Room temperature storage and cryopreservation of canine platelet concentrates

Kay Allyson From the Departments of Clinical Studies (Allyson, Abrams-Ogg) and Biomedical Sciences (Johnstone), Ontario Veterinary College, University of Guelph, Guelph, ON NIG 2WI, Canada.

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Anthony C. G. Abrams-Ogg From the Departments of Clinical Studies (Allyson, Abrams-Ogg) and Biomedical Sciences (Johnstone), Ontario Veterinary College, University of Guelph, Guelph, ON NIG 2WI, Canada.

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Ian B. Johnstone From the Departments of Clinical Studies (Allyson, Abrams-Ogg) and Biomedical Sciences (Johnstone), Ontario Veterinary College, University of Guelph, Guelph, ON NIG 2WI, Canada.

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SUMMARY

Objective

To determine whether in vitro viability and function, and microbiological sterility, of canine platelet concentrates (PC) could be retained during storage at 20 to 24 C (room temperature [RT]) for up to 7 days and cryopreservation for 6 months.

Animals

14 mature dogs.

Procedure

PC prepared by centrifugation of fresh blood were stored for 7 days at RT with continuous agitation. An aliquot of each was cryopreserved with 6% dimethyl sulfoxide at −74 C for 6 months. Fresh PC (day 0) were tested by microbial culture and measurement of platelet count, mean platelet volume, pH, glucose and lactate concentrations, lactate dehydrogenase activity, response to hypotonic stress, and aggregation. Tests were also performed on PC stored at RT on days 3, 5, and 7, and on the cryopreserved aliquots after thawing.

Results

After 7 days at RT, microbial growth was not evident, and decrease in platelet number was not significant. On the basis of pH and glucose and lactate concentrations, metabolic activity was maintained throughout RT storage. On the basis of mean platelet volume and lactate dehydrogenase activity, platelet swelling and membrane damage had occurred. Aggregatory responses decreased during RT storage, and platelets recovered poorly from hypotonic stress. After cryopreservation for 6 months, microbial growth was not evident, but platelet numbers were significantly decreased. Mean platelet volume and lactate dehydrogenase activity were significantly greater, compared with values for day-0 PC. Crypreserved platelets aggregated poorly and did not respond to hypotonic stress.

Conclusions

Platelet viability and microbiological sterility are retained in canine PC stored for 7 days at RT, but platelet function progressively decreases and day-7 platelets are substantially damaged. Crypreservation of PC results in considerable damage, compared with that of PC stored at RT.

Clinical Relevance

Similar to human PC, canine PC stored at RT for up to 5 days can be recommended for treatment. (Am J Vet Res 1997;58:1338–1347)

SUMMARY

Objective

To determine whether in vitro viability and function, and microbiological sterility, of canine platelet concentrates (PC) could be retained during storage at 20 to 24 C (room temperature [RT]) for up to 7 days and cryopreservation for 6 months.

Animals

14 mature dogs.

Procedure

PC prepared by centrifugation of fresh blood were stored for 7 days at RT with continuous agitation. An aliquot of each was cryopreserved with 6% dimethyl sulfoxide at −74 C for 6 months. Fresh PC (day 0) were tested by microbial culture and measurement of platelet count, mean platelet volume, pH, glucose and lactate concentrations, lactate dehydrogenase activity, response to hypotonic stress, and aggregation. Tests were also performed on PC stored at RT on days 3, 5, and 7, and on the cryopreserved aliquots after thawing.

Results

After 7 days at RT, microbial growth was not evident, and decrease in platelet number was not significant. On the basis of pH and glucose and lactate concentrations, metabolic activity was maintained throughout RT storage. On the basis of mean platelet volume and lactate dehydrogenase activity, platelet swelling and membrane damage had occurred. Aggregatory responses decreased during RT storage, and platelets recovered poorly from hypotonic stress. After cryopreservation for 6 months, microbial growth was not evident, but platelet numbers were significantly decreased. Mean platelet volume and lactate dehydrogenase activity were significantly greater, compared with values for day-0 PC. Crypreserved platelets aggregated poorly and did not respond to hypotonic stress.

Conclusions

Platelet viability and microbiological sterility are retained in canine PC stored for 7 days at RT, but platelet function progressively decreases and day-7 platelets are substantially damaged. Crypreservation of PC results in considerable damage, compared with that of PC stored at RT.

Clinical Relevance

Similar to human PC, canine PC stored at RT for up to 5 days can be recommended for treatment. (Am J Vet Res 1997;58:1338–1347)

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