Table 3. UV-vis imaging agents with QD or Au/Ag nanoparticles.
Imaging modality | Dye/contrast agent | Means of incorporation | Polymer components | Responsive size change | Responsive imaging property | Formulation method a | Size (nm) | Targeting group | Cells/in vivo work | Therapeutics | Ref. |
UV-vis | Fe3O4 QD | As core from which polymer was built on | Chitosan | pH | N/A | E | 160 | N/A | Uptake in L02 cells | Insulin | 67 |
UV-vis | QD | Electrostatic interaction and chemical crosslinks with polymer matrix | CM-dextran and PLL | N/A | N/A | D + E | 190 | N/A | N/A | N/A | 100 |
UV-vis | QD | Electrostatic interaction between HA and QD | HA | N/A | N/A | E | 50–120 | HA | Imaging of lymphatic vessels on ears of mice | N/A | 99 |
UV-vis | QD | In situ synthesis inside the nanogels | Chitosan and PMAA crosslinked with MBA | pH | Photoluminescence (PL) increase as pH decreases | A + D | 85–175 | N/A | Uptake and cytoxicity on mouse melanoma B16F10 cells | Temozolomide | 105 |
UV-vis | QD | Electrostatic interaction | Cholesterol-bearing amino-group-modified Pullulan | N/A | N/A | C + E | 38 | N/A | Uptake in HeLa cells | N/A | 102 |
UV-vis | QD | Electrostatic interaction between lysosome, QD and polymer | Carboxymethyl cellulose | N/A | PL decreases as pH decreases | D + E | 285 | — | Uptake and cytotoxicity on HepG2 & MCF-7 cells | Methotrexate | 101 |
NIR | QD | In situ synthesis inside the nanogels | HPC and PAA crosslinked wit MBA | pH and temperature | PL increases as pH decreases | A + D | 32–50 (pH 4.5) to 75–83 (pH 7.4) | N/A | Cytotoxicity on B16F10 cells | Temozolomide | 104 |
UV-vis | QD | As core from which polymer was built on | His-tagged polypeptides | pH, temperature and competitors | N/A | E | 40.2 | RGD | Uptake and cytotoxicity on HeLa cells | Dye ABDPSP & fluorescein sodium (model drugs) | 103 |
UV-vis | Carbon shell and magnetic core nanoparticles | As core from which polymer was built on | Poly(NIPAM-AAm) crosslinked with MBA | NIR/magnetic induced thermal responsive | PL increases as temperature increase | A + E | 320 (at 24 °C) | — | Cytotoxicity of B16F10 cells | Curcumin | 106 |
UV-vis | Ag NP | As core from which polymer was built on | Poly(NIPAM-AA) crosslinked with MBA | pH | Blue shift and increase in absorption intensity as pH decreases | A + E | ∼77 (pH 5.0) to ∼137 (pH 7.4) at 37 °C | — | Uptake and cytotoxicity on B16F10 cells | Dipyridamole | 114 |
UV-vis | Au NP | As core from which polymer was built on | P(NIPAAM-co-AAm) crosslinked with MBA | Visible light induced thermal responsive | N/A | A + E | >80 (37 °C) and ∼53 (25 °C) | N/A | Uptake and cytotoxicity of HeLa cells | 5-Fluorouracil | 110 |
UV-vis | Au–Ag NP | As core from which polymer was built on | PEG crosslinked with PEGMA | NIR induced thermal responsive | PL increases as temperature increases | A + E | 18–43 (37 °C) | HA | Uptake and cytotoxicity on B16F10 cells | Temozolomide | 111 |
UV-vis | Au–Ag NP | As core from which polymer was built on | PS crosslinked with DVB and PEG crosslinked with PEGMA | NIR induced thermal responsive | N/A | A + E | 22–37 (37 °C) | N/A | Uptake and cytotoxicity on B16F10 cells | Curcumin | 112 |
UV-vis | Au NP | In situ synthesis inside the nanogel | Lysosome–dextran | N/A | N/A | C | 190 | N/A | Uptake and cytotoxicity on KB cells | Doxorubicin | 114 |
UV-vis | Au NP | As core from which polymer was built on | Chitosan and PAA crosslinked with glutaldehyde | N/A | N/A | D + A | ∼120 | N/A | Uptake and cytotoxicity on HepG2 cells | N/A | 113 |
UV-vis | Au NP | In situ synthesis inside the nanogel | Chitosan | N/A | N/A | B | 80–230 | N/A | — | N/A | 115 |
a Formulation methods: refer to Fig. 1.