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阿米卡星在人体中的药理学。

Pharmacology of amikacin in humans.

作者信息

Bodey G P, Valdivieso M, Feld R, Rodriguez V

出版信息

Antimicrob Agents Chemother. 1974 May;5(5):508-12. doi: 10.1128/AAC.5.5.508.

DOI:10.1128/AAC.5.5.508
PMID:4462465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC429003/
Abstract

Amikacin is a new aminoglycoside antibiotic which is active in vitro against most isolates of gram-negative bacilli. A dose of 300 mg/m(2) intramuscularly produced a highest mean serum concentration of 25.4 mug/ml with a mean serum concentration of 3.1 mug/ml at 8 h. The same dose intravenously produced a highest mean serum concentration of 52.4 mug/ml with a mean serum concentration of 2.1 mug/ml at 8 h. The mean urinary excretion during the first 6 h was 75 and 66%, respectively. When amikacin was administered at a dose of 150 mg/m(2) every 6 h, there was evidence of some drug accumulation. A loading dose of 150 mg/m(2) administered intravenously over 30 min followed by 200 mg/m(2) administered as a continuous infusion every 6 h maintained serum concentrations of 8 mug/ml. No major toxicity was observed with any of these drug regimens.

摘要

阿米卡星是一种新型氨基糖苷类抗生素,在体外对大多数革兰氏阴性杆菌分离株具有活性。300mg/m²的肌肉注射剂量产生的最高平均血清浓度为25.4μg/ml,8小时时的平均血清浓度为3.1μg/ml。相同剂量静脉注射产生的最高平均血清浓度为52.4μg/ml,8小时时的平均血清浓度为2.1μg/ml。前6小时的平均尿排泄率分别为75%和66%。当每6小时以150mg/m²的剂量给予阿米卡星时,有药物蓄积的迹象。静脉注射150mg/m²的负荷剂量,持续30分钟,然后每6小时以200mg/m²的剂量持续输注,可维持血清浓度为8μg/ml。这些药物方案均未观察到重大毒性。

相似文献

1
Pharmacology of amikacin in humans.阿米卡星在人体中的药理学。
Antimicrob Agents Chemother. 1974 May;5(5):508-12. doi: 10.1128/AAC.5.5.508.
2
Amikacin pharmacokinetics in pediatric patients with malignancy.恶性肿瘤患儿的阿米卡星药代动力学
Antimicrob Agents Chemother. 1979 Dec;16(6):829-32. doi: 10.1128/AAC.16.6.829.
3
Clinical pharmacology of amikacin and kanamycin.阿米卡星和卡那霉素的临床药理学
J Infect Dis. 1976 Nov;134 SUPPL:S312-5. doi: 10.1093/infdis/135.supplement_2.s312.
4
Pharmacokinetic and clinical studies with amikacin, a new aminoglycoside antibiotic.新型氨基糖苷类抗生素阿米卡星的药代动力学及临床研究。
J Infect Dis. 1976 Nov;134 SUPPL:S316-22. doi: 10.1093/infdis/135.supplement_2.s316.
5
Disposition kinetics of amikacin in patients with renal impairment after intramuscular administration.肾功能损害患者肌内注射后阿米卡星的处置动力学
Int J Clin Pharmacol Ther Toxicol. 1982 Jun;20(6):271-5.
6
Bronchial secretion levels of amikacin.阿米卡星的支气管分泌物水平。
Antimicrob Agents Chemother. 1979 Dec;16(6):767-71. doi: 10.1128/AAC.16.6.767.
7
[Pharmacokinetics and clinical experience with amikacin. A new aminoglycoside antibiotic].
Dtsch Med Wochenschr. 1976 Sep 3;101(36):1312-7. doi: 10.1055/s-0028-1104263.
8
Amikacin concentration in the cerebrospinal fluid of children with acute bacterial meningitis.
J Int Med Res. 1979;7(1):45-51. doi: 10.1177/030006057900700107.
9
Influence of dose in the urinary excretion of amikacin.剂量对阿米卡星尿排泄的影响。
Int J Clin Pharmacol Ther Toxicol. 1984 Oct;22(10):538-42.
10
Distribution of amikacin in serum, muscle, and fat in children after a single intramuscular injection.单次肌内注射后阿米卡星在儿童血清、肌肉和脂肪中的分布情况。
Antimicrob Agents Chemother. 1977 Jun;11(6):1081-3. doi: 10.1128/AAC.11.6.1081.

