Mannose-poly(ethylene glycol)-linked SPION targeted to antigen presenting cells for magnetic resonance imaging on lymph node

• Published in: Carbohydrate polymers Vol. 92; no. 2; pp. 1586 - 1595
• Main Authors: Muthiah, Muthunarayanan, Vu-Quang, Hieu, Kim, You-Kyoung, Rhee, Joon Haeng, Kang, Sang Hyeon, Jun, Soo Youn, Choi, Yun-Jaie, Jeong, Yong Yeon, Cho, Chong-Su, Park, In-Kyu
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier Ltd 15.02.2013; Elsevier
• Subjects: Animals; Antigen-presenting cells; Antigen-Presenting Cells - metabolism; Applied sciences; Biocompatible Materials - chemistry; Biocompatible Materials - metabolism; Biological and medical sciences; crosslinking; Exact sciences and technology; Ferric Compounds - chemistry; Forms of application and semi-finished materials; hydrophilicity; image analysis; in vivo studies; intravenous injection; Investigative techniques, diagnostic techniques (general aspects); iron oxides; Lectins, C-Type - metabolism; lymph; Lymph node; lymph nodes; Lymph Nodes - cytology; Magnetic Resonance Imaging; Magnets - chemistry; Male; Mannans - chemistry; Mannose; Mannose - chemistry; Mannose receptor; Mannose-Binding Lectins - metabolism; Medical sciences; Mice; Miscellaneous; Miscellaneous. Technology; MR imaging; nanoparticles; Nanoparticles - chemistry; Polyethylene Glycols - chemistry; Polymer industry, paints, wood; Radiodiagnosis. Nmr imagery. Nmr spectrometry; Rats; receptors; Receptors, Cell Surface - metabolism; SPION; Technology of polymers; toxicity; Mannose receptor; Mannose; MR imaging; Lymph node; SPION; Antigen-presenting cells; Biological properties; Particle size; Surface reaction; Iron oxide; Hydrodynamic radius; Intravenous administration; Targeting; End group; Nanoparticle; Cytotoxicity; Amidation; Ethylene oxide polymer; Glycopolymer; Antigen presenting cell; Organic isothiocyanate; Manufacturing; Graft polymers; Aldose; Rodentia; Experimental study; Nuclear magnetic resonance imaging; In vitro; Chemical coupling; In vivo; Vertebrata; Chemical modification; Magnetic particles; Mammalia; Mouse; Animal; Superparamagnetic contrast agent
• ISSN: 0144-8617; 1879-1344
• DOI: 10.1016/j.carbpol.2012.11.011

► Mannose in the Mannose-PEG-SPION efficiently targets the APCs in lymph node. ► Mannose-PEG-SPION, after intravenous injection in rats, was tracked by MR imaging. ► The accumulation of Mannose-PEG-SPION in the lymph node was also confirmed by Prussian blue staining. ► Mannose-PEG-SPION was found to have a great potential for LN specific MR imaging. The aim of this study is to prepare biocompatible and targetable nanoparticles in lymph nodes (LNs) for lymph node-specific magnetic resonance (MR) imaging. Mannan-coated superparamagnetic iron oxide nanoparticles (SPIONs) (mannan-SPION), carboxylic mannan-coated SPION (CM-SPION), and β-glucan-coated SPION (Glucan-SPION) have been developed to target antigen-presenting cells (APCs), for lymph node detection by MR imaging. In this study, mannose-polyethylene glycol (PEG) was prepared by conjugating d-mannopyranosylphenyl isothiocyanate and amine-PEG-carboxyl. The 3-aminopropyltriethoxysilane (APTES)-activated SPION and the mannose-PEG were cross-linked to produce mannose-PEG-linked SPION (Mannose-PEG-SPION). Mannose-PEG-SPION carrying mannose on the surface were assumed efficient at targeting APCs through the specific interactions of the mannose tethered on the Mannose-PEG-SPION and the mannose receptors on the antigen presenting cells. The hydrophilic PEG corona layer in the Mannose-PEG-SPION could be prevented from aggregation during the systemic circulation with accompanying enhanced specificity and minimized systemic toxicity. The accumulation of SPION in the lymph nodes led to increased negative enhancement in the MR images. In the in vivo study, rats were injected intravenously with Mannose-PEG-SPION and PEG-SPION, as a control and then tracked by MR imaging after 1h, 2h, 3h, and 24h. MR imaging on lymph nodes clearly revealed the preferential uptake of Mannose-PEG-SPION in immune cell-rich lymph nodes. The predominant accumulation of Mannose-PEG-SPION in the lymph nodes was also confirmed by Prussian blue staining. Based on these results, Mannose-PEG-SPION shows great potential for lymph node-specific MR imaging.