Prostate cancer pet diagnostic reagents 68 ga-nota-ancp-psma and its preparation method and application
A technology of NOTA-ANCP-PSMA, 68ga-nota-ancp-psma, applied in the preparation methods of peptides, chemical instruments and methods, preparations for in vivo tests, etc. protection, etc.
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Embodiment 1
[0041] This embodiment provides a prostate cancer PET diagnostic reagent 68 The preparation method of Ga-NOTA-ANCP-PSMA, described method comprises the steps:
[0042] (S1) The precursor compound NOTA-ANCP-PSMA is synthesized by solid phase synthesis;
[0043] Preparation of compound 3
[0044] The synthetic route is shown below. Using Fmoc-Lys(Dde)-Wang Resin (compound 1) as the starting material, weigh 3g of the raw material with a substitution degree of 0.3mmol / g, add it to the reactor, add DMF, and soak for 30min. Then drain the DMF, add 3 times the volume of 20% Pip / DMF, and fill with nitrogen gas to remove Fmoc, react for 30 minutes, drain the 20% Pip / DMF, wash with DMF 5 times, and the ninhydrin detection shows dark blue. Add N,N'-succinimidyl carbonate (DSC), N,N-diisopropylethylamine (DIPEA) and 4-dimethylaminopyridine (DMAP) in proportion, and the input ratio is resin:DSC: DIPEA:DMAP=1:6:12:1, add an appropriate amount of DMF, and react for 1 h under the protectio...
Embodiment 2
[0059] In vitro stability assay:
[0060] 68 The radiochemical stability of Ga-NOTA-ANCP-PSMA was carried out in two systems of calf serum and phosphate buffer. PBS method: place in 0.5mL phosphate buffer (PBS, pH=7.4), place at 37°C, incubate for 30, 60, 90, 120, 150min, then use HPLC to measure its radiochemical purity to determine its in vitro stability. Serum method: place in 0.5mL calf serum solution, incubate at pH=7, 37°C. When incubated for 30, 60, 90, 120, and 150 min, the radiochemical purity was determined by HPLC to determine its in vitro stability.
[0061] like Figure 4 as shown, 68 The stability of Ga-NOTA-ANCP-PSMA in PBS system was good, and the radiochemical purity remained above 95.4% until 150 min. The in vitro stability results in the BSA system show that the radiochemical purity can be maintained at a level above 95% within 90 minutes, and then slightly decreased. illustrate 68 The stability of Ga-NOTA-ANCP-PSMA in BSA is poorer than that in PBS,...
Embodiment 3
[0063] Measurement of lipid-water partition coefficient:
[0064] Mark 68 Ga-NOTA-ANCP-PSMA was separated and purified by Sep-Pak C18 Cartridge, and eluted with 95% ethanol. The obtained marker was blown dry by dry nitrogen, and the obtained marker was dissolved in a 1.5mL EP tube (about 3.7MBq) using the same volume (0.5mL: 0.5mL) of n-octanol and phosphate buffer solution (pH=7.4) middle. Fully shake for 5 minutes, and centrifuge the layers in a centrifuge for 5 minutes at a speed of 2000 rpm. Take 100uL each of the organic phase and the aqueous phase in 1mL EP tubes, measure their radioactive counts in the well-type γ detector, and calculate the lipid-water partition coefficient P from the ratio of the radioactive counts of the organic phase and the aqueous phase. P=log (N o / N W )(N o and N W are the counts of the organic and aqueous phase samples, respectively). The operation was repeated 3 times, and the average value was taken as the lipid-water partition coeffi...
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