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本文引用的文献

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The influence of dosage form on the activity of a diuretic agent.剂型对利尿剂活性的影响。
Clin Pharmacol Ther. 1968 Sep-Oct;9(5):598-604. doi: 10.1002/cpt196895598.
2
To be taken as directed.按指示服用。
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Propranolol and polythiazide in treatment of hypertension.普萘洛尔与苄噻嗪治疗高血压
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Effect of alprenolol on blood pressure and plasma renin activity in hypertensive patients.心得舒对高血压患者血压及血浆肾素活性的影响。
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Pharmacokinetic studies on the selective beta1-receptor antagonist metoprolol in man.人用选择性β1受体拮抗剂美托洛尔的药代动力学研究。
J Pharmacokinet Biopharm. 1974 Aug;2(4):347-64. doi: 10.1007/BF01061407.
6
Absorption, metabolism, and excretion of hydrochlorothiazide.氢氯噻嗪的吸收、代谢及排泄
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Hydrochlorothiazide.氢氯噻嗪
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8
Combined pharmacokinetic and pharmacodynammc studies in man of the adrenergic beta1-receptor antagonist metoprolol.肾上腺素能β1受体拮抗剂美托洛尔在人体中的药代动力学和药效学联合研究。
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9
Comparative bioavailability and effect studies on metoprolol administered as ordinary and slow-release tablets in single and multiple doses.美托洛尔普通片与缓释片单剂量及多剂量给药的比较生物利用度和效应研究。
Acta Pharmacol Toxicol (Copenh). 1975;36(Suppl 5):45-58. doi: 10.1111/j.1600-0773.1975.tb03321.x.
10
Quantitative determination of metoprolol in plasma and urine by gas chromatography.气相色谱法定量测定血浆和尿液中的美托洛尔。
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美托洛尔与氢氯噻嗪复方片剂及氢氯噻嗪单独给药的生物利用度和处置情况。

Bioavailability and disposition of metoprolol and hydrochlorothiazide combined in one tablet and of separate doses of hydrochlorothiazide.

作者信息

Jordö L, Johnsson G, Lundborg P, Persson B A, Regärdh C G, Rönn O

出版信息

Br J Clin Pharmacol. 1979 Jun;7(6):563-7. doi: 10.1111/j.1365-2125.1979.tb04643.x.

DOI:10.1111/j.1365-2125.1979.tb04643.x
PMID:465277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1429665/
Abstract
  1. The plasma levels and the urinary excretion of hydrochlorothiazide (HCT) have been studied after administration of single doses of 12.5 and 25 mg of the drug in solution and in combination with 100 mg of the selective beta 1-adrenoreceptor antagonist metoprolol in a rapidly dissolving tablet. 2. Metoprolol did not significantly influence the bioavailability or the time-course of HCT. 3. HCT had no significant effect on the time-course or the plasma levels of metoprolol. The average half-life, 4.4 +/- 0.9 h, is about the same as previously observed for separate doses of this drug. 4. It seems unlikely that repeated doses of the combination product studied will lead to biopharmaceutic or pharmacokinetic interactions of clinical importance.
摘要
  1. 研究了单次服用12.5毫克和25毫克氢氯噻嗪(HCT)溶液剂以及与100毫克选择性β1肾上腺素能受体拮抗剂美托洛尔制成的速溶片后,HCT的血浆水平和尿排泄情况。2. 美托洛尔对HCT的生物利用度或时程没有显著影响。3. HCT对美托洛尔的时程或血浆水平没有显著影响。平均半衰期为4.4±0.9小时,与先前单独服用该药物时观察到的情况大致相同。4. 所研究的复方制剂重复给药似乎不太可能导致具有临床重要性的生物药剂学或药代动力学相互作用。