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

Nano self-assembly drug carrier microcapsule system

A nano-self-assembly and microcapsule technology, which is applied in the direction of microcapsules, capsule delivery, and drug combination, can solve the problems of high synthesis cost, reduced water solubility of drug molecules, and poor biocompatibility, and achieve large drug loads and biological Good compatibility, the effect of reducing toxic and side effects

Inactive Publication Date: 2015-03-18
CHENGDU LVKE HUATONG TECH
View PDF2 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] However, due to the complex structure of the polymer in the star polymer, the prepared drug carrier has problems such as poor biocompatibility, decreased drug loading capacity, and reduced water solubility of drug molecules on the surface of dendrimer.
In addition, dendrimer has a complex structure and high synthesis cost
These problems limit the application of star-shaped polymer nano-drug delivery system

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
  • Nano self-assembly drug carrier microcapsule system
  • Nano self-assembly drug carrier microcapsule system
  • Nano self-assembly drug carrier microcapsule system

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0044] ① Preparation of azide small molecule initiator

[0045]Step 1: Dissolve 5 mL of 2-chloroethoxyethanol in 25 mL of butanone, and add 4.5 g of NaN to the solution 3 , 2.5gBu 4 NI, 10 mg of dicyclohexane-18-crown-6, the mixture was heated to boiling and stirred for 24 hours. The mixture was filtered and the precipitate was rinsed thoroughly with acetone. The resulting mixed solution is the crude product of the product, after the mixed solution was concentrated, at 90 o C was distilled to obtain the pure product. The resulting 2-azidoethoxyethanol 1 H NMR (CDCl 3 ): 3.70 (t, 2 H, C H 2 OH), 3.65 (t, 2 H, HOCH 2 C H 2 O), 3.56 (t, 2H, N 3 CH 2 C H 2 O), 3.37 (t, 2H, C H 2 N 3 ), and 2.56 (s, 1H, OH).

[0046] Step 2: Dissolve 2g of 2-azidoethoxyethanol and 5.09g of α-chloroacyl chloride in 30mL of dichloromethane prepared in step 1, transfer the reaction system to ice, and dissolve 6.8g of dicyclohexyl The carbodiimide was slowly added to the reaction ...

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 nano self-assembly drug carrier microcapsule system which is prepared through following steps: (1) polymerizing phosphatidylcholine through an atom transfer radical polymerization method to obtain poly-phosphatidylcholine; (2) modifying the poly-phosphatidylcholine with a folic acid molecule; (3) polymerizing O-benzyl-L-tyrosine carboxylic acid anhydride through a ring-opening polymerization method to obtain poly-O-benzyl-L-tyrosine; (4) performing stem-grafting to the poly-O-benzyl-L-tyrosine with adriamycin through a hydrazone bond; (5) performing a bond-connecting process to the poly-phosphatidylcholine and the poly-O-benzyl-L-tyrosine in a click chemical manner to obtain a segmented copolymer; (6) dissolving the segmented copolymer in tetrahydrofuran and moving the solution to a dialysis bag, performing dialysis with pure water, and filtering a dialyzate through a filter membrane; and (7) freeze-drying a solution after filtration to obtain a medicine carrying micelle. The medicine carrying micelle has a double-layer core-shell structure of which an outer layer is hydrophilic poly-phosphatidylcholine and an inner layer is a drug molecule wrapping layer. The microcapsule belongs to nano-particles, can achieve targeted transmission of the drug and pH-sensitive releasing in cancer cells, is large in drug carrying amount and is good in stability. The targeted function can reduce toxic and side effects of the drug on normal tissue and organ.

Description

technical field [0001] The invention relates to a nanometer self-assembled drug carrier microcapsule system, in particular to a preparation method of a block polymer material drug carrier microcapsule with cancer cell targeting. The invention belongs to the field of polymer chemistry and polymer technology. Background technique [0002] Cancer has become the most important disease that endangers human health. One of the important methods to treat cancer is drug therapy. However, many anticancer drugs have defects such as insoluble in water and poor stability. For example, camptothecin, paclitaxel, doxorubicin, and 5-fluorouracil are difficult to be well utilized by organisms due to their poor solubility. Solving the problem of their water solubility is the key to the clinical application of such pharmaceutical preparations. In addition, most of the tumor treatment and diagnostic drugs have non-selective effects, and are often distributed in some normal tissues and organs, a...

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): A61K9/50A61K9/107A61K31/704A61K47/48C08G81/02C08G69/48C08F130/02C08F8/32A61P35/00
Inventor 不公告发明人
Owner CHENGDU LVKE HUATONG TECH
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