THIOLATED CHITOSAN AND PREPARATION METHOD THEREOF

Abstract

The invention discloses a thiolated chitosan and a preparation method thereof, which is chitosan co-modified by hydroxybutyl and sulfhydryl. The preparation method includes the following steps: firstly, hydroxybutyl is introduced into a chitosan molecular chain, and then sulfhydryl is introduced as a sulfhydryl moiety by a condensation reaction between free amino of hydroxybutyl chitosan and carboxyl of L-cysteine. An aqueous solution of the thiolated chitosan of the invention is in a solution state at low temperature, and can be flow-injected. When the temperature rises to around 37° C., a hydrogel can be formed. Due to the introduction of sulfhydryl, the antioxidant ability and tissue adhesion ability of the material are increased. The thiolated chitosan prepared according to the method may have wide application prospects in an aspect such as tissue engineering, drug delivery systems, cell culture, cosmetics, etc.

Claims

1. A thiolated chitosan, wherein the thiolated chitosan is a chitosan co-modified by hydroxybutyl and sulfhydryl.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0017] FIG. 1 is a photo of the temperature response test of a solution of chitosan HBC-SH co-modified by hydroxybutyl and sulfhydryl prepared according to the invention.

[0018] FIG. 2 is a broken line graph of the test results of the reducing ability of a solution of chitosan HBC-SH co-modified by hydroxybutyl and sulfhydryl prepared according to the invention.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0019] In order to further understand the invention, the thiolated chitosan provided by the invention will be described in detail below with reference to examples, but the invention is not limited to these examples. Non-substantial improvement and adjustment made by those skilled in the art under the core guiding notion of the invention still belong to the protection scope of the invention.

[0020] (I) Preparation of a Thiolated Chitosan

Example 1. Preparation of a Hydroxybutyl Chitosan HBC

[0021] (1) 20 g of chitosan was weighed, and was dissolved in 1000 ml of a 1% HCl aqueous solution followed by filtering. 1 mol/L of a NaOH solution was dropwise added to the filtrate to obtain a precipitate. The resulting precipitate was washed with distilled water until neutral. Desalination was performed with 70% ethanol. Dehydration was performed with 95% ethanol. A purified chitosan sample was obtained by drying at 50° C.

[0022] (2) 3 g of the purified chitosan was taken and dispersed in 30 ml of a 50% NaOH aqueous solution followed by stirring for 24 h and filtering. Excessive lye was squeezed out to obtain a solid. The obtained solid was added to 60 ml of an isopropanol aqueous solution (V.sub.isopropanol:V.sub.water=10:10) followed by stirring evenly. The temperature rose to 60° C. 80 ml of 1,2-epoxybutane was dropwise added, and the reaction was performed for 24 h. After cooling to room temperature, a 10% HCl aqueous solution was dropwise added to the reaction solution to adjust the pH of the system to neutrality. An insoluble substance was filtered off 3 times of the volume of ethanol was added to perform precipitation. Centrifugation, precipitation and drying were performed to obtain a hydroxybutyl chitosan HBC.

[0023] As for the preparation of hydroxybutyl chitosan HBC, reference can also be made to the preparation method disclosed in Chinese Patent 201110214776.X.

Example 2. Preparation of a Thiolated Chitosan HBC-SH

[0024] 0.5 g of the HBC prepared in Example 1 was accurately weighed, and was dissolved in 100 mL of a 0.05% acetic acid aqueous solution. 5 mmol of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride EDC.HCl and

[0025] N-hydroxysuccinimide NHS were added to the solution. Stirring was performed at room temperature for 0.5 h in the dark. 5 mmol of L-cysteine hydrochloride Cys.HCl was subsequently added. Stirring was performed at room temperature for 0.5 h in the dark. 1 M of sodium hydroxide was used to adjust the pH of the reaction liquid to 5, and the reaction was performed at room temperature for 24 h in the dark. After the reaction was completed, dialysis was performed with purified water in the dark for 3 days. The resulting dialysate was freeze-dried to obtain a thiolated chitosan HBC-SH-1.

