دورية أكاديمية

A randomized, phase I, double-blind, crossover study on pharmacokinetics of peppermint oil capsules in healthy volunteers: Enteric-coating versus colon-targeted-delivery

التفاصيل البيبلوغرافية
العنوان: A randomized, phase I, double-blind, crossover study on pharmacokinetics of peppermint oil capsules in healthy volunteers: Enteric-coating versus colon-targeted-delivery
المؤلفون: Weerts, Z.Z.R.M., Keszthelyi, D., Frijlink, H.W., Brouwers, J.R.B.J., Vork, L., Jonkers, D.M.A.E., Masclee, A.A.M.
المصدر: Weerts , Z Z R M , Keszthelyi , D , Frijlink , H W , Brouwers , J R B J , Vork , L , Jonkers , D M A E & Masclee , A A M 2016 , ' A randomized, phase I, double-blind, crossover study on pharmacokinetics of peppermint oil capsules in healthy volunteers : Enteric-coating versus colon-targeted-delivery ' , Neurogastroenterology and motility , vol. 28 , pp. 101 . https://doi.org/10.1111/nmo.12881Test
سنة النشر: 2016
المجموعة: University of Groningen research database
مصطلحات موضوعية: peppermint oil, placebo, adult, aged, antinociception, blood pressure monitoring, clinical article, clinical trial, controlled clinical trial, controlled study, crossover procedure, double blind procedure, elimination half-life, enteric coated tablet, exposure, female, heart rate, human, human tissue, irritable colon, male, microcapsule, odor, pharmacokinetics, plasma concentration-time curve, questionnaire, randomized controlled trial, safety, side effect, visually impaired person
الوصف: Peppermint oil (PO) has been shown to reduce abdominal pain in patients with Irritable Bowel Syndrome (IBS). Menthol, the main constituent of PO, induces intestinal smooth muscle relaxation and desensitizes nociceptive nerve afferents. Enteric-coated (EC PO) capsules that release PO mainly in the small intestine are commercially available. In order to increase local, colonic anti-nociception, a colon-targeted-delivery peppermint oil (CTD PO) capsule has been developed. The aim of this study was to compare pharmacokinetic parameters of both formulations and to evaluate safety and tolerability. In this randomized, double blind, placebo-controlled study, subjects received 182 mg of either EC PO or CTD PO in a crossover design with ≥14 days washout period in between. After baseline measurements and drug administration, blood samples to determine menthol-glucuronide (menthol is rapidly metabolized to menthol-glucuronide), blood pressure and heart rate measurements were collected at several time points. Side effects were evaluated using questionnaires. The primary outcome was Tmax: time to reach peak menthol-glucuronide concentration in plasma. Eight healthy volunteers (50% female), aged between 20 and 65 years (median 22.2, IQR 20.8-28.8) were included. The Tmax of CTD PO was significantly longer (in all volunteers) compared to EC PO with a median (IQR) of 360 (360-405) vs 180 (120-180) min, respectively, p <0.05. The Area Under the menthol-glucuronide plasma concentration time Curves were smaller with a median (IQR) of 2331 μg∗h/L (2006-2510) for CTD compared to 2623 μg∗h/L (2471-2920) for EC capsules, p <0.05. No significant differences were found in peak concentrations and elimination half-lives. No differences in vital signs or side effects were observed between both regimens. Remarkably, subjects noticed alterations in fecal odor after CTD PO but not after EC PO, again pointing to more distal delivery with CTD PO. In conclusion, the CTD PO has a significantly delayed peak menthol-glucuronide concentration, ...
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://research.rug.nl/en/publications/d5d137db-c7c6-46c0-8906-fb5cc609f492Test
DOI: 10.1111/nmo.12881
الإتاحة: https://doi.org/10.1111/nmo.12881Test
https://hdl.handle.net/11370/d5d137db-c7c6-46c0-8906-fb5cc609f492Test
https://research.rug.nl/en/publications/d5d137db-c7c6-46c0-8906-fb5cc609f492Test
https://pure.rug.nl/ws/files/78253908/A_randomized_phase_I_double_blind_crossover_study_on_pharmacokinetics.pdfTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.DFF3C98
قاعدة البيانات: BASE