Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluation
- Autores
- Juárez, Juliana; Cussa , jorgelina; Gómez Costa, Marcos Bruno
- Año de publicación
- 2025
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión aceptada
- Descripción
- The development of functional mesoporous carriers offers a promising strategy for enhancing the solubility and controlled release of poorly water-soluble drugs. This study aims to design and evaluate tert-butylamine-functionalized large-pore SBA-15 (LP-SBA-15) as an efficient carrier for loratadine (LORA). LP-SBA-15 was synthesized using a micelle-expanding agent and subsequently functionalized with TBA groups. Structural integrity and chemical modifications were confirmed through XRD, TEM, FTIR, and UV–Vis analyses. Nitrogen physisorption was used to assess textural changes after functionalization and drug loading. Drug loading content (DLC) and release profiles were determined spectrophotometrically, and release kinetics were modeled using Ritger–Peppas, Higuchi, and Weibull equations. The mesostructure was preserved after modification, while surface area and pore volume decreased, confirming successful functionalization. Drug loading capacity increased markedly from 22.5% (LP-SBA-15) to 62.5% (LPSBA-15-TBA). Release studies showed that unmodified LP-SBA-15 exhibited a rapid initial burst, whereas the TBA-functionalized material exhibited a gradual and sustained release. Kinetic fitting indicated a diffusion-controlled mechanism. LP-SBA-15-TBA proved to be a robust platform for loratadine delivery, combining high drug loading with sustained release. This strategy could improvetherapeutic efficacy, reduce dosing frequency, and enhance patient compliance.
Fil: Juárez, Juliana. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Cussa, Jorgelina. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Gómez Costa, Marcos Bruno. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Peer Reviewed - Fuente
- REVISTA DE CIENCIA DE MATERIALES, vol. 61 (págs. 2960-2974)
- Materia
-
Loratadine
LP-SBA-15
TBA
Drug delivery - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- Attribution-NonCommercial-NoDerivs 2.5 Argentina
- Repositorio
.jpg)
- Institución
- Universidad Tecnológica Nacional
- OAI Identificador
- oai:ria.utn.edu.ar:20.500.12272/15512
Ver los metadatos del registro completo
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Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluationJuárez, JulianaCussa , jorgelinaGómez Costa, Marcos BrunoLoratadineLP-SBA-15TBADrug deliveryThe development of functional mesoporous carriers offers a promising strategy for enhancing the solubility and controlled release of poorly water-soluble drugs. This study aims to design and evaluate tert-butylamine-functionalized large-pore SBA-15 (LP-SBA-15) as an efficient carrier for loratadine (LORA). LP-SBA-15 was synthesized using a micelle-expanding agent and subsequently functionalized with TBA groups. Structural integrity and chemical modifications were confirmed through XRD, TEM, FTIR, and UV–Vis analyses. Nitrogen physisorption was used to assess textural changes after functionalization and drug loading. Drug loading content (DLC) and release profiles were determined spectrophotometrically, and release kinetics were modeled using Ritger–Peppas, Higuchi, and Weibull equations. The mesostructure was preserved after modification, while surface area and pore volume decreased, confirming successful functionalization. Drug loading capacity increased markedly from 22.5% (LP-SBA-15) to 62.5% (LPSBA-15-TBA). Release studies showed that unmodified LP-SBA-15 exhibited a rapid initial burst, whereas the TBA-functionalized material exhibited a gradual and sustained release. Kinetic fitting indicated a diffusion-controlled mechanism. LP-SBA-15-TBA proved to be a robust platform for loratadine delivery, combining high drug loading with sustained release. This strategy could improvetherapeutic efficacy, reduce dosing frequency, and enhance patient compliance.Fil: Juárez, Juliana. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Fil: Cussa, Jorgelina. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Fil: Gómez Costa, Marcos Bruno. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Peer ReviewedSALTADOR2026-09-10T19:51:48Z2025info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articulopdfapplication/pdfREVISTA DE CIENCIA DE MATERIALES, vol. 61 (págs. 2960-2974) - ISSN 0022-2461 SPRINGER0022-2461https://hdl.handle.net/20.500.12272/15512REVISTA DE CIENCIA DE MATERIALES, vol. 61 (págs. 2960-2974)reponame:Repositorio Institucional Abierto (UTN)instname:Universidad Tecnológica Nacionalenginfo:eu-repo/semantics/openAccessAttribution-NonCommercial-NoDerivs 2.5 Argentinahttp://creativecommons.org/licenses/by-nc-nd/2.5/ar/JUAREZ, JULIANA ; CUSSA, JORGELINA ; GOMEZ COSTA, MARCOS BRUNOhttps://creativecommons.org/licenses/by-nc-nd/4.0/2026-09-24T12:44:13Zoai:ria.utn.edu.ar:20.500.12272/15512instacron:UTNInstitucionalhttp://ria.utn.edu.ar/Universidad públicaNo correspondehttp://ria.utn.edu.ar/oaigestionria@rec.utn.edu.ar; fsuarez@rec.utn.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:a2026-09-24 12:44:14.457Repositorio Institucional Abierto (UTN) - Universidad Tecnológica Nacionalfalse |
| dc.title.none.fl_str_mv |
Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluation |
| title |
Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluation |
| spellingShingle |
Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluation Juárez, Juliana Loratadine LP-SBA-15 TBA Drug delivery |
| title_short |
Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluation |
