Evidence map›Paper›PMID 39407632›Full record

ArticleMolecules (Basel, Switzerland)2024

Characterization and Crystal Structural Analysis of Novel Carvedilol Adipate and Succinate Ethanol-Solvated Salts.

Li Ye, Takayuki Furuishi, Takefumi Yamashita, Etsuo Yonemochi

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. 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
–field-weighted citation impact
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

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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.

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

4 authors.

Li YeDepartment of Physical Chemistry, School of Pharmacy and Pharmaceutical Sciences, Hoshi University, 2-4-41 Ebara, Shinagawa-ku 142-8501, Tokyo, Japan.
Takayuki FuruishiJuntendo University Faculty of Pharmacy, 6-8-1 Hinode, Urayasu 279-0013, Chiba, Japan.ORCID 0000-0002-5085-4683
Takefumi YamashitaDepartment of Physical Chemistry, School of Pharmacy and Pharmaceutical Sciences, Hoshi University, 2-4-41 Ebara, Shinagawa-ku 142-8501, Tokyo, Japan.
Etsuo YonemochiSchool of Pharmacy at Narita, International University of Health and Welfare, 4-3 Kozunomori, Narita 286-8686, Chiba, Japan.ORCID 0000-0001-5255-5129

Funding

Japan Society for the Promotion of Science 23K06220
6 · The paper itself

Abstract

Two ethanol-solvated adipate and succinate salts of carvedilol (CVD), a Biopharmaceutics Classification System class 2 drug, were synthesized by crystallizing ethanol with adipic acid (ADP) and succinic acid (SUA). Proton transfer from ADP and SUA to CVD and the presence of ethanol in the two novel compounds were confirmed using powder X-ray diffraction, Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, and single-crystal X-ray diffraction measurements. The two novel ethanol-solvated salts exhibited enhanced solubility and dissolution rates compared with pure carvedilol in phosphate buffer (pH 6.8). Additionally, the morphologies and attachment energies of the two novel compounds and pure CVD were calculated based on their single-crystal structures, revealing a correlation between attachment energy and dissolution rate.

Indexed as

AdipatesCarvedilolEthanolSolubilityCalorimetry, Differential ScanningCrystallizationCrystallography, X-RayMolecular StructurePropanolaminesSaltsSpectroscopy, Fourier Transform InfraredSuccinic AcidThermogravimetryX-Ray DiffractionAdipatesadipic acidCarvedilolEthanolPropanolaminesSaltsSuccinic Acidadipic acidattachment energycarvedilolcrystal structuremorphologysolubilitysuccinic acid

Identifiers

PMID39407632
PMCPMC11478148

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Registered trials

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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.