4.6 Article

Gum Arabic-Coated Magnetic Nanoparticles for Potential Application in Simultaneous Magnetic Targeting and Tumor Imaging

Journal

AAPS JOURNAL
Volume 11, Issue 4, Pages 693-699

Publisher

SPRINGER
DOI: 10.1208/s12248-009-9151-y

Keywords

brain tumor; drug delivery; gum arabic; magnetic nanoparticle; magnetic targeting

Funding

  1. NIH [CA114612, NS066945, GM007767]
  2. Hartwell Foundation Biomedical Research Award
  3. Ministry of Education, Science and Technology [R31-2008-000-10103-01]
  4. Chinese Program of Introducing Talents of Discipline to Universities [B06006]
  5. Fred W. Lyons Jr. and Rackham Pre-Doctoral Fellowships
  6. American Foundation of Pharmaceutical Education (AFPE)
  7. NATIONAL CANCER INSTITUTE [R01CA114612] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM007767] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS066945] Funding Source: NIH RePORTER

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Magnetic iron oxide nanoparticles (MNP) coated with gum arabic (GA), a biocompatible phytochemical glycoprotein widely used in the food industry, were successfully synthesized and characterized. GA-coated MNP (GA-MNP) displayed a narrow hydrodynamic particle size distribution averaging about 100 nm; a GA content of 15.6% by dry weight; a saturation magnetization of 93.1 emu/g Fe; and a superparamagnetic behavior essential for most magnetic-mediated applications. The GA coating offers two major benefits: it both enhances colloidal stability and provides reactive functional groups suitable for coupling of bioactive compounds. In vitro results showed that GA-MNP possessed a superior stability upon storage in aqueous media when compared to commercial MNP products currently used in magnetic resonance imaging (MRI). In addition, significant cellular uptake of GA-MNP was evaluated in 9L glioma cells by electron spin resonance (ESR) spectroscopy, fluorescence microscopy, and MRI analyses. Based on these findings, it was hypothesized that GA-MNP might be utilized as a MRI-visible drug carrier in achieving both magnetic tumor targeting and intracellular drug delivery. Indeed, preliminary in vivo investigations validate this clinical potential. MRI visually confirmed the accumulation of GA-MNP at the tumor site following intravenous administration to rats harboring 9L glioma tumors under the application of an external magnetic field. ESR spectroscopy quantitatively revealed a 12-fold increase in GA-MNP accumulation in excised tumors when compared to contralateral normal brain. Overall, the results presented show promise that GA-MNP could potentially be employed to achieve simultaneous tumor imaging and targeted intra-tumoral drug delivery.

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