However, when the concentration was ⩽25 μg/ml the growth curves were similar to the non-frozen control. This was also reflected in the doubling times for the cells. Although reduced (by 22 ± 2%, p = 0.09) these two groups were not significantly different from the non-frozen control ( Fig. 6). In contrast, the cells frozen using Me2SO were found to have an abnormally high

rate of growth. This was also reflected in the doubling time for the cells (Fig. 6), which for this group was significantly different from the non-frozen control during the test period (reduced by 41 ± 4%, p = 0.004). To determine the cell cryosurvival, the post-thaw viability of the cells was determined by flow cytometry using Annexin V-FITC and PI staining (Fig. 7). The percentage of viable cells was significantly higher for the cells frozen using Me2SO (80 ± 3%) than for either treatment using trehalose with selleck inhibitor or without PP-50 (60 ± 2%, and 44 ± 3%, respectively). The addition of PP-50 at 25 μg/ml during the incubation step, significantly enhanced viability (by a factor of 37 ± 7%, p = 0.002). For all the treatment groups tested, the majority of the non-viable cells were found to be necrotic rather than apoptotic. Perhaps the two most important criteria with which different methods of cell

cryopreservation should be judged are; cryosurvival AZD2014 purchase and retention of normal cell processes. The latter is thought to be particularly Vorinostat chemical structure important for both research and therapeutic applications. Here, a Me2SO-free cryopreservation protocol, using trehalose delivery utilising PP-50, was developed and assessed. The cell line SAOS-2 was used as a model for nucleated, adherent human cells. Calcein, like trehalose, is thought to be impermeable to the cell membrane. Calcein has therefore been used in previous studies to assess the extent

of delivery of hydrophilic species into cells [10] and [11]. The degree of calcein uptake in the presence of the PP-50 was less than that previously reported for the related polymer PP-75 [10] and [11]. In part, this may be explained by the presence of trehalose in the incubation media in the studies described above. This increase in osmotic pressure caused by the trehalose supplementation of the media, may have decreased the rate of endocytosis for the cells [34]. Endocytosis has previously been found to play an important role in the delivery of hydrophilic species into cells using the related polymer PP-75 [21]. However since the delivery of trehalose into human erythrocytes which do not perform endocytosis, has previously been demonstrated [27], delivery through the cell membrane may also be important. It was concluded that PP-50 was capable of delivering hydrophilic species, such as trehalose, into cells. It should be noted that the PP-50 appeared to increase the rate of uptake of hydrophilic species by endocytosis compared to the control (Fig. 1).