{"title":"用纯化的人纤维蛋白原制备血浆纤维蛋白原试验的质量控制材料。","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":"{\"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}","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
摘要
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。
Quality control material for plasma fibrinogen test produced from purified human fibrinogen.
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.