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二氢可待因(DHC)代谢物在二氢可待因相关死亡中的作用。

The role of dihydrocodeine (DHC) metabolites in dihydrocodeine-related deaths.

机构信息

Forensic Medicine and Science, Division, Faculty of Medicine, University of Glasgow, Glasgow, United Kingdom.

出版信息

J Anal Toxicol. 2010 Oct;34(8):476-90. doi: 10.1093/jat/34.8.476.

Abstract

The focus of this study was to report the blood and urine concentrations of dihydrocodeine (DHC) and its metabolites, dihydrocodeine-6-glucuronide (DHC6G), dihydromorphine (DHM), dihydromorphine-3-glucuronide (DHM3G), and dihydromorphine-6-glucuronide (DHM6G) in deaths involving DHC, and to report the range of concentrations detected in real cases in order to understand their contribution to DHC intoxication. Twenty-six positive postmortem cases were involved in the current study. Five cases were attributed solely to DHC intoxication, 13 cases to polydrug intoxication, and the remainder of the cases were unrelated to DHC (DHC has been detected but is unrelated to the cause of death). DHC and its glucuronide were detected in all cases investigated in blood and urine matrices. Unchanged parent drug is the most abundant analyte detected in blood samples mean and median of DHC/total DHC (DHC plus DHC6G) percentages were 63% and 72%, and DHC6G is the most abundant DHC metabolite in urine with a mean and median DHC6G/TDHC of 69% and 70%, respectively. Blood DHC concentrations ranged from 40 to 166,000 ng/mL and 200 to 159,000 ng/mL in urine. DHC6G concentrations in these cases ranged from 20 to 62,180 ng/mL in blood and 40 to 500,000 ng/mL in urine. However, DHM and its glucuronide were present at lower concentrations than DHC and its glucuronide. In the current study, it can be concluded that concentrations of DHC that cause death may be lower in polydrug intoxication. Concentrations found at autopsy overlapped between toxic and therapeutic concentrations because of the presence of other harmful substances, and death can occur with concentrations below lethal concentrations as reported in Case 1 (500 ng/mL). It has been suggested that DHM and DHM6G may play a major role in assessing the cause of death in cases where DHC is not detected and when it is detected in low concentrations. The current study does not support this hypothesis, and it can be seen clearly from the data reported here that DHM and its glucuronide were not detected where DHC was not detected. Toxic concentrations of DHM and DHM6G were identified in some of these cases; however, the concentration of DHC was enough to cause death on its own. It seems that DHM and DHM6G have less influence in causing death than the parent drug itself.

摘要

本研究的重点是报告涉及二氢可待因(DHC)的血液和尿液浓度及其代谢物二氢可待因-6-葡萄糖醛酸(DHC6G)、二氢吗啡(DHM)、二氢吗啡-3-葡萄糖醛酸(DHM3G)和二氢吗啡-6-葡萄糖醛酸(DHM6G)在涉及 DHC 的死亡案例中的浓度,并报告实际案例中检测到的浓度范围,以了解它们对 DHC 中毒的贡献。本研究涉及 26 例阳性尸检案例。其中 5 例仅归因于 DHC 中毒,13 例归因于多种药物中毒,其余病例与 DHC 无关(已检测到 DHC,但与死因无关)。在所研究的血液和尿液基质中均检测到 DHC 和其葡萄糖醛酸。未改变的母体药物是血液样本中最丰富的分析物,DHC/总 DHC(DHC 加 DHC6G)的平均值和中位数百分比分别为 63%和 72%,而尿液中 DHC6G 是最丰富的 DHC 代谢物,DHC6G/TDHC 的平均值和中位数分别为 69%和 70%。血液 DHC 浓度范围为 40 至 166,000ng/mL,尿液中为 200 至 159,000ng/mL。这些病例中 DHC6G 的浓度在血液中为 20 至 62,180ng/mL,尿液中为 40 至 500,000ng/mL。然而,DHM 和其葡萄糖醛酸的浓度低于 DHC 和其葡萄糖醛酸。在本研究中,可以得出结论,在多种药物中毒中,导致死亡的 DHC 浓度可能较低。由于存在其他有害物质,尸检中发现的浓度与治疗和毒性浓度重叠,并且正如案例 1(500ng/mL)中报告的那样,即使浓度低于致死浓度也可能导致死亡。有人提出,DHM 和 DHM6G 可能在 DHC 未检出或检出浓度较低时,在评估死亡原因方面发挥主要作用。本研究不支持这一假设,从这里报告的数据可以清楚地看出,在未检出 DHC 的情况下,DHM 和其葡萄糖醛酸也未检出。在这些病例中的一些病例中鉴定出 DHM 和 DHM6G 的毒性浓度;然而,DHC 的浓度足以单独导致死亡。似乎 DHM 和 DHM6G 对死亡的影响小于母体药物本身。

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