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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2012-01-01
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Online Access: | http://dx.doi.org/10.1100/2012/940541 |
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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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