Literature DB >> 23456098

Insights into drug precipitation kinetics during in vitro digestion of a lipid-based drug delivery system using in-line raman spectroscopy and mathematical modeling.

Cordula Stillhart1, Georgios Imanidis, Martin Kuentz.   

Abstract

PURPOSE: To determine drug precipitation during in vitro lipolysis of a lipid-based drug delivery system (LBDDS) using Raman spectroscopy as a real-time monitoring technique. A second aim was to describe the kinetics of lipolysis-triggered drug precipitation using a theoretical nucleation and growth model.
METHODS: A model LBDDS containing different concentration of fenofibrate was digested in vitro and drug precipitation was determined after ultracentrifugation and nanofiltration (off-line methods), as well as by Raman spectroscopy (in-line method). Subsequently, a theoretical nucleation and growth model was fitted to the obtained drug crystallization profiles by considering the lipolysis-triggered change in drug solubility.
RESULTS: Compared with standard off-line measurements, Raman spectroscopy enabled a more robust and highly time-resolved analysis of lipolysis-triggered drug precipitation. Although the formulation was rapidly digested, fenofibrate remained in a supersaturated state for several minutes before beginning to crystallize. The in vitro digestion results were in excellent agreement with the theoretical model (R (2)  > 0.976).
CONCLUSIONS: The combination of real-time Raman spectroscopy and mathematical modeling provided insights into the kinetics of lipolysis-triggered drug crystallization. This knowledge allows a better biopharmaceutical understanding and will, ultimately, lead to the improved development of lipid-based drug formulations.

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Year:  2013        PMID: 23456098     DOI: 10.1007/s11095-013-0999-2

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  48 in total

1.  Biorelevant media simulating fed state intestinal fluids: colloid phase characterization and impact on solubilization capacity.

Authors:  Karen Kleberg; Freja Jacobsen; Dimitris G Fatouros; Anette Müllertz
Journal:  J Pharm Sci       Date:  2010-08       Impact factor: 3.534

2.  Biorelevant in vitro dissolution testing of products containing micronized or nanosized fenofibrate with a view to predicting plasma profiles.

Authors:  Daniel Juenemann; Ekarat Jantratid; Christian Wagner; Christos Reppas; Maria Vertzoni; Jennifer B Dressman
Journal:  Eur J Pharm Biopharm       Date:  2010-11-11       Impact factor: 5.571

Review 3.  Characterising the behaviour of poorly water soluble drugs in the intestine: application of biorelevant media for solubility, dissolution and transport studies.

Authors:  Karen Kleberg; Jette Jacobsen; Anette Müllertz
Journal:  J Pharm Pharmacol       Date:  2010-11       Impact factor: 3.765

4.  Biopharmaceutical challenges associated with drugs with low aqueous solubility--the potential impact of lipid-based formulations.

Authors:  C M O'Driscoll; B T Griffin
Journal:  Adv Drug Deliv Rev       Date:  2007-11-06       Impact factor: 15.470

5.  Design of lipid-based formulations for oral administration of poorly water-soluble drugs: precipitation of drug after dispersion of formulations in aqueous solution.

Authors:  Kazi Mohsin; Michelle A Long; Colin W Pouton
Journal:  J Pharm Sci       Date:  2009-10       Impact factor: 3.534

6.  Excipient-mediated supersaturation stabilization in human intestinal fluids.

Authors:  Jan Bevernage; Thomas Forier; Joachim Brouwers; Jan Tack; Pieter Annaert; Patrick Augustijns
Journal:  Mol Pharm       Date:  2011-02-22       Impact factor: 4.939

7.  Separation and characterization of the colloidal phases produced on digestion of common formulation lipids and assessment of their impact on the apparent solubility of selected poorly water-soluble drugs.

Authors:  Greg A Kossena; Ben J Boyd; Christopher J H Porter; William N Charman
Journal:  J Pharm Sci       Date:  2003-03       Impact factor: 3.534

Review 8.  Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs.

Authors:  Christopher J H Porter; Natalie L Trevaskis; William N Charman
Journal:  Nat Rev Drug Discov       Date:  2007-03       Impact factor: 84.694

9.  Use of in vitro lipid digestion data to explain the in vivo performance of triglyceride-based oral lipid formulations of poorly water-soluble drugs: studies with halofantrine.

