Mishra Priya, Banga Ivneet, Tyagi Roshika, Munjal Tanya, Goel Aditya, Capalash Neena, Sharma Prince, Suri C R, Gandhi Sonu
Amity Institute of Biotechnology (AIB), Amity University Sector-125 Noida-201313 India
Amity Institute of Neuropsychology and Neurosciences (AINN), Amity University Sector-125 Noida-201313 India.
RSC Adv. 2018 Jun 26;8(41):23163-23170. doi: 10.1039/c8ra02018c. eCollection 2018 Jun 21.
Heroin use and addiction pose serious risks and side effects due to overdose. Quantification of heroin in biological samples is challenging due to rapid deacetylation of heroin to its active metabolites. In this study, we report the quantification of metabolic degradation of heroin by-products in biological urine samples. The presence of the drug was monitored after oral administration of heroin at different time intervals. Various biophysical techniques, such as high performance liquid chromatography (HPLC) and mass spectrometry (MS) were used to evaluate the presence of the drug. A competitive fluorescence based immunoassay was developed with a limit of detection (LOD) up to 0.01 ng mL and the IC value was 0.1 ng mL, while the dipstick assay shows a LOD up to 5 ng mL. Rapid detection of narcotic drugs was carried out for biological urine samples collected at various time points. Validation of the developed dipstick was carried out for the standard as well as the spiked urine samples by fluorescence based immunoassay (FIA), using anti-morphine antibodies. A strong correlation ( = 0.94) was obtained between the developed dipstick and FIA assay for biological urine samples collected at various time points. The developed immunochromatographic dipstick is highly sensitive, field applicable and cost effective, and can serve as a first choice for the monitoring of narcotic drugs in blood, urine and saliva in drug addicts and athletes.
由于过量使用,海洛因的使用和成瘾会带来严重风险和副作用。由于海洛因会迅速脱乙酰化为其活性代谢物,因此对生物样品中的海洛因进行定量分析具有挑战性。在本研究中,我们报告了生物尿液样本中海洛因副产物代谢降解的定量分析。在口服海洛因后的不同时间间隔监测药物的存在情况。使用了各种生物物理技术,如高效液相色谱(HPLC)和质谱(MS)来评估药物的存在。开发了一种基于竞争荧光的免疫测定法,检测限(LOD)高达0.01 ng/mL,IC值为0.1 ng/mL,而试纸条测定法的LOD高达5 ng/mL。对在不同时间点采集的生物尿液样本进行了麻醉药品的快速检测。通过基于荧光的免疫测定法(FIA),使用抗吗啡抗体,对开发的试纸条针对标准尿液样本和加标尿液样本进行了验证。对于在不同时间点采集的生物尿液样本,开发的试纸条与FIA测定法之间获得了很强的相关性(=0.94)。开发的免疫色谱试纸条高度灵敏、适用于现场且成本效益高,可作为监测吸毒者和运动员血液、尿液和唾液中麻醉药品的首选方法。