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硫酸卡那霉素与头孢唑林钠在实验性小肠绞窄性梗阻中的药代动力学

[Kanamycin sulfate and sodium cephazolin pharmacokinetics in experimental strangulation obstruction of the small intestine].

作者信息

Eriukhin I A, Poliak M S, Rukhliada N V

出版信息

Vestn Khir Im I I Grek. 1981 Jul;127(7):21-6.

PMID:7292844
Abstract

The experimental investigation of pharmacokinetic properties of kanamycin and cephazolin has shown the antibiotic to penetrate well into the blood, lymph, abdominal exudate. Transport of kanamycin in the wall of the strangulated intestine and its mesentery through the lymphatic system and by adsorption from the abdominal exudate is supposed to be possible. Normal concentration of the antibiotic was determined in the tissues around the strangulation zone. The concentration peak of both antibiotics was noted 1 hour after introduction in all the biosubstrates studied which may serve as an orientator for the optimal time of operation.

摘要

卡那霉素和头孢唑林药代动力学特性的实验研究表明,这两种抗生素能很好地渗透到血液、淋巴液和腹腔渗出液中。卡那霉素在绞窄性肠壁及其系膜中可能通过淋巴系统以及从腹腔渗出液中吸附进行转运。在绞窄区周围组织中测定到了抗生素的正常浓度。在所有研究的生物基质中,两种抗生素在注入后1小时均出现浓度峰值,这可为确定最佳手术时间提供参考。

相似文献

1
[Kanamycin sulfate and sodium cephazolin pharmacokinetics in experimental strangulation obstruction of the small intestine].硫酸卡那霉素与头孢唑林钠在实验性小肠绞窄性梗阻中的药代动力学
Vestn Khir Im I I Grek. 1981 Jul;127(7):21-6.
2
[Kanamycin pharmacokinetics in experimental small intestine obstruction].[实验性小肠梗阻中卡那霉素的药代动力学]
Antibiotiki. 1981 Mar;26(3):116-9.
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Occurrence of non-ototoxic antibiotic (cephazolin) in the inner ear.
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Lactate and glycerol released to the intestinal lumen reflect mucosal injury and permeability changes caused by strangulation obstruction.释放到肠腔内的乳酸和甘油反映了绞窄性肠梗阻引起的黏膜损伤和通透性变化。
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