4.6 Article

cRGD-Conjugated GdIO Nanoclusters for the Theranostics of Pancreatic Cancer through the Combination of T-1-T-2 Dual-Modal MRI and DTX Delivery

Journal

MOLECULES
Volume 28, Issue 16, Pages -

Publisher

MDPI
DOI: 10.3390/molecules28166134

Keywords

T-1-T-2; DTX; MRI; drug delivery; pancreatic cancer

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In this study, a gadolinium-doped iron oxide nanocluster with T1-T2 dual-mode imaging and targeted therapy was synthesized using iron acetylacetone and gadolinium acetylacetone as raw materials. The results showed that the synthesized material could actively target pancreatic cancer cells and exhibit excellent magnetic resonance enhancement, indicating its potential applications for the precise diagnosis and efficient treatment of pancreatic cancer.
Clinically, magnetic resonance imaging (MRI) often uses contrast agents (CAs) to improve image contrast, but single-signal MRI CAs are often susceptible to calcification, hemorrhage, and magnetic sensitivity. Herein, iron acetylacetone and gadolinium acetylacetone were used as raw materials to synthesize a T-1-T-2 dual-mode imaging gadolinium-doped iron oxide (GdIO) nanocluster. Moreover, to endow the nanoclusters with targeting properties and achieve antitumor effects, the cyclic Arg-Gly-Asp (cRGD) peptide and docetaxel (DTX) were attached to the nanocluster surface, and the efficacy of the decorated nanoclusters against pancreatic cancer was evaluated. The final synthesized material cRGD-GdIO-DTX actively targeted alpha v beta(3) on the surface of Panc-1 pancreatic cancer cells. Compared with conventional passive targeting, the enrichment of cRGD-GdIO-DTX in tumor tissues improved, and the diagnostic accuracy was significantly enhanced. Moreover, the acidic tumor microenvironment triggered the release of DTX from cRGD-GdIO-DTX, thus achieving tumor treatment. The inhibition of the proliferation of SW1990 and Panc-1 pancreatic cancer cells by cRGD-GdIO-DTX was much stronger than that by the untargeted GdIO-DTX and free DTX in vitro. In addition, in a human pancreatic cancer xenograft model, cRGD-GdIO-DTX considerably slowed tumor development and demonstrated excellent magnetic resonance enhancement. Our results suggest that cRGD-GdIO-DTX has potential applications for the precise diagnosis and efficient treatment of pancreatic cancer.

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