Rapid and Sensitive Determination of Udenafil in Plasma by LC-MS/MS for Intranasal Pharmacokinetic Study in Rats

被引:6
|
作者
Ku, Wan-Sung [1 ,2 ]
Cho, Hyun-Jong [1 ,2 ]
Yoon, In-Soo [1 ,2 ]
Kim, Jeong Hoon [3 ]
Cha, Bong-Jin [3 ]
Kim, Jung Sun [4 ]
Kim, Kyeong-Mi [5 ]
Kang, Shin-Kwon [5 ]
Chung, Suk-Jae [1 ,2 ]
Shim, Chang-Koo [1 ,2 ]
Kim, Dae-Duk [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[2] Seoul Natl Univ, Pharmaceut Sci Res Inst, Seoul 151742, South Korea
[3] Dong A Pharm Co Ltd, Gyeonggi Do 446905, South Korea
[4] Dongseo Univ, Div Hlth Sci, Pusan 617716, South Korea
[5] LCKorea Co Ltd, R&D Inst, Seoul 150102, South Korea
关键词
LC-MS/MS; udenafil; liquid liquid extraction; intranasal delivery; pharmacokinetics; PERFORMANCE LIQUID-CHROMATOGRAPHY; ACTIVE METABOLITE; SILDENAFIL; INHIBITOR; DA-8159; URINE;
D O I
10.1248/cpb.59.1083
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A rapid and sensitive analytical method for udenafil in rat plasma was developed and validated using liquid chromatography-tandem mass spectrometry (LC-MS/MS). This chromatographic procedure was then applied to the in viva pharmacokinetic studies in rats for determining the advantages of intranasal administration of the drug over oral administration. Using liquid liquid extraction (LLE), udenafil and the internal standard (IS) sildenafil were extracted with dichloromethane from 100 mu l of plasma samples. Chromatographic separation was performed using Pursuit XRS C-18 column (50 mm x2.1 mm, i.d., 3 mu m, Varian Inc., CA, U.S.A.) with an isocratic mobile phase consisting of acetonitrile and 10 mm ammonium acetate (90: 10, v/v) at a flow rate of 0.2 ml/min over a total run time of 2.5 min. Detection and quantification was performed by mass spectrometry using the multiple reaction-monitoring mode at m/z 517.4 -> 283.1 for udenafil and m/z 475.3 -> 4100.0 for IS. Results showed that the developed method was sensitive and specific for udenafil. Linearity was obtained in the range of 0.5-1000 ng/ml. The coefficient of variation of both intra- and inter-day validation were below 11.6% and the intra- and inter-day accuracy ranged from 91.5 to 109.9%. Udenatil concentration was successfully measured from plasma after intranasal as well as after intravenous or oral administration at clinical dose (1.67 mg/kg) in rats. Moreover, the T-max values obtained from pharmacokinetic studies suggested that administration of udenafil intranasally could be more effective than by the oral route.
引用
收藏
页码:1083 / 1088
页数:6
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