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

A kind of small molecule peptide and its preparation method and application as nanometer drug-carrying carrier

A technology of nano-drug loading and small molecule peptides, which is applied in the direction of nano-drugs, medical preparations containing active ingredients, nanotechnology, etc., can solve the problems of difficult self-assembly preparation, application limitations, poor material biocompatibility, etc., and achieve cost-effective Inexpensive, easy to purify, good biocompatibility effect

Active Publication Date: 2022-05-03
WEIFANG MEDICAL UNIV
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although some inorganic nanomaterials and polymer materials have made great progress in the treatment of tumors, some materials have poor biocompatibility, are difficult to degrade in vivo, and are difficult to self-assemble. Loading drugs, so that its clinical application is limited

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
  • A kind of small molecule peptide and its preparation method and application as nanometer drug-carrying carrier
  • A kind of small molecule peptide and its preparation method and application as nanometer drug-carrying carrier
  • A kind of small molecule peptide and its preparation method and application as nanometer drug-carrying carrier

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0058] Example 1: Ac-LVVLKKK(pY)-NH 2 Preparation of peptides

[0059] Step 1: Distill N,N-dimethylformamide (DMF) and piperidine solvents

[0060] Distill the purchased DMF solution under reduced pressure at 60°C to obtain pure DMF solvent; add a small amount of CaH to the purchased piperidine 2 Heating to reflux for 1-2 hours, receiving the fraction at the boiling point (106°C) to obtain pure piperidine solvent.

[0061] Step 2: Preparation of amino acids, resins, activators, capping agents, and deprotecting agents

[0062] Calculated on the polypeptide solid-phase synthesizer to prepare 0.25mmol / L Ac-LVVLKKK(pY)-NH 2 Amounts of amino acids and other reagents required:

[0063] Leu (leucine): 0.78 g dissolved in 11 mL DMF;

[0064] Lys (lysine): 1.50 g dissolved in 16 mL DMF;

[0065] Tyr(PO 3 h 2 ) (phosphorylated tyrosine): 2.67 g dissolved in 28 mL DMF

[0066] Val (valine): 0.75 g dissolved in 11 mL DMF;

[0067] Resin (loaded at 0.6 mmol / g): 0.417 g;

[0068]...

Embodiment 2

[0075] Example 2: Ac-LVVLKKK(pY)-NH 2 Preparation of drug-loaded carrier

[0076] Weigh 0.59 mg of peptide Ac-LVVLKKK(pY)-NH 2 , adding 1 mL of Hepes buffer (pH7.4) to obtain a peptide solution with a concentration of 0.5 mmol / L, sonicating for 10 min, and standing at room temperature for 24 h, the observation results of transmission electron microscopy (TEM) showed that the peptides had self-assembled at this time A spherical nanoparticle structure is formed, while some nanofibers ( image 3 ).

Embodiment 3

[0077] Example 3: Ac-LVVLKKK(pY)-NH 2 Changes in Self-Assembled Morphology of Drug Carriers Encapsulating DOX

[0078] The specific detection method is as follows:

[0079] Detection of self-assembly morphology (TEM) of drug-loaded peptides in Hepes buffer after adding DOX:

[0080] Prepare Ac-LVVLKKK(pY)-NH with concentrations of 0.1 mmol / L, 0.5 mmol / L and 1 mmol / L 2 Add 1 mL of each peptide solution, and add 0.02 mL of DOX respectively, so that the final concentration of DOX is 0.12 mg / mL. Sonicate for 10 min, place at room temperature for 24 h, and observe with TEM. The results showed that Ac-LVVLKKK(pY)-NH 2 Peptide solution, after adding DOX, the nanofibrous structure disappears, and finally self-assembles into spherical nanoparticles loaded with drugs, such as Figure 4 , Figure 5 , Image 6 shown.

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

No PUM Login to View More

Abstract

The invention discloses a small molecule peptide and its preparation method and application as a nano drug carrier. The structural formula of the peptide is Ac-LVVLKKK(pY)-NH 2 , can self-assemble into spherical nanoparticles in Hepes solution. The spherical nanoparticles formed by the peptide can be used as a drug-carrying carrier to pack insoluble antitumor drugs, reduce their toxic and side effects, and improve their bioavailability. The small molecular polypeptide designed in the present invention has enzyme responsiveness and the ability of self-assembly morphology transformation, can respond to the alkaline phosphatase overexpressed in the tumor microenvironment, and carry insoluble anti-tumor drugs to tumor cells. Under the induction, it transforms from spherical nanoparticles into nanofibers, releases anti-tumor drugs and prolongs the residence time of drugs in cells. The invention discloses the construction, preparation method and application of the peptide, and provides a new idea for the development of the nano drug loading system of chemotherapy drugs.

Description

technical field [0001] The invention relates to the technical field of nano-drug loading system and its preparation, in particular to a phosphatase-responsive small molecular peptide that can be used as a nano-drug loading carrier. Background technique [0002] Nanomaterials have a unique high-permeability long-retention (EPR) effect and can be effectively enriched in tumor cells. Therefore, as drug carriers for anti-tumor drugs, they have great potential in tumor treatment. Although some inorganic nanomaterials and polymer materials have made great progress in the treatment of tumors, some materials have poor biocompatibility, are difficult to degrade in vivo, and are difficult to self-assemble. Drug loading limits its clinical application. [0003] In recent years, the research of small molecular peptides in the construction of nano-drug delivery systems has attracted widespread attention. Peptide itself is one of the important components of organisms, with good biocompa...

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 Patents(China)
IPC IPC(8): C07K7/06A61K9/14A61K45/00A61K47/42A61P35/00B82Y5/00B82Y40/00
CPCC07K7/06A61K9/146A61K47/42A61K45/00A61P35/00B82Y40/00B82Y5/00
Inventor 白靖琨龚中英
Owner WEIFANG MEDICAL UNIV
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