Immobilized-enzyme reactors integrated with capillary electrophoresis for pharmaceutical research
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, přehledy
PubMed
28988452
DOI
10.1002/jssc.201700905
Knihovny.cz E-zdroje
- Klíčová slova
- capillary electrophoresis, drug metabolism, druggable enzymes, immobilized-enzyme reactors,
- MeSH
- design vybavení MeSH
- elektroforéza kapilární * MeSH
- enzymatické testy MeSH
- enzymy imobilizované chemie MeSH
- farmaceutický výzkum MeSH
- genom lidský MeSH
- kinetika MeSH
- léčivé přípravky MeSH
- lidé MeSH
- magnetismus MeSH
- proteomika MeSH
- reprodukovatelnost výsledků MeSH
- statická elektřina MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- enzymy imobilizované MeSH
- léčivé přípravky MeSH
Enzymes play an essential role in many aspects of pharmaceutical research as drug targets, drug metabolizers, enzyme drugs and more. In this specific field, enzyme assays are required to meet a number of specific requirements, such as low cost, easy automation, and high reliability. The integration of an immobilized-enzyme reactor to capillary electrophoresis represents a unique approach to fulfilling these criteria by combining the benefits of enzyme immobilization, that is, increased stability and repeated use, as well as the minute sample consumption, short analysis time, and efficient analysis provided by capillary electrophoresis. In this review, we summarize, analyze, and discuss published works where pharmaceutically relevant enzymes were used to prepare capillary electrophoresis-integrated immobilized-enzyme reactors in an online manner. The presented assays are divided into three distinct groups based on the drug-enzyme relationship. The first, more extensively studied group employs enzymes that are considered to be therapeutic targets, the second group of assays present tools to assess drug metabolism and the third group assesses enzyme drugs. Furthermore, we examine various methods of enzyme immobilization and their implications for assay properties.
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