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1
Comparative clinical pharmacology of amoxicillin and ampicillin administered orally.口服阿莫西林和氨苄西林的比较临床药理学
Antimicrob Agents Chemother. 1972 Jun;1(6):504-7. doi: 10.1128/AAC.1.6.504.
2
Pharmacokinetics of amoxicillin and ampicillin: crossover study of the effect of food.阿莫西林和氨苄西林的药代动力学:食物影响的交叉研究。
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3
Levels of antibiotic in human blood and interstitial fluid after oral administration of bacampicillin or phenoxymethyl penicillin and intravenous administration of amoxicillin or ampicillin.口服巴卡西林或苯氧甲基青霉素以及静脉注射阿莫西林或氨苄西林后人体血液和组织液中的抗生素水平。
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6
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Eur J Clin Pharmacol. 1985;29(4):495-502. doi: 10.1007/BF00613468.

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本文引用的文献

1
DICLOXACILLIN. IN VITRO AND PHARMACOLOGIC COMPARISONS WITH OXACILLIN AND CLOXACILLIN.双氯西林:与苯唑西林和氯唑西林的体外及药理学比较
Arch Intern Med. 1965 Sep;116:340-5. doi: 10.1001/archinte.1965.03870030020005.
2
Ampicillin activity in vitro and absorption and excretion in normal young men.氨苄西林在体外的活性以及在正常年轻男性体内的吸收与排泄。
Am J Med Sci. 1963 May;245:544-55.
3
Absorption and excretion of "Penbritin".“青霉素V钾片”的吸收与排泄
Br Med J. 1961 Jul 22;2(5246):198-200. doi: 10.1136/bmj.2.5246.198.
4
Pharmacological properties of hetacillin in the human.海他西林在人体中的药理特性。
Antimicrob Agents Chemother (Bethesda). 1965;5:947-50.
5
Clinical pharmacology of pivampicillin.匹氨西林的临床药理学
Antimicrob Agents Chemother (Bethesda). 1970;10:442-54.
6
-amino-p-hydroxybenzylpenicillin (BRL 2333), a new semisynthetic penicillin: absorption and excretion in man.α-氨基-对羟基苄青霉素(BRL 2333),一种新型半合成青霉素:人体中的吸收与排泄
Antimicrob Agents Chemother (Bethesda). 1970;10:427-30.
7
Time integral of drug concentration in the central (plasma) compartment.中央(血浆)室药物浓度的时间积分。
J Pharm Sci. 1970 May;59(5):722-3. doi: 10.1002/jps.2600590537.
8
Oral cephalexin and ampicillin: antimicrobial activity, recovery in urine, and persistence in blood of uremic patients.口服头孢氨苄和氨苄西林:尿毒症患者的抗菌活性、尿液中的回收率及血液中的持续时间
Ann Intern Med. 1970 Mar;72(3):349-56. doi: 10.7326/0003-4819-72-3-349.
9
Pharmacokinetics of ampicillin trihydrate, sodium ampicillin, and sodium dicloxacillin following intramuscular injection.三水合氨苄西林、氨苄西林钠和双氯西林钠肌肉注射后的药代动力学
J Pharm Sci. 1971 May;60(5):715-9. doi: 10.1002/jps.2600600511.
10
-amino-p-hydroxybenzylpenicillin (BRL 2333), a new semisynthetic penicillin: in vitro evaluation.α-氨基对羟基苄青霉素(BRL 2333),一种新型半合成青霉素:体外评估
Antimicrob Agents Chemother (Bethesda). 1970;10:411-5. doi: 10.1128/AAC.10.3.411.

口服阿莫西林和氨苄西林的比较临床药理学

Comparative clinical pharmacology of amoxicillin and ampicillin administered orally.

作者信息

Gordon C, Regamey C, Kirby W M

出版信息

Antimicrob Agents Chemother. 1972 Jun;1(6):504-7. doi: 10.1128/AAC.1.6.504.

DOI:10.1128/AAC.1.6.504
PMID:4680813
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC444250/
Abstract

Ampicillin and amoxicillin (alpha-amino-p-hydroxybenzyl penicillin) were administered orally in 500-mg doses to eight fasting volunteers in a comparative study in which pharmacokinetic techniques were used. The absorption of amoxicillin was significantly better, as demonstrated by a higher mean peak serum concentration of 7.6 mug/ml as compared to 3.2 mug/ml for ampicillin, an average "area under the curve" that was approximately double that of ampicillin, and an 8-hr urinary recovery for amoxicillin of 60% as compared to 34% for ampicillin. Serum half-lives were the same for the two antibiotics, with values of 60.3 (+/-3.3) min for ampicillin and 61.3 (+/-5.6) min for amoxicillin. The latter drug gave measurable concentrations in the blood at 8 hr in all of eight volunteers, as compared to only three of eight with ampicillin.

摘要

在一项采用药代动力学技术的对比研究中,给8名空腹志愿者口服500毫克剂量的氨苄西林和阿莫西林(α-氨基-对羟基苄青霉素)。阿莫西林的吸收明显更好,表现为平均血清峰值浓度更高,阿莫西林为7.6微克/毫升,而氨苄西林为3.2微克/毫升;平均“曲线下面积”约为氨苄西林的两倍;阿莫西林8小时尿回收率为60%,而氨苄西林为34%。两种抗生素的血清半衰期相同,氨苄西林为60.3(±3.3)分钟,阿莫西林为61.3(±5.6)分钟。8名志愿者服用阿莫西林后8小时血液中均可测得药物浓度,而服用氨苄西林的8名志愿者中只有3人在8小时后血液中可测得药物浓度。