聚乙二醇
三聚氯氰
超顺磁性
二乙烯基苯
分散聚合
乙二醇二甲基丙烯酸酯
磁性纳米粒子
甲基丙烯酸酯
化学
分散性
高分子化学
材料科学
微粒
PEG比率
乙二醇
吸附
比表面积
聚合
链霉亲和素
纳米颗粒
微球
戊二醛
丙烯酸
粒径
化学工程
表面改性
生物素化
乳液聚合
共聚物
磁粉探伤
聚丙烯酸
二乙烯三胺
聚乙烯醇
色谱法
单体
苯乙烯
悬浮聚合
大分子单体
配体(生物化学)
季戊四醇
作者
Yadong Zhang,Guangyu Wang,Yunli Li,Yaxuan Li,Yabing Zhang,Zhenhua Zhang
标识
DOI:10.1021/acsabm.6c01458
摘要
Magnetic microspheres immobilized with affinity ligands are highly efficient tools for immunoassays. Low non-specific adsorption and high affinity ligand loading capacity are crucial for the sensitivity of immunoassays, especially diagnostic allergen testing. This paper reports a carboxylated magnetic microsphere (PNFC@AA) via a multilayer cross-linked strategy. Monodisperse aminated polyglycidyl methacrylate (PGMA) microspheres were synthesized, followed by the incorporation of Fe3O4 nanoparticles through in situ coprecipitation. Polyacrylic acid (PAA) segments were then grafted onto the microsphere surface via surface radical polymerization using different crosslinkers, ultimately yielding magnetic PNFC@AA microspheres with high carboxyl loading. The prepared PNFC@AA microspheres exhibit uniform particle size, good monodispersity, and typical superparamagnetic properties. It was found that compared to divinylbenzene (DVB) and ethylene glycol dimethacrylate (EGDMA) crosslinkers, the hydrophilic crosslinker polyethylene glycol diacrylate (PEGDA) microspheres exhibited a larger specific surface area (19.17 m2/g), a higher carboxyl loading (655 μmol/g), and a stronger streptavidin (SA)-immobilized biotin binding capacity (2328 pmol/mg). In AMPPD chemiluminescent immunoassay (CLIA), these microspheres effectively suppressed non-specific adsorption, reduced background luminescence, and substantially improved the signal-to-noise ratio. Furthermore, the SA-coupling microspheres were successfully applied to the detection of specific IgE against four common allergens (house dust mite (Dermatophagoides farinae), German cockroach (Blatella germanica), milk, and egg), respectively, which effectively distinguished the sensitization levels of different allergens. This study provides a simple and efficient strategy for the design of high-performance immunodiagnostic carriers.
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