Literature DB >> 12367677

Determination of a new phosphodiesterase V inhibitor, DA-8159, in plasma and urine by high-performance liquid chromatography.

Hyun Joo Shim1, Eun Joo Lee, Young Hee Jung, So Hee Kim, Soon Hoe Kim, Moohi Yoo, Jong Won Kwon, Won Bae Kim, Myung Gull Lee.   

Abstract

A high-performance liquid chromatographic (HPLC) method using liquid-liquid extraction for sample preparation was developed for the determination of a new phosphodiesterase V inhibitor, DA-8159, in rat plasma and urine using sildenafil citrate as an internal standard. A 100 microl aliquot of 0.1 M Na(2)CO(3) (containing sildenafil citrate, 3 microg/ml as free sildenafil) and a 1 ml aliquot of ether were added to a 100 microl aliquot of biological samples (urine samples were diluted 20 times with distilled water). After vortex centrifugation at 9000 x g for 3 min, the ether layer was collected and dried under nitrogen gas. The residue was reconstituted with a 150 microl aliquot of the mobile phase, centrifuged, and a 100 microl aliquot of the supernatant was injected onto a reversed-phase column. The mobile phases, 20 mM KH(2)PO(4) (pH 4.7):acetonitrile (70:30, v/v for plasma and tissue samples, and 75:25, v/v for urine samples), were run at a flow rate of 1.0 ml/min. The column effluent was monitored by an ultraviolet detector set at 292 nm. The retention times for DA-8159 and the internal standard were approximately 10.7 and 9.1 min, respectively, in plasma and tissue samples and the corresponding values in urine samples were 47 and 33 min. The detection limits for DA-8159 in rat plasma and urine were 20 and 100 ng/ml, respectively. The coefficients of variation of the assay were generally low: below 10% for plasma and 9.9% for urine. No interferences from endogenous substances were found. Copyright 2002 Elsevier Science B.V.

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Year:  2002        PMID: 12367677     DOI: 10.1016/s0731-7085(02)00397-7

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  5 in total

1.  Effect of ketoconazole on the pharmacokinetics of udenafil in healthy Korean subjects.

Authors:  Kwang-Hee Shin; Yong-ju Chung; Bo-Hyung Kim; Tae-Eun Kim; Hwa-Sook Kim; Joo-Youn Cho; In-Jin Jang; Sang-Goo Shin; Kyung-Sang Yu
Journal:  Br J Clin Pharmacol       Date:  2010-03       Impact factor: 4.335

2.  Pharmacokinetic and pharmacodynamic consequences of inhibition of terazosin metabolism via CYP3A1 and/or 3A2 by DA-8159, an erectogenic, in rats.

Authors:  E Y Oh; S K Bae; J W Kwon; M You; D C Lee; M G Lee
Journal:  Br J Pharmacol       Date:  2007-03-12       Impact factor: 8.739

3.  Pharmacokinetic interaction between DA-8159, a new erectogenic, and metformin in rats: competitive inhibition of metabolism via hepatic CYP3A1/2.

Authors:  Y H Choi; S J Chung; M G Lee
Journal:  Br J Pharmacol       Date:  2008-01-21       Impact factor: 8.739

4.  Safety, tolerability and pharmacokinetics of udenafil, a novel PDE-5 inhibitor, in healthy young Korean subjects.

Authors:  Bo-Hyung Kim; Hyeong-Seok Lim; Jae-Yong Chung; Jung-Ryul Kim; Kyoung Soo Lim; Dong-Ryul Sohn; Joo-Youn Cho; Kyung-Sang Yu; Sang-Goo Shin; Jae-Seung Paick; In-Jin Jang
Journal:  Br J Clin Pharmacol       Date:  2008-03-03       Impact factor: 4.335

5.  Fabrication, appraisal, and transdermal permeation of sildenafil citrate-loaded nanostructured lipid carriers versus solid lipid nanoparticles.

Authors:  Yosra S R Elnaggar; Magda A El-Massik; Ossama Y Abdallah
Journal:  Int J Nanomedicine       Date:  2011-12-06
  5 in total

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