton, AB, Canada
关键词
Paclitaxel; nanoformulation; pluronic copolymer; self-assembled micelles; water-solubility; tumor suppression and hemolysis; CANCER-THERAPY; MULTIDRUG-RESISTANCE; LIPID NANOCAPSULES; POLYMERIC MICELLES; CREMOPHOR-EL; IN-VITRO; FORMULATION; DELIVERY; CELLS; NANOTECHNOLOGY;
D O I
10.1177/0885328217708458
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Surgery, chemotherapy, and radiotherapy are the three top cancer treatment modalities. Paclitaxel (PTX) is one of the most widely used chemotherapy drugs. However, its clinical applications have been significantly limited due to: (i) serious hemolysis effect of currently available commercial paclitaxel formulations and (ii) its water insolubility. An easy way to deliver paclitaxel by a new nanocarrier system using pluronic copolymers of P123/F68 and Sorbitan monopalmitate (Span 40) was reported in our previous research article. The characterization of the formulation and analysis of drug release and cellular uptake were also presented. In this article, we reported discoveries of our follow-up invivo antitumor and invitro hemolytic study discoveries. The experimental results showed that the nanoformulated PTX achieved much better tumor suppression performance while reducing hemolysis side effects. This newly formulated drug can significantly improve patient outcomes in cancer chemotherapy.
引用
收藏
页码:66 / 73
页数:8
相关论文
共 41 条
[1]   A quality monitoring program for red blood cell components: in vitro quality indicators before and after implementation of semiautomated processing [J].
Acker, Jason P. ;
Hansen, Adele L. ;
Kurach, Jayme D. R. ;
Turner, Tracey R. ;
Croteau, Ioana ;
Jenkins, Craig .
TRANSFUSION, 2014, 54 (10) :2534-2543
[2]   New frontiers in nanotechnology for cancer treatment [J].
Alexis, Frank ;
Rhee, June-Wha ;
Richie, Jerome P. ;
Radovic-Moreno, Aleksandar F. ;
Langer, Robert ;
Farokhzad, Omid C. .
UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2008, 26 (01) :74-85
[3]   Nanomedicine in cancer therapy: Innovative trends and prospects [J].
Blanco, Elvin ;
Hsiao, Angela ;
Mann, Aman P. ;
Landry, Matthew G. ;
Meric-Bernstam, Funda ;
Ferrari, Mauro .
CANCER SCIENCE, 2011, 102 (07) :1247-1252
[4]   Multifunctional Micellar Nanomedicine for Cancer Therapy [J].
Blanco, Elvin ;
Kessinger, Chase W. ;
Sumer, Baran D. ;
Gao, Jinming .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2009, 234 (02) :123-131
[5]   CDC25 phosphatases in cancer cells: key players? Good targets? [J].
Boutros, Rose ;
Lobjois, Valerie ;
Ducommun, Bernard .
NATURE REVIEWS CANCER, 2007, 7 (07) :495-507
[6]   Preparation and characterization of solid lipid nanospheres containing paclitaxel [J].
Cavalli, R ;
Caputo, O ;
Gasco, MR .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2000, 10 (04) :305-309
[7]  
Chao TC, 2005, INVEST NEW DRUG, V23, P171
[8]   Preparation, characterization and properties of sterically stabilized paclitaxel-containing liposomes [J].
Crosasso, P ;
Ceruti, M ;
Brusa, P ;
Arpicco, S ;
Dosio, F ;
Cattel, L .
JOURNAL OF CONTROLLED RELEASE, 2000, 63 (1-2) :19-30
[9]   Method for analysis of nanoparticle hemolytic properties in vitro [J].
Dobrovoiskaia, Marina A. ;
Clogston, Jeffrey D. ;
Neun, Barry W. ;
Hall, Jennifer B. ;
Patri, Anil K. ;
McNeil, Scott E. .
NANO LETTERS, 2008, 8 (08) :2180-2187
[10]   Programmed Hydrolysis in Designing Paclitaxel Prodrug for Nanocarrier Assembly [J].
Fu, Q. ;
Wang, Y. ;
Ma, Y. ;
Zhang, D. ;
Fallon, J. K. ;
Yang, X. ;
Liu, D. ;
He, Z. ;
Liu, F. .
SCIENTIFIC REPORTS, 2015, 5