氨基水杨酸
栓剂
医学
药代动力学
直肠炎
直肠
尿
溃疡性结肠炎
胃肠病学
生物利用度
直肠给药
解热药
内科学
泌尿科
药理学
止痛药
疾病
作者
Guy Aumais,Marc Lefebvre,Claude Tremblay,Alain Bitton,Florian Martin,Alain Giard,Majid Al Madi,Jean Spénard
标识
DOI:10.1046/j.1365-2036.2003.01409.x
摘要
Summary Objective : Patients with ulcerative proctitis may have rectal mucosal properties different from healthy volunteers. This project compared the pharmacokinetics of rectally administered mesalazine in these two populations. Methods : In two separate studies, nine patients with ulcerative proctitis and 16 healthy volunteers received a single 500 mg mesalazine suppository and then 500 mg every 8 h for 5 days. Blood samples were collected for 12 h in healthy volunteers and 30 h in patients, and urine for 24 h in healthy volunteers and 30 h in patients. Rectal biopsies were performed 8 h after the last dose. Results : After a single dose to patients, mean mesalazine half‐life (s.d.) was 5.0 (3.6) h. At steady‐state, means (s.d.) were 89.1 (78.9) ng/mL for C min , 361.1 (240.8) ng/mL for C max , and 7.1 (7.3) h for half‐life. Mean (range) rectal mesalazine concentrations were 167 (1.4–541.6) ng/mg tissue. After a single dose in healthy volunteers, mean (s.d.) half‐life was 4.0 (4.7) h. At steady‐state, means (s.d.) were 22.4 (61.6) ng/mL for C min , 359.4 (166.3) ng/mL for C max , and 0.9 (0.5) h for half‐life. Conclusion : Mesalazine is released in the rectum of patients, with a bioavailability of about 40%. Tissue distribution is also appreciable. Both parameters appear higher than in healthy volunteers.
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