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1
In vitro activity of ticarcillin against anaerobic bacteria compared with that of carbenicillin and penicillin.替卡西林对厌氧菌的体外活性与羧苄西林和青霉素的比较。
Antimicrob Agents Chemother. 1977 Feb;11(2):258-61. doi: 10.1128/AAC.11.2.258.
2
Susceptibility of the anaerobic bacteria, group D streptococci, Enterobacteriaceae, and Pseudomonas to semisynthetic penicillins: carbenicillin, piperacillin, and ticarcillin.厌氧细菌、D组链球菌、肠杆菌科细菌及假单胞菌对半合成青霉素(羧苄西林、哌拉西林及替卡西林)的敏感性
Antimicrob Agents Chemother. 1978 Nov;14(5):643-9. doi: 10.1128/AAC.14.5.643.
3
Comparative susceptibility of anaerobic bacteria to ticarcillin, cefoxitin, metronidazole, and related antimicrobial agents.厌氧细菌对替卡西林、头孢西丁、甲硝唑及相关抗菌药物的敏感性比较。
Antimicrob Agents Chemother. 1977 Apr;11(4):679-82. doi: 10.1128/AAC.11.4.679.
4
Comparative activity in vitro of ticarcillin, BL-P1654, and carbenicillin.替卡西林、BL-P1654和羧苄西林的体外比较活性
Antimicrob Agents Chemother. 1976 Aug;10(2):241-4. doi: 10.1128/AAC.10.2.241.
5
Comparative activity of mezlocillin, penicillin, ampicillin, carbenicillin, and ticarcillin against gram-positive bacteria and Haemophilus influenzae.美洛西林、青霉素、氨苄西林、羧苄西林和替卡西林对革兰氏阳性菌和流感嗜血杆菌的比较活性。
Antimicrob Agents Chemother. 1981 Dec;20(6):843-6. doi: 10.1128/AAC.20.6.843.
6
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Antimicrob Agents Chemother. 1976 Jan;9(1):89-90. doi: 10.1128/AAC.9.1.89.
7
BL-P1654, ticarcillin, and carbenicillin: in vitro comparison alone and in combination with gentamicin against Pseudomonas aeruginosa.BL-P1654、替卡西林和羧苄西林:单独及与庆大霉素联合应用对铜绿假单胞菌的体外比较
Antimicrob Agents Chemother. 1975 Mar;7(3):336-40. doi: 10.1128/AAC.7.3.336.
8
Antimicrobial activity and synergism of cefuroxime on anaerobic bacteria.头孢呋辛对厌氧菌的抗菌活性及协同作用
Chemotherapy. 1981;27(4):252-8. doi: 10.1159/000237988.
9
Comparison and evaluation of ticarcillin and carbenicillin using disk diffusion methods.使用纸片扩散法对替卡西林和羧苄西林进行比较与评价。
Antimicrob Agents Chemother. 1976 Apr;9(4):625-32. doi: 10.1128/AAC.9.4.625.
10
Susceptibility of anaerobic bacteria to 23 antimicrobial agents.厌氧菌对23种抗菌剂的敏感性。
Antimicrob Agents Chemother. 1976 Oct;10(4):736-52. doi: 10.1128/AAC.10.4.736.

引用本文的文献

1
Ticarcillin: a review of its pharmacological properties and therapeutic efficacy.替卡西林:其药理特性与治疗效果综述
Drugs. 1980 Nov;20(5):325-52. doi: 10.2165/00003495-198020050-00001.
2
In vitro activity of pipecolic acid amide of clindamycin (U-57930E) on anaerobic bacteria compared with those of clindamycin, cefoxitin, and chloramphenicol.与克林霉素、头孢西丁和氯霉素相比,克林霉素哌可酸酰胺(U-57930E)对厌氧菌的体外活性。
Antimicrob Agents Chemother. 1982 Aug;22(2):350-1. doi: 10.1128/AAC.22.2.350.
3
In vitro susceptibility of anaerobic bacteria to ciprofloxacin (Bay o 9867).厌氧菌对环丙沙星(拜奥9867)的体外敏感性
Antimicrob Agents Chemother. 1984 Nov;26(5):785-6. doi: 10.1128/AAC.26.5.785.
4
Augmentation of the in vitro activity of azlocillin against Bacteroides fragilis by clavulanic acid.棒酸增强阿洛西林对脆弱拟杆菌的体外活性。
Antimicrob Agents Chemother. 1984 Oct;26(4):606-7. doi: 10.1128/AAC.26.4.606.
5
Comparison of in vitro activity of moxalactam (LY127935) with cefazolin, amikacin, tobramycin, carbenicillin, piperacillin, and ticarcillin against 420 blood culture isolates.羟羧氧酰胺菌素(LY127935)与头孢唑林、阿米卡星、妥布霉素、羧苄西林、哌拉西林及替卡西林对420例血培养分离菌的体外活性比较
Antimicrob Agents Chemother. 1980 Mar;17(3):412-6. doi: 10.1128/AAC.17.3.412.
6
Antimicrobial drugs used in the management of anaerobic infections in children.用于治疗儿童厌氧菌感染的抗菌药物。
Drugs. 1983 Dec;26(6):520-9. doi: 10.2165/00003495-198326060-00004.
7
Susceptibility of anaerobic bacteria to nine antimicrobial agents and demonstration of decreased susceptibility of Clostridium perfringens to penicillin.厌氧菌对九种抗菌药物的敏感性以及产气荚膜梭菌对青霉素敏感性降低的证明。
Antimicrob Agents Chemother. 1981 Jan;19(1):51-5. doi: 10.1128/AAC.19.1.51.
8
In vitro activity of cefbuperazone, a new cephamycin, against anaerobic bacteria.新型头孢霉素头孢哌酮对厌氧菌的体外活性
Antimicrob Agents Chemother. 1985 Apr;27(4):640-2. doi: 10.1128/AAC.27.4.640.
9
Activity of difloxacin (A-56619) and A-56620 against clinical anaerobic bacteria in vitro.双氟沙星(A-56619)和A-56620对临床厌氧菌的体外活性。
Antimicrob Agents Chemother. 1987 Apr;31(4):619-21. doi: 10.1128/AAC.31.4.619.
10
Therapeutic evaluation of difloxacin (A-56619) and A-56620 for experimentally induced Bacteroides fragilis-associated intra-abdominal abscess.地氟沙星(A-56619)和A-56620对实验性诱导的脆弱拟杆菌相关性腹腔内脓肿的治疗评估。
Antimicrob Agents Chemother. 1986 Oct;30(4):574-6. doi: 10.1128/AAC.30.4.574.

