Comparative analysis of in vitro properties of platelets stored in three different platelet additive solutions: A pilot study
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Amit Ajay Pawar1, Deepak Kumar1, Sadana Usha Sree1
1Department of Immunohematology and Blood Transfusion, Armed Forces Medical College, Pune, Maharashtra, India.
Introduction:
Platelets are stored in plasma or in a combination of plasma and platelet additive solution (PAS). The use of PASs allows greater plasma recovery from whole blood, minimizes adverse effects, facilitates ABO-incompatible platelet transfusions, and supports the use of photochemical pathogen reduction technologies. This study evaluated and compared the in vitro properties of apheresis-derived platelets stored in three different PASs: Intersol (PAS-C), T PAS+ (PAS-E), and plasmalyte A with the help of biochemical and metabolic parameters and platelet surface markers.
Aim And Objectives:
The aim and objectives of this study were to compare in vitro properties of platelets stored in three different PASs.
Materials And Methods:
A comparative observational study was conducted for 1 year in which platelet concentrates (PCs) were collected using the apheresis technique and stored in three different PASs - Intersol (n = 10), T-PAS+ (n = 10), and plasmalyte A (n = 10). On day 1 and day 5, samples were collected from PCs and evaluated for change in their in vitro properties with the help of biochemical and metabolic parameters and platelet surface markers.
Results:
During the storage period of 5 days, swirling was maintained but the number of platelets decreased in all PASs. pH decreased significantly in T-PAS+ and Intersol. pO2 decreased significantly in T-PAS+ and pCO2 increased in T-PAS+ as well as plasmalyte A. Intersol showed higher lactate production and glucose metabolism. P-selectin increased significantly in Intersol and T-PAS+ but plasmalyte A showed the lowest increment in expression of Annexin V.
Conclusion:
T-PAS+ and plasmalyte A were found to be better alternatives to Intersol as PAS for PCs for storage as they promote better maintenance of platelets and lower platelet activation.

