Fabrication of Glucose-Sensitive Layer-by-Layer Films for Potential Controlled Insulin Release Applications

Self-regulated drug delivery systems (DDS) are potential alternative to the conventional method of introducing insulin to the body due to their controlled drug release mechanism. In this study, Layer-by-Layer technique was utlized to manufacture drug loaded, pH responsive thin films. Insulin was alt...

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Main Authors: Talusan Timothy Jemuel E., Usman Ken Aldren S., Payawan Leon M.
Format: Article
Language:English
Published: EDP Sciences 2015-01-01
Series:MATEC Web of Conferences
Online Access:http://dx.doi.org/10.1051/matecconf/20152703001
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spelling doaj-f036ec2f0e9d4ab4a5899f4d5053d0822021-02-02T08:22:28ZengEDP SciencesMATEC Web of Conferences2261-236X2015-01-01270300110.1051/matecconf/20152703001matecconf_iceim2015_03001Fabrication of Glucose-Sensitive Layer-by-Layer Films for Potential Controlled Insulin Release ApplicationsTalusan Timothy Jemuel E.0Usman Ken Aldren S.1Payawan Leon M.2Institute of Chemistry, University of the PhilippinesNatural Sciences Research Institute, University of the PhilippinesInstitute of Chemistry, University of the PhilippinesSelf-regulated drug delivery systems (DDS) are potential alternative to the conventional method of introducing insulin to the body due to their controlled drug release mechanism. In this study, Layer-by-Layer technique was utlized to manufacture drug loaded, pH responsive thin films. Insulin was alternated with pH-sensitive, [2-(dimethyl amino) ethyl aminoacrylate] (PDMAEMA) and topped of with polymer/glucose oxidase (GOD) layers. Similarly, films using a different polymer, namely Poly(Acrylic Acid) (PAA) were also fabricated. Exposure of the films to glucose solutions resulted to the production of gluconic acid causing a polymer conformation change due to protonation, thus releasing the embedded insulin. The insulin release was monitored by subjecting the dipping glucose solutions to Bradford Assay. Films exhibited a reversal in drug release profile in the presence of glucose as compared to without glucose. PAA films were also found out to release more insulin compared to that of the PDMAEMA films.The difference in the profile of the two films were due to different polymer-GOD interactions, since both films exhibited almost identical profiles when embedded with Poly(sodium 4-styrenesulfonate) (PSS) instead of GOD.http://dx.doi.org/10.1051/matecconf/20152703001
collection DOAJ
language English
format Article
sources DOAJ
author Talusan Timothy Jemuel E.
Usman Ken Aldren S.
Payawan Leon M.
spellingShingle Talusan Timothy Jemuel E.
Usman Ken Aldren S.
Payawan Leon M.
Fabrication of Glucose-Sensitive Layer-by-Layer Films for Potential Controlled Insulin Release Applications
MATEC Web of Conferences
author_facet Talusan Timothy Jemuel E.
Usman Ken Aldren S.
Payawan Leon M.
author_sort Talusan Timothy Jemuel E.
title Fabrication of Glucose-Sensitive Layer-by-Layer Films for Potential Controlled Insulin Release Applications
title_short Fabrication of Glucose-Sensitive Layer-by-Layer Films for Potential Controlled Insulin Release Applications
title_full Fabrication of Glucose-Sensitive Layer-by-Layer Films for Potential Controlled Insulin Release Applications
title_fullStr Fabrication of Glucose-Sensitive Layer-by-Layer Films for Potential Controlled Insulin Release Applications
title_full_unstemmed Fabrication of Glucose-Sensitive Layer-by-Layer Films for Potential Controlled Insulin Release Applications
title_sort fabrication of glucose-sensitive layer-by-layer films for potential controlled insulin release applications
publisher EDP Sciences
series MATEC Web of Conferences
issn 2261-236X
publishDate 2015-01-01
description Self-regulated drug delivery systems (DDS) are potential alternative to the conventional method of introducing insulin to the body due to their controlled drug release mechanism. In this study, Layer-by-Layer technique was utlized to manufacture drug loaded, pH responsive thin films. Insulin was alternated with pH-sensitive, [2-(dimethyl amino) ethyl aminoacrylate] (PDMAEMA) and topped of with polymer/glucose oxidase (GOD) layers. Similarly, films using a different polymer, namely Poly(Acrylic Acid) (PAA) were also fabricated. Exposure of the films to glucose solutions resulted to the production of gluconic acid causing a polymer conformation change due to protonation, thus releasing the embedded insulin. The insulin release was monitored by subjecting the dipping glucose solutions to Bradford Assay. Films exhibited a reversal in drug release profile in the presence of glucose as compared to without glucose. PAA films were also found out to release more insulin compared to that of the PDMAEMA films.The difference in the profile of the two films were due to different polymer-GOD interactions, since both films exhibited almost identical profiles when embedded with Poly(sodium 4-styrenesulfonate) (PSS) instead of GOD.
url http://dx.doi.org/10.1051/matecconf/20152703001
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