Suppr超能文献

静脉注射氨茶碱与志愿者长期口服缓释硝苯地平之间的相互作用。

The interaction between i.v. theophylline and chronic oral dosing with slow release nifedipine in volunteers.

作者信息

Jackson S H, Shah K, Debbas N M, Johnston A, Peverel-Cooper C A, Turner P

出版信息

Br J Clin Pharmacol. 1986 Apr;21(4):389-92. doi: 10.1111/j.1365-2125.1986.tb05212.x.

Abstract

Eight healthy volunteers received a 5 min i.v. infusion of lysine theophylline, equivalent to 197 mg anhydrous theophylline, both before (day 1) and during (day 5) steady state chronic oral dosing with slow release nifedipine 20 mg 12 hourly. A theophylline pharmacokinetic profile was performed on day 1 and day 5 and a nifedipine pharmacokinetic profile was performed on day 4 and day 5. The greatest difference in serum theophylline concentrations was seen at the first sampling time (5 min after completion of the infusion) with a mean concentration of 9.9 mg l-1 during nifedipine administration and 14.6 mg l-1 with theophylline alone. Thereafter, the difference fell to approximately 1 mg l-1 until 6 h when they became almost identical. Repeated measures analysis of variance using the theophylline serum concentrations at each of ten time points over 8 h as the repeated measures showed a small but significant effect of nifedipine (F(1,151) = 7.0, P less than 0.01) on serum theophylline concentrations. Mean volume of distribution (V) rose from 0.33 +/- 0.07 to 0.39 +/- 0.06 1 kg-1 corrected body weight (CBW) in the presence of nifedipine (t = 2.23, P = 0.052). Theophylline clearance, area under the curve to 8 h AUC (0-8), area under the curve to infinity AUC (0-infinity) and elimination half-life (t1/2) did not change appreciably. No statistically significant changes in nifedipine pharmacokinetics occurred in the presence of theophylline.

摘要

8名健康志愿者在稳态下每日两次口服20 mg缓释硝苯地平前(第1天)和服药期间(第5天),分别接受了5分钟的赖氨酸茶碱静脉输注,相当于197 mg无水茶碱。在第1天和第5天进行了茶碱药代动力学分析,在第4天和第5天进行了硝苯地平药代动力学分析。在首次采样时间(输注结束后5分钟)观察到血清茶碱浓度差异最大,硝苯地平给药期间平均浓度为9.9 mg l-1,单独使用茶碱时为14.6 mg l-1。此后,差异降至约1 mg l-1,直至6小时时两者几乎相同。使用8小时内十个时间点的每个时间点的茶碱血清浓度作为重复测量进行重复测量方差分析,结果显示硝苯地平对血清茶碱浓度有微小但显著的影响(F(1,151) = 7.0,P小于0.01)。在存在硝苯地平的情况下,分布容积(V)从0.33 +/- 0.07升至0.39 +/- 0.06 1 kg-1校正体重(CBW)(t = 2.23,P = 0.052)。茶碱清除率、至8小时曲线下面积AUC(0-8)、至无穷大曲线下面积AUC(0-无穷大)和消除半衰期(t1/2)没有明显变化。在存在茶碱的情况下,硝苯地平药代动力学没有发生统计学上的显著变化。

