摘要
目的建立Beagle犬血浆中间-尼索地平RP-HPLC测定方法,研究Beagle犬静脉注射间-尼索地平后体内药动学。方法色谱条件:Waters C18色谱柱(3.9 mm×300 mm,10μm);流动相:甲醇-水(64∶36);检测波长:236 nm;柱温:30℃;流速:1.0 mL·min-1。Beagle犬静脉注射间-尼索地平后定时取血,用RP-HPLC测定血浆药物浓度,3P97软件计算药动学参数。结果间-尼索地平在1.875~480μg·L-1内线性关系良好(r=0.999 9);Beagle犬静脉注射0.1,0.2,0.5 mg·kg-1间-尼索地平后药动学行为均符合二室模型,AUC与剂量呈正相关,t1/2α分别为6.32,7.07和16.0 min;t1/2β分别为136,149和137 min;Vc分别为4.4,6.7和10.3 L;CL分别为0.20,0.20和0.30 L·min-1。结论本方法操作简便,灵敏度高,稳定性好,可满足药动学研究需要。
Abstract
OBJECTIVE To establish a reversed phase high performance liquid chromatographic(RP-HPLC) method for the measurement of m-nisoldipine(m-Nis) in the plasma of Beagle dogs and to investigate the pharmacokinetics of m-Nis after an intravenous administration in Beagle dogs.METHODS The analysis was performed on a Waters C18 column(3.9 mm×300 mm, 10 μm)at 30 ℃ with the mobile phase of methanol-water(64∶36) at a flow rate of 1.0 mL·min-1.The detect wavelength was at 236 nm.The plasma samples were collected after an intravenous administration of m-Nis in Beagle dogs.The plasma concentrations of m-Nis were measured using HPLC method and the pharmacokinetic parameters were calculated by 3P97.RESULTS The calibration curve of m-Nis was linear in the range of 1.875~480(μg·L-1) with a correlation coefficient of 0.999 9.The plasma concentration-time curves of mNis were fitted with a two-compartment open pharmacokinetic model.The main pharmacokinetic parameters of m-Nis after a single dose of 0.1,0.2 and 0.5 mg·kg-1of m-Nis in Beagle dogs were: t1/2α 6.32,7.07 and 16.0 min;t1/2β 136,149 and 137 min;Vc 4.4,6.7 and 10.3 L;CL 0.20,0.20 and 0.30 L·min-1,respectively.CONCLUSION The method is sensitive,stable and easy to process.It is practical and suitable for the pharmacokinetic study of m-Nis.
关键词
间-尼索地平 /
反相高效液相色谱法 /
药动学
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Key words
m-nisodipine /
RP-HPLC /
pharmacokinetics
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张志清;王永利;李晓娜.
间-尼索地平Beagle犬静脉给药后体内药动学研究[J]. 中国药学杂志, 2006, 41(07): 535-537
ZHNG Zhi-qing;WNG Yong-li;LI Xio-n.
Pharmacokinetics of m-Nisoldipine After an Intravenous Administration in Beagle dogs [J]. Chinese Pharmaceutical Journal, 2006, 41(07): 535-537
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参考文献
[1] YUAN F Y, HUANG X Z. New type calcium channel blockers- m-nisoldipine and Nisodipine[J] . J Shenyang Coll Pharm(沈阳药学院学报), 1990, 7(1):58-59.
[2] LIU W H,FU S X,LI Y S. Antihypertensive effects of m-Nisoldipine and Nisoldipine on renal hypertensive rats and dogs[J] .Acta Pharmacol Sin(中国药理学报),1992, 13(1):31-35.
[3] ZHANG Y J, ZHANG G H, ZHANG Y L, et al. Underpressure effects of m-nisoldipine and nisoldipine on spontaneous hypertensive rats[J] .Acta Acad Med Hebei(河北医学院学报),1994, 15(3):135-137.
[4] FU S X,LI Y S,JIN C J,et al. Effects of m-Nisoldipine and Nisoldipine on hemodynamics in anesthetized dogs[J] . Acta Pharmacol Sin(中国药理学报),1988, 9(1):43-48.
[5] REN L M, LI Y S,FU S X,et al. Cardiovascular action of m-Nisoldipine in anesthetized rabbits and guinea pigs[J] . Acta Pharmacol Sin(中国药理学报),1988, 9(5):426.
[6] YUAN F Y, YAN T R, BAO C H, et al. Investigation of light stability of m-Nisoldipine [J] . Chin Pharm J(中国药学杂志),1989, 24(9):540-541.
[7] AHR H J, KRAUSE H P, SUWELACK D, et al. Pharmacokinetics of Nisoldipine[J] .Drug Res,1988,38(8):1100-1104.
[8] HUANG Y,FU S X,LI Y S. Pharmacokinetics of m-Nisoldipine in rabbits and rats[J] . Acta Pharmacol Sin(中国药理学报),1990,11(6):484-487.
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脚注
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