Identifier

etd-11152005-124419

Degree

Master of Science in Mechanical Engineering (MSME)

Department

Mechanical Engineering

Document Type

Thesis

Abstract

Cryopreservation of reproductive cells and tissues is a useful technique to deliver intact genomes, maximize the distribution of favorable genes, control disease spread. It is widely applied to many fields such as biology, medicine, ecology and agriculture. To optimize the cryopreservation procedure, the biophysical responses of reproductive tissues at different cooling conditions and in different mediums must be clearly understood. Here we studied the biophysical response during freezing of: 1) bovine sperm frozen at a cooling rate of 20 ˚C/min in three media: without cryopreservation agents(CPAs), with 0.7 M glycerol, and with 0.7 M glycerol along with 1.5 mg/ml of cholesterol-loaded cyclodextrin (CLC); 2) equine ovarian tissue cooled either at 40˚C/min or at 0.5˚C/min from 25˚ to 4˚C, and then cooled to subzero temperatures at 5 ˚C/min in the presence and absence of 0.85 M glycerol and 0.85 M dimethylsulfoxide; and 3) Macaca mulatta ovarian tissue cooled at 0.5˚C/min or 40˚C/min from 25˚ to 4˚C, and then cooled to subzero temperatures at 5 ˚C/min in the absence and presence of 0.85 M glycerol, 0.85 M dimethylsulfoxide and 0.85 Methylene glycol. For all the three reproductive systems, a shape-independent Differential Scanning Calorimeter (DSC) technique was used to measure the volumetric shrinkage during freezing. A model of water transport was then fitted to the experimentally obtained volumetric shrinkage data and the best fit membrane permeability parameters (Lpg and ELp) was yielded. For bovine sperm, Lpg ranged from 0.02 to 0.036 µm/min-atm and ELp ranged from 26.4 to 42.1 kcal/mol. The subzero water transport parameters of bovine sperm are significantly different from those reported in literature. The experimentally determined optimal rate of freezing bovine spermatozoa agrees quite closely with the theoretically calculated range, from 45 to 60 ˚C/min. For equine tissue samples, Lpg ranged from 0.06 to 0.73 µm/min-atm and ELp ranged from 6.1 to 54.2 kcal/mol. For rhesus ovarian tissue Lpg ranged from 0.7 to 0.15 µm/min-atm and ELp ranged from 22.1 to 32.1 kcal/mol. Data obtained for equine and macaque ovarian tissue data suggest that the optimal cryopreservationn rates are significantly dependent upon suprazero cooling conditions and choice of cryoprotective agent.

Date

2005

Document Availability at the Time of Submission

Release the entire work immediately for access worldwide.

Committee Chair

Ram Devireddy

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