Comparative bioavailability evaluation of erythromycin base and its salts and esters. I. Erythromycin estolate capsules versus enteric-coated erythromycin base tablets.
نویسندگان
چکیده
A randomized crossover study in 16 healthy volunteers given multiple doses of erythromycin base enteric-coated tablets or erythromycin estolate capsules revealed essentially no difference in the resultant plasma concentration of bioactive erythromycin. This similarity in bioactivity persisted despite the fact that total eryghromycin levels (bioactive erythromycin base plus bioinactive erythromycin propionate) were at least three times higher after administration of the estolate than after administration of the base.
منابع مشابه
Erythromycin: Pharmacokinetics, Bioavailability, Nonantimicrobial Activity, and Possible Mechanisms Associated with Adverse Reactions
The oral administration of crushed enteric-coated tablets of erythromycin base to foals suppressed the pulmonary inflammatory response induced by bronchoalveolar lavage. The systemic bioavailability of erythromycin base was low and variable (19.8 6 8.8%), likely as a result of degradation of a substantial portion of the administered dose to microbiologically inactive anhydroerythromycin in the ...
متن کاملBioavailability and stability of erythromycin delayed release tablets.
BACKGROUND Erythromycin is available as the free base, ethylsuccinate, estolate, stearate, gluceptate, and lactobionate derivatives. When given orally erythromycin and its derivatives except the estolate are inactivated to some extent by the gastric acid and poor absorption may result. OBJECTIVES To establish whether delayed release erythromycin tablets meet the bioequivalent requirement for ...
متن کاملInfluence of study design in assessing food effects on absorption of erythromycin base and erythromycin stearate.
We performed a series of six single-dose and multiple-dose studies to evaluate the effect of food on the absorption of erythromycin base and erythromycin stearate. When we used a single-dose design, we found that an unprotected erythromycin base preparation was absorbed extensively if a prolonged fast preceded administration of the drug. A shorter faster period (as occurs in clinical settings) ...
متن کاملtrihydroxy-3,5,7,9,11,13-hexamethyl-6-[[3,4,6- trideoxy-3-(dimethylamino)--D-xylo hexopyranosyl]oxy]-oxacyclo-tetradecane-2,10-dione. ERYTHROMYCIN CLINICAL PHARMACOLOGY Orally administered erythromycin base and its salts
Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerly Streptomyces erythraeus) and belongs to the macrolide group of antibiotics. It is basic and readily forms salts with acids but it is the base which is microbiologically active. Erythromycin base is (3R *, 4S *, 5S *, 6R *, 7R *, 9R *, 11R *, 12R *, 13S *, 14R *)-4 [(2,6-Dideoxy-3-C-methyl3-O-methyl--L-ribo-hexopyran...
متن کاملtrihydroxy-3,5,7,9,11,13-hexamethyl-6-[[3,4,6- trideoxy-3-(dimethylamino)--D-xylo- hexopyranosyl]oxy]-oxacyclo-tetradecane-2,10-dione. ERYTHROMYCIN CLINICAL PHARMACOLOGY Orally administered erythromycin base and its salts
Erythromycin is produced by a strain of Saccharopolyspora erythraea (formerly Streptomyces erythraeus) and belongs to the macrolide group of antibiotics. It is basic and readily forms salts with acids but it is the base which is microbiologically active. Erythromycin base is (3R *, 4S *, 5S *, 6R *, 7R *, 9R *, 11R *, 12R *, 13S *, 14R *)-4[(2,6-Dideoxy-3-C-methyl3-O-methyl--L-ribo-hexopyranos...
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ورودعنوان ژورنال:
- Journal of clinical pharmacology
دوره 20 7 شماره
صفحات -
تاریخ انتشار 1980