A kind of APD hybrid nano system and its construction method and application
A construction method and nanotechnology, applied in the fields of nanotechnology, nanotechnology, nanomedicine, etc., can solve the problems of easy aggregation of gold rods, complicated operation, tedious operation, etc., and achieve the advantages of cell endocytosis, simple preparation method, and cell entry efficiency. high effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0059] In this embodiment, left-handed DNA is also expressed as L-DNA, and "L-" is used to indicate left-handed.
[0060] In this example, the APD hybrid nanosystem is prepared through the following steps.
[0061] (1) Mix 3.7 mL of 0.1 mol / L CTAB and 150 μL of 0.01 mol / L HAuCl 4 After mixing, add 0.85mL deionized water, then add 0.3mL 0.01 mol / L ice NaBH in ice bath 4 Aqueous solution, 1200 r / min rapid stirring for 2 minutes, standing for 2 hours will immediately generate CTAB-coated gold seeds. Add 1.4 mL of the prepared gold seed solution into the gold nanorod growth solution, stir rapidly at 450 rpm for 2 minutes, let it stand for 12 hours, then centrifuge at 10,000 rpm for 10 minutes, and resuspend with 0.01 mol / L CTAB solution Gold nanorods, stored at room temperature for future use. The growth liquid is: 300mLCTAB, the concentration of the substance is 0.1 mol / liter; 16mLHAuCl 4 , the concentration of the substance is 0.01 mol / L; 3mLAgNO 3 , the concentration of th...
Embodiment 2
[0071] This example mainly illustrates the anti-nuclease degradation ability of the APD nanosystem.
[0072] Using the same method to prepare left-handed DNA tetrahedron and right-handed DNA tetrahedron, the preparation method is the same as step (2) of Example 1. Right-handed DNA (D-DNA) was used to prepare right-handed DNA tetrahedrons (D-TDNs), and the base sequence of D-DNA was the same as that of L-DNA. The preparation method of APD is the same as that of Example 1, and will not be repeated in this example. D-TDNs, L-TDNs and APD were mixed with deoxyribonucleotide enzymes, incubated at 37°C for 8h, and EDTA was added to terminate the enzymatic degradation reaction. Subsequently, heparin sodium was added to APD and enzyme to destroy the electrostatic interaction and release D-TDNs. The remaining samples were not treated with sodium heparin.
[0073] Using polyacrylamide gel electrophoresis test to observe the movement of the sample, the results are as follows Figure ...
Embodiment 3
[0075] This example is an example of preparation of a targeted APD nanosystem.
[0076] Synthesis of folic acid-mercapto-containing polylysine conjugates: Feed folic acid, mercapto-containing polylysine, EDC and NHS at a molar ratio of 1:1:1.5:1.5, dissolve in 20ml of dimethyl sulfoxide, and stir magnetically at room temperature 24 hours. Then the reaction solution was transferred to a dialysis bag with a cut-off molecular weight of 6000 Da, immersed in ultrapure water for dialysis for 24 hours. When the dialysis time expired, the moisture in the sample was removed by freeze-drying to obtain a folic acid-polylysine conjugate.
[0077] Follow the steps below to prepare the nanosystem:
[0078](1) Prepare gold nanorods of specific size by seed crystal growth method. Add 3.7 mL of 0.1 mol / L CTAB and 150 μL of 0.01 mol / L HAuCl 4 After mixing, add 0.85mL deionized water, then add 0.3mL 0.01 mol / L ice NaBH in ice bath 4 Aqueous solution, stirred rapidly at 1200rpm for 2min, and...
PUM
Property | Measurement | Unit |
---|---|---|
molecular weight | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com