From: Emerging nanobiotechnology for precise theranostics of hepatocellular carcinoma
Nanocarriers | Drugs | Target cell | Anticancer Mechanism | Outcomes | |
---|---|---|---|---|---|
Inorganic | Nanoshells | Sorafenib; Doxorubicin; Oxaliplatin | HepG2 | Photothermal therapy; Codelivery of drugs | Inhibit cell proliferation and minimize the resistance of HCC |
Inorgnic Nanofibers | Doxorubicin | SMMC-7721, H22 tumor | Delivery of drugs | Provide good tumor-targeting activity; Prolonged drug release with lower tumor cytotoxicity; Prevent tumor recurrence | |
Graphene Oxide-Based Nanocarriers | Doxorubicin | Hepatoma cells | Delivery of drugs | Exhibit a cytotoxic effect on liver cancer cells | |
Calcium NPs | Sorafenib; Doxorubicin; Immunosuppressive agents; Therapeutic genes | HepG2, HepG2/ADR,SMMC-7721,A549,BEL-7402 | Delivery of drugs and genes | Enhance anticancer effect with lower cytotoxicity | |
Metal oxide NPs (Iron, Zinc, Alumina) | Sorafenib; Doxorubicin; Paclitaxel; Therapeutic genes | Hep-2,HepG2,Hep3B,Hepa1-6,Huh-7,SMMC-7721 | Membrane disruption/ROS production; Delivery of drugs and genes; Magnetic field induces lysosomal leakage; Magnetic hyperthermia | Induce cytotoxicity and apoptosis of HCC cells; Efficient tumor imaging | |
Silver NPs | – | HT29,HepG2 | ROS formation/apoptosis induction; Disruption of intercellular proteins; Apoptosis through caspase expression | Induce apoptosis of HepG2 cells | |
Platinum NPs | – | HepG2 | Release of Pt(II) ions | Enhance antitumor activity with fewer side effects | |
Gold NPs | Cisplatin; Doxorubicin; Capecitabine; 5-FU; Therapeutic genes | HepG2 & resistant HepG2, HepG2-C3A, H22, HCC-LM3-fLuc, Huh-7, HepB3, HepB5, A549, MCF-7 | Cationic cellular uptake/oxidative stress; Cell uptake through peptide conjugation; Gold atom-intercellular protein interaction; c-Myc gene silencing by siRNA; Delivery of 5-FU; photothermal therapy; Immunotherapy, conjugation with SM5-1; Gold-protein interaction/Radiotherapy; miR-375 replacement therapy | Effectively inhibit the growth and resistance of HCC cells; Reduce toxicity systematically | |
Silica NPs | Doxorubicin; Cetuximab; Cisplatin; Therapeutic genes | H22SMMC-7721 cell lines, HepG2, PLC, BEL-7402, QGY7703 | Delivery of drugs; Suicide gene delivery and gene regulation; Magnetic hyperthermia; Photothermal therapy | Effective drug-releasing ability and efficient tumor-homing; Better antitumor activity; Reduce toxicity systematically | |
Selenium NPs | Doxorubicin; Baicalin Therapeutic genes | HegG2,HepG2215 | Delivery of drugs and genes | Inhibit tumor growth; Mitigate harmful effects from almost any drug at the delivery area | |
Janus NPs | Doxorubicin; Docetaxel | HepG2,H22 | Delivery of drugs; Photothermal therapy | Effectively enhance tumor targeting and internalization in selective and safe chemotherapy for multidimensional HCC theranostics | |
Magnetic Nanoclusters | Doxorubicin | HCC cell lines | Sustained drug loading and release; In vivo MRI of intra-tumoral delivery | Significantly enhance liver cancer cell death | |
Superparamagnetic Iron-Oxide NPs (SPIONs) | Doxorubicin; Curcumin | HCC cell lines,HepG2 | Delivery of drugs and as therapeutics themselves; Targeted MR imaging of HCC; Magnetic hyperthermia | Effectively inhibit HCC cell growth | |
