Synthesis and Antitumor Activity of Photosensitizer Eugenol Porphyrin Derivatives: A Combination Therapy of Chemotherapy and Photodynamic Therapy

Author:

Li Hui1ORCID,Tang Chen1ORCID,Liu Zhenhua1ORCID,Tian Zejie1ORCID,Shi Lei1ORCID,Yang Lingyan1ORCID,He Jun1ORCID,Ai Wenbin2ORCID,He Xufeng3ORCID,Liu Yunmei1ORCID

Affiliation:

1. Institute of Pharmacy & Pharmacology, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study University of South China Hengyang Hunan China

2. The Second Affiliated Hospital, Hengyang Medical School University of South China Henyang Hunan China

3. Health School of Nuclear Industry Nanhua Hospital, University of South China Huaihua Hunan China

Abstract

ABSTRACTPhotodynamic therapy (PDT) is a promising treatment for cancer. At present, the development of photosensitizers has become a hot spot for research at home and abroad. In this study, 20 porphyrin‐butylphenol compounds were synthesized, and the structures of the target compounds were analyzed by means of 1H NMR, IR, mass spectrometry, and other analytical methods. The quantum yield of the target compound as a photosensitizer for the production of singlet oxygen was determined by using a DPBF reactive oxygen probe (1,3‐diphenylisobenzofuran). The anticancer activity of the synthesized target compounds was studied using HepG2 cells and A549 cells. The results of the singlet oxygen experiments showed that the Zn metal chelated compound had better singlet oxygen production than the free‐base porphyrin. The cellular activity assays showed that the metal‐chelated compounds exhibited better in vitro antitumor activity.

Funder

Natural Science Foundation of Hunan Province

Publisher

Wiley

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