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两种氢氯噻嗪制剂的生物利用度。

Bioavailability of two hydrochlorothiazide preparations.

作者信息

Beermann B, Groschinsky-Grind M, Lindstrom B

出版信息

Eur J Clin Pharmacol. 1977 Mar 11;11(3):203-5. doi: 10.1007/BF00606411.

DOI:10.1007/BF00606411
PMID:576856
Abstract

Eight healthy volunteers received hydro-chlorothiazide 75 mg as Dichlotride and Esiderx. Maximal plasma levels were significantly (p less than 0.05) higher after Dichlotride than Esidrex, 512 +- 189 and 376 +- 70ng/ml, respectively. However, the bioavailability of the two brands of hydrochlorothiazide did not differ significantly as judged by comparison of the AUC0 leads to 9h and AUC0 leads to chi, and the urinary recovery of hydrochlorothiazide during 48 hrs.

摘要

八名健康志愿者服用了75毫克氢氯噻嗪,分别为双氢氯噻嗪片(Dichlotride)和依西太尔(Esiderx)。服用双氢氯噻嗪片后的最大血浆浓度显著(p<0.05)高于依西太尔,分别为512±189纳克/毫升和376±70纳克/毫升。然而,通过比较0至9小时的曲线下面积(AUC0→9h)、0至无穷大的曲线下面积(AUC0→∞)以及48小时内氢氯噻嗪的尿回收率判断,这两种品牌的氢氯噻嗪生物利用度无显著差异。

相似文献

1
Bioavailability of two hydrochlorothiazide preparations.两种氢氯噻嗪制剂的生物利用度。
Eur J Clin Pharmacol. 1977 Mar 11;11(3):203-5. doi: 10.1007/BF00606411.
2
Comparative bioavailability and pharmacokinetics of hydrochlorothiazide from oral tablet dosage forms, determined by plasma level and urinary excretion methods.通过血浆水平和尿排泄方法测定氢氯噻嗪口服片剂剂型的比较生物利用度和药代动力学。
Biopharm Drug Dispos. 1982 Oct-Dec;3(4):329-36. doi: 10.1002/bdd.2510030406.
3
Bioavailability of hydrochlorothiazide from tablets and suspensions.
J Pharm Sci. 1984 Mar;73(3):359-61. doi: 10.1002/jps.2600730317.
4
Malabsorption of hydrochlorothiazide following intestinal shunt surgery.肠道分流术后氢氯噻嗪吸收不良。
Clin Pharmacokinet. 1979 Jan-Feb;4(1):63-8. doi: 10.2165/00003088-197904010-00006.
5
Pharmacokinetics of hydrochlorothiazide in fasted and nonfasted subjects: a comparison of plasma level and urinary excretion methods.氢氯噻嗪在禁食和非禁食受试者中的药代动力学:血浆水平与尿排泄方法的比较
J Pharm Sci. 1982 Feb;71(2):245-8. doi: 10.1002/jps.2600710226.
6
[On the bioavailability of hydrochlorothiazide and triamterene from commercial drugs (author's transl)].
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8
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9
Gastrointestinal absorption of hydrochlorothiazide enhanced by concomitant intake of food.同时摄入食物可增强氢氯噻嗪的胃肠道吸收。
Eur J Clin Pharmacol. 1978 May 17;13(2):125-8. doi: 10.1007/BF00609756.
10
High-pressure liquid chromatographic determination of chlorothiazide and hydrochlorothiazide in plasma and urine: preliminary results of clinical studies.血浆和尿液中氯噻嗪及氢氯噻嗪的高效液相色谱测定:临床研究的初步结果
J Pharm Sci. 1981 Mar;70(3):291-5. doi: 10.1002/jps.2600700317.

引用本文的文献

1
Clinical pharmacokinetics of diuretics.利尿剂的临床药代动力学
Clin Pharmacokinet. 1980 May-Jun;5(3):221-45. doi: 10.2165/00003088-198005030-00003.
2
Pharmacokinetics of hydrochlorothiazide in relation to renal function.氢氯噻嗪的药代动力学与肾功能的关系。
Eur J Clin Pharmacol. 1983;24(5):661-5. doi: 10.1007/BF00542218.
3
Enhancement of the gastrointestinal absorption of hydrochlorothiazide by propantheline.丙胺太林增强氢氯噻嗪的胃肠道吸收。

本文引用的文献

1
The mechanism of action of chlorothiazide.氯噻嗪的作用机制。
Ann N Y Acad Sci. 1958 Feb 3;71(4):363-79. doi: 10.1111/j.1749-6632.1958.tb46763.x.
2
Effect of dissolution media on disintegration and dissolution of hydrochlorothiazide tablets.
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3
Gas chromatographic determination of furosemide in plasma using an extractive alkylation technique and an electron capture detector.采用萃取烷基化技术和电子捕获检测器,通过气相色谱法测定血浆中的呋塞米。
Eur J Clin Pharmacol. 1978 Jul 30;13(5):385-7. doi: 10.1007/BF00644613.
4
Bioavailability and disposition of metoprolol and hydrochlorothiazide combined in one tablet and of separate doses of hydrochlorothiazide.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。
Br J Clin Pharmacol. 1979 Jun;7(6):563-7. doi: 10.1111/j.1365-2125.1979.tb04643.x.
5
Malabsorption of hydrochlorothiazide following intestinal shunt surgery.肠道分流术后氢氯噻嗪吸收不良。
Clin Pharmacokinet. 1979 Jan-Feb;4(1):63-8. doi: 10.2165/00003088-197904010-00006.
6
Apparent dose-dependent absorption of chlorothiazide in dogs.
J Pharmacokinet Biopharm. 1979 Oct;7(5):463-70. doi: 10.1007/BF01062388.
J Chromatogr. 1974 Dec 4;101(1):219-21. doi: 10.1016/s0021-9673(01)94754-5.
4
Absorption, metabolism, and excretion of hydrochlorothiazide.氢氯噻嗪的吸收、代谢及排泄
Clin Pharmacol Ther. 1976 May;19(5 Pt 1):531-7. doi: 10.1002/cpt1976195part1531.