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

First comparison of commercial systems to prepare nanofat: technical performances and biological quality differ among obtained products.

Arcani R., Abellan M., Simoncini S., Dani V., Robert S., Zavarro A.

Laboratory Study, published in Sci Rep (2026) — 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
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
Laboratory Study
Journal
Sci Rep (2026)
Country
England
Reported sample size
—
Source database
PubMed
PMID
41720956
PMCID
PMC13022058
DOI
10.1038/s41598-026-40847-2

Abstract (original English)

Nanofat is a relatively recent fat grafting technique obtained involving the mechanical emulsification of adipose tissue whose preparation is produced at the patient's bedside. Although it was initially reported to improve skin quality in intradermal applications, it is now increasingly used in regenerative medicine. However, the absence of standardized protocols and the diversity of commercial devices result in nanofat products of variable quality. This study presents the first comprehensive comparison of nanofat obtained from different commercially available preparation systems, combining both their technical performance and biological characterization. Lipoaspirates from five healthy donors were processed using eight commercially available devices for nanofat production using emulsification or micronization techniques. The technical parameters included preparation time, ease of preparation and injection, volumetric yield, and residual aqueous fraction. Biological analyses included stromal vascular fraction isolation with evaluation of cell viability, viable nucleated cell yield, immunophenotypic cell subtype characterization and clonogenic capacity. These parameters were compared using a scoring model that enabled inter-kit ranking, integrating both a technical performance score and a biological quality score. Additionally, nanofat-conditioned media were collected for extrac

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
HumansAdipose TissueAdipocytesCell SurvivalExtracellular VesiclesFemaleRegenerative Medicine

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