Evidence map›Paper›PMID 41542046›Full record

ArticleResearch square2026

Wound Healing Activity of

Astri Rozanah Siregar

Abstract readPreprint
In one paragraph

Article in Research square, 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

1 author.

Astri Rozanah SiregarIPB University.ORCID 0009-0006-4909-7554

Funding

Research Training Center for Botanicals and Chronic Diseases in Tajikistan and IndonesiaD43TW009672 · FIC · RUTGERS, THE STATE UNIV OF N.J. · PI ILYA RASKIN · 2014 to 2026
$3.2M
FIC NIH HHS D43 TW009672
6 · The paper itself

Abstract

Background: Impaired wound healing is a major complication in diabetic patients. Currently available wound therapies may cause adverse effects, highlighting the need for safer, natural alternatives. This study evaluated the wound healing potential of Methods: Diabetic excision wound models were established and animals were divided into six groups: non-diabetic untreated wounds, diabetic untreated wounds, diabetic wounds treated with UCSME ointment at concentrations of 5%, 10%, and 20%, and diabetic wounds treated with betadine ointment. Wound healing was assessed through wound area reduction, epithelialization time, inflammatory and proliferative cell counts, angiogenesis, collagen deposition, and hydroxyproline content. Phytochemical composition and antioxidant activity were also analyzed. Results: UCSME ointment significantly accelerated wound closure, shortened epithelialization time, enhanced angiogenesis, re-epithelialization, collagen synthesis, and increased neutrophil, macrophage, and fibroblast counts compared to untreated diabetic controls (p < 0.05). A 5% concentration was sufficient to improve wound closure and proliferative cell responses, while 10% and 20% concentrations showed stronger effects on inflammatory response and angiogenesis. The 20% UCSME ointment produced the most pronounced improvements in angiogenesis, re-epithelialization, and hydroxyproline levels. UCSME contained high total phenolic (20.99%) and flavonoid (0.40%) contents and exhibited strong antioxidant activity (IC Conclusion: Topical UCSME effectively promotes wound healing in diabetic rats and represents a promising natural therapeutic candidate for diabetic wound management.

Indexed as

antioxidant activitydiabetic wound healingGC-MSLC-MS/MSphenolic compoundstopical ointmentUncaria callophylla

Identifiers

PMID41542046
PMCPMC12803335

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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.