A kind of nanocomposite and its preparation method and application
A nano-composite, gold nano-cages technology, applied in the fields of biotechnology and biomedical materials, to achieve the effects of avoiding drug poisoning, protecting drug toxicity damage, and inhibiting growth
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Embodiment 1
[0054] 1. Construction of Au-ODN
[0055] The oligonucleotide (ODN) sequence designed and synthesized in the present invention was purchased from Shanghai Jierui Bioengineering Co., Ltd. The 3' end of one chain of ODN was modified with a sulfhydryl group, and the sequence was as follows: 5'-GCAGCTCGAGCGCTGCGCACGCGT-SH-3'; its complementary sequence was: 3'-CGTCGAGCTCGCGACGCGTGCGCA-5'.
[0056] Gold nanocages (size, 50-100nm) purchased on the market were used to disperse them in phosphate buffer (pH7.0 or so) at a concentration of 0.1-0.5 mg / mL to prepare a gold nanocage solution;
[0057] Add the synthesized ODN to the gold nanocage solution according to the molar ratio of gold and double-stranded oligonucleotide (ODN) at 1:200 to 1:500. Under the action of sulfhydryl, ODN can effectively coordinate with the gold nanocage and bind to the nanocage; after adding the ODN, add an appropriate amount of NaCl solution to the solution to make the final concentration 0.1M; then contin...
Embodiment 2
[0060] 1. Drug capture by nanocomposite Au-ODN
[0061] The chemotherapy drug doxorubicin hydrochloride (DOX) was purchased from Aladdin Company.
[0062] Prepare a solution containing DOX in phosphate buffer solution, so that the concentration of DOX is about 1μM, and then prepare different concentrations of Au-ODN (0.4~3.8nM), add DOX to the Au-ODN solution, react for 30min, and invert for 3~ Mix 5 times.
[0063] The invention designs and synthesizes Au-ODN, which can specifically capture the chemotherapeutic drug doxorubicin (DOX) in the solution. After DOX is captured by Au-ODN, the fluorescence will be weakened or quenched, so it can be accurately detected by the fluorescence quantitative method. The ability of Au-OND to capture DOX. The result is as image 3 as shown in a.
[0064] 2. Stability of Au-ODN in DNase I
[0065] Au-ODN is resuspended in phosphate buffer solution at a concentration of 1-3nM, and then DOX is added to the solution at a final concentration ...
Embodiment 3
[0067] Flow cytometry and laser confocal microscopy were used to detect the entry of Au-ODN into normal liver cells, and CCK8 method was used to detect the protective effect of Au-DON on the viability of normal liver cells under chemotherapy drug treatment. The specific operation is as follows:
[0068] 1. Detection by flow cytometry and confocal laser microscopy
[0069] (1) Normal liver cells QSG-7701 and L02 were mixed with 1×10 4 The density of each well was inoculated in 12-well plates respectively. After 24 hours of culture, Au-ODN resuspended in culture medium was added to the cell culture plate at a concentration of 5-20 μM. The ODN was labeled with fluorescent dye FAM, and the culture was continued for 0 ~4h, and real-time monitoring of Au-ODN entering liver cells by flow cytometry, the results are as follows Figure 4 shown.
[0070] At the end of the culture, the culture medium was aspirated, and the cells were washed 2-3 times with phosphate buffer to remove the...
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