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Penetration of cefazolin, ceftriaxone, cefoperazone, and ceftazidime into human gallbladder tissue and bile.

作者信息

Berger S A, Levy Y, Halevy A, Gorea A, Orda R

出版信息

World J Surg. 1988 Oct;12(5):641-4. doi: 10.1007/BF01655872.

DOI:10.1007/BF01655872
PMID:3072775
Abstract
摘要

相似文献

1
Penetration of cefazolin, ceftriaxone, cefoperazone, and ceftazidime into human gallbladder tissue and bile.
World J Surg. 1988 Oct;12(5):641-4. doi: 10.1007/BF01655872.
2
Penetration of ceftriaxone and cefoperazone into bile and gallbladder tissue in patients with acute cholecystitis.
Dig Dis Sci. 1992 Nov;37(11):1691-3. doi: 10.1007/BF01299860.
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Comparative study of the effects of four cephalosporins against Escherichia coli in vitro and in vivo.四种头孢菌素对大肠杆菌体内外作用的比较研究
Antimicrob Agents Chemother. 1990 Oct;34(10):1932-7. doi: 10.1128/AAC.34.10.1932.
4
The effect of obstruction on the biliary excretion of cefoperazone and ceftazidime.
J Antimicrob Chemother. 1990 Mar;25(3):399-406. doi: 10.1093/jac/25.3.399.
5
[Determination of cefoperazone levels of the serum, bile and the gallbladder wall].[血清、胆汁及胆囊壁中头孢哌酮水平的测定]
Med Welt. 1983 Mar 18;34(11):345-6.
6
Determination of cephazolin, ceftazidime, and ceftriaxone distribution in nucleus pulposus.测定髓核中头孢唑林、头孢他啶和头孢曲松的分布。
Arch Orthop Trauma Surg. 2012 Jul;132(7):969-73. doi: 10.1007/s00402-012-1514-7. Epub 2012 Apr 12.
7
Penetration of third-generation cephalosporins into human peritoneal tissue.第三代头孢菌素在人体腹膜组织中的穿透情况。
Chemotherapy. 1989;35(5):326-9. doi: 10.1159/000238689.
8
Ceftazidime concentration in gallbladder tissue and excretion in bile.头孢他啶在胆囊组织中的浓度及胆汁排泄情况。
Antimicrob Agents Chemother. 1988 Oct;32(10):1588-9. doi: 10.1128/AAC.32.10.1588.
9
Tissue penetration characteristics of ceftizoxime and cefazolin in human bile and gallbladder wall.头孢唑肟和头孢唑林在人胆汁和胆囊壁中的组织穿透特性。
J Antimicrob Chemother. 1982 Nov;10 Suppl C:117-20. doi: 10.1093/jac/10.suppl_c.117.
10
Cefoperazone concentrations in bile and gall bladder wall after intravenous administration.静脉给药后胆汁和胆囊壁中的头孢哌酮浓度。
Antimicrob Agents Chemother. 1980 Dec;18(6):980-2. doi: 10.1128/AAC.18.6.980.

引用本文的文献

1
Ceftriaxone: an update of its use in the management of community-acquired and nosocomial infections.头孢曲松:其在社区获得性感染和医院感染管理中应用的最新情况
Drugs. 2002;62(7):1041-89. doi: 10.2165/00003495-200262070-00005.
2
Penetration of ceftriaxone and cefoperazone into bile and gallbladder tissue in patients with acute cholecystitis.
Dig Dis Sci. 1992 Nov;37(11):1691-3. doi: 10.1007/BF01299860.

本文引用的文献

1
Pharmacokinetic studies of ceftazidime in serum, bone, bile, tissue fluid and peritoneal fluid.
J Antimicrob Chemother. 1981 Sep;8 Suppl B:293-7.
2
Biliary excretion of cephalosporins in rats: influence of molecular weight.大鼠体内头孢菌素的胆汁排泄:分子量的影响。
Antimicrob Agents Chemother. 1980 May;17(5):842-6. doi: 10.1128/AAC.17.5.842.
3
Antibacterial activity of ceftriaxone (Ro 13-9904), a beta-lactamase-stable cephalosporin.头孢曲松(Ro 13 - 9904)的抗菌活性,一种对β-内酰胺酶稳定的头孢菌素。
Antimicrob Agents Chemother. 1981 Mar;19(3):414-23. doi: 10.1128/AAC.19.3.414.
4
Biliary excretion and pharmacokinetics of cefoperazone in humans.头孢哌酮在人体中的胆汁排泄及药代动力学
J Antimicrob Chemother. 1983 Jul;12(1):27-37. doi: 10.1093/jac/12.1.27.
5
Cefoperazone concentrations in bile and gall bladder wall after intravenous administration.静脉给药后胆汁和胆囊壁中的头孢哌酮浓度。
Antimicrob Agents Chemother. 1980 Dec;18(6):980-2. doi: 10.1128/AAC.18.6.980.
6
Comparison of ceftazidime concentrations in bile and serum.头孢他啶在胆汁和血清中的浓度比较。
Antimicrob Agents Chemother. 1983 Jul;24(1):104-6. doi: 10.1128/AAC.24.1.104.
7
The excretion of antibiotics by the biliary tract.抗生素经胆道的排泄。
Surg Gynecol Obstet. 1984 Jun;158(6):601-7.
8
Cefotaxime and desacetyl cefotaxime in human bile.人胆汁中的头孢噻肟和去乙酰头孢噻肟。
Infection. 1983 Mar-Apr;11(2):118-20. doi: 10.1007/BF01641077.
9
Ceftriaxone: renal and biliary excretion and effect on the colon microflora.头孢曲松:肾脏和胆汁排泄及对结肠微生物群的影响。
J Antimicrob Chemother. 1982 Sep;10(3):207-15. doi: 10.1093/jac/10.3.207.
10
Comparative activity of ampicillin and seven cephalosporins against group D streptococci.氨苄西林与七种头孢菌素对D组链球菌的活性比较
J Clin Pathol. 1974 Oct;27(10):828-31. doi: 10.1136/jcp.27.10.828.