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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1073/pnas.1322651111</dc:identifier><dc:language>eng</dc:language><dc:creator>Timko, B.P.</dc:creator><dc:creator>Arruebo, M.</dc:creator><dc:creator>Shankarappa, S.A.</dc:creator><dc:creator>McAlvin, J.B.</dc:creator><dc:creator>Okonkwo, O.S.</dc:creator><dc:creator>Mizrahi, B.</dc:creator><dc:creator>Stefanescu, C.F.</dc:creator><dc:creator>Gomez, L.</dc:creator><dc:creator>Zhu, J.</dc:creator><dc:creator>Zhu, A.</dc:creator><dc:creator>Santamaria, J.</dc:creator><dc:creator>Langer, R.</dc:creator><dc:creator>Kohane, D.S.</dc:creator><dc:title>Near-infrared-actuated devices for remotely controlled drug delivery</dc:title><dc:identifier>ART-2014-85449</dc:identifier><dc:description>A reservoir that could be remotely triggered to release a drug would enable the patient or physician to achieve on-demand, reproducible, repeated, and tunable dosing. Such a device would allow precise adjustment of dosage to desired effect, with a consequent minimization of toxicity, and could obviate repeated drug administrations or device implantations, enhancing patient compliance. It should exhibit low off-state leakage to minimize basal effects, and tunable on-state release profiles that could be adjusted from pulsatile to sustained in real time. Despite the clear clinical need for a device that meets these criteria, none has been reported to date to our knowledge. To address this deficiency, we developed an implantable reservoir capped by a nanocomposite membrane whose permeability was modulated by irradiation with a near-infrared laser. Irradiated devices could exhibit sustained on-state drug release for at least 3 h, and could reproducibly deliver short pulses over at least 10 cycles, with an on/off ratio of 30. Devices containing aspart, a fast-acting insulin analog, could achieve glycemic control after s.c. implantation in diabetic rats, with reproducible dosing controlled by the intensity and timing of irradiation over a 2-wk period. These devices can be loaded with a wide range of drug types, and therefore represent a platform technology that might be used to address a wide variety of clinical indications.</dc:description><dc:date>2014</dc:date><dc:source>http://zaguan.unizar.es/record/60874</dc:source><dc:doi>10.1073/pnas.1322651111</dc:doi><dc:identifier>http://zaguan.unizar.es/record/60874</dc:identifier><dc:identifier>oai:zaguan.unizar.es:60874</dc:identifier><dc:identifier.citation>Proceedings of the National Academy of Sciences 111, 4 (2014), 1349-1354</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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