A kind of nano drug system targeting tumor and preparation method thereof
A nano-drug and tumor technology, applied in the field of tumor-targeting nano-drug system and its preparation, can solve the problems of affecting the overall stability of the drug-carrying system, instability of black scale nano-materials, and difficulty in storage, and achieve good tumor targeting. Sex, prolong blood circulation time, improve the effect of stability
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Embodiment 1
[0042] The nano drug system is characterized by structural formula: Zn-BP-P-Apt / D NSs, and its preparation method comprises the following steps:
[0043] A. Disperse 3mg of black phosphorus crystal powder in 16ml of 1-methyl-2-pyrrolidone, and then use the probe to sonicate the mixture for 6 hours under ice bath conditions, ultrasonic power 600W, on / off cycle, The on / off cycle time is: 3 s / 3 s, the obtained brown suspension is centrifuged at 2000 rpm for 10 minutes, the supernatant is collected, and centrifuged at 10000 rpm for more than 10 minutes to collect the precipitate , to prepare BP NSs for use.
[0044] B. Dissolving 700ug of Apt-SH with an optical density of 20OD in 0.8ml tris buffer; wherein the tris content in the tris buffer is 10 mM / ml, pH = 7.4; then add 1.6mg of NH 2- PEG-MAL and 20ug of TCEP, stirred for 2 hours in the dark to obtain NH 2 - PEG-Apt solution;
[0045] C. Add 1.6mg of BP NSs to the NH obtained in the previous step 2 -PEG-Apt solution, s...
Embodiment 2
[0049] The nano drug system is characterized by structural formula: Zn-BP-P-Apt / D NSs, and its preparation method comprises the following steps:
[0050] A. Disperse 8mg of black phosphorus crystal powder in 24ml of 1-methyl-2-pyrrolidone, then put the mixture under ice bath conditions, use the probe to sonicate for 12 hours, ultrasonic power 800 W, on / off cycle , the on / off cycle time is: 4s / 6 s, the obtained brown suspension is centrifuged at 4000 rpm for 20 minutes, the supernatant is collected, and centrifuged at 10000 rpm or more for more than 10 minutes, the precipitate is collected, BP NSs were prepared and used for later use.
[0051] B. Dissolving 1300ug of Apt-SH with an optical density of 20OD in 1.4ml tris buffer; wherein the tris content in the tris buffer is 10 mM / ml, pH = 7.4; then add 2.5 mg of NH 2 - PEG-MAL and 60ug of TCEP, stirred for 5 hours in the dark to obtain NH 2 - PEG-Apt solution;
[0052] C. Add 2.4mg of BP NSs to the NH obtained in the prev...
Embodiment 3
[0056] The nano drug system is characterized by structural formula: Zn-BP-P-Apt / D NSs, and its preparation method comprises the following steps:
[0057] A. Disperse 5mg of black phosphorus crystal powder in 20ml of 1-methyl-2-pyrrolidone, and then put the mixture in an ice bath, use a probe to sonicate for 8 hours, ultrasonic power 700 W, on / off cycle , the on / off cycle time is: 2 s / 4 s, the obtained brown suspension is centrifuged at 2000-4000 rpm for 10-20 minutes, the supernatant is collected, and centrifuged again at 10000 rpm for 10 minutes Above, the precipitate was collected to prepare BP NSs for future use.
[0058] B. Dissolving 1000ug of Apt-SH with an optical density of 20OD in 1ml tris buffer; wherein the tris content in the tris buffer is 10 mM / ml, pH = 7.4; then add 2mg parts by weight of NH 2 - PEG-MAL and 40ug of TCEP, stirred for 2-5 hours in the dark to obtain NH 2 - PEG-Apt solution;
[0059] C. Add 160-240 parts by weight of BP NSs to the NH obtaine...
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