Circular dichroism in functional quality evaluation of medicines.

Han Yao, Evelien Wynendaele, Xiaolong Xu, Anne Kosgei, Bart De Spiegeleer
Author Information
  1. Han Yao: Drug Quality and Registration (DruQuaR) Group, Department of Pharmaceutical Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460 , 9000 Ghent, Belgium.
  2. Evelien Wynendaele: Drug Quality and Registration (DruQuaR) Group, Department of Pharmaceutical Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460 , 9000 Ghent, Belgium.
  3. Xiaolong Xu: Drug Quality and Registration (DruQuaR) Group, Department of Pharmaceutical Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460 , 9000 Ghent, Belgium.
  4. Anne Kosgei: Drug Quality and Registration (DruQuaR) Group, Department of Pharmaceutical Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460 , 9000 Ghent, Belgium.
  5. Bart De Spiegeleer: Drug Quality and Registration (DruQuaR) Group, Department of Pharmaceutical Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460 , 9000 Ghent, Belgium. Electronic address: Bart.DeSpiegeleer@UGent.be.

Abstract

Circular dichroism (CD) is a non-destructive and powerful technique for providing structure and ligand interaction information of small molecules as well as biotechnological medicines. While CD is a well-established technique in biomedical research, and different types and variants of CD do exist, the focus of this review is on the pharmaceutical quality control (QC) aspects of the classic electronic CD (ECD). The basic principles of the CD technique are initially described, followed by a systematic literature research on pharmaceutical aspects encompassing chiral small molecules, bio-polymers (i.e. proteins, peptides and nucleic acids), medicine-biotarget interaction (i.e. small molecule-albumin interaction, protein-receptor interaction and peptide-biotarget interaction) and medicine changes (i.e. chemical modification, biosimilar/bio-better with stability and aggregation). In addition, unstructured literature was also included covering the use of CD mainly in discovery and fundamental research, but which might shift towards the pharmaceutical QC field as well in the future.

Keywords

MeSH Term

Circular Dichroism
Ligands
Nucleic Acids
Peptides
Pharmaceutical Preparations
Proteins
Quality Control

Chemicals

Ligands
Nucleic Acids
Peptides
Pharmaceutical Preparations
Proteins

Word Cloud

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