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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Series: | MATEC Web of Conferences |
Online Access: | http://dx.doi.org/10.1051/matecconf/20152703001 |
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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 |
work_keys_str_mv |
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