Bierer D W
Health and Personal Care Division, Procter & Gamble Company, Cincinnati, Ohio 45241.
Rev Infect Dis. 1990 Jan-Feb;12 Suppl 1:S3-8. doi: 10.1093/clinids/12.supplement_1.s3.
Pepto-Bismol, which contains bismuth subsalicylate (BSS) as the active ingredient, has been marketed in the United States for more than 80 years. In the gastrointestinal tract, BSS is converted to salicylic acid and insoluble bismuth salts. The salicylate portion of BSS is extensively absorbed (greater than 90%) and excreted in urine. The maximal daily dose of Pepto-Bismol (4.2 g of BSS) results in peak concentrations of salicylate in plasma considerably below the level of salicylate toxicity. In contrast, little bismuth from BSS is absorbed from the gastrointestinal tract (less than .005%). Extended dosing of Pepto-Bismol (3.14 g of BSS/d) for up to 6 weeks produced a mean concentration of bismuth in blood of 16.1 +/- 7.9 ng/g, considerably below concentrations in blood that have been reported to cause neurotoxicity. Neurotoxicity studies in animals and human safety data indicate that Pepto-Bismol can be used safely for its acute indications and for up to 3-4 weeks of extended dosing.
必奇(Pepto-Bismol)以碱式水杨酸铋(BSS)作为活性成分,在美国已销售80多年。在胃肠道中,BSS会转化为水杨酸和不溶性铋盐。BSS中的水杨酸部分被大量吸收(超过90%)并经尿液排出。必奇的最大日剂量(4.2克BSS)导致血浆中水杨酸的峰值浓度远低于水杨酸中毒水平。相比之下,BSS中的铋很少从胃肠道吸收(低于0.005%)。在必奇连续给药(3.14克BSS/天)长达6周的情况下,血液中铋的平均浓度为16.1±7.9纳克/克,远低于据报道会导致神经毒性的血液浓度。动物神经毒性研究和人类安全数据表明,必奇可安全用于急性适应症以及长达3至4周的连续给药。