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Antipseudomonal agents exhibit differential pharmacodynamic interactions with human polymorphonuclear leukocytes against established biofilms of Pseudomonas aeruginosa.抗假单胞菌药物与人类多形核白细胞针对铜绿假单胞菌已形成的生物膜表现出不同的药效学相互作用。
Antimicrob Agents Chemother. 2015 Apr;59(4):2198-205. doi: 10.1128/AAC.04934-14. Epub 2015 Feb 2.
3
The role of schedule of antibiotic therapy on the neutropenic patient.抗生素治疗方案在中性粒细胞减少患者中的作用。
Infection. 1980;Suppl 1:75-81. doi: 10.1007/BF01644940.
4
Rapid, specific microbiological assay for amikacin (BB-K8).阿米卡星(BB-K8)的快速、特异性微生物学测定法。
Antimicrob Agents Chemother. 1974 Oct;6(4):498-500. doi: 10.1128/AAC.6.4.498.
5
Penetration of amikacin into the aphakic eye.阿米卡星在无晶状体眼中的穿透情况。
Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1975 Aug 4;196(1):85-94. doi: 10.1007/BF00410030.
6
Effect of renal failure and dialysis on the serum concentration of the aminoglycoside amikacin.肾衰竭和透析对氨基糖苷类药物阿米卡星血清浓度的影响。
Antimicrob Agents Chemother. 1976 Sep;10(3):464-6. doi: 10.1128/AAC.10.3.464.
7
Ototoxicity of amikacin.阿米卡星的耳毒性。
Antimicrob Agents Chemother. 1976 Jun;9(6):956-61. doi: 10.1128/AAC.9.6.956.
8
Distribution of gentamicin and amikacin in rabbit tissues.庆大霉素和阿米卡星在兔组织中的分布。
Antimicrob Agents Chemother. 1977 Jun;11(6):974-7. doi: 10.1128/AAC.11.6.974.
9
Effects of gestational age, birth weight, and hypoxemia on pharmacokinetics of amikacin in serum of infants.胎龄、出生体重和低氧血症对婴儿血清中阿米卡星药代动力学的影响。
Antimicrob Agents Chemother. 1977 Jun;11(6):1027-32. doi: 10.1128/AAC.11.6.1027.
10
Pharmacokinetics of amikacin during hemodialysis and peritoneal dialysis.阿米卡星在血液透析和腹膜透析期间的药代动力学。
Antimicrob Agents Chemother. 1977 Feb;11(2):214-8. doi: 10.1128/AAC.11.2.214.

本文引用的文献

1
Effect of the concentrations of magnesium and calcium on the in-vitro susceptibility of Pseudomonas aeruginosa to gentamicin.镁和钙浓度对铜绿假单胞菌体外对庆大霉素敏感性的影响。
J Infect Dis. 1971 Dec;124 Suppl:S37-45. doi: 10.1093/infdis/124.supplement_1.s37.
2
Colonization with gentamicin-resistant Pseudomonas aeruginosa, pyocine type 5, in a burn unit.在一个烧伤病房中出现对庆大霉素耐药的5型绿脓杆菌定植。
J Infect Dis. 1971 Dec;124 Suppl:S18-23. doi: 10.1093/infdis/124.supplement_1.s18.
3
In vitro studies of BB-K8, a new aminoglycoside antibiotic.新型氨基糖苷类抗生素BB-K8的体外研究
Antimicrob Agents Chemother. 1973 Aug;4(2):186-92. doi: 10.1128/AAC.4.2.186.
4
BB-K 8, a new semisynthetic aminoglycoside antibiotic.
J Antibiot (Tokyo). 1972 Dec;25(12):695-708. doi: 10.7164/antibiotics.25.695.
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Microbiological evaluation of BB-K 8, a new semisynthetic aminoglycoside.
J Antibiot (Tokyo). 1972 Dec;25(12):709-31. doi: 10.7164/antibiotics.25.709.