Current antiviral drugs and their analysis in biological materials-Part I: Antivirals against respiratory and herpes viruses
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Review
PubMed
28755849
DOI
10.1016/j.jpba.2017.06.071
PII: S0731-7085(17)31205-0
Knihovny.cz E-resources
- Keywords
- Antivirals, Chromatography, HIV, Hepatitis viruses, Herpes viruses, Mass spectrometry, Respiratory viruses, Sample preparation,
- MeSH
- Antiviral Agents analysis therapeutic use MeSH
- Biological Factors analysis MeSH
- Herpesviridae drug effects metabolism MeSH
- Herpesviridae Infections drug therapy metabolism MeSH
- Respiratory Tract Infections drug therapy metabolism MeSH
- Humans MeSH
- Tandem Mass Spectrometry methods MeSH
- Virus Diseases drug therapy MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Antiviral Agents MeSH
- Biological Factors MeSH
This review article is the first in the series providing an overview of currently used antiviral drugs and presenting contemporary approaches to their analysis. Large number of available antivirals and their structural variability makes this task very challenging. Trying to cover this topic comprehensively while maintaining reasonable size of the article, the review is presented in two parts. For the purpose of the overall review, antivirals were divided into four groups: (i) antivirals against herpes viruses, (ii) antivirals against respiratory viruses, (iii) antivirals against hepatitis viruses, and (iv) antivirals against HIV. Part one is devoted to the groups (i) and (ii) and also concerns the key features of the bioanalytical method. The mechanisms of action of antivirals against respiratory and herpes viruses and their use in clinical practice are briefly outlined, and the analytical methods for selected representatives of each class are described in more detail. The methods developed for the determination of drugs from these classes mostly include conventional procedures. In contrast, current trends such as UHPLC are used rarely and proper method validation based on requirements of bioanalytical guidelines can be often considered insufficient.
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