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1
In vitro activity of LY127935.LY127935的体外活性。
Antimicrob Agents Chemother. 1979 Oct;16(4):503-9. doi: 10.1128/AAC.16.4.503.
2
Comparative activities of the oxa-beta-lactam LY127935, cefotaxime, cefoperazone, cefamandole, and ticarcillin against multiply resistant gram-negative bacilli.氧杂β-内酰胺类LY127935、头孢噻肟、头孢哌酮、头孢孟多和替卡西林对多重耐药革兰氏阴性杆菌的比较活性。
Antimicrob Agents Chemother. 1980 Feb;17(2):273-9. doi: 10.1128/AAC.17.2.273.
3
Moxalactam (LY127935), a new semisynthetic 1-oxa-beta-lactam antibiotic with remarkable antimicrobial activity: in vitro comparison with cefamandole and tobramycin.莫西拉酸(LY127935),一种新型半合成1-氧杂-β-内酰胺抗生素,具有显著的抗菌活性:与头孢孟多和妥布霉素的体外比较。
Antimicrob Agents Chemother. 1980 Apr;17(4):750-6. doi: 10.1128/AAC.17.4.750.
4
In vitro activity of LY127935, a new 1-oxa cephalosporin, against aerobic gram-negative bacilli.新型1-氧杂头孢菌素LY127935对需氧革兰氏阴性杆菌的体外活性
Antimicrob Agents Chemother. 1979 Dec;16(6):864-8. doi: 10.1128/AAC.16.6.864.
5
Activity of cefamandole and other cephalosporins against aerobic and anaerobic bacteria.头孢孟多及其他头孢菌素对需氧菌和厌氧菌的活性。
Antimicrob Agents Chemother. 1976 May;9(5):852-5. doi: 10.1128/AAC.9.5.852.
6
Comparison of the in vitro activities of HR756 with cephalothin, cefoxitin, and cefamandole.HR756与头孢噻吩、头孢西丁和头孢孟多的体外活性比较。
Antimicrob Agents Chemother. 1978 Dec;14(6):876-9. doi: 10.1128/AAC.14.6.876.
7
Antimicrobial activity of cefmenoxime (SCE-1365).头孢甲肟(SCE - 1365)的抗菌活性
Antimicrob Agents Chemother. 1981 Mar;19(3):454-60. doi: 10.1128/AAC.19.3.454.
8
Piperacillin (T-1220), a new semisynthetic penicillin: in vitro antimicrobial activity comparison with carbenicillin, ticarcillin, ampicillin, cephalothin, cefamandole and cefoxitin.哌拉西林(T - 1220),一种新型半合成青霉素:与羧苄西林、替卡西林、氨苄西林、头孢噻吩、头孢孟多和头孢西丁的体外抗菌活性比较
J Antibiot (Tokyo). 1977 Dec;30(12):1107-14. doi: 10.7164/antibiotics.30.1107.
9
Susceptibility of anaerobic bacteria to cefoperazone and other beta-lactam antibiotics.
Clin Ther. 1980;3(Spec Issue):34-8.
10
In vitro activity of LY127935.LY127935的体外活性。
Antimicrob Agents Chemother. 1979 Sep;16(3):287-92. doi: 10.1128/AAC.16.3.287.

引用本文的文献

1
The Chemical Relationship Among Beta-Lactam Antibiotics and Potential Impacts on Reactivity and Decomposition.β-内酰胺类抗生素之间的化学关系及其对反应活性和分解的潜在影响。
Front Microbiol. 2022 Mar 24;13:807955. doi: 10.3389/fmicb.2022.807955. eCollection 2022.
2
Depth distributions of bacteria for the Pseudomonas aeruginosa-infected burn wounds treated by methylene blue-mediated photodynamic therapy in rats: effects of additives to photosensitizer.经亚甲蓝介导的光动力疗法治疗的铜绿假单胞菌感染烧伤创面细菌的深度分布:光敏剂添加剂的影响。
J Biomed Opt. 2022 Jan;27(1). doi: 10.1117/1.JBO.27.1.018001.
3
Comparative in vitro activity of new beta-lactam antibiotics against anaerobic bacteria.新型β-内酰胺类抗生素对厌氧菌的体外活性比较
Antimicrob Agents Chemother. 1981 Nov;20(5):600-9. doi: 10.1128/AAC.20.5.600.
4
Synergism between aminoglycosides and cephalosporins with antipseudomonal activity: interaction index and killing curve method.具有抗假单胞菌活性的氨基糖苷类药物与头孢菌素之间的协同作用:相互作用指数和杀菌曲线法
Antimicrob Agents Chemother. 1982 Nov;22(5):743-52. doi: 10.1128/AAC.22.5.743.
5
Differences in susceptibilities of species of the Bacteroides fragilis group to several beta-lactam antibiotics: indole production as an indicator of resistance.脆弱拟杆菌群不同菌种对几种β-内酰胺类抗生素敏感性的差异:吲哚产生作为耐药性的指标
Antimicrob Agents Chemother. 1982 Oct;22(4):628-34. doi: 10.1128/AAC.22.4.628.
6
Comparative susceptibilities of clinical isolates of Serratia marcescens to newer cephalosporins, alone and in combination with various aminoglycosides.粘质沙雷氏菌临床分离株对新型头孢菌素单独及与各种氨基糖苷类联合使用时的敏感性比较。
Antimicrob Agents Chemother. 1980 Nov;18(5):651-5. doi: 10.1128/AAC.18.5.651.
7
Penetration of moxalactam and cefazolin into atrial appendage after simultaneous intramuscular or intravenous administration.同时肌内或静脉给药后,莫西拉坦和头孢唑林在心房附件中的渗透情况。
Antimicrob Agents Chemother. 1982 Aug;22(2):201-3. doi: 10.1128/AAC.22.2.201.
8
Comparative in vitro study of temocillin (BRL 17421), a new penicillin.新型青霉素替莫西林(BRL 17421)的体外比较研究
Antimicrob Agents Chemother. 1982 Apr;21(4):641-5. doi: 10.1128/AAC.21.4.641.
9
Comparative in vitro study of SQ26,776.SQ26,776的体外对比研究。
Antimicrob Agents Chemother. 1982 Feb;21(2):294-8. doi: 10.1128/AAC.21.2.294.
10
[N-formimidoyl-thienamycin: in vitro activity in bacteria with resistance to beta-lactam antibiotics or gentamicin].[N-甲脒基硫霉素:对β-内酰胺类抗生素或庆大霉素耐药细菌的体外活性]
Infection. 1982 Nov-Dec;10(6):361-70. doi: 10.1007/BF01642300.