Example 3. Preparation of a Thiolated Chitosan HBC-SH

[0026] 0.5 g of the HBC prepared in Example 1 was accurately weighed, and was dissolved in 100 mL of a 0.05% acetic acid aqueous solution. 5 mmol of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride EDC.HCl and N-hydroxysuccinimide NHS were added to the solution. Stirring was performed at room temperature for 0.5 h in the dark. 10 mmol of L-cysteine hydrochloride Cys.HCl was subsequently added. Stirring was performed at room temperature for 0.5 h in the dark. 1 M of sodium hydroxide was used to adjust the pH of the reaction liquid to 5, and the reaction was performed at room temperature for 24 h in the dark. After the reaction was completed, dialysis was performed with purified water in the dark for 3 days. The resulting dialysate was freeze-dried to obtain a thiolated chitosan HBC-SH-2.

Example 4. Preparation of a Thiolated Chitosan HBC-SH

[0027] 0.5 g of the HBC prepared in Example 1 was accurately weighed, and was dissolved in 100 mL of a 0.05% acetic acid aqueous solution. 5 mmol of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride EDC.HCl and N-hydroxysuccinimide NHS were added to the solution. Stirring was performed at room temperature for 0.5 h in the dark. 15 mmol of L-cysteine hydrochloride Cys.HCl was subsequently added. Stirring was performed at room temperature for 0.5 h in the dark. 1 M of sodium hydroxide was used to adjust the pH of the reaction liquid to 5, and the reaction was performed at room temperature for 24 h in the dark. After the reaction was completed, dialysis was performed with purified water in the dark for 3 days. The resulting dialysate was freeze-dried to obtain a thiolated chitosan HBC-SH-3.

[0028] (II) Temperature Response Test

[0029] Test method: A certain amount of HBC-SH-2 was weighed and dissolved in purified water at 4° C. to formulate a 5% HBC-SH-2 solution. The solution was placed at 4° C. and 37° C. many times.

[0030] Conclusion: The results are shown in FIG. 1. The solution is a transparent solution at 4° C. and a transparent gel at 37° C. Moreover, the transition is reversible with temperature changes, indicating that the aqueous solution of the thiolated chitosan has temperature responsiveness.

[0031] (III) Sulfhydryl Content Test

[0032] Test method: The content of free sulfhydryl in thiolated chitosan was determined with an Ellman's reagent (DTNB) using the content of sulfhydryl demarcated by L-cysteine hydrochloride Cys.HCl as a standard curve.

[0033] Conclusion: The results are shown in the following table. The content of sulfhydryl in thiolated chitosan prepared according to different preparation methods is different to some extent.

TABLE-US-00001 Sample No. Sulfhydryl content HBC-SH-1 0.0951 mmol/g HBC-SH-2 0.1447 mmol/g HBC-SH-3 0.1603 mmol/g

[0034] (IV) Reducing Ability Test

[0035] Test principle: A sample with the reducing ability can reduce Fe′ of potassium ferricyanide to Fe′ (potassium ferrocyanide), and the Fe′ (potassium ferrocyanide) further generates Prussian blue {Fe.sub.4[Fe(CN).sub.6}.sub.3 with maximum absorbance at 700 nm under the reaction with ferric chloride.

[0036] Test method: 1) The thiolated chitosan (HBC-SH-3) samples with various concentrations was formulated with purified water, respectively 0 mg/ml, 10 mg/ml, 20 mg/ml, 50 mg/ml and 100 mg/ml. 2) 1 ml of each concentration sample was taken and put into a test tube. 2.5 ml of a potassium ferricyanide solution [K.sub.3Fe(CN).sub.6, 1%], and 2.5 ml of sodium phosphate buffer (0.2 M, pH 6.6) were added successively. After mixing evenly, the mixture was incubated at 50° C. for 20 min. Then 2.5 ml of trichloroacetic acid (10%) and 0.5 ml of ferric chloride (FeC1.sub.3, 0.1%) were added successively. The absorbance value of the mixture was measured at 700 nm.

[0037] Conclusion: The results are shown in FIG. 2. The thiolated chitosans with different concentrations have absorbance values at 700 nm after treatment, indicating that the sulfhydryl modified hydroxybutyl chitosan exhibits a certain reducing ability.