Table 2. Mechanism of Nano-theranostics therapies exerted on cells .
| Action | Temperature Elevation | Mechanisms | Ref | |
| Photo thermal therapy | NA | L-SPR: It is a collective oscillation. It is mediated with light scattered absorption. The absorbed light (as an energy) is dissipated as local heat. The light excites the free electrons (present in the internalized NTs) converts light into heat. | 6,7 | |
| Photo dynamic therapy | NA | The photosensitizer in the material generates the ROS, like singlet oxygen (1O2), free radicals and peroxides on excitation of NT material with NIR light. The ROS is cytotoxic in nature. It causes irreversible damage to tumour tissues, called as photodynamic effect. | 8,9 | |
| Hyperthermia | Lysosomal damage | 41°C to 46°C | Increases sensitivity of tumour without affecting the protein synthesis. It activates the apoptosis by expressing or inducing proteins | 7 |
| Thermal ablation | Cell necrosis | 46°C to 70°C | The elevated temperature modifies biomolecules; denatures proteins, to lose their activity; and melts the lipid | 7 |
| Nano photo thermolysis | Dual action necrosis with oncosis | NA | Temperature elevation results in micro explosion at the surface of NTs with no heat transfer to the surrounding tissue. It causes an irreversible cell damage by expulsion from the nanoparticle surface or generated ultrasonic shock | 7 |
|
LANTCET [Laser-activated nano-thermolysis as cell elimination technology] |
Activation by reaction of vapor and plasmon resonance | NA | The vapor bubbles generated due to plasmon resonance effect of NTs, disrupts the cancer cell membrane and cytoskeleton through mechanical forces | 7 |
Abbreviations: L-SPR, localized surface plasmon resonance; ROS, reactive oxygen species; NA, not applicable; NIR, near infra-red.