Targeted Cancer Therapy With Novel High Drug-Loading Nanocrystals

被引:145
作者
Liu, Feng [1 ]
Park, Ji-Young [1 ]
Zhang, Yong [1 ]
Conwell, Christine [1 ]
Liu, Yang [1 ]
Bathula, Surendar Reddy [1 ]
Huang, Leaf [1 ]
机构
[1] Univ N Carolina, Div Mol Pharmaceut, Eshelman Sch Pharm, Chapel Hill, NC 27599 USA
关键词
target; nanocrystal; high drug loading; cancer therapy; P-GLYCOPROTEIN; PACLITAXEL; MICELLES; DELIVERY; FORMULATION; RESISTANCE; GROWTH; TAXOL;
D O I
10.1002/jps.22112
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A novel nanocrystal formulation of hydrophobic drugs has been developed for cancer therapy The new method, called a three-phase nanoparticle engineering technology (3PNET), includes three phases: phase 1, amorphous precipitate; phase 2, hydrated amorphous aggregate; and phase 3, stabilized nanocrystal The 3PNET has been applied to two anticancer drugs, paclitaxel (PTX) and camptothecin (CPT), using Pluronic F127 (F127) polymer as a single excipient. The nanocrystals encapsulated over 99% of the drug with a high ratio of drug to excipient The nanocrystal formulation of PTX did not induce hemolysis at pharmacologically relevant concentrations. Antitumor activity in two tumor models, human lung cancer and murine breast cancer, demonstrated that intravenously injected nanocrystals significantly inhibited the tumor growth. The nanocrystals also showed significant therapeutic effects via oral administration In addition, the nanocrystals could be further modified for targeted delivery of PTX by conjugating a folate ligand to F127. The new nanomedicine formulations show clear potential for clinical development because of the excellent antitumor activity, low toxicity, and the ease of scale-up manufacture The formulation method may apply to other hydrophobic drugs (C) 2010 Wiley-Liss, Inc and the American Pharmacists Association J Pharm Sci 99 3542-3551,2010
引用
收藏
页码:3542 / 3551
页数:10
相关论文
共 27 条
[1]  
Abeylath SC, 2008, EXPERT OPIN DRUG DEL, V5, P931, DOI [10.1517/17425247.5.9.931, 10.1517/17425247.5.9.931 ]
[2]   Patents and nanomedicine [J].
Bawa, Raj .
NANOMEDICINE, 2007, 2 (03) :351-374
[3]   A PRELIMINARY RISK-BENEFIT ASSESSMENT OF PACLITAXEL [J].
BITTON, RJ ;
FIGG, WD ;
REED, E .
DRUG SAFETY, 1995, 12 (03) :196-208
[4]   Conditioning following powder micronization:: Influence on particle growth of salbutamol sulfate [J].
Brodka-Pfeiffer, K ;
Häusler, H ;
Grass, P ;
Langguth, P .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2003, 29 (10) :1077-1084
[5]   Polymeric micelles for drug delivery [J].
Croy, S. R. ;
Kwon, G. S. .
CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (36) :4669-4684
[6]   The effects of Pluronic block copolymers on the aggregation state of nystatin [J].
Croy, SR ;
Kwon, GS .
JOURNAL OF CONTROLLED RELEASE, 2004, 95 (02) :161-171
[7]   Polyethylene glycol-phosphatidylethanolamine conjugate (PEG-PE)-based mixed micelles: Some properties, loading with paclitaxel, and modulation of P-glycoprotein-mediated efflux [J].
Dabholkar, Rupa D. ;
Sawant, Rishikesh M. ;
Mongayt, Dimitriy A. ;
Devarajan, Padma V. ;
Torchilin, Vladimir P. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 315 (1-2) :148-157
[8]   Phase I dose escalation and pharmacokinetic study of pluronic polymer-bound doxorubicin (SP 1049C) in patients with advanced cancer [J].
Danson, S ;
Ferry, D ;
Alakhov, V ;
Margison, J ;
Kerr, D ;
Jowle, D ;
Brampton, M ;
Halbert, G ;
Ranson, M .
BRITISH JOURNAL OF CANCER, 2004, 90 (11) :2085-2091
[9]  
Dhanikula AB, 2004, AAPS J, V6
[10]  
Escobar-Chávez JJ, 2006, J PHARM PHARM SCI, V9, P339