内蒙古医学杂志
內矇古醫學雜誌
내몽고의학잡지
INNER MONGOLIA MEDICAL JOURNAL
2015年
3期
286-288
,共3页
血小板%低温保存%质量分析
血小闆%低溫保存%質量分析
혈소판%저온보존%질량분석
platelet%cryopreservation%qualitative analysis
目的:探讨低温条件保存血小板的最佳方法。方法随机选取10人份血小板,在5%二甲基亚砜(DM SO )的条件下分别放入低温冰箱(-80℃)及液氮中冷冻保存。分别检测经两种方式保存2月后的血小板计数(PL T )、血小板平均体积(M PV )、血小板体积分布宽度(PDW )、PH值、乳酸脱氢酶(LDH )浓度、磷脂酰丝氨酸(PS )阳性率及CD62 p阳性率。结果两组低温保存复温后的血小板与新鲜血小板相比PH值无显著差异( P>0.05),PL T、M PV、PDW、LDH、PS阳性率及CD62 p阳性率均有显著差异( P<0.05)。两组低温保存方式间各项指标比较均无显著差异(P>0.05)。结论液氮及低温冰箱保存均会在一定程度上损伤血小板,两种保存方式比较无明显区别。
目的:探討低溫條件保存血小闆的最佳方法。方法隨機選取10人份血小闆,在5%二甲基亞砜(DM SO )的條件下分彆放入低溫冰箱(-80℃)及液氮中冷凍保存。分彆檢測經兩種方式保存2月後的血小闆計數(PL T )、血小闆平均體積(M PV )、血小闆體積分佈寬度(PDW )、PH值、乳痠脫氫酶(LDH )濃度、燐脂酰絲氨痠(PS )暘性率及CD62 p暘性率。結果兩組低溫保存複溫後的血小闆與新鮮血小闆相比PH值無顯著差異( P>0.05),PL T、M PV、PDW、LDH、PS暘性率及CD62 p暘性率均有顯著差異( P<0.05)。兩組低溫保存方式間各項指標比較均無顯著差異(P>0.05)。結論液氮及低溫冰箱保存均會在一定程度上損傷血小闆,兩種保存方式比較無明顯區彆。
목적:탐토저온조건보존혈소판적최가방법。방법수궤선취10인빈혈소판,재5%이갑기아풍(DM SO )적조건하분별방입저온빙상(-80℃)급액담중냉동보존。분별검측경량충방식보존2월후적혈소판계수(PL T )、혈소판평균체적(M PV )、혈소판체적분포관도(PDW )、PH치、유산탈경매(LDH )농도、린지선사안산(PS )양성솔급CD62 p양성솔。결과량조저온보존복온후적혈소판여신선혈소판상비PH치무현저차이( P>0.05),PL T、M PV、PDW、LDH、PS양성솔급CD62 p양성솔균유현저차이( P<0.05)。량조저온보존방식간각항지표비교균무현저차이(P>0.05)。결론액담급저온빙상보존균회재일정정도상손상혈소판,량충보존방식비교무명현구별。
Objective To explore the best way of platelet cryopreservation .Methods Selected 1 0 fresh platelet -rich plasmas (FPRPs) with 5% DMSO were cryopreserved in the -8 0 ℃ hypothermia refrigerator and liquid nitrogen for 2 months .The aliquots were thawed by 3 7 ℃ water bath for analysis .The markers observed included platelet account ,mean platelet volume ,platelet distribute width ,pH ,LDH ,phosphoryl serine express and CD6 2 p express .Results All the indexes between the two groups of cryopreservation method had no signifi-cant difference( P>0 .0 5 ) .Compared with fresh platelets ,PH had no significant difference in two groups of cryopreservated platelets(P>0 .05 ) .PLT ,MPV ,PDW ,LDH ,PS express and CD62p express had significant difference( P<0 .0 5 ) .Conclusion To some extent ,both the -8 0 ℃ hypothermia refrigerator and liquid nitro-gen cryopreservation were damaged platelet .There are no obvious difference between the two kinds of cryop-reservation methods .