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结肠递送胶囊对5-氨基水杨酸的应用及对比格犬口服给药后药代动力学特征的评价。

Application of a colon delivery capsule to 5-aminosalicylic acid and evaluation of the pharmacokinetic profile after oral administration to beagle dogs.

作者信息

Takaya T, Sawada K, Suzuki H, Funaoka A, Matsuda K, Takada K

机构信息

Department of Pharmaceutics and Pharmacokinetics, Kyoto Pharmaceutical University, Japan.

出版信息

J Drug Target. 1997;4(5):271-6. doi: 10.3109/10611869708995842.

Abstract

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.

摘要

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。

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