Skip to main navigation Skip to search Skip to main content

Manganese-Templated Nontrivial Structures for MRI and Therapy

  • Farah Benyettou
  • , Thirumurugan Prakasam
  • , Mostafa Khair
  • , Osama Abdullah
  • , Matteo Lusi
  • , Haidee Paterson
  • , Maryam Alkaabi
  • , Sneha Thomas
  • , Rainer Straubinger
  • , Nosayba Al Damook
  • , Maylis Boitet
  • , Mamoun Abelbaki
  • , Judalyn Del Monte
  • , Diana Yu
  • , Rick E. Heinz
  • , Sheri L. Holmen
  • , Edward Hsu
  • , Carlos Platas-Iglesias
  • , Gennaro Esposito
  • , Ali Trabolsi
  • New York University Abu Dhabi
  • University of Utah
  • University of A Coruna

Research output: Contribution to journalArticlepeer-review

Abstract

Manganese (Mn)-based metal–organic architectures offer a unique avenue for integrating magnetic resonance imaging (MRI) and cancer therapy within a single molecular platform. We report three topologically distinct Mn-templated structures─Mn-[2]Catenate (Mn-[2]C), Mn-Trefoil Knot (Mn-TK), and Mn-Borromean Rings (Mn-BR)─that combine high relaxivity with tumor-selective cytotoxicity. The design leverages their geometrical complexity and electropositive, pH-labile coordination framework to ensure kinetic stability and lipophilicity at physiological pH while enabling Mn2+ release in the acidic tumor microenvironment. Among the three, Mn-BR and Mn-TK exhibit superior longitudinal relaxivities (r1 = 10.1 and 6.8 mM–1.s–1 at 3 T) and produce bright T1-weighted contrast exceeding that of Gd-DTPA and Mn-DPDP. In vitro, they show high cancer selectivity and potency in glioblastoma (U251-MG) cells, with IC50 values of 3.0 ± 0.9 μM (Mn-BR) and 5.6 ± 1.9 μM (Mn-TK), outperforming cisplatin (12.7 ± 2.5 μM) while sparing normal cells (SI > 3.9 for Mn-TK; SI > 9.4 for Mn-BR). Mechanistically, their uptake proceeds via energy-dependent endocytosis─caveolae-mediated for Mn-TK and clathrin/macropinocytosis-driven for Mn-BR─culminating in lysosomal acidification, pH-triggered disassembly, Mn2+ release, ROS accumulation, and caspase-dependent apoptosis. In vivo, Mn-TK and Mn-BR achieve tumor-specific accumulation, strong MRI contrast, and pronounced growth inhibition in subcutaneous glioblastoma models, while Mn-[2]C shows minimal selectivity and higher systemic toxicity. Importantly, in a spontaneous orthotopic glioblastoma model, both Mn-TK and Mn-BR provided robust BBB permeability and persistent, tumor-specific MRI enhancement, confirming their potential for precise MRI-guided tumor visualization. This research marks a major leap forward in medical nanotechnology, unveiling a new class of metal–organic structures that seamlessly integrates imaging and therapy. By unlocking their full potential, these structures promise to revolutionize MRI diagnostics, precision medicine, and next-generation cancer treatments, paving the way for unparalleled clinical outcomes.

Original languageEnglish
Pages (from-to)15529-15549
Number of pages21
JournalJournal of the American Chemical Society
Volume148
Issue number15
DOIs
Publication statusPublished - 22 Apr 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Manganese-Templated Nontrivial Structures for MRI and Therapy'. Together they form a unique fingerprint.

Cite this