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dc.contributor.author
Nunes, Adenia Mirela Alves  
dc.contributor.author
de Oliveira Alves Júnior, José  
dc.contributor.author
Springer, Valeria Haydee  
dc.contributor.author
Júnior, João Augusto Oshiro  
dc.date.available
2025-03-31T14:01:07Z  
dc.date.issued
2024-08  
dc.identifier.citation
Nunes, Adenia Mirela Alves; de Oliveira Alves Júnior, José; Springer, Valeria Haydee; Júnior, João Augusto Oshiro; Intelligent Systems based on Cyclodextrins for the Treatment of Breast Cancer; Bentham Science Publishers; Current Pharmaceutical Design; 30; 30; 8-2024; 2345-2363  
dc.identifier.issn
1381-6128  
dc.identifier.uri
http://hdl.handle.net/11336/257687  
dc.description.abstract
The incidence of breast cancer has been increasing over the last four decades, although the mortality rate has decreased. Endocrine therapy and chemotherapy are the most used options for cancer treatment but several obstacles are still attributed to these therapies. Smart materials, such as nanocarriers for targeting, delivery and release of active ingredients, sensitive to intrinsic-stimuli (pH-responsive, redox-responsive, enzyme- responsive, and thermo-responsive) and extrinsic-stimuli (ultrasound-responsive, magnetic-responsive, light-responsive) have been studied as a novel strategy in breast cancer therapy. Cyclodextrins (CDs) are used in the design of these stimuli-responsive drug carrier and delivery systems, either through inclusion complexes with hydrophobic molecules or covalent bonds with large structures to generate new materials. The present work aims to gather and integrate recent data from in vitro and in vivo preclinical studies of CD-based stimuli- responsive systems to contribute to the research in treating breast cancer. All drug carriers showed high in vitro release rates in the presence of a stimulus. The stimuli-responsive nanoplatforms presented biocompatibility and satisfactory results of IC50, inhibition of cell viability and antitumor activity against several breast cancer cell lines. Additionally, these systems led to a significant reduction in drug dosages, which encouraged possible clinical studies for better alternatives to traditional antitumor therapies.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Bentham Science Publishers  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
RESPONSIVE SYSTEMS  
dc.subject
CANCER CELLS  
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EXTRINSIC STIMULUS  
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INTRINSIC STIMULUS  
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NANOCARRIERS  
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POLYMERIC SYSTEMS  
dc.subject.classification
Otras Ciencias de la Salud  
dc.subject.classification
Ciencias de la Salud  
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Intelligent Systems based on Cyclodextrins for the Treatment of Breast Cancer  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2024-12-26T13:37:46Z  
dc.journal.volume
30  
dc.journal.number
30  
dc.journal.pagination
2345-2363  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Oak Park  
dc.description.fil
Fil: Nunes, Adenia Mirela Alves. Universidade Estadual da Paraiba; Brasil  
dc.description.fil
Fil: de Oliveira Alves Júnior, José. Universidade Estadual da Paraiba; Brasil  
dc.description.fil
Fil: Springer, Valeria Haydee. Universidad Nacional del Sur. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina  
dc.description.fil
Fil: Júnior, João Augusto Oshiro. Universidade Estadual da Paraiba; Brasil  
dc.journal.title
Current Pharmaceutical Design  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.eurekaselect.com/231614/article  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.2174/0113816128291108240613094515