Antisense oligonucleotide probe contrast agent marked by superparamagnetism iron oxide and production of the same
A technology of antisense oligonucleotides and anti-oligonucleotides, which is applied in the direction of nuclear magnetic resonance/magnetic resonance imaging contrast agents, etc., can solve the problem of not being able to display antisense activity, and achieve clear anatomical structure, spatial and temporal resolution High, good contrast effect
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Embodiment 1
[0030] Embodiment 1 preparation method
[0031] A non-limiting preparation method of the contrast agent of the present invention: comprising the following steps:
[0032] (1). Preparation of the carrier: one-step co-precipitation method is used to complete the synthesis of ferric oxide. The reaction principle is: Fe 2+ +2Fe 3+ +8OH - → Fe 3 o 4 +4H 2 O; adding dextran while synthesizing ferric oxide to obtain the ferric oxide carrier of the outsourcing dextran;
[0033] (2). The synthesis of the antisense oligonucleotide fragment of the c-erbB2 oncogene whose oligonucleotide sequence is CTCCATGGTGCTCAC. The antisense oligonucleotides in the examples were provided by Shanghai Sangong Co., Ltd.
[0034] (3). Synthesis of contrast agent: the specific steps are: the ferric iron tetroxide carrier coated with dextran obtained in the purification step (1): take 250 μL of the carrier after passing through the column; add 10 μL of 0.1M sodium periodate, The hydroxyl group of th...
Embodiment 2
[0036] Embodiment 2 biological and physical properties detection:
[0037] Referring to accompanying drawing 2, among the figure 5 sample wells are in order from left to right: No. 1, No. 2 holes are antisense oligonucleotide standard 1ug, 3ug, No. 3 hole is contrast agent of the present invention, No. 4, No. 2 5 wells are the carrier and antisense oligonucleotide mixture. It can be seen from the figure that the contrast agent of the present invention has a high degree of purification and stable properties.
[0038] Refer to accompanying drawing 3, wherein figure A is antisense oligonucleotide standard product spectrum, figure B is carrier spectrum, their peak shape is good, there is no interference of miscellaneous peak. Figure C is the mixture of carrier and antisense oligonucleotides. The two are completely separated, and the peak shape is good without tailing. The recovery rate is 100%, which proves that the gel column used in this experiment can be used for contrast agen...
Embodiment 3
[0040] Embodiment 3 Magnetic property detection:
[0041] Referring to accompanying drawing 5, by oscillating sample magnetometer and magnetic resonance detection, the saturation magnetization of the sample is 69.32875emu / g Fe, the specific saturation magnetization is 68.41215emu / g, the specific residual magnetization is 30.4753emu / g, and the remanence is 19.25782Gs, the relaxation rate is 0.154×10 6 mol -1 sec -1 . The magnetization curve is a single curve passing through the origin, indicating that the contrast agent of the present invention has superparamagnetism.
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