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Anchoring of Nanocomposites Based on Novel Metal Nanocomplexes/Nanocarbonaceous Surfaces and Assessing Their In Vivo Anticancer Effects on Ehrlich Ascites Tumor

Author name : HEBA BASSIONY ALI ABD ELHALIM GHANEM
Publication Date : 2022-11-15
Journal Name : ACS Omega

Abstract

ABSTRACT: Nanotechnology is the study of materials’ unique
properties at the nanoscale. Nanomedicine is the application of
nanotechnology in medicine, which has been utilized to treat some
common diseases, such as cancer. The aim of the present work is
to synthesize the cadmium (Cd) nanocomplex using paracetamol
as a ligand with a molar ratio of 1:2 M/L that was characterized by
different physicochemical methods and to explore the effect of the
synthesized Cd nanocomplex on the immune system and the redox
status of the body and their anticancer effects on Ehrlich ascites
carcinoma (EAC) induced in mice. Eighty female albino mice were
separated into Group I: control; Group II: EAC; Group III: EAC
treated with a low-dose Cd nanocomplex; and Group IV: EAC treated with a high-dose Cd nanocomplex. Interleukin-6 (IL-6), NLR
family pyrin domain containing 3 (NLRP3), and 8-hydroxy 2-deoxyguanosine (8-OHdG) levels were assessed by enzyme-linked
immunosorbent assay (ELISA). Peroxynitrite level and glutathione peroxidase activity were assessed by spectrophotometry. NRF2
mRNA expression, cadmium content, and liver and renal toxicity were estimated. Results: There was a significant increase in IL-6,
NLRP3, 8-OHdG, peroxynitrite, and NRF2 mRNA expressions and in the glutathione peroxidase activity in EAC treated with lowand high-dose Cd nanocomplexes. However, the EAC treated with high-dose Cd nanocomplex group showed significant liver and
renal toxicity. Conclusion: Cadmium nanocomplex has anticancer effects on EAC induced in mice via its effects on the immune
system and redox status as well as pyroptosis and epigenetic instability of the body, while high doses of Cd nanocomplex can cause
liver and renal toxicity.

Keywords

Nanocompositesو Ehrlich Ascites Tumor

Publication Link

https://pubmed.ncbi.nlm.nih.gov/36406541/

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