4.6 Article

Heparin-Superparamagnetic Iron Oxide Nanoparticles for Theranostic Applications

期刊

MOLECULES
卷 27, 期 20, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27207116

关键词

superparamagnetic iron oxide nanoparticles (SPION); heparin; heparanase; theranostic; paclitaxel; dopamine; toxicity; metastasis

资金

  1. Italian Ministry of University and Research (MIUR) through the Dipartimenti di Eccellenza 2019 grant

向作者/读者索取更多资源

In this study, a heparin-based nanoparticle system was successfully developed by engineering superparamagnetic iron oxide nanoparticles (SPIONs) with an organic coating composed of low molecular weight heparin (LMWH) and bovine serum albumin (BSA). The system showed promising potential for targeted theranostic applications and demonstrated enhanced antitumor effects when loaded with the chemotherapeutic agent paclitaxel (PTX). Furthermore, the nanoparticles exhibited effective inhibition on the heparanase enzyme and showed comparable relaxivity values to commercial contrast agents, indicating their potential in magnetic resonance imaging (MRI).
In this study, superparamagnetic iron oxide nanoparticles (SPIONs) were engineered with an organic coating composed of low molecular weight heparin (LMWH) and bovine serum albumin (BSA), providing heparin-based nanoparticle systems (LMWH@SPIONs). The purpose was to merge the properties of the heparin skeleton and an inorganic core to build up a targeted theranostic nanosystem, which was eventually enhanced by loading a chemotherapeutic agent. Iron oxide cores were prepared via the co-precipitation of iron salts in an alkaline environment and oleic acid (OA) capping. Dopamine (DA) was covalently linked to BSA and LMWH by amide linkages via carbodiimide coupling. The following ligand exchange reaction between the DA-BSA/DA-LMWH and OA was conducted in a biphasic system composed of water and hexane, affording LMWH@SPIONs stabilized in water by polystyrene sulfonate (PSS). Their size and morphology were investigated via dynamic light scattering (DLS) and transmission electron microscopy (TEM), respectively. The LMWH@SPIONs' cytotoxicity was tested, showing marginal or no toxicity for samples prepared with PSS at concentrations of 50 mu g/mL. Their inhibitory activity on the heparanase enzyme was measured, showing an effective inhibition at concentrations comparable to G4000 (N-desulfo-N-acetyl heparin, a non-anticoagulant and antiheparanase heparin derivative; Roneparstat). The LMWH@SPION encapsulation of paclitaxel (PTX) enhanced the antitumor effect of this chemotherapeutic on breast cancer cells, likely due to an improved internalization of the nanoformulated drug with respect to the free molecule. Lastly, time-domain NMR (TD-NMR) experiments were conducted on LMWH@SPIONs obtaining relaxivity values within the same order of magnitude as currently used commercial contrast agents.

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