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Article

A novel blood-pooling MR contrast agent: Carboxymethyl-diethylaminoethyl dextran magnetite

  • Authors:
    • Akinaga Sonoda
    • Norihisa Nitta
    • Keiko Tsuchiya
    • Ayumi Nitta‑Seko
    • Shinichi Ohta
    • Hideji Otani
    • Kiyoshi Murata
  • View Affiliations / Copyright

    Affiliations: Department of Radiology, Shiga University of Medical Science, Otsu, Shiga 520‑2192, Japan
  • Pages: 5195-5198
    |
    Published online on: October 21, 2016
       https://doi.org/10.3892/mmr.2016.5874
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Abstract

Gadofosveset trisodium is available as a prolonged pooling vascular contrast agent for magnetic resonance imaging. As gadolinium (Gd)-based agents may increase the risk for nephrogenic systemic fibrosis in patients with severe renal insufficiency, the present study synthesized carboxymethyl-diethylaminoethyl dextran magnetite (CMEADM) particles as a blood-pooling, non-Gd‑based contrast agent. CMEADM particles carry a negative or positive charge due to the binding of amino and carboxyl groups to the hydroxyl group of dextran. The present study evaluated whether the degree of charge alters the blood‑pooling time. The evaluation was performed by injecting four groups of three Japanese white rabbits each with CMEADM‑, CMEADM2‑, CMEADM+ (surface charges: ‑10.4, ‑41.0 and +9.6 mV, respectively) or with ultrasmall superparamagnetic iron oxide (USPIO; ‑11.5 mV). The relative signal intensity (SIrel) of each was calculated using the following formula: SIrel = (SI post‑contrast ‑ SI pre‑contrast / SI pre‑contrast) x 100. Following injection with the CMEADMs, but not with USPIO, the in vivo pooling time was prolonged to >300 min. No significant differences were attributable to the electric charge among the CMEADM‑, CMEADM2‑ or and CMEADM+ particles when analyzed with analysis of variance and Tukey's HSD test. Taken together, all three differently‑charged CMEADM2 particles exhibited prolonged vascular enhancing effects, compared with the USPIO. The degree of charge of the contrast agents used in the present study did not result in alteration of the prolonged blood pooling time.
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Copy and paste a formatted citation
Spandidos Publications style
Sonoda A, Nitta N, Tsuchiya K, Nitta‑Seko A, Ohta S, Otani H and Murata K: A novel blood-pooling MR contrast agent: Carboxymethyl-diethylaminoethyl dextran magnetite. Mol Med Rep 14: 5195-5198, 2016.
APA
Sonoda, A., Nitta, N., Tsuchiya, K., Nitta‑Seko, A., Ohta, S., Otani, H., & Murata, K. (2016). A novel blood-pooling MR contrast agent: Carboxymethyl-diethylaminoethyl dextran magnetite. Molecular Medicine Reports, 14, 5195-5198. https://doi.org/10.3892/mmr.2016.5874
MLA
Sonoda, A., Nitta, N., Tsuchiya, K., Nitta‑Seko, A., Ohta, S., Otani, H., Murata, K."A novel blood-pooling MR contrast agent: Carboxymethyl-diethylaminoethyl dextran magnetite". Molecular Medicine Reports 14.6 (2016): 5195-5198.
Chicago
Sonoda, A., Nitta, N., Tsuchiya, K., Nitta‑Seko, A., Ohta, S., Otani, H., Murata, K."A novel blood-pooling MR contrast agent: Carboxymethyl-diethylaminoethyl dextran magnetite". Molecular Medicine Reports 14, no. 6 (2016): 5195-5198. https://doi.org/10.3892/mmr.2016.5874
Copy and paste a formatted citation
x
Spandidos Publications style
Sonoda A, Nitta N, Tsuchiya K, Nitta‑Seko A, Ohta S, Otani H and Murata K: A novel blood-pooling MR contrast agent: Carboxymethyl-diethylaminoethyl dextran magnetite. Mol Med Rep 14: 5195-5198, 2016.
APA
Sonoda, A., Nitta, N., Tsuchiya, K., Nitta‑Seko, A., Ohta, S., Otani, H., & Murata, K. (2016). A novel blood-pooling MR contrast agent: Carboxymethyl-diethylaminoethyl dextran magnetite. Molecular Medicine Reports, 14, 5195-5198. https://doi.org/10.3892/mmr.2016.5874
MLA
Sonoda, A., Nitta, N., Tsuchiya, K., Nitta‑Seko, A., Ohta, S., Otani, H., Murata, K."A novel blood-pooling MR contrast agent: Carboxymethyl-diethylaminoethyl dextran magnetite". Molecular Medicine Reports 14.6 (2016): 5195-5198.
Chicago
Sonoda, A., Nitta, N., Tsuchiya, K., Nitta‑Seko, A., Ohta, S., Otani, H., Murata, K."A novel blood-pooling MR contrast agent: Carboxymethyl-diethylaminoethyl dextran magnetite". Molecular Medicine Reports 14, no. 6 (2016): 5195-5198. https://doi.org/10.3892/mmr.2016.5874
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