Table 4.
Natural Compound | Drug Delivery System | Findings | Ref. |
---|---|---|---|
Resveratrol | Peptide and Sucrose Liposomes | Prolonged drug-release in vitro; Breast cancer (MCF-7) cells growth inhibition (IC50 = 20.89 μmol/L); Apoptosis; Tumor growth inhibition in mice bearing breast cancer (Dose = 10 mg/kg) | [128] |
Sulfobutylether-β-cyclodextrin | Improved stability; Longer half-life; Significant cytotoxic potential against non-small cell lung cancer; Suitable for pulmonary delivery | [117] | |
Gold Nanoparticles | Optimal cellular uptake; Superior cytotoxic effects on breast, pancreatic, and prostate cancers | [129] | |
Curcumin | Silver-Decorated Melanin-like Polydopamine/Mesoporous Silica Composites |
Improved chemotherapeutic efficiency against human cervical cancer cells (HeLa) and Taxol-resistant non-small cell lung cells (A549/TAX); Desirable biocompatibility; Low hemolytic activity | [124] |
Liposomes | Potent cytotoxic effect against human MiaPaCa pancreatic cancer cells (IC50 = 17.5 µM); suppression of tumor growth in tumor-bearing nude mice (Dose = 20 mg/kg); Potent antiangiogenic effect | [130] | |
Cyclodextrins | Enhanced delivery; Improved therapeutic efficacy against lung cancer in vitro and in vivo | [131] | |
EGCG | Deformable Liposomal Formulation | Increased drug-release; Optimal formulation for topical delivery in skin cancer prevention | [132] |
Folic acid and polyethylene glycol (PEG)-modified Nanoparticles | Inhibition of MCF-7 cells proliferation in a dose-dependent manner; Enhances targeting ability and efficacy of the drug | [133] | |
Quercetin | Lipid Nanoparticles | Sustained release; Inhibition of the MCF-7 breast cancer cells growth; Increased ROS production; Increased apoptotic and necrotic indexes in MCF-7 cells | [134] |
Polymeric Nanoparticles | Enhanced efficacy in cancer therapy; Reduced tumor volume in breast and lung-bearing mice; | [135] | |
Rutin | Proniosomal Gel | High biocompatibility of the gel on the 3D reconstructed human epidermis; Lack of irritant and phototoxic potential; Preferential cytotoxic effect of the drug on melanoma cells (IC50 = 8.601 µM) | [136] |
β-cyclodextrins and hydroxypropyl-β-cyclodextrins | Increased antioxidant activity; Antiproliferative and pro-apoptotic effect against B164A5 murine melanoma cells | [137] | |
Betulinic acid | Gamma-cyclodextrins | Improved antiproliferative activity in vitro on metastatic and non-metastatic B164A5 melanoma cells; G0/G1 cell-cycle arrest; Reduced in vivo tumor development | [46] |
Magnetoliposomes | Enhanced antitumor activity when breast adenocarcinoma MDA-MB-231 cells and a microtubule assembly modulatory activity under hypertermic conditions; | [127] | |
Silver Nanocolloids | Augmented anticancer effect against lung A549 and liver HepG2 cancer cell lines; Cell type- and time-dependent cytotoxic effect | [138] | |
Artemisinin
(Artesunate) |
Chitosan Magnetic Nanoparticles |
Enhanced accumulation of nanoparticles in the 4T1 breast tumor tissues of BALB/c mice model | [139] |
pH-Responsive Lipid Nanoparticles | Inhibition of the breast cancer cells growth; down-regulation of the anti-apoptotic protein survivin, and cyclin D1; down-regulation of the oncogenic proteins HER2 and HER3; Reduced expression of the epidermal growth factor receptor (EGFR or HER1) | [140] | |
Ginseng | Ginsenoside Rb1/Protopanaxadiol Nanoparticles | High encapsulation efficiency, drug loading capacity, and slow release kinetics; Lack of hemolytic effect; Superior in vitro anticancer activity on murine Lewis lung carcinoma | [141] |
Ginsenoside-based multifunctional liposomal delivery system | Successful delivery of the bioactive combination drugs and internalization into gastric cancer cells; Suppressed gastric cancer tumor growth | [142] |