Photodynamic therapy (PDT) is a promising therapeutic modality based on the combined use of light and photosensitizers (PSs) and approved for treating several types of cancers. Thio-heterocyclic naphthalimide-based PSs are particularly attractive as phototheranostic agents, combining fluorescence imaging for diagnosis with reactive oxygen species (ROS)-mediated cytotoxicity for treatment. However, no effective conjugation strategy for simultaneously endowing naphthalimides with water solubility and efficient ROS production ability currently exists. Herein, novel water-soluble, heavy atom-free thioxanthene-fused naphthalimide–polyamine conjugates 1–4 have been developed. Structural variation in the polyamine moiety, including chain length and nitrogen content, allowed the fine-tuning of key properties. Conjugates 2 and 3 exhibited (i) favorable photophysical and fluorescent properties, (ii) enhanced water solubility, (iii) improved photodynamic efficacy against MCF-7 breast cancer cells, and (iv) negligible dark toxicity. This novel class of thioxanthene-fused naphthalimide–polyamine conjugates provides a promising conjugation strategy for improving the drug-like properties of PSs.

Uliassi, E., Rossi, M., Giosia, M.D., Conti, A., Calvaresi, M., Rhoden, K.J., et al. (2026). Novel Water-Soluble, Heavy Atom-Free Thioxanthene-Fused Naphthalimide-Polyamine Phototheranostic Conjugates. CHEMMEDCHEM, 21(15), 1-12 [10.1002/cmdc.70403].

Novel Water-Soluble, Heavy Atom-Free Thioxanthene-Fused Naphthalimide-Polyamine Phototheranostic Conjugates

Uliassi, Elisa;Giosia, Matteo Di;Conti, Amalia;Calvaresi, Matteo;Rhoden, Kerry J;Bolognesi, Maria Laura
2026

Abstract

Photodynamic therapy (PDT) is a promising therapeutic modality based on the combined use of light and photosensitizers (PSs) and approved for treating several types of cancers. Thio-heterocyclic naphthalimide-based PSs are particularly attractive as phototheranostic agents, combining fluorescence imaging for diagnosis with reactive oxygen species (ROS)-mediated cytotoxicity for treatment. However, no effective conjugation strategy for simultaneously endowing naphthalimides with water solubility and efficient ROS production ability currently exists. Herein, novel water-soluble, heavy atom-free thioxanthene-fused naphthalimide–polyamine conjugates 1–4 have been developed. Structural variation in the polyamine moiety, including chain length and nitrogen content, allowed the fine-tuning of key properties. Conjugates 2 and 3 exhibited (i) favorable photophysical and fluorescent properties, (ii) enhanced water solubility, (iii) improved photodynamic efficacy against MCF-7 breast cancer cells, and (iv) negligible dark toxicity. This novel class of thioxanthene-fused naphthalimide–polyamine conjugates provides a promising conjugation strategy for improving the drug-like properties of PSs.
2026
Uliassi, E., Rossi, M., Giosia, M.D., Conti, A., Calvaresi, M., Rhoden, K.J., et al. (2026). Novel Water-Soluble, Heavy Atom-Free Thioxanthene-Fused Naphthalimide-Polyamine Phototheranostic Conjugates. CHEMMEDCHEM, 21(15), 1-12 [10.1002/cmdc.70403].
Uliassi, Elisa; Rossi, Michele; Giosia, Matteo Di; Conti, Amalia; Calvaresi, Matteo; Rhoden, Kerry J; Bolognesi, Maria Laura
File in questo prodotto:
File Dimensione Formato  
ChemMedChem - 2026 - Uliassi - Novel Water‐Soluble Heavy Atom‐Free Thioxanthene‐Fused Naphthalimide Polyamine.pdf

accesso aperto

Tipo: Versione (PDF) editoriale / Version Of Record
Licenza: Licenza per Accesso Aperto. Creative Commons Attribuzione (CCBY)
Dimensione 2.04 MB
Formato Adobe PDF
2.04 MB Adobe PDF Visualizza/Apri
cmdc70403-sup-0001-suppdata-s1.pdf

accesso aperto

Tipo: File Supplementare
Licenza: Licenza per Accesso Aperto. Creative Commons Attribuzione (CCBY)
Dimensione 2.05 MB
Formato Adobe PDF
2.05 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/1084567
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
  • OpenAlex ND
social impact