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不同剂型土霉素制剂的生物利用度与溶出度

Bioavailability and dissolution of different formulations of oxytetracycline preparations.

作者信息

Hart A, Barber H E, Calvey T N

出版信息

Br J Clin Pharmacol. 1975 Jun;2(3):277-80. doi: 10.1111/j.1365-2125.1975.tb01588.x.

Abstract

1 The concentration of oxytetracycline in plasma was studied by microbiological assay after oral administration of five different preparations of the antibiotic. None of these preparations had been studied previously. 2 There was a statistically significant correlation between the time required for 50% dissolution at pH 2 and biological availability, as assessed by the peak plasma level or the area under the plasma concentration-time curve. 3 The mean bioavailability of oxytetracycline was greatest with preparations of the hydrochloride, and with film-coated tablets of the dihydrate. In contrast, sugar-coated tablets of oxytetracycline dihydrate were associated with poorer dissolution characteristics and reduced biological availability.

摘要
  1. 通过微生物测定法研究了口服五种不同制剂的土霉素后血浆中土霉素的浓度。这些制剂此前均未被研究过。2. 如通过血浆峰值水平或血浆浓度-时间曲线下面积所评估的,在pH 2条件下50%溶解所需时间与生物利用度之间存在统计学上的显著相关性。3. 土霉素的平均生物利用度在盐酸盐制剂和二水合物薄膜包衣片的情况下最高。相比之下,土霉素二水合物糖衣片的溶解特性较差且生物利用度降低。

相似文献

2
Bioavailability of oxytetracycline dihydrate tablets in dogs.土霉素二水合物片在犬体内的生物利用度。
J Vet Pharmacol Ther. 1981 Mar;4(1):11-3. doi: 10.1111/j.1365-2885.1981.tb00704.x.

本文引用的文献

4
Cross-over study of ten tetracycline preparations.十种四环素制剂的交叉研究。
Eur J Clin Pharmacol. 1973 Jun;6(1):64-8. doi: 10.1007/BF00561804.
5
Biological availability and in vitro release from oral oxytetracycline and tetracycline preparations.
Acta Pharmacol Toxicol (Copenh). 1973;33(2):138-56. doi: 10.1111/j.1600-0773.1973.tb01517.x.

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