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First-pass effect and intrinsic clearance of propranolol and pindolol in the isolated perfused rat liver.

Basset Hm, A H Robins

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Abstract

This study investigated the first-pass effect (E) and total hepatic intrinsic clearance (Clint) of propranolol and pindolol by means of an isolated rat liver perfusion model. It was shown that propranolol has a highly significantly greater E and Clint than pindolol. These marked differences between the drugs may be accounted for by the strong initial binding of propranolol to liver sites, a phenomenon possibly related to the greater lipid solubility of propranolol compared with pindolol.

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This study investigated the first-pass effect (E) and total hepatic intrinsic clearance (Clint) of propranolol and pindolol by means of an isolated rat liver perfusion model. It was shown that propranolol has a highly significantly greater E and Clint than pindolol. These marked differences between the drugs may be accounted for by the strong initial binding of propranolol to liver sites, a phenomenon possibly related to the greater lipid solubility of propranolol compared with pindolol.

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Available abstract

This study investigated the first-pass effect (E) and total hepatic intrinsic clearance (Clint) of propranolol and pindolol by means of an isolated rat liver perfusion model. It was shown that propranolol has a highly significantly greater E and Clint than pindolol. These marked differences between the drugs may be accounted for by the strong initial binding of propranolol to liver sites, a phenomenon possibly related to the greater lipid solubility of propranolol compared with pindolol.

Key concepts: Pindolol, Propranolol, Medicine, Pharmacology, Perfusion, Internal medicine, Endocrinology

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First-pass effect and intrinsic clearance of propranolol and pindolol in the isolated perfused rat liver. — Research Paper | ScholarLens