Preparation of Temperature-Responsive Antibody-Nanoparticles by RAFT-Mediated Grafting from Polymerization

被引:1
|
作者
Yoshihara, Erika [1 ,2 ]
Nabil, Ahmed [1 ,3 ,4 ]
Mochizuki, Shinichi [5 ]
Iijima, Michihiro [6 ]
Ebara, Mitsuhiro [1 ,2 ,7 ]
机构
[1] Natl Inst Mat Sci NIMS, Res Ctr Funct Mat RCFM, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
[2] Univ Tsukuba, Grad Sch Pure & Appl Sci, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058577, Japan
[3] Beni Suef Univ, Fac Postgrad Studies Adv Sci PSAS, Biotechnol & Life Sci Dept, Bani Suwayf 62511, Egypt
[4] Egyptian Liver Res Inst & Hosp ELRIAH, Mansoura 35511, Egypt
[5] Univ Kitakyushu, Fac Environm Engn, 1-1 Hibikino, Kitakyushu, Fukuoka 8080135, Japan
[6] Oyama Coll, Natl Inst Technol, Oyama Coll NIT, Dept Mat Chem & Bioengn, 771 Nakakuki, Oyama 3230806, Japan
[7] Tokyo Univ Sci, Grad Sch Ind Sci & Technol, Shinjuku Ku, 1-3 Kagurazaka, Tokyo 1620825, Japan
关键词
polymer-protein conjugates; grafting from; temperature-responsive; RAFT; precipitation polymerization; CONJUGATE; STREPTAVIDIN; RECOGNITION; ENRICHMENT;
D O I
10.3390/polym14214584
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Herein, we report the preparation of temperature-responsive antibody-nanoparticles by the direct polymerization of N-isopropylacrylamide (NIPAAm) from immunoglobulin G (IgG). To this end, a chain transfer agent (CTA) was introduced into IgG, followed by the precipitation polymerization of NIPAAm in an aqueous medium via reversible addition-fragmentation chain transfer polymerization above the lower critical solution temperature (LCST). Consequently, antibody-polymer particles with diameters of approximately 100-200 nm were formed. Owing to the entanglement of the grafted polymers via partial chemical crosslinking, the antibody-nanoparticles maintained their stability even at temperatures below the LCST. Further, the dispersed nanoparticles could be collected by thermal precipitation above the LCST. Additionally, the antibody-nanoparticles formulation could maintain its binding constant and exhibited a good resistance against enzymatic treatment. Thus, the proposed antibody-nanoparticles can be useful for maximizing the therapeutic potential of antibody-drug conjugates or efficacies of immunoassays and antibody recovery and recycling.
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页数:14
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