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1
The absorption of cimetidine before and during maintenance treatment with cimetidine and the influence of a meal on the absorption of cimetidine--studies in patients with peptic ulcer disease.西咪替丁维持治疗前后的吸收情况以及进餐对西咪替丁吸收的影响——对消化性溃疡病患者的研究
Br J Clin Pharmacol. 1979 Jan;7(1):23-31. doi: 10.1111/j.1365-2125.1979.tb00892.x.
2
Pharmacokinetics of cimetidine after single doses and during continuous treatment.西咪替丁单次给药及持续治疗期间的药代动力学。
Clin Pharmacokinet. 1981 Jul-Aug;6(4):306-15. doi: 10.2165/00003088-198106040-00005.
3
Impaired cimetidine absorption due to antacids and metoclopramide.抗酸剂和甲氧氯普胺导致西咪替丁吸收受损。
Eur J Clin Pharmacol. 1981;20(3):225-8. doi: 10.1007/BF00544602.
4
Tiotidine and cimetidine--kinetics and dynamics.替奥替丁与西咪替丁——动力学与动态学
Clin Pharmacol Ther. 1981 Feb;29(2):198-202. doi: 10.1038/clpt.1981.31.
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Oral and intravenous pharmacokinetics of cimetidine in liver cirrhosis.西咪替丁在肝硬化患者中的口服及静脉药代动力学
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6
Cimetidine clearance and bioavailability in hepatic cirrhosis.西咪替丁在肝硬化中的清除率和生物利用度。
Clin Pharmacol Ther. 1981 Feb;29(2):191-7. doi: 10.1038/clpt.1981.30.
7
Elimination of oral cimetidine in chronic renal failure and during haemodialysis.慢性肾功能衰竭及血液透析期间口服西咪替丁的消除情况。
Br J Clin Pharmacol. 1980 Jun;9(6):585-92. doi: 10.1111/j.1365-2125.1980.tb01084.x.
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Cimetidine bioavailability after massive small bowel resection.大量小肠切除术后西咪替丁的生物利用度。
Clin Pharm. 1982 Nov-Dec;1(6):558-61.
9
Pharmacokinetics and pharmacodynamics of oral and intravenous cimetidine in seriously ill patients.口服和静脉注射西咪替丁在重症患者中的药代动力学和药效学
J Clin Pharmacol. 1990 Jun;30(6):568-71. doi: 10.1002/j.1552-4604.1990.tb03622.x.
10
Short- and long-term treatment with cimetidine in peptic ulcer disease and the pharmacokinetics of cimetidine.西咪替丁在消化性溃疡疾病中的短期和长期治疗以及西咪替丁的药代动力学
Scand J Gastroenterol Suppl. 1979;55:96-106.

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1
Repurposing drugs in oncology (ReDO)-cimetidine as an anti-cancer agent.肿瘤学中药物的重新利用(ReDO)——西咪替丁作为一种抗癌药物
Ecancermedicalscience. 2014 Nov 26;8:485. doi: 10.3332/ecancer.2014.485. eCollection 2014.
2
Multiple peaking phenomena in pharmacokinetic disposition.药代动力学处置中的多重峰现象。
Clin Pharmacokinet. 2010 Jun;49(6):351-77. doi: 10.2165/11319320-000000000-00000.
3
Regional gastrointestinal absorption of ranitidine in the rat.雷尼替丁在大鼠体内的区域性胃肠道吸收
Pharm Res. 1995 Sep;12(9):1311-5. doi: 10.1023/a:1016269522828.
4
Intestinal uptake of cimetidine and ranitidine in rats.西咪替丁和雷尼替丁在大鼠肠道中的摄取
Pharm Res. 1994 Nov;11(11):1599-604. doi: 10.1023/a:1018961805118.
5
Gastric pH influences the appearance of double peaks in the plasma concentration-time profiles of cimetidine after oral administration in dogs.胃内pH值会影响犬口服西咪替丁后血浆浓度-时间曲线中双峰的出现情况。
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6
Concurrent administration of cimetidine and enteric-coated prednisolone: effect on plasma levels of prednisolone.西咪替丁与肠溶衣泼尼松龙同时给药:对泼尼松龙血浆水平的影响。
Br J Clin Pharmacol. 1980 Jul;10(1):87-9. doi: 10.1111/j.1365-2125.1980.tb00506.x.
7
Elimination of oral cimetidine in chronic renal failure and during haemodialysis.慢性肾功能衰竭及血液透析期间口服西咪替丁的消除情况。
Br J Clin Pharmacol. 1980 Jun;9(6):585-92. doi: 10.1111/j.1365-2125.1980.tb01084.x.
8
Pharmacokinetics and bioavailability of cimetidine in gastric and duodenal ulcer patients.西咪替丁在胃溃疡和十二指肠溃疡患者中的药代动力学及生物利用度
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9
Effect of cimetidine on the absorption of orally administered tetracycline.西咪替丁对口服四环素吸收的影响。
Br J Clin Pharmacol. 1980 Feb;9(2):153-8. doi: 10.1111/j.1365-2125.1980.tb05826.x.
10
Is the measurement of blood cimetidine levels useful?测量血液中西咪替丁水平有用吗?
Br J Clin Pharmacol. 1981 Sep;12(3):417-21. doi: 10.1111/j.1365-2125.1981.tb01237.x.

