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头孢尼西在人肺组织和淋巴结中的渗透情况。

Penetration of cefonicid into human lung tissue and lymph nodes.

作者信息

Cazzola M, Polverino M, Guidetti E, Santangelo G, Paizis G, Monaco G, D'Amato G, Girbino G

机构信息

Division of Occupational Pulmonary Disease and Respiratory Allergy, A. Cardarelli Hospital, Naples, Italy.

出版信息

Chemotherapy. 1990;36(5):325-31. doi: 10.1159/000238784.

Abstract

The present study was undertaken in order to investigate the penetration of cefonicid, a long-acting parenteral cephalosporin, with enhanced activity against most gram-positive and gram-negative pathogens, into human lung tissue and lymph nodes in patients undergoing open thoracotomy. Samples of lung tissue, lymph nodes and serum were obtained at various times after a single intramuscular dose of 1 g. The concentration of cefonicid was assayed by an agar diffusion method with Bacillus subtilis used as the test organism. The mean concentrations of cefonicid in serum at 2, 4, 8, 12 and 24 h after the injection were 91.5, 66.1, 35.7, 21.8 and 2.9 micrograms/ml, respectively. The mean levels of cefonicid into the hilar lymph nodes at the same times were 22.3, 18.7, 12.0, 6.9 and 1.5 micrograms/ml, respectively, while its concentrations in lung tissue were lower than those in lung lymph nodes up to the 12th hour (12.1, 14.6, 7.8, 5.4 and 1.9 micrograms/ml, respectively). Our results show that cefonicid was well distributed in interstitial fluid from which pulmonary lymph is formed and that its concentrations in lung tissue and lymph nodes were sufficient to inhibit most pathogens involved in respiratory tract infections. This finding was considered important, because it demonstrated that the high binding by plasma protein of cefonicid did not prevent it from entering lung tissue and fluids in useful quantities.

摘要

本研究旨在调查头孢尼西(一种长效胃肠外头孢菌素,对大多数革兰氏阳性和革兰氏阴性病原体具有增强的活性)在接受开胸手术的患者的人肺组织和淋巴结中的渗透情况。在单次肌内注射1克后,于不同时间获取肺组织、淋巴结和血清样本。采用以枯草芽孢杆菌为测试生物的琼脂扩散法测定头孢尼西的浓度。注射后2、4、8、12和24小时血清中头孢尼西的平均浓度分别为91.5、66.1、35.7、21.8和2.9微克/毫升。同时,肺门淋巴结中头孢尼西的平均水平分别为22.3、18.7、12.0、6.9和1.5微克/毫升,而在第12小时之前其在肺组织中的浓度低于肺淋巴结中的浓度(分别为12.1、14.6、7.8、5.4和1.9微克/毫升)。我们的结果表明,头孢尼西在形成肺淋巴的间质液中分布良好,并且其在肺组织和淋巴结中的浓度足以抑制大多数呼吸道感染所涉及的病原体。这一发现被认为很重要,因为它表明头孢尼西与血浆蛋白的高结合并不妨碍其以有效量进入肺组织和体液。

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