Evidence map›Paper›PMID 36678907›Full record

ArticlePharmaceutics2023

The Effect of the Particle Size Reduction on the Biorelevant Solubility and Dissolution of Poorly Soluble Drugs with Different Acid-Base Character.

Dóra Csicsák, Rita Szolláth, Szabina Kádár, Rita Ambrus, Csilla Bartos, Emese Balogh, István Antal, István Köteles, Petra Tőzsér, Vivien Bárdos and 5 more

Abstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

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

20 citing papers in PubMed.

  1. Review
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  20. Effects ofFood science & nutrition · 2023
    Article
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

15 authors.

Dóra CsicsákDepartment of Pharmaceutical Chemistry, Semmelweis University, 9 Hőgyes Endre Street, 1092 Budapest, Hungary.
Rita SzolláthDepartment of Pharmaceutical Chemistry, Semmelweis University, 9 Hőgyes Endre Street, 1092 Budapest, Hungary.
Szabina KádárDepartment of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, 3 Műegyetem Rkp., 1111 Budapest, Hungary.
Rita AmbrusInstitute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, 6 Eötvös Street, 6720 Szeged, Hungary.ORCID 0000-0001-5496-1710
Csilla BartosInstitute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, 6 Eötvös Street, 6720 Szeged, Hungary.ORCID 0000-0003-4457-5298
Emese BaloghDepartment of Pharmaceutics, Semmelweis University, 7 Hőgyes Endre Street, 1092 Budapest, Hungary.
István AntalDepartment of Pharmaceutics, Semmelweis University, 7 Hőgyes Endre Street, 1092 Budapest, Hungary.ORCID 0000-0002-5434-201X
István KötelesDepartment of Pharmaceutical Chemistry, Semmelweis University, 9 Hőgyes Endre Street, 1092 Budapest, Hungary.ORCID 0000-0002-1678-233X
Petra TőzsérDepartment of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, 3 Műegyetem Rkp., 1111 Budapest, Hungary.
Vivien BárdosDepartment of Pharmaceutical Chemistry, Semmelweis University, 9 Hőgyes Endre Street, 1092 Budapest, Hungary.
Péter HorváthDepartment of Pharmaceutical Chemistry, Semmelweis University, 9 Hőgyes Endre Street, 1092 Budapest, Hungary.ORCID 0000-0001-7149-4173
Enikő BorbásDepartment of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, 3 Műegyetem Rkp., 1111 Budapest, Hungary.
Krisztina Takács-NovákDepartment of Pharmaceutical Chemistry, Semmelweis University, 9 Hőgyes Endre Street, 1092 Budapest, Hungary.
Bálint SinkóPion Inc., 10 Cook Street, Billerica, MA 01821, USA.
Gergely VölgyiDepartment of Pharmaceutical Chemistry, Semmelweis University, 9 Hőgyes Endre Street, 1092 Budapest, Hungary.ORCID 0000-0001-8990-3916

Funding

National Research, Development, and Innovation Fund of Hungary Grant TKP2021-EGA-02New National Excellence program of the Ministry for Innovation and Technology ÚNKP-21-4
6 · The paper itself

Abstract

Particle size reduction is a commonly used process to improve the solubility and the dissolution of drug formulations. The solubility of a drug in the gastrointestinal tract is a crucial parameter, because it can greatly influence the bioavailability. This work provides a comprehensive investigation of the effect of the particle size, pH, biorelevant media and polymers (PVA and PVPK-25) on the solubility and dissolution of drug formulations using three model compounds with different acid-base characteristics (papaverine hydrochloride, furosemide and niflumic acid). It was demonstrated that micronization does not change the equilibrium solubility of a drug, but it results in a faster dissolution. In contrast, nanonization can improve the equilibrium solubility of a drug, but the selection of the appropriate excipient used for nanonization is essential, because out of the two used polymers, only the PVPK-25 had an increasing effect on the solubility. This phenomenon can be explained by the molecular structure of the excipients. Based on laser diffraction measurements, PVPK-25 could also inhibit the aggregation of the particles more effectively than PVA, but none of the polymers could hold the nanonized samples in the submicron range until the end of the measurements.

Indexed as

biorelevant mediadissolutionparticle sizereal-time monitoringsolubility

Identifiers

PMID36678907
PMCPMC9865396

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.