Authors:  Christopher J H Porter; Ann Marie Kaukonen; Agnes Taillardat-Bertschinger; Ben J Boyd; Jacquelyn M O'Connor; Glenn A Edwards; William N Charman
Journal:  J Pharm Sci       Date:  2004-05       Impact factor: 3.534

10.  Comparative study on digestive lipase activities on the self emulsifying excipient Labrasol, medium chain glycerides and PEG esters.

Authors:  Sylvie Fernandez; Vincent Jannin; Jean-David Rodier; Nicolas Ritter; Bruno Mahler; Frédéric Carrière
Journal:  Biochim Biophys Acta       Date:  2007-03-02
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  10 in total

1.  A new in vitro lipid digestion - in vivo absorption model to evaluate the mechanisms of drug absorption from lipid-based formulations.

Authors:  Matthew F Crum; Natalie L Trevaskis; Hywel D Williams; Colin W Pouton; Christopher J H Porter
Journal:  Pharm Res       Date:  2015-12-24       Impact factor: 4.200

2.  Biopharmaceutical modeling of drug supersaturation during lipid-based formulation digestion considering an absorption sink.

Authors:  Cordula Stillhart; Georgios Imanidis; Brendan T Griffin; Martin Kuentz
Journal:  Pharm Res       Date:  2014-06-25       Impact factor: 4.200

3.  Quantifying In Vivo Luminal Drug Solubilization -Supersaturation-Precipitation Profiles to Explain the Performance of Lipid Based Formulations.

Authors:  Yusuke Tanaka; Erin Tay; Tri-Hung Nguyen; Christopher J H Porter
Journal:  Pharm Res       Date:  2020-02-03       Impact factor: 4.200

Review 4.  Lipid-associated oral delivery: Mechanisms and analysis of oral absorption enhancement.

Authors:  Oljora Rezhdo; Lauren Speciner; Rebecca Carrier
Journal:  J Control Release       Date:  2016-08-09       Impact factor: 9.776

Review 5.  The Precipitation Behavior of Poorly Water-Soluble Drugs with an Emphasis on the Digestion of Lipid Based Formulations.

Authors:  Jamal Khan; Thomas Rades; Ben Boyd
Journal:  Pharm Res       Date:  2015-11-23       Impact factor: 4.200

6.  Suitability of Artificial Membranes in Lipolysis-Permeation Assays of Oral Lipid-Based Formulations.

Authors:  Oliver J Hedge; Christel A S Bergström
Journal:  Pharm Res       Date:  2020-05-20       Impact factor: 4.200

7.  Low-Frequency Raman Scattering Spectroscopy as an Accessible Approach to Understand Drug Solubilization in Milk-Based Formulations during Digestion.

Authors:  Malinda Salim; Sara J Fraser-Miller; Ka Rlis Be Rziņš; Joshua J Sutton; Gisela Ramirez; Andrew J Clulow; Adrian Hawley; Stéphane Beilles; Keith C Gordon; Ben J Boyd
Journal:  Mol Pharm       Date:  2020-02-03       Impact factor: 4.939

8.  Small-volume in vitro lipid digestion measurements for assessing drug dissolution in lipid-based formulations using SAXS.

Authors:  Nafia F Khan; Malinda Salim; Syaza Y Binte Abu Bakar; Kurt Ristroph; Robert K Prud'homme; Adrian Hawley; Ben J Boyd; Andrew J Clulow
Journal:  Int J Pharm X       Date:  2022-02-09

Review 9.  Models for Predicting Drug Absorption From Oral Lipid-Based Formulations.

Authors:  Linda C Alskär; Christel A S Bergström
Journal:  Curr Mol Biol Rep       Date:  2015-10-07

10.  Impact of Drug Physicochemical Properties on Lipolysis-Triggered Drug Supersaturation and Precipitation from Lipid-Based Formulations.

Authors:  Linda C Alskär; Janneke Keemink; Jenny Johannesson; Christopher J H Porter; Christel A S Bergström
Journal:  Mol Pharm       Date:  2018-09-07       Impact factor: 4.939

  10 in total

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