Journal
TALANTA
Volume 234, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.talanta.2021.122614
Keywords
Fluorescence; Trypsin; Cyt C; Thiamine; Cobaltic prussian blue analogs
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Funding
- National Key Research and Development Program of China [2018YFD1100503]
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The presented fluorometry assay allows for the quantitative detection of trypsin with good repeatability and selectivity, with detection and quantification limits of 0.15 and 0.50 μg/mL, respectively. Accurate results were obtained through the detection of trypsin in practical serum and urine samples.
A fluorometry assay for trypsin sensitive determination has been presented. The fluorescence of the system at 370/445 nm is derived from thiochrome obtained by in-situ oxidation of thiamine. Based on the inner filter effect, cytochrome C (Cyt C) can quench the fluorescence at 445 nm effectively. Cyt C is specifically hydrolyzed by trypsin through an enzymatic reaction, giving rise to the enhancement of the fluorescence intensity. The change value of fluorescence intensity is proportional to trypsin concentration, which is successfully used for trypsin quantitative detection. This method exhibits good repeatability and selectivity with a detection limit of 0.15 mu g mL(-1) and a quantification limit of 0.50 mu g mL(-1) for trypsin sensing. Moreover, it is applied to detect trypsin in practical serum and urine samples with accurate results. The proposed assay is not only a promising candidate for trypsin determination in practical application but also a potentially valuable tool in urine comprehensive analysis and disease diagnosis.
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