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酶法测定快速测量抗逆转录病毒药物浓度。

Enzymatic Assay for Rapid Measurement of Antiretroviral Drug Levels.

机构信息

Department of Mechanical Engineering, University of Washington, Seattle, Washington 98195, United States.

Center for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.

出版信息

ACS Sens. 2020 Apr 24;5(4):952-959. doi: 10.1021/acssensors.9b02198. Epub 2020 Apr 15.

Abstract

Poor adherence to pre-exposure prophylaxis (PrEP) and antiretroviral therapy (ART) can lead to human immunodeficiency virus (HIV) acquisition and emergence of drug-resistant infections, respectively. Measurement of antiviral drug levels provides objective adherence information that may help prevent adverse health outcomes. Gold-standard drug-level measurement by liquid chromatography/mass spectrometry is centralized, heavily instrumented, and expensive and is thus unsuitable and unavailable for routine use in clinical settings. We developed the REverSe TRanscrIptase Chain Termination (RESTRICT) assay as a rapid and accessible measurement of drug levels indicative of long-term adherence to PrEP and ART. The assay uses designer single-stranded DNA templates and intercalating fluorescent dyes to measure complementary DNA (cDNA) formation by reverse transcriptase in the presence of nucleotide reverse transcriptase inhibitor drugs. We optimized the RESTRICT assay using aqueous solutions of tenofovir diphosphate (TFV-DP), a metabolite that indicates long-term adherence to ART and PrEP, at concentrations over 2 orders of magnitude above and below the clinically relevant range. We used dilution in water as a simple sample preparation strategy to detect TFV-DP spiked into whole blood and accurately distinguished TFV-DP drug levels corresponding to low and high PrEP adherences. The RESTRICT assay is a fast and accessible test that could be useful for patients and clinicians to measure and improve ART and PrEP adherence.

摘要

抗逆转录病毒治疗药物(ART)和暴露前预防(PrEP)依从性差,分别可导致人类免疫缺陷病毒(HIV)感染和耐药感染的出现。抗病毒药物水平的测量可提供客观的依从性信息,有助于预防不良健康结局。通过液相色谱/质谱法进行的金标准药物水平测量是集中化的,需要大量仪器,且费用昂贵,因此不适合也无法在临床环境中常规使用。我们开发了逆转录酶链终止(RESTRICT)检测法,作为一种快速、可及的药物水平测量方法,可提示 PrEP 和 ART 的长期依从性。该检测法使用设计的单链 DNA 模板和嵌入型荧光染料,在存在核苷酸逆转录酶抑制剂药物的情况下,测量逆转录酶形成的互补 DNA(cDNA)。我们使用浓度超过临床相关范围 2 个数量级的替诺福韦二磷酸(TFV-DP)水溶液优化了 RESTRICT 检测法,TFV-DP 是一种指示长期 ART 和 PrEP 依从性的代谢物。我们使用稀释水作为简单的样品制备策略,检测掺入全血的 TFV-DP,并准确区分对应低和高 PrEP 依从性的 TFV-DP 药物水平。RESTRICT 检测法是一种快速、可及的检测方法,可用于患者和临床医生测量和改善 ART 和 PrEP 的依从性。

相似文献

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Enzymatic Assay for Rapid Measurement of Antiretroviral Drug Levels.酶法测定快速测量抗逆转录病毒药物浓度。
ACS Sens. 2020 Apr 24;5(4):952-959. doi: 10.1021/acssensors.9b02198. Epub 2020 Apr 15.

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