Chemistry and Drug Metabolism, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, 251 Bayview Boulevard, Suite 200 Room 05A-721, Baltimore, MD, 21224, USA.
Anal Bioanal Chem. 2014 Jan;406(3):785-92. doi: 10.1007/s00216-013-7524-7. Epub 2013 Dec 1.
Analyte stability is an important factor in urine test interpretation, yet cannabinoid stability data are limited. A comprehensive study of Δ(9)-tetrahydrocannabinol (THC), 11-hydroxy-THC (11-OH-THC), 11-nor-9-carboxy-THC (THCCOOH), cannabidiol, cannabinol, THC-glucuronide, and THCCOOH-glucuronide stabilities in authentic urine was completed. Urine samples after ad libitum cannabis smoking were pooled to prepare low and high pools for each study participant; baseline concentrations were measured within 24 h at room temperature (RT), 4 °C and -20 °C. Stability at RT, 4 °C and -20 °C was evaluated by Friedman tests for up to 1 year. THCCOOH, THC-glucuronide, and THCCOOH-glucuronide were quantified in baseline pools. RT THCCOOH baseline concentrations were significantly higher than -20 °C, but not 4 °C baseline concentrations. After 1 week at RT, THCCOOH increased, THCCOOH-glucuronide decreased, but THC-glucuronide was unchanged. In RT low pool, total THCCOOH (THCCOOH + THCCOOH-glucuronide) was significantly lower after 1 week. At 4 °C, THCCOOH was stable 2 weeks, THCCOOH-glucuronide 1 month and THC-glucuronide for at least 6 months. THCCOOH was stable frozen for 1 year, but 6 months high pool results were significantly higher than baseline; THC-glucuronide and THCCOOH-glucuronide were stable for 6 months. Total THCCOOH was stable 6 months at 4 °C, and frozen 6 months (low) and 1 year (high). THC, cannabidiol and cannabinol were never detected in urine; although not detected initially, 11-OH-THC was detected in 2 low and 3 high pools after 1 week at RT. Substantial THCCOOH-glucuronide deconjugation was observed at RT and 4 °C. Analysis should be conducted within 3 months if non-hydrolyzed THCCOOH or THCCOOH-glucuronide quantification is required.
分析物稳定性是尿液检测解释的一个重要因素,但大麻素稳定性数据有限。本研究全面考察了 Δ(9)-四氢大麻酚 (THC)、11-羟基-THC (11-OH-THC)、11-去甲-9-羧酸-THC (THCCOOH)、大麻二酚、大麻酚、THC 葡萄糖醛酸苷和 THCCOOH 葡萄糖醛酸苷在真实尿液中的稳定性。对随意吸食大麻后的尿液样本进行混合,为每位研究参与者制备低浓度和高浓度尿液样本;在室温 (RT)、4°C 和 -20°C 下,在 24 小时内测量基线浓度。通过 Friedman 检验评估 RT、4°C 和 -20°C 下的稳定性,最长可达 1 年。在基线样本中定量检测 THCCOOH、THC 葡萄糖醛酸苷和 THCCOOH 葡萄糖醛酸苷。RT 条件下的 THCCOOH 基线浓度明显高于 -20°C,但与 4°C 基线浓度无差异。RT 条件下 1 周后,THCCOOH 增加,THCCOOH 葡萄糖醛酸苷减少,但 THC 葡萄糖醛酸苷无变化。在 RT 低浓度尿液样本中,1 周后总 THCCOOH(THCCOOH+THCCOOH 葡萄糖醛酸苷)显著降低。4°C 条件下,THCCOOH 稳定 2 周,THCCOOH 葡萄糖醛酸苷稳定 1 个月,THC 葡萄糖醛酸苷至少稳定 6 个月。THCCOOH 冷冻 1 年稳定,6 个月时高浓度样本结果显著高于基线;THC 葡萄糖醛酸苷和 THCCOOH 葡萄糖醛酸苷 6 个月稳定。4°C 时,6 个月时总 THCCOOH 稳定,6 个月和 1 年冷冻时总 THCCOOH 稳定。THC、大麻二酚和大麻酚在尿液中从未检出;尽管最初未检出,但在 RT 条件下放置 1 周后,2 个低浓度尿液样本和 3 个高浓度尿液样本中检出 11-OH-THC。在 RT 和 4°C 条件下观察到大量 THCCOOH 葡萄糖醛酸苷去结合。如果需要检测非水解 THCCOOH 或 THCCOOH 葡萄糖醛酸苷的定量分析,应在 3 个月内进行。