Unrivalled Stromal Cells.
Autologous fat grafting is a minimally invasive, non-surgical procedure in which adipose tissue, rich in mesenchymal stem cells is harvested from the stomach or leg, processed to create a fat rich in stem cells, and finally injected to add volume and healing; giving long-term - if not permanent - results. By simply using existing fat tissue for regeneration, it provides a long-term - if not permanent - treatment that has almost a zero risk of adverse reaction.
Lipoaspiration
First, the adipose tissue is harvested from the patient, consisting of triglyceride, the fat layer, the tumescent solution and RBC remnant.
Micronization
The triglyceride and tumescence is discarded and the fat is cut with the specially designed microlyzer blades. The solution can be processed to be millifat, microfat and nanofat, which have different properties.
Injection
After processing through the correct number of microlyzers, the adipose is injected for the procedure. Milifat is a thick fat used for filling applications, microfat is used for deep wrinkles and general aesthetic appearance, and nanofat is used for superficial dermal and hair regeneration.
STUDIES AND RESEARCH
Unlike similar systems, Lipomine's patented microlyzer technology cuts the adupose with greater precision and mazimises tissue vitality and the number of free SVF cells in its field.
*At IFATS 2019 Marseille, France Congress, taken from Dr. Jeremy Magalon's unbiased benchmark presentation.
For Osteogenic, Chondrogenic and Adipogenic Differentiation
The differentiation adipose-derived mesenchymal stem cells (ADMSC) obtained from Microlyzer technology is as follows. Adipogenz was demonstrated by the accumulation of lipid vacuoles stained with Oil Red O. Chondrogenesis was demonstrated by accumution of sulfated proteoglycan-rich matrix stained with Safranin-O. Osteogenesis was demonstrated by Alizarin Red staining of extracellular matrix calcification.
For Osteogenic, Chondrogenic and Adipogenic Differentiation
The differentiation adipose-derived mesenchymal stem cells (ADMSC) obtained from Microlyzer technology is as follows. Adipogenz was demonstrated by the accumulation of lipid vacuoles stained with Oil Red O. Chondrogenesis was demonstrated by accumution of sulfated proteoglycan-rich matrix stained with Safranin-O. Osteogenesis was demonstrated by Alizarin Red staining of extracellular matrix calcification.
BEFORE AND AFTER PHOTOS
One session of the Lipomine Kit.
Before
After
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