DNA (deoxyribonucleic acid) nano system for tumor targeting as well as preparation method and application of DNA nano system
A tumor-targeting, nanotechnology, applied in the field of tumor-targeted DNA nanosystems and its preparation, can solve the problems of limited nanosystems, low targeting efficiency, and poor therapeutic effects, and achieve expanded application range and easy penetration , combined with fast effects
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Embodiment 1
[0064] This embodiment provides a DNA nanosystem for tumor targeting, the preparation method of which is as follows:
[0065] (1) Preparation of two-dimensional DNA nanosheets
[0066] A long scaffold chain is mixed with the pre-designed stapled short chain and the upper and lower capture chains, cooled by PCR program, and assembled according to the principle of base complementary pairing to obtain a two-dimensional DNA nanosheet structure. The scaffold chain is the M13 genome, and the staple short chain is a nucleic acid sequence complementary to the scaffold chain. The upper and lower capture strands are used to hybridize two different functional groups, respectively.
[0067] The specific operation is: mix the scaffold chain, staple short chain, upper capture chain and lower capture chain with TAE-Mg at a ratio of 1:5:5:5 2+ In the solution (Tris-Base, 40mM; acetic acid, 20mM; EDTA, 2mM; magnesium acetate, 12.5mM; pH 8.0), the temperature was raised to 95°C, and then slow...
Embodiment 2
[0079] This embodiment provides a DNA nanosystem for tumor targeting. The difference between its preparation method and Example 1 is that the photosensitizer Ce6 in step (4) is replaced by the fluorescent dye indocyanine green (ICG), thereby To obtain the SA-ICG coupling product, the specific operation is as follows:
[0080] SA was dissolved in PBS to make a 200 μM stock solution, and NHS-activated indocyanine green was dissolved in DMSO to make a 6 mM ICG-NHS stock solution. Mix 100 μL SA stock solution with 20 μL ICG-NHS stock solution and shake at 25° C. for 2 h. After the reaction was completed, excess ICG was removed using a desalting column with a molecular weight cut-off of 40 KDa to obtain a SA-ICG coupling product.
[0081] Refer to Example 1 for other steps.
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