Evidence map›Paper›PMID 37266689›Full record

ArticleJournal of molecular modeling2023

Competitive formation of molecular inclusion complexes of chlordecone and β-hexachlorocyclohexane with natural cyclodextrins: DFT and molecular dynamics study.

Anthuan Ferino-Pérez, Queiroz Portorreal, Juan J Gamboa-Carballo, Babak Minofar, Sarra Gaspard, Ulises J Jaúregui-Haza

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Article in Journal of molecular modeling, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 4 countries.

Anthuan Ferino-PérezDepartment of Chemistry, KU Leuven, B-3001, Louvain, Belgium.
Queiroz PortorrealInstituto Tecnológico de Santo Domingo (INTEC), Avenida de los Próceres #49, Los Jardines del Norte 10602, Santo Domingo, Dominican Republic.
Juan J Gamboa-CarballoLaboratory of Inorganic Chemistry (LAC), Department of Chemistry and Applied Biosciences (D-CHAB), Federal Institute of Technologies (ETH), Vladimir-Prelog-Weg 1, 8093, Zurich, Switzerland.
Babak MinofarDepartment of Chemistry, Faculty of Science, University of South Bohemia in Ceske Budejovice, Branisovska 31, 370 05, Ceske Budejovice, Czech Republic.
Sarra GaspardLaboratoire COVACHIMM2E EA 3592, Université des Antilles, BP 250, Pointe à Pitre Guadeloupe (FWI), France.
Ulises J Jaúregui-HazaInstituto Tecnológico de Santo Domingo (INTEC), Avenida de los Próceres #49, Los Jardines del Norte 10602, Santo Domingo, Dominican Republic. ulises.jauregui@intec.edu.do.
Instituto Tecnológico de Santo Domingo · DOKU Leuven · BEUniversité des Antilles · GPUniversity of South Bohemia in České Budějovice · CZ

Funding

CAPES, Guadeloupe Project DetDePestInstituto Tecnológico de Santo Domingo CIMPest-CBA-330810-2018-P-1
6 · The paper itself

Abstract

contextChlordecone (CLD) and β-hexachlorocyclohexane (β-HCH) are chlorinated pesticides that coexist as persistent organic pollutants in the groundwater of several countries in the Caribbean, being an environmental issue. This work evaluates theoretically the competitive formation of host-guest complexes pesticides@cyclodextrines (CDs) as an alternative for water purification and selective separation of pesticides.

methodsQuantum mechanical calculations based on density functional theory (DFT) and classical molecular dynamics (MD) simulations were used to achieve information on geometries, energies, structure, and dynamics of guest-host complexes in the gas phase, implicit solvent medium, and in aqueous solutions.

resultsDFT studies showed that interactions of both pesticides with CDs are mediated by steric factors and guided by maximization of the hydrophobic interactions either with the other pesticide or with the CD cavity's inner atoms. MD results corroborate the formation of stable complexes of both pesticides with the studied CDs. α-CD exhibited a preference for the smaller β-HCH molecule over the CLD that could not perturb the formed complex.

conclusionsThe simulation of competitive formation with γ-CD illustrated that this molecule could accommodate both pesticides inside its cavity. These results suggest that CDs with smaller cavity sizes such as α-CD could be used for selective separation of β-HCH from CLD in water bodies, while γ-CD could be used for methods that aim to remove both pesticides at the same time.

Indexed as

CyclodextrinsDFTMolecular dynamicsMolecular inclusion complexesPesticides

Identifiers

PMID37266689
OpenAlexW4379093995

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.