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Time-Insensitive Fluorescent Sensor for Human Serum Albumin and Its Unusual Red Shift
Author(s) -
Sara E. Smith,
J.M. Williams,
Shin Ando,
Kazunori Koide
Publication year - 2014
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/ac5001256
Subject(s) - bromocresol green , chemistry , bromocresol purple , human serum albumin , fluorescence , dichlorofluorescein , absorption (acoustics) , fluorescence spectroscopy , serum albumin , colorimetry , chromatography , analytical chemistry (journal) , biochemistry , optics , reactive oxygen species , physics
The concentration of human serum albumin (HSA) indicates the health state of individuals and is routinely measured by UV spectroscopy with bromocresol. However, this method tends to overestimate HSA, and more critically, depends highly on the timing, in seconds, of the measurements. Here, we report an analog of 2',7'-dichlorofluorescein that can be used as a fluorescent sensor to quantify HSA in human sera. The accuracy of this new method proved superior to that of bromocresol when an international standard serum sample was analyzed. This method is more convenient than the bromocresol method because it allows for fluorescence measurements during a >15 min period. Colorimetric analysis was also performed to further investigate the effects of the binding of the sensor to HSA. These spectroscopic studies suggest that absorption and emission changes upon HSA binding may be due to the dehydration of the dye and/or stabilization of the tritylic cation species.

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