Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug Delivery
Mesoporous silica nanoparticles have been reported as suitable drug carriers, but their successful delivery to target tissues following systemic administration remains a challenge. In the present work, ultrasound-induced inertial cavitation was evaluated as a mechanism to promote their extravasation...
| Authors: | , , , , , , |
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| Format: | article |
| Publication Date: | 2017 |
| Country: | España |
| Institution: | Universidad Complutense de Madrid (UCM) |
| Repository: | Docta Complutense |
| Language: | English |
| OAI Identifier: | oai:docta.ucm.es:20.500.14352/18311 |
| Online Access: | https://hdl.handle.net/20.500.14352/18311 |
| Access Level: | Open access |
| Keyword: | 546 615.46 Extravasation Nanoparticle Delivery Cavitation Mesoporous Silica Nanoparticles Materiales Química inorgánica (Farmacia) Tecnología farmaceútica 3312 Tecnología de Materiales |
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Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug DeliveryParis, J.L.Mannaris, ChristophorosCabañas Criado, María VictoriaCarlisle, RobertManzano García, MiguelVallet Regí, María Dulce NombreCoussios, Constantin C.546615.46ExtravasationNanoparticle DeliveryCavitationMesoporous Silica NanoparticlesMaterialesQuímica inorgánica (Farmacia)Tecnología farmaceútica3312 Tecnología de MaterialesMesoporous silica nanoparticles have been reported as suitable drug carriers, but their successful delivery to target tissues following systemic administration remains a challenge. In the present work, ultrasound-induced inertial cavitation was evaluated as a mechanism to promote their extravasation in a flow-through tissue mimicking agarose phantom. Two different ultrasound frequencies, 0.5 or 1.6 MHz, with pressures in the range 0.5-4 MPa were used to drive cavitation activity which was detected in real time. The optimal ultrasound conditions identified were employed to deliver dye-loaded nanoparticles as a model for drug-loaded nanocarriers, with the level of extravasation evaluated by fluorescence microscopy. The same nanoparticles were then co-injected with submicrometric polymeric cavitation nuclei as a means to promote cavitation activity and decrease the required in-situ acoustic pressure required to attain extravasation. The overall cavitation energy and penetration of the combination was compared to mesoporous silica nanoparticles alone. The results of the present work suggest that combining mesoporous silica nanocarriers and submcrometric cavitation nuclei may help enhance the extravasation of the nanocarrier, thus enabling subsequent sustained drug release to happen from those particles already embedded in the tumour tissue.ElsevierUniversidad Complutense de Madrid20172017-12-1220172017-12-12journal articlehttp://purl.org/coar/resource_type/c_6501info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/20.500.14352/18311reponame:Docta Complutenseinstname:Universidad Complutense de Madrid (UCM)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:docta.ucm.es:20.500.14352/183112026-06-02T12:44:21Z |
| dc.title.none.fl_str_mv |
Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug Delivery |
| title |
Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug Delivery |
| spellingShingle |
Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug Delivery Paris, J.L. 546 615.46 Extravasation Nanoparticle Delivery Cavitation Mesoporous Silica Nanoparticles Materiales Química inorgánica (Farmacia) Tecnología farmaceútica 3312 Tecnología de Materiales |
| title_short |
Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug Delivery |
| title_full |
Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug Delivery |
| title_fullStr |
Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug Delivery |
| title_full_unstemmed |
Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug Delivery |
| title_sort |
Ultrasound-Mediated Cavitation-Enhanced Extravasation of Mesoporous Silica Nanoparticles for Controlled-Release Drug Delivery |
| dc.creator.none.fl_str_mv |
Paris, J.L. Mannaris, Christophoros Cabañas Criado, María Victoria Carlisle, Robert Manzano García, Miguel Vallet Regí, María Dulce Nombre Coussios, Constantin C. |
| author |
Paris, J.L. |
| author_facet |
Paris, J.L. Mannaris, Christophoros Cabañas Criado, María Victoria Carlisle, Robert Manzano García, Miguel Vallet Regí, María Dulce Nombre Coussios, Constantin C. |
| author_role |
author |
| author2 |
Mannaris, Christophoros Cabañas Criado, María Victoria Carlisle, Robert Manzano García, Miguel Vallet Regí, María Dulce Nombre Coussios, Constantin C. |
| author2_role |
author author author author author author |
| dc.contributor.none.fl_str_mv |
Universidad Complutense de Madrid |
| dc.subject.none.fl_str_mv |
546 615.46 Extravasation Nanoparticle Delivery Cavitation Mesoporous Silica Nanoparticles Materiales Química inorgánica (Farmacia) Tecnología farmaceútica 3312 Tecnología de Materiales |
| topic |
546 615.46 Extravasation Nanoparticle Delivery Cavitation Mesoporous Silica Nanoparticles Materiales Química inorgánica (Farmacia) Tecnología farmaceútica 3312 Tecnología de Materiales |
| description |
Mesoporous silica nanoparticles have been reported as suitable drug carriers, but their successful delivery to target tissues following systemic administration remains a challenge. In the present work, ultrasound-induced inertial cavitation was evaluated as a mechanism to promote their extravasation in a flow-through tissue mimicking agarose phantom. Two different ultrasound frequencies, 0.5 or 1.6 MHz, with pressures in the range 0.5-4 MPa were used to drive cavitation activity which was detected in real time. The optimal ultrasound conditions identified were employed to deliver dye-loaded nanoparticles as a model for drug-loaded nanocarriers, with the level of extravasation evaluated by fluorescence microscopy. The same nanoparticles were then co-injected with submicrometric polymeric cavitation nuclei as a means to promote cavitation activity and decrease the required in-situ acoustic pressure required to attain extravasation. The overall cavitation energy and penetration of the combination was compared to mesoporous silica nanoparticles alone. The results of the present work suggest that combining mesoporous silica nanocarriers and submcrometric cavitation nuclei may help enhance the extravasation of the nanocarrier, thus enabling subsequent sustained drug release to happen from those particles already embedded in the tumour tissue. |
| publishDate |
2017 |
| dc.date.none.fl_str_mv |
2017 2017-12-12 2017 2017-12-12 |
| dc.type.none.fl_str_mv |
journal article http://purl.org/coar/resource_type/c_6501 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/20.500.14352/18311 |
| url |
https://hdl.handle.net/20.500.14352/18311 |
| dc.language.none.fl_str_mv |
Inglés eng |
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Inglés |
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eng |
| dc.rights.none.fl_str_mv |
open access http://purl.org/coar/access_right/c_abf2 |
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info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 |
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openAccess |
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application/pdf |
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Elsevier |
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Elsevier |
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reponame:Docta Complutense instname:Universidad Complutense de Madrid (UCM) |
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Universidad Complutense de Madrid (UCM) |
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Docta Complutense |
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Docta Complutense |
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