SC301 Clinic Stem Cell Research Center · Cell Processing Facility License No. 139
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HomeSVF Isolation Process
( Process )

How SVF is isolated

Five steps from the moment fat enters the research center until it returns to the operating room. The conditions for each step are the values reported in Dr. Shin Dong-jin's paper (Annals of Plastic Surgery, 2023).

Why every step matters

Not "was SVF used?" but "how was it isolated?"

SVF (stromal vascular fraction) is a mixture of many cell types found in adipose tissue, including adipose-derived stem cells, endothelial progenitor cells, pericytes and fibroblasts. Separating these cells from fat cells takes several steps of physical and chemical processing.

Even small changes in temperature, processing time, centrifugal force, or the type and concentration of reagents change how many cells are obtained and how active they are. That is why, when results are discussed, the process used and how precisely the cells were isolated are treated as more important variables than whether SVF was used at all. A 2026 meta-analysis (Jefri et al., 893 patients) also found that differences in graft retention rate varied with the isolation method.

The research center standardizes this process, repeats it under the same conditions every time, and keeps a record of each step. SVF isolation alone takes 1 hour 20 minutes to 1 hour 40 minutes, and the whole surgery takes 3 hours on average.

Centrifuge fitted with buckets for different tube sizes
( 5 Steps )

Step by step

Fat leaves the operating room, passes through the research center and returns to the operating room. The number badges show the conditions reported in the paper (Annals of Plastic Surgery, 2023); actual conditions are adjusted within the protocol range according to the amount and condition of the fat.

Operating room01 Harvesting
Operating room05 Mixing & injection
SVF isolation 1 h 20 min – 1 h 40 minWhole surgery, average 3 hours
  1. 01Operating room

    Fat harvesting

    Tumescent infusionCannula aspiration

    A tumescent solution of saline, local anesthetic and a hemostatic agent is infused into the fat layer of the abdomen or thighs, and the fat is then aspirated with a dedicated cannula. Reducing physical damage to the fat cells is the starting point for SVF quality later on.

    The harvested fat enters the research center's clean area through the pass box.

  2. Centrifuge installed inside a biosafety cabinet to reduce the risk of contamination.
    02Research center

    Purification

    300 g3 min

    The harvested fat is centrifuged to remove liquid components such as blood and tumescent fluid, leaving only pure adipose tissue.

    A set amount of this is set aside for SVF isolation.

  3. Oil layerFat cellsAqueous layer(saline, etc.)SVF (stem cells)Adipose-derived stemcells (ADSCs)FibroblastsImmune cellsMicrovascular endothelial cellsMuscle cells
    03Research center

    SVF isolation

    500 g3 min

    When the purified fat is centrifuged again, differences in density separate it into a fat-cell layer and an SVF layer.

    The SVF layer (pellet) that settles at the bottom is carefully collected.

  4. Cell counter that records cell number and viability as figures.
    04Research center

    Cell counting

    68–99 million cellsViability measured

    After the concentration is adjusted to the volume to be used, a cell counter measures the number of viable cells and the viability rate, which are recorded for each patient.

    The number of cells per injection is based on published breast cases. These figures are used for graft planning and for graft retention data analysis.

  5. 05Research center → Operating room

    Mixing & injection

    9 : 0.5 fat : SVFNo outside contractor

    Purified fat and SVF are mixed at a set ratio to make the final product used for grafting. The ratio is planned according to the purpose of the procedure and the treatment area.

    The finished product never leaves the building; it goes straight to the operating room next door and is injected the same day.

View the five steps as a table
StepWhat happensPurposeEquipment
1. Fat harvestingTumescent infusion, then cannula aspirationObtain source fat with minimal cell damage—
2. PurificationCentrifugation at 300 g · 3 minObtain pure adipose tissueCentrifuge
3. SVF isolationCentrifugation at 500 g · 3 min, SVF layer collectedObtain SVF cellsCentrifuge
4. Cell countingCell number and viability measuredObtain data for graft planningCell counter
5. Mixing & injectionFat + SVF at about 9 : 0.5Complete the final graft, same-day injection—

Source: Shin DJ. Ann Plast Surg. 2023;90(4):380–384 (Methods section) · SC301 Clinic research note "SVF Isolation Process" (2026-09-15). Photos taken at the SC301 Clinic Stem Cell Research Center.

Environment

The conditions this process requires

SVF consists of living cells, so the environment in which the process takes place affects the result. These are the four conditions the research center provides.

01

Aseptic environment

If the cell-processing space is contaminated, the risk of infection and foreign-body reactions rises. The research center carries out the process in a pressure-controlled clean area, with a pass box and a centrifuge inside a biosafety cabinet. See the clean area

02

Government-licensed facility

The facility holds Cell Processing Facility License No. 139 (Ministry of Food and Drug Safety) and is a Designated Advanced Regenerative Medicine Institution, No. 재생-1-0049 (Ministry of Health and Welfare). See licenses & designations

03

One-stop, in-house

From harvesting to isolation and mixing, nothing is sent to an outside facility. Cells lose activity the longer they stay outside the body, so everything is completed the same day in the research center next to the operating room.

04

Dedicated research staff

Automated equipment alone does not do the job. Researchers with master's or doctoral degrees and more than 10 years of experience perform and record each step themselves. See the research team

FAQ

Frequently asked questions about the process

To watch it on video, see the SVF extraction video (YouTube, Korean).

Does a higher cell count always lead to a better result?

A higher cell count can favor graft retention, but cell count alone does not determine the result. The characteristics of the cells and the condition of the graft site, as well as post-operative care and lifestyle during recovery, can also significantly affect graft retention. It is therefore important to secure enough cells and to follow appropriate post-operative care. Article on graft retention rate

Is it a problem if it takes a long time from harvesting to grafting?

In cell processing, precision and expertise in the isolation process matter as much as saving time. At SC301, specialized research staff isolate and process the cells by hand, following set procedures and conditions that take the characteristics of the cells into account.

The research center is also located right next to the operating room, which cuts unnecessary transfer and waiting time, and the entire process from harvesting to grafting is managed systematically.

Medically reviewed by Dr. Shin Dong-jin (Chief Director, SC301 Clinic · Medical License No. 44215). This content is provided for information about the process and was written in compliance with the Medical Service Act and related laws. Actual process conditions and results may vary depending on the condition of each individual's fat.

( Next )

Isolated cells are recorded as numbers

The cell numbers and viability rates measured in step 4 have built up into about 9,000 graft retention records since 2007. How this data became published papers is shown on the Research page.