Unowsky J, Behl C R, Beskid G, Sattler J, Halpern J, Cleeland R
Department of Pharmacology and Chemotherapy, Hoffmann-La Roche, Nutley, N.J.
Chemotherapy. 1988;34(4):272-6. doi: 10.1159/000238580.
The rat enteral and rabbit rectal models were utilized to study the effect of Capmul (medium chain glycerides) on the absorption of a selection of beta-lactam and aminoglycoside antibiotics. All tested non-orally available beta-lactam antibiotics (cefamandole, cefotaxime, moxalactam, cefoxitin, mezlocillin, carumonam, penicillin G and amdinocillin) showed increased absorption enterally in rats and rectally in rabbits when formulated with Capmul. The orally available beta-lactam antibiotics, cephalexin and cephradine, were not enhanced in their enteral or rectal absorption by Capmul in the two model systems. Ampicillin absorption was enhanced rectally and enterally by Capmul. Rectal absorption of the aminoglycoside antibiotics, tobramycin and gentamycin, was enhanced by Capmul while enteral absorption was not.
采用大鼠肠内和家兔直肠模型,研究了Capmul(中链甘油酯)对多种β-内酰胺类抗生素和氨基糖苷类抗生素吸收的影响。所有测试的非口服可用β-内酰胺类抗生素(头孢孟多、头孢噻肟、莫西沙星、头孢西丁、美洛西林、卡芦莫南、青霉素G和氨曲南)与Capmul配制成制剂后,在大鼠肠内和家兔直肠中的吸收均增加。在这两种模型系统中,口服可用的β-内酰胺类抗生素头孢氨苄和头孢拉定,其肠内或直肠吸收未因Capmul而增强。氨苄西林的直肠和肠内吸收均因Capmul而增强。Capmul增强了氨基糖苷类抗生素妥布霉素和庆大霉素的直肠吸收,但未增强其肠内吸收。