Process for preparing concentrated platelets through improved albuginea method
A platelet and buffy coat technology, applied in blood transfusion devices, suction devices, etc., can solve problems such as failure to meet quality requirements, waste of blood resources, low platelet recovery rate, etc., and achieve the effect of improving recovery rate and ensuring stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] The optimization of embodiment 1 centrifugation process
[0025] 180 bags of 400 mL whole blood were randomly divided into 9 groups. On the basis of the centrifugation parameters of the traditional buffy coat method, the relative centrifugal force was gradually adjusted, and 9 different centrifugation schemes were adopted. See Table 1 for details. PC is prepared by the modified buffy coat method: the raw whole blood is kept at a constant temperature of 22±2°C for 2 hours on average, centrifuged for 16 minutes, and the buffy coat is separated, and then the buffy coat is kept at a constant temperature of 22±2°C for 2 hours or 12 hours (generally It is said to stand still for 2 hours. In some cases, the main reason is that when the blood collection vehicle returns the blood sample at night, we usually first let it stand for 2 hours and then perform the first centrifugation to separate the buffy membrane, then let it stand for 12 hours, and perform the second in the next mor...
Embodiment 2
[0035] Embodiment 2 different whole blood volume groups
[0036] 30 bags of 300mL whole blood were prepared by the modified buffy coat method, and centrifugation scheme 6 was used to prepare PC, and the experimental data of PC prepared by centrifugation scheme 6 in 20 bags of 400mL whole blood were compared and analyzed. The results can be seen in Table 3,
[0037] Whole blood of 400mL and 300mL was used to prepare PC, and there was no statistically significant difference in platelet concentration between the groups before preparation (p>0.05). The recovery rate of PC prepared from 400mL whole blood was higher than that of 300mL whole blood, and the difference was statistically significant (p<0.05) See Table 3.
[0038] Table 3 Differences in the recovery rate of platelets prepared from whole blood with different blood volumes
[0039]
[0040] Note: compared with the 300mL whole blood group P a <0.05
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


