Preparation method and application of nucleic acid spherical nanoparticle medicine
A nanoparticle and nucleic acid technology, used in nanomedicine, drug combination, drug delivery, etc., can solve the problem of low delivery efficiency, and achieve the effect of not easy to degrade, good stability, and inhibition of translation
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[0046] Preparation method of DNA NPs-18 nt: Mix 500 nM DNA-18 nt and 45 μM disulfide monomer compound in 20 mM Tris-HCl buffer (pH = 7.5) at 37°C for 15 min. Subsequently, unreacted DNA and disulfide monomer compounds were removed by dialysis in water for 48 h to finally obtain DNA NPs-18 nt. The particle size of the DNA NPs-18nt synthesized in this example is about 50 nm. To optimize the assembly conditions, different concentrations of disulfide monomer compounds were added to Tris-HCl buffer (pH = 7.5) containing 5 μM DNA-18 nt (N / P = 1~15).
[0047] In Example 1, survivin mRNA was used as the target positive-sense RNA, wherein Random DNA, DNA-18 nt and its positive-sense RNA—survivin mRNA sequences are shown in Table 1.
[0048] The sequence list of DNA and sense RNA adopted in the embodiment and comparative example of table 1
[0049]
[0050] Note: The target sequence of the survivin probe is the NO.305-NO.321 base interval of survivin mRNA with a total length of 265...
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