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英国用于抗球蛋白试验的低离子强度溶液的pH值、电导率和渗透压摩尔浓度。

The pH, conductivity and osmolality of low ionic strength solutions used within the U.K. for the antiglobulin test.

作者信息

Phillips P K, Bebbington C

机构信息

UK External Quality Assessment Scheme, National Institute for Biological Standards and Control, Potters Bar, U.K.

出版信息

Transfus Med. 1991 Sep;1(3):155-8. doi: 10.1111/j.1365-3148.1991.tb00024.x.

Abstract

Low ionic strength solutions (LISS) for use in the antiglobulin test were obtained from 356 U.K. laboratories. Of the 324 laboratories using LISS to suspend the test red cells and who returned details of their LISS technique, 15 used unequal proportions of red cell suspension and serum despite the LISS being formulated for use with equal proportions. Of the 22 laboratories mixing LISS with serum and red cells suspended in a normal ionic strength medium, four used a LISS preparation formulated for a LISS-suspension technique and three used a commercially available LISS-addition preparation using proportions of red cells, serum and LISS not recommended by the manufacturer. The mean (standard deviation) pH, conductivity and osmolality of the 334 LISS preparations for LISS-suspension was 6.9 (0.2), 4.1 (0.4) mS/cm and 298 (15) mmole/kg, respectively. It is suggested that attention should be paid to the osmolality and, particularly, conductivity during the preparation of LISS because values were observed that were clearly outside the acceptable range cited in the Guidelines for the Blood Transfusion Services in the United Kingdom, i.e. pH 6.7 +/- 0.2, conductivity 3.7 +/- 0.3 mS/cm and osmolality 295 +/- 5 mmole/kg.

摘要

用于抗球蛋白试验的低离子强度溶液(LISS)取自356家英国实验室。在324家使用LISS悬浮试验红细胞并反馈其LISS技术细节的实验室中,尽管LISS是按等比例使用配制的,但有15家使用了不等比例的红细胞悬液和血清。在22家将LISS与悬浮于正常离子强度介质中的血清和红细胞混合的实验室中,有4家使用了为LISS悬浮技术配制的LISS制剂,3家使用了市售的LISS添加制剂,但其红细胞、血清和LISS的比例并非制造商所推荐。用于LISS悬浮的334种LISS制剂的平均(标准差)pH值、电导率和渗透压分别为6.9(0.2)、4.1(0.4)mS/cm和298(15)mmol/kg。建议在制备LISS时应关注渗透压,尤其是电导率,因为观察到的值明显超出了英国输血服务指南中规定的可接受范围,即pH值6.7±0.2、电导率3.7±0.3 mS/cm和渗透压295±5 mmol/kg。

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