研究目的
To develop a highly sensitive electrochemical biosensor for the therapeutic drug monitoring (TDM) of indinavir (IDV), a protease inhibitor antiretroviral drug, in human serum samples, to prevent adverse effects of its first-pass metabolism and optimize dosage regimes.
研究成果
The CYP3A4|TGA-PdTeQD|Cyst|Au biosensor demonstrated high sensitivity and suitability for measuring very low concentrations of IDV, making it applicable for therapeutic drug monitoring in patients, especially those who are ultra-rapid metabolisers. The biosensor's performance in human serum samples indicates its potential for clinical diagnostic applications.
研究不足
The biosensor's storage stability and reproducibility need optimization, as the response decreased with storage time in the refrigerator, indicating possible denaturation of the enzyme.
1:Experimental Design and Method Selection:
The study involved the preparation of an electrochemical biosensor by depositing a thin film of CYP3A4 and TGA-PdTeQD on a cysteamine-functionalised gold disk electrode using thiol and carbodiimide covalent bonding chemistries. Cyclic voltammetry was used to determine the electrochemical signatures of the biosensor.
2:Sample Selection and Data Sources:
Human serum samples spiked with IDV were used to test the biosensor's applicability in real samples.
3:List of Experimental Equipment and Materials:
Equipment included an EG & G Princeton Applied Research 273A Potentiostat/Galvanostatic, Nicolet Evolution 100 UV-Visible Spectrophotometer, Horiba NanoLog? 3-22-TRIAX, PerkinElmer Model 100 FT-IR Spectrophotometer, and Horiba XploRA? Tabletop Confocal Raman Microscope. Materials included palladium chloride, thioglycolic acid, sodium hydroxide, sodium borohydride, hydrogen chloride, EDC, NHS, sodium phosphate monobasic dehydrate, disodium hydrogen phosphate dibasic, cysteamine, human serum, and human cytochrome P450-3A4 enzyme.
4:Experimental Procedures and Operational Workflow:
The biosensor was prepared by functionalizing a gold disk electrode with cysteamine, activating it with EDC/NHS, depositing TGA-PdTeQD, and then immobilizing CYP3A4 enzyme. The biosensor was characterized by CV and calibrated for its responses to IDV.
5:Data Analysis Methods:
The sensitivity, linear range, and limit of detection of the biosensor were determined from the CV responses at the characteristic reduction peak potential value of ?0.26 V.
独家科研数据包,助您复现前沿成果,加速创新突破
获取完整内容