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Updated: Aug 7, 2026

Measuring Fast Calcium Fluxes in Cardiomyocytes
Published on: November 29, 2011
Changes in canine ionised calcium under three storage conditions
S F Brennan1, J O'donovan, C T Mooney
1Department of Small Animal Clinical Studies, Faculty of Veterinary Medicine, University College Dublin, Belfield, Ireland.
Insights
Aerobic blood collection is suitable for measuring ionized calcium concentration (iCa) within 10 minutes and up to 48 hours. However, iCa levels decrease over time regardless of storage conditions.
Area of Science:
- Veterinary Clinical Pathology
- Biochemistry
- Analytical Chemistry
Background:
- Accurate measurement of ionized calcium concentration (iCa) is crucial in veterinary diagnostics.
- Standard blood collection and storage protocols can influence iCa and pH values.
- Assessing the stability of iCa in collected samples is essential for retrospective analysis.
Purpose of the Study:
- To evaluate iCa and pH in aerobically collected blood samples.
- To compare iCa and pH in heparinized whole blood and plasma after 48 hours under various storage conditions.
- To determine the feasibility of retrospective iCa measurement.
Main Methods:
- Blood samples from 17 dogs were analyzed for iCa and pH using a blood gas analyzer.
- Samples were collected aerobically into heparinized syringes and plain syringes (transferred to tubes).
- Analyses were performed within 10 minutes, and remaining samples were stored at room temperature or 4°C for 48 hours.
Main Results:
- No significant difference in iCa or pH between aerobic and anaerobic collection methods within 10 minutes.
- A decrease in iCa concentration was observed at 48 hours across all storage conditions.
- pH changes did not consistently correlate with iCa concentration changes over the storage period.
Conclusions:
- Aerobically collected samples are suitable for immediate and 48-hour iCa measurement under the tested conditions.
- Retrospective analysis of iCa is possible, but a decrease in concentration should be considered.
- Further studies may be needed to optimize storage protocols for long-term iCa stability.
Objectives:
To determine the ionised calcium concentration following aerobic collection of blood and to compare ionised calcium concentration and pH of heparinised whole blood and plasma at 48 hours following collection under three different storage conditions to assess if ionised calcium concentration can be measured retrospectively.
Methods:
Blood was collected from 17 dogs for analysis of ionised calcium concentration and pH using a Rapidpoint 400 (Bayer) blood gas analyser. Blood was collected into a commercial preheparinised syringe and into a plain syringe, with subsequent transfer to a commercially available heparinised sample tube. Samples were analysed within 10 minutes, and the remainder was divided for storage. One aliquot was set-aside at room temperature for 48 hours, and the other was immediately centrifuged and the plasma divided for storage at room temperature and at 4 degrees C for 48 hours each. In all samples, ionised calcium concentration and pH were measured again at 48 hours after storage.
Results:
There was no significant difference in ionised calcium concentration or pH between anaerobically and aerobically collected heparinised whole blood analysed within 10 minutes of collection. At 48 hours, ionised calcium concentrations had decreased under all storage conditions irrespective of the direction of pH change.
Clinical Significance:
Ionised calcium concentration can be measured in aerobically collected samples within 10 minutes and at 48 hours after collection under the conditions described.
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