本文引用的文献

1
Susceptibility of Enterobacter to cefamandole: evidence for a high mutation rate to resistance.肠杆菌对头孢孟多的敏感性:耐药高突变率的证据。
Antimicrob Agents Chemother. 1976 Jun;9(6):970-4. doi: 10.1128/AAC.9.6.970.
2
Evaluation of a dispensing instrument (Dynatech MIC-2000) for preparing microtiter antibiotic plates and testing their potency during storage.评估一种用于制备微量滴定抗生素平板并检测其储存期间效力的分配仪器(Dynatech MIC - 2000)。
Antimicrob Agents Chemother. 1978 May;13(5):842-4. doi: 10.1128/AAC.13.5.842.

LY127935的体外活性。

In vitro activity of LY127935.

作者信息

Fass R J

出版信息

Antimicrob Agents Chemother. 1979 Oct;16(4):503-9. doi: 10.1128/AAC.16.4.503.

DOI:10.1128/AAC.16.4.503
PMID:518080
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC352889/
Abstract

LY127935 is a unique new beta-lactam antibiotic. Its activity against 536 clinical isolates was studied by using microdilution methods of susceptibility testing and compared with the activities of cefamandole, cefoxitin, and cephalothin. The lowest concentrations required to inhibit at least 90% of strains tested (MIC(90)s) of LY127935 for Staphylococcus aureus, Streptococcus pyogenes, Streptococcus agalactiae, and Streptococcus pneumoniae ranged from 2 to 8 mug/ml. The MIC(90)s for other staphylococci and streptococci were higher. The MIC(90)s for Enterobacteriaceae and Pseudomonas species ranged from 0.12 to 8 mug/ml and 8 to >32 mug/ml, respectively. The MIC(90)s for anaerobes ranged from 2 to >32 mug/ml. As determined by MIC(90)s, LY127935 was consistently the least active antibiotic against facultatively anaerobic gram-positive cocci and the most active against aerobic and facultatively anaerobic gram-negative bacilli. Its position with respect to activity against anaerobes varied from being the most active against Bacteroides fragilis and Clostridium perfringens to the least active against anaerobic cocci. In a population of multidrug-resistant isolates, concentrations of 8 mug or less of LY127935 per ml inhibited 82% of Enterobacteriaceae; concentrations of 32 mug or less per ml inhibited 100% of Enterobacteriaceae and 40% of P. aeruginosa. Increasing the inoculum size by 100-fold did not increase the minimal inhibitory concentrations of LY127935 or cefoxitin but did increase minimal inhibitory concentrations of cefamandole and cephalothin for some Enterobacteriaceae. All four drugs were bactericidal; minimal bactericidal concentrations were the same or one concentration higher than minimal inhibitory concentrations for 91 to 96% of strains tested. The broad spectrum and marked in vitro activity of LY127935 make it a promising new antibiotic.

摘要

LY127935是一种独特的新型β-内酰胺抗生素。采用微量稀释法药敏试验研究了其对536株临床分离菌的活性,并与头孢孟多、头孢西丁和头孢噻吩的活性进行了比较。LY127935对金黄色葡萄球菌、化脓性链球菌、无乳链球菌和肺炎链球菌抑制至少90%受试菌株所需的最低浓度(MIC90s)为2至8μg/ml。其他葡萄球菌和链球菌的MIC90s较高。肠杆菌科细菌和假单胞菌属的MIC90s分别为0.12至8μg/ml和8至>32μg/ml。厌氧菌的MIC90s为2至>32μg/ml。根据MIC90s测定,LY127935始终是对兼性厌氧革兰氏阳性球菌活性最低的抗生素,而对需氧和兼性厌氧革兰氏阴性杆菌活性最高。其对厌氧菌的活性地位有所不同,对脆弱拟杆菌和产气荚膜梭菌活性最高,而对厌氧球菌活性最低。在多药耐药分离菌群体中,每毫升8μg或更低浓度的LY127935可抑制82%的肠杆菌科细菌;每毫升32μg或更低浓度可抑制100%的肠杆菌科细菌和40%的铜绿假单胞菌。将接种量增加100倍不会增加LY127935或头孢西丁的最低抑菌浓度,但会增加某些肠杆菌科细菌对头孢孟多和头孢噻吩的最低抑菌浓度。所有四种药物均具有杀菌作用;91%至96%受试菌株的最低杀菌浓度与最低抑菌浓度相同或高一个浓度。LY127935的广谱和显著体外活性使其成为一种有前景的新型抗生素。