Evidence map›Paper›PMID 38623980›Full record

ArticleCurrent pharmaceutical biotechnology2025

A Novel Approach of Polyvinyl Alcohol/Acrylic Acid Based Hydrogels for Controlled Delivery of Diclofenac Sodium.

Muhammad Suhail, Syed Faisal Badshah, I-Hui Chiu, Arif Ullah, Arshad Khan, Hamid Ullah, Noorah Saleh Al-Sowayan, Ming-Jun Tsai, Pao-Chu Wu

Abstract read
PubMed Publisher
In one paragraph

Article in Current pharmaceutical biotechnology, 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
1.2field-weighted citation impact, top 25% 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

9 authors at 5 institutions in 4 countries.

Muhammad SuhailSchool of Pharmacy, Kaohsiung Medical University, Kaohsiung, 80708, Taiwan.
Syed Faisal BadshahDepartment of Pharmacy, Faculty of Medical and Health Sciences, University of Poonch Rawalakot, Azad Jammu and Kashmir, 10250, Pakistan.
I-Hui ChiuSchool of Pharmacy, Kaohsiung Medical University, Kaohsiung, 80708, Taiwan.
Arif UllahDepartment of Pharmacy, University of Science and Technology Bannu, Bannu, 28100, Pakistan.
Arshad KhanDepartment of Pharmaceutics, Faculty of Pharmacy, Khawaja Fareed Campus (Railway Road), The Islamia University of Bahawalpur, Bahawalpur, 63100, Pakistan.
Hamid UllahSchool of Pharmacy, Kaohsiung Medical University, Kaohsiung, 80708, Taiwan.
Noorah Saleh Al-SowayanDepartment of Biology, College of Pharmacy, Qassim University, Buraydah, Saudi Arabia.
Ming-Jun TsaiSchool of Pharmacy, Kaohsiung Medical University, Kaohsiung, 80708, Taiwan.
Pao-Chu WuSchool of Pharmacy, Kaohsiung Medical University, Kaohsiung, 80708, Taiwan.
Kaohsiung Medical University · TWIslamia University of Bahawalpur · PKQassim University · SAUniversity of Azad Jammu and Kashmir · PKUniversity of Science and Technology Bannu · PK

Funding

National Science and Technology Council of Taiwan NSTC 112-2320-B-037-014-MY3
6 · The paper itself

Abstract

AIM AND

objectiveThe aim of this study was to prepare polyvinyl alcohol/acrylic acid (PVA/AA) hydrogels for the controlled release of diclofenac sodium as controlled release carriers to overcome not only the side effects of diclofenac sodium but also sustain its release for an extended period.

backgroundDiclofenac sodium is employed for relieving pain and fever. The half-life of diclofenac sodium is very short (1-2 h). Hence, multiple intakes of diclofenac sodium are required to maintain a constant pharmacological action. Multiple GI adverse effects are produced as a result of diclofenac sodium intake.

methodsA free radical polymerization technique was used for crosslinking PVA with AA in the presence of APS. EGDMA was used as a cross-linker. FTIR and XRD confirmed the preparation and loading of the drug by prepared hydrogels. An increase in the thermal stability of PVA was shown by TGA and DSC analysis. Surface morphology was investigated by SEM. Similarly, water penetration and drug loading were demonstrated by porosity and drug loading studies. The pH-sensitive nature of PVA/AA hydrogels was investigated at different pH values by swelling and drug release studies.

resultsThe development and drug loading of PVA/AA hydrogels were confirmed by FTIR and XRD analysis. TGA and DSC indicated high thermal stability of prepared hydrogels as compared to unreacted PVA. SEM indicated a hard and compact network of developed hydrogels. The swelling and drug release studies indicated maximum swelling and drug release at high pH as compared to low pH values, indicating the pH-sensitive nature of prepared hydrogels. Moreover, we demonstrated that drug release was sustained for a prolonged time in a controlled pattern by prepared hydrogels by comparing the drug release of the developed hydrogels with the commercial product Cataflam.

conclusionThe results indicated that prepared PVA/AA hydrogels can be used as an alternative approach for the controlled delivery of diclofenac sodium.

Indexed as

AcrylatesAnti-Inflammatory Agents, Non-SteroidalDiclofenacDrug CarriersHydrogelsPolyvinyl AlcoholDelayed-Action PreparationsDrug Delivery SystemsDrug LiberationHydrogen-Ion ConcentrationSpectroscopy, Fourier Transform InfraredAcrylatesacrylic acidAnti-Inflammatory Agents, Non-SteroidalDelayed-Action PreparationsDiclofenacDrug CarriersHydrogelsPolyvinyl AlcoholDrug delivery systemsdrug release studieshydrogelspolymer polyvinyl alcohol (PVA).porosityswelling

Identifiers

PMID38623980
OpenAlexW4394833152

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.