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1.
Int J Legal Med ; 130(3): 711-21, 2016 May.
Article in English | MEDLINE | ID: mdl-26739323

ABSTRACT

To assess the effects of cannabis on the ability required to ride a bicycle, repetitive practical cycling tests and medical examinations were carried out before and after inhalative consumption of cannabis. A maximum of three joints with body weight-adapted THC content (300 µg THC per kg body weight) could be consumed by each test subject. Fourteen regular cannabis-consuming test subjects were studied (12 males, 2 females). In summary, only a few driving faults were observed even under the influence of very high THC concentrations. A defined THC concentration that leads to an inability to ride a bicycle cannot be presented. The test subjects showed only slight distinctive features that can be documented using a medical test routinely run for persons under suspicion of driving under the influence of alcohol or drugs.


Subject(s)
Bicycling , Cannabis , Marijuana Smoking , Adult , Driving Under the Influence , Dronabinol/analogs & derivatives , Dronabinol/blood , Female , Humans , Male , Young Adult
2.
Eur J Pediatr ; 175(7): 1019-21, 2016 Jul.
Article in English | MEDLINE | ID: mdl-26691719

ABSTRACT

UNLABELLED: We report on two patients who ingested psychoactive scopolamine that was synthesized at home from butylscopolamine (Buscopan®), which is available as over-the-counter antispasmodic in nearly 100 countries worldwide. Patient 1 presented with severe central anticholinergic toxidrome, while patient 2 suffered from minor symptoms. An empty blister of Buscopan® was found in the patients' home, but initially was not suspected to be causative for the observed central anticholinergic symptoms, as Buscopan® is not able to pass the blood-brain barrier in its native form. Only later, the information by third parties and a Google search helped to identify homemade scopolamine derived from Buscopan® as the responsible agent in these two cases. Retrospectively, scopolamine could be detected in serum and urine of both patients, while it was absent in one control after ingestion of native Buscopan®. CONCLUSION: Over-the-counter drugs can be used to synthesize psychoactives with means that are available in every household. Such knowledge can spread via social media and internet discussion boards long before appearing in medical literature. While typical clinical presentation often enables clinicians to adequately identify and treat specific toxidromes, these sources of information need to be increasingly taken into account by medical professionals for identification of its causative agent. This potential of Buscopan® might gain importance as an easily accessible source of psychoactive scopolamine. WHAT IS KNOWN: • Substances with central anticholinergic effects are known for their hallucinogenic potential and may be used as psychoactives. What is New: • The over-the-counter antispasmodic butylscopolamine (Buscopan®) can be abused to synthesize anticholinergic, psychoactive scopolamine at home with means that are available in every household.


Subject(s)
Anticholinergic Syndrome/diagnosis , Butylscopolammonium Bromide/adverse effects , Parasympatholytics/adverse effects , Scopolamine/adverse effects , Adolescent , Butylscopolammonium Bromide/analysis , Designer Drugs/analysis , Humans , Male , Nonprescription Drugs/adverse effects , Parasympatholytics/analysis , Scopolamine/analysis
3.
Forensic Sci Int ; 215(1-3): 110-3, 2012 Feb 10.
Article in English | MEDLINE | ID: mdl-21511420

ABSTRACT

UNLABELLED: Objective Chloroprene, 2-chloro-1,3 butadiene, is a volatile synthetic liquid. The chloroprene monomer is extremely reactive and is used for the production of latexes and synthetic rubber such as Neoprene. Up to now an acute lethal human exposure has been described only once in the literature [19]. The intoxication is associated with nervous system depression, pulmonary edema, narcosis, and respiratory arrest. Case report A 29-year-old chemistry company worker was found unconscious in an empty vessel (depth: 3m) used for chloroprene. The man was dressed in shoes, trousers, a helmet and a respiratory mask. The upper part of the body was unclothed. In spite of reanimation, the man died three hours later in a hospital. MATERIAL AND METHODS: All analyses were performed by headspace gas chromatography (HS/GC/FID). In addition, brain, muscle and myocardial muscle were analysed by headspace GC-MS. Results and discussion Autopsy findings: The cause of death could not be determined as the macromorphological findings were unspecific. Toxicology findings The calibration curve of chloroprene in serum shows linearity from 1.0 to 200 µg/ml (r(2)=0.9999) using benzene as internal standard. The LOD is 0.28 µg/ml, the LLOQ is 0.99 µg/ml. Tissues and body fluids were stored at -20 °C till the analysis. Chloroprene was quantified after addition of benzene as the internal standard. It was found in nearly all tissues and body fluids except in the urine and lung. The highest concentrations were detected in the kidney, liver, myocardial muscle and especially in the brain. Furthermore, hexanal was found in all samples except in the urine. The amount of hexanal in some specimens is high, especially in the lung, bile, gastric content and myocardial muscle. Conclusion We assume that a significant amount of chloroprene was not only inhaled but also absorbed through the skin because the man wore a respiratory mask. Presumably the accident would not have happened if the works safety protocols had been followed. The reason why high concentrations of hexanal were found in the tissues could not be clarified.


Subject(s)
Chloroprene/poisoning , Accidents, Occupational , Adult , Aldehydes/analysis , Brain/pathology , Brain Chemistry , Chloroprene/analysis , Chloroprene/pharmacokinetics , Chromatography, Gas , Forensic Toxicology , Humans , Kidney/chemistry , Kidney/pathology , Liver/chemistry , Lung/pathology , Male , Myocardium/chemistry , Tissue Distribution
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