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. 2017 Mar 28;18(4):709. doi: 10.3390/ijms18040709

Table 1.

Nanosized delivery systems for anti-inflammatory polyphenols.

Bioactive Principle Nanovector Type of Delivery System Experimental Model Reference
Quercetin
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Nanoparticles NP of soya lecithin, Tween-80 and PEG In vivo (rats) [76]
PLGA NP containing quercetin In vitro [78]
Eudragit-polyvinyl alcohol quercetin-loaded NP In vitro [79]
Quercetin-PLGA NP In vivo (rats) [80]
Nanocapsules Lipid-coated NC In vitro [77,78]
Quercetin-PLGA NC
Resveratrol
Inline graphic
Nanoparticles PLGA NP containing resveratrol In vivo (Wistar male rats) [82]
Eudragit RL 100 NP In vitro/In vivo [83]
Carboxymethyl chitosan NP In vitro/In vivo (rats) [84]
Solid lipid nanoparticles SLN with a controlled release profile In vitro [85]
Resveratrol loaded SLN In vivo (Wistar male rats) [86]
Cyclodextrins CD-based nanosponges In vitro [87]
Ellagic acid
Inline graphic
Nanoparticles Ellagic acid-loaded PLGA NP In vitro [88]
PLGA-PCL ellagic acid NP In vivo (rats with induced nephrotoxicity) [89]
Curcumin
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Nanoparticles Hydrogel/glass In vivo (rats with post-traumatic osteoarthritis) [96]
Nanoemulsions o/w nanoemulsion containing curcumin in the oil phase In vitro [98]
Lipid nanoparticles Lecithin liposomes In vivo (rats) [100]

NP, nanoparticles; PEG, polyethylene glycol; PLGA, polylactic-co-glycolic acid; NC, nanocapsules; SLN, solid lipid nanoparticles; CD, cyclodextrins; PCL, polycaprolactone; o/w, oil in water.