Article ID Journal Published Year Pages File Type
1232291 Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2012 6 Pages PDF
Abstract

To know the interaction of amphiphilic drugs nortriptyline hydrochloride (NOT) and promazine hydrochloride (PMZ) with serum albumins (i.e., human serum albumin (HSA) and bovine serum albumin (BSA)), techniques of UV–visible, fluorescence, and circular dichroism (CD) spectroscopies are used. The binding affinity is more in case of PMZ with both the serum albumins. The quenching rate constant (kq) values suggest a static quenching process for all the drug–serum albumin interactions. The UV–visible results show that the change in protein conformation of PMZ–serum albumin interactions are more prominent as compared to NOT–serum albumin interactions. The CD results also explain the conformational changes in the serum albumins on binding with the drugs. The increment in %α-helical structure is slightly more for drug–BSA complexes as compared to drug–HSA complexes.

Graphical abstractFluorescence emission spectra of native HSA and HSA–NOT complexes, excited at 280 nm.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Drugs promazine and nortriptyline form complexes with HSA and BSA. ► The binding affinity of promazine is more than nortriptyline with the serum albumins. ► Secondary structure induction by the drugs is more in BSA as compared to HSA.

Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
Authors
, , , , ,