相似文献

1
The interaction between i.v. theophylline and chronic oral dosing with slow release nifedipine in volunteers.
Br J Clin Pharmacol. 1986 Apr;21(4):389-92. doi: 10.1111/j.1365-2125.1986.tb05212.x.
2
The bioavailability and pharmacokinetics of slow release nifedipine during chronic dosing in volunteers.
Br J Clin Pharmacol. 1986 Apr;21(4):385-8. doi: 10.1111/j.1365-2125.1986.tb05211.x.
4
[Interactions of theophylline and nifedipine].
Z Erkr Atmungsorgane. 1990;174(2):97-103.
5
Influence of chronic dosing on theophylline clearance.
Br J Clin Pharmacol. 1984 May;17(5):525-30. doi: 10.1111/j.1365-2125.1984.tb02385.x.
7
Effect of nifedipine and theophylline in asthma.
Clin Pharmacol Ther. 1986 Aug;40(2):195-8. doi: 10.1038/clpt.1986.163.
8
Pharmacokinetic studies of nifedipine and digoxin co-administration.
Int J Clin Pharmacol Ther Toxicol. 1986 Jan;24(1):39-42.
9
Pharmacokinetic properties of a new sustained-release theophylline preparation.
Int J Clin Pharmacol Ther Toxicol. 1983 Feb;21(2):69-72.

引用本文的文献

1
Targeting the Warburg effect for cancer treatment: Ketogenic diets for management of glioma.
Semin Cancer Biol. 2019 Jun;56:135-148. doi: 10.1016/j.semcancer.2017.12.011. Epub 2017 Dec 30.
3
Calcium antagonists. Drug interactions of clinical significance.
Drug Saf. 1995 Sep;13(3):157-87. doi: 10.2165/00002018-199513030-00003.
4
The bioavailability and pharmacokinetics of slow release nifedipine during chronic dosing in volunteers.
Br J Clin Pharmacol. 1986 Apr;21(4):385-8. doi: 10.1111/j.1365-2125.1986.tb05211.x.
5
Selective inhibitory effects of nifedipine and verapamil on oxidative metabolism: effects on theophylline.
Br J Clin Pharmacol. 1988 Mar;25(3):397-400. doi: 10.1111/j.1365-2125.1988.tb03319.x.
6
Effect of nifedipine on serum theophylline concentrations and asthma control.
Thorax. 1987 Oct;42(10):794-6. doi: 10.1136/thx.42.10.794.
7
Pharmacokinetic interactions with calcium channel antagonists (Part II).
Clin Pharmacokinet. 1991 Dec;21(6):448-60. doi: 10.2165/00003088-199121060-00005.
9
Pharmacokinetic interactions between theophylline and other medication (Part II).
Clin Pharmacokinet. 1991 Feb;20(2):135-50. doi: 10.2165/00003088-199120020-00005.

本文引用的文献

1
Verapamil-digoxin interaction.
N Engl J Med. 1980 Jul 17;303(3):160. doi: 10.1056/NEJM198007173030316.
2
Pharmacokinetic interaction between theophylline and erythromycin.
Br J Clin Pharmacol. 1982 Oct;14(4):495-9. doi: 10.1111/j.1365-2125.1982.tb02018.x.
3
Predictability of theophylline levels.
Drug Intell Clin Pharm. 1982 Sep;16(9):695-7. doi: 10.1177/106002808201600910.
4
Effect of nifedipine on digoxin kinetics in healthy subjects.
Clin Pharmacol Ther. 1982 Nov;32(5):562-5. doi: 10.1038/clpt.1982.203.
6
STRIPE: an interactive computer program for the analysis of drug pharmacokinetics.
J Pharmacol Methods. 1983 May;9(3):193-9. doi: 10.1016/0160-5402(83)90038-4.
7
The first pass metabolism of nifedipine in man.
Br J Clin Pharmacol. 1984 Dec;18(6):951-4. doi: 10.1111/j.1365-2125.1984.tb02569.x.
8
Digoxin plasma concentrations and nifedipine.
Lancet. 1981 Apr 11;1(8224):844-5. doi: 10.1016/s0140-6736(81)92727-6.
9
SIMP: a computer program in BASIC for nonlinear curve fitting.
J Pharmacol Methods. 1985 Dec;14(4):323-9. doi: 10.1016/0160-5402(85)90008-7.
10
The bioavailability and pharmacokinetics of slow release nifedipine during chronic dosing in volunteers.
Br J Clin Pharmacol. 1986 Apr;21(4):385-8. doi: 10.1111/j.1365-2125.1986.tb05211.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验