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Toxic potential evaluation of optical contact lenses based on bacterial cellulose with addition of drug-cyclodextrin complexes coated with organ

Grant number: 12/12594-0
Support type:Scholarships in Brazil - Scientific Initiation
Effective date (Start): September 01, 2012
Effective date (End): March 31, 2016
Field of knowledge:Biological Sciences - Genetics - Mutagenesis
Principal researcher:Ticiana Sidorenko de Oliveira Capote
Grantee:Fernanda Coelho
Home Institution: Faculdade de Odontologia (FOAr). Universidade Estadual Paulista (UNESP). Campus de Araraquara. Araraquara , SP, Brazil


This project is part of a larger research project ever awarded by the Regular Research Grants FAPESP (Process 2011/11810-8). In the last years, biotechnology has advanced in the development of biomaterials for tissue regeneration and for their utilization as medical devices. In this context, reabsorbed membranes have shown promising results in tissue regeneration that can be used in the healing of skin wounds, grafts, drug delivery systems, and tissue engineering. The Institute of Chemistry at Araraquara - IQ UNESP has developed composites based on bacterial cellulose (BC) for utilization as contact lenses (patent deposited). During the preparation of the lenses, in order to increase the transparency, it is intended to recover the lenses with a hybrid organic-inorganic composite (which contains aluminum alkoxide nanoparticles and GPTMS (glicidoxipropiltrimetoxisilano). Drugs like ciprofloxacin and sodium diclofenac will be incorporated into these contact lenses to improve their therapeutic properties. However, in order to ensure the safe use of these composites by the medical device industry, it is necessary to evaluate whether they have cytotoxic, genotoxic, and mutagenic activities. This important partnership among researchers from the IQ, FOAr (Araraquara - UNESP), and the University of São Paulo (USP) will evaluate the cytotoxic, genotoxic, and mutagenic potential of these biomaterials. Besides cytotoxicity, it is very important to evaluate the genotoxic and mutagenic potential of these biomaterials, because, if the biomaterials provide such risks, they can induce cellular modifications in the surrounding tissue, with possible progression to tumor formation (carcinogenesis). In vitro tests will be performed to verify if the materials have cytotoxic (XTT and clonogenic survival tests), genotoxic (comet), and mutagenic (micronucleus) potentials. Statistical analysis will be used to assess whether the biomaterials are cytotoxic, genotoxic, and/ or mutagenic. This information is essential for the safe release of the biomaterial in future employment in the medical device industry.(AU)

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