Green Synthesis of Genistein‐Fortified Zinc Ferrite Nanoparticles as a Potent Hepatic Cancer Inhibitor: Validation through Experimental and Computational Studies

Author:

Otuechere Chiagoziem A.12,Neupane Netra P.2,Adewuyi Adewale3,Pathak Prateek24ORCID,Novak Jurica56ORCID,Grishina Maria4ORCID,Khalilullah Habibullah7,Jaremko Mariusz8,Verma Amita2ORCID

Affiliation:

1. Department of Biochemistry Faculty of Basic Medical Sciences Redeemer's University 232101 Ede Nigeria

2. Bioorganic and Medicinal Chemistry Research Laboratory Department of Pharmaceutical Sciences Sam Higginbottom University of Agriculture Technology and Sciences 211007 Prayagraj India

3. Department of Chemical Sciences Faculty of Natural Sciences Redeemer's University 232101 Ede Nigeria

4. Laboratory of Computational Modeling of Drugs Higher Medical and Biological School South Ural State University 454008 Chelyabinsk Russia

5. Department of Biotechnology University of Rijeka 51000 Rijeka Croatia

6. Center for Artificial Intelligence and Cybersecurity University of Rijeka 51000 Rijeka Croatia

7. Department of Pharmaceutical Chemistry and Pharmacognosy Unaizah College of Pharmacy Qassim University 51911 Unayzah Saudi Arabia

8. Smart-Health Initiative (SHI) and Red Sea Research Center (RSRC) Division of Biological and Environmental Sciences and Engineering (BESE) King Abdullah University of Science and Technology (KAUST) 23955-6900 Thuwal Saudi Arabia

Abstract

AbstractIn hepatic cancer, precancerous nodules account for damage and inflammation in liver cells. Studies have proved that phyto‐compounds based on biosynthetic metallic nanoparticles display superior action against hepatic tumors. This study targeted the synthesis of genistein‐fortified zinc ferrite nanoparticles (GENP) trailed by anticancer activity assessment against diethylnitrosamine and N‐acetyl‐2‐aminofluorene induced hepatic cancer. The process of nucleation was confirmed by UV/VIS spectrophotometry, X‐ray beam diffraction, field‐emission scanning electron microscopy, and FT‐IR. An in vitro antioxidant assay illustrated that the leaves of Pterocarpus mildbraedii have strong tendency as a reductant and, in the nanoformulation synthesis, as a natural capping agent. A MTT assay confirmed that GENP have a strong selective cytotoxic potential against HepG2 cancer cells. In silico studies of genistein exemplified the binding tendency towards human matrix metalloproteinase comparative to the standard drug marimastat. An in vivo anticancer evaluation showed that GENP effectively inhibit the growth of hepatic cancer by interfering with hepatic and non‐hepatic biochemical markers.

Funder

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Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

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