Organic | Chitin and chitosan-based NPs | Doxorubicin | HepG2,H22,LO2,HU7,SMMC-7721 | Delivery of drugs; mRNA apoptotic gene expression | Kill HCC cell lines; Higher antitumor activity; Stronger fluorescent intensity shown in tumor tissue |
Polysaccharide NPs | Doxorubicin; Paclitaxel | HepG2,H22,SMMC-7721 | Delivery of drugs | Intrinsic liver targeting capability to incorporate multiple targeting and therapeutic approaches | |
Micelles | Sorafenib Doxorubicin | HCC cell lines, HepG2 | Provides specific targeted action against HCC | Good tumor growth inhibition and overall survival rate | |
Albumin NPs; Peptide NPs | Doxorubicin; Paclitaxel; Therapeutic genes | HepG2,Huh7 | Delivery of drugs and genes | Significantly enhance antitumor efficiency in HCC | |
Other polymer NPs | Doxorubicin; 10-hydroxycamptothecin; Therapeutic genes | HepG2,Hep3B,Hepa-1.6,C3A,SK-HEP-1 | Delivery of drugs and genes; Photothermal therapy | Multi-functionality of DDS in specific antitumor therapy | |
Organic Nanofibers | Cisplatin; Doxorubicin; Therapeutic genes | HCC cell lines,EMT6 | Delivery of drugs and genes | Provide good tumor-targeting activity; Significantly inhibit metastasis and tumor growth of liver cancer cells; Prevent tumor recurrence | |
Carbon Nanotubes | Doxorubicin | HCC cell lines,SMMC-7721,H22 | Delivery of drugs; Specific cancer imaging and selectivity of HCC; Photothermal therapy | Kill HCC cell lines; Repress liver cancer growth | |
Carbon Dots (CDs) | Doxorubicin | HepG2,HL-7702 | Delivery of drugs; Active anticancer effects through direct pyrolysis of an organic therapeutic; Restrains migration for adjuvant therapy; Increased efficiency of radiotherapy | Multi-functionality of DDS in specific antitumor therapy | |
Liposomes | Cisplatin; Sorafenib; Doxorubicin; 5-FU; Therapeutic genes | HepG2,H22 | Delivery of drugs and genes | Longer imaging time and higher signal enhancement; Good inhibition of cell growth | |
Lipid NPs; Vesicle NPs | Sorafenib; Doxorubicin; Therapeutic genes | HepG2, Hep3B, Huh7 | Delivery of drugs and genes | Significantly enhanced antitumor effects Efficiency in HCC | |
Hydrogel NPs | Cisplatin; Therapeutic genes | HepG2, Hep3B, H22 | Delivery of drugs and genes | Efficient intracellular drug release and subsequent induction of tumor cell death | |
Dendrimer | Doxorubicin | HepG2 | Enhance the uptake of drug; Increases the cytotoxicity and anticancer effect | Better antitumor efficiency | |
Polyethylene glycol (PEG) NPs | Sorafenib; Vandetanib | HepG2, BEL7402 | Delivery of drugs | Capability of producing promising drug delivery | |
Polylactic-Co-Glycolic Acid (PLGA) NPs | Sorafenib; Selumetinib; Docetaxel Brucine; Therapeutic genes | HepG2,Hep3B, HCC1, SK-Hep1, JHH-7,BEL7402,SK-Hep1,HL-7702 | Delivery of and genes | Increase drug loading capacity and biocompatibility; Effectively suppress tumor cell proliferation; Improve antitumor efficiency | |
Metal–organic frameworks (MOF) NPs | Dihydroartemisinin | HepG2,HCT116,MCF-7 | Delivery of drugs | Enhanced antitumor efficiency in HCC with low cytotoxicity and side effects | |
Upconversion NPs | doxorubicin and hydroxycamptothecin(HCPT) | HepG2 | Phothermal therapy; codelivery of drugs | Multimodal antitumor function in reducing tumor volume to almost zero in vivo |