{"title":"Quality control material for plasma fibrinogen test produced from purified human fibrinogen.","authors":"Masahiro Okuda, Yahiro Uemura, Noriyuki Tatsumi","doi":"10.1155/S1463924603000142","DOIUrl":null,"url":null,"abstract":"<p><p>Plasma fibrinogen measurement is a routine laboratory procedure commonly performed on automated coagulation analysers. Its determination is quantitative, not quantitative. Yet, a lack of precision has been an issue for fibrinogen measurement. A control material derived from plasma comprises many proteins, inhibitors and fatty acids, any or all of which can interfere in the fibrinogen assay. This study has attempted to develop a quality control material using purified human fibrinogen and has compared measurement precision between both purified and plasma materials. Purified fibrinogen was prepared using Cohn fraction 1 and glycine precipitation. Purified fibrinogen clottability was greater than 95%, with no main plasma proteins, lipids or fibrinogen degradation products observed. Two purified control materials were lyophilized at normal (2.30 g l(-1)) and abnormal (1.20 g l(-1)) levels of fibrinogen concentration. Precision was evaluated using a liquid-type reagent, Thrombocheck Fib(L), on automated coagulation analysers. Coefficient of variation for within-run, intraday and between-day precision of the purified materials was 0.7-3.5%. In comparison, the coefficient of variation for plasma materials ranged from 1.2 to 5.3%. These results suggest that materials prepared from purified fibrinogen can be useful to laboratory quality control by improving overall precision of fibrinogen measurement and are applicable to automated coagulation analysers.</p>","PeriodicalId":15248,"journal":{"name":"Journal of Automated Methods & Management in Chemistry","volume":"25 4","pages":"79-85"},"PeriodicalIF":0.0000,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/S1463924603000142","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Automated Methods & Management in Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/S1463924603000142","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
Plasma fibrinogen measurement is a routine laboratory procedure commonly performed on automated coagulation analysers. Its determination is quantitative, not quantitative. Yet, a lack of precision has been an issue for fibrinogen measurement. A control material derived from plasma comprises many proteins, inhibitors and fatty acids, any or all of which can interfere in the fibrinogen assay. This study has attempted to develop a quality control material using purified human fibrinogen and has compared measurement precision between both purified and plasma materials. Purified fibrinogen was prepared using Cohn fraction 1 and glycine precipitation. Purified fibrinogen clottability was greater than 95%, with no main plasma proteins, lipids or fibrinogen degradation products observed. Two purified control materials were lyophilized at normal (2.30 g l(-1)) and abnormal (1.20 g l(-1)) levels of fibrinogen concentration. Precision was evaluated using a liquid-type reagent, Thrombocheck Fib(L), on automated coagulation analysers. Coefficient of variation for within-run, intraday and between-day precision of the purified materials was 0.7-3.5%. In comparison, the coefficient of variation for plasma materials ranged from 1.2 to 5.3%. These results suggest that materials prepared from purified fibrinogen can be useful to laboratory quality control by improving overall precision of fibrinogen measurement and are applicable to automated coagulation analysers.
血浆纤维蛋白原测量是一项常规的实验室程序,通常在自动凝血分析仪上进行。它的决定是定量的,而不是定量的。然而,纤维蛋白原测量缺乏精度一直是一个问题。来源于血浆的对照物质包括许多蛋白质、抑制剂和脂肪酸,其中任何一种或全部可以干扰纤维蛋白原测定。本研究试图利用纯化的人纤维蛋白原开发一种质量控制材料,并比较了纯化材料和血浆材料的测量精度。采用Cohn馏分1和甘氨酸沉淀法制备纯化纤维蛋白原。纯化纤维蛋白原的可凝性大于95%,未观察到主要血浆蛋白、脂质或纤维蛋白原降解产物。两种纯化的对照材料在正常(2.30 g l(-1))和异常(1.20 g l(-1))水平的纤维蛋白原浓度下冻干。在自动凝血分析仪上使用液体型试剂,血栓检查Fib(L)来评估精度。纯化物质的运行内、日内、日间精密度变异系数为0.7 ~ 3.5%。相比之下,等离子体材料的变异系数在1.2 ~ 5.3%之间。这些结果表明,纯化纤维蛋白原制备的材料可用于实验室质量控制,提高纤维蛋白原测量的整体精度,并适用于自动凝血分析仪。