Stability evaluation of Gd chelates for macromolecular MRI contrast agents

MAGMA. 2020 Aug;33(4):527-536. doi: 10.1007/s10334-019-00805-8. Epub 2019 Dec 10.

Abstract

Objective: We try to establish designs for the macromolecular agents possessing high Gd3+-chelating stability, because free Gd3+ ion released from Gd chelates is known as a risk factor to cause toxic side effects and a safety concern.

Materials and methods: We prepared three types of Gd-based macromolecular MRI contrast agents from a synthetic polymer (poly(glutamic acid) homopolymer or poly(ethylene glycol)-b-poly(lysine) block copolymer) and a chelating moiety (DO3A or DOTA) having two strategic designs for high chelate stability. Then, we examine the in vitro Gd3+-chelate stability of these macromolecular MRI contrast agents.

Results: The prepared macromolecular agents exhibited the same or higher Gd3+-chelate stability as/than did Gd-DOTA that possesses the highest Gd3+-chelate stability among the approved small-MW Gd-chelate MRI contrast agent.

Discussion: Our macromolecular design was considered to work well for high Gd3+-chelate stability.

Keywords: Chelating stability; Contrast agent; Gd-chelate; Macromolecular contrast agent; Polymeric micelle.

MeSH terms

  • Chelating Agents / pharmacology*
  • Contrast Media / pharmacology*
  • Gadolinium / chemistry*
  • Heterocyclic Compounds, 1-Ring / chemistry
  • Macromolecular Substances / chemistry
  • Magnetic Resonance Imaging / methods*
  • Magnetic Resonance Spectroscopy
  • Polyethylene Glycols / chemistry
  • Polyglutamic Acid / chemistry
  • Polylysine / chemistry
  • Risk Factors
  • Solubility*
  • Water / chemistry

Substances

  • 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid
  • Chelating Agents
  • Contrast Media
  • Heterocyclic Compounds, 1-Ring
  • Macromolecular Substances
  • Water
  • 1,4,7,10-tetraazacyclododecane- 1,4,7,10-tetraacetic acid
  • Polylysine
  • Polyglutamic Acid
  • Polyethylene Glycols
  • Gadolinium