Literature DB >> 20852776

Pharmacologically active compounds in the environment and their chirality.

Barbara Kasprzyk-Hordern1.   

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).

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Year:  2010        PMID: 20852776     DOI: 10.1039/c000408c

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  28 in total

1.  Structure-guided RP-HPLC chromatography of diastereomeric α-helical peptide analogs substituted with single amino acid stereoisomers.

Authors:  Yibing Huang; Ling Pan; Lianjing Zhao; Colin T Mant; Robert S Hodges; Yuxin Chen
Journal:  Biomed Chromatogr       Date:  2013-10-11       Impact factor: 1.902

2.  Ecotoxicological evaluation of propranolol hydrochloride and losartan potassium to Lemna minor L. (1753) individually and in binary mixtures.

Authors:  Aline A Godoy; Fábio Kummrow; Paulo Augusto Z Pamplin
Journal:  Ecotoxicology       Date:  2015-04-07       Impact factor: 2.823

3.  Electric-field-induced assembly and propulsion of chiral colloidal clusters.

Authors:  Fuduo Ma; Sijia Wang; David T Wu; Ning Wu
Journal:  Proc Natl Acad Sci U S A       Date:  2015-05-04       Impact factor: 11.205

Review 4.  Analysis of stereoselective drug interactions with serum proteins by high-performance affinity chromatography: A historical perspective.

Authors:  Zhao Li; David S Hage
Journal:  J Pharm Biomed Anal       Date:  2017-01-11       Impact factor: 3.935

5.  Characterization, crystallization and preliminary X-ray diffraction analysis of an (S)-specific esterase (pfEstA) from Pseudomonas fluorescens KCTC 1767: enantioselectivity for potential industrial applications.

Authors:  Seulgi Kim; Tri Duc Ngo; Kyeong Kyu Kim; T Doohun Kim
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2012-10-30

6.  Stereoselective Activity of 1-Propargyl-4-styrylpiperidine-like Analogues That Can Discriminate between Monoamine Oxidase Isoforms A and B.

Authors:  Damijan Knez; Natalia Colettis; Luca G Iacovino; Matej Sova; Anja Pišlar; Janez Konc; Samo Lešnik; Josefina Higgs; Fabiola Kamecki; Irene Mangialavori; Ana Dolšak; Simon Žakelj; Jurij Trontelj; Janko Kos; Claudia Binda; Mariel Marder; Stanislav Gobec
Journal:  J Med Chem       Date:  2020-01-22       Impact factor: 7.446

7.  Highly efficient electro-oxidation catalyst under ultra-low voltage for degradation of aspirin.

Authors:  Xiaolei Kang; Wei Sun; Limei Cao; Ji Yang
Journal:  Environ Sci Pollut Res Int       Date:  2017-09-22       Impact factor: 4.223

8.  Vectorial Electron Spin Filtering by an All-Chiral Metal-Molecule Heterostructure.

Authors:  Chetana Badala Viswanatha; Johannes Stöckl; Benito Arnoldi; Sebastian Becker; Martin Aeschlimann; Benjamin Stadtmüller
Journal:  J Phys Chem Lett       Date:  2022-06-30       Impact factor: 6.888

Review 9.  A review of combined sewer overflows as a source of wastewater-derived emerging contaminants in the environment and their management.

Authors:  Bruce Petrie
Journal:  Environ Sci Pollut Res Int       Date:  2021-04-29       Impact factor: 4.223

10.  Helical springs as a color indicator for determining chirality and enantiomeric excess.

Authors:  Katsuhiro Maeda; Daisuke Hirose; Mai Nozaki; Yoichi Shimizu; Taro Mori; Kentaro Yamanaka; Koji Ogino; Tatsuya Nishimura; Tsuyoshi Taniguchi; Munetsugu Moro; Eiji Yashima
Journal:  Sci Adv       Date:  2021-06-30       Impact factor: 14.136

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