Spectrofluorimetric determination of human serum albumin using terbium-danofloxacin probe.

Spectrofluorimetric determination of human serum albumin using terbium-danofloxacin probe.
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DOI:
10.1100/2012/940541
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发表时间:
2012
影响因子:
--
通讯作者:
Jouyban A
Jouyban A
中科院分区:
其他
文献类型:
--
作者:
Ramezani AM;Manzoori JL;Amjadi M;Jouyban A

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建立了以铽-达氟沙星(Tb 3 +-Dano)为荧光探针测定人血清白蛋白(HSA)和牛血清白蛋白(BSA)的荧光分析方法。这些蛋白质显著增强Tb 3 +-Dano复合物在545 nm处的荧光强度,并且增强的Tb 3 +-Dano荧光强度与蛋白质(HSA和BSA)的浓度成正比。在pH = 7.8,[Tb 3 +] = 8.5 × 10 - 5 mol L-1,[Dano] = 1.5 × 10 - 4 mol L-1时,HSA的最大响应值为1.5 × 10 - 4 mol L-1。BSA、HSA标准品溶液和HSA血浆样品的校准图分别在0.2 × 10−6 − 1.3 × 10−6 mol L−1、0.2 × 10−6 − 1.4 × 10−6 mol L−1和0.2 × 10−6 − 1 × 10−6 mol L−1范围内呈线性。BSA、HSA和HSA血浆样品的检测限(S/N = 3)分别为8.7 × 10−8 mol L−1、6.2 × 10−8 mol L−1和8.1 × 10−8 mol L−1。使用大量真实的生物血浆样品检查了该方法的适用性,并与紫外光谱参考方法进行了比较。结果表明,该方法可作为生物样品中白蛋白测定的一种简便、实用、灵敏的替代方法。
A spectrofluorimetric method is proposed for the determination of human serum albumin (HSA) and bovine serum albumin (BSA) using terbium-danofloxacin (Tb3+-Dano) as a fluorescent probe. These proteins remarkably enhance the fluorescence intensity of the Tb3+-Dano complex at 545 nm, and the enhanced fluorescence intensity of Tb3+-Dano is proportional to the concentration of proteins (HSA and BSA). Optimum conditions for the determination of HSA were investigated and found that the maximum response was observed at: pH = 7.8, [Tb3+] = 8.5 × 10−5 mol L−1, [Dano] = 1.5 × 10−4 mol L−1. The calibration graphs for standard solutions of BSA, HSA, and plasma samples of HSA were linear in the range of 0.2 × 10−6 − 1.3 × 10−6 mol L−1, 0.2 × 10−6 − 1.4 × 10−6 mol L−1, and 0.2 × 10−6 − 1 × 10−6 mol L−1, respectively. The detection limits (S/N = 3) for BSA, HSA, and plasma sample of HSA were 8.7 × 10−8 mol L−1, 6.2 × 10−8 mol L−1, and 8.1 × 10−8 mol L−1, respectively. The applicability of the method was checked using a number of real biological plasma samples and was compared with the UV spectrometric reference method. The results was showed that the method could be regarded as a simple, practical, and sensitive alternative method for determination of albumin in biological samples.
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