Production method of probe molecule for recognizing tumor cell by specificity
A technology of tumor cells and probe molecules, which is applied in the field of nanomaterials and biology, can solve the problems of complex process, large particle size and shedding of quantum dots, and achieve the effect of improving stability, low toxicity and good biocompatibility
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Embodiment 1
[0028] Embodiment 1: polyethylene glycol-folic acid (NH 2 -PEG-FA) Synthesis 1
[0029] Equimolar folic acid and polyethylene glycol with amino groups on both sides are dissolved in DMSO, then N, N'-dicyclohexylcarboimide (DCC) is added in an equimolar amount with polyethylene glycol-folic acid, and Add triethylamine in an equimolar amount to polyethylene glycol-folic acid, and react at room temperature for 3 hours. After the mixed solution was centrifuged, the supernatant was dialyzed against a pH=6 buffer solution, and then dialyzed against deionized water. After removal of the solvent, a pale yellow solid was obtained.
Embodiment 2
[0030] Embodiment 2: polyethylene glycol-folic acid (NH 2 -PEG-FA) Synthesis 2
[0031] Equimolar folic acid and polyethylene glycol with amino groups on both sides are dissolved in DMSO, then N, N'-dicyclohexylcarboimide (DCC) is added in an equimolar amount with polyethylene glycol-folic acid, and Add triethylamine in an equimolar amount to polyethylene glycol-folic acid, and react at room temperature for 6 hours. After the mixed solution was centrifuged, the supernatant was dialyzed against a pH=9 buffer solution, and then dialyzed against deionized water. After removal of the solvent, a pale yellow solid was obtained.
Embodiment 3
[0032] Embodiment 3: polyethylene glycol-folic acid (NH 2 -PEG-FA) Synthesis 3
[0033] Equimolar folic acid and polyethylene glycol with amino groups on both sides are dissolved in DFM, then N, N'-dicyclohexylcarboimide (DCC) is added in an equimolar amount to polyethylene glycol-folic acid, and Add triethylamine in an equimolar amount to polyethylene glycol-folic acid, and react at room temperature for 9 hours. After the mixed solution was centrifuged, the supernatant was dialyzed against a buffer solution with pH=10, and then dialyzed against deionized water. After removal of the solvent, a pale yellow solid was obtained.
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