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Investigation of Diffusion Characteristics through Microfluidic Channels for Passive Drug Delivery Applications

Microfluidics has many drug delivery applications due to the ability to easily create complex device designs with feature sizes reaching down to the 10s of microns. In this work, three different microchannel designs for an implantable device are investigated for treatment of ocular diseases such as...

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Autores principales: Goudie, Marcus J., Ghuman, Alyssa P., Collins, Stephanie B., Pidaparti, Ramana M., Handa, Hitesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899604/
https://www.ncbi.nlm.nih.gov/pubmed/27313895
http://dx.doi.org/10.1155/2016/7913616
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author Goudie, Marcus J.
Ghuman, Alyssa P.
Collins, Stephanie B.
Pidaparti, Ramana M.
Handa, Hitesh
author_facet Goudie, Marcus J.
Ghuman, Alyssa P.
Collins, Stephanie B.
Pidaparti, Ramana M.
Handa, Hitesh
author_sort Goudie, Marcus J.
collection PubMed
description Microfluidics has many drug delivery applications due to the ability to easily create complex device designs with feature sizes reaching down to the 10s of microns. In this work, three different microchannel designs for an implantable device are investigated for treatment of ocular diseases such as glaucoma, age-related macular degeneration (AMD), and diabetic retinopathy. Devices were fabricated using polydimethylsiloxane (PDMS) and soft lithography techniques, where surface chemistry of the channels was altered using 2-[methoxy(polyethyleneoxy)propyl]trimethoxysilane (PEG-silane). An estimated delivery rate for a number of common drugs was approximated for each device through the ratio of the diffusion coefficients for the dye and the respective drug. The delivery rate of the model drugs was maintained at a physiological condition and the effects of channel design and surface chemistry on the delivery rate of the model drugs were recorded over a two-week period. Results showed that the surface chemistry of the device had no significant effect on the delivery rate of the model drugs. All designs were successful in delivering a constant daily dose for each model drug.
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spelling pubmed-48996042016-06-16 Investigation of Diffusion Characteristics through Microfluidic Channels for Passive Drug Delivery Applications Goudie, Marcus J. Ghuman, Alyssa P. Collins, Stephanie B. Pidaparti, Ramana M. Handa, Hitesh J Drug Deliv Research Article Microfluidics has many drug delivery applications due to the ability to easily create complex device designs with feature sizes reaching down to the 10s of microns. In this work, three different microchannel designs for an implantable device are investigated for treatment of ocular diseases such as glaucoma, age-related macular degeneration (AMD), and diabetic retinopathy. Devices were fabricated using polydimethylsiloxane (PDMS) and soft lithography techniques, where surface chemistry of the channels was altered using 2-[methoxy(polyethyleneoxy)propyl]trimethoxysilane (PEG-silane). An estimated delivery rate for a number of common drugs was approximated for each device through the ratio of the diffusion coefficients for the dye and the respective drug. The delivery rate of the model drugs was maintained at a physiological condition and the effects of channel design and surface chemistry on the delivery rate of the model drugs were recorded over a two-week period. Results showed that the surface chemistry of the device had no significant effect on the delivery rate of the model drugs. All designs were successful in delivering a constant daily dose for each model drug. Hindawi Publishing Corporation 2016 2016-05-26 /pmc/articles/PMC4899604/ /pubmed/27313895 http://dx.doi.org/10.1155/2016/7913616 Text en Copyright © 2016 Marcus J. Goudie et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Goudie, Marcus J.
Ghuman, Alyssa P.
Collins, Stephanie B.
Pidaparti, Ramana M.
Handa, Hitesh
Investigation of Diffusion Characteristics through Microfluidic Channels for Passive Drug Delivery Applications
title Investigation of Diffusion Characteristics through Microfluidic Channels for Passive Drug Delivery Applications
title_full Investigation of Diffusion Characteristics through Microfluidic Channels for Passive Drug Delivery Applications
title_fullStr Investigation of Diffusion Characteristics through Microfluidic Channels for Passive Drug Delivery Applications
title_full_unstemmed Investigation of Diffusion Characteristics through Microfluidic Channels for Passive Drug Delivery Applications
title_short Investigation of Diffusion Characteristics through Microfluidic Channels for Passive Drug Delivery Applications
title_sort investigation of diffusion characteristics through microfluidic channels for passive drug delivery applications
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899604/
https://www.ncbi.nlm.nih.gov/pubmed/27313895
http://dx.doi.org/10.1155/2016/7913616
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