4.6 Article

Development of superior nanotheranostic agents with indocyanine green-conjugated poly(styrene-alt-maleic acid) nanoparticles for tumor imaging and phototherapy

Journal

JOURNAL OF MATERIALS CHEMISTRY B
Volume 11, Issue 28, Pages 6560-6566

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3tb00764b

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Developing safe and high-quality theranostic agents for cancer treatment is crucial. In this study, the clinical indocyanine green (ICG) was coupled with biocompatible poly(styrene-alt-maleic anhydride) (PSMAn) to obtain PSMAn-ICG polymer. The self-assembly of its hydrolyzed product in water resulted in ICG-conjugated poly(styrene-alt-maleic acid) nanoparticles (PSMA-ICG NPs). These NPs demonstrated good solubility and stability in aqueous solutions, high photostability, and reduced damage to red blood cells, highlighting the importance of PSMA coupling. Furthermore, the PSMA-ICG NPs showed significant tumor targeting and long-term imaging capabilities, as well as potent photothermal therapy when combined with near-infrared laser irradiation. Overall, this study provides promising phototheranostic agents for clinical applications.
Developing safe, high-quality theranostic agents for cancer treatment is of great clinical value. In this work, for the first time, the clinical indocyanine green (ICG) is coupled with the biocompatible poly(styrene-alt-maleic anhydride) (PSMAn) to obtain the PSMAn-ICG polymer. The self-assembly of its hydrolyzed product in water results in ICG-conjugated poly(styrene-alt-maleic acid) nanoparticles (PSMA-ICG NPs). Intriguingly, the NPs have many advantages, including good solubility and stability in aqueous solutions, high photostability and decreased hemolytic damage to red blood cells, highlighting the importance of PSMA coupling. More interestingly, PSMA-ICG NPs significantly promote tumor targeting and enable long-term imaging of tumors. Furthermore, the administration of PSMA-ICG NPs in combination with near-infrared laser irradiation provides superior potency in the photothermal therapy of tumors. Furthermore, 9-amino-sialic acid (Sia)-coated PSMA-ICG NPs are fabricated, further enhancing tumor imaging and phototherapy. This is the first report of PSMA-NIR conjugates achieving tumor reduction in mice. Overall, this study provides novel phototheranostic agents with broad clinical transformation prospects.

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