The emergence of nanotechnology-based drug delivery systems
has revolutionized cancer treatment by enabling targeted therapeutic approaches
that can specifically accumulate within tumor tissues while minimizing
off-target effects. Epidermal growth factor receptor (EGFR)-targeted gelatin
nanoparticles represent a promising approach for cancer therapy through
selective drug delivery to EGFR-overexpressing tumour cells. A better
understanding of the biological barriers and the pathophysiological principles
of GE11- modified tumor-targeting nanoparticles will be promoted, especially
through the study of the targeting delivery process of GE11 peptide-modified
liposomes. This research paper comprehensively examines the observation methods
and analytical processes for characterizing EGFR-targeted gelatin
nanoparticles, focusing on their synthesis, modification, and therapeutic
applications. The study evaluates various characterisation techniques including
transmission electron microscopy (TEM), scanning electron microscopy (SEM),
dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FTIR),
and in vitro cellular assays. The methodology encompasses both experimental
design principles and analytical protocols based on established practices in
the literature. Secondary data analysis was conducted through a comprehensive
review of recent literature published between 2020-2024. A total of 40
peer-reviewed publications were systematically analyzed to extract quantitative
data on nanoparticle properties, targeting efficiency, and therapeutic
outcomes. Primary data analysis encompasses original research findings from
laboratory studies conducted to evaluate EGFR-targeted gelatin nanoparticle
systems. The analysis includes experimental data from nanoparticle synthesis,
characterisation, and biological evaluation studies. Primary data analysis
reveals that GE11 peptide-modified gelatin nanoparticles demonstrate enhanced
cellular uptake in EGFR-positive cancer cell lines, with particle sizes ranging
from 150-300 nm and encapsulation efficiencies exceeding 85%. Secondary data
analysis from recent studies indicates significant therapeutic improvements,
with targeted formulations showing 60-75% greater efficacy compared to
non-targeted controls in various cancer models. The findings demonstrate that
multi-modal characterization approaches are essential for optimizing
EGFR-targeted gelatin nanoparticle systems, providing critical insights for
translating these therapeutic platforms from laboratory research to clinical applications.
The successful translation of these research findings into clinical
applications has the potential to significantly improve outcomes for cancer
patients while reducing treatment-related side effects.
Author(s) Details
Huda Begam
Department of Chemistry, RKDF University, Gandhi Nagar, Bhopal (M.P.)
462033, India.
Please see the book here :- https://doi.org/10.9734/bpi/msraa/v11/6292
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