Welling P G, Koch P A, Lau C C, Craig W A
Antimicrob Agents Chemother. 1977 Mar;11(3):462-9. doi: 10.1128/AAC.11.3.462.
The influence of various test meals and fluid volumes on the relative bioavailability of commercial formulations of doxycycline hyclate and tetracycline hydrochloride was studied in healthy human volunteers. Serum levels of tetracycline were uniformly reduced by approximately 50% by all test meals, whereas serum levels of doxycycline were reduced by 20%. The reduction of tetracycline serum levels will likely be of clinical significance. The bioavailability of each drug was almost identical from an oral solution and from capsules in fasted subjects. The rate of doxycycline absorption was reduced when capsules were administered with a small volume of water, but the overall efficiency of absorption of both drugs was essentially independent of co-administered fluid volume. The use of 8-h serum data provides a reliable estimate of drug bioavailability for tetracycline and, to a lesser extent, for doxycycline.
在健康人类志愿者中研究了各种试验餐和液体量对盐酸多西环素和盐酸四环素商业制剂相对生物利用度的影响。所有试验餐均使四环素的血清水平均匀降低约50%,而多西环素的血清水平降低20%。四环素血清水平的降低可能具有临床意义。在禁食受试者中,每种药物从口服溶液和胶囊中的生物利用度几乎相同。当胶囊与少量水一起服用时,多西环素的吸收速率降低,但两种药物的总体吸收效率基本上与同时给予的液体量无关。使用8小时血清数据可为四环素以及在较小程度上为多西环素的药物生物利用度提供可靠估计。