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OtherBASIC SCIENCE INVESTIGATIONS

Gelatin-Based Plasma Expander Effectively Reduces Renal Uptake of 111In-Octreotide in Mice and Rats

Julliëtte E.M. van Eerd, Erik Vegt, Jack F.M. Wetzels, Frans G.M. Russel, Rosalinde Masereeuw, Frans H.M. Corstens, Wim J.G. Oyen and Otto C. Boerman
Journal of Nuclear Medicine March 2006, 47 (3) 528-533;
Julliëtte E.M. van Eerd
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Erik Vegt
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Jack F.M. Wetzels
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Frans G.M. Russel
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Rosalinde Masereeuw
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Frans H.M. Corstens
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Wim J.G. Oyen
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Otto C. Boerman
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  • FIGURE 1. 
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    FIGURE 1. 

    Biodistribution data obtained 20 h after intravenous injection of 111In-octreotide in rats. Groups of 4 rats received 0.5 mL of PBS, 0.5 mL of lysine (80 mg), or 0.5 mL of Gelofusine (20 mg) intravenously 2–5 min before injection of 111In-octreotide. Results are presented as mean %ID/g; error bars indicate SDs. **P < 0.01.

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    FIGURE 2. 

    Biodistribution data obtained with various plasma expanders 20 h after intravenous injection of 111In-octreotide in rats. Rats received PBS, lysine (80 mg), Gelofusine (20 mg), Voluven (20 mg), Rheomacrodex (30 mg), or Haemaccel (17.5 mg) (0.5 mL intravenously) 2–5 min before injection of 111In-octreotide. Results are presented as mean %ID/g; error bars indicate SDs. *P < 0.05. **P < 0.01.

  • FIGURE 3. 
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    FIGURE 3. 

    111In-Octreotide uptake in kidneys of rats (4 per group) 20 h after injection. Rats received PBS or Gelofusine (20 mg) (0.5 mL intravenously) 3, 15, or 60 min before injection of 111In-octreotide. Results are presented as mean %ID/g; error bars indicate SDs. *P < 0.05. **P < 0.01.

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    TABLE 1

    111In-Octreotide Biodistribution at 20 Hours After Injection*

    Mean ± SD %ID/g in:
    RatsMice
    OrganPBSLysineGelofusinePBSLysineGelofusine
    Blood0.01 ± 0.000.00 ± 0.000.00 ± 0.000.02 ± 0.010.02 ± 0.000.03 ± 0.00
    Muscle0.005 ± 0.000.01 ± 0.000.01 ± 0.000.01 ± 0.000.01 ± 0.000.01 ± 0.00
    Lungs0.01 ± 0.000.01 ± 0.000.01 ± 0.000.59 ± 0.120.79 ± 0.250.69 ± 0.10
    Spleen0.04 ± 0.000.03 ± 0.000.05 ± 0.010.10 ± 0.010.08 ± 0.060.11 ± 0.01
    Kidneys1.36 ± 0.140.88 ± 0.08†0.73 ± 0.15†1.47 ± 0.381.23 ± 0.19‡0.58 ± 0.23†
    Adrenal glands0.72 ± 0.200.69 ± 0.270.97 ± 0.300.13 ± 0.010.12 ± 0.030.18 ± 0.04
    Pancreas0.39 ± 0.050.27 ± 0.05‡0.40 ± 0.050.08 ± 0.010.08 ± 0.010.08 ± 0.02
    Liver0.04 ± 0.010.03 ± 0.010.04 ± 0.000.10 ± 0.010.10 ± 0.020.11 ± 0.02
    Intestine0.06 ± 0.030.08 ± 0.050.06 ± 0.040.09 ± 0.020.10 ± 0.020.11 ± 0.02
    • ↵* PBS, lysine, or Gelofusine was injected 2–5 min before injection of radiolabel. Biodistribution data were collected at 20 h after intravenous injection of 111In-octreotide in rats or mice. Groups of 4 rats received 0.5 mL of PBS or Gelofusine (20 mg). Groups of 5 mice received 0.1 mL of PBS or Gelofusine (4 mg).

    • ↵† P < 0.01.

    • ↵‡ P < 0.05.

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Journal of Nuclear Medicine: 47 (3)
Journal of Nuclear Medicine
Vol. 47, Issue 3
March 2006
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Gelatin-Based Plasma Expander Effectively Reduces Renal Uptake of 111In-Octreotide in Mice and Rats
Julliëtte E.M. van Eerd, Erik Vegt, Jack F.M. Wetzels, Frans G.M. Russel, Rosalinde Masereeuw, Frans H.M. Corstens, Wim J.G. Oyen, Otto C. Boerman
Journal of Nuclear Medicine Mar 2006, 47 (3) 528-533;

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Gelatin-Based Plasma Expander Effectively Reduces Renal Uptake of 111In-Octreotide in Mice and Rats
Julliëtte E.M. van Eerd, Erik Vegt, Jack F.M. Wetzels, Frans G.M. Russel, Rosalinde Masereeuw, Frans H.M. Corstens, Wim J.G. Oyen, Otto C. Boerman
Journal of Nuclear Medicine Mar 2006, 47 (3) 528-533;
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