Preparation method and application of nucleic acid spherical nano particle drug
A nanoparticle and nucleic acid technology, which is applied in the direction of drug combinations, pharmaceutical formulas, medical preparations of non-active ingredients, etc., can solve the problems of low delivery efficiency, achieve the effects of not easy to degrade, good stability, and increase local effective concentration
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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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