Ryan J R, Riley W A, Vargas R, Offen W W, Gruber C M
Clin Pharmacol Ther. 1987 Jul;42(1):28-32. doi: 10.1038/clpt.1987.103.
The effects of plain and enteric-coated fenoprofen calcium (Nalfon, Dista, Indianapolis, Ind.) on gastrointestinal microbleeding were studied in 32 normal male volunteers in a randomized, open-label, parallel trial at two inpatient research facilities. A 1-week placebo (baseline) period preceded 2 weeks of fenoprofen therapy (enteric coated or plain, 600 mg q.i.d.). Fecal blood loss was measured by 51Cr-tagged erythrocyte assay and averaged over days 4 to 7 (baseline) and 11 to 14 and 18 to 21 (active therapy). At one center gastrointestinal irritation was evaluated endoscopically before and after active therapy. Endoscopy showed both formulations to cause mucosal damage not evident by subject-reported symptoms. Four of the 16 subjects developed asymptomatic duodenal ulcers. Mean daily fecal blood loss was significantly lower (P = 0.03) with enteric-coated (mean +/- SD, 1.104 +/- 0.961 ml/day) than with plain fenoprofen calcium (mean +/- SD, 1.686 +/- 0.858 ml/day), suggesting that tolerance of fenoprofen can be improved with administration in an enteric-coated form.
在两个住院研究机构对32名正常男性志愿者进行了一项随机、开放标签、平行试验,研究普通型和肠溶型芬洛芬钙(萘普生,迪斯塔公司,印第安纳波利斯,印第安纳州)对胃肠道微出血的影响。在为期2周的芬洛芬治疗(肠溶型或普通型,每日4次,每次600毫克)之前有1周的安慰剂(基线)期。通过51铬标记红细胞测定法测量粪便失血量,并计算第4至7天(基线)以及第11至14天和第至21天(积极治疗期)的平均值。在一个中心,在积极治疗前后通过内镜评估胃肠道刺激情况。内镜检查显示两种制剂均会导致黏膜损伤,而受试者报告的症状并未显示出这种损伤。16名受试者中有4人出现无症状十二指肠溃疡。肠溶型芬洛芬钙(平均值±标准差,1.104±0.961毫升/天)的平均每日粪便失血量显著低于普通型芬洛芬钙(平均值±标准差,1.686±0.858毫升/天)(P = 0.03),这表明以肠溶型给药可提高对芬洛芬的耐受性。