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N,N-dimethylpentylone poisoning: Clinical manifestations, analytical detection, and metabolic characterization.
Leung, H S; Tang, Magdalene H Y; Tong, H F; Chong, Y K.
Affiliation
  • Leung HS; Hospital Authority Toxicology Reference Laboratory, Princess Margaret Hospital, Hong Kong; Chemical Pathology Laboratory, Princess Margaret Hospital, Hong Kong.
  • Tang MHY; Hospital Authority Toxicology Reference Laboratory, Princess Margaret Hospital, Hong Kong.
  • Tong HF; Hospital Authority Toxicology Reference Laboratory, Princess Margaret Hospital, Hong Kong; Chemical Pathology Laboratory, Princess Margaret Hospital, Hong Kong.
  • Chong YK; Hospital Authority Toxicology Reference Laboratory, Princess Margaret Hospital, Hong Kong; Chemical Pathology Laboratory, Princess Margaret Hospital, Hong Kong. Electronic address: cyk280a@ha.org.hk.
Forensic Sci Int ; 361: 112116, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38905907
ABSTRACT

INTRODUCTION:

The proliferation of new psychoactive substances (NPS) poses a significant challenge to clinical and forensic toxicology laboratories. N,N-dimethylpentylone, a novel synthetic cathinone, has emerged as a public health concern. The aims of this study are to describe the clinical presentation of N,N-dimethylpentylone poisoning, to describe detection methods, and to deduce its metabolic pathways.

METHODS:

Clinical data was collected and reviewed retrospectively from patients with confirmed N,N-dimethylpentylone exposure. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to identify N,N-dimethylpentylone and its metabolites in urine samples. The metabolic pathway was characterised by comparison of the detected substances with reference standards.

RESULTS:

Eight cases were included in the case series. Seven different metabolites of N,N-dimethylpentylone were identified in in vivo patient urine samples, where the two major metabolic pathways were proposed to be opening of the 5-membered ring and reduction of carboxide. All patients presented with neuropsychiatric and/or cardiovascular symptoms. Co-ingestion with other substances was reported in all cases. One patient requiring intensive care was described in detail. All patients eventually recovered. The analytical method allowed the simultaneous identification of N,N-dimethylpentylone, pentylone and bisdesmethyl-N,N-dimethylpentylone, as well as other drugs of abuse in patient samples.

CONCLUSION:

N,N-dimethylpentylone appears to be less potent than its metabolite pentylone. Co-ingestion with other drugs of abuse is common. Poisoning cases have neuropsychiatric and cardiovascular manifestations. An updated and comprehensive laboratory method is needed for its detection.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychotropic Drugs / Tandem Mass Spectrometry Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Forensic Sci Int Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychotropic Drugs / Tandem Mass Spectrometry Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Forensic Sci Int Year: 2024 Document type: Article