Dual pH- and temperature-responsive protein nanoparticles

被引:27
|
作者
Matsumoto, Nicholas M. [1 ,2 ]
Buchman, George W. [3 ]
Rome, Leonard H. [2 ,4 ]
Maynard, Heather D. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Calif Nanosyst Inst, Los Angeles, CA 90095 USA
[3] Paragon Bioserv Inc, Baltimore, MD 21201 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Multiply responsive; Vault; Nanoparticle; Conjugate; VAULT RIBONUCLEOPROTEIN-PARTICLES; DRUG-DELIVERY; MAGNETIC NANOPARTICLES; POLYMERIC NANOPARTICLES; N-ISOPROPYLACRYLAMIDE; CANCER-THERAPY; ACRYLIC-ACID; CORE; MICROGELS; PLATFORM;
D O I
10.1016/j.eurpolymj.2015.01.043
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Multiply responsive protein nanoparticles are interesting for a variety of applications. Herein, we describe the synthesis of a vault nanoparticle that responds to both temperature and pH. Specifically, poly(N-isopropylacrylamide-co-acrylic acid) with a pyridyl disulfide end group was prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization. The polymer had a lower critical solution temperature (LCST) of 31.9 degrees C at pH 5, 44.0 degrees C at pH 6 and above 60 degrees C at pH 7. The polymer was conjugated to human major vault protein (hMVP), and the resulting nanoparticle was analyzed by UV-Vis, dynamic light scattering (DLS) and electron microscopy. The data demonstrated that the poly(N-isopropylacrylamide-co-acrylic acid)-vault conjugate did not respond to temperatures below 60 degrees C at pH 7, while the nanoparticles reversibly aggregated at pH 6. Furthermore, it was shown that the vault nanoparticle structure remained intact for at least three heat and cooling cycles. Thus, these dually responsive nanoparticles may serve as a platform for drug delivery and other applications. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:532 / 539
页数:8
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