“…This pentacyclic triterpenoid inhibits NF-š
B activation for anti-inflammatory activity. [42] When tested in a Panc02 ectopic xenograft mouse model, these nanoparticles circulated longer, accumulated more at the tumor sites, and inhibited tumor growth better than the uncoated nanoparticle Payload PLGA PTX, [45] rapamycin, [32] DOX, [46] Celastrol, [ 34,47] ICG, [48] membrane-bound gadolinium-lipid, [49] tacrolimus, [28] carfilzomib, [38] PTX, [39] Chitosan or chitosan-gelatine crosslinked polymers atorvastatin, [35] ChS [50] Silk fibroin ferulic acid [51] PEGylated poly(š½-amino ester) nanoparticles PTX [52] DOPE/DSPE-PEG liposome emtansine [26] Gold nanoclusters, nanoshell, or nanocage cholorin e6 and indoximod, [53] DOX, [53] cyanine 7 [54] Mesoporous silica IR780 (a photothermal and imaging agent), [55] DOX [ 25,56] Metal-organic framework nanoparticles mitoxantrone and siRNA, [57] glucose oxidase and chloroperoxidase [33] Magnetic nanoclusters simvastatin, [58] siRNA, [59] Gallium nanoswimmers DOX [60] HSA nanoparticles Pt(lau) (a laurate-functionalized Pt(IV) prodrug) [61] Bismuth selenide nanoparticles quercetin [41] a) PLGA = poly(lactic-co-glycolic acid), PTX = paclitaxel, DOX = doxorubicin, ICG = indocyanine green, ChS = chondroitin sulfate, DOPE = 1,2-dioleoyl-sn-glycero-3phoshoethanolamine, DSPE-PEG = distearoylphosphatidylethanolamine-poly(ethylene glycol), siRNA = small interfering RNA, HAS = human serum albumin.…”