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 (Tb(3+)-Dano) as a fluorescent probe. These proteins remarkably enhance the fluorescence intensity of the Tb(3+)-Dano complex at 545 nm, and the enhanced fluorescence intensity of Tb(3+)-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, [Tb(3+)] = 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.