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High-Quality Lipoaspirate Following 1470-nm Radial Emitting Laser-Assisted Liposuction.
Shapira, Eyal; Plonski, Lori; Menashe, Shaked; Ofek, Andre; Rosenthal, Adaya; Brambilla, Massimiliano; Goldenberg, Gary; Haimowitz, Sahar; Heller, Lior.
Affiliation
  • Shapira E; From the Department of Plastic Surgery, Shamir Medical Center, Zerifin, Israel.
  • Plonski L; From the Department of Plastic Surgery, Shamir Medical Center, Zerifin, Israel.
  • Menashe S; From the Department of Plastic Surgery, Shamir Medical Center, Zerifin, Israel.
  • Ofek A; From the Department of Plastic Surgery, Shamir Medical Center, Zerifin, Israel.
  • Rosenthal A; From the Department of Plastic Surgery, Shamir Medical Center, Zerifin, Israel.
  • Brambilla M; Department of the Health of the Woman, Child and Neonate, Fondazione IRCSS Ospedale Maggiore, Milan, Italy.
  • Goldenberg G; Department of Dermatology, Icahn School of Medicine at Mount Sinai Hospital, Mount Sinai, NY.
  • Haimowitz S; Prostate Cancer Research Laboratory, Department of Urology, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Heller L; From the Department of Plastic Surgery, Shamir Medical Center, Zerifin, Israel.
Ann Plast Surg ; 89(6): e60-e68, 2022 12 01.
Article in En | MEDLINE | ID: mdl-36416705
ABSTRACT

BACKGROUND:

Laser-assisted liposuction (LAL) has been used to maximize viable adipocyte yields in lipoaspirates, although optimizing tissue processing methods is still a challenge. A high-quality lipoaspirate has been a key factor for extended graft longevity.

OBJECTIVE:

To assess the viability and potency of stromal vascular fraction (SVF) cells and adipose-derived stem cells (ASCs) in fat samples from lipoaspirates harvested with a novel 1470-nm diode, radial emitting LAL platform. Two processing methods, enzymatic and nonenzymatic, were compared.

METHODS:

Laser-assisted liposuction lipoaspirates harvested from 10 subjects were examined for cell viability after processing by enzymatic or nonenzymatic methods. Isolated SVF cells were cultured with an ASC-permissive medium to assess their viability and proliferation capacity by cell proliferation assay. Flow cytometric analysis with ASC-specific markers, gene expression levels, and immunofluorescence for ASC transcription factors were also conducted.

RESULTS:

Lipoaspirates showed high SVF cell viability of 97% ± 0.02% and 98% ± 0.01%, averaged SVF cell count of 8.7 × 10 6 ± 3.9 × 10 6 and 9.4 × 10 6 ± 4.2 × 10 6 cells per mL, and averaged ASC count of 1 × 10 6 ± 2.2 × 10 5 and 1.2 × 10 6 ± 5 × 10 5 cells per mL in nonenzymatic and enzymatic methods, respectively. The ASC-specific markers, gene expression levels, and immunofluorescence for ASC transcription factors confirmed the adipose origin of the cells.

CONCLUSIONS:

The laser lipoaspirates provide a high yield of viable and potent SVF cells and ASCs through both nonenzymatic and enzymatic processes. Improved purity of the harvested lipoaspirate and high ASC content are expected to result in extended graft longevity. Furthermore, eliminating enzymatic digestion may provide advantages, such as reducing process time, cost, and regulatory constraints.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lipectomy Limits: Humans Language: En Journal: Ann Plast Surg Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lipectomy Limits: Humans Language: En Journal: Ann Plast Surg Year: 2022 Document type: Article