ArticleNanomedicine (London, England)2026
Sodium alginate functionalized biocompatible selenium nanocarriers loaded trans-resveratrol for mitochondrial targeted HepG2 hepatocellular carcinoma inhibition study.
Article in Nanomedicine (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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9 authors.
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Abstract
aimsTo investigate the use of sodium alginate (SA) for functionalization of selenium nanoparticles (SA@Se NPs) in developing biocompatible nanocarrier to enhance stability, mitochondrial targeting and anticancer efficacy of trans-resveratrol (TRV).
methodsSA@Se NPs were synthesized by chemical reduction method and characterized to evaluate their crystalline structure by X-ray diffraction (XRD), particle size and surface charge. Synthesized SA@Se NPs were evaluated for cumulative TRV release. Cytotoxicity of TRV-SA@Se was assessed against HepG2 and HEK-293T cells by WST-8 assay. Superoxide anion detecton by staining with MitoSOX and calorimmetrically caspases-9/3 activities were evaluated in HepG2 cells.
resultsSA@Se NPs demonstrated the spherical morphology with an average particle size of 23 nm having surface charge -33.65 ± 1.94 mV which slightly neutralized to -27.43 ± 2.11 mV by TRV encapsulation. SA@Se NPs exhibited 64.55 ± 4.5% encapsulation efficiency for TRV and showed cumulative release 74.38 ± 3.75% at pH 5.0 over 24 h. TRV-SA@Se NPs exhibited anticancer activity against HepG2 cells having IC
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