A comparative anticancer analysis of Iron Oxide nanoparticles of Hippophae rhamnoides and Cichorium intybus found in the Karakoram Range of Gilgit Baltistan against liver cancer targeting the RhoA gene
ObjectiveThe current research work focused on the evaluation of of and Fe O NPs against liver cancer cell line (HepG2) by performing antiproliferative assay targeting the gene and apoptotic pathway genes and proteins.MethodsFe O NPs were synthesized using extracts of and and characterized by UV-Vis...
Saved in:
Published in | Drug development and industrial pharmacy p. 1 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
10.09.2024
|
Subjects | |
Online Access | Get more information |
Cover
Loading…
Summary: | ObjectiveThe current research work focused on the evaluation of of
and
Fe
O
NPs against liver cancer cell line (HepG2) by performing antiproliferative assay targeting the
gene and apoptotic pathway genes and proteins.MethodsFe
O
NPs were synthesized using extracts of
and
and characterized by UV-Vis spectroscopy, FTIR, SEM/EDS and XRD. MTT assay was used to study cytotoxicity against the HepG2 cells. Real-time qPCR and ELISA were used for the gene and protein analysis.ResultsAn absorbance peak at 300 nm for
and 289 nm for
nanoparticles were observed by UV-Vis analysis. The FTIR bands of
Fe
O
NPs suggested the presence of aldehydes, alcohols and polyols whereas bands of
Fe
O
NPs suggested the presence of carboxyl groups, hydroxyl groups, alkynes and amines. The size of Fe
O
NPs was found to be 27 ± 5nm for
and 84 ± 4nm for
The IC
value of 41.69 µM for
and 71.04 µM for
Fe
O
NPs compared to plant extract (78.10 µM and 96.03 µM for
and
respectively
were found against HepG2 cells. The gene expression and protein levels of
were decreased whereas those of
and
were found increased.ConclusionNanoparticles and extract of
were found more effective as compared to
which was evident by the results of cytotoxicity and analysis of studied genes and proteins. |
---|---|
ISSN: | 1520-5762 |
DOI: | 10.1080/03639045.2024.2400209 |