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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Multifunctional antitumor magnetite/chitosan-l-glutamic acid (core/shell) nanocomposites

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Autor(es):
Santos, Daniela P. [1] ; Adolfina Ruiz, M. [2] ; Gallardo, Visitacion [2] ; Zanoni, Maria Valnice B. [1] ; Arias, Jose L. [2]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] UNESP, Univ Sao Paulo State, Inst Chem, BR-14801970 Araraquara, SP - Brazil
[2] Univ Granada, Fac Pharm, Dept Pharm & Pharmaceut Technol, E-18071 Granada - Spain
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: JOURNAL OF NANOPARTICLE RESEARCH; v. 13, n. 9, p. 4311-4323, SEP 2011.
Citações Web of Science: 16
Resumo

The development of anticancer drug delivery systems based on biodegradable nanoparticles has been intended to maximize the localization of chemotherapy agents within tumor interstitium, along with negligible drug distribution into healthy tissues. Interestingly, passive and active drug targeting strategies to cancer have led to improved nanomedicines with great tumor specificity and efficient chemotherapy effect. One of the most promising areas in the formulation of such nanoplatforms is the engineering of magnetically responsive nanoparticles. In this way, we have followed a chemical modification method for the synthesis of magnetite/chitosan-l-glutamic acid (core/shell) nanostructures. These magnetic nanocomposites (average size a parts per thousand 340 nm) exhibited multifunctional properties based on its capability to load the antitumor drug doxorubicin (along with an adequate sustained release) and its potential for hyperthermia applications. Compared to drug surface adsorption, doxorubicin entrapment into the nanocomposites matrix yielded a higher drug loading and a slower drug release profile. Heating characteristics of the magnetic nanocomposites were investigated in a high-frequency alternating magnetic gradient: a stable maximum temperature of 46 A degrees C was successfully achieved within 40 min. To our knowledge, this is the first time that such kind of stimuli-sensitive nanoformulation with very important properties (i.e., magnetic targeting capabilities, hyperthermia, high drug loading, and little burst drug release) has been formulated for combined antitumor therapy against cancer. (AU)

Processo FAPESP: 07/07914-7 - Aplicação de poli ácido glutâmico no estudo de conjugados poliméricos para sistema de liberação controlada de drogas.
Beneficiário:Daniela Pereira dos Santos
Linha de fomento: Bolsas no Brasil - Pós-Doutorado