Evolution of the NBOMes: 25C- and 25B- Sold as 25I-NBOMe
Larissa K. Laskowski, Faesal Elbakoush, Jessica Calvo, Gina Exantus-Bernard, Jane Fong, Justin L. Poklis, Alphonse Poklis, Lewis S. Nelson
Journal of Medical Toxicology November 12, 2014 DOI: 10.1007/s13181-014-0445-9 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Case report Peer reviewed |
|---|---|
| Sample size | 2 |
| Population | Adolescents with NBOMe intoxication |
| Intervention | Benzodiazepines |
| Keywords | Anesthesia Pharmacology |
| Citations | 39 |
| Key findings | Two adolescents who reported using 25I-NBOMe were confirmed by mass spectrometry to have ingested 25C-NBOMe and 25B-NBOMe, respectively. Both presented with seizures and muscle rigidity, with one case showing extreme CPK elevation. The authors propose that laboratory confirmation can reveal unexpected NBOMe variants and contribute to epidemiological data. |
Abstract
IntroductionThe NBOMes (N-benzyl-oxy-methyl derivatives of known 2C phenylethylamines) are a new and growing class of potent synthetic stimulants. Case reports provide the bulk of available safety and clinical data for clinicians. We report two cases of NBOMe intoxication with 25C-NBOMe (the first lab-confirmed US case) and 25B-NBOMe, respectively, both confirmed via triple quadrapole mass spectrometry.Case reportsCase 1: A 16-year-old girl had a generalized seizure after reported use of 25I-NBOMe. She presented with altered mental status, lower extremity rigidity, and elevated CPK (6042 U/L). Despite treatment with benzodiazepines, her lower extremity rigidity persisted and CPK peaked at 47,906 U/L. She was discharged on hospital day 8. Serum and urine specimens confirmed presence of 25C-NBOMe. Case 2: A 15-year-old boy developed bizarre behavior after reported use of 25I-NBOMe. In the ED, he had two generalized seizures and persistent muscle rigidity. CPK peaked at 429 U/L. Seizures were managed with benzodiazepines, and he was discharged within 24 h. Serum specimens revealed 25B-NBOMe.DiscussionNBOMes are amphetamine derivatives and highly potent 5-HT(2A) receptor agonists. Clinical manifestations are a product of enhanced central sympathetic and serotonergic tone. We report two cases of NBOMe intoxication in patients who believed they used 25I-NBOME, while lab confirmation proved otherwise. Whether unique clinical manifestations are specific to the NBOMe variant, dose, route of administration, or other factors is unknown. Laboratory confirmation may play a role in identifying unexpected NBOMe variants, while contributing to the epidemiologic data on these novel substances.
Citations in the library
Cited by 20
- Pharmacology and Toxicology of N-Benzylphenethylamine ("NBOMe") Hallucinogens. Current Topics in Behavioral Neurosciences 2017
- DARK Classics in Chemical Neuroscience: NBOMes ACS Chemical Neuroscience October 28, 2019
- Measuring inhibition of monoamine reuptake transporters by new psychoactive substances (NPS) in real-time using a high-throughput, fluorescence-based assay. Toxicology in Vitro December 1, 2017
- Locomotor and discriminative stimulus effects of four novel hallucinogens in rodents. Behavioural Pharmacology August 1, 2017
- In vitro phase I metabolism of three phenethylamines 25D‐NBOMe, 25E‐NBOMe and 25N‐NBOMe using microsomal and microbial models Drug Testing and Analysis July 3, 2018
and 15 more in the library