分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2015年
9期
1272-1277
,共6页
Mn掺杂ZnS量子点%免疫球蛋白G%金纳米粒子%磷光
Mn摻雜ZnS量子點%免疫毬蛋白G%金納米粒子%燐光
Mn참잡ZnS양자점%면역구단백G%금납미입자%린광
Manganese doped zinc sulfide quantum dots%Immunoglobulin G%Gold nanoparticals%Phosphorescence
通过Mn掺杂ZnS量子点表面的羧基与人IgG表面的氨基进行酰胺缩合,制备了人IgG功能化的Mn掺杂ZnS量子点( IgG-QDs)。通过金纳米粒子和羊抗人IgG之间的静电相互作用,合成了羊抗人IgG功能化的金纳米粒子。利用IgG-QDs和羊抗人IgG功能化的金纳米粒子之间的荧光共振能量转移效应,建立了人血清中人IgG的室温磷光检测新方法。本方法的线性范围为1~10μg/mL,检出限为0.45μg/mL。由于引入了室温磷光检测,本方法有效避免了机体自发荧光和基质散射光等背景信号的干扰,成功实现了人血清样品中人IgG的检测。
通過Mn摻雜ZnS量子點錶麵的羧基與人IgG錶麵的氨基進行酰胺縮閤,製備瞭人IgG功能化的Mn摻雜ZnS量子點( IgG-QDs)。通過金納米粒子和羊抗人IgG之間的靜電相互作用,閤成瞭羊抗人IgG功能化的金納米粒子。利用IgG-QDs和羊抗人IgG功能化的金納米粒子之間的熒光共振能量轉移效應,建立瞭人血清中人IgG的室溫燐光檢測新方法。本方法的線性範圍為1~10μg/mL,檢齣限為0.45μg/mL。由于引入瞭室溫燐光檢測,本方法有效避免瞭機體自髮熒光和基質散射光等揹景信號的榦擾,成功實現瞭人血清樣品中人IgG的檢測。
통과Mn참잡ZnS양자점표면적최기여인IgG표면적안기진행선알축합,제비료인IgG공능화적Mn참잡ZnS양자점( IgG-QDs)。통과금납미입자화양항인IgG지간적정전상호작용,합성료양항인IgG공능화적금납미입자。이용IgG-QDs화양항인IgG공능화적금납미입자지간적형광공진능량전이효응,건립료인혈청중인IgG적실온린광검측신방법。본방법적선성범위위1~10μg/mL,검출한위0.45μg/mL。유우인입료실온린광검측,본방법유효피면료궤체자발형광화기질산사광등배경신호적간우,성공실현료인혈청양품중인IgG적검측。
IgG functionalized Mn doped ZnS quantum dots ( IgG-QDs ) were fabricated via the amide condensation between the carboxy groups on the surface of Mn doped ZnS quantum dots and the amino groups on the surface of IgG. The IgG antibody functionalized Au nanoparticals were synthesized via the electrostatic interaction between the Au nanoparticals and IgG antibody. Based on the fluorescence resonance energy transfer effect between the IgG-QDs and the IgG antibody functionalized Au nanoparticals, the IgG-QDs could be applied for low background phosphorescent sensing of IgG with the linear range of 1-10 μg/mL and the limit of detection of 0. 45 μg/mL. The proposed method was successfully applied to detect IgG in human serum without the disturbance of the background fluorescence and scattered light.