Table 2.
Drug | Iron oxide-based nanoparticle systems |
Purpose | Experimental system | Results | Ref. |
---|---|---|---|---|---|
Adriamycin | Nanoparticles conjugated with multidrug resistance protein inhibitors | Combination treatment | In vivo experiments with human chronic myeloid leukemia cell lines | Significant decrease in tumor sizes | [158] |
Bleomycin | Coprecipitated chitosan-coated nanoparticles | Drug delivery | Release kinetics. Cellular experiments conducted in HeLa cells | Effective release. Increased drug activity found in nanoparticle– drug conjugated systems | [142] |
Bortezomib | Coprecipitated nanoparticles coated with covalently attached carboxymethyl dextran | Combination treatment | Cellular experiments with resistant and nonresistant cell lines | Combination treatment with MFH more effective in both resistant and nonresistant cell lines when compared with hot water | [160] |
Carboplatin | Iron nanopowder in chitosan nanoparticles | Combination treatment | In vivo studies for liver carcinoma | Higher survival rates with combination therapy | [156] |
Cisplatin | Nanoparticles coated with adsorbed starch polymers | Combination treatment | Cellular combination experiments using BP6 rat sarcoma cells | Combination treatment more effective | [148] |
Magnetic nanoparticles encapsulated in poly(glycolic acid) nanoparticles | Drug delivery by polymer biodegradation and heat | Drug release using microwave pulses | Effective actuated drug release | [145] | |
Nanoparticles prepared by electrochemical deposition | MDR inhibitors | In vitro studies with SKOV-3/DPP cells | Enhanced accumulation of platinum using nanoparticles | [146] | |
Coprecipitated nanoparticles coated with adsorbed starch polymers | Drug delivery | Release kineticsc | Cisplatin desorption after magnetic field application | [149] | |
Porous hollow nanoparticles functionalized with herceptin | Targeted release | Release kinetics and in vitro cellular studies with SK-BR-03 cells | Release kinetics controlled by pH. Significant cytotoxicity found | [150] | |
Carbon-encapsulated nanoparticles | Combination treatment | Release and cellular studies with DU-145 cells | Combination treatment was effective | [147] | |
Coprecipitated nanoparticles coated with adsorbed carboxymethyl dextran | Combination treatment | Cellular efficacy studies using Caco-2. Compared with hot water hyperthermia | Treatment sequence is important. Significant differences between heating methods | [151] | |
Nanoparticles coated with crosslinked starch | Drug delivery | Release kinetics | Release profiles influenced by crosslinking density, pH and temperature | [141] | |
Coprecipitated gold-coated nanoparticles | Drug delivery/targeted delivery | Cellular studies with resistant and native A2780 cells | Cisplatin-coated nanoparticles demonstrated higher activity | [139] | |
Coprecipated nanoparticles coated with poly(lactic acid) | Drug delivery | Loading and release kinetics | Effective drug loading. Half of loaded drug was released | [138] | |
Coprecipitated nanoparticles coated with adsorbed carboxymethyl dextran | Combination treatment/understanding of potentiation mecahnisms | Cellular studies using Caco-2 | No cytoprotective role from copper when used with MFH. Higher platinum uptake and membrane permeability with MFH when compared with hot water | [152] | |
Concanavalin A | Coprecipitated chitosan-coated nanoparticles | Drug delivery | Release kinetics. Cellular experiments conducted in HeLa cells | Increased drug activity found in nanoparticle–drug conjugated systems | [142] |
Cyclophosphamide | Citrate-coated nanoparticles | MRI contrast/combination treatment | In vivo experiments in mammary adenocarcinoma | Lifespan of mice significantly improved. MRI enhancement observed | [155] |
CO3O4−Fe3O4 hybrid nanoparticles | Drug delivery | Release kinetics. Cellular experiments conducted in mouse fibroblast | Controlled release was achieved. Particles were not cytotoxic | [143] | |
Geldanamycin | Micrometer-sized particles | Combination treatment | In vitro and in vivo studies using B16 melanoma | In vivo, 55% remission in treated group | [157] |
Gemcitabine | Coprecipitated nanoparticles coated with a polyelectrolyte complex of poly(acrylic acid), chitosan and folic acid | Drug delivery | Release kinetics. Cellular experiments with PRF-5, DLD-1 and MDA-231 cell lines | Nanoparticles delivered the drug to the nuclei of cells | [144] |
Melphalan | Adsorbed dextran-coated nanoparticles | MRI contrast/combination treatment | In vivo experiments in P388 tumors, Ehlich carcinoma and Lewis carcinoma | Lifespan of mice significantly improved. MRI enhancement observed | [154] |
Paclitaxel | Nanoparticles encapsulated in liposomes | Combination treatment | Release kinetics. Cellular experiments with HeLa cells | Combination treatment more effective | [159] |
Selol | Encapsulated magnetic nanoparticles in poly(lactic)-co-glycolic acid nanoparticles | Drug delivery | Cellular studies using B16–F10 cells | Loaded particles produced higher cell cytotoxicity | [140] |
Quercetin | Combination treatment | In vivo experiments with a melanoma model | Combination treatment more effective | [169] |
MDR: Multidrug-resistance; MFH: Magnetic fluid hyperthermia.