Evidence map›Paper›PMID 40277687›Full record

ArticleGels (Basel, Switzerland)2025

Pharmacological Behavior of Propylene Glycol/Polyvinyl Alcohol Hydrogel Incorporating Indomethacin Nanocrystals in the Skin.

Hiroko Otake, Fumihiko Ogata, Yosuke Nakazawa, Manju Misra, Masanobu Tsubaki, Naohito Kawasaki, Noriaki Nagai

Abstract read
In one paragraph

Article in Gels (Basel, Switzerland), 2025. 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

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

7 authors.

Hiroko OtakeFaculty of Pharmacy, Kindai University, 3-4-1, kowakae, Higahi-Osaka 577-8502, Osaka, Japan.
Fumihiko OgataFaculty of Pharmacy, Kindai University, 3-4-1, kowakae, Higahi-Osaka 577-8502, Osaka, Japan.ORCID 0000-0002-2755-8341
Yosuke NakazawaFaculty of Pharmacy, Keio University, 1-5-30 Shibakoen, Tokyo 105-8512, Japan.ORCID 0000-0002-2226-1944
Manju MisraDepartment of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Opposite Air Force Station, Palaj Basan Road, Village Palaj, Gandhinagar 382355, Gujarat, India.
Masanobu TsubakiLaboratory of Pharmacotherapy, Kagawa School of Pharmaceutical Sciences, Tokushima Bunri University, 1314-1 Shido, Sanuki 769-2193, Kagawa, Japan.
Naohito KawasakiFaculty of Pharmacy, Kindai University, 3-4-1, kowakae, Higahi-Osaka 577-8502, Osaka, Japan.ORCID 0000-0002-9412-0868
Noriaki NagaiFaculty of Pharmacy, Kindai University, 3-4-1, kowakae, Higahi-Osaka 577-8502, Osaka, Japan.ORCID 0009-0007-1266-038X

Funding

Takeda Science Foundation Pharmaceutical Research Grants 2024068087
6 · The paper itself

Abstract

backgroundWe previously reported that carbopol hydrogels incorporating indomethacin nanoparticles (IMC NPs) improved the low permeability and bioavailability of skin formulations in transdermal drug delivery systems. However, the combination of NPs with other types of hydrogels has not been sufficiently explored to date. Therefore, this study investigated propylene glycol (PG)/polyvinyl alcohol (PVA) hydrogel as an alternative base to carbopol hydrogel for incorporating IMC NPs.

methodsIMC NPs were prepared using bead milling treatment, and these NPs were incorporated into PG/PVA hydrogel (IMC-NP@PG/PVA hydrogel). The IMC concentration was measured using the HPLC method, and seven-week-old Wistar rats were used to evaluate skin absorption.

resultsBead milling reduced the IMC particle size in the PG/PVA hydrogels to the nanoscale (30-200 nm) without altering its crystalline form. The IMC-NP@PG/PVA hydrogel exhibited enhanced uniformity, solubility, and drug release compared to the IMC microparticle-loaded PG/PVA hydrogel (IMC-MP@PG/PVA hydrogel), with a 1.44-fold greater area under the concentration-time curve. Transdermal permeability studies revealed that IMC-NP@PG/PVA had 2.36-fold higher absorption than the IMC-MP@PG/PVA hydrogel, with dissolved IMC permeating the skin. Pharmacokinetics in the rats showed significantly increased plasma levels, absorption rates, and bioavailability for IMC-NP@PG/PVA, demonstrating its superior delivery efficiency. Moreover, the skin absorption of IMC-NP@PG/PVA was higher than that of carbopol hydrogel.

conclusionsThese findings highlight the potential of PG/PVA hydrogels as an effective base for transdermal drug delivery systems based on NPs.

Indexed as

hydrogelindomethacinnanocrystalpolyvinyl alcoholpropylene glycoltransdermal drug delivery system

Identifiers

PMID40277687
PMCPMC12027185

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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.