Section for Drug Abuse Research, Dept. of Forensic Sciences, Division of Laboratory Medicine, Oslo University Hospital, Oslo, Norway.
Department of Pharmaceutical Biosciences, School of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, Norway.
Addiction. 2021 Nov;116(11):3104-3112. doi: 10.1111/add.15492. Epub 2021 May 3.
To study whether the preparation procedure, and its acidic and heating conditions, used by heroin users to prepare heroin for intravenous administration affects the final composition of the fluid to be injected.
Samples from different seizures of illegal heroin provided by the Norwegian police were prepared by adding water and ascorbic acid before heating under controlled conditions in the laboratory. Further, three seizures were prepared with different amounts of ascorbic or citric acid relative to their diacetylmorphine content. Pure diacetylmorphine base or salt was also submitted to the procedure applying two different heating intensities. The seizures and the final product after preparation were analysed for diacetylmorphine, 6-acetylmorphine and morphine using liquid chromatography with tandem mass spectrometry (LC-MS-MS).
After preparation, a decrease of 19.8% (25th and 75th percentiles = -29.2 and -15.3) in the initial diacetylmorphine content was observed. Both the 6-acetylmorphine and morphine content increased but, due to their low content in the initial product, diacetylmorphine still represented 83.9% (25th and 75th percentiles = 77.3 and 88.0) of the sum of these three opioids in the final solution. The loss of water during preparation caused an increase in the concentration of diacetylmorphine, 6-acetylmorphine and morphine, depending on the heating intensity applied. The content of these opioids was affected by the quantity and type of acid added in relation to the heroin purity and the level of diacetylmorphine dissolved being proportional to the amount of ascorbic acid, but not citric acid, in the sample with high heroin purity.
Preparation of heroin for intravenous injection appears to change the amount or concentration of diacetylmorphine and its active metabolites, 6-acetylmorphine and morphine in the final product, depending on heroin purity, amount and type of acid used or heating conditions. These circumstances can contribute to unintentional variations in the potency of the final injected solution, and therefore affect the outcome after injection.
研究海洛因使用者为静脉注射准备海洛因时所采用的准备程序及其酸性和加热条件是否会影响待注射液体的最终成分。
由挪威警方提供的不同批次非法海洛因样品,在实验室中进行控制条件下加水和抗坏血酸添加,然后加热。此外,三个批次根据其二乙酰吗啡含量添加不同量的抗坏血酸或柠檬酸。还将纯二乙酰吗啡碱或盐进行了该程序处理,应用了两种不同的加热强度。采用液相色谱-串联质谱法(LC-MS-MS)对缴获物和准备后的最终产物进行二乙酰吗啡、6-乙酰吗啡和吗啡分析。
准备后,初始二乙酰吗啡含量下降了 19.8%(25 百分位数和 75 百分位数=-29.2 和-15.3)。6-乙酰吗啡和吗啡的含量均增加,但由于初始产物中的含量较低,二乙酰吗啡仍占最终溶液中这三种阿片类药物总和的 83.9%(25 百分位数和 75 百分位数=77.3 和 88.0)。准备过程中水分的损失导致二乙酰吗啡、6-乙酰吗啡和吗啡的浓度增加,具体取决于应用的加热强度。添加的酸的量和类型以及海洛因的纯度会影响这些阿片类药物的含量,而溶解的二乙酰吗啡水平与样品中抗坏血酸的量成正比,但与柠檬酸不成比例,在高纯度海洛因样品中。
为静脉注射准备海洛因的过程似乎会改变最终产物中二乙酰吗啡及其活性代谢物 6-乙酰吗啡和吗啡的数量或浓度,具体取决于海洛因纯度、使用的酸的量和类型或加热条件。这些情况可能导致最终注射溶液效力的意外变化,从而影响注射后的结果。