Gene medicine for inhibiting lung cancer metastasis and pulmonary metastases
A drug and gene technology, applied in the field of gene medicine based on recombinant adeno-associated virus and tumor angiogenesis inhibitory gene, can solve the problems of low concentration of anti-tumor angiogenesis factors and inability to better play the purpose of treating tumors in target organs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0072] Preparation of rAAV2 / 2-eGFP
[0073] The composition of the expression frame of the eGFP expression plasmid is as follows: the promoter is CMV enhancer / chicken β-actin promoter, eGFPcDNA, polyA, WPRE. The two ends of the expression box are AAV2ITR.
[0074] Prepare recombinant virus by calcium phosphate-free helper virus multi-plasmid method: co-transfect 293 cells with eGFP expression plasmid, AV helper plasmid, and rAAV2 helper plasmid, harvest cells after 60-72 hours, and use sodium deoxycholate (0.5%) Cleave with benzonase (30u / ml), centrifuge (3000g 30min) to remove cell debris, and cesium chloride gradient centrifuge to obtain recombinant virus rAAV2 / 2-eGFP, which is purified by chromatography.
Embodiment 2
[0076] rAAV2 / 1-eGFP, rAAV2 / 3-eGFP, rAAV2 / 4-eGFP, rAAV2 / 5-eGFP, rAAV2 / 6-eGFP, rAAV2 / 7-eGFP, rAAV2 / 8-eGFP, rAAV2 / 9-eGFP, rAAV2 / Preparation of 10-eGFP and rAAV2 / 11-eGFP
[0077] Referring to the steps in Example 1, the rAAV2 helper plasmids were replaced with rAAV1, rAAV3, rAAV4, rAAV5, rAAV6, rAAV7, rAAV8, rAAV9, rAAV10, and rAAV11, and the remaining operations were the same as in Example 1 to obtain 11 different serotypes of rAAV viruses.
Embodiment 3
[0079] Screening for lung-tropic rAAV serotypes
[0080] The titers of the various serotypes of rAAV obtained in Example 2 were determined by Real-PCR method. The primers used were designed according to the sequence of WPRE, respectively WPRE-F (5'-TGGCGTGGTGTGCACTGT) and WPRE-R (5'-GTTCCGCCGTGGCAATAG).
[0081] LLC cells or HLEC cells were seeded into 24-well plates and cultured overnight. Add the various serotype rAAV viruses that contain embodiment 2 and obtain respectively (MOI 10 4 ) serum-free medium, after incubation for 5 hours, it was replaced with normal medium. After 72 hours, the cells were observed with a fluorescent microscope, and the cells were sorted with a flow cytometer, and the transduction efficiency was calculated (n=3).
[0082] Table 3 Transduction efficiency of different serotypes of rAAV to LLC cells or HLEC cells
[0083] rAAV serotype
[0084] It can be seen that the transduction efficiency of various serotypes of rAAV to LLC cells or ...
PUM
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