首页|CdTe/CdS量子点对木犀草素与人血清白蛋白结合力的影响

CdTe/CdS量子点对木犀草素与人血清白蛋白结合力的影响

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用还原型谷胱甘肽( GSH)作硫源和稳定剂在水相中合成了生物相容性好、量子产率高的核壳型CdTe/CdS半导体量子点;同时模拟人体内生理环境,研究了CdTe/CdS量子点( QDs)对木犀草素与人血清白蛋白( HSA)相互作用的影响。结果表明, CdTe/CdS QDs可有规律地猝灭HSA荧光;在CdTe/CdS QDs存在条件下,木犀草素可使HSA荧光最大发射波长从341 nm红移到347 nm,红移程度明显大于无QDs存在时,同时木犀草素与HSA的表观结合常数和结合位点数均有增加,即CdTe/CdS QDs使木犀草素与HSA的结合力增强。
The Preparation and Application of CdTe/CdS Core-shell Quantum Dots
Biocompatible and high luminescence CdTe/CdS core -shell quantum dots ( QDs ) were synthesized in aqueous solution using glutathione ( GSH) as sulfur source and stabilizer.Further, luteolin was studied for the affinities for human serum albumin ( HSA) in the presence and absence of CdTe/CdS QDs, respectively.Results revealed that the fluorescence intensities of HSA decreased remarkably with increasing concentration of QDs.Luteolin resulted in obvious red-shift of the maximum emission of HSA from 341 nm to 347 nm in the presence of QDs and the extent of red -shift induced by luteolin was much bigger than that in the absence of QDs.The binding constants and the number of binding sites per HSA molecule ( n) both increased.Thus, the binding affinities of luteolin for HSA increased in the presence of CdTe/CdS QDs.

CdTe/CdS QDsluteolinhuman serum albuminaffinitiesfluorescence quenching

王维维、杜迎翔

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中国药科大学分析化学教研室,江苏 南京 210009

中国药科大学药物质量与安全预警教育部重点实验室,江苏 南京 210009

中国药科大学现代中药教育部重点实验室,江苏 南京 210009

CdTe/CdS QDs 木犀草素 人血清白蛋白 结合力 荧光猝灭

2014

广州化工
广州市化工行业协会 广州市化学化工学会 广州市化学工业研究所

广州化工

影响因子:0.358
ISSN:1001-9677
年,卷(期):2014.(16)
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