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Glucan derivative, method for preparing same, and additive for preparing medicament

A technology of glucan and derivatives is applied in the field of amphiphilic glucan derivatives, additives for preparing pharmaceuticals, and glucan derivatives, and can solve the problems of difficult synthesis, strong hemolysis, and uncertain grafting position.

Active Publication Date: 2020-05-19
SHANGHAI TUFA MEDICAL TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The above-mentioned amphiphilic derivatives of dextran that have been disclosed have some shortcomings, such as: the grafting position of the hydrophobic group on the dextran is uncertain, the hemolytic property is strong, and the synthesis is difficult, etc.

Method used

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  • Glucan derivative, method for preparing same, and additive for preparing medicament
  • Glucan derivative, method for preparing same, and additive for preparing medicament
  • Glucan derivative, method for preparing same, and additive for preparing medicament

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0070] Embodiment 1. Dextran derivatives of formula I-1-1 and formula I-1-2

[0071] In this embodiment, a dextran derivative is provided, which has the structure shown in formula I-1 or formula I-2.

[0072]

[0073] The preparation method of the above-mentioned dextran derivatives is to mix the amino derivatives of diglyceride and dextran in the solution according to the molar ratio of 1:1-10:1, and generate the target product after reductive amination reaction. Wherein, the said diglycerides contain fatty acid chains with 10-20 carbon atoms. In this embodiment, the preparation method includes the following steps:

[0074] a. Steps for preparing amino derivatives of diglycerides

[0075] making the di-fatty acid glyceride react with excess compound 1 at room temperature under the action of an activator to obtain an amino derivative of the di-fatty acid glyceride;

[0076] In this step, the di-fatty acid glyceride is at least one of 1,2-difatty acid glyceride or 1,3-dif...

Embodiment 2

[0085] Example 2. Specific Dextran Derivatives

[0086] In this example, dextran derivatives with different average molecular weights of dextran and different fatty acid glycerides were used to prepare dextran derivatives, and the obtained dextran derivatives were respectively labeled, as shown in Table 1 below.

[0087] Table 1. Dextran and corresponding dextran derivatives with different average molecular weights

[0088]

[0089]

[0090] The above compounds have the following general formula

[0091]

[0092] Wherein, the value range of n and o is 8-20, preferably 14-16; and, n and o may be the same or different values.

[0093] Those skilled in the art can understand that the glyceryl distearate described in Table 1 may be glyceryl distearate or glyceryl 1,3-distearate or a mixture of both.

[0094] In this example, according to the dextran and diglycerides listed in Table 1, the dextran derivatives were prepared according to the following specific steps to obt...

Embodiment 3

[0098] Embodiment 3. Comparative Examples

[0099] In this example, octadecylamine is used as a hydrophobic group to bond to the reducing end of dextran with an average molecular weight of 10,000 to obtain a dextran derivative DEX10K-OCA, which is A one-tailed dextran derivative.

[0100] The specific preparation method of the dextran derivative DEX10K-OCA is as follows.

[0101] Take 0.1mmol of 1.0g of dextran and put it in a dry flask, add 20ml of anhydrous DMSO, heat and stir at 60°C until dissolved; add 0.5mmol of 135mg of octadecylamine, heat and stir at 75°C until dissolved, add 0.3ml of glacial acetic acid , heated and stirred for 2 hours. A DMSO solution (2 ml) containing 0.45 mmol of sodium triacetoxyborohydride was added, and the reaction was continued to stir at room temperature for 2 hours.

[0102] Repeatedly filter the reaction solution until it becomes clear, add the filtrate to about 5 times the amount of ethanol to cause precipitation, filter, take the filt...

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Abstract

The invention discloses a glucan derivative and an additive containing the glucan derivative. The glucan derivative has a structure as shown in formula I which is described in the specification. According to the glucan derivative disclosed by the invention, two fatty acid ester groups are bonded to the tail end reduction end of dextran bya proper linking group, so that the amphiphilic glucan derivative disclosed by the invention is provided witha double-tail structure, and then the amphiphilic derivative with good biodegradability and good surface activity is obtained and can be widely appliedto pharmaceutical preparations.

Description

technical field [0001] The invention relates to the field of pharmacy, in particular to a dextran derivative, especially an amphipathic dextran derivative, and an additive for preparing medicaments containing the dextran derivative. Background technique [0002] Surfactant refers to a substance that can significantly reduce the surface tension of a liquid, and its chemical structure contains both hydrophilic and hydrophobic groups. Surfactants are widely used and can be used in solubilization, emulsification, wetting, decontamination, sterilization, defoaming and foaming, etc. Polymer surfactants generally refer to a relative molecular mass of 10 3 ~10 6 of surfactants. Compared with low-molecular-weight surfactants, high-molecular-weight surfactants are weaker in reducing surface tension, but have good solubilizing, emulsifying, thickening, foam-stabilizing, and film-forming properties. Polymer surfactants can be classified into natural polymer surfactants (including se...

Claims

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Application Information

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IPC IPC(8): C08B37/02A61K9/107A61K47/36
CPCC08B37/0021A61K47/36A61K9/1075
Inventor 赵谦翁伟宇黄建明徐晓珍朱沪光梁婷婷
Owner SHANGHAI TUFA MEDICAL TECH CO LTD
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