From: Emerging nanotechnology-based therapeutics to combat multidrug-resistant cancer
S. No | Nanoparticles (NPs) | Chemotherapeutic drugs | Experimental model | Mechanism of action | Refs |
---|---|---|---|---|---|
Nanomicelles | |||||
1 | TAT-TPGS-PEG-b-P(ALA) nanomicelles | Doxorubicin | Human breast cancer (MCF-7 and MCF-7/ADR cells) | Inhibition of P-gp efflux pump and intracellular drug retention and enhanced cytotoxicity | [303] |
2 | Folic acid conjugated P(OEGMA300)-st-P(HEMA-g-LA) nanomicelles | Doxorubicin | Human cervical cancer (HeLa cells) | Enhanced intracellular drug accumulation and tumor microenvironment-triggered drug release and cytotoxicity | [304] |
3 | Polycarbonate based NO nanomicelles | Doxorubicin | Human breast cancer (MCF-7/DOXR cells) | Nitric oxide-mediated P-gp inhibition, intracellular drug accumulation and cytotoxicity | [305] |
4 | Nitrate functionalized TPGS nanomicelles | Doxorubicin, adjudin and nitric oxide | Human breast cancer (MCF-7/ADR cells), murine mammary carcinoma (4T1 cells) and BALB/c mice | Controlled drug release, enhanced cytotoxicity, P-gp inhibition, reduction in tumor growth and reversal of MDR | [306] |
5 | Poly (β-amino ester) polymer-based nanomicells | Doxorubicin | Human breast cancer (MCF-7 and MCF-7/ADR cells) | Inhibition of P-gp efflux pump by polymer, lysosomal escape and intracellular drug retention | [307] |
6 | FA-Chitosan coated nanomicelles | siRNA and Doxorubicin | Murine breast cancer (4T1, 4T1/MDR cells) and 4T1/MDR xenograft mice | Elevated intracellular drug accumulation and downregulation of MDR1 gene for the suppression of tumor growth | [308] |
7 | Thermosensitive Hydrogel | Doxorubicin and Docetaxel | Murine CT-26 cell line and CT-26 xenograft mice model | Sustained drug release and enhanced retention and antitumor activity with minimized inherent side effects in mice | [309] |
8 | Lysine linked d-α-TPGS2000 succinate (PLV2K) nanomicelles | Doxorubicin | Human colorectal adenocarcinoma cell line (Caco-2 cells) | Elevated intracellular accumulation of doxorubicin by uncompetitive P-gp ATP base inhibition | [310] |
9 | Polyvinyl caprolactam-polyvinyl acetate-polyethylene micelles (Soluplus®) | Doxorubicin | Human breast cancer (MCF-7 and MCF-7/DOX cells) and nude BALB/c mice | Inhibition pf P-gp drug efflux and alteration in membrane fluidity further enhance the intracellular drug retention and associated toxicity with antitumor activity | [311] |
10 | PEG-PE/VitaminE nanoemulsion | Paclitaxel and curcumin | Human ovarian cancer cell lines (SKOV3 and SKOV3TR cells) and female nude mice | Bioavailable curcumin inhibits the NF-κB and also acts as an inhibitor for P-gp efflux transporters and elevated intracellular paclitaxel | [146] |
11 | PCL-PEG nanomicelles | Doxorubicin and siHIF | Prostate cancer (PC-3) cells and xenograft mice | siHIF-mediated MDR1 gene silencing, disruption of angiogenesis and enhanced intracellular doxorubicin levels | [174] |
12 | Pluronic (P-105) based nanomicelles | Doxorubicin and Ruboxyl | Human leukemia cell line (HL-60 cells), Human ovarian cancer cell lines (A2780S and A2780/ADR cells) | Surfactant-based nanomicelles facilitate the delivery of drugs to resistant cells and also enhance their intracellular retention | [312] |
Nanoemulsion | |||||
13 | Nanoemulsion | Paeonol | Human colorectal adenocarcinoma (Caco-2 cell lines) and male SD rats | Nanoemulsions bypass P-gp efflux pumps and suppress tumor growth | [313] |
14 | Folate conjugated nanoemulsion | Docetaxel | Human epithelial cell lines (KB-WT and KB-PR10 cells) and C57BL/6Â J transgenic mouse | Bypasses efflux pumps and downregulates P-gp efflux with enhanced antitumor activity | [314] |
15 | Amphiphilic dendrimer | Doxorubicin | Human breast Cancer (MCF-7S, MCF-7R cells), Human prostate cancer (PC-3 cells), Human hepatocarcinoma (HepG2 cells), Human cervical cancer (HeLa cells) and Mice models (NSG mice and C57BL/6 mice) | EPR-mediated efficient doxorubicin delivery prevents systemic toxicity and overcomes drug resistance | [315] |
16 | Capryol 90- nanoemulsion | Paclitaxel | Human colorectal cancer (Caco-2 cells) | Inhibit P-gp efflux and enhance drug retention and associated toxicity | [316] |
17 | Flaxseed oil-DSPE-PEG2000) nanoemulsion | Curcumin and Paclitaxel | Ovarian cancer (SKOV and SKOV3TR) cells | Inhibit NF-κB activity and downregulate P-gp expression with elevated intracellular drug retention | [317] |
18 | Polyalkylcyanoacrylate NPs | Cyclosporin A and Doxorubicin | Mouse leukemia (P388/ADR cells) | Inhibition of P-gp efflux pump by cyclosporine A with enhanced doxorubicin retention and associated cytotoxicity | [318] |