Evidence map›Paper›PMID 41602186›Full record

ArticleRSC advances2026

Novel pH-responsive pectin-based hybrid smart hydrogels for in vitro drug release and in vivo wound healing applications.

Hirra Manzoor, Nasima Arshad, Muhammad A U R Qureshi, Sher Qadar

Abstract read
In one paragraph

Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Hirra ManzoorDepartment of Chemistry Allama Iqbal Open University Islamabad Pakistan nasimaa2006@yahoo.com nasima.arshad@aiou.edu.pk hirramanzoor@gmail.com aneesqureshi287@gmail.com sherqadar@gmail.com.
Nasima ArshadDepartment of Chemistry Allama Iqbal Open University Islamabad Pakistan nasimaa2006@yahoo.com nasima.arshad@aiou.edu.pk hirramanzoor@gmail.com aneesqureshi287@gmail.com sherqadar@gmail.com.ORCID https://orcid.org/0000-0002-4257-9909
Muhammad A U R QureshiDepartment of Chemistry Allama Iqbal Open University Islamabad Pakistan nasimaa2006@yahoo.com nasima.arshad@aiou.edu.pk hirramanzoor@gmail.com aneesqureshi287@gmail.com sherqadar@gmail.com.
Sher QadarDepartment of Chemistry Allama Iqbal Open University Islamabad Pakistan nasimaa2006@yahoo.com nasima.arshad@aiou.edu.pk hirramanzoor@gmail.com aneesqureshi287@gmail.com sherqadar@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite their exceptional biocompatibility and non-toxicity, pectin-based hydrogels suffer from poor mechanical strength, water sensitivity and high instability, which limit their utilization in the biomedical sector. Therefore, main objective behind this study was to develop integrated pectin-based hydrogel system to improve mechanical and structural properties of hydrogels for biomedical applications. Multifunctional hydrogels were formulated to integrate the gel-forming capabilities and biocompatibility of polyvinyl alcohol (PVA) and pectin, with the crosslinking and structural reinforcement of 3-aminopropyltriethoxysilane (APTES), and the antimicrobial and drug-loading capabilities of graphene oxide (GO) fillers. Using varied GO concentrations, pectin/PVA/APTES/GO hydrogel series PPG (-2.5, -5, -7.5, and -10) was synthesized, and samples' structural integrity, amorphous nature, porous morphology, and thermal stability were characterized. The hydrogels demonstrated high cell viability, biodegradation, and antibacterial activity, and their swelling in distilled water (DW) reached a maximum value of 3300% in 120 min. The greatest degree of swelling was observed at pH 8 in both buffered and non-buffered solutions. Following the Higuchi, zero-order, and Korsmeyer-Peppas models for controlled release kinetics, 91.44% of levofloxacin (LVX) was released from the drug-loaded hydrogel (DPPG) within 3.5 hours in a PBS (pH 7.4) solution. Furthermore,

Identifiers

PMID41602186
PMCPMC12833731

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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.