Please use this identifier to cite or link to this item: http://ir.futminna.edu.ng:8080/jspui/handle/123456789/1006
Title: Application of Gold Nanoparticles for Improved drug efficiency.
Authors: Shittu, O. K.
Bankole, M.T
Abdulkareem, S. A
Abubakre, O. K
Ubaka, A.U
Keywords: medicine
nanotechnology
nanoparticle
bioreduction
nanodrug
lincomycin
Issue Date: 29-Aug-2017
Publisher: Advances in natural sciences nanoscience and nanotechnology
Citation: O. K Shittu, M.T Bankole, S. A Abdulkareem, O. K Abubakre , A.U Ubaka (2017). Application of Gold Nanoparticles for Improved drug efficiency. Advances in natural sciences nanoscience and nanotechnology 8: 035014
Series/Report no.: 8;035014
Abstract: Due to increasing resistance of microorganisms towards current antibiotics, there is a need for new or enhanced antibiotics. Nanotechnology is a technology that enhances the use of gold nanoparticles (AuNP) in area of medical applications, especially as a drug carrier for targeted drug delivery. In this research, AuNPs was synthesized using biological method via bioreduction of Piper guineense aqueous leaf extract on tetra gold chloride, characterized using UV–Vis spectrophometer, DLS, TEM/EDS and FTIR. The synthesized AuNPs was covalently functionalized with polyethylene glycol and encapsulated with Lincomycin and in vitro dissolution methods was used to evaluate the potential performance of the formulated nanodrug. The nanodrug has highest release efficiency at the 9th minutes (23.4 mg ml−1 for 40 °C) and (29.5 mg ml−1 for 60 °C) compared with the non-nanodrug. The antibacterial potential of the nanodrug was seen on the gram-positive bacteria of Staphylococcus aureus and Streptococcus pyogenes with highest inhibitions of 18 mm (at 40 °C) and 16 mm (at 60 °C) for S. aureus, and 16 mm for S. pyogenes (both at 40 °C and 60 °C). The bacteria growth inhibition continued and lasted for 15 min, while that of non-nanodrug lasted for 9 min with lesser growth inhibition compared to the formulated nanodrug. This work shows that the presence of the AuNPs increased the release efficiency of lincomycin even at a lower concentration and also bacteria growth inhibition thereby suggesting the effectiveness of the nanodrug formulation.
URI: http://repository.futminna.edu.ng:8080/jspui/handle/123456789/1006
Appears in Collections:Biochemistry

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