Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory Environments
Luminescent nanoparticles are innovative tools for medicine, allowing the imaging of cells and tissues, and, at the same time, carrying and releasing different types of molecules. We explored and compared the loading/release ability of diclofenac (COX-2 antagonist), in both undoped-and luminescent T...
| Authors: | , , , , , , , , |
|---|---|
| Format: | article |
| Status: | Published version |
| Publication Date: | 2022 |
| Country: | España |
| Institution: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repository: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/334094 |
| Online Access: | http://hdl.handle.net/10261/334094 |
| Access Level: | Open access |
| Keyword: | Inflammation treatment Diclofenac-loaded nanoparticles apatite Tb3+-doped apatite Luminescence Cytocompatibility Apatite |
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Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory EnvironmentsCano Plá, Sandra MaríaD’Urso, AnnaritaFernández-Sánchez, Jorge F.Colangelo, DonatoChoquesillo-Lazarte, DuaneFerracini, RicardoBosetti, MichelaPrat, MariaGómez-Morales, JaimeInflammation treatmentDiclofenac-loaded nanoparticlesapatiteTb3+-doped apatiteLuminescenceCytocompatibilityApatiteLuminescent nanoparticles are innovative tools for medicine, allowing the imaging of cells and tissues, and, at the same time, carrying and releasing different types of molecules. We explored and compared the loading/release ability of diclofenac (COX-2 antagonist), in both undoped-and luminescent Terbium (Tb)-doped citrate-coated carbonated apatite nanoparticles at different temperatures (25, 37, 40 °C) and pHs (7.4, 5.2). The cytocompatibility was evaluated on two osteosarcoma cell lines and primary human osteoblasts. Biological effects of diclofenac-loadednanoparticles were monitored in an in vitro osteoblast’s cytokine–induced inflammation model by evaluating COX-2 mRNA expression and production of PGE2. Adsorption isotherms fitted the multilayer Langmuir-Freundlich model. The maximum adsorbed amounts at 37 °C were higher than at 25 °C, and particularly when using the Tb-doped particles. Diclofenac-release efficiencies were higher at pH 5.2, a condition simulating a local inflammation. The luminescence properties of diclofenac-loaded Tb-doped particles were affected by pH, being the relative luminescence intensity higher at pH 5.2 and the luminescence lifetime higher at pH 7.4, but not influenced either by the temperature or by the diclofenac-loaded amount. Both undoped and Tb-doped nanoparticles were cytocompatible. In addition, diclofenac release increased COX-2 expression and decreased PGE2 production in an in vitro inflammation model. These findings evidence the potential of these nanoparticles for osteo-localized delivery of anti-inflammatory drugs and the possibility to localize the inflammation, characterized by a decrease in pH, by changes in luminescence.We thank Universidad Jorge Tadeo Lozano (Utadeo), National Natural Parks, and the Corales de Profundidad Natural National Park (CPNNP) for their funding and support. The results are products of UTADEO’s projects Ecología y biología del pez león en dos ambientes contrastantes del Caribe colombiano. Fase V (código 822-15-17) and Invasiones biológicas en ambientes tropicales marinos: el caso del pez león (código 901-17-18), and they are within the framework of the subprogram Handling of invading species in the CPNNP. We would like to thank Deibis Seguro from Scuba Cartagena and the Diving Division and Rescue of the National Navy for their support in the capture field trips. Observations with ROV and drifting cameras were made within the projects PRY-BEM-012-14 and Mapeo de la distribución del ensamblaje de Madracis spp., which were funded by Invemar, ANH, and National Parks. We would like to thank Gabriel Navas Suárez and Adriana Bermúdez Tobón for their support in the laboratories of Universidad de Cartagena. Christian Sánchez Díaz prepared the cartography. We would also like to thank the undergraduate and graduate students that cooperated with sample processing, especially Nireth Sierra Sabalza, Shirly Bello Escobar, María Castellanos Jiménez, Margui Almario García, María Rodríguez, and Zuleima Vides Pedrozo. ASM received funding from MincienciasMultidisciplinary Digital Publishing InstituteConsejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]2023202320222023info:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501Publisher's versioninfo:eu-repo/semantics/publishedVersionhttp://hdl.handle.net/10261/334094reponame:DIGITAL.CSIC. Repositorio Institucional del CSICinstname:Consejo Superior de Investigaciones Científicas (CSIC)Ingléshttp://dx.doi.org/10.3390/nano12030562Síinfo:eu-repo/semantics/openAccessoai:digital.csic.es:10261/3340942026-05-22T06:33:51Z |
| dc.title.none.fl_str_mv |
Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory Environments |
| title |
Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory Environments |
| spellingShingle |
Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory Environments Cano Plá, Sandra María Inflammation treatment Diclofenac-loaded nanoparticles apatite Tb3+-doped apatite Luminescence Cytocompatibility Apatite |
| title_short |
Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory Environments |
| title_full |
Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory Environments |
| title_fullStr |
Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory Environments |
| title_full_unstemmed |
Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory Environments |
| title_sort |
Biomimetic Citrate-Coated Luminescent Apatite Nanoplatforms for Diclofenac Delivery in Inflammatory Environments |
| dc.creator.none.fl_str_mv |
Cano Plá, Sandra María D’Urso, Annarita Fernández-Sánchez, Jorge F. Colangelo, Donato Choquesillo-Lazarte, Duane Ferracini, Ricardo Bosetti, Michela Prat, Maria Gómez-Morales, Jaime |
| author |
Cano Plá, Sandra María |
| author_facet |
Cano Plá, Sandra María D’Urso, Annarita Fernández-Sánchez, Jorge F. Colangelo, Donato Choquesillo-Lazarte, Duane Ferracini, Ricardo Bosetti, Michela Prat, Maria Gómez-Morales, Jaime |
| author_role |
author |
| author2 |
D’Urso, Annarita Fernández-Sánchez, Jorge F. Colangelo, Donato Choquesillo-Lazarte, Duane Ferracini, Ricardo Bosetti, Michela Prat, Maria Gómez-Morales, Jaime |
| author2_role |
author author author author author author author author |
| dc.contributor.none.fl_str_mv |
Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72] |
| dc.subject.none.fl_str_mv |
Inflammation treatment Diclofenac-loaded nanoparticles apatite Tb3+-doped apatite Luminescence Cytocompatibility Apatite |
| topic |
Inflammation treatment Diclofenac-loaded nanoparticles apatite Tb3+-doped apatite Luminescence Cytocompatibility Apatite |
| description |
Luminescent nanoparticles are innovative tools for medicine, allowing the imaging of cells and tissues, and, at the same time, carrying and releasing different types of molecules. We explored and compared the loading/release ability of diclofenac (COX-2 antagonist), in both undoped-and luminescent Terbium (Tb)-doped citrate-coated carbonated apatite nanoparticles at different temperatures (25, 37, 40 °C) and pHs (7.4, 5.2). The cytocompatibility was evaluated on two osteosarcoma cell lines and primary human osteoblasts. Biological effects of diclofenac-loadednanoparticles were monitored in an in vitro osteoblast’s cytokine–induced inflammation model by evaluating COX-2 mRNA expression and production of PGE2. Adsorption isotherms fitted the multilayer Langmuir-Freundlich model. The maximum adsorbed amounts at 37 °C were higher than at 25 °C, and particularly when using the Tb-doped particles. Diclofenac-release efficiencies were higher at pH 5.2, a condition simulating a local inflammation. The luminescence properties of diclofenac-loaded Tb-doped particles were affected by pH, being the relative luminescence intensity higher at pH 5.2 and the luminescence lifetime higher at pH 7.4, but not influenced either by the temperature or by the diclofenac-loaded amount. Both undoped and Tb-doped nanoparticles were cytocompatible. In addition, diclofenac release increased COX-2 expression and decreased PGE2 production in an in vitro inflammation model. These findings evidence the potential of these nanoparticles for osteo-localized delivery of anti-inflammatory drugs and the possibility to localize the inflammation, characterized by a decrease in pH, by changes in luminescence. |
| publishDate |
2022 |
| dc.date.none.fl_str_mv |
2022 2023 2023 2023 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article http://purl.org/coar/resource_type/c_6501 Publisher's version info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10261/334094 |
| url |
http://hdl.handle.net/10261/334094 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
http://dx.doi.org/10.3390/nano12030562 Sí |
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info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.publisher.none.fl_str_mv |
Multidisciplinary Digital Publishing Institute |
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Multidisciplinary Digital Publishing Institute |
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reponame:DIGITAL.CSIC. Repositorio Institucional del CSIC instname:Consejo Superior de Investigaciones Científicas (CSIC) |
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Consejo Superior de Investigaciones Científicas (CSIC) |
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DIGITAL.CSIC. Repositorio Institucional del CSIC |
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DIGITAL.CSIC. Repositorio Institucional del CSIC |
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