However, DMSO is also toxic and its

addition and removal is a complex process associated with potentially detrimental DZNeP osmotic shock to the cells (Luciano et al., 2009). So the reduction of the DMSO concentration is necessary. Also, the use of fetal bovine serum (FBS) is under constant discussion by regulatory authorities (Korhonen, 2007), as there is the risk of transmitting potentially infectious agents, for example the bovine spongiform encephalopathy virus (Will et al., 1996 and Bradley, 2004), to the cell samples. Many infectious agents like bacteria and viruses are even capable of surviving at the low temperatures (− 160 °C) that are routinely used for the storage of cell stocks (Bielanski et al., 2003 and Hubalek, 2003). FBS is a natural and undefined mixture of different growth factors and nutrients, impeding a standardized and reproducible cell preparation and assay evaluation. The Cancer Vaccine Consortium of the Sabin Vaccine Institute (CVC/SVI) reported that serum choice among their participants was responsible for suboptimal performance in one of their international Enzyme Linked Immuno Spot (ELISpot) proficiency panels (Janetzki et al., 2008). Obtaining reliable results in functional assays requires intensive selleck chemical and time-consuming pretesting of FBS to identify batches with low background reactivity and optimal antigen-response.

Also, strict import restrictions on FBS prevent an unlimited exchange of frozen samples. Ideally,

media should be free of all undefined Edoxaban additives and possible sources of contamination, which means avoiding all animal-derived products. Our aim in this study was to compare different approaches for achieving xeno-free or chemically defined, standardized and reproducible cryopreservation protocols. We tested: two completely protein-free and fully chemically defined media, already resulting in efficient cryopreservation of different adult stem cell types (Zeisberger et al., 2011); a medium containing bovine serum albumin (BSA) fraction V, a defined and widely accepted substitute for FBS (Germann et al., 2011), and a medium containing human serum albumin (HSA) as xeno-free alternative (Liu et al., 2010). Several serum-free cryopreservation media and methods have already been developed and distributed on the market as GMP-compliant or -amenable products (Grein et al., 2010, Holm et al., 2010 and Liu et al., 2010), but none of them are completely protein-free. The protein-free media, used in the present study, were specifically designed to compensate for the damaging effects of low temperatures under xeno-free and chemically defined conditions (Gonzalez Hernandez and Fischer, 2007). The immediate effects of freezing and thawing on cell membranes and organelles, e.g.