Titre :

Oral colon delivery platform based on a novel combination approach: design concept and preliminary evaluation

Auteur(s) :

Moutaharrik, Saliha [Auteur]
Università degli Studi di Milano = University of Milan [UNIMI]
Maroni, Alessandra [Auteur]
Università degli Studi di Milano = University of Milan [UNIMI]
Melocchi, Alice [Auteur]
Università degli Studi di Milano = University of Milan [UNIMI]
Zema, Lucia [Auteur]
Università degli Studi di Milano = University of Milan [UNIMI]
Foppoli, Anastasia [Auteur]
Università degli Studi di Milano = University of Milan [UNIMI]
Cerea, Matteo [Auteur]
Università degli Studi di Milano = University of Milan [UNIMI]
Palugan, Luca [Auteur]
Università degli Studi di Milano = University of Milan [UNIMI]
Neut, Christel [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Siepmann, Florence [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Siepmann, Juergen [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Gazzaniga, Andrea [Auteur]
Università degli Studi di Milano = University of Milan [UNIMI]

Titre de la revue :

Journal of Drug Delivery Science and Technology

Nom court de la revue :

J. Drug Deliv. Sci. Technol.

Numéro :

66

Pagination :

102919

Date de publication :

2021-12-01

ISSN :

1773-2247

Mot(s)-clé(s) en anglais :

High-amylose starch
Oral colon delivery
Spray-coating
Hydroxypropyl cellulose
Hydroxylpropyl methylcellulose
Combined time-pH-and microbiota-dependent approach

Discipline(s) HAL :

Sciences du Vivant [q-bio]

Résumé en anglais : [en]

An oral colon delivery platform based on a novel combination strategy, leveraging multiple physiological characteristics of the intestine, is proposed. The system comprises a drug core, a water-swellable/soluble inner layer ...
Lire la suite >An oral colon delivery platform based on a novel combination strategy, leveraging multiple physiological characteristics of the intestine, is proposed. The system comprises a drug core, a water-swellable/soluble inner layer based on a hydrophilic cellulose derivative and an enteric outer layer (Eudragit® S) containing a microbially-degradable polysaccharide (high-amylose starch, Amylo N460), acting synergistically to prevent early release in the small intestine on the one hand, and release failure on the other. The Eudragit® S:Amylo N460 solid weight ratio in the external coating was 7:3; triethyl citrate and glyceryl monostearate were used as a plasticizer and an anti-tacking agent, respectively. The outer Eudragit® S/Amylo N460 layer was applied in a fluid bed using hydro-alcoholic or aqueous coating formulations. Two types of “inner” systems were studied: (i) Drug-loaded tablets coated with a low-viscosity hydroxypropyl methylcellulose (by aqueous spray-coating), and (ii) hydroxypropyl cellulose capsules prepared by injection-molding (filled with paracetamol as an analytical tracer). The obtained dosage forms were thoroughly characterized, including in vitro release measurements in various media. In all cases, pulsatile release profiles were obtained after medium change from 0.1 N HCl to phosphate buffer pH 7.4, with lag phases depending on the type and preparation technique of the hydrophilic polymer layer. The role of the microbiota on the release performance was explored in simulated colonic fluid (SCF), consisting in culture medium inoculated with fecal samples from inflammatory bowel disease patients. Clear differences in drug release were observed in SCF versus culture medium free of feces, indicating the effect of microbial degradation.Lire moins >

Langue :

Anglais

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

CHU Lille
Inserm
Université de Lille

Collections :

• Advanced Drug Delivery Systems (ADDS) - U1008
• Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286

Équipe(s) de recherche :

U1008

Date de dépôt :

2022-04-13T07:12:16Z
2024-02-14T14:33:23Z