Regions Hospital, Emergency Medicine, 640 Jackson St, St. Paul, MN 55101, USA.
Clin Toxicol (Phila). 2011 Nov;49(9):810-4. doi: 10.3109/15563650.2011.615064. Epub 2011 Oct 5.
No information exists on therapeutic or toxic concentrations of tetrahydrozoline, which has been reported to be used in drug facilitated sexual assaults. The primary aim of this investigation was to establish baseline therapeutic serum and urine concentrations in a sample of healthy volunteers.
Ten healthy volunteers consented to have two drops of Original Visine® eye drops (0.05% tetrahydrozoline solution) placed directly into the conjunctival sac of each eye, 30 s apart, at times 0, 4, 8, and 12 h. Blood and urine samples were then collected at 2, 5, 9, 13, and 24 h post-application and analyzed for concentrations. Tetrahydrozoline concentrations are described using measures of central tendency and dispersion at each time point, with predictions of serum and urine concentrations over time calculated using a linear mixed effects regression model.
Tetrahydrazoline concentrations were detectable in both serum and urine after therapeutic ocular administration. The mean serum half-life of tetrahydrozoline was approximately 6 h. Systemic absorption varied among subjects, with the maximum serum concentrations ranging from 0.068 to 0.380 ng/ml. At 24 h, all patients had detectable urine concentrations of tetrahydrozoline (range = 13?210 ng/ml).
When used as directed by the manufacturer for therapeutic ocular administration, tetrahydrozoline concentrations were detectable in both serum and urine up to 12 h after the last administered dose. A concentration greatly exceeding the 95% confidence interval of drug present during therapeutic ocular use may be suggestive of illegal adulterant use or accidental or suicidal overdose.
目前尚无四氢唑啉的治疗或中毒浓度的相关信息,有报道称该药被用于药物辅助性侵。本研究的主要目的是在健康志愿者样本中确定基线治疗血清和尿液浓度。
10 名健康志愿者同意在 0、4、8 和 12 小时分别将两滴 Original Visine®眼药水(0.05%四氢唑啉溶液)直接滴入双眼的结膜囊中,每滴间隔 30 秒。随后在给药后 2、5、9、13 和 24 小时采集血液和尿液样本,并分析浓度。在每个时间点使用集中趋势和离散度描述四氢唑啉浓度,并使用线性混合效应回归模型预测血清和尿液浓度随时间的变化。
在治疗性眼部给药后,血清和尿液中均可检测到四氢唑啉。四氢唑啉的平均血清半衰期约为 6 小时。个体间的全身吸收情况不同,最大血清浓度范围为 0.068 至 0.380ng/ml。在 24 小时时,所有患者的尿液中均能检测到四氢唑啉(范围为 13?210ng/ml)。
按照制造商的指示用于治疗性眼部给药时,最后一次给药后 12 小时内,血清和尿液中均可检测到四氢唑啉。浓度大大超过治疗性眼部使用时药物的 95%置信区间可能提示非法添加物使用或意外或自杀性过量。