Carbenicillin Prodrugs: Kinetics of Intestinal Absorption Competing Degradation of the α-Esters of Carbenicillin and Prediction of Prodrug Absorbability from Quantitative Structure-Absorption Rate Relationship
Author:
Publisher
Elsevier BV
Subject
Pharmaceutical Science
Reference13 articles.
1. Preparation, hydrolysis, and oral absorption of .alpha.-carboxy esters of carbenicillin
2. Carbenicillin Prodrugs: Stability Kinetics of α-phenyl and α-indanyl Esters in Aqueous Solution
3. Gi Absorption of β-Lactam Antibiotics III: Kinetic Evidence for In Situ Absorption of Ionized Species of Monobasic Penicillins and Cefazolin from the Rat Small Intestine and Structure-Absorption Rate Relationships
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1. Penicillins;Antimicrobial Agents;2014-04-30
2. Prediction of oral drug absorption in humans by theoretical passive absorption model;International Journal of Pharmaceutics;2005-04
3. Role of the monocarboxylic acid transport system in the intestinal absorption of an orally active β-lactam prodrug: carindacillin as a model;International Journal of Pharmaceutics;1999-11
4. Synthesis and Properties of Disodium Tetraethyleneglycol-bis-(α-carboxybenzylpenicillin);Drug Development and Industrial Pharmacy;1999-01
5. (D) Routes of delivery: Case studies;Advanced Drug Delivery Reviews;1992-03
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