A kind of dna nano controlled release drug delivery molecule that can be used for breast cancer and other tumors and its application
A drug delivery and molecular technology, applied in the direction of antineoplastic drugs, drug combinations, pharmaceutical formulations, etc., can solve the problems of unseen patents, etc., and achieve the effects of good biocompatibility, avoiding damage, and controllable release
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Embodiment 1
[0033] figure 1 Schematic diagram of the construction of the DNA nano-controlled release siRNA delivery system. Take 1 μL single-stranded DNA (10 μM) each for Prism-1, Prism-2, Prism-3, Prism-4, Prism-5, Prism-6, and 1 μL single-stranded siRNA (10 μM) with P-7 sequences linked at both ends , and 1 μL of another complementary siRNA single strand (10 μM) were added to 12 μL of PBS (8 mM Na 2 HPO 4 , 0.137mM NaCl, 2mM NaH 2 PO 4 , pH7.2-7.4) solution. When fluorescent observation is required for subsequent experiments, the corresponding single strands with fluorescent modifications can be used. The mixed solution was placed in a PCR machine, and the temperature was slowly and uniformly cooled from 95°C to 4°C within 6.5 hours, that is, the temperature was lowered by 1°C in about 4 minutes and 18s, so as to realize the self-assembly of nucleic acids. A single strand of DNA can self-assemble into a three-dimensional DNA hexahedron through complementary base pairing. image 3...
Embodiment 2
[0038] figure 1 Schematic diagram of the construction of the DNA nano-controlled release siRNA delivery system. Each take 1 μL of single-stranded DNA (10 μM) Prism-1-PEG, Prism-2-PEG, Prism-3-PEG, Prism-4-PEG, Prism-5-PEG, Prism-6-PEG, and, and 1 μL of two The siRNA single strand (10 μM) with the P-7 sequence connected at the end, and 1 μL of another complementary siRNA single strand (10 μM) were added to 12 μL PBS (8 mM Na 2 HPO 4 , 0.137mM NaCl, 2mM NaH 2 PO 4 , pH7.2-7.4) solution. When fluorescent observation is required for subsequent experiments, the corresponding single strands with fluorescent modifications can be used. The mixed solution was placed in a PCR machine, and the temperature was slowly and uniformly cooled from 95°C to 4°C within 6.5 hours, that is, the temperature was lowered by 1°C in about 4 minutes and 18s, so as to realize the self-assembly of nucleic acids. A single strand of DNA can self-assemble into a three-dimensional DNA hexahedron through ...
Embodiment 3
[0043] figure 1 Schematic diagram of the construction of the DNA nano-controlled release siRNA delivery system. Take 1 μL each of single-stranded DNA (10 μM) Prism-1-S, Prism-2-PEG, Prism-3-S, Prism-4-S, Prism-5-PEG, Prism-6-S, and 1 μL of both ends ligation siRNA single strand (10 μM) with P-7 sequence, and 1 μL of another complementary siRNA single strand (10 μM) were added to 12 μL PBS (8 mM Na 2 HPO 4 , 0.137mM NaCl, 2mM NaH 2 PO 4 , pH7.2-7.4) solution. When fluorescent observation is required for subsequent experiments, the corresponding single strands with fluorescent modifications can be used. The mixed solution was placed in a PCR machine, and the temperature was slowly and uniformly cooled from 95°C to 4°C within 6.5 hours, that is, the temperature was lowered by 1°C in about 4 minutes and 18s, so as to realize the self-assembly of nucleic acids. A single strand of DNA can self-assemble into a three-dimensional DNA hexahedron through complementary base pairing....
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