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

Cationic gene vector with high transfection efficiency and low cytotoxicity and preparation method thereof

A technology of transfection efficiency and cytotoxicity, applied in the field of new biomedical materials, can solve problems such as poor repeatability and complicated preparation methods, and achieve low cytotoxicity, high transfection efficiency, and great application prospects

Active Publication Date: 2018-08-10
CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
View PDF4 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although these methods can reduce cytotoxicity to a certain extent, their preparation methods are complicated and have poor reproducibility

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
  • Cationic gene vector with high transfection efficiency and low cytotoxicity and preparation method thereof
  • Cationic gene vector with high transfection efficiency and low cytotoxicity and preparation method thereof
  • Cationic gene vector with high transfection efficiency and low cytotoxicity and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0029] The present invention also provides a method for preparing a cationic gene carrier with high transfection efficiency and low cytotoxicity, comprising the following steps:

[0030] A) will C 8 h 17 N 3 .HCl and 1-hydroxybenzotriazole are added to the N,N-dimethylformamide solution of p-toluenesulfonyl and tert-butoxycarbonyl double-protected arginine for activation;

[0031] B) adding an aqueous solution of linear poly-α-lysine to the activated solution in step A) for reaction;

[0032] The molar ratio of the linear poly-α-lysine to p-toluenesulfonyl-protected arginine is 1: (5-120);

[0033] C) Dialyzing and freeze-drying the solution after the reaction in the step B) in sequence to obtain an intermediate product;

[0034] D) Reacting the intermediate product under the condition of trifluoroacetic acid, adding anhydrous ether for precipitation, vacuum drying and dialysis to obtain the cationic gene carrier.

[0035] In the present invention, arginine (Boc-Arg (Tos)...

Embodiment 1

[0050] The preparation of embodiment 1PLL-Arg (Tos)

[0051] Linear poly-α-lysine was dissolved in deionized water, and p-toluenesulfonyl and tert-butoxycarbonyl double-protected arginine (Boc-Arg(Tos)) was dissolved in DMF. Add EDC.HCl and HOBT to the Boc-Arg (Tos) solution to activate the reaction at room temperature for 1 h, then slowly add the aqueous solution of PLL to the above mixture, and react at room temperature for 72 h. The reaction mixture was dialyzed and lyophilized. Then the lyophilized product was reacted under the condition of trifluoroacetic acid for 4 h, concentrated in vacuo, settled by adding anhydrous ether, vacuum-dried, dialyzed and lyophilized to obtain the white solid product PLL-Arg(Tos).

[0052] The grafting ratios of poly-α-lysine grafted to tosyl-protected arginine (Arg(Tos)) are listed in Table 1.

[0053] Table 1 The corresponding relationship between the molar ratio of raw materials and the molecular weight of products

[0054] Ca...

Embodiment 2

[0056] 1) Using PLL-Arg (Tos) to mediate the in vitro transfection of pGL3 (luciferase plasmid) and pEGFPN1 (green fluorescent protein plasmid) to MCF-7 cells

[0057] (1) Culture of MCF-7 cells

[0058] MCF-7 cells were cultured in fetal calf serum medium containing 10% volume fraction at a set temperature of 37°C and 5% volume fraction of CO 2 cultured in a constant temperature incubator.

[0059] (2) Cell transfection

[0060] 24 hours before transfection, cells in the logarithmic growth phase were taken, digested with trypsin, and diluted with 10% fetal calf serum culture medium, according to 1×10 4 The density of cells / well was plated in a 96-well cell culture plate, and placed in a culture temperature of 37°C with a volume fraction of 5% CO 2 Cultured in a constant temperature incubator until the cells reached 80-90% confluence. During transfection, after compounding the carrier / rhoDNA complex for 20 minutes, the amount of 0.2 μg ρDNA / well was added to the 96-well ce...

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
Concentrationaaaaaaaaaa
Login to View More

Abstract

The invention provides a cationic gene vector with high transfection efficiency and low cytotoxicity. The cationic gene vector comprises linear poly-alpha-lysine (PLL) and tosyl protected arginine (Arg(Tos)) grafted on linear poly-alpha-lysine, wherein the molar ratio of linear poly-alpha-lysine to tosyl protected arginine is 1 to (5 to 120). The optimal transfection efficiency of the cation genevector PLL-Arg(Tos) is more than ten times of the optimal transfection efficiency of a cationic gene vector gold standard PEI25k; when the cationic gene vector PLL-Arg(Tos) has the optimal transfection efficiency, the survival rate in cells is 90 percent or above. Furthermore, the optimal gene silencing efficiency of the PLL-Arg(Tos) on HuH-7Luc capable of constantly expressing luciferase can reach 80 percent or above. The invention further provides a preparation method of the cation vector with high transfection efficiency and low cytotoxicity.

Description

technical field [0001] The invention belongs to the technical field of biomedical new materials, in particular to a cationic gene carrier with high transfection efficiency and low cytotoxicity and a preparation method thereof. Background technique [0002] At present, gene therapy, as a new treatment method, has attracted increasing attention in the treatment of cancer and genetic diseases. Gene therapy refers to a new technology that introduces healthy foreign genes into recipient cells, that is, target cells, to correct or compensate diseases caused by gene defects or abnormalities, so as to achieve therapeutic purposes. [0003] However, gene therapy requires an effective gene carrier. Among gene vectors, cationic gene vectors are attracting more and more attention. Among cationic gene carriers, PEI25k is the "gold standard" of cationic gene carriers. Although PEI25k has high transfection efficiency, it has severe cytotoxicity, which limits its clinical application, se...

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
IPC IPC(8): C12N15/87C12N15/85C08G63/91
CPCC08G63/912C12N15/85C12N15/87C12N2800/107
Inventor 田华雨方华攀林琳郭兆培陈杰孙平杰陈学思
Owner CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
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