Melander A
Clin Pharmacokinet. 1978 Sep-Oct;3(5):337-51. doi: 10.2165/00003088-197803050-00001.
Food intake exerts a complex influence on the bioavailability of drugs. It may interfere not only with tablet disintegration, drug dissolution and drug transit through the gastrointestinal tract, but may also affect the metabolic transformation of drugs in the gastrointestinal wall and in the liver. Different food components can have different effects, and food may interact in opposite ways, even with drugs that are chemically related. Therefore, the net effect of food on drug bioavailability can be predicted only by direct clinical studies of the drug in question. As judged mainly from single meal, single dose studies, food intake enhances the bioavailability of several different drugs, such as propranolol, metoprolol, hydrallazine, hydrochlorothiazide, canrenone (from spironolactone), nitrofurantoin, erythromycin (stearate), dicoumarol, phenytoin and carbamazepine, but reduces that of drugs such as isoniazid, rifampicin, tetracycline, penicillin and ampicillin, while having no consistent effect on the bioavailability of metronidazole, oxazepam, melperone, propylthiouracil, sulphasomidine and sulphonylureas. For some drugs such as digoxin and paracetamol, the rate but not the extent of absorption is reduced. Food may enhance bioavailability even though, or rather because, the rate of gastric emptying is reduced; this is apparently the case with hydrochlorothiazide and nitrofurantoin. The food induced enhancement of bioavailability of propranolol, metoprolol and hydrallazine is probably due to reduced first pass metabolism of these drugs, while food induced improvement of drug dissolution may explain the enhanced bioavailability of carbamazepine, canrenone, dicoumarol and phenytoin. An increased gastrointestinal pH may be in part the cause of the food induced reduction of the bioavailability of drugs such as isoniazid and tetracycline. In addition to single meal effects, repeated intake of protein-rich meals enhance, while carbohydrate-rich meals reduce, the rate of oxidation of antipyrine and theophylline. Moreover, intake of charcoal broiled meat markedly accelerates the oxidation of phenacetin and variably accelerates elimination of theophylline. Thus, food and its components and contaminants may have both short and long term effects on both the absorptive and biotransformation processes influencing systemic availability of drugs.
食物摄入对药物的生物利用度具有复杂的影响。它不仅可能干扰片剂崩解、药物溶解以及药物在胃肠道中的转运,还可能影响药物在胃肠道壁和肝脏中的代谢转化。不同的食物成分可能有不同的作用,甚至与化学结构相关的药物,食物也可能产生相反的相互作用。因此,食物对药物生物利用度的净效应只能通过对相关药物进行直接的临床研究来预测。主要从单餐、单剂量研究判断,食物摄入可提高几种不同药物的生物利用度,如普萘洛尔、美托洛尔、肼屈嗪、氢氯噻嗪、坎利酮(来自螺内酯)、呋喃妥因、红霉素(硬脂酸盐)、双香豆素、苯妥英和卡马西平,但会降低异烟肼、利福平、四环素、青霉素和氨苄西林等药物的生物利用度,而对甲硝唑、奥沙西泮、美哌隆、丙硫氧嘧啶、磺胺索嘧啶和磺脲类药物的生物利用度没有一致的影响。对于某些药物,如地高辛和对乙酰氨基酚,吸收速率降低但吸收程度不变。即使胃排空速率降低,食物也可能提高生物利用度;氢氯噻嗪和呋喃妥因显然就是这种情况。食物引起的普萘洛尔、美托洛尔和肼屈嗪生物利用度提高可能是由于这些药物的首过代谢降低,而食物引起的药物溶解改善可能解释了卡马西平、坎利酮、双香豆素和苯妥英生物利用度的提高。胃肠道pH值升高可能部分是食物引起异烟肼和四环素等药物生物利用度降低的原因。除了单餐效应外,重复摄入富含蛋白质的餐食会提高,而富含碳水化合物的餐食会降低安替比林和茶碱的氧化速率。此外,摄入炭烤肉类会显著加速非那西丁的氧化,并不同程度地加速茶碱的消除。因此,食物及其成分和污染物可能对影响药物全身利用度的吸收和生物转化过程产生短期和长期影响。