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Drug Release Evaluation of Mesoporous TiO2: A Nano Carrier for Duloxetine

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Part of the book series: Communications in Computer and Information Science ((CCIS,volume 341))

Abstract

Mesoporous TiO2 was synthesized solvothermally, but its XRD pattern proved little randomly arranged mesopores. Its DRS-UV-Vis spectrum showed characteristic band gap excitation just below 400 nm and oxygen to metal charge transfer close to 250 nm. It was loaded with the model drug duloxetine (DX) by wet method. Locked-in drug within the mesopores of TiO2 was confirmed by XRD, DRS-UV-Vis and FT-IR techniques. About 11% loading of drug was verified by UV-Vis spectroscopy. The study of drug release showed two stages of burst release between 0 and 12 h and beyond that slow extended release of DX occurred. The total burst release was equal to 20%, and even at the end of 40 h the total release was equal to 90%. Hence, mesoporous TiO2 was established as a viable, biocompatible DX reservoir for its controlled release. The same mesoporous TiO2 could be convenient for the release of potentially toxic drugs which require small and extended dose.

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© 2012 Springer-Verlag Berlin Heidelberg

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Ganesh, M., Hemalatha, P., Peng, M.M., Cha, W.S., Palanichamy, M., Jang, H.T. (2012). Drug Release Evaluation of Mesoporous TiO2: A Nano Carrier for Duloxetine. In: Kim, Th., Ramos, C., Abawajy, J., Kang, BH., Ślęzak, D., Adeli, H. (eds) Computer Applications for Modeling, Simulation, and Automobile. MAS ASNT 2012 2012. Communications in Computer and Information Science, vol 341. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-35248-5_33

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  • DOI: https://doi.org/10.1007/978-3-642-35248-5_33

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-35247-8

  • Online ISBN: 978-3-642-35248-5

  • eBook Packages: Computer ScienceComputer Science (R0)

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