Boone D J, Duncan P H, MacNeil M L, Smith B F, Houston B, Hearn T L
Clin Chem. 1984 Jan;30(1):33-7.
More than 300 laboratories participated in an interlaboratory survey of creatine kinase (CK, EC 2.7.3.2) determinations in which they analyzed seven lyophilized samples for total CK and CK isoenzymes and furnished information about their methodology. The samples were not necessarily intended to mimic typical patients' specimens but rather to determine the analytical ability of the laboratories to distinguish isoenzyme fraction CK-MB from CK-BB and to detect small but abnormal amounts of CK-BB. For total CK measurement, most laboratories used an NADP+ reduction method monitored at 340 nm (89%), and reported results in units per liter (U/L) (99%) at either 30 degrees C (34%) or 37 degrees C (60%). Despite the variety of analytical conditions, most laboratories (89%) correctly reported results within their normal range for all samples. The 287 laboratories that reported isoenzyme distributions in the samples used either cellulose acetate (37%) or agarose (44%) electrophoresis, ion-exchange chromatography (9%), or immunoinhibition (7%). Results from laboratories that used nonspecific CK-MB immunoinhibition techniques were biased when a significant amount of CK-BB isoenzyme was present.
300多个实验室参与了一项肌酸激酶(CK,EC 2.7.3.2)测定的实验室间调查,在该调查中,他们分析了7个冻干样本的总CK和CK同工酶,并提供了有关其方法的信息。这些样本不一定旨在模拟典型患者的标本,而是为了确定实验室区分CK-MB同工酶组分与CK-BB以及检测少量但异常的CK-BB的分析能力。对于总CK测量,大多数实验室使用在340nm处监测的NADP +还原法(89%),并在30℃(34%)或37℃(60%)下以每升单位(U/L)报告结果(99%)。尽管分析条件多种多样,但大多数实验室(89%)正确报告了所有样本在其正常范围内的结果。报告样本中同工酶分布的287个实验室使用了醋酸纤维素(37%)或琼脂糖(44%)电泳、离子交换色谱法(9%)或免疫抑制法(7%)。当存在大量CK-BB同工酶时,使用非特异性CK-MB免疫抑制技术的实验室结果存在偏差。