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1.
J Microencapsul ; 31(3): 254-61, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24124883

RESUMO

A series of graft copolymers consisting of polystyrene backbone with biocompatible side chains based on (co)polymers of l-lactic acid and glycolic acid were synthesised by combination two controlled polymerisations, namely, nitroxide mediated radical polymerisation (NMRP) and ring opening polymerisation (ROP) with "Click" chemistry. The main goal of this work was to design new biodegradable microspheres using obtained graft copolymers for long-term sustained release of imatinib mesylate (IMM) as a model drug. The IMM loaded microspheres of the graft copolymers, polystyrene-g-poly(lactide-co-glycolide) (PS-g-PLLGA), polystyrene-g-poly(lactic acid) (PS-g-PLLA) and poly(lactic-coglycolic acid) (PLLGA) were then prepared by a modified water-in-oil-in-water (w1/o/w2) double emulsion/solvent evaporation technique. The optimised microspheres were characterised by particle size, encapsulation efficiency, and surface morphology also; their degradation and release properties were studied in vitro. The degradation studies of three different types of microspheres showed that the PS backbone of the graft copolymers slows down the degradation rate compared to PLLGA.


Assuntos
Microesferas , Poliglactina 910/química , Poliestirenos/química , Química Click , Preparações de Ação Retardada/química , Preparações de Ação Retardada/farmacocinética , Preparações de Ação Retardada/farmacologia , Emulsões , Tamanho da Partícula , Poliglactina 910/farmacocinética , Poliglactina 910/farmacologia , Poliestirenos/farmacocinética , Poliestirenos/farmacologia
2.
J Mater Sci Mater Med ; 24(1): 147-53, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23053813

RESUMO

Poly(lactic-co-glycolic acid) microspheres loaded with imatinib mesylate has been developed as a new therapeutic strategy to prevent craniopharyngioma recurrence. Microspheres composed of different lactic/glycolic acid ratios, molecular weights and drug compositions were synthesized and loaded with imatinib mesylate by modified double-emulsion/solvent evaporation technique and subsequently characterized by particle-size distribution, scanning electron microscopy, encapsulation efficiency and in vitro drug release. Inhibitory potential of imatinib containing microspheres on tumor neovascularization was investigated on craniopharyngioma tumor samples by rat cornea angiogenesis assay. Results showed that microspheres in different LA:GA ratios [LA:GA 50:50 (G50), 75:25 (G25), 85:15 (G15)] considerably reduced neovascularization induced by recurrent tumor samples in an in vivo angiogenesis assay (P < 0.01). Our data indicate that local delivery of imatinib mesylate to the post-surgical tumoral cavity using biodegradable microspheres may be a promising biologically selective approach to prevent the recurrence of craniopharyngiomas, via inhibition of neovascularization.


Assuntos
Antineoplásicos/administração & dosagem , Benzamidas/administração & dosagem , Craniofaringioma/irrigação sanguínea , Ácido Láctico , Microesferas , Neovascularização Patológica/prevenção & controle , Piperazinas/administração & dosagem , Ácido Poliglicólico , Pirimidinas/administração & dosagem , Cromatografia Líquida de Alta Pressão , Mesilato de Imatinib , Copolímero de Ácido Poliláctico e Ácido Poliglicólico , Espectrofotometria Ultravioleta
3.
Biomacromolecules ; 13(9): 2680-91, 2012 Sep 10.
Artigo em Inglês | MEDLINE | ID: mdl-22866988

RESUMO

The generation and fabrication of nanoscopic structures are of critical technological importance for future implementations in areas such as nanodevices and nanotechnology, biosensing, bioimaging, cancer targeting, and drug delivery. Applications of carbon nanotubes (CNTs) in biological fields have been impeded by the incapability of their visualization using conventional methods. Therefore, fluorescence labeling of CNTs with various probes under physiological conditions has become a significant issue for their utilization in biological processes. Herein, we demonstrate a facile and additional fluorophore-free approach for cancer cell-imaging and diagnosis by combining multiwalled CNTs with a well-known conjugated polymer, namely, poly(p-phenylene) (PP). In this approach, PP decorated with poly(ethylene glycol) (PEG) was noncovalently (π-π stacking) linked to acid-treated CNTs. The obtained water self-dispersible, stable, and biocompatible f-CNT/PP-g-PEG conjugates were then bioconjugated to estrogen-specific antibody (anti-ER) via -COOH functionalities present on the side-walls of CNTs. The resulting conjugates were used as an efficient fluorescent probe for targeted imaging of estrogen receptor overexpressed cancer cells, such as MCF-7. In vitro studies and fluorescence microscopy data show that these conjugates can specifically bind to MCF-7 cells with high efficiency. The represented results imply that CNT-based materials could easily be fabricated by the described approach and used as an efficient "fluorescent probe" for targeting and imaging, thereby providing many new possibilities for various applications in biomedical sensing and diagnosis.


Assuntos
Materiais Biocompatíveis/síntese química , Corantes Fluorescentes/síntese química , Imagem Molecular/métodos , Sondas Moleculares/síntese química , Nanotubos de Carbono/química , Polietilenoglicóis/síntese química , Polímeros/síntese química , Adenocarcinoma/metabolismo , Adenocarcinoma/patologia , Anticorpos/química , Materiais Biocompatíveis/metabolismo , Neoplasias da Mama/metabolismo , Neoplasias da Mama/patologia , Estrogênios/metabolismo , Feminino , Corantes Fluorescentes/metabolismo , Humanos , Imunoconjugados/química , Células MCF-7 , Microscopia Eletrônica de Transmissão , Sondas Moleculares/metabolismo , Polietilenoglicóis/metabolismo , Polímeros/metabolismo , Espectroscopia de Infravermelho com Transformada de Fourier , Análise Espectral Raman , Água
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