体育科学
體育科學
체육과학
SPORT SCIENCE
2015年
1期
93-97
,共5页
河春姬%杨声%董颖%张力思%景晶%徐友宣%吴侔天
河春姬%楊聲%董穎%張力思%景晶%徐友宣%吳侔天
하춘희%양성%동영%장력사%경정%서우선%오모천
异体血液回输%血型抗原%流式细胞仪%方法验证
異體血液迴輸%血型抗原%流式細胞儀%方法驗證
이체혈액회수%혈형항원%류식세포의%방법험증
homologous blood transfusion%blood antigen%flow cytometer%validation
目的:血液回输能够迅速增加机体红细胞数,增强有氧运动能力,提高运动成绩。采用流式细胞技术对异体血液回输的检测方法进行适用性验证研究,以证明该技术检测异体血液回输的可靠性和可操作性。研究方法:应用流式细胞技术,通过检测血液中荧光标记的红细胞血型抗原表达形式的方法,追踪是否存在微量的异体红细胞群,并判断是否接受异体血液回输。3名检测员使用流式细胞仪对46例不同比例(0~5%)体外混合的全血进行8种红细胞血型抗原的检测。结果:本研究对该方法的特异性、灵敏度、精密度、稳定性等进行评估。此方法检测无假阳性结果;可准确检测不低于3%的异体输血量,灵敏度较高;经细胞稳定液处理4~8℃储存的样品在4周内重复检测结果一致,3名检测员检测的结果一致。结论:流式细胞技术检测异体血液回输的方法准确可靠,符合实验室国际标准(ISO‐17025)认证和验证要求,已通过中国合格评定认可委员会认可,并应用于常规和奥运会等大型赛事的异体血液回输兴奋剂检测。
目的:血液迴輸能夠迅速增加機體紅細胞數,增彊有氧運動能力,提高運動成績。採用流式細胞技術對異體血液迴輸的檢測方法進行適用性驗證研究,以證明該技術檢測異體血液迴輸的可靠性和可操作性。研究方法:應用流式細胞技術,通過檢測血液中熒光標記的紅細胞血型抗原錶達形式的方法,追蹤是否存在微量的異體紅細胞群,併判斷是否接受異體血液迴輸。3名檢測員使用流式細胞儀對46例不同比例(0~5%)體外混閤的全血進行8種紅細胞血型抗原的檢測。結果:本研究對該方法的特異性、靈敏度、精密度、穩定性等進行評估。此方法檢測無假暘性結果;可準確檢測不低于3%的異體輸血量,靈敏度較高;經細胞穩定液處理4~8℃儲存的樣品在4週內重複檢測結果一緻,3名檢測員檢測的結果一緻。結論:流式細胞技術檢測異體血液迴輸的方法準確可靠,符閤實驗室國際標準(ISO‐17025)認證和驗證要求,已通過中國閤格評定認可委員會認可,併應用于常規和奧運會等大型賽事的異體血液迴輸興奮劑檢測。
목적:혈액회수능구신속증가궤체홍세포수,증강유양운동능력,제고운동성적。채용류식세포기술대이체혈액회수적검측방법진행괄용성험증연구,이증명해기술검측이체혈액회수적가고성화가조작성。연구방법:응용류식세포기술,통과검측혈액중형광표기적홍세포혈형항원표체형식적방법,추종시부존재미량적이체홍세포군,병판단시부접수이체혈액회수。3명검측원사용류식세포의대46례불동비례(0~5%)체외혼합적전혈진행8충홍세포혈형항원적검측。결과:본연구대해방법적특이성、령민도、정밀도、은정성등진행평고。차방법검측무가양성결과;가준학검측불저우3%적이체수혈량,령민도교고;경세포은정액처리4~8℃저존적양품재4주내중복검측결과일치,3명검측원검측적결과일치。결론:류식세포기술검측이체혈액회수적방법준학가고,부합실험실국제표준(ISO‐17025)인증화험증요구,이통과중국합격평정인가위원회인가,병응용우상규화오운회등대형새사적이체혈액회수흥강제검측。
Objective :Blood transfusion could increase red blood cells (RBCs ) rapidly and may enhance endurance performance significantly .A validation was carried out to prove the reliabili‐ty and operability of the detection of homologous blood transfusion with flow cytometry tech‐nology .Method :Homologous blood transfusion was detected using flow cytometry technique to observe the presence of different RBCs phenotypes of eight different antigens in a blood sam‐ple .The analysis of 46 blood samples containing different percentages (0 ~ 5% ) of homolo‐gous RBCs was carried out by three independent analysts .Results :The method afforded satis‐factory results in terms of robustness ,sensitivity ,specificity ,precision and stability .No false positive results were observed .All samples contained 3% homologous RBCs were unambigu‐ously detected .These samples were stable over 4 weeks after using cell stable buffer at 4 ~8℃ .Conclusion :This method fulfils the ISO‐17025 accreditation and has been accredited by China National Accreditation Service for Conformity Assessment (CNAS ) .The method has been successfully utilized to the detection of homologous blood transfusion in major events and routine doping‐control samples .