LysetTM is manufactured by Sclavo Diagnostics International S.r.l. on Biorigen S.r.l. licence

BOOST YOUR CELL CULTURE TODAY FOR THE EXPERIMENTS OF TOMORROW

an “off the shelf”, fully standardized and lyophilized, human platelet derived cell culture supplement.

XENO-FREE COMPONENTS OF HUMAN ORIGIN

is being utilized to replace animal and human serum such as Fetal Bovine Serum (FBS) in culture medium formulation for different types of cells.

CELL SUPPLEMENT OBTAINED BY THE COMBINATION OF TWO COMPONENTS

the possibility of mixing the two supplement components (PL, human platelet lysate from Platelet Rich Plasma and AD, human Platelet Poor Plasma) in different percentages, allows the supplement customization and optimization for each cell type.

Applications

Growth factors isolated from human blood platelets are significantly more efficient than fetal bovine serum (FBS) or fetal calf serum (FCS), which are widely used as growth supplements for cell culture. In many cases, hPL increases cell proliferation and number of doublings that cells can perform in culture by a factor of 3 to 7 and hence represent a significant productivity gain. The features and advantages of blood platelets growth factors in cell culture have already been demonstrated in small volume R&D laboratories. Lyset™ makes these growth factors available to the Biotech industry in regenerative medicine (Autologous Cells Implantation) and in biopharmaceuticals manufacturing monoclonal antibody-based drugs, vaccines, interferons.

Fetal bovine serum (FBS) is the most widely used additive for cell culture media because of its high content of growth promoting factors and components that have been shown to satisfy specific metabolic requirements for the culture of cell.

FBS presents several disadvantages (see also D. Brunner et al.. References N° 6)

  • The high variability between different FBS batches is time consuming and expensive for the selection of the best performing serum.
  • FBS, as well as the products coming from bovine source, are not advised, especially in cultures for therapy applications, due to the risk of prion, zoonose and viral contaminations, including bovine spongiform encephalopathy, also commonly known as “ mad-cow-disease”.
  • The FBS production requires each year that more than 1’000’000 bovine fetuses must be harvested from pregnant cows sent to the slaughter. Fetuses are extracted from the cows and fetal blood is punctured in the beating heart in the unanaesthetised fetus creating an ethical concern.
  • Recent concerns about the global supply versus demand of FBS creating a demand for alternatives.

Human Platelet lysate has demonstrated to be a new and efficient cell culture supplement and been evaluated with reference to FBS but it offers more than a substitute to FBS due to its influence on the cell properties.

PDGF was detected in the hPL but was not present in FBS. The platelet lysate medium demonstrated lack of microorganisms, mycoplasma and endotoxins. In general the platelet lysate medium supported cell growth and maintained viabilities superior to FBS. Productivity studies of antibodies (hybridomas) and transferrin (hepatocytes) showed enhanced production in platelet-derived medium in comparison with FBS.

PRP and hPL have been used in cell culture and have demonstrated similar activity on growth and proliferation of cells in cell culture.

The platelet lysate has been investigated in culture studies (cell growth, viability and product formation) towards a number of target cells including, but not limited to myelomas, hybridomas, hepatocytes, chondrocytes, mesenchymal stem cells, fibroblasts and epithelial cells.

Example: hPL effect on human articular chondrocytes proliferation

Human articular chondrocytes were cultured in 10% FCS (control) or 5% hPL supplemented medium and the cell population doublings were evaluated at different time points. hPL expanded cells showed a higher proliferation potential compared to the FCS expanded cells.

Values represent the number of doublings obtained at 80% confluence in the culture time period range (n = 3 primary cultures).

Human articular chondrocytes expanded in culture in the presence of Lyset™

Chondrogenic potential of Human articular chondrocytes expanded "in vitro" in the presence of Lyset™: Toluidin blue metachromatic staining of a cell pellet culture