4.7 Article

Two- and three-way chemometric analyses for investigation of interactions of acarbose with normal and glycated human serum albumin: Developing a novel biosensing system

Journal

MICROCHEMICAL JOURNAL
Volume 160, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.microc.2020.105675

Keywords

Acarbose; Human serum albumin; Glycated human serum albumin; Biosensing

Funding

  1. research council of Kermanshah University of Medical Sciences

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This research project investigates the interactions of acarbose with normal human serum albumin and glycated HSA using chemometrics assisted-electrochemical and spectroscopic techniques. By combining various analytical methods and chemometric algorithms, the study sheds light on the binding mechanisms between ACB and HSA/GHSA. Additionally, a novel electrochemical technique was developed for the determination of GHSA as a potential biomarker in diabetes, showing successful validation using synthetic and real samples.
In this project, our research group has performed an interesting work in which interactions of acarbose (ACB) with normal human serum albumin (HSA) and glycated HSA (GHSA) have been investigated by chemometrics assisted-electrochemical and spectroscopic techniques. To have a deep insight to the interactions of ACB with HSA and GHSA, different electrochemical and spectroscopic techniques were used to monitor ACB-HSA and ACB-GHSA interactions and analyzed by multivariate curve resolution alternating least squares (MCR-ALS), MCR-BANNDS and EQUISPEC as efficient chemometric algorithms. Then, molecular docking techniques were used to extract more information which helped us to better justify binding of ACB with HSA and GHSA. After obtaining qualitative and quantitative information and justification of the ACB-HSA and ACB-GHSA interactions, a novel electrochemical technique was developed for exploiting second-order advantage from differential pulse voltammetric data for determination of GHSA as a potential biomarker in diabetes in the presence of HSA. Calibration and validation of the developed system showed us that our system was successful in determination of GHSA in synthetic and real samples.

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