Level D· Scientific groundwork from lab and animal studiesAnimal StudyPubMed

Photoresponsive Multifunctional Nanoplatform Based on ADSC-Exos Coated BPQDs Demonstrates Effective Antibacterial Properties and Induces Macrophage Polarization for Infected Wound Healing.

Wang C., Chen J., Guo J., Li G., Yi K., Jiang T.

Animal Study on Chronic Wound, Chronic Inflammation, published in Adv Healthc Mater (2025) — summary generated from the PubMed abstract.

Open my reading list
Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
Read the A–D evidence level guide

This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Animal Study
Journal
Adv Healthc Mater (2025)
Country
Germany
Reported sample size
—
Source database
PubMed
PMID
40692515
DOI
10.1002/adhm.202501044
Citations
1

Abstract (original English)

Bacterial infections and the disturbance of immune microenvironment contribute to chronic non-healing wounds. Macrophage polarization and phenotypic transition play a critical role in modulating the immune microenvironment of wounds. To address these intertwined challenges of bacterial burden and immune dysregulation, an innovative multifunctional therapeutic nanoplatform is developed that integrates black phosphorus quantum dots (BPQDs) into exosomes derived from adipose stem cells (BPQDs@EXOs). In vitro experiments show that the platform exhibited broad-spectrum photothermal antibacterial properties, efficient ROS scavenging ability, and the effect of promoting M2 macrophage polarization. In infected wound models, BE + NIR promotes wound healing by eradicating bacterial infection, attenuating ROS levels, promoting M2 macrophage polarization and accelerating re-epithelialization. Mechanistic insights from deep transcriptomic analyses on day 4 and day 10 confirm that the BE nanoplatform downregulates the expression of proinflammatory genes, upregulates the expression of wound-healing genes, and induces cell proliferation. Overall, this novel approach effectively integrates photothermal antibacterial properties, macrophage polarization regulation and anti-inflammatory effects, thereby creating an optimal immune environment and providing a comprehensive solution to the challenges

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is preclinical work; animal or laboratory results cannot be applied to humans.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

How we grade evidence
Wound HealingAnti-Bacterial AgentsMacrophagesAnimalsMiceQuantum DotsExosomesReactive Oxygen SpeciesStem CellsAdipose Tissue

Browse all related research

Filter the research library by this study's title keywords, author, or publication year.

Related research