Using zeta potential to study the ionisation behaviour of polymers employed in modified-release dosage forms and estimating their pKa

A range of enteric polymers is used in pharmaceutical industry for developing gastro-resistant formulations. It is generally implied that these coatings are interchangeable due to similar dissolution pH thresholds reported by suppliers. Despite rapid dissolution in compendial phosphate buffers, thes...

Full description

Bibliographic Details
Main Authors: Joao A.C. Barbosa, Malaz S.E. Abdelsadig, Barbara R. Conway, Hamid A. Merchant
Format: Article
Language:English
Published: Elsevier 2019-12-01
Series:International Journal of Pharmaceutics: X
Online Access:http://www.sciencedirect.com/science/article/pii/S2590156719300386
_version_ 1811270577298604032
author Joao A.C. Barbosa
Malaz S.E. Abdelsadig
Barbara R. Conway
Hamid A. Merchant
author_facet Joao A.C. Barbosa
Malaz S.E. Abdelsadig
Barbara R. Conway
Hamid A. Merchant
author_sort Joao A.C. Barbosa
collection DOAJ
description A range of enteric polymers is used in pharmaceutical industry for developing gastro-resistant formulations. It is generally implied that these coatings are interchangeable due to similar dissolution pH thresholds reported by suppliers. Despite rapid dissolution in compendial phosphate buffers, these products can take up to 2 h to disintegrate in-vivo in the human small intestine. The factors primarily responsible for such variability in dissolution of these polymeric coatings are the differences in ionisation of acidic functional groups on polymer chains and their interplay with ions and buffer species present in gastrointestinal fluids. In this study, we aim to develop a novel, simple and inexpensive technique that can be used under various in-vitro conditions to study the ionisation behaviour of commonly used polymers (EUDRAGIT-E100, L100, S100, HPMC AS-LF, AS-HF, HP-50, HP-55) and to estimate their pKa. Moreover, this method was successfully applied to study the ionisation behaviour of a range of natural polymers (Guar, Tara, locust bean, Konjac gums, gum Arabic, citrus pectin, chitosan and alginate) and their pKa was also estimated. The proposed method would allow a better understanding of the dissolution behaviour of these polymers within gastrointestinal tract and will aid rational design of modified release dosage forms. Keywords: pKa, Ionisation, Enteric, Gastro-resistant, Modified-release, Zeta-potential, Charge, Dissolution
first_indexed 2024-04-12T22:04:27Z
format Article
id doaj.art-dbffe91c0a2242c788181d43ed56207e
institution Directory Open Access Journal
issn 2590-1567
language English
last_indexed 2024-04-12T22:04:27Z
publishDate 2019-12-01
publisher Elsevier
record_format Article
series International Journal of Pharmaceutics: X
spelling doaj.art-dbffe91c0a2242c788181d43ed56207e2022-12-22T03:15:00ZengElsevierInternational Journal of Pharmaceutics: X2590-15672019-12-011Using zeta potential to study the ionisation behaviour of polymers employed in modified-release dosage forms and estimating their pKaJoao A.C. Barbosa0Malaz S.E. Abdelsadig1Barbara R. Conway2Hamid A. Merchant3Department of Pharmacy, School of Applied Sciences, University of Huddersfield, Queensgate, Huddersfield HD1 3DH, United KingdomDepartment of Pharmacy, School of Applied Sciences, University of Huddersfield, Queensgate, Huddersfield HD1 3DH, United KingdomDepartment of Pharmacy, School of Applied Sciences, University of Huddersfield, Queensgate, Huddersfield HD1 3DH, United KingdomCorresponding author.; Department of Pharmacy, School of Applied Sciences, University of Huddersfield, Queensgate, Huddersfield HD1 3DH, United KingdomA range of enteric polymers is used in pharmaceutical industry for developing gastro-resistant formulations. It is generally implied that these coatings are interchangeable due to similar dissolution pH thresholds reported by suppliers. Despite rapid dissolution in compendial phosphate buffers, these products can take up to 2 h to disintegrate in-vivo in the human small intestine. The factors primarily responsible for such variability in dissolution of these polymeric coatings are the differences in ionisation of acidic functional groups on polymer chains and their interplay with ions and buffer species present in gastrointestinal fluids. In this study, we aim to develop a novel, simple and inexpensive technique that can be used under various in-vitro conditions to study the ionisation behaviour of commonly used polymers (EUDRAGIT-E100, L100, S100, HPMC AS-LF, AS-HF, HP-50, HP-55) and to estimate their pKa. Moreover, this method was successfully applied to study the ionisation behaviour of a range of natural polymers (Guar, Tara, locust bean, Konjac gums, gum Arabic, citrus pectin, chitosan and alginate) and their pKa was also estimated. The proposed method would allow a better understanding of the dissolution behaviour of these polymers within gastrointestinal tract and will aid rational design of modified release dosage forms. Keywords: pKa, Ionisation, Enteric, Gastro-resistant, Modified-release, Zeta-potential, Charge, Dissolutionhttp://www.sciencedirect.com/science/article/pii/S2590156719300386
spellingShingle Joao A.C. Barbosa
Malaz S.E. Abdelsadig
Barbara R. Conway
Hamid A. Merchant
Using zeta potential to study the ionisation behaviour of polymers employed in modified-release dosage forms and estimating their pKa
International Journal of Pharmaceutics: X
title Using zeta potential to study the ionisation behaviour of polymers employed in modified-release dosage forms and estimating their pKa
title_full Using zeta potential to study the ionisation behaviour of polymers employed in modified-release dosage forms and estimating their pKa
title_fullStr Using zeta potential to study the ionisation behaviour of polymers employed in modified-release dosage forms and estimating their pKa
title_full_unstemmed Using zeta potential to study the ionisation behaviour of polymers employed in modified-release dosage forms and estimating their pKa
title_short Using zeta potential to study the ionisation behaviour of polymers employed in modified-release dosage forms and estimating their pKa
title_sort using zeta potential to study the ionisation behaviour of polymers employed in modified release dosage forms and estimating their pka
url http://www.sciencedirect.com/science/article/pii/S2590156719300386
work_keys_str_mv AT joaoacbarbosa usingzetapotentialtostudytheionisationbehaviourofpolymersemployedinmodifiedreleasedosageformsandestimatingtheirpka
AT malazseabdelsadig usingzetapotentialtostudytheionisationbehaviourofpolymersemployedinmodifiedreleasedosageformsandestimatingtheirpka
AT barbararconway usingzetapotentialtostudytheionisationbehaviourofpolymersemployedinmodifiedreleasedosageformsandestimatingtheirpka
AT hamidamerchant usingzetapotentialtostudytheionisationbehaviourofpolymersemployedinmodifiedreleasedosageformsandestimatingtheirpka