Literature DB >> 2291875

Absolute bioavailability and pharmacokinetics of medifoxamine in healthy humans.

S Saleh1, A Johnston, P Turner.   

Abstract

Medifoxamine is a new monoamine re-uptake inhibiting antidepressant drug. Twelve volunteers received 100 mg by i.v. infusion over 15 min and 500 mg by mouth fasting. The treatments were given 1 week apart in a randomised cross-over design. Venous blood samples (10 ml) were taken at intervals for 24 h for h.p.l.c. measurement of serum medifoxamine. A biexponential decline of serum medifoxamine concentration was observed after intravenous administration in all subjects and similar terminal elimination half-lives were observed following both routes, indicating that oral absorption is not rate-limiting. The absolute bioavailability of oral medifoxamine was 21%.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2291875      PMCID: PMC1368255          DOI: 10.1111/j.1365-2125.1990.tb03823.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  2 in total

1.  Determination of medifoxamine in plasma and urine by high-performance liquid chromatography.

Authors:  S Saleh; A Johnston; M Chanon; P Turner
Journal:  J Chromatogr       Date:  1989-11-10

2.  STRIPE: an interactive computer program for the analysis of drug pharmacokinetics.

Authors:  A Johnston; R C Woollard
Journal:  J Pharmacol Methods       Date:  1983-05
  2 in total
  2 in total

1.  The pharmacokinetics and pharmacodynamics of medifoxamine after oral administration in healthy elderly volunteers.

Authors:  N Gainsborough; M L Nelson; V Maskrey; C G Swift; S H Jackson
Journal:  Eur J Clin Pharmacol       Date:  1994       Impact factor: 2.953

Review 2.  Individual variation in first-pass metabolism.

Authors:  Y K Tam
Journal:  Clin Pharmacokinet       Date:  1993-10       Impact factor: 6.447

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.