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Unaltered serum propranolol binding by meal-induced variations in fatty acids.

作者信息

Naranjo C A, Sellers E M, Khouw V

出版信息

Br J Clin Pharmacol. 1982 Apr;13(4):575-6. doi: 10.1111/j.1365-2125.1982.tb01425.x.

DOI:10.1111/j.1365-2125.1982.tb01425.x
PMID:7066174
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1402056/
Abstract
摘要

相似文献

1
Unaltered serum propranolol binding by meal-induced variations in fatty acids.膳食诱导的脂肪酸变化对血清普萘洛尔结合无影响。
Br J Clin Pharmacol. 1982 Apr;13(4):575-6. doi: 10.1111/j.1365-2125.1982.tb01425.x.
2
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3
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PKQuest: a general physiologically based pharmacokinetic model. Introduction and application to propranolol.PKQuest:一种基于生理学的通用药代动力学模型。普萘洛尔的介绍与应用
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2
Individual variation in first-pass metabolism.首过代谢的个体差异。
Clin Pharmacokinet. 1993 Oct;25(4):300-28. doi: 10.2165/00003088-199325040-00005.
3
Mechanisms and variations in the food effect on propranolol bioavailability.
Eur J Clin Pharmacol. 1990;38(5):469-75. doi: 10.1007/BF02336686.

本文引用的文献

1
Titration of free fatty acids of plasma: a study of current methods and a new modification.血浆游离脂肪酸的滴定:当前方法研究及一种新改良方法
J Lipid Res. 1960 Apr;1:199-202.
2
Fatty acids modulation of meal-induced variations in diazepam free fraction.脂肪酸对餐食诱导的地西泮游离分数变化的调节作用。
Br J Clin Pharmacol. 1980 Sep;10(3):308-10. doi: 10.1111/j.1365-2125.1980.tb01763.x.
3
Variability in heparin effect on serum drug binding.肝素对血清药物结合作用的变异性。
Clin Pharmacol Ther. 1980 Oct;28(4):545-50. doi: 10.1038/clpt.1980.201.
4
Effects of caffeine on plasma free fatty acids, urinary catecholamines, and drug binding.咖啡因对血浆游离脂肪酸、尿儿茶酚胺及药物结合的影响。
Clin Pharmacol Ther. 1980 Sep;28(3):398-403. doi: 10.1038/clpt.1980.179.
5
Effect of heparin administration on plasma binding of benzodiazepines.肝素给药对苯二氮䓬类药物血浆结合的影响。
Br J Clin Pharmacol. 1980 Feb;9(2):171-5. doi: 10.1111/j.1365-2125.1980.tb05829.x.
6
Diurnal fluctuations in triglyceride, free fatty acids, and insulin during sucrose consumption and insulin infusion in man.人体在摄入蔗糖和输注胰岛素期间甘油三酯、游离脂肪酸及胰岛素的昼夜波动情况。
J Clin Invest. 1971 Mar;50(3):583-91. doi: 10.1172/JCI106528.
7
Diurnal patterns of triglycerides, free fatty acids, blood sugar, and insulin during carbohydrate-induction in man and their modification by nocturnal suppression of lipolysis.人体在碳水化合物诱导期间甘油三酯、游离脂肪酸、血糖和胰岛素的昼夜模式及其通过夜间抑制脂肪分解的改变。
J Clin Invest. 1973 Mar;52(3):732-40. doi: 10.1172/JCI107235.
8
The disposition of propranolol. 3. Decreased half-life and volume of distribution as a result of plasma binding in man, monkey, dog and rat.普萘洛尔的处置。3. 由于人、猴、狗和大鼠体内的血浆结合作用,半衰期和分布容积降低。
J Pharmacol Exp Ther. 1973 Jul;186(1):114-22.
9
Plasma protein binding of basic drugs. I. Selective displacement from alpha 1-acid glycoprotein by tris(2-butoxyethyl) phosphate.碱性药物的血浆蛋白结合。I. 磷酸三(2-丁氧基乙基)酯对α1-酸性糖蛋白的选择性置换作用
Clin Pharmacol Ther. 1977 Nov;22(5 Pt 1):539-44.
10
Altered drug binding due to the use of indwelling heparinized cannulas (heparin lock) for sampling.由于使用留置肝素化插管(肝素锁)进行采样导致药物结合改变。
Clin Pharmacol Ther. 1979 Jan;25(1):103-7. doi: 10.1002/cpt1979251103.