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Updated: Apr 13, 2026

Anticancer Metal Complexes: Synthesis and Cytotoxicity Evaluation by the MTT Assay
Published on: November 10, 2013
Fluorophores to fighters: BODIPY-metal complexes as next-gen anticancer prodrugs
Twara Kikani1, Krutika Patel1, Sonal Thakore1
1Department of Chemistry, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara 390 002, India. chemistry2797@yahoo.com.
Abstract:
Metal-coordinated complexes have been employed as effective anti-cancer agents with cis-platin being the foundation for the development of metal-based therapeutics. However, their use is greatly limited by their systemic toxicity, drug resistance and non-targeted approach. Progressing drug resistance has led to the use of combinatorial approaches for a multifaceted attack on cancer. Photodynamic therapy (PDT) is a clinically approved adjuvant chemotherapy that involves the use of a photosensitizer (PS), light and endogenous molecular oxygen (3O2). Boron-dipyrromethene (BODIPY) dyes are a class of fluorophores that serve as promising PSs with excellent light-activated reactive oxygen species (ROS) generating capacity (for PDT) and light-to-heat conversion (for PTT) causing the thermal ablation of cancer cells. Conjugating a metal-based drug along with a PS and a targeting ligand to design a prodrug acts as a "magic packet" to target various cancers. This review elaborates the advances in the development of metallo-prodrugs adorned with a BODIPY cage as cancer theranostics. It highlights the engineering marvel of constructing prodrugs with high specificity and organelle-targeting ability.
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