本文引用的文献

1
Ticarcillin therapy of infections.替卡西林治疗感染
Antimicrob Agents Chemother. 1973 Oct;4(4):427-31. doi: 10.1128/AAC.4.4.427.
2
[Ticarcillin: in-vitro activity and pharmacokinetics (author's transl)].替卡西林:体外活性与药代动力学(作者译)
Dtsch Med Wochenschr. 1974 Nov 29;99(48):2460-4. doi: 10.1055/s-0028-1108155.
3
Clinical and laboratory investigations on ticarcillin, an anti-pseudomonal antibiotic.替卡西林(一种抗假单胞菌抗生素)的临床与实验室研究。
Chemotherapy. 1974;20(1):45-51. doi: 10.1159/000221790.
4
Comparative in vitro activity and clinical pharmacology of ticarcillin and carbenicillin.替卡西林和羧苄西林的体外活性及临床药理学比较
Antimicrob Agents Chemother. 1975 Oct;8(4):457-62. doi: 10.1128/AAC.8.4.457.
5
Susceptibility of Anaerobic bacteria to carbenicillin, cefoxitin, and related drugs.厌氧菌对羧苄青霉素、头孢西丁及相关药物的敏感性。
J Infect Dis. 1975 Apr;131(4):417-22. doi: 10.1093/infdis/131.4.417.

替卡西林对厌氧菌的体外活性与羧苄西林和青霉素的比较。

In vitro activity of ticarcillin against anaerobic bacteria compared with that of carbenicillin and penicillin.

作者信息

Roy I, Bach V, Thadepalli H

出版信息

Antimicrob Agents Chemother. 1977 Feb;11(2):258-61. doi: 10.1128/AAC.11.2.258.

DOI:10.1128/AAC.11.2.258
PMID:848931
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC351964/
Abstract

A total of 334 clinical anaerobic isolates were tested in an anaerobic glove box by the agar dilution technique for susceptibility to clinically achievable levels of ticarcillin, carbenicillin, and penicillin. Thirty-two micrograms or less of penicillin per milliliter inhibited 91% of all strains, whereas 100 mug of carbenicillin and ticarcillin per ml inhibited 95 and 98%, respectively. A total of 82% (85 strains) of Bacteroides were inhibited by penicillin, and 93 and 96% were inhibited by carbenicillin and ticarcillin, respectively. Thirteen (24%) of 55 strains of Bacteroides fragilis tested were resistant to 32 mug of penicillin per ml, and 6 (11%) and 3 (5%) were resistant to 100 mug of carbenicillin and ticarcillin per ml, respectively. Within the therapeutic range, ticarcillin was the most effective of the three penicillins tested against B. fragilis subsp. fragilis.

摘要

采用琼脂稀释法,在厌氧手套箱中对总共334株临床厌氧菌分离株进行测试,以检测它们对临床可达到浓度的替卡西林、羧苄西林和青霉素的敏感性。每毫升32微克或更低浓度的青霉素可抑制所有菌株的91%,而每毫升100微克的羧苄西林和替卡西林分别可抑制95%和98%。总共82%(85株)的拟杆菌属菌株被青霉素抑制,分别有93%和96%被羧苄西林和替卡西林抑制。在测试的55株脆弱拟杆菌中,有13株(24%)对每毫升32微克的青霉素耐药,分别有6株(11%)和3株(5%)对每毫升100微克的羧苄西林和替卡西林耐药。在治疗范围内,替卡西林是所测试的三种青霉素中对脆弱拟杆菌脆弱亚种最有效的。