Poly(glycidyl methacrylate) grafted CdSe quantum dots by surface-initiated atom transfer radical polymerization: Novel synthesis, characterization, properties, and cytotoxicity studies

被引:24
作者
Bach, Long Giang [1 ]
Islam, Md. Rafiqul [1 ]
Lee, Doh Chang [2 ]
Lim, Kwon Taek [1 ]
机构
[1] Pukyong Natl Univ, Dept Imaging Syst Engn, Pusan 608737, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, KAIST Inst Nanocentury KINC, Taejon 305701, South Korea
关键词
CdSe quantum dots; Polymer; Nanohybrids; ATRP; Imaging materials; Biotin; Cytotoxicity; COVALENT IMMOBILIZATION; NANOPARTICLES; NANOCRYSTALS; FABRICATION; STABILITY; CAPSULES; CANCER;
D O I
10.1016/j.apsusc.2013.06.142
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A novel approach for the synthesis of poly(glycidyl methacrylate) grafted CdSe quantum dot (QDs) (PGMA-g-CdSe) was developed. The PGMA-g-CdSe nanohybrids were synthesized by the surface-initiated atom transfer radical polymerization of glycidyl methacrylate from the surface of the strategic initiator, CdSe-BrIB QDs prepared by the interaction of 2-bromoisobutyryl bromide (BrIB) and CdSe-OH QDs. The structure, morphology, and optical property of the PGMA-g-CdSe nanohybrids were analyzed by FT-IR, XPS, TGA,XRD, TEM, and PL. The as-synthesized PGMA-g-CdSe nanohybrids having multi-epoxide groups were employed for the direct coupling of biotin via ring-opening reaction of the epoxide groups to afford the Biotin-f-PGMA-g-CdSe nanobioconjugate. The covalent immobilization of biotin onto PGMA-g-CdSe was confirmed by FT-IR, XPS, and EDX. Biocompatibility and imaging properties of the Biotin-f-PGMA-g-CdSe were investigated by MU bioassay and PL analysis, respectively. The cell viability study suggested that the biocompatibility was significantly enhanced by the functionalization of CdSe QDs by biotin and PGMA. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:546 / 553
页数:8
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