Spectrofluorimetric Determination of Human Serum Albumin Using Terbium-Danofloxacin Probe

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...

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Main Authors: Amir M. Ramezani, Jamshid L. Manzoori, Mohammad Amjadi, Abolghasem Jouyban
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/2012/940541
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spelling doaj-eb1bd9f4923446298c95f312dc9ad71b2020-11-25T01:52:39ZengHindawi LimitedThe Scientific World Journal1537-744X2012-01-01201210.1100/2012/940541940541Spectrofluorimetric Determination of Human Serum Albumin Using Terbium-Danofloxacin ProbeAmir M. Ramezani0Jamshid L. Manzoori1Mohammad Amjadi2Abolghasem Jouyban3Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, IranDepartment of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, IranDepartment of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, IranDrug Applied Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz 51664, IranA 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.http://dx.doi.org/10.1100/2012/940541
collection DOAJ
language English
format Article
sources DOAJ
author Amir M. Ramezani
Jamshid L. Manzoori
Mohammad Amjadi
Abolghasem Jouyban
spellingShingle Amir M. Ramezani
Jamshid L. Manzoori
Mohammad Amjadi
Abolghasem Jouyban
Spectrofluorimetric Determination of Human Serum Albumin Using Terbium-Danofloxacin Probe
The Scientific World Journal
author_facet Amir M. Ramezani
Jamshid L. Manzoori
Mohammad Amjadi
Abolghasem Jouyban
author_sort Amir M. Ramezani
title Spectrofluorimetric Determination of Human Serum Albumin Using Terbium-Danofloxacin Probe
title_short Spectrofluorimetric Determination of Human Serum Albumin Using Terbium-Danofloxacin Probe
title_full Spectrofluorimetric Determination of Human Serum Albumin Using Terbium-Danofloxacin Probe
title_fullStr Spectrofluorimetric Determination of Human Serum Albumin Using Terbium-Danofloxacin Probe
title_full_unstemmed Spectrofluorimetric Determination of Human Serum Albumin Using Terbium-Danofloxacin Probe
title_sort spectrofluorimetric determination of human serum albumin using terbium-danofloxacin probe
publisher Hindawi Limited
series The Scientific World Journal
issn 1537-744X
publishDate 2012-01-01
description 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.
url http://dx.doi.org/10.1100/2012/940541
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