Injectable poly(organophosphazene)-camptothecin conjugate hydrogels: Synthesis, characterization, and antitumor activities

被引:34
作者
Cho, Jung-Kyo [1 ,2 ]
Chun, ChanJu [4 ]
Kuh, Hyo-Jeong [3 ]
Song, Soo-Chang [1 ]
机构
[1] Korea Inst Sci & Technol, Ctr Biomat, Biomed Res Inst, Seoul 136791, South Korea
[2] Univ Sci & Technol, Dept Biomol Sci, Taejon, South Korea
[3] Catholic Univ Korea, Dept Biomed Sci, Seoul, South Korea
[4] Chonnam Natl Univ, Coll Pharm, Kwangju, South Korea
关键词
Antitumor activity; Poly(organophosphazene); Thermosensitive hydrogel; Polymer-drug conjugate; Stability of camptothecin; POLYMER THERAPEUTICS; SPACER GROUPS; CAMPTOTHECIN; CANCER; POLYPHOSPHAZENES; EFFICACY; DELIVERY;
D O I
10.1016/j.ejpb.2012.04.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The objective of this study is to develop an effective polymer therapeutics involving camptothecin (CPT) with enhanced efficacy and lessened systemic side-toxicity for cancer treatment. Polymer-CPT conjugates (PCCs), which consisted of CPT-20-glycinate and poly(organophosphazene) bearing carboxylic acid, were synthesized, characterized for physicochemical properties, in vitro degradation and CPT release behaviors from the PCC, and evaluated their anticancer activity. The aqueous solutions of all these PCCs showed a thermo-responsive sol-gel transition behavior for injectable application near room temperature. The CPT incorporated into the hydrogel was proven to be stable in vitro over 15 days. The in vitro cytotoxicity of the PCC was verified to be effective against four kinds of human cancer cell lines. The in vivo anticancer activity study with HT-29 colon cancer cell xenografted mice showed that the intratumorally injected PCC hydrogel inhibited the tumor growth more effectively relative to CPT alone (-29% vs. 130% in tumor size). Crown Copyright (C) 2012 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:582 / 590
页数:9
相关论文
共 31 条
[1]   Ion and pH Effect on the Lower Critical Solution Temperature Phase Behavior in Neutral and Acidic Poly(organophosphazene) Counterparts [J].
Ahn, Sungsook ;
Monge, Estela C. ;
Song, Soo-Chang .
LANGMUIR, 2009, 25 (04) :2407-2418
[2]   POLY[(AMINO-ACID-ESTER)PHOSPHAZENES] - SYNTHESIS, CRYSTALLINITY, AND HYDROLYTIC SENSITIVITY IN SOLUTION AND THE SOLID-STATE [J].
ALLCOCK, HR ;
PUCHER, SR ;
SCOPELIANOS, AG .
MACROMOLECULES, 1994, 27 (05) :1071-1075
[3]  
[Anonymous], 1961, CHEM AMINO ACIDS
[4]   Synthesis and characterization of biodegradable thermosensitive neutral and acidic poly(organophosphazene) gels bearing carboxylic acid group [J].
Cho, Jung-Kyo ;
Lee, Sun Mi ;
Kim, Chang Won ;
Song, Soo-Chang .
JOURNAL OF POLYMER RESEARCH, 2011, 18 (04) :701-713
[5]   Doxorubicin-polyphosphazene conjugate hydrogels for locally controlled delivery of cancer therapeutics [J].
Chun, ChangJu ;
Lee, Sun M. ;
Kim, Chang W. ;
Hong, Ki-Yun ;
Kim, Sang Y. ;
Yang, Han K. ;
Song, Soo-Chang .
BIOMATERIALS, 2009, 30 (27) :4752-4762
[6]   Thermosensitive poly(organophosphazene)-paclitaxel conjugate gels for antitumor applications [J].
Chun, Changlu ;
Lee, Sun Mi ;
Kim, Sang Yoon ;
Yang, Han Kwang ;
Song, Soo-Chang .
BIOMATERIALS, 2009, 30 (12) :2349-2360
[7]   The dawning era of polymer therapeutics [J].
Duncan, R .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (05) :347-360
[8]   Fabrication of nanomicelle with enhanced solubility and stability of camptothecin based on α,β-poly[(N-carboxybutyl)-L-aspartamide]-camptothecin conjugate [J].
Fan, Naiqian ;
Duan, Kongrong ;
Wang, Chengyun ;
Liu, Shunying ;
Luo, Shufang ;
Yu, Jiahui ;
Huang, Jin ;
Li, Yaping ;
Wang, Daxin .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2010, 75 (02) :543-549
[9]   Synthesis and In Vivo Antitumor Efficacy of PEGylated Poly(L-lysine) Dendrimer-Camptothecin Conjugates [J].
Fox, Megan E. ;
Guillaudeu, Steve ;
Frechet, Jean M. J. ;
Jerger, Katherine ;
Macaraeg, Nichole ;
Szoka, Francis C. .
MOLECULAR PHARMACEUTICS, 2009, 6 (05) :1562-1572
[10]   Camptothecin-20-PEG ester transport forms: the effect of spacer groups on antitumor activity [J].
Greenwald, RB ;
Pendri, A ;
Conover, CD ;
Lee, C ;
Choe, YH ;
Gilbert, C ;
Martinez, A ;
Xia, J ;
Wu, DC ;
Hsue, M .
BIOORGANIC & MEDICINAL CHEMISTRY, 1998, 6 (05) :551-562