Table 1.
2D NSs | Surface Functionalization |
Targeting Ligand | Drug | LC (mg or μg)/EE (%) | Size (nm) | ζ Potential (mV) | Synergistic Effect | Cancer Type | Treatment Days | TGI Rates (%)/Observation after the Treatment |
Reference | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
BP | DOX | 950% (in wt) | 281 ± 9.5 | 1.5 | CTX/PTT/PDT | Breast cancer (4T1 cells) | 14 | 95.5% | [91] | |||
PAMAM | HA | 95% | 291 ± 4.17 | −5.83 ± 2.31 | CTX/PTT | Reduction in tumor size | [92] | |||||
CaP | 53.6% | 181.5 | −15.5 | CTX | Breast cancer (MCF-7 cells) | 18 | 85% | [93] | ||||
HA | MTX | 2.6% | 276 | −18 | CTX/PTT | Breast cancer (4T1 cells) | 10 | Inhibit tumor growth | [94] | |||
MoS2 | PEG | DOX | ~69% | 150 | −7.17 ± 1.8 | Sarcoma (S180 cells) | 14 | Decrease in tumor volume | [95] | |||
CuS | 162.3 mg | 114.5 | −5.3 ± 1.5 | - | [96] | |||||||
PEI, PEG, α-LA | FA, BSA | 185 mg | 196 | 6.8 | Breast cancer (MCF-7 cells) | 20 | Inhibit tumor growth | [97] | ||||
Liposome | 104.4% | 250 | −38.26 | Breast cancer (4T1 cells) | 2 | [98] | ||||||
CS, CMC, SPIONs | 95.69% | 429.07 ± 3.538 | −59.01 ± 3.629 | 14 | [99] | |||||||
Ti3C2 | HA | 84.2% | 178 ± 32.4 | −20.71 ± 1.5 | CTX/PTT/PDT | Colorectal cancer (HCT-116 cells) | 16 | Tumor disappearance and no metastasis/recurrence | [100] | |||
CP | MET | 96.2% | 310 | −20 | Breast cancer (MDA-MB-231 cells) | [101] | ||||||
PDA, PEG-GNRs | DOX | 95.88% | 250 | −22.1 ± 1.2 | CTX/PTT | - | [102] | |||||
LDHs | AuNPs | FA-TCS | 94.6% | 100–180 | −52.4 | Breast cancer (MCF7 cells) | - | Increased % of cell death at the G0/G1 phase | [103] | |||
BSA | 5-FU | 56.4% ± 7.4% | 172.4 ± 10.6 | −14.0 | CTX | Colorectal cancer (HCT-116 cells) | 18 | Significant and effective inhibition of tumor growth | [104] | |||
ABX | 93.2% ± 5.2% | |||||||||||
ICG | - | 99.6% ± 0.1% | 38.8 ± 1.8 | 33.9 ± 0.9 | CTX/PTT/PDT | Breast cancer (4T1 cells) | 12 | [105] | ||||
5-FU and CD-siRNA | 22.60% (in wt) | 89 | 38.9 | CTX | Breast cancer (MCF7 cells) | - | Suppresses cell growth | [106] | ||||
Gal | Cur | 31% | 116.1 ± 35.9 | 10.0 ± 0.7 | Hepatocellular cancer (HepG2 cells) | - | [107] | |||||
BSA | 5-FU | - | 41.2 ± 5.4 | - | CTX/PTT | Colon cancer (HCT-116 cells) | 24 | Induces cancer cell death with no sign of recurrence | [108] | |||
MTX | 42% ± 0.25% | 104 | - | CTX | Cervical cancer (C33A cells) | 4 | Tumor growth suppression | [109] | ||||
FA | DOX | 3.6 mg/mg (w/w) | 60–100 | −3.2 | Oral epidermal cancer (KB cells) | - | Predominant apoptosis of cancer cells | [110] | ||||
PDA | - | 125 | −14.61 | CDT/PTT | Lung cancer (A549 cells) | - | [111] | |||||
F-CDs | 212.6 μg/g | 137 | 39.7 | CTX | HeLa cells | - | Enhanced cytotoxicity | [112] |