Free Content Enantiomer Analysis of A New Street Drug, 3,4-Methylenedioxy-N-methyl-butanamine, in Rat Urine

Authors: Nagai T.1; Matsushima K.2; Suzuki A.1; Saotome A.1; Kurosu A.1; Nihei H.2; Kuroyanagi K.3; Tokudome S.1

Source: Journal of Analytical Toxicology, Volume 26, Number 2, March 2002 , pp. 104-109(6)

Publisher: Preston Publications

Buy & download fulltext article:

Free content The full text is free.

View now:
PDF 112.1kb 

Abstract:

A new street drug, 3,4-methylenedioxy-N-methyl-butanamine (MBDB), has been found in Japan recently. The stereoisomer monitoring and the urinary excretion kinetics are not determined in biological fluids even though abused MBDB is a racemic form [enantiomer ratio (-/+) = 1.00]. The present studies were done by high-performance liquid chromatography (HPLC) equipped with a chiral activity column at 40°C using urine specimens from five Wistar rats. Urine samples were collected over six time intervals after a single oral administration of racemic MBDB (30 mg/kg). Unchanged MBDB and 3,4-methylenedioxybutanamine (BDB), an N-demethylated metabolite, were found in the rats' urine. Each enantiomer of MBDB and BDB was monitored (peak resolution > 1.00) by HPLC analysis within 30 min. For both MBDB and BDB, the (+)-isomers were excreted a little more than the (-)-isomers. The stereoselective disposition of BDB was more remarkable than that of MBDB and was observed in the urine throughout the study (p < 0.05). The urinary excretion of MBDB showed significant difference between the two enantiomers from 4 to 20 h (p < 0.05). The amount of MBDB excreted up to 24 h was 34.7 ± 2.8% of the administered dose: 17.6 ± 1.4% for (+)-isomer and 17.1 ± 1.5% for (-)-isomer. The amount of BDB was 4.9 ± 1.0%; 2.9 ± 0.6% for (+)-isomer and 2.0 ± 0.4% for (-)-isomer. The enantiomer ratio (-/+) of MBDB and BDB was 1.00 or a little smaller. The ratio (-/+) of MBDB changed from 1.00 ± 0.02 to 0.88 ± 0.09 by 24 h, and that of BDB from 0.68 ± 0.03 to 0.78 ± 0.02. The ratio (-/+) for MBDB and BDB accumulated up to 24 h was 0.97 ± 0.01 and 0.70 ± 0.06, respectively, and the total ratio (-/+) of the two substances was 0.93 ± 0.02 (p < 0.05). These findings suggested that the stereoselective disposition of racemic MBDB was different from that of 3,4-dimethylenedioxyamphetamine and 3,4-dimethylenedioxymethamphetamine and was similar to that of methamphetamine.

Language: English

Document Type:

Affiliations: 1: Department of Legal Medicine, Dokkyo University School of Medicine, 880, Kitakobayashi, Mibu, Tochigi 321-0293, Japan 2: Department of Legal Medicine, Dokkyo University School of Medicine, 880, Kitakobayashi, Mibu, Tochigi 321-0293, Japan; Scientific Crime Detection Laboratory, Tochigi Prefectural Police Headquarters, Utsunomiya, Tochigi 320-8510, Japan 3: Tokyo Medical Examiners' Office, Otsuka 4-21-18, Bunkyo-ku, Tokyo 112-0012, Japan

Publication date: 2002-03-01

More about this publication?
  • The Journal of Analytical Toxicology (JAT), established in 1977 and published 9 times a year, is the international source covering a broad range of clinical, forensic, and industrial laboratory topics regarding the isolation, identification, and quantitation of potentially toxic substances.

    With an emphasis on practical application, JAT articles provide improved and novel techniques for use in clinical, forensic, workplace, sports testing (doping), and other toxicology laboratories. Articles describe newly developed methods in immunoassay testing, gas chromatography, liquid chromatography, mass spectrometry, atomic absorption spectrometry, solid and liquid phase extraction techniques, and other analytical approaches. Worldwide readership includes toxicologists, pathologists, chemists, clinicians, researchers, and educators working in medical examiner and law enforcement laboratories, hospitals, university and independent analytical laboratories, as well as the drug manufacturing industry.

    Each year in October, we publish a special issue from the Society of Forensic Toxicologists.

    JAT, as determined by ISI Citation Index, is one of the two most referenced international journals in forensic science.

  • Subscribe to this Title
  • ingentaconnect is not responsible for the content or availability of external websites
Related content

Tools

Key

Free Content
Free content
New Content
New content
Open Access Content
Open access content
Subscribed Content
Subscribed content
Free Trial Content
Free trial content

Text size:

A | A | A | A
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages. print icon Print this page