Hoeprich P D, Merry J M, Gunther R, Franti C E
Antimicrob Agents Chemother. 1987 Aug;31(8):1234-7. doi: 10.1128/AAC.31.8.1234.
The passage of antifungal agents into pulmonary parenchyma was studied in normal sheep prepared by cannulation of the right external jugular vein and the efferent duct of the right caudal mediastinal lymph node. Five sheep were given single, sequential, intravenous injections of flucytosine, ketoconazole, BAY n 7133, amphotericin B methyl ester, and amphotericin B. Venous blood plasma and pulmonary lymph were collected before infusion and from 5 min to 24 h postinfusion; the concentrations of the drugs were assayed by a well-agar diffusion method. All drugs appeared promptly in the pulmonary lymph and disappeared at approximately exponential rates from both liquids. The lymph/plasma ratios of the drug concentrations did not differ between flucytosine and the two azoles but were lower for both polyenes. Binding by plasma proteins did not appear to be a determinant of pulmonary entry.
通过右颈外静脉插管和右尾纵隔淋巴结输出管制备正常绵羊,研究抗真菌药物进入肺实质的情况。给五只绵羊依次单次静脉注射氟胞嘧啶、酮康唑、BAY n 7133、两性霉素B甲酯和两性霉素B。在输注前以及输注后5分钟至24小时收集静脉血浆和肺淋巴;采用琼脂扩散法测定药物浓度。所有药物均迅速出现在肺淋巴中,并以近似指数的速率从两种液体中消失。氟胞嘧啶与两种唑类药物的药物浓度淋巴/血浆比值无差异,但两种多烯类药物的该比值较低。血浆蛋白结合似乎不是肺部摄取的决定因素。