一种新的苯二氮卓免疫分析法的B-303验证,改进了葡萄糖醛酸化苯二氮卓的检测

IF 6.3 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Imir Metushi
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We tested the precision of the immunoassay systems by taking a positive and negative sample and running over a total of 20 runs. We tested 120 patient samples using both the current Benzodiazepine Plus and the new Benzodiasepines II immunoassays across three laboratory testing sites. The cut off used for a positive result was 200 ng/mL. A query was conducted to review the number of positive and negative benzodiazepine results 3 months prior to converting to the Benzodiazepine II version of the assay and 3 months after. Results The assay was precise 100% of the times using both negative and positive samples across all three- testing sites. A total of 59 positive samples and a total of 61 negative samples by the old Benzodiazpines II immunoassay were used for patient correlation. The 59 positive samples using the old Benzodiazepine plus immunoassay were also positive by the new Bensoziazepine II immunoassay. We noticed that from the 61 negative samples as classified by the old Benzodiazepine Plus immunoassay, 8 samples tested positive when run on the new Benzodiasepine II immunoassay. These 8 samples were confirmed by mass spectrometry to be true positive. We noticed that the 8 true positive samples had the following analytes: Sample 1, alprazolam at 59 ng/mL and a-OH alprazolam at 64 ng/L; Sample 2, alprazolam at 99 ng/mL and a-OH alprazolam at 36 ng/mL; Sample 3, a-OH midazolam at 377 ng/mL; Sample 4, lorazepam at 650 ng/mL; Sample 5, lorazepam at 370 ng/mL; Sample 6, lorazepam at 1659 ng/mL; Sample 7, lorazepam at 726 ng/mL; Sample 8, lorazepam at 34 ng/mL, alprazolam at 22 ng/mL, a-OH alprazolam at 17 mg/mL, 7-aminoclonazepam at 241 ng/mL. Our query identified that in the prior month before converting to Benzodiazepine Plus IMA the rate of positive Benzodiazepine IMA screens was 8%, and 3 months after converting to the Benzodiazepine Plus IMA the rate of a positive benzodiazepine screen increased to 15%. 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引用次数: 0

