Erythrocytes as a Slow Release Carrier System for Propranolol and its Prodrugs
Author:
Affiliation:
1. Drug Development Group, Department of Pharmaceutical Sciences, Aston University, Birmingham B4 7ET
Publisher
Oxford University Press (OUP)
Subject
Pharmaceutical Science,Pharmacology
Link
http://academic.oup.com/jpp/article-pdf/38/Supplement_12/117P/37763950/j.2042-7158.1986.tb14345.x.pdf
Reference1 articles.
1. Encapsulation of drugs in intact erythrocytes: An intravenous delivery system
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1. Residence time distributions of solutes in the perfused rat liver using a dispersion model of hepatic elimination: 2. Effect of pharmacological agents, retrograde perfusions, and enzyme inhibition on evans blue, sucrose, water, and taurocholate;Journal of Pharmacokinetics and Biopharmaceutics;1990-06
2. Residence time distributions of solutes in the perfused rat liver using a dispersion model of hepatic elimination: 1. Effect of changes in perfusate flow and albumin concentration on sucrose and taurocholate;Journal of Pharmacokinetics and Biopharmaceutics;1990-06
3. Availability predictions by hepatic elimination models for Michaelis-Menten kinetics;Journal of Pharmacokinetics and Biopharmaceutics;1989-12
4. Role of the red blood cell in drug metabolism;Biopharmaceutics & Drug Disposition;1988-07
5. Prodrugs of propranolol: hydrolysis and intramolecular aminolysis of various propranolol esters and an oxazolidin-2-one derivative;International Journal of Pharmaceutics;1988-03
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