BIOAVAILABILITY OF 5-AMINOSALICYLIC ACID FROM SLOW-RELEASE 5-AMINOSALICYLIC ACID DRUG AND SULFASALAZINE IN NORMAL-CHILDREN

被引:22
作者
CHRISTENSEN, LA
FALLINGBORG, J
JACOBSEN, BA
ABILDGAARD, K
RASMUSSEN, HH
RASMUSSEN, SN
HANSEN, SH
机构
[1] AALBORG HOSP,DEPT SURG GASTROENTEROL,DK-9000 AALBORG,DENMARK
[2] ROYAL DANISH SCH PHARM,DEPT ORGAN CHEM,DK-2100 COPENHAGEN,DENMARK
关键词
MESALAZINE; PHARMACOKINETICS; STEADY STATE;
D O I
10.1007/BF01296106
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The bioavailability of a controlled release 5-aminosalicylic acid preparation (Pentasa) was investigated in nine healthy children after a medication period of six days (1000 mg/day) and compared with sulfasalazine (Salazopyrin) (2000 mg/day). The local bioavailability in the distal gut lumen, reflected by the 5-aminosalicylic acid concentration in the fecal water, showed comparable values after Pentasa (4.44 mmol/liter) and Salazopyrin (6.25 mmol/liter). The concentration of N-acetyl-5-ASA was significantly higher after Pentasa, reflecting the more proximal release of 5-aminosalicylic acid compared with Salazopyrin. No relation was found between the 5-aminosalicylic acid fecal water concentration and the 5-aminosalicylic acid dose per kilogram of body weight. The urinary excretion of 5-aminosalicylic acid and N-acetyl-5-aminosalicylic acid was higher after Pentasa than after Salazopyrin (32% vs 25%). Dose interval plasma concentration curves showed low values after both preparations. Based on the concept that the fecal water concentration is decisive for the efficacy of 5-aminosalicylic acid in distal inflammatory bowel disease, Pentasa treatment offers a relevant alternative in cases of Salazopyrin intolerance or allergy in children. The higher systemic bioavailability from Pentasa warrants monitoring of the renal function.
引用
收藏
页码:1831 / 1836
页数:6
相关论文
共 28 条
[1]
A CONTROLLED-STUDY OF FECAL DISTRIBUTION IN ULCERATIVE-COLITIS AND PROCTITIS [J].
ALLISON, MC ;
DICK, R ;
POUNDER, RE .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1987, 22 (10) :1277-1280
[2]
AZADKHAN AK, 1977, LANCET, V2, P892
[3]
BINDER V, 1981, SCAND J GASTROENTERO, V16, P1122
[4]
STEADY-STATE KINETICS OF 5-AMINOSALICYLIC ACID AND SULFAPYRIDINE DURING SULFASALAZINE PROPHYLAXIS IN ULCERATIVE-COLITIS [J].
BONDESEN, S ;
NIELSEN, OH ;
SCHOU, JB ;
JENSEN, PH ;
LASSEN, LB ;
BINDER, V ;
KRASILNIKOFF, PA ;
DANO, P ;
HANSEN, SH ;
RASMUSSEN, SN ;
HVIDBERG, EF .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1986, 21 (06) :693-700
[5]
NEPHROTOXIC LESIONS FROM 5-AMINOSALICYLIC ACID [J].
CALDER, IC ;
FUNDER, CC ;
TANGE, JD ;
HAM, KN ;
GREEN, CR .
BMJ-BRITISH MEDICAL JOURNAL, 1972, 1 (5793) :152-+
[6]
RELEASE OF 5-AMINOSALICYLIC ACID FROM PENTASA DURING NORMAL AND ACCELERATED INTESTINAL TRANSIT-TIME [J].
CHRISTENSEN, LA ;
SLOT, O ;
SANCHEZ, G ;
BOSERUP, J ;
RASMUSSEN, SN ;
BONDESEN, S ;
HANSEN, SH ;
HVIDBERG, EF .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1987, 23 (03) :365-369
[7]
CHRISTENSEN LA, 1990, ALIMENT PHARM THERAP, V4, P523
[8]
MAINTENANCE OF REMISSION IN ULCERATIVE-COLITIS WITH ORAL PREPARATION OF 5-AMINOSALICYLIC ACID [J].
DEW, MJ ;
HUGHES, P ;
HARRIES, AD ;
WILLIAMS, G ;
EVANS, BK ;
RHODES, J .
BMJ-BRITISH MEDICAL JOURNAL, 1982, 285 (6347) :1012-1012
[9]
COLONIC RELEASE OF 5-AMINO SALICYLIC-ACID FROM AN ORAL PREPARATION IN ACTIVE ULCERATIVE-COLITIS [J].
DEW, MJ ;
RYDER, REJ ;
EVANS, N ;
EVANS, BK ;
RHODES, J .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1983, 16 (02) :185-187
[10]
Hanauer S, 1989, GASTROENTEROLOGY, V96, pA195