Table 1.
phytochemicals |
nanoparticles |
experiments |
||||
---|---|---|---|---|---|---|
name | name/components | size (nm) | EE | model/treatments | main outcomes | refs |
trans-resveratrol | solid lipid nanoparticles | 248 | 79.9 | model: Wistar male diabetic rats | ↓ fasting glucose sugar | 133 |
treatment: oral administration of 10 mg/kg/day of resveratrol in SLN form or free form for 1 month | ↓ insulin resistance | |||||
↓ serum oxidative stress status | ||||||
↓ Snap23, Stx4 and Vamp2 level in muscle | ||||||
PLGA nanoparticles | 176 | 97.2 | model: HepG2 hepatocytes | ↑ stability, water solubility and bioactivity of resveratrol | 134 | |
treatment: 12.5, 25, 50, and 100 μM of resveratrol in PLGA form or free form for 24h. | ↓ lipogenesis | |||||
↓ lipolysis | ||||||
↓ hepatocellular proliferation and lipid accumulation | ||||||
galactosylated PLGA nanoparticles | 108.4 | 97.2 | model: Caco-2 cells for uptake study | ↑ Caco-2 cellular uptake of resveratrol | 135 | |
mouse macrophage cell line RAW 264.7 for anti-inflammation study | ↓ TNF-α and IL-6 expressions | |||||
treatment: 20 μg/mL of resveratrol in PLGA form or free form. | ||||||
EGCG | lipid nanoparticles; phosphatidylcholine, kolliphor HS15, a-tocopherol acetate, EGCG, and 1-(palmitoyl)-2-(5-keto-6-octene-dioyl) phosphatidylcholine (KOdiA-PC) | 108 | 96.0 | model: human monocytic | ↑ EGCG stability | 80 |
THP-1 cells | ↑ sustained release of EGCG | |||||
treatment: free or nano-EGCG at EGCG dose of 5, 10, 20, and 40 μg/mL in combination with 40 μg protein/mL of oxLDL for 18 h | ↑ binding affinity to and uptake by macrophages | |||||
↑ macrophage EGCG content | ||||||
↓ macrophage MCP-1 mRNA levels and protein secretion | ||||||
chitosan–tripolyphosphate nanoparticles of EGCG (EGCG is encapsulated into self-assembled nanoparticles made of chitosan and aspartic acid) | 100 | 25.0 | model: male New Zealand white rabbits | ↓ TC | 84 | |
treatment: free or nano-EGCG (7 mL of 0.5% aqueous acetic acid) at EGCG dose of 100 mg/day for 5 weeks. | ↓ TG | |||||
↓ HDL | ||||||
↓ LDL | ||||||
soy lecithin, glyceryl tridecanoate, glyceryl tripalmitate, and Kolliphor HS15 | 45- 50 | 99.0 | model: THP-1-derived | ↑ EGCG stability | 81 | |
macrophages | ↑ sustained release of EGCG | |||||
treatment: free or nano-EGCG at EGCG dose of 5 μM, 10 μM and 20 μM were tested | ↑ cellular bioavailability of EGCG | |||||
↓ TC content in macrophages | ||||||
↓ MCP-1 expression in macrophages | ||||||
soy PC, surfactant Kolliphor HS15, and (+)-α-tocopherol acetate | 104 | 95.0 | Model: male 6-week old LDLr−/− mice | ↓ secretion of inflammatory factors in mouse peritoneal macrophages | 77 | |
treatment: free or nano-EGCG at EGCG dose of 25 mg/kg/body weight EGCG per week for 22 weeks | ↓ lesion surface areas of aortic arches | |||||
curcumin | turmeric extract-loaded nanoemulsions | 136–138 | 88.0 | Model: Balb/c mice | ↓ SREBP-1 | 110 |
treatment: oral administration of free or nanocurcumin at a curcumin dose of 300 mg/kg/day 3 times/week for 9 weeks | ↓ PPARγ2 | |||||
↓ Cleaved caspase-3 | ||||||
↓ PARP in the liver | ||||||
polylactide-poly(ethylene glycol) (PLA–PEG) copolymer nanoparticles | 100–150 | 98.3 | model: albino rats (STZ-induced diabetic) | ↓ NF-κB activation | 113 | |
treatment: oral administration of free or nanocurcumin at a curcumin dose of 20 mg/kg/day | ↓ COX-2 and TGF-β expression | |||||
↑ PPARγ expression | ||||||
PLGA based nanoparticles | 237 ± 6 | 66.0 | model: Sprague–Dawley rats (STZ induced diabetic) | ↓ CRP, IL-6, TNF-α | 136 | |
treatment: oral administration of nanocurcumin at a curcumin dose of 100 mg/kg/day for 15 days. | ↓ plasma TG and TC | |||||
↑ HDL-cholesterol | ||||||
quercetin | succinylated chitosan-alginate core—shell-corona nanoparticles | 91.58 ± 1.14 | 95.0 | model: Male Wistar rats (STZ induced diabetic) | ↓ TG | 11 |
treatment: oral administration of free or nanoquercetin at a quercetin dose of 100 mg/kg/day for 28 days | ↓ TC | |||||
↓ AST, ALT and ALP levels | ||||||
PLGA nanoparticles | 179.9 ± 11.2 | 86.0 | model: Sprague–Dawley rats (STZ induced diabetic) | ↓ blood glucose levels (similar effect to free quercetin although with a lower dose and frequency) | 129 | |
treatment: oral administration of free or nanoquercetin at a quercetin dose of 150 mg/kg every day for free group and every 5th day for NP group for 15 days |
Abbreviations: SLN, solid lipid nanoparticles; EE, encapsulation efficiency; EGCG, epigallocatechin gallate; oxLDL, oxidized low density lipoprotein; MCP-1, monocyte chemotactic proteins-1; NP, nanoparticle; HDL, high-density lipoprotein; LDL, low-density lipoprotein; PC, phosphatidylcholine; Snap23, synaptosomal-associated protein 23; Stx4, Syntaxin4; Vamp2, vesicle-associated membrane protein 2; R, resveratrol; SREBP1c, sterol regulatory element-binding protein-1c; PPAR, peroxisome proliferator-activated receptors; PARP, poly(ADP-ribose) polymerase; STZ, streptozotocin; NF-κB, suppressing nuclear factor-kappa B; COX-2, cyclooxygenase-2; TGF, tumor growth factor; CRP, C-reactive protein; IL-6, interleukin-6; TNFα, Tumor Necrosis Factor; TG, triglycerides; TC, total cholesterol; AST, aspartate transaminase; ALT, alanine transaminase; ALP, alkaline phosphatase.