AI Article Synopsis

  • - A special drug made from platinum called a prodrug was created, which can be activated by red light to help treat cancer by making it produce a type of oxygen that can kill cancer cells.
  • - This drug works well in cancer cells, specifically in some types of cervical and breast cancer, but doesn’t affect healthy cells much, showing it’s safe for normal tissue.
  • - It gets to the parts of the cell that are important for energy and stress responses and causes the cancer cells to die by making them stop growing and function poorly.

Article Abstract

A cisplatin-based platinum(iv) prodrug, [Pt(NH)Cl(OH)( )], having as a red-light active boron-dipyrromethene (BODIPY) pendant, was synthesized and characterized and its application as a chemo--photodynamic therapy agent was studied. as the ligand precursor is structurally characterized. The complex displayed an intense absorption band near 650 nm ( ∼ 8.8 × 10 dm mol cm) in 1 : 1 (v/v) DMSO/DPBS. It showed an emission band at 674 nm ( = 630 nm) with a fluorescence quantum yield ( ) value of 0.37. In red light (600-720 nm), it generated singlet oxygen as evidenced from the 1,3-diphenylisobenzofuran (DPBF) titration experiment giving a singlet oxygen quantum yield ( ) value of 0.28 in DMSO. The mechanistic pUC19 DNA photocleavage study and singlet oxygen sensor green (SOSG) assay ascertained its ability to generate singlet oxygen in both extracellular and intracellular media by a type-II photo-process. The complex exhibited high stability in the dark, but on red-light irradiation, it displayed rapid activation in the presence of a reducing environment. It displayed remarkable apoptotic photocytotoxicity with half-maximal inhibitory concentration (IC) ranging from 0.58 to 0.76 μM in human cervical cancer (HeLa) and breast cancer (MCF-7) cells with a respective photo-cytotoxicity index value of >172 and >131. The photodynamic activity was significantly less in non-cancerous human peripheral lung epithelial (HPL1D) cells. The emissive complex showed localization in the mitochondria and endoplasmic reticulum (ER) with a similar Pearson's correlation coefficient value, making it a dual organelle-targeted therapeutic agent. JC-1, fluo-4-AM and annexin V-FITC/propidium iodide assays in HeLa cells showed cellular apoptosis by arresting cells in the sub-G1 phase mitochondrial dysfunction and ER stress.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749958PMC
http://dx.doi.org/10.1039/d2md00225fDOI Listing

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