| title_full |
Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluation |
| title_fullStr |
Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluation |
| title_full_unstemmed |
Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluation |
| title_sort |
Functional LP-SBA-15/tert-butylamine nanocarriers for loratadine: synthesis, characterization, and controlled release evaluation |
| dc.creator.none.fl_str_mv |
Juárez, Juliana Cussa , jorgelina Gómez Costa, Marcos Bruno |
| author |
Juárez, Juliana |
| author_facet |
Juárez, Juliana Cussa , jorgelina Gómez Costa, Marcos Bruno |
| author_role |
author |
| author2 |
Cussa , jorgelina Gómez Costa, Marcos Bruno |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
Loratadine LP-SBA-15 TBA Drug delivery |
| topic |
Loratadine LP-SBA-15 TBA Drug delivery |
| dc.description.none.fl_txt_mv |
The development of functional mesoporous carriers offers a promising strategy for enhancing the solubility and controlled release of poorly water-soluble drugs. This study aims to design and evaluate tert-butylamine-functionalized large-pore SBA-15 (LP-SBA-15) as an efficient carrier for loratadine (LORA). LP-SBA-15 was synthesized using a micelle-expanding agent and subsequently functionalized with TBA groups. Structural integrity and chemical modifications were confirmed through XRD, TEM, FTIR, and UV–Vis analyses. Nitrogen physisorption was used to assess textural changes after functionalization and drug loading. Drug loading content (DLC) and release profiles were determined spectrophotometrically, and release kinetics were modeled using Ritger–Peppas, Higuchi, and Weibull equations. The mesostructure was preserved after modification, while surface area and pore volume decreased, confirming successful functionalization. Drug loading capacity increased markedly from 22.5% (LP-SBA-15) to 62.5% (LPSBA-15-TBA). Release studies showed that unmodified LP-SBA-15 exhibited a rapid initial burst, whereas the TBA-functionalized material exhibited a gradual and sustained release. Kinetic fitting indicated a diffusion-controlled mechanism. LP-SBA-15-TBA proved to be a robust platform for loratadine delivery, combining high drug loading with sustained release. This strategy could improvetherapeutic efficacy, reduce dosing frequency, and enhance patient compliance. Fil: Juárez, Juliana. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina. Fil: Cussa, Jorgelina. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina. Fil: Gómez Costa, Marcos Bruno. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina. Peer Reviewed |
| description |
The development of functional mesoporous carriers offers a promising strategy for enhancing the solubility and controlled release of poorly water-soluble drugs. This study aims to design and evaluate tert-butylamine-functionalized large-pore SBA-15 (LP-SBA-15) as an efficient carrier for loratadine (LORA). LP-SBA-15 was synthesized using a micelle-expanding agent and subsequently functionalized with TBA groups. Structural integrity and chemical modifications were confirmed through XRD, TEM, FTIR, and UV–Vis analyses. Nitrogen physisorption was used to assess textural changes after functionalization and drug loading. Drug loading content (DLC) and release profiles were determined spectrophotometrically, and release kinetics were modeled using Ritger–Peppas, Higuchi, and Weibull equations. The mesostructure was preserved after modification, while surface area and pore volume decreased, confirming successful functionalization. Drug loading capacity increased markedly from 22.5% (LP-SBA-15) to 62.5% (LPSBA-15-TBA). Release studies showed that unmodified LP-SBA-15 exhibited a rapid initial burst, whereas the TBA-functionalized material exhibited a gradual and sustained release. Kinetic fitting indicated a diffusion-controlled mechanism. LP-SBA-15-TBA proved to be a robust platform for loratadine delivery, combining high drug loading with sustained release. This strategy could improvetherapeutic efficacy, reduce dosing frequency, and enhance patient compliance. |
| publishDate |
2025 |
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2025 2026-09-10T19:51:48Z |
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info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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acceptedVersion |
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REVISTA DE CIENCIA DE MATERIALES, vol. 61 (págs. 2960-2974) - ISSN 0022-2461 SPRINGER 0022-2461 https://hdl.handle.net/20.500.12272/15512 |
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REVISTA DE CIENCIA DE MATERIALES, vol. 61 (págs. 2960-2974) - ISSN 0022-2461 SPRINGER 0022-2461 |
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https://hdl.handle.net/20.500.12272/15512 |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
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info:eu-repo/semantics/openAccess Attribution-NonCommercial-NoDerivs 2.5 Argentina http://creativecommons.org/licenses/by-nc-nd/2.5/ar/ JUAREZ, JULIANA ; CUSSA, JORGELINA ; GOMEZ COSTA, MARCOS BRUNO https://creativecommons.org/licenses/by-nc-nd/4.0/ |
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openAccess |
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Attribution-NonCommercial-NoDerivs 2.5 Argentina http://creativecommons.org/licenses/by-nc-nd/2.5/ar/ JUAREZ, JULIANA ; CUSSA, JORGELINA ; GOMEZ COSTA, MARCOS BRUNO https://creativecommons.org/licenses/by-nc-nd/4.0/ |
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SALTADOR |
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