Evidence map›Paper›PMID 35557697›Full record

ArticleACS omega2022

Crystal Forms of the Antihypertensive Drug Irbesartan: A Crystallographic, Spectroscopic, and Hirshfeld Surface Analysis Investigation.

Andrea Mariela Araya-Sibaja, Cinira Fandaruff, Ana María Guevara-Camargo, Felipe Vargas-Huertas, William J Zamora, José Roberto Vega-Baudrit, Teodolito Guillén-Girón, Mirtha Navarro-Hoyos, Paola Paoli, Patrizia Rossi and 1 more

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2022. 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
1.4field-weighted citation impact, top 19% 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, 5 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

11 authors at 6 institutions in 4 countries.

Andrea Mariela Araya-SibajaLaboratorio Nacional de Nanotecnología LANOTEC-CeNAT-CONARE, Pavas, 1174-1200 San José, Costa Rica.ORCID https://orcid.org/0000-0001-9809-6079
Cinira FandaruffUniversidade Federal de Santa Catarina, Campus Universitário, Trindade, CCS, Bloco J/K, 89040970 Florianópolis, Brazil.
Ana María Guevara-CamargoLaboratorio Nacional de Nanotecnología LANOTEC-CeNAT-CONARE, Pavas, 1174-1200 San José, Costa Rica.
Felipe Vargas-HuertasLaboratorio Bioactividad para el Desarrollo Sustentable BIODESS, Escuela de Química, Universidad de Costa Rica, San Pedro de Montes de Oca, 2060 San José, Costa Rica.ORCID https://orcid.org/0000-0002-6270-0403
William J ZamoraGrupo CBio3, Escuela de Química, Universidad de Costa Rica, San Pedro de Montes de Oca, 2060 San José, Costa Rica.ORCID https://orcid.org/0000-0003-4029-4528
José Roberto Vega-BaudritLaboratorio Nacional de Nanotecnología LANOTEC-CeNAT-CONARE, Pavas, 1174-1200 San José, Costa Rica.ORCID https://orcid.org/0000-0002-2002-1744
Teodolito Guillén-GirónEscuela de Ciencia e Ingeniería de los Materiales, Tecnológico de Costa Rica, Cartago 159-7050, Costa Rica.
Mirtha Navarro-HoyosLaboratorio Bioactividad para el Desarrollo Sustentable BIODESS, Escuela de Química, Universidad de Costa Rica, San Pedro de Montes de Oca, 2060 San José, Costa Rica.ORCID https://orcid.org/0000-0003-2115-4677
Paola PaoliDepartment of Industrial Engineering, University of Firenze, Via S. Marta 3, 50139 Firenze, Italy.ORCID https://orcid.org/0000-0002-2408-4590
Patrizia RossiDepartment of Industrial Engineering, University of Firenze, Via S. Marta 3, 50139 Firenze, Italy.ORCID https://orcid.org/0000-0002-6316-338X
William JonesDepartment of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.ORCID https://orcid.org/0000-0002-4690-4852
Universidad de Costa Rica · CRUniversity of Florence · ITInstituto Tecnológico de Costa Rica · CRUniversidade Federal de Santa Catarina · BRUniversidad Nacional · CRUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The design of new pharmaceutical solids with improved physical and chemical properties can be reached through in-detail knowledge of the noncovalent intermolecular interactions between the molecules in the context of crystal packing. Although crystallization from solutions is well-known for obtaining new solids, the effect of some variables on crystallization is not yet thoroughly understood. Among these variables, solvents are noteworthy. In this context, the present study aimed to investigate the effect of ethanol (EtOH), acetonitrile (MeCN), and acetone (ACTN) on obtaining irbesartan (IBS) crystal forms with 2,3-dibromosuccinic acid. Crystal structures were solved by single-crystal diffraction, and the intermolecular interactions were analyzed using the Hirshfeld surfaces analysis. The characterization of physicochemical properties was carried out by powder X-ray diffraction, Fourier transform infrared spectroscopy (FT-IR), thermal analysis, and solution-state NMR techniques. Two different IBS salts were obtained, one from MeCN and ACTN (compound

Identifiers

PMID35557697
PMCPMC9089371
OpenAlexW4224289583

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.