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丙磺舒可增强阿洛西林和头孢尼西在骨组织中的渗透。

Azlocillin and cefonicid penetration into bone enhanced by probenecid.

作者信息

Summersgill J T, Harrod L G, Raff M J

出版信息

Antimicrob Agents Chemother. 1984 Sep;26(3):292-4. doi: 10.1128/AAC.26.3.292.

Abstract

Azlocillin (AZL) and cefonicid (CFD) penetration into rabbit humerus and scapula was evaluated with and without concomitantly administered probenecid. Groups of animals received either 70 mg of AZL intravenously or 20 mg of CFD intramuscularly per kg of body weight; other groups were pretreated with 40 mg of probenecid per kg before the administration of antibiotics. Peak levels of AZL in the sera of animals not receiving probenecid were 76.0 micrograms/ml at 30 min and declined to 7.7 micrograms/ml by 2.0 h. Maximum concentrations in bone were 2.7 micrograms/g in the humerus and 7.1 micrograms/g in the scapula at 1 h. Pretreatment with probenecid significantly elevated levels of AZL in both serum and bone while increasing the half-life in serum from 0.44 to 0.65 h. Maximum drug concentrations in bones of probenecid-pretreated animals were 3.9 and 11.7 micrograms/g in the humerus and scapula, respectively, with detectable levels persisting in bone for up to 4 h. The peak level of CFD alone in serum was 36.7 micrograms/ml at 30 min and declined to 0.86 micrograms/ml at 8 h. Maximum concentrations in bone were 0.66 micrograms/g in the humerus at 1 h and 1.8 micrograms/g in the scapula at 2 h. Pretreatment with probenecid significantly elevated levels of CFD in both serum and bone while increasing the half-life in serum from 1.4 to 2.94 h. Pretreatment with probenecid achieved maximum concentrations of 1.7 and 2.8 micrograms/g in the humerus and scapula, respectively. Detectable levels of CFD persisted in the humerus for up to 4 h and in the scapula for 8 h.

摘要

在伴用或不伴用丙磺舒的情况下,评估了阿洛西林(AZL)和头孢尼西(CFD)在兔肱骨和肩胛骨中的渗透情况。动物分组,每组每千克体重静脉注射70毫克阿洛西林或肌肉注射20毫克头孢尼西;其他组在给予抗生素前,每千克体重先用40毫克丙磺舒预处理。未接受丙磺舒的动物血清中阿洛西林的峰值水平在30分钟时为76.0微克/毫升,到2.0小时时降至7.7微克/毫升。1小时时,肱骨中骨内的最大浓度为2.7微克/克,肩胛骨中为7.1微克/克。丙磺舒预处理显著提高了血清和骨中阿洛西林的水平,同时使血清中的半衰期从0.44小时增加到0.65小时。丙磺舒预处理动物的骨中最大药物浓度在肱骨和肩胛骨中分别为3.9和11.7微克/克,骨中可检测水平持续长达4小时。单独使用头孢尼西时,血清中的峰值水平在30分钟时为36.7微克/毫升,8小时时降至0.86微克/毫升。1小时时,肱骨中骨内的最大浓度为0.66微克/克,2小时时肩胛骨中为1.8微克/克。丙磺舒预处理显著提高了血清和骨中头孢尼西的水平,同时使血清中的半衰期从1.4小时增加到2.94小时。丙磺舒预处理在肱骨和肩胛骨中分别达到最大浓度1.7和2.8微克/克。头孢尼西的可检测水平在肱骨中持续长达4小时,在肩胛骨中持续8小时。

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本文引用的文献

1
Kinetics and renal handling of cefonicid.头孢尼西的动力学及肾脏处理过程
Clin Pharmacol Ther. 1981 Nov;30(5):587-93. doi: 10.1038/clpt.1981.208.
3
Osteomyelitis: the past decade.骨髓炎:过去十年
N Engl J Med. 1980 Aug 14;303(7):360-70. doi: 10.1056/NEJM198008143030703.
7
International clinical experience with azlocillin.阿洛西林的国际临床经验。
J Antimicrob Chemother. 1983 May;11 Suppl B:215-22. doi: 10.1093/jac/11.suppl_b.215.
8
Treatment of serious Pseudomonas infections with azlocillin.
J Antimicrob Chemother. 1983 May;11 Suppl B:153-8. doi: 10.1093/jac/11.suppl_b.153.
9
The use of azlocillin to treat serious infections.阿洛西林用于治疗严重感染。
J Antimicrob Chemother. 1983 May;11 Suppl B:141-7. doi: 10.1093/jac/11.suppl_b.141.

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