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Synthesis and Evaluation of Novel meso-Tetraphenyltetrabenzoporphyrins for Photodynamic Therapy.
Liang, Hong-Yu; Jiang, Ying; Song, Zhi-Bing; Namulinda, Tabbisa; Chen, Pei-Ran; Chen, Zhi-Long; Yan, Yi-Jia.
Afiliação
  • Liang HY; Department of Pharmaceutical Science & Technology, Donghua University, Shanghai 201620, China.
  • Jiang Y; Department of Pharmaceutical Science & Technology, Donghua University, Shanghai 201620, China.
  • Song ZB; Department of Pharmaceutical Science & Technology, Donghua University, Shanghai 201620, China.
  • Namulinda T; Department of Pharmaceutical Science & Technology, Donghua University, Shanghai 201620, China.
  • Chen PR; Department of Pharmaceutical Science & Technology, Donghua University, Shanghai 201620, China.
  • Chen ZL; Department of Pharmaceutical Science & Technology, Donghua University, Shanghai 201620, China.
  • Yan YJ; Department of Pharmacy, Huadong Hospital, Fudan University, Shanghai 200040, China.
ACS Med Chem Lett ; 15(7): 1109-1117, 2024 Jul 11.
Article em En | MEDLINE | ID: mdl-39015270
ABSTRACT
To discover effective photosensitizers for photodynamic therapy (PDT), a series of new meso-tetraphenyltetrabenzoporphyrin (m-Ph4TBP) derivatives were designed, prepared, and characterized. All m-Ph4TBPs own two characteristic absorption bands in the range of 450-500 and 600-700 nm and have the ability to generate singlet oxygen upon photoexcitation. Most of the m-Ph4TBPs demonstrated high photoactivity, among which compounds I4, I6, I12, and I13 induced apoptosis and also exhibited excellent photodynamic activities in vivo. Nonetheless, the liver organs of the I4 and I6-PDT groups showed clear calcifications, whereas the liver tissues of the other PDT groups showed no calcification. It was indicated that compared to phenolic m-Ph4TBPs, glycol m-Ph4TBPs exhibited superior biological safety in mice. According to comprehensive evaluations, m-Ph4TBP I12 displayed excellent photodynamic antitumor efficacy and biological safety and can be regarded as a promising antitumor drug candidate.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article