Super-hydrophilic zwitterionic poly(carboxybetaine) and amphiphilic non-ionic poly(ethylene glycol) for stealth nanoparticles

被引:295
作者
Cao, Zhiqiang [1 ]
Jiang, Shaoyi [1 ]
机构
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
基金
美国国家科学基金会;
关键词
Polyethylene glycol; Zwitterions; Non-fouling; Protein conjugation; Liposome; Drug delivery; SELF-ASSEMBLED MONOLAYERS; PROTEIN ADSORPTION; DRUG-DELIVERY; MOLECULAR SIMULATION; BLOCK-COPOLYMERS; IN-VIVO; THERAPEUTIC APPLICATIONS; POLYMERIC NANOPARTICLES; LIPOSOMAL DOXORUBICIN; PHOSPHOLIPID-BILAYERS;
D O I
10.1016/j.nantod.2012.08.001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This review compares two types of non-fouling polymers, the widely used nonionic poly(ethylene glycol) (PEG) and the recently established zwitterionic poly(carboxybetaine) (PCB), for their use in creating stealth nanoparticles (NPs) for drug delivery and protein protection. While both types of polymers exhibit reasonable non-fouling properties, such as good protein and colloidal stability and extended blood circulation time in vivo, amphiphilic PEG has negative effects on proteins and NPs due to its hydrophobic nature, including reduced protein bioactivity, instability of assembled NPs, and lipid bilayer destabilization. These problems can be overcome by super-hydrophilic PCB. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:404 / 413
页数:10
相关论文
共 102 条
[1]   Self-porating polymersomes of PEG-PLA and PEG-PCL: hydrolysis-triggered controlled release vesicles [J].
Ahmed, F ;
Discher, DE .
JOURNAL OF CONTROLLED RELEASE, 2004, 96 (01) :37-53
[2]   Biodegradable polymersomes loaded with both paclitaxel and doxorubicin permeate and shrink tumors, inducing apoptosis in proportion to accumulated drug [J].
Ahmed, Fariyal ;
Pakunlu, Refika I. ;
Brannan, Aaron ;
Bates, Frank ;
Minko, Tamara ;
Discher, Dennis E. .
JOURNAL OF CONTROLLED RELEASE, 2006, 116 (02) :150-158
[3]   The formation of biodegradable polymeric micelles from newly synthesized poly(aspartic acid)-block-polylactide AB-type diblock copolymers [J].
Arimura, H ;
Ohya, Y ;
Ouchi, T .
MACROMOLECULAR RAPID COMMUNICATIONS, 2004, 25 (06) :743-747
[4]   Synthesis and characterization of PLGA nanoparticles [J].
Astete, Carlos E. ;
Sabliov, Cristina M. .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2006, 17 (03) :247-289
[5]  
Avgoustakis Konstantinos, 2004, Current Drug Delivery, V1, P321, DOI 10.2174/1567201043334605
[6]   Hydration of phospholipid bilayers in the presence and absence of cholesterol [J].
Bach, D ;
Miller, IR .
CHEMISTRY AND PHYSICS OF LIPIDS, 2005, 136 (01) :67-72
[7]  
Bach D., 1998, BIOCHIM BIOPHYS ACTA, V1386, P216
[8]   Polysialic Acid-Based Micelles for Encapsulation of Hydrophobic Drugs [J].
Bader, Rebecca A. ;
Silvers, Angela L. ;
Zhang, Nan .
BIOMACROMOLECULES, 2011, 12 (02) :314-320
[9]   INTERACTION OF PEG-PHOSPHOLIPID CONJUGATES WITH PHOSPHOLIPID - IMPLICATIONS IN LIPOSOMAL DRUG-DELIVERY [J].
BEDUADDO, FK ;
HUANG, L .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 16 (2-3) :235-247
[10]   Lipid chain length effect on the phase behaviour of PCs/PEG:2000-PEs mixtures.: A spin label electron spin resonance and spectrophotometric study [J].
Belsito, S ;
Bartucci, R ;
Sportelli, L .
BIOPHYSICAL CHEMISTRY, 2001, 93 (01) :11-22