本文引用的文献

1
Inhibition of gastric acid secretion by cimetidine in patients with duodenal ulcer.西咪替丁对十二指肠溃疡患者胃酸分泌的抑制作用。
N Engl J Med. 1975 Aug 21;293(8):371-5. doi: 10.1056/NEJM197508212930802.
2
High-pressure liquid chromatographic analysis of cimetidine, a histamine H2-receptor antagonist, in blood and urine.
J Pharm Sci. 1977 Aug;66(8):1148-50. doi: 10.1002/jps.2600660825.
3
Pharmacological evaluation of cimetidine, a new histamine H2-receptor antagonist, in healthy man.新型组胺H2受体拮抗剂西咪替丁在健康人体中的药理学评价。
Br J Clin Pharmacol. 1975 Dec;2(6):481-6. doi: 10.1111/j.1365-2125.1975.tb00564.x.
4
Influence of a meal on the absorption of cimetidine. A new histamine H2-receptor antagonist.
Digestion. 1976;14(2):127-32. doi: 10.1159/000197917.
5
Inhibition of food-stimulated gastric acid secretion by cimetidine.西咪替丁对食物刺激的胃酸分泌的抑制作用。
Gut. 1976 Mar;17(3):161-8. doi: 10.1136/gut.17.3.161.

西咪替丁维持治疗前后的吸收情况以及进餐对西咪替丁吸收的影响——对消化性溃疡病患者的研究

The absorption of cimetidine before and during maintenance treatment with cimetidine and the influence of a meal on the absorption of cimetidine--studies in patients with peptic ulcer disease.

作者信息

Bodemar G, Norlander B, Fransson L, Walan A

出版信息

Br J Clin Pharmacol. 1979 Jan;7(1):23-31. doi: 10.1111/j.1365-2125.1979.tb00892.x.

DOI:10.1111/j.1365-2125.1979.tb00892.x
PMID:760739
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1429608/
Abstract

1 The absorption of a single oral dose of cimetidine taken on a fasting stomach or together with a meal was studied in 28 patients before and during 12 weeks treatment with cimetidine. 2 No significant changes in bioavailability were seen during treatment measured as the area under the blood concentration curve (AUC). 3 AUC after a single dose of 400 mg cimetidine was 2.05 times the area after a 200 mg dose. 4 There was a good correlation between AUC and the dose of cimetidine given corrected for body weight (r=0.89). 5 There was no difference in bioavailability if 200 mg cimetidine was taken on a fasting stomach or together with a beef steak meal. 6. During fasting conditions there was a peak in blood concentration at about one hour followed by a second unexplained peak during the third to fifth hour after dose administration. 7 With food the initial rise in blood concentrations was slower and there was only one peak occurring about 2 h after dose administration.

摘要
  1. 在28名患者中,研究了空腹或与餐同服单次口服西咪替丁后的吸收情况,研究时间为西咪替丁治疗前及治疗12周期间。

  2. 以血药浓度曲线下面积(AUC)衡量,治疗期间生物利用度未见显著变化。

  3. 单次服用400mg西咪替丁后的AUC是服用200mg剂量后面积的2.05倍。

  4. AUC与根据体重校正后的西咪替丁给药剂量之间存在良好相关性(r = 0.89)。

  5. 空腹服用200mg西咪替丁或与牛排餐同服时,生物利用度无差异。

  6. 在禁食条件下,给药后约1小时血药浓度出现峰值,随后在给药后第三至第五小时出现第二个无法解释的峰值。

  7. 进食后血药浓度的初始上升较慢,给药后约2小时仅出现一个峰值。