corrole and methylphenylsulfide

Recent work has highlighted the potential of metallocorroles as versatile platforms for the development of drugs and imaging agents, since the bioavailability, physicochemical properties and therapeutic activity can be dramatically altered by metal ion substitution and/or functional group replacement. Significant advances in cancer treatment and imaging have been reported based on work with a water-soluble bis-sulfonated gallium corrole in both cellular and rodent-based models. We now show that cytotoxicities increase in the order Ga < Fe < Al < Mn < Sb < Au for bis-sulfonated corroles; and, importantly, that they correlate with metallocorrole affinities for very low density lipoprotein (VLDL), the main carrier of lipophilic drugs. As chemotherapeutic potential is predicted to be enhanced by increased lipophilicity, we have developed a novel method for the preparation of cell-penetrating lipophilic metallocorrole/serum-protein nanoparticles (NPs). Cryo-TEM revealed an average core metallocorrole particle size of 32 nm, with protein tendrils extending from the core (conjugate size is ~100 nm). Optical imaging of DU-145 prostate cancer cells treated with corrole NPs (≤100 nM) revealed fast cellular uptake, very slow release, and distribution into the endoplasmic reticulum (ER) and lysosomes. The physical properties of corrole NPs prepared in combination with transferrin and albumin were alike, but the former were internalized to a greater extent by the transferrin-receptor-rich DU-145 cells. Our method of preparation of corrole/protein NPs may be generalizable to many bioactive hydrophobic molecules to enhance their bioavailability and target affinity.

Topics: Cell Line, Tumor; Chromatography, Gas; Chromatography, High Pressure Liquid; Cryoelectron Microscopy; Endoplasmic Reticulum; Flow Cytometry; Humans; Hydrogen Peroxide; Lysosomes; Magnetic Resonance Spectroscopy; Male; Microscopy, Atomic Force; Microscopy, Electrochemical, Scanning; Nanoparticles; Oxidation-Reduction; Porphyrins; Sulfides

The electronic and structural features of (oxo)manganese(V) corroles and their catalyzed oxygen atom transfers to thioanisole in different spin states have been investigated by the B3LYP functional calculations. Calculations show that these corrole-based oxidants and their complexes with thioanisole generally have the singlet ground state, and their triplet forms are also accessible in consideration of the spin-orbit coupling interaction. Due to strong d-π conjugation interactions between Mn and the corrole ring arising from the π electron donation of the corrole moiety, the five-coordinated Mn approximately has the stable 18-electron configuration. The predicted free energy barriers for the singlet oxygen atom transfer reactions are generally larger than 22 kcal mol(-1), while the spin flip in reaction may remarkably increase the reactivity. In particular, the bromination on β-pyrrole carbon atoms of the meso-substituted (oxo)manganese(V) corrole strikingly enhances the spin-orbit coupling interaction and results in the dramatic increase of reactivity. The multiple spin changes are predicted to be involved in the low-energy reaction pathway. The present results show good agreement with the experimental observation and provide a detailed picture for the oxygen atom transfer reaction induced by the (oxo)manganese(V) corroles.

Topics: Manganese Compounds; Oxides; Oxygen; Porphyrins; Quantum Theory; Sulfides; Thermodynamics