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Arab Journal of Nuclear Sciences and Applications
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Volume Volume 51 (2018)
ahmed, A., badr, Y. (2018). Improvement of 6-mercaptopurine Efficiency by Encapsulated in Chitosan Nanoparticles. Arab Journal of Nuclear Sciences and Applications, 51(4), 181-186. doi: 10.21608/ajnsa.2018.2630.1040
amna hussein ahmed; yehia abd elhameed badr. "Improvement of 6-mercaptopurine Efficiency by Encapsulated in Chitosan Nanoparticles". Arab Journal of Nuclear Sciences and Applications, 51, 4, 2018, 181-186. doi: 10.21608/ajnsa.2018.2630.1040
ahmed, A., badr, Y. (2018). 'Improvement of 6-mercaptopurine Efficiency by Encapsulated in Chitosan Nanoparticles', Arab Journal of Nuclear Sciences and Applications, 51(4), pp. 181-186. doi: 10.21608/ajnsa.2018.2630.1040
ahmed, A., badr, Y. Improvement of 6-mercaptopurine Efficiency by Encapsulated in Chitosan Nanoparticles. Arab Journal of Nuclear Sciences and Applications, 2018; 51(4): 181-186. doi: 10.21608/ajnsa.2018.2630.1040

Improvement of 6-mercaptopurine Efficiency by Encapsulated in Chitosan Nanoparticles

Article 19, Volume 51, Issue 4, October 2018, Page 181-186  XML PDF (440.38 K)
Document Type: Original Article
DOI: 10.21608/ajnsa.2018.2630.1040
Authors
amna hussein ahmed email 1; yehia abd elhameed badr2
1lecturer assistant at NILES,Cairo university
2professor At NIES, cairo university
Abstract
6-mercaptopurine is a cytotoxic and immunosuppressant drug. The use of this drug is limited due to its poor bioavailability and short plasma half-life. Chitosan nanoparticles exhibit great interest for nanomedicine, biomedical engineering and development of new therapeutic drug release systems with improved bioavailability, increased specificity and sensitivity, and reduced pharmacological toxicity. The main objective of this study is to formulate 6mercaptopurine (6MP) encapsulated chitosan nanoparticles (6-MP-CNPs) using with Tripolyphosphate (TPP) as cross-linker for anti-cancer therapy in order to enhance cytotoxcicty and bioavailability . Chitosan nanoparticles exhibited a small particle
size and a high surface charge .The prepared nanoparticles were characterized by transmission electron microscopy, zeta potential. The average particle size determined through TEM was found to be 90 ± 10 nm and after encapsulation the particle size show an obvious increase. Zeta potential 26.2±6.35 mV. 6-MP-CNPs showed enhancement in cellular inhibition of breast cancer cell line MCF7 compared to free 6MP.
Keywords
Key words:Chitosan Nanoprtices; 6 mercaptopurine; Cytotoxicity; Drug delivery
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