摘要

A sensitive procedure for the quantification of total protein bovine serum albumen (BSA) in human serum was presented with sequential injection sampling and fluorometric detection. A few microliters of sample and fluorescamine solutions were aspirated into the holding coil to facilitate the reaction of protein with fluorescamine by giving rise to a blue-green-fluorescent derivative. The derivative was afterwards excited by a 400 nm radiation from a UV radiator, and the emitted fluorescence was monitored at the wavelength of 470 run. By loading 5.0 mu l of sample and 4.0 mu l of fluorescamine solution 0.075% (m/v), a linear calibration graph was obtained within 0.3-12.5 mu g ml(-1), and a detection limit (36) of 0.1 mu g ml(-1) was achieved, along with a sampling frequency of 40 h(-1) and a R.S.D. value of 2.1% at the 5.0 mu g ml(-1) levels. Protein contents in human serums were analyzed by using the present procedure, and reasonable agreements were obtained with those obtained by a documented spectrophotometric (Biuret) method.