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Cryopreservation Method (cryopreservation + method)
Selected AbstractsThe current status of sperm cryopreservation of the endangered Probarbus jullieni (Sauvage) in MalaysiaJOURNAL OF APPLIED ICHTHYOLOGY, Issue 5 2010P. C. Chew Summary The objective of this study was to develop a cryopreservation method in Probarbus jullieni sperm, an endangered riverine fish species in Southeast Asia, including the optimization of an extender solution (14 extender formulations were tested) and selecting a cryoprotectant (five types of agents and methanol were used at concentrations (v/v) of 5, 7.5, 9, 10, 12, 15 and 20%). The semen to diluent ratios tested were as follow: 1 : 1, 1 : 2, 1 : 3, 1 : 4, 1 : 5, 1 : 7, 1 : 9, 1 : 14, 1 : 19, 1 : 24 and 1 : 49. Vapour exposure duration was set at 5, 10, 15 and 20 min while the distance between sample and liquid nitrogen (LN2) during the vapour exposure was designed at 3, 3.5, 4, 5 and 6 cm. Further, the time frame for thawing was set at 6, 7, 8, 10, 20 and 30 s. The optimum protocol was by using CF-HBSS (pH 7.5, osmolality 285 ± 10 mOsmol kg,1) in combination with methanol at 9% (v/v); sperm to diluents ratio between 1 : 3 to 1 : 5; vapour exposure for 5 min or 10 min, with samples placed at 3.5 cm or 4 cm above LN2 and thawing at 40°C for 7 s. The mean of pre-frozen and post-thaw sperm motility was 80.1 ± 13.6% (n = 43) and 49.6 ± 16.4% (n = 43) respectively. The reproductive characteristics of P. jullieni during its spawning season were addressed in present work. Cryopreserved sperm was found to have lower fertilization ability (4.2 ± 2.5%, n = 1050) and hatching rate (1.6 ± 1.2%, n = 1050) compared with fresh sperm (fertilization 77.7 ± 6.2%, n = 1050; hatching 64.7 ± 7.7%, n = 1050). The resulted problems and constraints encountered in the process of sperm cryopreservation of the species studied were also reported in this paper. [source] Semen cryopreservation in the Salmonidae and in the Northern pikeAQUACULTURE RESEARCH, Issue 3 2000F. Lahnsteiner The present paper summarizes the data on a semen cryopreservation method for the Salmonidae (Oncorhynchus mykiss, Salmo trutta f. lacustris, Salvelinus fontinalis, Salvelinus alpinus, Salmo trutta f. fario, Hucho hucho, Coregonus lavaretus, Thymallus thymallus) and for the Northern pike (Esox lucius) published during recent years. It describes (1) methods used for the determination of sperm viability; (2) the protective efficiency of substances specifically for protection of internal and external parts of cells and the process of extender development; (3) the freezing, thawing and fertilization conditions; and (4) the tolerable deviations from the freezing protocol for more easy application. Finally, biomarkers are reported that predict the suitability of semen for cryopreservation and the quality of frozen,thawed semen. [source] Cryopreservation of Fibroblasts Immobilized Within a Porous Scaffold: Effects of Preculture and Collagen Coating of Scaffold on Performance of Three-Dimensional CryopreservationARTIFICIAL ORGANS, Issue 7 2010Hirotoshi Miyoshi Abstract As a preliminary investigation to establish a cryopreservation method suited for bioartificial livers (BALs), three-dimensional (3-D) cryopreservation experiments with fibroblasts were performed, in which the cells were firstly seeded into a porous scaffold, and the scaffold containing the cells was then cryopreserved. After thawing, 65% of the initially applied cells were still attached to the scaffold, and this efficiency was significantly higher than that in the control experiments (39%), in which fibroblasts cryopreserved in a suspension were seeded into the scaffold. This higher efficiency was mainly caused by higher immobilization efficiency at the time of cell seeding (83%) than in the controls (54%). Collagen coating of the scaffold in the 3-D cryopreservation enhanced immobilization efficiency at the time of cell seeding, and 1-day precultures before the 3-D cryopreservation considerably improved cell growth after thawing. From these favorable results, this 3-D cryopreservation method may become useful for developing BALs. [source] Enhancement of cell recovery for dissociated human embryonic stem cells after cryopreservationBIOTECHNOLOGY PROGRESS, Issue 3 2010Xia Xu Abstract Due to widespread applications of human embryonic stem (hES) cells, it is essential to establish effective protocols for cryopreservation and subsequent culture of hES cells to improve cell recovery. We have developed a new protocol for cryopreservation of dissociated hES cells and subsequent culture. We examined the effects of new formula of freezing solution containing 7.5% dimethylsulfoxide (DMSO) (v/v %) and 2.5% polyethylene glycol (PEG) (w/v %) on cell survival and recovery of hES cells after cryopreservation, and further investigated the role of the combination of Rho-associated kinase (ROCK) inhibitor and p53 inhibitor on cell recovery during the subsequent culture. Compared with the conventional slow-freezing method which uses 10% DMSO as a freezing solution and then cultured in the presence of ROCK inhibitor at the first day of culture, we found out that hES cell recovery was significantly enhanced by around 30 % (P < 0.05) by the new freezing solution. Moreover, at the first day of post-thaw culture, the presence of 10 ,M ROCK inhibitor (Y-27632) and 1 ,M pifithrin-, together further significantly improved cell recovery by around 20% (P < 0.05) either for feeder-dependent or feeder-independent culture. hES cells remained their undifferentiated status after using this novel protocol for cryopreservation and subsequent culture. Furthermore, this protocol is a scalable cryopreservation method for handling large quantities of hES cells. © 2009 American Institute of Chemical Engineers Biotechnol. Prog., 2010 [source] | ||||||||||