Evidence map›Paper›PMID 42252294›Full record

ArticleScientific reports2026

Engineered novel dually cross-linked hydrogel system embedded with Apigenin-cyclodextrin complex for surgical wound healing.

Zakir Ali, Fatima Zahid, Ainy Butt, Muhammad Owais Ahmad, Ali H Alamri, Adel Al Fatease, Zahrah Ali Asiri, Nabil K Alruwaili, Muhammad Aamir Zohaib, Fakhar Ud Din

Abstract read
In one paragraph

Article in Scientific reports, 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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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

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3 · Its place in the literature

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4 · The record

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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

10 authors.

Zakir AliNanomedicine Research Group, Department of Pharmacy, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Fatima ZahidNanomedicine Research Group, Department of Pharmacy, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Ainy ButtNanomedicine Research Group, Department of Pharmacy, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan.
Muhammad Owais AhmadHerbion Pharmaceutical Pakistan (Pvt) Ltd, Islamabad Plant, Islamabad, Pakistan.
Ali H AlamriDepartment of Pharmaceutics, College of Pharmacy, King Khalid University, 62529, Abha, Saudi Arabia.
Adel Al FateaseDepartment of Pharmaceutics, College of Pharmacy, King Khalid University, 62529, Abha, Saudi Arabia.
Zahrah Ali AsiriDepartment of Pharmaceutics, College of Pharmacy, King Khalid University, 62529, Abha, Saudi Arabia.
Nabil K AlruwailiPharmacy Department, Alnahda College, Riyadh, Kingdom of Saudi Arabia.
Muhammad Aamir ZohaibCollege of Pharmaceutical Sciences, Soochow University, Dushu Lake Campus, Ren'nai Lu, Suzhou, 215000, Jiangsu Province, China.
Fakhar Ud DinNanomedicine Research Group, Department of Pharmacy, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad, 45320, Pakistan. fudin@qau.edu.pk.

Funding

Higher Education Commision, Pakistan 20-14604/ NRPU/R&D/HEC/2021Higher Education Commision, Pakistan 520-149873-2MD6-118
6 · The paper itself

Abstract

Surgical wounds present a critical clinical challenge often requiring advanced therapeutic strategies to accelerate healing and enhance tissue regeneration. Herein, we engineered novel dually cross-linked hydrogel system incorporating an Apigenin-β-cyclodextrin (API-βCD) inclusion complex for enhanced wound therapy. First, the API-βCD inclusion complex was prepared and characterized comprehensively through nuclear magnetic resonance (NMR) and Fourier transform infrared (FTIR) spectroscopy, X-ray diffractometry (XRD), scanning electron microscopy (SEM), molecular docking and phase solubility studies. Then, dually cross-linked hydrogel matrix embedded with the API-βCD complex was synthesized and assessed for comprehensive structural, mechanical and physiochemical properties. In vitro release, ex vivo permeation, cell viability, antibacterial activity, wound closure and anti-inflammatory cells analyses of the API-βCD hydrogel were performed. Results confirmed the formation of successful inclusion complex. Phase solubility study demonstrated 66.8 ~ fold increase in the aqueous solubility of API. FTIR analysis confirmed successful crosslinking within the hydrogel matrix. Moreover, API-βCD hydrogel exhibited enhanced mechanical properties, porous architecture and optimal swelling and degradation behaviors. In vitro and ex vivo studies demonstrated sustained release, minimal permeation and enhanced disposition (57%) of API in skin layers, higher cell viability, and augmented antibacterial potential. Additionally, API-βCD hydrogel demonstrated significantly accelerated wound healing with 97% wound closure and noticeable downregulation of inflammatory parameters, such as TNF-α and IL-1β. These results concluded that API-βCD hydrogel may improve the solubility, dissolution of API and holds promising potential for regenerative wound management.

Indexed as

Apigeninbeta-CyclodextrinsHydrogelsWound HealingAnimalsAnti-Bacterial AgentsCell SurvivalHumansMolecular Docking SimulationSolubilitySpectroscopy, Fourier Transform InfraredAnti-Bacterial AgentsApigeninbeta-CyclodextrinsbetadexHydrogelsApigeninHydrogel systemPolygalacturonic acidSolubilityWound healing

Identifiers

PMID42252294
PMCPMC13328717

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LicenceCC BY-NC-ND
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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.