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Model 5050

Manufactured by Eckert & Ziegler
Sourced in Germany

The Model 5050 is a laboratory equipment designed for general use. It measures 20 cm x 15 cm x 10 cm and weighs approximately 3 kg. The device is powered by a 120V AC power source.

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3 protocols using model 5050

1

Radiolabeled Tracer Identification and Purification

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Analytical radio-HPLC was used to identify the product of each synthesis (via co-injection with reference standard) and to isolate pure products to confirm the Rf value of the product bands in radio-TLC. The radio-HPLC system setup comprised a Smartline HPLC system (Knauer, Berlin, Germany) equipped with a degasser (Model 5050), pump (Model 1000), UV detector (254 nm; Eckert & Ziegler, Berlin, Germany) and gamma-radiation detector, and counter (B-FC- 4100 and BFC-1000; Bioscan, Inc., Poway, CA, USA). All HPLC separations used a C18 Gemini column (Kinetex, 250 × 4.6 mm, 5 µm, Phenomenex, Torrance, CA, USA). Using a mobile phase of 3:1 H2O:MeCN with 0.1% TFA (v/v) and a flow rate of 1.0 mL/min, the retention time of [18F]Flumazenil was 11 min. For [18F]PBR06, the retention time was 8 min using a mobile phase of 60:40 (v/v) MeCN:20 mM sodium phosphate buffer (pH = 5.8) with a flow rate of 1.5 mL/min. [18F]Fallypride samples were separated with a mobile phase of 60% MeCN in 25 mM HN4HCO2 with 1% TEA (v/v) and a flow rate of 1.5 mL/min resulting in a retention time of 4.5 min. [18F]FEPPA samples were separated with a mobile phase of 70:30 v/v H2O:EtOH with 0.1% H3PO4 at 0.8 mL/min, giving a retention time of 15.5 min.
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2

Radio-HPLC Analysis of Radiopharmaceuticals

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Radio-HPLC was used to analyze crude radiopharmaceuticals and to perform tests for radiochemical and chemical purity and radiochemical identity of TLC-purified batches of radiopharmaceuticals. The radio-HPLC system setup comprised a Smartline HPLC system (Knauer, Berlin, Germany) equipped with a degasser (Model 5050), pump (Model 1000), UV detector (254 nm; Eckert & Ziegler, Berlin, Germany), gamma-radiation detector (BFC-4100, Bioscan, Inc., Poway, CA, USA), and counter (BFC-1000; Bioscan, Inc., Poway, CA, USA). A C18 Gemini column was used for separations (250 × 4.6 mm, 5 µm, Phenomenex, Torrance, CA, USA). [18F]PBR-06 samples were separated with a mobile phase of 60:40 (v/v) MeCN:20 mM sodium phosphate buffer (pH = 5.8) at a flow rate of 1.5 mL/min resulting in a retention time for [18F]PBR-06 of 6.5 min. [18F]Fallypride samples were separated with a mobile phase of 60% MeCN in 25 mM NH4HCO2 with 1% TEA (v/v) at a flow rate of 1.5 mL/min resulting in a retention time for [18F]Fallypride of 5.8 min.
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3

Radiolabeled Fallypride Characterization

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As a performance comparison, some crude [18F]Fallypride microscale reactions were analyzed with radio-TLC and radio-HPLC. The radio-HPLC system setup comprised a Smartline HPLC system (Knauer, Berlin, Germany) equipped with a degasser (Model 5050), pump (Model 1000), UV detector (254 nm; Eckert & Ziegler, Berlin, Germany), gamma-radiation detector (BFC-4100, Bioscan, Inc., Poway, CA, USA), and counter (BFC-1000; Bioscan, Inc., Poway, CA, USA). A C18 Gemini column was used for separations (250 × 4.6 mm, 5 μm, Phenomenex, Torrance, CA, USA). Samples were separated with a mobile phase of 60% MeCN in 25 mM NH4HCO2 with 1% TEA (v/v) and a flow rate of 1.5 mL/min resulting in a retention time for [18F]Fallypride of 5.8 min.
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