Literature DB >> 25964103

Fasted-state simulated intestinal fluid "FaSSIF-C", a cholesterol containing intestinal model medium for in vitro drug delivery development.

Pooneh Khoshakhlagh1, Raphael Johnson1, Peter Langguth1, Thomas Nawroth1, Lars Schmueser2,3, Nadja Hellmann3, Heinz Decker3, Noemi Kinga Szekely4.   

Abstract

A set of biorelevant media "fasted-state simulated intestinal fluid with cholesterol (FaSSIF-C)" for the in vitro study of intestinal drug dissolution in the duodenum was developed. These contain cholesterol at the same levels as in human bile: the cholesterol content of FaSSIF-7C is equivalent to healthy female, FaSSIF-10C to healthy male persons, and FaSSIF-13C to several disease cases that lead to gallstones. The fluids were studied in three aspects: biocompatibility, intestinal nanostructure, and solubilizing power of hydrophobic drugs of the BCS class II. The biocompatibility study showed no toxic effects in a Caco-2 cell system. The drug-solubilizing capacity toward Fenofibrate, Danazol, Griseofulvin, and Carbamazepine was assessed as example. It varied with the cholesterol content widely from a fourfold improvement to a twofold reduction. The nanostructure study by dynamic light scattering and small-angle neutron scattering indicated vesicles as the main component of FaSSIF-C in equilibrium (>1 h), but at high cholesterol content, larger particles were observed as a minor contribution. The neutron experiments indicated the presence of complex micelle-vesicle mixtures, even after 1 h development of fed-state bile model to FaSSIF. The results indicate that cholesterol affects some drugs in solubilization and particle size in intestinal model fluids.
© 2015 Wiley Periodicals, Inc. and the American Pharmacists Association.

Entities:  

Keywords:  Caco-2 cells; DLS; FaSSIF; SANS; biorelevant media; drug solubility; in vitro models; light-scattering; lipids; micelle

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Substances:

Year:  2015        PMID: 25964103     DOI: 10.1002/jps.24470

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  4 in total

1.  Evolution of Choice of Solubility and Dissolution Media After Two Decades of Biopharmaceutical Classification System.

Authors:  Nadia Bou-Chacra; Katherine Jasmine Curo Melo; Ivan Andrés Cordova Morales; Erika S Stippler; Filippos Kesisoglou; Mehran Yazdanian; Raimar Löbenberg
Journal:  AAPS J       Date:  2017-05-17       Impact factor: 4.009

2.  Topography of Simulated Intestinal Equilibrium Solubility.

Authors:  Claire Dunn; Jeremy Perrier; Ibrahim Khadra; Clive G Wilson; Gavin W Halbert
Journal:  Mol Pharm       Date:  2019-04-16       Impact factor: 4.939

3.  Selection of In Vivo Predictive Dissolution Media Using Drug Substance and Physiological Properties.

Authors:  Deanna M Mudie; Nasim Samiei; Derrick J Marshall; Gregory E Amidon; Christel A S Bergström
Journal:  AAPS J       Date:  2020-01-27       Impact factor: 4.009

4.  Dual Level Statistical Investigation of Equilibrium Solubility in Simulated Fasted and Fed Intestinal Fluid.

Authors:  Bayan E Ainousah; Jeremy Perrier; Claire Dunn; Ibrahim Khadra; Clive G Wilson; Gavin Halbert
Journal:  Mol Pharm       Date:  2017-11-15       Impact factor: 4.939

  4 in total

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