Evidence mapPaperPMID 41348417Full record

ReviewArchives of pharmacal research2026

Exploration of recent advancements of nanoparticle-based therapeutics emphasis on diabetic-related chronic wound management: a comprehensive review.

Esraa M Elshazly, Mona G Arafa, Samia A Nour

Abstract readReview
In one paragraph

Review in Archives of pharmacal research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
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

3 authors.

Esraa M ElshazlyDepartment of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, The British University in Egypt, Cairo, Egypt.
Mona G ArafaDepartment of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, The British University in Egypt, Cairo, Egypt. mona.arafa@bue.edu.eg.
Samia A NourDepartment of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Cairo university, Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The skin is frequently subjected to injuries and disorders encompassing both acute and chronic wounds. Chronic wounds, including diabetic wounds, pose significant clinical problems due to prolonged and ineffective healing processes. Traditional therapies are associated with many limitations. In this regard, nanoparticles (NPs)-based drug delivery systems have emerged as promising solutions for improving chronic wound healing and to overcome the drawbacks of conventional approaches. Furthermore, the functionalization of these NPs through surface modification can increase the overall therapeutic performance. Incorporating them into advanced dosage form maximizes the therapeutic impact. Although their therapeutic promise is high, clinical translation of nanoparticles is hindered by challenges such as manufacturing problems with scaling up production of lipid nanoparticles and the regulatory difficulties related to nanoparticle characterization, such as compliance with FDA criteria for size variation. The current review endeavored to explore the most recently developed nanotechnology-based therapeutic agents that are used in diabetic chronic wound healing, especially SLNs. It also discusses the various surface modification strategies that can enhance therapeutic effectiveness. Further, to maximize the overall efficacy of the drug delivery system and to improve wound healing outcomes, the incorporation of NPs into advanced dosage forms such as thermoresponsive gels has a huge impact. This review also serves as a database for the methodology of collecting the required data, screening, and selection in addition to the pathways from NPs preclinical studies to the stages of clinical approval; moreover, NPs manufacturing and scaling-up feasibility.

Indexed as

Diabetes MellitusNanoparticle Drug Delivery SystemNanoparticlesWound HealingAnimalsChronic DiseaseDrug Delivery SystemsHumansNanoparticle Drug Delivery SystemDiabetic chronic wound healingNanoparticlesPreclinical and clinical studiesRegulatory approachScaling up feasibilitySolid lipid nanoparticlesThermo-responsive gel

Identifiers

PMID41348417
PMCPMC12913279

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.