Literature DB >> 9166128

Experimental exposure of male volunteers to N-methyl-2-pyrrolidone (NMP): acute effects and pharmacokinetics of NMP in plasma and urine.

B Akesson1, K Paulsson.   

Abstract

OBJECTIVES: To study the acute effects of exposure to the increasingly used solvent, N-methyl-2-pyrrolidone (NMP) in male volunteers. Further, to determine the NMP concentration in plasma and urine during and after the exposure.
METHODS: Six male volunteers were exposed for eight hours on four different days to 0, 10, 25, and 50 mg/m3 NMP. Plasma was collected and urine was sampled during and after the exposure. Changes in nasal volume were measured by acoustic rhinometry and in airway resistance by spirometry.
RESULTS: The eight-hour experimental exposure to 10, 25, and 50 mg/m3 did not induce discomfort to eyes or upper airways. Acute changes in nasal volume were not found, and no changes in the spirometric data could be registered. The elimination curves suggested a non-linear pattern and at the end of exposure showed mean (range) half lifes of NMP in plasma of about 4.0 (2.9-5.8) hours and in urine 4.5 (3.5-6.6) hours. The unmetabolised NMP found in urine samples collected during exposure and at the subsequent 44 hours corresponded to about 2% of the calculated absorbed dose. At the end of the exposure there was a close correlation between exposures and the plasma concentration and urinary excretion of NMP.
CONCLUSIONS: NMP was absorbed through the respiratory tract and readily eliminated from the body, mainly by biotransformation to other compounds. Exposure to 10, 25, or 50 mg/m3 NMP did not cause nose, eye, or airway irritation. Thus, NMP is a mild irritant.

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Year:  1997        PMID: 9166128      PMCID: PMC1128696          DOI: 10.1136/oem.54.4.236

Source DB:  PubMed          Journal:  Occup Environ Med        ISSN: 1351-0711            Impact factor:   4.402


  8 in total

1.  Isolation and identification of the major urinary metabolite of N-methylpyrrolidinone in the rat.

Authors:  D A Wells; A A Hawi; G A Digenis
Journal:  Drug Metab Dispos       Date:  1992 Jan-Feb       Impact factor: 3.922

2.  The role of acoustic rhinometry in studying the nasal cycle.

Authors:  E W Fisher; G K Scadding; V J Lund
Journal:  Rhinology       Date:  1993-06       Impact factor: 3.681

3.  Effects of prenatal exposure to N-methylpyrrolidone on postnatal development and behavior in rats.

Authors:  U Hass; S P Lund; J Elsner
Journal:  Neurotoxicol Teratol       Date:  1994 May-Jun       Impact factor: 3.763

4.  Epidemiology Standardization Project (American Thoracic Society).

Authors:  B G Ferris
Journal:  Am Rev Respir Dis       Date:  1978-12

5.  Percutaneous absorption of co-administered N-methyl-2-[14C]pyrrolidinone and 2-[14C]pyrrolidinone in the rat.

Authors:  I Midgley; A J Hood; L F Chasseaud; C J Brindley; S Baughman; G Allan
Journal:  Food Chem Toxicol       Date:  1992-01       Impact factor: 6.023

6.  Irritant cutaneous reactions to N-methyl-2-pyrrolidone (NMP).

Authors:  H L Leira; A Tiltnes; K Svendsen; L Vetlesen
Journal:  Contact Dermatitis       Date:  1992-09       Impact factor: 6.600

7.  Disposition and metabolism of double-labeled [3H and 14C] N-methyl-2-pyrrolidinone in the rat.

Authors:  D A Wells; G A Digenis
Journal:  Drug Metab Dispos       Date:  1988 Mar-Apr       Impact factor: 3.922

8.  The acute oral toxicity and primary ocular and dermal irritation of selected N-alkyl-2-pyrrolidones.

Authors:  J M Ansell; J A Fowler
Journal:  Food Chem Toxicol       Date:  1988-05       Impact factor: 6.023

  8 in total
  7 in total

1.  Ambient monitoring and biomonitoring of workers exposed to N-methyl-2-pyrrolidone in an industrial facility.

Authors:  Michael Bader; Wolfgang Rosenberger; Thomas Rebe; Stephen A Keener; Thomas H Brock; Hans-Jürgen Hemmerling; Renate Wrbitzky
Journal:  Int Arch Occup Environ Health       Date:  2005-12-15       Impact factor: 3.015

2.  Oxidation suppression during hydrothermal phase reversion allows synthesis of monolayer semiconducting MoS2 in stable aqueous suspension.

Authors:  Zhongying Wang; Yin-Jia Zhang; Muchun Liu; Andrew Peterson; Robert H Hurt
Journal:  Nanoscale       Date:  2017-05-04       Impact factor: 7.790

3.  Human experimental exposure to N-methyl-2-pyrrolidone (NMP): toxicokinetics of NMP, 5-hydroxy- N-methyl-2-pyrrolidone, N-methylsuccinimide and 2-hydroxy- N-methylsuccinimide (2-HMSI), and biological monitoring using 2-HMSI as a biomarker.

Authors:  B A G Jönsson; B Akesson
Journal:  Int Arch Occup Environ Health       Date:  2003-04-03       Impact factor: 3.015

4.  Dermal absorption and urinary elimination of N-methyl-2-pyrrolidone.

Authors:  Michael Bader; Stephen A Keener; Renate Wrbitzky
Journal:  Int Arch Occup Environ Health       Date:  2005-10-12       Impact factor: 3.015

5.  Biological monitoring and health effects of low-level exposure to N-methyl-2-pyrrolidone: a cross-sectional study.

Authors:  Vincent Haufroid; Veronika K Jaeger; Stefan Jeggli; Rolf Eisenegger; Alfred Bernard; Drita Friedli; Dominique Lison; Philipp Hotz
Journal:  Int Arch Occup Environ Health       Date:  2014-08       Impact factor: 3.015

6.  Organic solvents as vehicles for precipitating liquid embolics: a comparative angiotoxicity study with superselective injections of swine rete mirabile.

Authors:  O Dudeck; O Jordan; K T Hoffmann; A F Okuducu; K Tesmer; T Kreuzer-Nagy; D A Rüfenacht; E Doelker; R Felix
Journal:  AJNR Am J Neuroradiol       Date:  2006-10       Impact factor: 3.825

7.  Exposure to multiple low-level chemicals in relation to reproductive hormones in premenopausal women involved in liquid crystal display manufacture.

Authors:  Ching-Chun Lin; Chia-Ning Huang; Jung-Der Wang; Yaw-Huei Hwang; Ruei-Hao Shie; Yu-Yin Chang; Shao-Ping Weng; Pau-Chung Chen
Journal:  Int J Environ Res Public Health       Date:  2013-04-03       Impact factor: 3.390

  7 in total

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