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Labrasol® is an efficacious intestinal permeation enhancer across rat intestine: Ex vivo and in vivo rat studies.
- Source :
-
Journal of controlled release : official journal of the Controlled Release Society [J Control Release] 2019 Sep 28; Vol. 310, pp. 115-126. Date of Electronic Publication: 2019 Aug 08. - Publication Year :
- 2019
-
Abstract
- Labrasol® ALF (Labrasol®), is a non-ionic surfactant excipient primarily used as a solubilising agent. It was investigated here as an intestinal permeation enhancer in isolated rat colonic mucosae in Ussing chamber and in rat in situ intestinal instillations. Labrasol® comprises mono-, di- and triglycerides and mono- and di- fatty acid esters of polyethylene glycol (PEG)-8 and free PEG-8, with caprylic (C <subscript>8</subscript> )- and capric acid (C <subscript>10</subscript> ) as the main fatty acids. Source components of Labrasol® as well as Labrasol® modified with either C <subscript>8</subscript> or C <subscript>10</subscript> as the sole fatty acid components were also tested to determine which element of Labrasol® was responsible for its permeability-enhancing properties. Labrasol® (4, 8 mg/mL) enhanced the transport of the paracellular markers, [ <superscript>14</superscript> C] mannitol, FITC-dextran 4000, and FITC-insulin across colonic mucosae. The enhancement was non-damaging, transient, and molecular weight-dependent. The PEG ester fraction of Labrasol® also had enhancing properties. When insulin was administered with Labrasol® in instillations, it had a relative bioavailability of 7% in jejunum and 12% in colon. C <subscript>8</subscript> - and C <subscript>10</subscript> versions of Labrasol® and the PEG ester fraction also induced similar bioavailability values in jejunal instillations: 6, 5 and 7% respectively. Inhibition of lipases in instillations did not reduce the efficacy of Labrasol®, suggesting that its mechanism as a PE is not simply due to liberated medium chain fatty acids. Labrasol® acts as an efficacious intestinal permeation enhancer and has potential for use in oral formulations of macromolecules and BCS Class III molecules.<br /> (Copyright © 2019 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Colon metabolism
Excipients pharmacokinetics
Glycerides pharmacokinetics
In Vitro Techniques
Intestinal Mucosa metabolism
Jejunum metabolism
Male
Rats
Rats, Wistar
Tight Junctions drug effects
Tight Junctions metabolism
Colon drug effects
Excipients pharmacology
Glycerides pharmacology
Intestinal Absorption drug effects
Intestinal Mucosa drug effects
Jejunum drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1873-4995
- Volume :
- 310
- Database :
- MEDLINE
- Journal :
- Journal of controlled release : official journal of the Controlled Release Society
- Publication Type :
- Academic Journal
- Accession number :
- 31401199
- Full Text :
- https://doi.org/10.1016/j.jconrel.2019.08.008