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040 _aEG-GICUC
_beng
_cEG-GICUC
_dEG-GICUC
_erda
041 0 _aeng
_beng
_bara
049 _aDeposit
082 0 4 _a591.35
_221
092 _a591.35
_221
097 _aM.Sc
099 _aCai01.12.21.M.Sc.2023.Re.E
100 0 _aReem Maged Ahmed Sheta,
_epreparation.
245 1 0 _aEstimation of the safety and antitumor activity of silver doped hydroxyapatite nanoparticles in mice /
_cby Reem Maged Ahmed Sheta ; supervised by Ass. Prof. Hanan Ramadan Hamad, Prof. Gehan Safwat ElHusseiny.
246 1 5 _aﺗﻘدﯾر اﻟﺳﻼﻣﺔ واﻟﻧﺷﺎط اﻟﻣﺿﺎد ﻟﻠورم ﻣن ﺟزﯾﺋﺎت ھﯾدروﻛﺳﯾﺑﺎﺗﯾت اﻟﻧﺎﻧوﯾﺔ اﻟﻣطﻌﻣﺔ ﺑﺎﻟﻔﺿﺔ ﻓﻲ اﻟﻔﺋران
264 0 _c2023.
300 _a135 pages :
_billustrations ;
_c25 cm. +
_eCD.
336 _atext
_2rdacontent
337 _aUnmediated
_2rdamedia
338 _avolume
_2rdacarrier
502 _aThesis (M.Sc.)-Cairo University, 2023.
504 _aBibliography: pages 119-131.
520 _aCurrently, the main therapies for treating cancer are associated with a variety of side effects. Accordingly, researchers are focusing on the use of nanotherapy to develop a highly novel, less toxic and extremely efficient therapeutic agents for cancer treatment. Silver doped Hydroxyapatite nanoparticles (Ag:HAp-NPs) have shown effective at treating both infections and cancerous tumors while being non- cytotoxic to normal healthy cells in vitro. Therefore, this study was undertaken to estimate the safety and anti-tumor activity of silver doped hydroxyapatite nanoparticles in mice in vivo. Regarding the antitumor activity, concurrent administration of Ag:HAp-NPs caused a significant decrease in tumor volume and weight. Additionally, it showed a high elevation of intracellular ROS generation as well as MDA levels within tumor tissues and lead to the induction of DNA breaks. The high production of intracellular ROS generation, and the oxidative stress induction by Ag:HAp-NPs within tumor tissues confirmed a decrease in GSH and GPx levels. Significant elevation of P53 and HO-1 gene and decrease in Hsp70 and Kras was observed as well. Additionally, the percentage of necrotic tissue in tumor- induced groups and % of degenerated tumor cells after treatment with Ag:HAp-NPs were significantly elevated. Regarding the safety of Ag:HAp- NPs, it was shown to be safe and non-genotoxic. This was confirmed by the non-significant changes in TL and TM in the bone marrow and liver tissues. It was further confirmed by the observed non- significant changes in the MDA and TAC levels as well as the SOD activity in the liver among the safety groups, except for high dosage level. Moreover, histological examinations demonstrated that Silver doped Hydroxyapatite nanoparticles have mild toxicity on kidney and liver tissues with minimal inflammatory reactions associated with the presence of Ag:HAp-NPs in contrast with Cisplatin. In conclusion, silver doped hydroxyapatite nanoparticles have a potential anticancer activity against induced solid tumors in mice and demonstrated a higher level of safety for the liver, kidney and bone marrow tissues, making Ag:HAp-NPs a promising anti-tumor agent.
520 _aﺣﺎﻟًﯿﺎ،ﺗﺮﺗﺒﻂ اﻟﻌﻼﺟﺎت اﻟﺮﺋﯿﺴﯿﺔ ﻟﻌﻼج اﻟﺴﺮطﺎن ﺑﻤﺠﻤﻮﻋﺔ ﻣﺘﻨﻮﻋﺔﻣﻦاﻵﺛﺎر اﻟﺠﺎﻧﺒﯿﺔ.وﻓًﻘﺎ ﻟﺬﻟﻚ،ﯾﺮﻛﺰا ﻟﺒﺎﺣﺜﻮن ﻋﻠﻰ اﺳﺘﺨﺪام اﻟﻌﻼج ﺑﺎﻟﻨﺎﻧﻮ ﻟﺘﻄﻮﯾﺮ ﻋﻮاﻣﻞ ﻋﻼﺟﯿﺔ ﺟﺪﯾﺪة ﻟﻠﻐﺎﯾﺔ ؤاﻗﻞ ﺳﻤﯿﺔ وﻓﻌﺎﻟﺔ ﻟﻠﻐﺎﯾﺔ ﻟﻌﻼج اﻟﺴﺮطﺎن.ٔاظﮭﺮت ﺟﺰﯾﺌﺎت ھﯿﺪروﻛﺴﯿﺒﺎﺗﯿﺖ اﻟﻨﺎﻧﻮﯾﺔ اﻟﻤﻄﻌﻤﺔ ﺑﺎﻟﻔﻀﺔ)Ag: HAp-NPs( ﻓﻌﺎﻟﯿﺘﮭﺎ ﻓﻲ ﻋﻼج ﻛﻞ ﻣﻦ اﻻﻟﺘﮭﺎﺑﺎت واﻷورام اﻟﺴﺮطﺎﻧﯿﺔ ﺑﯿﻨﻤﺎ ﺗﻜﻮن ﻏﯿﺮﺳﺎﻣﺔ ﻟﻠﺨﻼﯾﺎ اﻟﺴﻠﯿﻤﺔ ﻣﻌﻤﻠﯿﺎ in vitro .ﻟﺬﻟﻚ،ٔ اﺟﺮﯾﺖ ھﺬه اﻟﺪراﺳﺔ ﻟﺘﻘﺪﯾﺮ اﻟﺴﻼﻣﺔ واﻟﻨﺸﺎط اﻟﻤﻀﺎد ﻟﻠﻮرم ﻣﻦ ﻟﺠﺴﯿﻤﺎت ھﯿﺪروﻛﺴﯿﺒﺎﺗﯿﺖ اﻟﻨﺎﻧﻮﯾﺔ اﻟﻤﻄﻌﻤﺔ ﺑﺎﻟﻔﻀﺔ ﻓﻲ اﻟﻔﺌﺮان ﻓﻲ اﻟﺠﺴﻢ اﻟﺤﻲ in vivo .ﻓﯿﻤﺎ ﯾﺘﻌﻠﻖ ﺑﺎﻟﻨﺸﺎط اﻟﻤﻀﺎد ﻟﻠﻮرم، ﺗﺴﺒﺐ اﻹ ﻋﻄﺎء اﻟﻤﺘﺰاﻣﻦ ﻟـ Ag: HAp-NPs ﻓﻲ اﻧﺨﻔﺎض ﻛﺒﯿﺮ ﻓﻲ ﺣﺠﻢ ووزن اﻟﻮرم. ﺑﺎﻹﺿﺎﻓﺔٕ اﻟﻰ ذﻟﻚ اظﮭﺮ ارﺗﻔﺎﻋﺎ ﻛﺒیرا ﻓﻲﺗﻮﻟﯿﺪ ROSداﺧﻞ اﻟﺨﻼﯾﺎ وﻛﺬﻟﻚ ﻣﺴﺘﻮﯾﺎتMDA داﺧل أﻧﺴﺠﺔ اﻟﻮرم وﯾٔﻮديٕ اﻟﻰ ﺗﺤﺮﯾﺾ ﻓﻮاﺻﻞ اﻟﺤﻤﺾاﻟﻨﻮوي.ٔ اﻛﺪ اﻹﻧﺘﺎج اﻟﻌﺎﻟﻲﻟﺘﻮﻟﯿﺪ ROS داﺧﻞ اﻟﺨﻼﯾﺎ، وﺗﺤﺮﯾﺾ اﻹﺟﮭﺎد اﻟﺘﺄﻛﺴﺪي ﺑﻮاﺳﻄﺔ Ag: HAp-NPs داﺧﻞٔ اﻧﺴﺠﺔاﻟﻮرم اﻧﺨﻔﺎﺿا ﻓﻲ ﻣﺴﺘﻮﯾﺎت GSHو.GPxﻛﻤﺎ ﻟﻮﺣﻆ ارﺗﻔﺎع ﻛﺒﯿﺮ ﻓﻲ ﺟﯿﻦP53وHO-1واﻧﺨﻔﺎضﻓﻲ Hsp70وKras.ﺑﺎﻹﺿﺎﻓﺔٕ اﻟﻰذﻟﻚ،ﺗﻢ رﻓﻊ ﻧﺴﺒﺔ اﻷﻧﺴﺠﺔ اﻟﻤﯿﺘﺔ ﻓﻲ اﻟﻤﺠﻤﻮﻋﺎت اﻟﺘﻲ ﯾﺴﺒﺒﮭﺎ اﻟﻮرم وﻧﺴﺒﺔ اﻟﺨﻼﯾﺎ اﻟﺴﺮطﺎﻧﯿﺔاﻟﻤﺘﺪھﻮرةﺑﻌﺪاﻟﻌﻼج Ag: HAp-NPsﺑﺸﻜﻞﻣﻠﺤﻮظ.ﻓﯿﻤﺎﯾﺘﻌﻠﻖﺑﺴﻼﻣﺔ :Ag HAp-NPs،ﻓﻘﺪﺛﺒﺖٔ اﻧﮭﺎ ٓاﻣﻨﺔوﻏﯿﺮﺳﺎﻣﺔﻟﻠﺠﯿﻨﺎت.ﺗﻢﺗﺄﻛﯿﺪذﻟﻚﻣﻦﺧﻼل اﻟﺘﻐﯿﯿﺮات ﻏﯿﺮاﻟﻤﮭﻤﺔﻓﻲTLوTMﻓﻲﻧﺨﺎع اﻟﻌﻈﺎم ؤاﻧﺴﺠﺔاﻟﻜﺒﺪ.ﺗﻢ ﺗﺄﻛﯿﺪذﻟﻚٔای ًﺿﺎﻣﻦ ﺧﻼل اﻟﺘﻐﯿﯿﺮات ﻏﯿﺮاﻟﻤﻠﺤﻮظﺔ ﻓﻲﻣﺴﺘﻮﯾﺎت MDAوTACﺑﺎﻹﺿﺎﻓﺔٕ اﻟﻰﻧﺸﺎطSODﻓﻲاﻟﻜﺒﺪ
530 _aIssues also as CD.
546 _aText in English and abstract in Arabic & English.
650 0 _aGenetics
653 0 _aSilver doped hydroxyapatite
_acancer
_amice
_aantitumor
_aoxidative stress and safety
700 0 _aHanan Ramadan Hamad,
_ethesis advisor.
700 0 _aGehan Safwat El Husseiny,
_ethesis advisor.
900 _b28-09-2023
_cHanan Ramadan Hamad
_cGehan Safwat El Husseiny
_dAhmed Emam Dakroury
_UCairo University
_FFaculty of Science
_DDepartment of Zoology
905 _aHanan
942 _2ddc
_cTH
_e21
_n0
999 _c165719
_d165719