Influence of Pharmaceutical Formulation on the Mucosal Concentration of 5-Aminosalicylic Acid and <i>N</i>-Acetylmesalamine in Japanese Patients with Ulcerative Colitis
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- Yamamoto Yuki
- Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital Department of Clinical Pharmacology and Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Kyushu University
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- Masuda Satohiro
- Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital Department of Clinical Pharmacology and Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Kyushu University Department of Pharmacy, Kyushu University Hospital
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- Nakase Hiroshi
- Department of Gastroenterology and Hepatology, Sapporo Medical University School of Medicine Department of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University
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- Matsuura Minoru
- Department of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto University
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- Maruyama Shihoko
- Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital
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- Hisamatsu Tadakazu
- The Third Department of Internal Medicine, Kyorin University School of Medicine Department of Internal Medicine, Toho University Sakura Medical Center
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- Suzuki Yasuo
- Department of Internal Medicine, Toho University Sakura Medical Center
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- Matsubara Kazuo
- Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital
Bibliographic Information
- Other Title
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- Influence of Pharmaceutical Formulation on the Mucosal Concentration of 5-Aminosalicylic Acid and N-Acetylmesalamine in Japanese Patients with Ulcerative Colitis
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Abstract
<p>The efficacy of 5-aminosalicylic acid (5-ASA) as the first-line therapy for ulcerative colitis (UC) is determined by the extent of drug delivery to the inflamed region. Moreover, differences among the various formulations influence delivery of the drug. In this study, we examined the clinical significance of colonic mucosal concentrations of 5-ASA and N-acetylmesalamine (Ac-5-ASA) in UC patients receiving a pH-dependent or time-dependent release formulation of 5-ASA. The subjects were 67 patients with UC who were treated with a pH-dependent or time-dependent formulation of 5-ASA between December 2011 and April 2014. A retrospective observational analysis of clinical outcomes was performed using the clinical activity index (CAI) obtained on the day of biopsy. Colonic mucosal concentrations of 5-ASA and Ac-5-ASA in biopsy samples were measured by LC-tandem mass spectrometry/mass spectrometry. Patients who were treated with the pH-dependent formulation had higher colon mucosal concentrations of 5-ASA than those who were treated with the time-dependent formulation. Additionally, 5-ASA concentration was significantly higher in patients with CAI scores ≤3. A higher concentration of Ac-5-ASA was achieved with the time-dependent formulation than with the pH-dependent formulation. Furthermore, patients with CAI scores ≤3 had higher concentrations of 5-ASA than those with CAI scores ≥4. The colonic mucosal concentration of 5-ASA in patients with UC is influenced by the pharmaceutical formulation and the remission status of UC.</p>
Journal
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- Biological and Pharmaceutical Bulletin
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Biological and Pharmaceutical Bulletin 42 (1), 81-86, 2019-01-01
The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390845713035154432
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- NII Article ID
- 130007542208
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- NII Book ID
- AA10885497
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- ISSN
- 13475215
- 09186158
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- NDL BIB ID
- 029410906
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- PubMed
- 30369547
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
- KAKEN
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- Abstract License Flag
- Disallowed