{"title":"品多洛尔:与其他β -肾上腺素受体阻滞剂的药代动力学比较。","authors":"J. Meier","doi":"10.1185/03007997709110145","DOIUrl":null,"url":null,"abstract":"SummaryThe pharmacokinetic properties of the 9 most frequently studied beta-adrenoceptor blocking agents (alprenolol, atenolol, metoprolol, oxprenolol, pindolol, practolol, propranolol, sotalol and timolol) are compared. Some pharmacokinetic parameters were found to be similar or not relevantly different in this group of drugs, e.g. the rate and amount of absorption, distribution volume, elimination half-life, total clearance and total urinary excretion. However, some other pharmacokinetic parameters, such as daily dosage, oral bioavailability, first-pass effect and the ratio of renal versus hepatic clearance, were surprisingly different. A good correlation between systemic availability and urinary excretion of unchanged drug could be demonstrated for the beta-adrenoceptor blocking agents.The pharmacokinetic comparison shows that pindolol has some relevant advantages. Due to the moderate metabolism, a negligible first-pass effect results which yields a high oral bioavailability and leads to small inter-in...","PeriodicalId":75385,"journal":{"name":"Acta medica Scandinavica. Supplementum","volume":"606 1","pages":"65-70"},"PeriodicalIF":0.0000,"publicationDate":"2009-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1185/03007997709110145","citationCount":"22","resultStr":"{\"title\":\"Pindolol: a pharmacokinetic comparison with other beta-adrenoceptor blocking agents.\",\"authors\":\"J. Meier\",\"doi\":\"10.1185/03007997709110145\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"SummaryThe pharmacokinetic properties of the 9 most frequently studied beta-adrenoceptor blocking agents (alprenolol, atenolol, metoprolol, oxprenolol, pindolol, practolol, propranolol, sotalol and timolol) are compared. Some pharmacokinetic parameters were found to be similar or not relevantly different in this group of drugs, e.g. the rate and amount of absorption, distribution volume, elimination half-life, total clearance and total urinary excretion. However, some other pharmacokinetic parameters, such as daily dosage, oral bioavailability, first-pass effect and the ratio of renal versus hepatic clearance, were surprisingly different. A good correlation between systemic availability and urinary excretion of unchanged drug could be demonstrated for the beta-adrenoceptor blocking agents.The pharmacokinetic comparison shows that pindolol has some relevant advantages. Due to the moderate metabolism, a negligible first-pass effect results which yields a high oral bioavailability and leads to small inter-in...\",\"PeriodicalId\":75385,\"journal\":{\"name\":\"Acta medica Scandinavica. Supplementum\",\"volume\":\"606 1\",\"pages\":\"65-70\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1185/03007997709110145\",\"citationCount\":\"22\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta medica Scandinavica. Supplementum\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1185/03007997709110145\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta medica Scandinavica. Supplementum","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1185/03007997709110145","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Pindolol: a pharmacokinetic comparison with other beta-adrenoceptor blocking agents.
SummaryThe pharmacokinetic properties of the 9 most frequently studied beta-adrenoceptor blocking agents (alprenolol, atenolol, metoprolol, oxprenolol, pindolol, practolol, propranolol, sotalol and timolol) are compared. Some pharmacokinetic parameters were found to be similar or not relevantly different in this group of drugs, e.g. the rate and amount of absorption, distribution volume, elimination half-life, total clearance and total urinary excretion. However, some other pharmacokinetic parameters, such as daily dosage, oral bioavailability, first-pass effect and the ratio of renal versus hepatic clearance, were surprisingly different. A good correlation between systemic availability and urinary excretion of unchanged drug could be demonstrated for the beta-adrenoceptor blocking agents.The pharmacokinetic comparison shows that pindolol has some relevant advantages. Due to the moderate metabolism, a negligible first-pass effect results which yields a high oral bioavailability and leads to small inter-in...