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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
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