Method for preparation of hybrid amphiphilic star copolymer nano micelles
Hybrid amphiphilic star copolymer nano micelles are prepared in the invention. Cage shaped octa(γ-aminopropyl) silsesquioxanes is selected as the inorganic part, and L-glutamic benzyl ester—five membered ring anhydride is ring-opening polymerized by the initiation of amino groups on the surface of cage shaped octa(γ-aminopropyl) silsesquioxanes, producing copolymers with cage shaped octa(γ-aminopropyl) silsesquioxanes as nucleus and poly (L-glutamic-benzyl ester) as arms. The copolymers reacts with monomethoxy poly (ethylene glycol) carboxylic acid by condensation. Finally, the benzyl groups in the side chains of poly (L-glutamic acid-benzyl ester) are converted into hydrazine groups by acylhydrazination to obtain hybrid amphiphilic star copolymer nano micelles. The micelles can load doxorubicin, they are safe to human body and have good application prospects.
1. A method of preparing hybrid amphiphilic star copolymer micelles comprising:
(1) preparing monomers by:
mixing L-glutamic benzyl ester with tetrahydrofuran to form a mixture,
heating the mixture and dissolving L-glutamic benzyl ester in the tetrahydrofuran to form a solution,
adding triphosgene to the solution to carry out a reaction under protection of N 2 until the solution becomes transparent,
driving out HCl gas and phosgene produced in the reaction with continuous entry of N 2 ,
adding the transparent solution to anhydrous petroleum ether in excess amount and obtaining white needle like crystal product in an ice bath,
purifying the white needle like crystal product with tetrahydrofuran and/or anhydrous petroleum ether to obtain a purified product,
isolating the purified product through filtration to obtain an isolated product, and
vacuum drying the isolated product to obtain L-glutamic benzyl ester—five membered ring anhydride (NCA);
(2) ring-opening polymerizing of NCA by:
mixing and stirring cage shaped octa(γ-aminopropyl) silsesquioxanes, anhydrous dichloromethane and the L-glutamic benzyl ester—five membered ring anhydride obtained in step ( 1 ) under protection of N 2 to initiate ring-opening polymerization and obtain a copolymeric product, and
isolating, washing, and drying the copolymeric product (labeled as Si-PBLG);
( 3 ) conducting condensation reaction by:
dissolving the Si-PBLG obtained in step (2) in chloroform to obtain dissolved Si-PBLG,
reacting the dissolved Si-PBLG with monomethoxy polyethylene glycol carboxylic acid (coded as CH 3 O-PEG-COOH) in presence of 1-(3-dimethylamino propyl)-3-ethylcarbodiimide hydrochloride and N-hydroxy succinimide as catalysts to obtain a hybrid amphiphilic star copolymer (labeled as Si-PBLG-PEG), and
purifying the Si-PBLG-PEG by precipitation with ether, re-dissolution, dialysis, and freeze-drying to obtain purified Si-PBLG-PEG;
(4) conducting acylhydrazination reaction by:
mixing the purified Si-PBLG-PEG obtained in step (3) with hydrazine hydrate solution and 1,4-dioxane and carrying out a refluxing reaction to obtain a reaction solution, and
dialyzing the reaction solution to obtain the hybrid amphiphilic star copolymer nano micelles.
2. The method of claim 1 wherein in step (2), molar ratio of cage shaped octa(γ-aminopropyl) silsesquioxanes to L-glutamic benzyl ester—five membered ring anhydride is 1:40, 1:50, 1:60, 1:70, or 1:80, and the corresponding hybrid amphiphilic star copolymer nano micelles so obtained are labeled as HNM-1, HNM-2, HNM-3, HNM-4 and HNM-5, respectively.
3. The method of claim 1 wherein in step (3), number-average molecular weight of monomethoxy polyethylene glycol carboxylic acid is 620.
4. The method of claim 1 , wherein in step (3), weight ratio of Si-PBLG to monomethoxy polyethylene glycol carboxylic acid is 1:0.5, 1:1, or 1:2.
5. The method of claim 1 , wherein in step (3), weight ratio of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride to N-hydroxy succinimide is 2:1, and combined weight of the two makes up 30% of the weight of Si-PBLG.
6. The method of claim 1 , wherein in step (4), weight ratio of the hybrid amphiphilic star copolymer Si-PBLG-PEG to the hydrazine hydrate solution is 2.4:1˜1.6:1.
7. The method of claim 1 , wherein in step (4), concentration of the hydrazine hydrate solution is 80%.
8. The method of claim 1 , wherein in step (4), volume of 1,4-dioxane is the same as the hydrazine hydrate solution.
9. A method for preparing drug-loaded hybrid amphiphilic star-shaped copolymer nano micelles comprising:
1) freeze drying hybrid amphiphilic star copolymer micelles prepared based on claim 1 to obtain dried powder,
2) adding the dried powder to an excess dimethyl sulfoxide solution containing doxorubicin hydrochloride to obtain a first mixture,
3) adding triethylamine to the first mixture obtained in step 2) for neutralizing hydrochloric acid in doxorubicin hydrochloride to obtain a second mixture containing nano micelles,
4) removing free doxorubicin on the surface of the nano micelles by dialysis in deionized water at room temperature to obtain a third mixture, and
5) freeze drying the third mixture of step 4) to obtain the drug-loaded hybrid amphiphilic star copolymer nano micelles.