Glutaraldehyde-crosslinked Naringenin-loaded Albumin Nanoparticles (GNANPs) induce antimicrobial properties and apoptosis in gastric cancer cells

戊二醛 抗菌剂 细胞凋亡 柚皮素 化学 白蛋白 癌症 纳米颗粒 癌细胞 药理学 微生物学 生物化学 医学 纳米技术 抗氧化剂 生物 类黄酮 色谱法 材料科学 有机化学 内科学
作者
Murugan A. Munusamy,Muruganantham Bharathi,Abdullah A. Alarfaj,Samer Hasan Hussein‐Al‐Ali,Ravichandran Nagaiya,Sarathbabu Subbarayan
出处
期刊:Toxicology in Vitro [Elsevier BV]
卷期号:106: 106037-106037 被引量:4
标识
DOI:10.1016/j.tiv.2025.106037
摘要

An assessment of the anticancer activity of Glutaraldehyde-crosslinked Naringenin-loaded Albumin Nanoparticles (GNANPs) against gastric cancer cells was the purpose of this study. The increasing prevalence of gastric cancer and the limitations of conventional therapies necessitate novel approaches that combine targeted drug delivery with therapeutic efficacy. Several techniques were used to characterize the synthesized GNANPs, including UV–visible spectroscopy, X-ray diffractometer (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), Fourier transform infrared (FT-IR), dynamic light scattering (DLS), and photoluminescence (PL). They were evaluated for their antimicrobial properties, cytotoxicity, ROS accumulation, apoptotic activity, and oxidative stress markers against AGS cells. The characterization analyses indicated the existence of Glutaraldehyde-crosslinked Naringenin-loaded Albumin Nanoparticles with an oval-shaped morphology and an average particle size of 127.80 nm. The existence of several elements and functional groups in the GNANPs was also detected using EDX and FT-IR analyses, respectively. The synthesized GNANPs have shown exceptional antibacterial activities by effectively inhibiting the growth of several infections. The treatment of GNANPs efficiently inhibited the growth of AGS cells. Fluorescence staining studies showed increased apoptosis and oxidative stress markers in AGS cells treated with synthesized Glutaraldehyde-crosslinked Naringenin-loaded Albumin Nanoparticles, indicating their potential as a viable cancer treatment option. • The synthesis and characterization of naringenin-loaded albumin-glutaraldehyde nanoparticles, revealing their presence of various elements and functional groups • The anticancer activities of Albumin-Naringenin NPs against gastric cancer cells via inhibited cell growth and increased apoptosis. • The antimicrobial properties of the synthesized Albumin-Naringenin NPs, which effectively inhibited the growth of various pathogens. • Synthesized Albumin-Naringenin NPs demonstrated potential as a viable option for treating gastric cancer.
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