Takaya T, Sawada K, Suzuki H, Funaoka A, Matsuda K, Takada K
Department of Pharmaceutics and Pharmacokinetics, Kyoto Pharmaceutical University, Japan.
J Drug Target. 1997;4(5):271-6. doi: 10.3109/10611869708995842.
Pressure-controlled colon delivery capsule (PCC) containing 5-aminosalicylic acid (5-ASA) for the treatment of inflammatory bowel disease (IBD) was prepared and evaluated by an in vivo experiment using beagle dogs. As a reference drug, sulfasalazine (SASP), prodrug of 5-ASA, was used as a plain gelatin capsule preparation. After the oral administration of SASP at the does of 25.0 mg/kg, the mean time when the plasma 5-ASA concentration reaches to its maximum (Tmax) was 9.0 hr. In the case of 5-ASA administered in PCC, at the doses of 12.5 and 25.0 mg/kg, Tmaxs were 5.3 and 5.3 hr, respectively. Although the time for the first appearance of 5-ASA into the systemic circulation was almost the same value between SASP capsule and PCC containing 5-ASA, longer Tmax was observed from SASP capsule than from PCC. These results suggest that this 5-ASA preparation would be an useful dosage form for the therapy of IBD from the point of avoiding the side effect of sulfapyridine, one of the metabolites of SASP.
制备了含5-氨基水杨酸(5-ASA)的压力控制型结肠给药胶囊(PCC),用于治疗炎症性肠病(IBD),并通过使用比格犬进行的体内实验进行评估。作为参比药物,5-ASA的前体药物柳氮磺胺吡啶(SASP)制成普通明胶胶囊制剂。以25.0mg/kg的剂量口服SASP后,血浆5-ASA浓度达到最大值的平均时间(Tmax)为9.0小时。对于以PCC形式给药的5-ASA,在12.5mg/kg和25.0mg/kg的剂量下,Tmax分别为5.3小时和5.3小时。尽管5-ASA首次进入体循环的时间在SASP胶囊和含5-ASA的PCC之间几乎相同,但SASP胶囊的Tmax比PCC更长。这些结果表明,从避免SASP代谢产物之一磺胺吡啶的副作用的角度来看,这种5-ASA制剂将是治疗IBD的一种有用剂型。