Experimental and Modeling Study of Drug Release from HPMC-Based Erodible Oral Thin Films

In this work hydroxypropyl methylcellulose (HPMC) fast-dissolving thin films for oral administration are investigated. Furosemide (Class IV of the Biopharmaceutical Classification System) has been used as a model drug for in vitro release tests using three different set-ups: the Franz cell, the mill...

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Main Authors: Alessandra Adrover, Gabriele Varani, Patrizia Paolicelli, Stefania Petralito, Laura Di Muzio, Maria Antonietta Casadei, Ingunn Tho
Format: Article
Language:English
Published: MDPI AG 2018-11-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/10/4/222
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author Alessandra Adrover
Gabriele Varani
Patrizia Paolicelli
Stefania Petralito
Laura Di Muzio
Maria Antonietta Casadei
Ingunn Tho
author_facet Alessandra Adrover
Gabriele Varani
Patrizia Paolicelli
Stefania Petralito
Laura Di Muzio
Maria Antonietta Casadei
Ingunn Tho
author_sort Alessandra Adrover
collection DOAJ
description In this work hydroxypropyl methylcellulose (HPMC) fast-dissolving thin films for oral administration are investigated. Furosemide (Class IV of the Biopharmaceutical Classification System) has been used as a model drug for in vitro release tests using three different set-ups: the Franz cell, the millifluidic flow-through device, and the paddle type dissolution apparatus (USP II). In order to enable drug incorporation within HPMC films, a multifunctional excipient, hydroxypropyl-<inline-formula> <math display="inline"> <semantics> <mi>&#946;</mi> </semantics> </math> </inline-formula>-cyclodextrin (HP-<inline-formula> <math display="inline"> <semantics> <mi>&#946;</mi> </semantics> </math> </inline-formula>-CD) has been included in the formulation, and the influence of HP-<inline-formula> <math display="inline"> <semantics> <mi>&#946;</mi> </semantics> </math> </inline-formula>-CD on film swelling, erosion, and release properties has been investigated. Mathematical models capable of describing the swelling and release processes from HPMC erodible thin films in different apparatuses have been developed. In particular, we propose a new model for the description of drug transport and release in a Franz cell that accounts for the effect of the unavoidable imperfect mixing of the receptor chamber.
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spelling doaj.art-d61076e5e6894309bda29161425455812022-12-22T04:23:06ZengMDPI AGPharmaceutics1999-49232018-11-0110422210.3390/pharmaceutics10040222pharmaceutics10040222Experimental and Modeling Study of Drug Release from HPMC-Based Erodible Oral Thin FilmsAlessandra Adrover0Gabriele Varani1Patrizia Paolicelli2Stefania Petralito3Laura Di Muzio4Maria Antonietta Casadei5Ingunn Tho6Dipartimento di Ingegneria Chimica, Materiali e Ambiente, Sapienza Universitá di Roma, Via Eudossiana 18, 00184 Rome, ItalyDipartimento di Ingegneria Chimica, Materiali e Ambiente, Sapienza Universitá di Roma, Via Eudossiana 18, 00184 Rome, ItalyDipartimento di Chimica e Tecnologie del Farmaco, Sapienza Universitá di Roma, Piazzale Aldo Moro 5, 00185 Rome, ItalyDipartimento di Chimica e Tecnologie del Farmaco, Sapienza Universitá di Roma, Piazzale Aldo Moro 5, 00185 Rome, ItalyDipartimento di Chimica e Tecnologie del Farmaco, Sapienza Universitá di Roma, Piazzale Aldo Moro 5, 00185 Rome, ItalyDipartimento di Chimica e Tecnologie del Farmaco, Sapienza Universitá di Roma, Piazzale Aldo Moro 5, 00185 Rome, ItalySection of Pharmaceutics and Social Pharmacy, Department of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, 0316 Oslo, NorwayIn this work hydroxypropyl methylcellulose (HPMC) fast-dissolving thin films for oral administration are investigated. Furosemide (Class IV of the Biopharmaceutical Classification System) has been used as a model drug for in vitro release tests using three different set-ups: the Franz cell, the millifluidic flow-through device, and the paddle type dissolution apparatus (USP II). In order to enable drug incorporation within HPMC films, a multifunctional excipient, hydroxypropyl-<inline-formula> <math display="inline"> <semantics> <mi>&#946;</mi> </semantics> </math> </inline-formula>-cyclodextrin (HP-<inline-formula> <math display="inline"> <semantics> <mi>&#946;</mi> </semantics> </math> </inline-formula>-CD) has been included in the formulation, and the influence of HP-<inline-formula> <math display="inline"> <semantics> <mi>&#946;</mi> </semantics> </math> </inline-formula>-CD on film swelling, erosion, and release properties has been investigated. Mathematical models capable of describing the swelling and release processes from HPMC erodible thin films in different apparatuses have been developed. In particular, we propose a new model for the description of drug transport and release in a Franz cell that accounts for the effect of the unavoidable imperfect mixing of the receptor chamber.https://www.mdpi.com/1999-4923/10/4/222erodible thin filmsHPMCcyclodextrinsfurosemideFranz cellUSP IImillifluidic flow-through deviceerosion
spellingShingle Alessandra Adrover
Gabriele Varani
Patrizia Paolicelli
Stefania Petralito
Laura Di Muzio
Maria Antonietta Casadei
Ingunn Tho
Experimental and Modeling Study of Drug Release from HPMC-Based Erodible Oral Thin Films
Pharmaceutics
erodible thin films
HPMC
cyclodextrins
furosemide
Franz cell
USP II
millifluidic flow-through device
erosion
title Experimental and Modeling Study of Drug Release from HPMC-Based Erodible Oral Thin Films
title_full Experimental and Modeling Study of Drug Release from HPMC-Based Erodible Oral Thin Films
title_fullStr Experimental and Modeling Study of Drug Release from HPMC-Based Erodible Oral Thin Films
title_full_unstemmed Experimental and Modeling Study of Drug Release from HPMC-Based Erodible Oral Thin Films
title_short Experimental and Modeling Study of Drug Release from HPMC-Based Erodible Oral Thin Films
title_sort experimental and modeling study of drug release from hpmc based erodible oral thin films
topic erodible thin films
HPMC
cyclodextrins
furosemide
Franz cell
USP II
millifluidic flow-through device
erosion
url https://www.mdpi.com/1999-4923/10/4/222
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