Literature DB >> 28648070

Magnetic Resonance Imaging Quantification of Fasted State Colonic Liquid Pockets in Healthy Humans.

Kathryn Murray1, Caroline L Hoad1,2, Deanna M Mudie3, Jeff Wright1, Khaled Heissam1, Nichola Abrehart1, Susan E Pritchard2, Salem Al Atwah1, Penny A Gowland2, Martin C Garnett4, Gregory E Amidon5, Robin C Spiller1, Gordon L Amidon5, Luca Marciani1.   

Abstract

The rate and extent of drug dissolution and absorption from solid oral dosage forms is highly dependent on the volume of liquid in the gastrointestinal tract (GIT). However, little is known about the time course of GIT liquid volumes after drinking a glass of water (8 oz), particularly in the colon, which is a targeted site for both locally and systemically acting drug products. Previous magnetic resonance imaging (MRI) studies offered novel insights on GIT liquid distribution in fasted humans in the stomach and small intestine, and showed that freely mobile liquid in the intestine collects in fairly distinct regions or "pockets". Based on this previous pilot data, we hypothesized that (1) it is possible to quantify the time course of the volume and number of liquid pockets in the undisturbed colon of fasted healthy humans following ingestion of 240 mL, using noninvasive MRI methods; (2) the amount of freely mobile water in the fasted human colon is of the order of only a few milliliters. Twelve healthy volunteers fasted overnight and underwent fasted abdominal MRI scans before drinking 240 mL (∼8 fluid ounces) of water. After ingesting the water they were scanned at frequent intervals for 2 h. The images were processed to quantify freely mobile water in the total and regional colon: ascending, transverse, and descending. The fasted colon contained (mean ± SEM) 11 ± 5 pockets of resting liquid with a total volume of 2 ± 1 mL (average). The colonic fluid peaked at 7 ± 4 mL 30 min after the water drink. This peak fluid was distributed in 17 ± 7 separate liquid pockets in the colon. The regional analysis showed that pockets of free fluid were found primarily in the ascending colon. The interindividual variability was very high; the subjects showed a range of number of colonic fluid pockets from 0 to 89 and total colonic freely mobile fluid volume from 0 to 49 mL. This is the first study measuring the time course of the number, regional location, and volume of pockets of freely mobile liquid in the undisturbed colon of fasted humans after ingestion of a glass of water. Novel insights into the colonic fluid environment will be particularly relevant to improve our understanding and design of the in vivo performance of controlled release formulations targeted to the colon. The in vivo quantitative information presented here can be input into physiologically based mechanistic models of dissolution and absorption, and can be used in the design and set up of novel in vitro performance tools predictive of the in vivo environment.

Entities:  

Keywords:  MRI; bioperformance; controlled release; delayed release; dissolution; intestinal water; large bowel

Mesh:

Substances:

Year:  2017        PMID: 28648070     DOI: 10.1021/acs.molpharmaceut.7b00095

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  9 in total

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Review 2.  Application of In Vivo Imaging Techniques and Diagnostic Tools in Oral Drug Delivery Research.

Authors:  Stefan Senekowitsch; Philipp Schick; Bertil Abrahamsson; Patrick Augustijns; Thomas Gießmann; Hans Lennernäs; Christophe Matthys; Luca Marciani; Xavier Pepin; Alan Perkins; Maximilian Feldmüller; Sarah Sulaiman; Werner Weitschies; Clive G Wilson; Maura Corsetti; Mirko Koziolek
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Review 3.  Formulation predictive dissolution (fPD) testing to advance oral drug product development: An introduction to the US FDA funded '21st Century BA/BE' project.

Authors:  Bart Hens; Patrick D Sinko; Nicholas Job; Meagan Dean; Jozef Al-Gousous; Niloufar Salehi; Robert M Ziff; Yasuhiro Tsume; Marival Bermejo; Paulo Paixão; James G Brasseur; Alex Yu; Arjang Talattof; Gail Benninghoff; Peter Langguth; Hans Lennernäs; William L Hasler; Luca Marciani; Joseph Dickens; Kerby Shedden; Duxin Sun; Gregory E Amidon; Gordon L Amidon
Journal:  Int J Pharm       Date:  2018-06-23       Impact factor: 5.875

Review 4.  Nanocomposite systems for precise oral delivery of drugs and biologics.

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Journal:  Drug Deliv Transl Res       Date:  2021-02-03       Impact factor: 4.617

5.  Application of In Vivo MRI Imaging to Track a Coated Capsule and Its Disintegration in the Gastrointestinal Tract in Human Volunteers.

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Review 6.  In Vitro Methodologies for Evaluating Colon-Targeted Pharmaceutical Products and Industry Perspectives for Their Applications.

Authors:  Mauricio A García; Felipe Varum; Jozef Al-Gousous; Michael Hofmann; Susanne Page; Peter Langguth
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7.  Mechanistic modeling of gastrointestinal motility with integrated dissolution for simulating drug absorption.

Authors:  Kevin C Johnson
Journal:  ADMET DMPK       Date:  2020-06-09

8.  Modelling and Simulation of the Drug Release from a Solid Dosage Form in the Human Ascending Colon: The Influence of Different Motility Patterns and Fluid Viscosities.

Authors:  Michael Schütt; Konstantinos Stamatopoulos; Hannah K Batchelor; Mark J H Simmons; Alessio Alexiadis
Journal:  Pharmaceutics       Date:  2021-06-10       Impact factor: 6.321

9.  Measurement of fasted state gastric antral motility before and after a standard bioavailability and bioequivalence 240 mL drink of water: Validation of MRI method against concomitant perfused manometry in healthy participants.

Authors:  Khaled Heissam; Nichola Abrehart; Caroline L Hoad; Jeff Wright; Alex Menys; Kathryn Murray; Paul M Glover; Geoffrey Hebbard; Penny A Gowland; Jason Baker; William L Hasler; Robin C Spiller; Maura Corsetti; James G Brasseur; Bart Hens; Kerby Shedden; Joseph Dickens; Deanna M Mudie; Greg E Amidon; Gordon L Amidon; Luca Marciani
Journal:  PLoS One       Date:  2020-11-11       Impact factor: 3.240

  9 in total

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