Pharmacologically active compounds in the environment and their chirality
- PMID: 20852776
- DOI: 10.1039/c000408c
Pharmacologically active compounds in the environment and their chirality
Abstract
Pharmacologically active compounds including both legally used pharmaceuticals and illicit drugs are potent environmental contaminants. Extensive research has been undertaken over the recent years to understand their environmental fate and toxicity. The one very important phenomenon that has been overlooked by environmental researchers studying the fate of pharmacologically active compounds in the environment is their chirality. Chiral drugs can exist in the form of enantiomers, which have similar physicochemical properties but differ in their biological properties such as distribution, metabolism and excretion, as these processes (due to stereospecific interactions of enantiomers with biological systems) usually favour one enantiomer over the other. Additionally, due to different pharmacological activity, enantiomers of chiral drugs can differ in toxicity. Furthermore, degradation of chiral drugs during wastewater treatment and in the environment can be stereoselective and can lead to chiral products of varied toxicity. The distribution of different enantiomers of the same chiral drug in the aquatic environment and biota can also be stereoselective. Biological processes can lead to stereoselective enrichment or depletion of the enantiomeric composition of chiral drugs. As a result the very same drug might reveal different activity and toxicity and this will depend on its origin and exposure to several factors governing its fate in the environment. In this critical review a discussion of the importance of chirality of pharmacologically active compounds in the environmental context is undertaken and suggestions for directions in further research are made. Several groups of chiral drugs of major environmental relevance are discussed and their pharmacological action and disposition in the body is also outlined as it is a key factor in developing a full understanding of their environmental occurrence, fate and toxicity. This review will be of interest to environmental scientists, especially those interested in issues associated with environmental contamination with pharmacologically active compounds and chiral pollutants. As the review will outline current state of knowledge on chiral drugs, it will be of value to anyone interested in the phenomenon of chirality, chiral drugs, their stereoselective disposition in the body and environmental fate (212 references).
Similar articles
-
Chiral toxicology: it's the same thing...only different.Toxicol Sci. 2009 Jul;110(1):4-30. doi: 10.1093/toxsci/kfp097. Epub 2009 May 4. Toxicol Sci. 2009. PMID: 19414517 Review.
-
Chiral pesticides: identification, description, and environmental implications.Rev Environ Contam Toxicol. 2012;217:1-74. doi: 10.1007/978-1-4614-2329-4_1. Rev Environ Contam Toxicol. 2012. PMID: 22350557 Review.
-
Stereoselectivity in drug metabolism.Expert Opin Drug Metab Toxicol. 2007 Apr;3(2):149-58. doi: 10.1517/17425255.3.2.149. Expert Opin Drug Metab Toxicol. 2007. PMID: 17428147 Review.
-
Illicit drugs: contaminants in the environment and utility in forensic epidemiology.Rev Environ Contam Toxicol. 2011;210:59-110. doi: 10.1007/978-1-4419-7615-4_3. Rev Environ Contam Toxicol. 2011. PMID: 21170703 Review.
-
Chirality of pollutants--effects on metabolism and fate.Appl Microbiol Biotechnol. 2004 Apr;64(3):300-16. doi: 10.1007/s00253-003-1511-4. Epub 2004 Jan 10. Appl Microbiol Biotechnol. 2004. PMID: 14716466 Review.
Cited by
-
Chiral Polythiophenes: Part I: Syntheses of Monomeric Precursors.Molecules. 2021 Jul 10;26(14):4205. doi: 10.3390/molecules26144205. Molecules. 2021. PMID: 34299480 Free PMC article. Review.
-
Advances in Immunomodulatory Mesoporous Silica Nanoparticles for Inflammatory and Cancer Therapies.Biomolecules. 2024 Aug 25;14(9):1057. doi: 10.3390/biom14091057. Biomolecules. 2024. PMID: 39334825 Free PMC article. Review.
-
Unusual enantioselective cytoplasm-to-nucleus translocation and photosensitization of the chiral Ru(II) cationic complex via simple ion-pairing with lipophilic weak acid counter-anions.Nucleic Acids Res. 2023 Apr 24;51(7):3041-3054. doi: 10.1093/nar/gkad155. Nucleic Acids Res. 2023. PMID: 36938880 Free PMC article.
-
Effects of chirality on the antifungal potency of methylated succinimides obtained by Aspergillus fumigatus biotransformations. comparison with racemic ones.Molecules. 2013 May 15;18(5):5669-83. doi: 10.3390/molecules18055669. Molecules. 2013. PMID: 23676473 Free PMC article.
-
Chromatographic Studies of Protein-Based Chiral Separations.Separations. 2016 Sep;3(3):27. doi: 10.3390/separations3030027. Epub 2016 Sep 5. Separations. 2016. PMID: 28344977 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials