Histopathology, pharmacokinetics and estimation of interleukin-6 levels of Moringa oleifera leaves extract-functionalized selenium nanoparticles against rats induced hepatocellular carcinoma

Ebrahem, EMM; Sayed, GH; Gad, GNA; Kurls Ekram Anwer; Selim, AA;

Abstract


Background: Hepatocellular carcinoma (HCC) is one of the most dangerous cancers in all the world. This study focused on prevention and therapy of hepatocellular carcinoma (HCC) using Moringa oleifera extract combined with vitamin C and selenium in a nanoplatform (MO/asc.-Se-NPs). Results: Full characterization of MO/asc.-Se-NPs was performed by using different analytical techniques (TEM, DLS, zeta-sizer), and its antioxidant capacity was measured by DPPH assay. Biodistribution study was performed with the aid of radiolabeling technique using technetium-99m in normal albino mice. HCC was induced in Wister albino rats to evaluate the efficiency of MO/asc.-Se-NPs in the treatment of HCC. The biomarker analysis (ALT, AST and ALB) shows improvement in its values in prevention and treated groups by using MO/asc.-Se NP. The levels of inflammatory marker interleukin 6 (IL6 tissue homogenate) was improved by decreasing its values in these two groups also. Histology section of tissue liver showed alleviation in treated and prevention groups. Conclusions: In conclusion, MO/asc.-Se-NPs can be used as a potential agent for prevention and treatment of HCC after further preclinical studies.


Other data

Title Histopathology, pharmacokinetics and estimation of interleukin-6 levels of Moringa oleifera leaves extract-functionalized selenium nanoparticles against rats induced hepatocellular carcinoma
Authors Ebrahem, EMM; Sayed, GH; Gad, GNA; Kurls Ekram Anwer ; Selim, AA
Keywords Moringa oleifera;Se-NPs;Hepatocellular carcinoma;Interleukin-6;Tc-99m-complexation;IN-VIVO ANTIOXIDANT;LIVER-DAMAGE;INFLAMMATION;INJURY;VITRO
Issue Date 2022
Publisher BMC
Journal CANCER NANOTECHNOLOGY 
ISSN 1868-6958
DOI 10.1186/s12645-022-00123-0
Scopus ID 2-s2.0-85130409803
Web of science ID WOS:000798418900001

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