摘要

新的罗氏苯二氮卓类免疫分析法使用了一种机载β -葡萄糖醛酸酶,可以提高对葡萄糖醛酸化苯二氮卓类药物的检测。我们在三个实验室测试地点评估并验证了这种新的检测方法:1)社区医院,2)第四护理医疗中心和3)外展参考实验室。方法新的联机数据苯二氮卓类免疫测定(IMA)使用与其前身相同的校定剂和对照,但在其试剂之一中包含ß-葡糖苷酸酶。这种添加有助于从苯二氮卓类缀合物中水解葡萄糖醛酸盐,并改善苯二氮卓类葡萄糖醛酸盐的检测。任何不一致的样品都用液相色谱-质谱法进行确认。我们通过采集阳性和阴性样本,总共运行20次来测试免疫测定系统的精度。我们在三个实验室测试点使用当前的苯二氮卓Plus和新的苯二氮卓II免疫分析法对120例患者样本进行了测试。阳性结果的切断液为200 ng/mL。在转换为苯二氮卓II版本的分析之前3个月和之后3个月,对苯二氮卓阳性和阴性结果的数量进行了查询。结果在所有三个检测点使用阴性和阳性样品时,测定的准确度为100%。采用旧的苯二氮卓类药物免疫分析法共59份阳性样本和61份阴性样本进行患者相关性分析。59例使用旧苯二氮卓类药物加免疫分析法的阳性样本,新苯二氮卓类药物ⅱ免疫分析法也呈阳性。我们注意到,在61份用旧的苯二氮卓Plus免疫分析法分类的阴性样本中,8份用新的苯二氮卓II免疫分析法检测呈阳性。质谱分析证实8份样品为真阳性。我们注意到8个真阳性样品中含有以下分析物:样品1,阿普唑仑59 ng/mL和a-OH阿普唑仑64 ng/L;样品2,阿普唑仑99 ng/mL和a-OH阿普唑仑36 ng/mL;样品3,a-OH咪达唑仑377 ng/mL;样品4,劳拉西泮650 ng/mL;样品5,劳拉西泮370 ng/mL;样品6,劳拉西泮1659 ng/mL;样品7,劳拉西泮726 ng/mL;样品8,劳拉西泮34 ng/mL,阿普唑仑22 ng/mL, a-OH阿普唑仑17 mg/mL, 7-氨基氯硝西泮241 ng/mL。我们的查询发现,在转换为苯二氮卓类药物加IMA前一个月,苯二氮卓类药物加IMA筛查阳性率为8%,转换为苯二氮卓类药物加IMA 3个月后,苯二氮卓类药物筛查阳性率增加到15%。结论通过增加β -葡糖苷酶的板载水解步骤,提高了苯二氮卓类药物的检出率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
B-303 Validation of a New Benzodiazepine Immunoassay with Improved Detection of Glucuronidated Benzodiazepines
Background The new Roche benzodiazepines II immunoassay utilizes an on board beta-glucuronidase enzyme that should enhance detection of glucuronidated benzodiazepines. We evaluated and validated this new assay across three laboratory testing sites: 1) a community hospital, 2) a quaternary-care medical center and a 3) outreach reference laboratory. Methods The new ONLINE DAT Benzodiazepines II immunoassay (IMA) utilizes the same calibrators and controls as its predecessor but it includes a ß-glucuronidase enzyme in one of its reagents. This addition should help hydrolize glucuronide from its benzodiazepine conjugates and improve the detection of benzodiazepine glucuronides. Any samples that were discordant were run by liquid chromatography-mass spectrometry for confirmation. We tested the precision of the immunoassay systems by taking a positive and negative sample and running over a total of 20 runs. We tested 120 patient samples using both the current Benzodiazepine Plus and the new Benzodiasepines II immunoassays across three laboratory testing sites. The cut off used for a positive result was 200 ng/mL. A query was conducted to review the number of positive and negative benzodiazepine results 3 months prior to converting to the Benzodiazepine II version of the assay and 3 months after. Results The assay was precise 100% of the times using both negative and positive samples across all three- testing sites. A total of 59 positive samples and a total of 61 negative samples by the old Benzodiazpines II immunoassay were used for patient correlation. The 59 positive samples using the old Benzodiazepine plus immunoassay were also positive by the new Bensoziazepine II immunoassay. We noticed that from the 61 negative samples as classified by the old Benzodiazepine Plus immunoassay, 8 samples tested positive when run on the new Benzodiasepine II immunoassay. These 8 samples were confirmed by mass spectrometry to be true positive. We noticed that the 8 true positive samples had the following analytes: Sample 1, alprazolam at 59 ng/mL and a-OH alprazolam at 64 ng/L; Sample 2, alprazolam at 99 ng/mL and a-OH alprazolam at 36 ng/mL; Sample 3, a-OH midazolam at 377 ng/mL; Sample 4, lorazepam at 650 ng/mL; Sample 5, lorazepam at 370 ng/mL; Sample 6, lorazepam at 1659 ng/mL; Sample 7, lorazepam at 726 ng/mL; Sample 8, lorazepam at 34 ng/mL, alprazolam at 22 ng/mL, a-OH alprazolam at 17 mg/mL, 7-aminoclonazepam at 241 ng/mL. Our query identified that in the prior month before converting to Benzodiazepine Plus IMA the rate of positive Benzodiazepine IMA screens was 8%, and 3 months after converting to the Benzodiazepine Plus IMA the rate of a positive benzodiazepine screen increased to 15%. Conclusion Our results indicate that the new version of the assay, by using the addition of the on board hydrolysis step with beta glucuronidase greatly enhances the detection rate of benzodiazepines.
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来源期刊
Clinical chemistry
Clinical chemistry 医学-医学实验技术
CiteScore
11.30
自引率
4.30%
发文量
212
审稿时长
1.7 months
期刊介绍: Clinical Chemistry is a peer-reviewed scientific journal that is the premier publication for the science and practice of clinical laboratory medicine. It was established in 1955 and is associated with the Association for Diagnostics & Laboratory Medicine (ADLM). The journal focuses on laboratory diagnosis and management of patients, and has expanded to include other clinical laboratory disciplines such as genomics, hematology, microbiology, and toxicology. It also publishes articles relevant to clinical specialties including cardiology, endocrinology, gastroenterology, genetics, immunology, infectious diseases, maternal-fetal medicine, neurology, nutrition, oncology, and pediatrics. In addition to original research, editorials, and reviews, Clinical Chemistry features recurring sections such as clinical case studies, perspectives, podcasts, and Q&A articles. It has the highest impact factor among journals of clinical chemistry, laboratory medicine, pathology, analytical chemistry, transfusion medicine, and clinical microbiology. The journal is indexed in databases such as MEDLINE and Web of Science.
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