首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Quality Assurance Program for Clinical Measurement of Antiretrovirals: AIDS Clinical Trials Group Proficiency Testing Program for Pediatric and Adult Pharmacology Laboratories
【2h】

Quality Assurance Program for Clinical Measurement of Antiretrovirals: AIDS Clinical Trials Group Proficiency Testing Program for Pediatric and Adult Pharmacology Laboratories

机译:抗逆转录病毒药物临床检测的质量保证计划:儿科和成人药理学实验室的AIDS临床试验小组能力验证计划

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Clinical trials designed to compare antiretroviral regimens, investigate therapeutic drug monitoring, or measure pharmacometrics often include protease inhibitors (PIs), nonnucleoside reverse transcriptase inhibitors (NNRTIs), and nucleoside reverse transcriptase inhibitors, requiring the measurement of these antiretrovirals in plasma. Within the adult and pediatric AIDS Clinical Trials Group (ACTG), a network of Pharmacology Support Laboratories (PSLs) is a component of the group laboratory infrastructure and conducts these types of pharmacologic assays. The adult ACTG has developed a comprehensive quality assurance program for the conduct of clinical pharmacology protocols, one component of which is the antiretroviral proficiency testing (PT) program that has been implemented between the adult and pediatric pharmacology laboratories of the ACTG. PT testing samples were prepared and distributed in July 2001, February 2002, and July 2002. High, medium, and low concentrations of PIs (indinavir, saquinavir, amprenavir, lopinavir, ritonavir, and nelfinavir) and NNRTIs (nevirapine and efavirenz) were added to drug-free EDTA plasma and distributed, on dry ice, to eight ACTG PSLs. One testing laboratory used liquid chromatography-tandem mass spectrometry, and seven used high-performance liquid chromatography-UV analysis. A result was considered acceptable if it was within 20% deviation of the assigned concentration. For all concentrations of PIs evaluated, 96% of samples tested (430 of 448 measurements) met the acceptance criteria. For both NNRTIs, 100% of samples tested (140 of 140 measurements) met the acceptance criteria. In conclusion, the PT program results presented demonstrate excellent interlaboratory agreement for all antiretrovirals tested and provide support for the merger of plasma concentration data among laboratories for large clinical trials.
机译:旨在比较抗逆转录病毒疗法,研究治疗药物监测或衡量药理学的临床试验通常包括蛋白酶抑制剂(PIs),非核苷逆转录酶抑制剂(NNRTIs)和核苷逆转录酶抑制剂,需要在血浆中测量这些抗逆转录病毒药物。在成人和儿童艾滋病临床试验小组(ACTG)中,药理支持实验室(PSL)网络是该小组实验室基础设施的组成部分,并进行这些类型的药理测定。成人ACTG已制定了用于临床药理学方案的全面质量保证计划,其中一个组成部分是已在ACTG的成人和儿科药理实验室之间实施的抗逆转录病毒能力测试(PT)程序。制备了PT测试样品并分别于2001年7月,2002年2月和2002年7月分发。添加了高,中和低浓度的PI(indinavir,saquinavir,amprenavir,lopinavir,ritonavir和nelfinavir)和NNRTIs(nevirapine和efavirenz)。加入无毒品的EDTA血浆,并在干冰上分配到八个ACTG PSL。一个测试实验室使用液相色谱-串联质谱法,而七个使用高效液相色谱-UV分析法。如果结果与指定浓度的偏差在20%以内,则认为该结果可接受。对于所评估的所有浓度的PI,96%的测试样品(448个测量中的430个)均达到了接受标准。对于两种NNRTI,测试的样本中有100%(140个测量中的140个)符合接受标准。总之,提出的PT计划结果证明了所有测试的抗逆转录病毒药物之间的优良实验室间一致性,并为大型临床试验中实验室之间血浆浓度数据的合并提供了支持。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号