Evaluation of a Methylcellulose and Hyaluronic Acid Hydrogel as a Vehicle for Rectal Delivery of Biologics

Biologics have changed the management of Inflammatory Bowel Disease (IBD), but there are concerns regarding unexpected systemic toxicity and loss of therapeutic response following administration by injection. Local delivery of biologics directly to the inflamed mucosa via rectal enema administration...

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Main Authors: Andreea Aprodu, Julia Mantaj, Bahijja Raimi-Abraham, Driton Vllasaliu
Format: Article
Language:English
Published: MDPI AG 2019-03-01
Series:Pharmaceutics
Subjects:
Online Access:http://www.mdpi.com/1999-4923/11/3/127
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spelling doaj-c7f635c5e8b44119bfcdd838404bcc042020-11-24T22:28:49ZengMDPI AGPharmaceutics1999-49232019-03-0111312710.3390/pharmaceutics11030127pharmaceutics11030127Evaluation of a Methylcellulose and Hyaluronic Acid Hydrogel as a Vehicle for Rectal Delivery of BiologicsAndreea Aprodu0Julia Mantaj1Bahijja Raimi-Abraham2Driton Vllasaliu3Faculty of Life Sciences & Medicine, School of Cancer and Pharmaceutical Sciences, King’s College London, London SE1 9NH, UKFaculty of Life Sciences & Medicine, School of Cancer and Pharmaceutical Sciences, King’s College London, London SE1 9NH, UKFaculty of Life Sciences & Medicine, School of Cancer and Pharmaceutical Sciences, King’s College London, London SE1 9NH, UKFaculty of Life Sciences & Medicine, School of Cancer and Pharmaceutical Sciences, King’s College London, London SE1 9NH, UKBiologics have changed the management of Inflammatory Bowel Disease (IBD), but there are concerns regarding unexpected systemic toxicity and loss of therapeutic response following administration by injection. Local delivery of biologics directly to the inflamed mucosa via rectal enema administration addresses the problems associated with systemic administration. Hydrogels are potentially useful delivery vehicles enabling rectal administration of biologics. Here, we prepared a hydrogel system based on methylcellulose (MC) and hyaluronic acid (HA), which possesses mucosal healing properties, incorporating a model macromolecular drug, namely (fluorescently-labeled) bovine serum albumin (BSA). The BSA-loaded MCHA hydrogel showed temperature-dependent gelation (liquid-like at 20 °C and gel-like at 37 °C) and shear thinning behavior, with these being important and desirable characteristics for rectal application (enabling easy application and retention). BSA release from the MCHA system at 37 °C was linear, with 50% of the loaded drug released within 2 h. The system demonstrated acceptable toxicity towards intestinal (colon) Caco-2 epithelial cells, even at high concentrations. Importantly, application of the BSA-loaded MCHA hydrogel to polarized Caco-2 monolayers, with or without an exemplar absorption enhancer, resulted in transintestinal permeability of BSA. The study therefore indicates that the MCHA hydrogel shows potential for topical (rectal) delivery of biologics in IBD.http://www.mdpi.com/1999-4923/11/3/127biologicsbiologics deliveryhyaluronic acidhydrogelsinflammatory bowel diseaseintestinal deliverymethylcellulose (MC)
collection DOAJ
language English
format Article
sources DOAJ
author Andreea Aprodu
Julia Mantaj
Bahijja Raimi-Abraham
Driton Vllasaliu
spellingShingle Andreea Aprodu
Julia Mantaj
Bahijja Raimi-Abraham
Driton Vllasaliu
Evaluation of a Methylcellulose and Hyaluronic Acid Hydrogel as a Vehicle for Rectal Delivery of Biologics
Pharmaceutics
biologics
biologics delivery
hyaluronic acid
hydrogels
inflammatory bowel disease
intestinal delivery
methylcellulose (MC)
author_facet Andreea Aprodu
Julia Mantaj
Bahijja Raimi-Abraham
Driton Vllasaliu
author_sort Andreea Aprodu
title Evaluation of a Methylcellulose and Hyaluronic Acid Hydrogel as a Vehicle for Rectal Delivery of Biologics
title_short Evaluation of a Methylcellulose and Hyaluronic Acid Hydrogel as a Vehicle for Rectal Delivery of Biologics
title_full Evaluation of a Methylcellulose and Hyaluronic Acid Hydrogel as a Vehicle for Rectal Delivery of Biologics
title_fullStr Evaluation of a Methylcellulose and Hyaluronic Acid Hydrogel as a Vehicle for Rectal Delivery of Biologics
title_full_unstemmed Evaluation of a Methylcellulose and Hyaluronic Acid Hydrogel as a Vehicle for Rectal Delivery of Biologics
title_sort evaluation of a methylcellulose and hyaluronic acid hydrogel as a vehicle for rectal delivery of biologics
publisher MDPI AG
series Pharmaceutics
issn 1999-4923
publishDate 2019-03-01
description Biologics have changed the management of Inflammatory Bowel Disease (IBD), but there are concerns regarding unexpected systemic toxicity and loss of therapeutic response following administration by injection. Local delivery of biologics directly to the inflamed mucosa via rectal enema administration addresses the problems associated with systemic administration. Hydrogels are potentially useful delivery vehicles enabling rectal administration of biologics. Here, we prepared a hydrogel system based on methylcellulose (MC) and hyaluronic acid (HA), which possesses mucosal healing properties, incorporating a model macromolecular drug, namely (fluorescently-labeled) bovine serum albumin (BSA). The BSA-loaded MCHA hydrogel showed temperature-dependent gelation (liquid-like at 20 °C and gel-like at 37 °C) and shear thinning behavior, with these being important and desirable characteristics for rectal application (enabling easy application and retention). BSA release from the MCHA system at 37 °C was linear, with 50% of the loaded drug released within 2 h. The system demonstrated acceptable toxicity towards intestinal (colon) Caco-2 epithelial cells, even at high concentrations. Importantly, application of the BSA-loaded MCHA hydrogel to polarized Caco-2 monolayers, with or without an exemplar absorption enhancer, resulted in transintestinal permeability of BSA. The study therefore indicates that the MCHA hydrogel shows potential for topical (rectal) delivery of biologics in IBD.
topic biologics
biologics delivery
hyaluronic acid
hydrogels
inflammatory bowel disease
intestinal delivery
methylcellulose (MC)
url http://www.mdpi.com/1999-4923/11/3/127
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