Detalhes do Documento

Zeolite structures loading with an anticancer compound as drug delivery systems

Autor(es): Amorim, Ricardo cv logo 1 ; Vilaça, Natália cv logo 2 ; Martinho, Olga cv logo 3 ; Reis, R. M. cv logo 4 ; Sardo, Mariana cv logo 5 ; Rocha, João cv logo 6 ; Fonseca, António Manuel cv logo 7 ; Baltazar, Fátima cv logo 8 ; Neves, Isabel C. cv logo 9

Data: 2012

Identificador Persistente: http://hdl.handle.net/1822/23807

Origem: RepositóriUM - Universidade do Minho


Descrição
The authors are thankful to Dr. A. S. Azevedo for collecting the powder diffraction data. Two different structures of zeolites, faujasite (FAU) and Linde type A (LTA), were studied to investigate their suitability for drug delivery systems (DDS). The zeolites in the sodium form (NaY and NaA) were used as hosts for encapsulation of α-cyano-4- hydroxycinnamic acid (CHC). CHC, an experimental anticancer drug, was encapsulated in both zeolites by diffusion in liquid phase. These new drug delivery systems, CHC@zeolite, were characterized by spectroscopic techniques (FTIR, 1H NMR, 13C and 27Al solidstate MAS NMR, and UV−vis), chemical analysis, powder X-ray diffraction (XRD) and scanning electron microscopy (SEM). The effect of the zeolites and CHC@zeolite drug deliveries on HCT-15 human colon carcinoma cell line viability was evaluated. Both zeolites alone revealed no toxicity to HCT-15 cancer cells. Importantly, CHC@zeolite exhibit an inhibition of cell viability up to 585-fold, when compared to the non-encapsulated drug. These results indicate the potential of the zeolites for drug loading and delivery into cancer cells to induce cell death
Tipo de Documento Artigo
Idioma Inglês
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