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Controlled Cisplatin Delivery from Ureasil-PEO1900 Hybrid Matrix
  • Universidade Estadual Paulista (UNESP)
  • Synchrotron SOLEIL LOrme Merisiers
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
  • French CORECUB agency
Sponsorship Process Number: 
French CORECUB agency: 564/07
The ability of assembling inorganic, organic, and even bioactive components ill a single material unfolds all exciting direction in the development of novel Multifunctional hybrid materials. Recently, we have observed that the hydrophilic/hydrophobic character of the organic polymeric moieties determines the swelling/diffusion control of the drug release. In this work, the antitumor cisplatin (CisPt) molecules incorporated into the ureasil-PEO (poly(ethylene oxide)) hybrid material Was used as a probe for the in Situ and simultaneous UV-vis and Raman spectroscopies monitoring of the kinetics of both the water uptake as well as the CisPt release by the hybrid matrix. Drug molecules were incorporated during the hydrolysis and polycondensation steps. The monolithic xerogel were analyzed by X-ray absorption spectroscopy and differential scanning calorimetry, while the drug release properties were monitored by Raman its well as UV-vis spectroscopies. The results show that the molecular structure of the CisPt is preserved in the one pot sol-gel route used in synthesizing the CisPt-loaded PEO 1900 hybrid. The in Situ monitoring of water uptake clearly points Out the key contribution of the osmotic How oil the stepped profile of the CisPt delivered from the PEO 1900 hybrid matrix.
Issue Date: 
Journal of Physical Chemistry B. Washington: Amer Chemical Soc, v. 114, n. 10, p. 3461-3466, 2010.
Time Duration: 
Amer Chemical Soc
Access Rights: 
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Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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