Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System

The contamination of drug residues, including chiral ones, is not acceptable in earth’s ecosystem. The dynamicity of enantiomers of thalidomide and its derivatives (3-methyl thalidomide, 3-ethyl thalidomide, and 3-butyl thalidomide) was ascertained at supramolecular level in water-sediment system us...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: ALI, IMRAN (author)
مؤلفون آخرون: GUPTA, VINOD K. (author), ABOUL-ENEIN, HASSAN Y. (author), unknown (author)
التنسيق: article
منشور في: 2009
الموضوعات:
الوصول للمادة أونلاين:https://eprints.kfupm.edu.sa/id/eprint/136162/1/Chirality_Prf_Gupta.pdf
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author ALI, IMRAN
author2 GUPTA, VINOD K.
ABOUL-ENEIN, HASSAN Y.
unknown
author2_role author
author
author
author_facet ALI, IMRAN
GUPTA, VINOD K.
ABOUL-ENEIN, HASSAN Y.
unknown
author_role author
dc.creator.none.fl_str_mv ALI, IMRAN
GUPTA, VINOD K.
ABOUL-ENEIN, HASSAN Y.
unknown
dc.date.none.fl_str_mv 2009-05-27
2020
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv https://eprints.kfupm.edu.sa/id/eprint/136162/1/Chirality_Prf_Gupta.pdf
(2009) Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System. Wiley InterScience.
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv https://eprints.kfupm.edu.sa/id/eprint/136162/
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Chemistry
dc.title.none.fl_str_mv Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System
dc.type.none.fl_str_mv Article
PeerReviewed
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description The contamination of drug residues, including chiral ones, is not acceptable in earth’s ecosystem. The dynamicity of enantiomers of thalidomide and its derivatives (3-methyl thalidomide, 3-ethyl thalidomide, and 3-butyl thalidomide) was ascertained at supramolecular level in water-sediment system using solid phase extraction (SPE) and stereoselective HPLC. Enantiomeric separation of these drugs was carried out on Ceramosphere RU-2 (25 cm 3 0.46 cm, particle size 50 lm) chiral column using pure ethanol (1.0 ml/min) as eluent at 230 nm detection. Retention times, capacity, separation, and resolution factors of the enantiomers of these drugs were in the range of 20.0–36.0, 2.08–3.93, 1.35–1.57, and 1.0–2.0 min, respectively. Percentage recoveries of the enantiomers in SPE were in the range of 90.0 to 95.0 in water-sediment system. Langmuir and Freundlich model were best fitted for dynamic equilibrium concentrations at different experimental parameters. Thalidomide and its derivatives follow first-order kinetics at dynamic equilibrium. The rate constants of chiral interconversions were 0.390 and 0.385 days21 for S- and R-enantiomers, respectively. The uptake of thalidomide by sediment is quite good and of endothermic nature indicating good self-purifi-cation capacity of the nature for such toxic species. Chirality 00:000–000, 2009. VVC 2009 Wiley-Liss, Inc.
eu_rights_str_mv openAccess
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identifier_str_mv (2009) Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System. Wiley InterScience.
language_invalid_str_mv en
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spelling Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment SystemALI, IMRANGUPTA, VINOD K.ABOUL-ENEIN, HASSAN Y.unknownChemistryThe contamination of drug residues, including chiral ones, is not acceptable in earth’s ecosystem. The dynamicity of enantiomers of thalidomide and its derivatives (3-methyl thalidomide, 3-ethyl thalidomide, and 3-butyl thalidomide) was ascertained at supramolecular level in water-sediment system using solid phase extraction (SPE) and stereoselective HPLC. Enantiomeric separation of these drugs was carried out on Ceramosphere RU-2 (25 cm 3 0.46 cm, particle size 50 lm) chiral column using pure ethanol (1.0 ml/min) as eluent at 230 nm detection. Retention times, capacity, separation, and resolution factors of the enantiomers of these drugs were in the range of 20.0–36.0, 2.08–3.93, 1.35–1.57, and 1.0–2.0 min, respectively. Percentage recoveries of the enantiomers in SPE were in the range of 90.0 to 95.0 in water-sediment system. Langmuir and Freundlich model were best fitted for dynamic equilibrium concentrations at different experimental parameters. Thalidomide and its derivatives follow first-order kinetics at dynamic equilibrium. The rate constants of chiral interconversions were 0.390 and 0.385 days21 for S- and R-enantiomers, respectively. The uptake of thalidomide by sediment is quite good and of endothermic nature indicating good self-purifi-cation capacity of the nature for such toxic species. Chirality 00:000–000, 2009. VVC 2009 Wiley-Liss, Inc.2009-05-272020ArticlePeerReviewedinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://eprints.kfupm.edu.sa/id/eprint/136162/1/Chirality_Prf_Gupta.pdf (2009) Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System. Wiley InterScience. enhttps://eprints.kfupm.edu.sa/id/eprint/136162/info:eu-repo/semantics/openAccessoai::1361622020-12-31T09:18:14Z
spellingShingle Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System
ALI, IMRAN
Chemistry
status_str publishedVersion
title Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System
title_full Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System
title_fullStr Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System
title_full_unstemmed Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System
title_short Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System
title_sort Supramolecular Dynamics of Thalidomide and its Derivatives in Water-Sediment System
topic Chemistry
url https://eprints.kfupm.edu.sa/id/eprint/136162/1/Chirality_Prf_Gupta.pdf