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

• Published in: Journal of Chromatography B Vol. 797; no. 1; pp. 111 - 129
• Main Authors: Bertucci, C, Bartolini, M, Gotti, R, Andrisano, V
• Format: Book Review Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 25-11-2003
• Subjects: Bio-polymers, immobilized; Biopolymers - chemistry; Chromatography, High Pressure Liquid - methods; Drug-binding constants; Electrophoresis, Capillary - methods; High-throughput screening; Pharmaceutical Preparations - chemistry; Reviews; Stereoisomerism; PNMT; SAP; QSRR; DTT; NSAID; High-throughput screening; DBH; Drug-binding constants; BSA; UF; TTR; NAChRs; CE-FA; HSA; NMDA; HPLC; ODS; CEC; AChE; BGE; CE; HPFA; ACE; VACE; CIM; MS; MR-SP; FAC; AGP; HPALC; PGA; EDTA; GS; GnT-V; Bio-polymers, immobilized; IMER; Reviews; IAM; Glut-P; GABA; Pgp; VP; FA; HD; GAPDH; OXH
• ISSN: 1570-0232; 1873-376X
• DOI: 10.1016/j.jchromb.2003.08.033

This review addresses the use of high-performance liquid chromatography (HPLC) and capillary electrophoresis (CE) as affinity separation methods to characterise drugs or potential drugs–bio-polymer interactions. Targets for the development of new drugs such as enzymes (IMERs), receptors, and membrane proteins were immobilized on solid supports. After the insertion in the HPLC system, these immobilized bio-polymers were used for the determination of binding constants of specific ligands, substrates and inhibitors of pharmaceutical interest, by frontal analyses and zonal elution methods. The most used bio-polymer immobilization techniques and methods for assessing the amount of active immobilized protein are reported. Examples of increased stability of immobilized enzymes with reduced amount of used protein were shown and the advantages in terms of recovery for reuse, reproducibility and on-line high-throughput screening for potential ligands are evidenced. Dealing with the acquisition of relevant pharmacokinetic data, examples concerning human serum albumin binding studies are reviewed. In particular, papers are reported in which the serum carrier has been studied to monitor the enantioselective binding of chiral drugs and the mutual interaction between co-administered drugs by CE and HPLC. Finally CE, as merging techniques with very promising and interesting application of microscale analysis of drugs’ binding parameters to immobilized bio-polymers is examined.