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Picoliter‐volume inkjet printing into planar microdevice reservoirs for low‐waste, high‐capacity drug loading
Oral delivery of therapeutics is the preferred route for systemic drug administration due to ease of access and improved patient compliance. However, many therapeutics suffer from low oral bioavailability due to low pH and enzymatic conditions, poor cellular permeability, and low residence time. Mic...
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Published in: | Bioengineering & translational medicine 2017-03, Vol.2 (1), p.9-16 |
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creator | Fox, Cade B. Nemeth, Cameron L. Chevalier, Rachel W. Cantlon, Joshua Bogdanoff, Derek B. Hsiao, Jeff C. Desai, Tejal A. |
description | Oral delivery of therapeutics is the preferred route for systemic drug administration due to ease of access and improved patient compliance. However, many therapeutics suffer from low oral bioavailability due to low pH and enzymatic conditions, poor cellular permeability, and low residence time. Microfabrication techniques have been used to create planar, asymmetric microdevices for oral drug delivery to address these limitations. The geometry of these microdevices facilitates prolonged drug exposure with unidirectional release of drug toward gastrointestinal epithelium. While these devices have significantly enhanced drug permeability in vitro and in vivo, loading drug into the micron‐scale reservoirs of the devices in a low‐waste, high‐capacity manner remains challenging. Here, we use picoliter‐volume inkjet printing to load topotecan and insulin into planar microdevices efficiently. Following a simple surface functionalization step, drug solution can be spotted into the microdevice reservoir. We show that relatively high capacities of both topotecan and insulin can be loaded into microdevices in a rapid, automated process with little to no drug waste. |
doi_str_mv | 10.1002/btm2.10053 |
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However, many therapeutics suffer from low oral bioavailability due to low pH and enzymatic conditions, poor cellular permeability, and low residence time. Microfabrication techniques have been used to create planar, asymmetric microdevices for oral drug delivery to address these limitations. The geometry of these microdevices facilitates prolonged drug exposure with unidirectional release of drug toward gastrointestinal epithelium. While these devices have significantly enhanced drug permeability in vitro and in vivo, loading drug into the micron‐scale reservoirs of the devices in a low‐waste, high‐capacity manner remains challenging. Here, we use picoliter‐volume inkjet printing to load topotecan and insulin into planar microdevices efficiently. Following a simple surface functionalization step, drug solution can be spotted into the microdevice reservoir. We show that relatively high capacities of both topotecan and insulin can be loaded into microdevices in a rapid, automated process with little to no drug waste.</description><identifier>ISSN: 2380-6761</identifier><identifier>EISSN: 2380-6761</identifier><identifier>DOI: 10.1002/btm2.10053</identifier><identifier>PMID: 28503662</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Advantages ; Bioavailability ; Biological products ; drug delivery ; Drug delivery systems ; Drug dosages ; Epithelium ; Hydrogels ; Inkjet printing ; Insulin ; Medical wastes ; Methods ; microdevices ; nanobiotechnology ; Nanotechnology ; Permeability ; Rapid Communication ; Reservoirs ; Silicon wafers ; topotecan</subject><ispartof>Bioengineering & translational medicine, 2017-03, Vol.2 (1), p.9-16</ispartof><rights>2017 The Authors. Bioengineering & Translational Medicine is published by Wiley Periodicals, Inc. on behalf of The American Institute of Chemical Engineers</rights><rights>2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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However, many therapeutics suffer from low oral bioavailability due to low pH and enzymatic conditions, poor cellular permeability, and low residence time. Microfabrication techniques have been used to create planar, asymmetric microdevices for oral drug delivery to address these limitations. The geometry of these microdevices facilitates prolonged drug exposure with unidirectional release of drug toward gastrointestinal epithelium. While these devices have significantly enhanced drug permeability in vitro and in vivo, loading drug into the micron‐scale reservoirs of the devices in a low‐waste, high‐capacity manner remains challenging. Here, we use picoliter‐volume inkjet printing to load topotecan and insulin into planar microdevices efficiently. Following a simple surface functionalization step, drug solution can be spotted into the microdevice reservoir. We show that relatively high capacities of both topotecan and insulin can be loaded into microdevices in a rapid, automated process with little to no drug waste.</description><subject>Advantages</subject><subject>Bioavailability</subject><subject>Biological products</subject><subject>drug delivery</subject><subject>Drug delivery systems</subject><subject>Drug dosages</subject><subject>Epithelium</subject><subject>Hydrogels</subject><subject>Inkjet printing</subject><subject>Insulin</subject><subject>Medical wastes</subject><subject>Methods</subject><subject>microdevices</subject><subject>nanobiotechnology</subject><subject>Nanotechnology</subject><subject>Permeability</subject><subject>Rapid Communication</subject><subject>Reservoirs</subject><subject>Silicon wafers</subject><subject>topotecan</subject><issn>2380-6761</issn><issn>2380-6761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNp9kctuEzEUhi1ERau2Gx4AWWKDECm-jD32BgkqLpWKYFHWlmOfSRxmxsH2JMqOR-AZeRIcUqrCgpWP7U-fzjk_Qo8puaCEsJfzMrB9JfgDdMK4IjPZSvrwXn2MznNeEUKopJyr5hE6ZkoQLiU7QflzcLEPBdLP7z82sZ8GwGH8uoKC1ymMJYyLei8Rr3s72oSH4FL0sAkOcIIMaRNDyriLCfdxWx1bmwu8wMuwWNabs2vrQtlhn6ZFJayvwjN01Nk-w_nteYq-vHt7c_lhdv3p_dXl6-uZ463iM6Uon8u2o153klvSeuGI8iCcb0RnGwKMALj64gTnnlPLtecCOm-J1pzyU_Tq4F1P8wG8g7Ek25s612DTzkQbzN8_Y1iaRdwY0TCp6F7w7FaQ4rcJcjFDyA76ugqIUzZUaU1p0zZNRZ_-g67ilMY6nmFMaSG1lrpSzw9UXWLOCbq7Zigx-zjNPk7zO84KP7nf_h36J7wK0AOwDT3s_qMyb24-soP0F3s-r-Y</recordid><startdate>201703</startdate><enddate>201703</enddate><creator>Fox, Cade B.</creator><creator>Nemeth, Cameron L.</creator><creator>Chevalier, Rachel W.</creator><creator>Cantlon, Joshua</creator><creator>Bogdanoff, Derek B.</creator><creator>Hsiao, Jeff C.</creator><creator>Desai, Tejal A.</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>M7S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201703</creationdate><title>Picoliter‐volume inkjet printing into planar microdevice reservoirs for low‐waste, high‐capacity drug loading</title><author>Fox, Cade B. ; 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subjects | Advantages Bioavailability Biological products drug delivery Drug delivery systems Drug dosages Epithelium Hydrogels Inkjet printing Insulin Medical wastes Methods microdevices nanobiotechnology Nanotechnology Permeability Rapid Communication Reservoirs Silicon wafers topotecan |
title | Picoliter‐volume inkjet printing into planar microdevice reservoirs for low‐waste, high‐capacity drug loading |
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