Contrast enhancement of the brain by folate-conjugated gadolinium-diethylenetriaminepentaacetic acid-human serum albumin nanoparticles by magnetic resonance imaging.

  • Huedayi Korkusuz
  • Karsten Ulbrich
  • Verena Bihrer
  • Katerina Welzel
  • Valery Chernikov
  • Thomas Knobloch
  • Sabine Petersen
  • Frank Huebner
  • Hanns Ackermann
  • Svetlana Gelperina
  • Yuecel Korkusuz
  • Wolfgang Kromen
  • Renate Hammerstingl
  • Jörg Haupenthal
  • Jens Fiehler
  • Stefan Zeuzem
  • Jörg Kreuter
  • Thomas J Vogl
  • Albrecht Piiper

Abstract

Different from regular small molecule contrast agents, nanoparticle-based contrast agents have a longer circulation time and can be modified with ligands to confer tissue-specific contrasting properties. We evaluated the tissue distribution of polymeric nanoparticles (NPs) prepared from human serum albumin (HSA), loaded with gadolinium-diethylenetriaminepentaacetic acid (Gd-DTPA) (Gd-HSA-NP), and coated with folic acid (FA) (Gd-HSA-NP-FA) in mice by magnetic resonance imaging (MRI). FA increases the affinity of the Gd-HSA-NP to FA receptor-expressing cells. Clinical 3 T MRI was used to evaluate the signal intensities in the different organs of mice injected with Gd-DTPA, Gd-HSA-NP, or Gd-HSA-NP-FA. Signal intensities were measured and standardized by calculating the signal to noise ratios. In general, the NP-based contrast agents provided stronger contrasting than Gd-DTPA. Gd-HSA-NP-FA provided a significant contrast enhancement (CE) in the brain (p ?=? .0032), whereas Gd-DTPA or Gd-HSA-NP did not. All studied MRI contrast agents showed significant CE in the blood, kidney, and liver (p < .05). Gd-HSA-NP-FA elicited significantly higher CE in the blood than Gd-HSA-NP (p ?=? .0069); Gd-HSA-NP and Gd-HSA-NP-FA did not show CE in skeletal muscle and gallbladder; Gd-HSA-NP, but not Gd-HSA-NP-FA, showed CE in the cardiac muscle. Gd-HSA-NP-FA has potential as an MRI contrast agent in the brain.

Bibliografische Daten

OriginalspracheEnglisch
Aufsatznummer4
ISSN1535-3508
StatusVeröffentlicht - 2012
pubmed 22954143