A sort of 18 F-labeled polypeptide tumor apoptosis detection reagent and its preparation method and application
A labeling, 18f-ambf3-gdevd technology, applied in the fields of radiopharmaceuticals and nuclear medicine, can solve the problems of long labeling time, harsh reaction conditions, and complicated steps
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Embodiment 1
[0051] Synthesis of Example 1 Labeled Precursor
[0052] The synthetic route of labeled precursor 1 described in this example is as follows:
[0053]
[0054] The synthesis of the labeled precursor 1 described in this example comprises the following steps:
[0055] (1) Connecting amino acids: Weigh 2-chlorotrityl chloride resin (544mg, Loading value: 1.106mmol / g) into a three-way sand core funnel, then add 10mL of dichloromethane (DCM) solvent, shake for 10min , drain the solvent;
[0056] Fmoc-L-aspartic acid beta-tert-butyl ester (272mg, 0.662mmol) was weighed and dissolved in 3mL DMF solvent, then DIPEA (200μL, 1.212mmol) was added, ultrasonically dissolved and added to a sand core funnel to react with the resin, and Shake at room temperature for 2 h; then drain the solvent, and add 7 mL of solution R (chromatographically pure DMF: CH 3 OH:DIPEA=17:2:1) Wash and shake in the three-way sand core funnel for 10min, drain the solvent, then wash with 7mL DMF solvent, then ...
Embodiment 2
[0077] Embodiment 2 polypeptide compound 18 F-AmBF 3 - Synthesis of GDEVD
[0078] Electron bombardment of oxygen-enriched water H 2 18 O, get 18 F ion, adsorbed by anion exchange column (QMA) 18 For F ions, use 300 μL of pyridazine (pH=2.5) buffer to 18 F ions were eluted from the QMA column, transferred to a 1 mL labeled reaction tube, added 10-20 μL (25 mmol / L, dissolved in DMF) of the labeled precursor compound 1 prepared in Example 1, and heated at 80 °C 30min reaction to get the peptide compound 18 F-AmBF 3 -GDEVD, denoted as probe 18 F-1.
[0079] Dilute a small amount of radioactive solution, and detect the labeling of the precursor by radioactive high-performance liquid phase. Add 20 mL of deionized water to the reaction solution for dilution, pass through a C18 column (SepPak plus C-18), wash with deionized water (10 mL) three times, and finally use 0.5 mL of ethanol to rinse the labeled product into a vial, add 4.5 Dilute with mL deionized water (ethanol ...
experiment example
[0083] 1. Determination of stability in PBS and serum
[0084] In order to simulate the in vivo environment, the 18 Stability of F-1 in PBS (pH=7.4) and serum. Take 4 parts of 400 μL PBS (pH=7.4) buffer and 100 μL labeled product 18 The F-1 solutions were mixed separately and heated at 37°C for 0.5, 1, 2, 3 and 4 h, respectively. A small amount of solution was taken for dilution, and the stability of the labeled product was detected by radioactive high-performance liquid phase.
[0085] Take 4 aliquots of 400 μL FBS and 100 μL labeled product 18 The F-1 solutions were mixed separately and incubated at 37°C for 0.5, 1, 2, 3 and 4 hours respectively. After the time point, 500 μL of acetonitrile was added, centrifuged at 12,000 g / min for 5 min with a high-speed centrifuge, and the supernatant was taken, and the stability of the labeled product was detected by radioactive high-performance liquid chromatography.
[0086] Detection of different incubation time points by radioac...
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