Table 1 Types of photothermal agents (PTAs) and their implications

From: Avenues for integrating photothermal therapy in cancer clinic

Photothermal Agents

Examples

Advantages

Disadvantages

Organic dye compounds

Indocyanine green (ICG)117,118, Prussian blue119,120,121,122 IR dyes like BF2123,124, IR780, IR800, IR825, Porphysome125

• Excellent PCE

• Thermostable

• Used for photoacoustic imaging purpose

• Photobleaching

• Instability

• Solvent toxicity

• Poor tumour targeting ability

Carbon nanomaterials

Carbon nanotubes126,127,128,129,Graphene and graphene oxide130,131

• Excellent biocompatibility

• Better bioavailability

• Enhanced cargo-loading capacity

• Lower PCE

• Poor biodegradability

• Toxicity

• Complex synthesis methods

Metal-based agents

Zinc-based gold nanocomposite132,133, Copper-based NPs132,134,135,136, Gold nanostructures137,138,139, Plasmonic gold nanostars139,140,141,142, Plasmonic gold semi-shells143, SPIONS144,145

• Excellent PCE

• Easier surface modification

• Thermostable

• Non-toxic

• Enhanced specificity

• Stability concerns (potential for aggregation)

• Immunotoxicity

• Limited selectivity

Conjugate-based agents

Polypyrrole nanomaterials146,147,

Conjugated polymers30,46,148, Carbon-silica nanocomposites149, Gold-decorated melanin nanoparticles118, Lanthanide ion-based up-conversion nanomaterial150, Biomimetic gold nanoformulation151

• Enhanced PCE

• Increased tumour targeting and accumulation

• Multimodal imaging support

• Versatile surface modifications

• Often complex synthesis and characterization procedures

• Toxicity concerns

• Limited thermostability