Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Thrombin-responsive DNA (deoxyribonucleic acid) nano machine as well as preparation method and application thereof

A technology of nanomachines and thrombin, which is applied in the field of nanomedicine to achieve the effects of drug protection, uniform size, and improved enrichment capacity

Active Publication Date: 2022-03-01
NANJING UNIV OF POSTS & TELECOMM
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The excellent properties of the above DNA nanostructures have brought new opportunities for the development of precise thrombolytic drugs in vivo. The precise drug delivery scheme of DNA nanostructures for in vivo thrombolytic therapy has not been recorded in the prior art.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Thrombin-responsive DNA (deoxyribonucleic acid) nano machine as well as preparation method and application thereof
  • Thrombin-responsive DNA (deoxyribonucleic acid) nano machine as well as preparation method and application thereof
  • Thrombin-responsive DNA (deoxyribonucleic acid) nano machine as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0049] The preparation method of the DNA nanomachine of embodiment 1 thrombin response

[0050] In this embodiment, the DNA nanomachine preparation method comprises the following steps:

[0051] Step 1: Preparation of rectangular flat DNA nanostructures

[0052] The raw materials for preparation include: M13mp18 template strands shown in SEQ ID NO:1 and short DNA strands, the short DNA strands include: DNA staple strands with 156 sequences, 24 DNAs with sequences shown in SEQ ID NO:3-26 Capture strand, 12 kinds of DNA "lock" strands with sequences shown in SEQ ID NO:28-39, the above DNA strands were mixed in 1×TAE / Mg 2+ In the buffer, the total volume after mixing is 100 μL, the template strand concentration is 10 nM, the short DNA strands of each sequence are added in equal amounts and in excess, and the total concentration of short DNA strands is 80 nM;

[0053] Among them, the DNA staple strands of 156 sequences are selected from the "Supporting information" of the docume...

Embodiment 2

[0062] Example 2: Regulation of DNA nanomachines in response to thrombin environments in different concentration ranges

[0063]The DAN "lock" chain used in Example 1 is a sequence that is not completely complementary to the thrombin aptamer chain, and is a DAN "lock" chain that mismatches two bases. By modifying the DNA "lock" chain The number of matching bases can change its stability when it is complementary to the thrombin aptamer chain, thereby regulating the DNA nanomachine response to the thrombin concentration in different concentration ranges; it is confirmed by experiments that corresponding to Example 1, it is completely complementary and only The DAN "lock" chain with a mismatch of 1 base can also realize the response of DNA nanomachines to thrombin, and the mismatch of 1 base is the sixth in the repeated sequence 5'-AAAACACCAACC-3' in the "lock" chain A base is replaced by a T base; no mismatch base, that is, the sixth A base of the repeat sequence 5'-AAAACACCAACC...

experiment example 1

[0064] Experimental Example 1: Evaluation of Thrombus Targeting Effect of Tubular DNA Nanomachines

[0065] A certain dose of Cy5.5 fluorescent labeling, according to the tubular DNA nanomachines constructed under the condition of DNA "lock" strand mismatch of 2 bases as described in Example 1, was injected into C57 / BL6 mice through the tail vein After 20 min, the lung tissue was isolated and observed by IVIS in vivo fluorescence imaging to evaluate the thrombus targeting effect of the tubular DNA nanomachine. The result is as image 3 As shown, compared with the control group, that is, Cy5.5-labeled single-stranded DNA and fluorescently-labeled rectangular flat DNA nanostructures, the ratio of Cy5.5 / FITC fluorescence intensity in the tubular DNA nanomachine treatment group was higher than that in the rectangular flat DNA nanostructure treatment group. More than 2.1 times, it shows that the tubular DNA nanomachine provided by the present invention can protect the drug as a dr...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
diameteraaaaaaaaaa
Login to View More

Abstract

The invention provides a preparation method and application of a thrombin-responsive DNA nano-machine. The nano-machine comprises a DNA nano-structure, a thrombolytic drug (tPA) compound and a thrombin aptamer chain structure, a tPA molecular drug is accurately loaded through arranged DNA capture chains, a controllable DNA molecular lock catch chain is utilized, and a third thrombin aptamer chain is added, so that the DNA nanostructure can be locked, and the tPA drug is entrapped in the DNA nanostructure. The DNA nano-machine disclosed by the invention can be used as a nano-scale molecular machine for loading tPA thrombolytic drugs, has high thrombin responsiveness, and can effectively respond to a thrombin environment at a thrombus part and accurately release thrombin, so that thrombolytic treatment is effectively transported to the thrombus part, and the thrombolytic effect is improved. The novel thrombolysis machine is accurate in drug loading, controllable in release and high in thrombolysis effect.

Description

technical field [0001] The invention belongs to the technical field of nanomedicine, and in particular relates to a thrombin-responsive DNA nanomachine and its preparation method and application, in particular to a thrombin-responsive DNA nanomachine and its preparation method and application. Background technique [0002] Currently, the standard therapy for the treatment of ischemic stroke and other thrombosis-related diseases in the clinic is intravenous injection of tissue plasminogen activator tPA within 3 to 4.5 hours after the onset of symptoms. tPA can catalyze the conversion of plasminogen into plasmin, and after intravenous injection of tPA, it will rapidly decompose the fibrin network to achieve the purpose of thrombolysis. However, the current use of tPA therapy in thrombotic patients still has the disadvantages of high risk of bleeding complications, short cycle life, and low targeting. Therefore, the precise delivery of tPA to the thrombus site and the on-deman...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): A61K47/54A61K38/49A61P7/02B82Y5/00B82Y40/00
CPCA61K47/549A61K38/49A61P7/02B82Y5/00B82Y40/00
Inventor 晁洁高宇汪联辉印珏王思雨
Owner NANJING UNIV OF POSTS & TELECOMM
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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