Interaction between DNA and Drugs Having Protonable Basic Groups: Characterization through Affinity Constants, Drug Release Kinetics, and Conformational Changes
This paper reports the in vitro characterization of the interaction between the phosphate groups of DNA and the protonated species of drugs with basic groups through the determination of the affinity constants, the reversibility of the interaction, and the effect on the secondary structure of the ma...
Main Authors: | Liliana P. Alarcón, Yolima Baena, Rubén H. Manzo |
---|---|
Format: | Article |
Language: | English |
Published: |
Österreichische Apotheker-Verlagsgesellschaft m. b. H.
2017-01-01
|
Series: | Scientia Pharmaceutica |
Subjects: | |
Online Access: | http://www.mdpi.com/2218-0532/85/1/1 |
Similar Items
-
Determination of the Absolute Configurations of Chiral Drugs Using Chiroptical Spectroscopy
by: Prasad L. Polavarapu
Published: (2016-08-01) -
Cellulosic fraction of rice bran fibre alters the conformation and inhibits the activity of porcine pancreatic lipase
by: Jing Qi, et al.
Published: (2015-12-01) -
Biological and structural properties’ interpretation on antitumour drug 3-(2-aminoethyl) indole (tryptamine) using molecular spectroscopy and computational tools
by: K. Hemachandran, et al.
Published: (2019-12-01) -
Activated Charge-Reversal Polymeric Nano-System: The Promising Strategy in Drug Delivery for Cancer Therapy
by: Yichen Hu, et al.
Published: (2016-04-01) -
Conformational Changes in DNA upon Ligand Binding Monitored by Circular Dichroism
by: Cammy K.-M. Chen, et al.
Published: (2012-03-01)