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Polyethylene glycol-chitosan-curcumin polymer, drug-loaded nano particles thereof and preparation method thereof

A technology of chitosan polymer and polyethylene glycol, applied in the direction of nanotechnology, nanotechnology, nanomedicine, etc., can solve the problem of not being able to prevent the partial release of curcumin

Active Publication Date: 2018-12-18
HUNAN NORMAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Based on this, it is necessary to provide a polyethylene glycol-chitosan-curcumin polymer and its Drug-loaded nanoparticles and preparation methods

Method used

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  • Polyethylene glycol-chitosan-curcumin polymer, drug-loaded nano particles thereof and preparation method thereof
  • Polyethylene glycol-chitosan-curcumin polymer, drug-loaded nano particles thereof and preparation method thereof
  • Polyethylene glycol-chitosan-curcumin polymer, drug-loaded nano particles thereof and preparation method thereof

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preparation example Construction

[0045] A preparation method of polyethylene glycol-chitosan-curcumin polymer, comprising the following steps:

[0046] Reaction of curcumin with succinic anhydride produces carboxylated curcumin.

[0047] After the carboxyl group of carboxylated curcumin is activated, it reacts with chitosan solution to generate curcumin-chitosan polymer.

[0048] After the carboxyl group of carboxylated polyethylene glycol is activated, react with the acetic acid solution of curcumin-chitosan polymer under a protective gas atmosphere for 48h to 96h, and purify to obtain polyethylene glycol-chitosan-curcumin polymer.

[0049] A kind of polyethylene glycol-chitosan-curcumin nanoparticle provided by the invention is to take polyethylene glycol (mPEG), succinic anhydride (SA), chitosan, curcumin as raw material, and the molar ratio is 1:1.2 The reaction of curcumin with succinic anhydride first synthesizes carboxylated curcumin (CURS), and in the presence of a catalyst, the carboxylated curcumin...

Embodiment 1

[0062] Embodiment 1: the chemical synthesis of polyethylene glycol-chitosan-curcumin polymer (PCC)

[0063] Its synthetic route is:

[0064]

[0065] 1) Synthesis of curcumin-chitosan (CCS) polymer

[0066] 2g (5.4mmol) of CUR, 0.65g (6.5mmol) of SA and 0.66g (5.4mmol) of DMAP were dissolved in 20ml of DMSO, and the reaction was stirred at 50-60°C for 48h. The reaction solution was dripped into 100ml of cold diethyl ether, stirred while dripping, and a yellow precipitate was precipitated, filtered by suction, washed with 50ml of cold diethyl ether each time, and carried out three times. The obtained yellow solid was vacuum-dried at room temperature to obtain pure yellow CURS. Dissolve 0.72g CURS and 0.20g DMAP in 10ml DMSO and stir at room temperature for 2h to activate CURS. Weigh chitosan 1.0g and dissolve in 10ml of 1% acetic acid aqueous solution (the molar ratio of CURS to chitosan unit is about 1:4), drop the activated CURS reaction liquid into the chitosan solutio...

Embodiment 2

[0069] Example 2: FTIR Spectroscopy of CUR, mPEG, CS, CCS and PCC Polymers

[0070] Take a small amount of solid CUR, mPEG, CS, CCS, and PCC and mix them evenly with infrared-dried potassium bromide powder (mass ratio is about 1:200), grind them carefully, press them into a transparent sample film, and place them in an infrared spectrometer to measure infrared spectrum.

[0071] FTIR spectra of (a) CUR, (b) mPEG, (c) CS, (d) CCS and (e) PCC polymers are shown in figure 1 . with CUR( figure 1 a) and CS ( figure 1 b) Compared to CCS ( figure 1 The infrared spectrum of c) maintains the characteristic absorption peak at 1558cm-1, which comes from the N-H bond of -NH2 at 1597cm-1 in CS, and a stronger peak appears at 1728cm-1, which is The C=O bond stretching vibration peak in the ester bond formed between CUR and CS indicates the successful esterification reaction between CUR and CS. In PCC ( figure 1 In the spectrum of e), the C=O stretching vibration peak of the amide bon...

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Abstract

The invention discloses a polyethylene glycol-chitosan-curcumin polymer, drug-loaded nano particles thereof and a preparation method thereof. The polyethylene glycol-chitosan-curcumin polymer is capable of grafting curcumin as a hydrophobic group to a framework material of nanoparticles, helps to form nanoparticles, forms a novel dosage form of curcumin, and acts as a carrier of other hydrophobicanticancer drugs to achieve the purpose of the combined medication. The polyethylene glycol-chitosan-curcumin nanoparticles are the novel dosage form of curcumin, which can be used as the carrier forother hydrophobic anticancer drugs to achieve controlled release of drugs. The nanoparticles have good biocompatibility and long circulation, and escape from the phagocytosis of a reticuloendothelialsystem. can be used as a co-delivery system for delivery of curcumin and other hydrophobic anti-tumor drugs to reach the combined medication, can improve the treatment by regulating different signaling pathways, also helps to minimize the occurrence of multidrug resistance at a large degree, and inhibits tumor growth.

Description

technical field [0001] The present invention relates to a nano-preparation, in particular to a polyethylene glycol-chitosan-curcumin, especially to a preparation method of polyethylene glycol-chitosan-curcumin nanoparticles, a drug-loaded polyethylene glycol - Chitosan - Curcumin nanoparticles and preparation method. Background technique [0002] The nanoparticle drug delivery system is the most important component of the drug delivery system (Drug Delivery System, DDS), because it has many advantages, such as increasing the solubility and stability of poorly soluble drugs, and achieving sustained drug release after in vivo administration. And controlled release, as well as the "passive targeting" effect based on the EPR effect (Enhanced Permeability and Retention Effect), so it has been widely used in the field of biomedicine. Polymer micelle nanoparticles formed by self-assembly of amphiphilic polymers in water are a very potential drug-loaded nanoparticles. The drug is ...

Claims

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Application Information

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IPC IPC(8): A61K47/61A61K47/60A61K47/69A61K31/12A61K45/06A61P35/00C08B37/08C08G81/00C08J3/12B82Y5/00
CPCA61K31/12A61K45/06B82Y5/00C08B37/003C08G81/00C08J3/12C08J2305/08C08J2387/00A61K2300/00
Inventor 陶晓军巫放明杨小平陈瑶
Owner HUNAN NORMAL UNIVERSITY
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