Evidence map›Paper›PMID 42239586›Full record

ArticleRSC advances2026

Engineering matrix-embedded dual-drug eluting biodegradable surgical sutures for prophylaxis against surgical site infections.

Garba Mohammed Khalid, Neel Anil Chaudhary, Nura Hassan, Lubabah Rahman, Shahnaz Kashif, Gunjan V Jahakar, Mouhamad Khoder

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. 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.

Garba Mohammed KhalidSchool of Life Sciences, Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University Penrhyn Road Kingston upon Thames KT1 2EE UK.ORCID https://orcid.org/0000-0003-4045-7702
Neel Anil ChaudharySchool of Life Sciences, Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University Penrhyn Road Kingston upon Thames KT1 2EE UK.
Nura HassanSchool of Life Sciences, Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University Penrhyn Road Kingston upon Thames KT1 2EE UK.
Lubabah RahmanSchool of Life Sciences, Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University Penrhyn Road Kingston upon Thames KT1 2EE UK.
Shahnaz KashifSchool of Life Sciences, Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University Penrhyn Road Kingston upon Thames KT1 2EE UK.
Gunjan V JahakarSchool of Life Sciences, Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University Penrhyn Road Kingston upon Thames KT1 2EE UK.
Mouhamad KhoderSchool of Life Sciences, Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University Penrhyn Road Kingston upon Thames KT1 2EE UK.ORCID https://orcid.org/0000-0002-7640-471X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite advances in aseptic technique and conventional antimicrobial prophylaxis, surgical site infections (SSIs) remain a leading cause of postoperative morbidity, mortality, and healthcare costs globally. Traditional sutures merely approximate tissue and can harbour microorganisms that drive the emergence of multidrug-resistant pathogens. Thus, SSIs contribute significantly to the spread of antimicrobial resistance (AMR). To address this dual challenge, this study focuses on developing and characterize biodegradable, multi-drug-eluting sutures capable of localised delivery of two therapeutic agents to prevent infection and promote wound healing. Two clinically relevant therapeutic agents, levofloxacin (broad-spectrum antibiotic) and ibuprofen (an anti-inflammatory), were incorporated into biodegradable polycaprolactone (PCL) polymer. Placebo (F1), levofloxacin-only (F2), and dual-drug (F3) biodegradable sutures conforming to the USP 2-0 size specification were successfully fabricated using solvent-free hot-melt extrusion technology. Solid-state analyses (DSC and PXRD), as well as FTIR and Raman spectroscopy, confirmed that the drugs were amorphous and molecularly dispersed in the suture.

Identifiers

PMID42239586
PMCPMC13227474

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Registered trials

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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.