Abstract
A novel fluorometric method for the determination of L-asparaginase, an enzyme crucial in cancer therapy and food industry applications, is presented. This sensitive and selective approach utilizes L-asparagine and two pH-sensitive carbon dots (blue-N-CDs and red-N-CDs) as probes. The interaction between L-asparagine and L-asparaginase liberates ammonia, causing an increase in pH. This pH change simultaneously decreases the fluorescence of blue-N-CDs while enhancing the emission of red-N-CDs, enabling ratiometric detection of L-asparaginase. Comprehensive characterization of both carbon dots and investigation of their response mechanism towards L-asparaginase were conducted using ultraviolet–visible spectrophotometry, fluorescence spectroscopy, and transmission electron microscopy (TEM) imaging techniques. The designed approach demonstrates outstanding linearity (20 to 2000 U L -1) and a low detection limit (6.95 U L -1) for L-asparaginase quantification. Moreover, when tested to human serum samples, the detection system exhibits outstanding selectivity and high recovery rates (96.15% to 99.75%) with low standard deviation, underscoring its suitability for practical implementation in clinical diagnostics.
| Original language | English |
|---|---|
| Article number | 125161 |
| Journal | Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy |
| Volume | 325 |
| Early online date | 19 Sept 2024 |
| DOIs | |
| Publication status | Published - 15 Jan 2025 |
Bibliographical note
Note: This research was supported by the Researchers Supporting Project (number RSPD2024R563) at King Saud University, Riyadh, Saudi Arabia.Keywords
- Biological sciences
- pH-sensitive
- Fluorometric
- L-asparaginase
- Ratiometric
- Carbon dots
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