Quantitative structure–(chromatographic) retention relationships

K Héberger - Journal of chromatography A, 2007 - Elsevier
Since the pioneering works of Kaliszan (R. Kaliszan, Quantitative Structure–
Chromatographic Retention Relationships, Wiley, New York, 1987; and R. Kaliszan …

In silico prediction of drug‐binding strengths to human serum albumin

G Colmenarejo - Medicinal research reviews, 2003 - Wiley Online Library
Abstract Drug binding to Human Serum Albumin (HSA) is an area of intense research. The
pharmacokinetics and pharmacodynamics of drugs are strongly affected by their binding to …

In vitro, in silico and integrated strategies for the estimation of plasma protein binding. A review

G Lambrinidis, T Vallianatou… - Advanced drug delivery …, 2015 - Elsevier
Plasma protein binding (PPB) strongly affects drug distribution and pharmacokinetic
behavior with consequences in overall pharmacological action. Extended plasma protein …

Stereoselective binding of chiral drugs to plasma proteins

Q Shen, L Wang, H Zhou, H Jiang, L Yu… - Acta Pharmacologica …, 2013 - nature.com
Chiral drugs show distinct biochemical and pharmacological behaviors in the human body.
The binding of chiral drugs to plasma proteins usually exhibits stereoselectivity, which has a …

[图书][B] Affinity chromatography

S Magdeldin - 2012 - books.google.com
Most will agree that one major achievement in the bio-separation techniques is affinity
chromatography. This coined terminology covers a myriad of separation approaches that …

Characterization of drug–protein interactions in blood using high‐performance affinity chromatography

DS Hage, A Jackson, MR Sobansky… - Journal of separation …, 2009 - Wiley Online Library
The binding of drugs with proteins in blood, serum, or plasma is an important process in
determining the activity, distribution, rate of excretion, and toxicity of drugs in the body. High …

Optimal collision energy is an eligible molecular descriptor to boost structural annotation: an application for chlorogenic acid derivatives-focused chemical profiling

Y Cao, C Chai, A Chang, X Xu, Q Song, W Liu… - … of Chromatography A, 2020 - Elsevier
Tandem mass spectrometry (MS/MS), in particular high-resolution MS/MS, is able to provide
element compositions and substructures for the detected signals. However, it is still …

Characterization of drug interactions with serum proteins by using high-performance affinity chromatography

DS Hage, J Anguizola, O Barnaby… - Current drug …, 2011 - ingentaconnect.com
The binding of drugs with serum proteins can affect the activity, distribution, rate of excretion,
and toxicity of pharmaceutical agents in the body. One tool that can be used to quickly …

Drug affinity to immobilized target bio-polymers by high-performance liquid chromatography and capillary electrophoresis

C Bertucci, M Bartolini, R Gotti, V Andrisano - Journal of Chromatography B, 2003 - Elsevier
This review addresses the use of high-performance liquid chromatography (HPLC) and
capillary electrophoresis (CE) as affinity separation methods to characterise drugs or …

Automated Ligand- and Structure-Based Protocol for in Silico Prediction of Human Serum Albumin Binding

ML Hall, WL Jorgensen… - Journal of chemical …, 2013 - ACS Publications
Plasma protein binding has a profound impact on the pharmacokinetic and
pharmacodynamic properties of many drug candidates and is thus an integral component of …