A method for separating and purifying epothilone d based on molecular imprinting

A technology of epothilone and molecular imprinting, which is applied in the biological field, can solve the problems of complex operation, high cost of filler, and high cost, and achieve the effect of simple operation, good separation effect, and low cost

Active Publication Date: 2021-04-20
NANJING TECH UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

② Epothilone has no cytotoxic activity of paclitaxel
However, the high cost in its production process has become a problem that people need to solve urgently.
In addition to factors such as low yield of the producing bacteria, long growth cycle, and susceptibility to infection, there are also major factors in the isolation and purification of epothilone
Because the expression product of S. cellulosus has complex and diverse components, the difficulty of separation and purification of epothilone is greatly increased.
[0004] At present, the methods for the separation and purification of epothilone mainly include: Sephadex combined with PHPLC separation and purification route, its purity can reach more than 90%, but the recovery rate is low, only about 75%, and the cost of filler is high. The operation is relatively complicated; the C18 normal pressure reverse column chromatography separation and purification route has a recovery rate of 80% and a purity of 85%, and its packing cost is high and the recovery rate is low; the ion exchange column chromatography separation and purification route , the recovery rate can reach 90%, but the purity of 60% is far from meeting the requirements of practical application

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] The invention provides a method for template molecule selection, the specific steps are as follows

[0038] Template molecules include EpoA, EpoB, EpoD and two or more of them in a 1:1 mixture. Take 0.1 mmol of template molecules, mix template molecules, functional monomers and cross-linking agents in a molar ratio of 1:4:20, add 50ml porogen is polymerized under certain conditions to obtain a polymer. Weigh 40 mg of the polymers prepared from the above different template molecules into a 10 ml centrifuge tube, add 8 ml of EpoD standard substance with a concentration of 50 mg / L for adsorption, and measure the adsorption amount A of EpoD. The polymer without template molecules was used as the control group to adsorb EpoD, and the adsorption amount B was measured. Determine the optimal template molecule with the A / B value as the reference standard (the larger the A / B value, the better the adsorption effect of the polymer obtained by adding the template molecule on EpoD)....

Embodiment 2

[0042] The invention provides a method for determining the ratio of a template molecule to a crosslinking agent, and the specific steps are as follows:

[0043] On the basis of Example 1, the amount of template molecules added is 0.1 mmol, the amount of functional monomers added is 0.4 mmol, and the molar ratios of template molecules and crosslinking agents are 1:5, 1:10, 1:15, 1:20 , 1:25 and 1:30. Add 50ml porogen to polymerize under certain conditions to obtain a polymer. Weigh 40mg of the polymer prepared by the above different template molecules into a 10ml centrifuge tube, add 8ml of EpoD standard substance with a concentration of 50mg / L for adsorption, and measure the adsorption amount A of EpoD 模板分子:交联剂 . The polymer without template molecules was used as the control group to adsorb EpoD, and the adsorption amount B was measured 模板分子:交联剂 . Use the size of A / B value as the reference standard to determine the best template molecule (A / B 模板分子:交联剂 The larger the value...

Embodiment 3

[0048] The invention provides a method for determining the ratio of template molecules and functional monomers, the specific steps are as follows:

[0049] On the basis of Examples 1 and 2, the added amount of the template molecule was 0.1 mmol, the added amount of the functional monomer was 0.2, 0.4, 0.6, 0.8, and 1.0 mmol, and the added amount of the crosslinking agent was 2 mmol. Add 50ml porogen to polymerize under certain conditions to obtain a polymer. Weigh 40mg of the polymer prepared by the above different template molecules into a 10ml centrifuge tube, add 8ml of EpoD standard substance with a concentration of 50mg / L for adsorption, and measure the adsorption amount A of EpoD 模板分子:功能单体 . The polymer without template molecules was used as the control group to adsorb EpoD, and the adsorption amount B was measured 模板分子:功能单体 . Use the size of A / B value as the reference standard to determine the best template molecule (A / B 模板分子:功能单体 The larger the value, the better th...

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Abstract

The invention discloses a method for separating and purifying Epothilone D based on molecular imprinting. The EpoD molecular imprinting polymer is soaked in a small amount of pure methanol, loaded into a separation column, and methanol-acetic acid, methanol, and methanol-deionized water are sequentially used Rinse the column, vacuum compact the column; dissolve the EpoD crude product in 20-80% methanol aqueous solution, and add it to the installed column; after standing for 20-50min, rinse the column to remove the interference, and further reduce the interference of impurities; Use 10-90% methanol PBS solution as the eluent to elute the column, so that EpoD is completely dissolved in the eluent, collect the eluate and spin evaporate to dryness, and redissolve in pure methanol to obtain a purified EpoD methanol solution. Compared with the existing separation and purification methods, the method is simple, convenient and low in cost, and at the same time, it is specific adsorption in the epothilone D adsorption process, which can achieve better separation effect. It provides possibility for further separation and purification of epothilone D.

Description

technical field [0001] The invention belongs to the field of biotechnology, and in particular relates to a method for separating and purifying epothilone D based on molecular imprinting. Background technique [0002] Epothilone (epothilone) is a class of macrolide compounds, first reported in 1993 by G. Höfle et al. of the German National Center for Biotechnology (GBF). Epothilone can be isolated from the fermentation liquid of the Myxobacteria suborder S. cellulosus strain, and its main components are Epothilone A and B. The biological activities of epothilone A, B and D on cancer cells are equivalent to or even stronger than paclitaxel, especially epothilone B, whose activity is 10-100 times stronger than paclitaxel. The activity of epothilone will be greatly improved after the substitution of methyl on the C12 position and the replacement of the C12-C13 double bond with an epoxy group. Epothilones have superior anti-tumor properties than paclitaxel: ① Epothilones are mo...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07D417/06C08F222/38C08F220/56C08J9/26
CPCC07D417/06C08F220/56C08F222/385C08J9/26
Inventor 虞龙张娣饶远张宁李市场
Owner NANJING TECH UNIV
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