医学信息
醫學信息
의학신식
MEDICAL INFORMATION
2014年
13期
181-182
,共2页
林颢%孙杰聪%李广盛%郑锦畅%魏波
林顥%孫傑聰%李廣盛%鄭錦暢%魏波
림호%손걸총%리엄성%정금창%위파
富血小板血浆%TGF-β%离心
富血小闆血漿%TGF-β%離心
부혈소판혈장%TGF-β%리심
Platelet rich plasma%TGF-β%Centrifugation
目的探索应用不同的离心速度来制备的富血小板血浆(platelet rich plasma,PRP)中TGF生长因子的含量,并做相关分析,尝试阐明制备PRP最合适的离心次数及速度。方法采集自愿者外周血200ml,应用EDTA抗凝,4o保存以备用。应用全自动血液分析仪进行血小板计数,采用二次离心法(不同的离心速度、时间)分离出PRP,再次用全自动血液分析仪进行血小板计数,然后用ELISA法检测所得的PRP中的TGF-β的浓度。结果外周血中的血小板浓度为146.36×109L,PRP的血小板浓度为(757.27±55.07)×109L。 PRP中的TGF-β浓度为(737.68±62.7)ng/ml。其中以900g,10min,700g,10min,这个离心速度与时间组合所得的PRP血小板浓度及TGF-β浓度最高(881.5×109L,824.2 ng/ml)。结论 PRP的制备的质量与离心速度,离心时间密切相关,合适的离心速度,时间可以得到高浓度并富含生长因子的PRP。
目的探索應用不同的離心速度來製備的富血小闆血漿(platelet rich plasma,PRP)中TGF生長因子的含量,併做相關分析,嘗試闡明製備PRP最閤適的離心次數及速度。方法採集自願者外週血200ml,應用EDTA抗凝,4o保存以備用。應用全自動血液分析儀進行血小闆計數,採用二次離心法(不同的離心速度、時間)分離齣PRP,再次用全自動血液分析儀進行血小闆計數,然後用ELISA法檢測所得的PRP中的TGF-β的濃度。結果外週血中的血小闆濃度為146.36×109L,PRP的血小闆濃度為(757.27±55.07)×109L。 PRP中的TGF-β濃度為(737.68±62.7)ng/ml。其中以900g,10min,700g,10min,這箇離心速度與時間組閤所得的PRP血小闆濃度及TGF-β濃度最高(881.5×109L,824.2 ng/ml)。結論 PRP的製備的質量與離心速度,離心時間密切相關,閤適的離心速度,時間可以得到高濃度併富含生長因子的PRP。
목적탐색응용불동적리심속도래제비적부혈소판혈장(platelet rich plasma,PRP)중TGF생장인자적함량,병주상관분석,상시천명제비PRP최합괄적리심차수급속도。방법채집자원자외주혈200ml,응용EDTA항응,4o보존이비용。응용전자동혈액분석의진행혈소판계수,채용이차리심법(불동적리심속도、시간)분리출PRP,재차용전자동혈액분석의진행혈소판계수,연후용ELISA법검측소득적PRP중적TGF-β적농도。결과외주혈중적혈소판농도위146.36×109L,PRP적혈소판농도위(757.27±55.07)×109L。 PRP중적TGF-β농도위(737.68±62.7)ng/ml。기중이900g,10min,700g,10min,저개리심속도여시간조합소득적PRP혈소판농도급TGF-β농도최고(881.5×109L,824.2 ng/ml)。결론 PRP적제비적질량여리심속도,리심시간밀절상관,합괄적리심속도,시간가이득도고농도병부함생장인자적PRP。
Objective To detect the concentration of TGF-β in platelet rich plasma (PRP) that was prepared under dif erent centrifugal force and time, and make a related analysis. Aiming to investigate the most appropriate centrifugal force and time for preparing PRP. Methods Collect 200ml peripheral blood from volunteers, anticoagulated it with EDTA at stored at 4℃ for later use. Ful-automatic blood analyzer was used for the platelet counting, isolated the PRP by quadratic centrifugation (with dif erent centrifugal force and time),then counted the platelet again with full-automatic blood analyzer. The concentration of TGF-β in PRP was detected by ELISA detection. Results The concentration of platelet in peripheral blood was 146.36í109/L, and in PRP was (757.27±55.07)í109L.The concentration of TGF-β in PRP was (737.68±62.7)ng/ml.We found that the concentration of TGF-β in PRP that isolated under 900g,10min combined with 700g,10min was the highest (881.5í10)9/L,824.2 ng/ml).Conclusion The quality of PRP the preparation is closely related to the centrifugal force and time. The appropriate centrifugation and time is more likely to a get high concentration of PRP that rich in growth factors.