| Grant number: | 14/16727-0 |
| Support Opportunities: | Scholarships in Brazil - Master |
| Start date: | April 01, 2015 |
| End date: | October 31, 2016 |
| Field of knowledge: | Health Sciences - Pharmacy - Pharmaceutical Technology |
| Agreement: | Coordination of Improvement of Higher Education Personnel (CAPES) |
| Principal Investigator: | Priscyla Daniely Marcato Gaspari |
| Grantee: | Ivana Pereira Santos Carvalho |
| Host Institution: | Faculdade de Ciências Farmacêuticas de Ribeirão Preto (FCFRP). Universidade de São Paulo (USP). Ribeirão Preto , SP, Brazil |
Abstract Carcinoma of the urinary bladder (CB) is the second most common malignancy of the urinary tract. In Brazil there are about 3200 deaths per year resulting from this type of cancer. Currently, the main CB therapies include immunotherapy with BCG and chemotherapy. But the effectiveness of these therapies is low, have a high recurrence rate and several adverse effects. Thus, there is a demand for novel therapeutic strategies such as the use of compounds extracted from plants such as glycoalkaloids, solasonine and solamargine, extracted from the fruit of the plant Solanum lycocarpum. These glycoalkaloids have antioxidant and anticarcinogenic properties acting in different interesting molecular mechanisms for cancer therapy. However, intravesical administration of drugs in the treatment of CB is a challenge, since the drugs have low permeability in the urothelium, low residence time in the bladder, due to periodic bladder emptying and filling. Furthermore, several administrations are needed, which causes high incidences of infections and local pain. Thus, a strategy to overcome these challenges is the application of nanomedicine, especially, the sustained release systems. In this line, this project aims at the development and characterization of Solid Lipid Nanoparticles (SLN) as carrier systems of extract of S. lycocarpum, in order to obtain a nanostructured system for intravesical therapy of bladder cancer. The NLS will be prepared by microemulsion and sonication method. The particles will be characterized regarding the size and zeta potential by photon correlation spectroscopy, morphology by atomic force microscopy and crystallinity by differential scanning calorimetry. In addition, the encapsulation efficiency and the mucoadhesive property of the NLS will be evaluated. The effectiveness of the developed nanostructured systems will be evaluated for cytotoxicity assays in vitro in cells of bladder cancer using 2D and 3D cell culture model. (AU) | |
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