Level D· Scientific groundwork from lab and animal studiesAnimal StudyPubMedOpen access

Adaptive Gelatin Microspheres Enhanced Stem Cell Delivery and Integration With Diabetic Wounds to Activate Skin Tissue Regeneration.

Shi M., Gao Y., Lee L., Song T., Zhou J., Yan L.

Animal Study on Diabetic Foot, Chronic Wound, published in Front Bioeng Biotechnol (2022) — summary generated from the PubMed abstract.

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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
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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
Front Bioeng Biotechnol (2022)
Country
Switzerland
Reported sample size
—
Source database
PubMed
PMID
35433645
PMCID
PMC9011108
DOI
10.3389/fbioe.2022.813805
Citations
32

Abstract (original English)

The delayed and complicated diabetic wound healing raises clinical and social concerns. The application of stem cells along with hydrogels is an attractive therapeutic approach. However, low cell retention and integration hindered the performance. Herein, gelatin microspheres were fabricated for local delivery of adipose-derived stem cells (from rats, rADSCs), and the effect of rADSCs with microspheres on diabetic wound healing was examined. Uniform, well-dispersed microspheres were fabricated using the microfluidic technique. Due to geometry differences, the proteinase degradation rate for microspheres was four times that of the bulk hydrogel. The obtained gelatin microspheres supported cell's adhesion and proliferation and provided a suitable microenvironment for rADSC survival. For in vivo animal tests, rADSCs were labeled with CM-Dil for tracking purposes. Microspheres were well embedded in the regenerated tissue and demonstrated good biocompatibility and an adaptive biodegradation rate. Histological examination revealed rADSC-loaded gelatin microspheres that significantly accelerated wound healing via promoting M2 macrophage polarization, collagen deposition, angiogenesis associated with peripheral nerve recovery, and hair follicle formation. Notably, the relative fluorescence intensity around the hair follicle was 17-fold higher than that of the blank group, indicating rA

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.

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