2021
DOI: 10.1016/j.pdpdt.2021.102259
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Emerging hybrid biomaterials for oxidative stress induced photodynamic therapy

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Cited by 6 publications
(4 citation statements)
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“…[27][28][29][30][31][32][33] Mesoporous silica nanoparticles (MSN) are among the most promising theranostic platforms for cancer imaging and therapy. [34][35][36][37][38][39][40][41][42][43][44] Caged drugs/contrast agents in MSN by chemical functionalization protect their intrinsic properties, promote aqueous solubility, and increase tumoral accumulation. [34][35][36][37][38][39][40][41][42][43] Also, the mesoporous structure and high surface-to-volume ratios of MSNs increase the drug/contrast agent loading and delivery efficiencies.…”
Section: Introductionmentioning
confidence: 99%
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“…[27][28][29][30][31][32][33] Mesoporous silica nanoparticles (MSN) are among the most promising theranostic platforms for cancer imaging and therapy. [34][35][36][37][38][39][40][41][42][43][44] Caged drugs/contrast agents in MSN by chemical functionalization protect their intrinsic properties, promote aqueous solubility, and increase tumoral accumulation. [34][35][36][37][38][39][40][41][42][43] Also, the mesoporous structure and high surface-to-volume ratios of MSNs increase the drug/contrast agent loading and delivery efficiencies.…”
Section: Introductionmentioning
confidence: 99%
“…[34][35][36][37][38][39][40][41][42][43][44] Caged drugs/contrast agents in MSN by chemical functionalization protect their intrinsic properties, promote aqueous solubility, and increase tumoral accumulation. [34][35][36][37][38][39][40][41][42][43] Also, the mesoporous structure and high surface-to-volume ratios of MSNs increase the drug/contrast agent loading and delivery efficiencies. 42,43 Recently, Meng and Nel developed lipid bilayer-coated MSN (silicasomes) for intratumoral delivery of chemotherapeutics such as oxaliplatin, gemcitabine, or paclitaxel to the Kras-derived pancreatic cancer in mice.…”
Section: Introductionmentioning
confidence: 99%
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“…HS induces endothelial cell injury through oxidative stress, which stimulates reactive oxygen species (ROS) generation, lipid peroxidation and DNA damage ( 6 ). ROS are by-products of oxygen metabolism, including superoxide anions, hydrogen peroxide and hydroxyl radicals ( 7 ). ROS target proteins, polysaccharides, DNA and lipids and increase the rate of cell damage ( 8 ).…”
Section: Introductionmentioning
confidence: 99%