Evidence map›Paper›PMID 42077907›Full record

ArticleACS omega2026

Complexation of Citalopram with β‑Cyclodextrin, Mono-subetadex, and Subetadex: Phase Solubility, Hummel-Dreyer, Affinity Capillary Electrophoresis, ITC, and NMR Studies.

Dóra V Ujj, Petr Kasal, Ida Fejős, Szabolcs Béni, József Kardos, Gábor Benkovics, Erika Bálint, Béla Mátravölgyi

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Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

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

8 authors.

Dóra V UjjDepartment of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem rkp. 3, Budapest H-1111, Hungary.
Petr KasalInstitute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Národni 3, Prague 1 CZ-110 00, Czech Republic.
Ida FejősDepartment of Pharmacognosy, Semmelweis University, Üllői út 26, Budapest H-1085, Hungary.
Szabolcs BéniIntegrative Health and Environmental Analysis Research Laboratory, Department of Analytical Chemistry, Institute of Chemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/a, Budapest H-1117, Hungary.
József KardosELTE NAP Neuroimmunology Research Group, Department of Biochemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/C, Budapest H-1117, Hungary.ORCID https://orcid.org/0000-0002-2135-2932
Gábor BenkovicsDepartment of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem rkp. 3, Budapest H-1111, Hungary.
Erika BálintDepartment of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem rkp. 3, Budapest H-1111, Hungary.ORCID https://orcid.org/0000-0002-5107-7089
Béla MátravölgyiDepartment of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem rkp. 3, Budapest H-1111, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclodextrins (CDs) have a number of important properties, such as chiral separation or the enhancing of water solubility of various substances. In the present study the complexation properties of sugammadex analog CDs, such as subetadex (SBX) and mono-subetadex (monoSBX) were investigated and compared with the native β-CD. The complexation features were investigated at pH 7.4 using citalopram, a selective serotonin reuptake inhibitor antidepressant, as a model compound. The stability constants were investigated by phase-solubility test, the Hummel-Dreyer (HD) method, affinity capillary electrophoresis, and ITC and the different analytical techniques were comprehensively evaluated and compared. The NMR studies supported the results from the investigated techniques and the complex structure was characterized by ROESY NMR studies. The phase-solubility study yielded results that deviated from the other three techniques, with monoSBX showing the highest stability constant. In the case of the HD method, the value of stability constants significantly differed from ACE and ITC, but the trend of CD stability followed the same order (β-CD < monoSBX < SBX). The ACE and ITC methods gave very similar results for β-CD and monoSBX, with some deviations for SBX, although still within the same order of magnitude. Based on the results ACE and ITC appear to be the most reliable techniques for determining CD-guest stability constants.

Identifiers

PMID42077907
PMCPMC13130130

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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.