Biodegradable block copolymers for delivery of proteins and water-insoluble drugs

被引:476
作者
Zentner, GM
Rathi, R
Shih, C
McRea, JC
Seo, MH
Oh, H
Rhee, BG
Mestecky, J
Moldoveanu, Z
Morgan, M
Weitman, S
机构
[1] MacroMed Inc, Sandy, UT 84070 USA
[2] Samyang Inc, Seoul 110725, South Korea
[3] Univ Alabama, Birmingham, AL USA
[4] Univ Utah, PDEF, Salt Lake City, UT USA
[5] IDD, San Antonio, TX USA
关键词
copolymers; thermal gels; biodegradable; controlled release; proteins; paclitaxel;
D O I
10.1016/S0168-3659(01)00276-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Release of several drugs from new ABA-type biodegradable thermal gels, ReGel(R), including proteins and conventional molecules, are presented. These are biodegradable, biocompatible polymers that demonstrate reverse thermal gelation properties. Organic solvents are not used in the synthesis, purification, or formulation of these polymers. The unique characteristics of ReGel(R) hinge on the following two key properties: (1) ReGel(R) is a water soluble, biodegradable polymer at temperatures below the gel transition temperature; (2) ReGel(R) forms a water-insoluble gel once injected. This is consistent with a hydrophobically bonded gel state where all interactions are physical, with no covalent crosslinking. An increase in viscosity of approximately 4 orders of magnitude accompanies the sol-gel transition. The gel forms a controlled release drug depot with delivery times ranging from 1 to 6 weeks. ReGel(R)'s inherent ability to solubilize (400 to >2000-fold) and stabilize poorly soluble and sensitive drugs, including proteins is a substantial benefit. The gel provided excellent control of the release of paclitaxel for approximately 50 days. Direct intratumoral injection of ReGel(R)/paclitaxel (OncoGel(TM)) results in a slow clearance of paclitaxel from the injection sire with minimal distribution into any organ. Efficacies equivalent to maximum tolerated systemic dosing were observed at OncoGel(TM) doses that were 10-fold lower. Data on protein release (pGH, G-CSF, insulin, rHbsAg) and polymer biocompatibility are discussed. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:203 / 215
页数:13
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