Bioorthogonal Photoactivation of 2‐Nitrobenzyl Caged Doxorubicin Anticancer Prodrugs on Gold Nanostars

Bioorthogonal chemistry that can be controlled through near-infrared (NIR) light is a promising route to therapeutics. This study proposes a method to intracellularly photoactivate prodrugs using plasmonic gold nanostars (AuNSt) and NIR irradiation. Two strategies are followed. On one hand, doxorubicin (Dox) masked with a 2-nitrobenzyl carbamate (proDox<sub>1</sub>) is used as a photoactivatable prodrug. In the second strategy, a photolabile Dox prodrug (proDox<sub>2</sub>) obtained by modification of Dox with 2-nitrobenzyl diol bearing a disulfide is attached to the AuNSt surface. Under NIR irradiation AuNSt induce local electromagnetic field enhancement, leading to photocleavage of the 2-nitrobenzyl moiety in both proDox<sub>1</sub> and proDox<sub>2</sub>, and subsequent Dox release. Near field enhancement by excitation of surface plasmons in AuNSt is sufficient to record the surface-enhanced Raman scattering (SERS) spectra of proDox<sub>1</sub> and proDox<sub>2</sub>. The therapeutic potential of this bioorthogonal photoactivation strategy is confirmed in vitro and in vivo using a mouse model of human melanoma. NIR-activated AuNSt induce in vivo the intracellular release of Dox and subsequent cancer cell death, thus reducing tumor growth at low irradiation power density to avoid undesired photothermal effects. These results demonstrate that AuNSt are suitable platforms for NIR light-triggered drug delivery in cancer therapy.

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Journal
Advanced Materials
Published
2025-09-09
DOI
https://doi.org/10.1002/adma.202510898
Primary Topic
Gold and Silver Nanoparticles Synthesis and Applications
Type
article
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article

Bioorthogonal Photoactivation of 2‐Nitrobenzyl Caged Doxorubicin Anticancer Prodrugs on Gold Nanostars

Roberto Cao‐Milán, Judith Langer, Félix Sancenón, María Alfonso et al.
Advanced Materials
Gold and Silver Nanoparticles Synthesis and Applications
article

Bioorthogonal Photoactivation of 2‐Nitrobenzyl Caged Doxorubicin Anticancer Prodrugs on Gold Nanostars

Roberto Cao‐Milán, Judith Langer, Félix Sancenón, María Alfonso, Andy Hernández‐Montoto, Juan José Esteve‐Moreno, Mónica Gorbe, José Manuel Terrés, Luis M. Liz‐Marzán, Óscar F. Silvestre, Carlos Renero‐Lecuna, Alba García‐Fernández, Andrea Escudero, Ramón Martínez‐Máñez, Eva María Nieto Garrido, Javier Ibáñez
article en

Abstract

Bioorthogonal chemistry that can be controlled through near-infrared (NIR) light is a promising route to therapeutics. This study proposes a method to intracellularly photoactivate prodrugs using plasmonic gold nanostars (AuNSt) and NIR irradiation. Two strategies are followed. On one hand, doxorubicin (Dox) masked with a 2-nitrobenzyl carbamate (proDox<sub>1</sub>) is used as a photoactivatable prodrug. In the second strategy, a photolabile Dox prodrug (proDox<sub>2</sub>) obtained by modification of Dox with 2-nitrobenzyl diol bearing a disulfide is attached to the AuNSt surface. Under NIR irradiation AuNSt induce local electromagnetic field enhancement, leading to photocleavage of the 2-nitrobenzyl moiety in both proDox<sub>1</sub> and proDox<sub>2</sub>, and subsequent Dox release. Near field enhancement by excitation of surface plasmons in AuNSt is sufficient to record the surface-enhanced Raman scattering (SERS) spectra of proDox<sub>1</sub> and proDox<sub>2</sub>. The therapeutic potential of this bioorthogonal photoactivation strategy is confirmed in vitro and in vivo using a mouse model of human melanoma. NIR-activated AuNSt induce in vivo the intracellular release of Dox and subsequent cancer cell death, thus reducing tumor growth at low irradiation power density to avoid undesired photothermal effects. These results demonstrate that AuNSt are suitable platforms for NIR light-triggered drug delivery in cancer therapy.

Advanced Materials
Ikerbasque (ES), University of Havana (CU), CIC biomaGUNE (ES), Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (ES), Centro de Investigacion Principe Felipe (ES), Instituto de Investigación Sanitaria La Fe (ES), Universitat Politècnica de València (ES), Universidade de Vigo (ES), University of Otago (NZ)
Generalitat Valenciana, Ministerio de Ciencia e Innovación, Instituto de Salud Carlos III, European Regional Development Fund, Agencia Estatal de Investigación
Openalex Percentile: Top 84%
Gold and Silver Nanoparticles Synthesis and Applications
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