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ATP-sensitive fluorescent probe liposome with tumor targeting and tracking functions, preparation method and application thereof

A tumor-targeting, fluorescent probe technology, applied in liposome delivery, preparations for in vivo tests, medical preparations of non-active ingredients, etc., can solve the problem of no active targeting, short PEG chain, high signal To achieve the effect of improving tumor targeting efficiency, increasing fluorescence intensity, and improving signal-to-noise ratio

Active Publication Date: 2019-01-25
SICHUAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

As a fluorescent probe, the micelles can be effectively delivered in vivo, enter cells, and have a high signal-low background ratio, excellent selectivity and biocompatibility, but there are the following problems: 1. Only rely on the enhanced penetration of nanometer size and The retention (EPR) effect reaches the tumor site, without active targeting, and the targeting efficiency is poor. The article does not provide in vivo targeting experiment data; 2. The PEG chain is too short to achieve the effect of prolonging the internal circulation; 3. It is necessary to synthesize oligo-containing Hybrid molecules of nucleotides, polyethylene glycol and di-fatty acyl lipids, with many synthetic steps, difficult synthesis and complex purification operations

Method used

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  • ATP-sensitive fluorescent probe liposome with tumor targeting and tracking functions, preparation method and application thereof
  • ATP-sensitive fluorescent probe liposome with tumor targeting and tracking functions, preparation method and application thereof
  • ATP-sensitive fluorescent probe liposome with tumor targeting and tracking functions, preparation method and application thereof

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Experimental program
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Effect test

Embodiment 1

[0043] The preparation method of the ATP-sensitive fluorescent probe liposome with tumor targeting and tracing functions described in this example is as follows:

[0044] (1) Dissolve cRGD-cys and distearoylphosphatidylethanolamine-polyethylene glycol 2000-maleimide (DSPE-PEG2000-Mal) in a molar ratio of 1:1 in methanol to obtain a mixed solution. The amount of methanol used is The concentration of DSPE-PEG2000-Mal in the mixed solution is 1mmol / L. The resulting mixed solution was magnetically stirred at room temperature for 12 hours to react, and after the reaction was completed, the solvent in the reaction solution was removed by rotary evaporation under reduced pressure to obtain the distearoylphosphatidylethanolamine-polyethylene glycol 2000 ( cRGD-DSPE-PEG2000);

[0045] (2) Dissolve cRGD-DSPE-PEG2000, lecithin and cholesterol prepared in step (1) in a molar ratio of 5:65:35 in a composite solvent obtained by mixing chloroform and methanol at a volume ratio of 3:1 to obt...

Embodiment 2

[0052] (1) Dissolve Her2-cys and dimyristoylphosphatidylethanolamine-polyethylene glycol 2000-maleamide (DMPE-PEG2000-Mal) in methanol at a molar ratio of 1:1 to obtain a mixed solution. The amount of methanol used is The concentration of DMPE-PEG2000-Mal in the mixed solution is 10mmol / L. The resulting mixed solution was magnetically stirred at room temperature for 24 hours to react, and after the reaction was completed, the solvent in the reaction solution was removed by rotary evaporation under reduced pressure to obtain Her2-coupled dimyristoylphosphatidylethanolamine-polyethylene glycol 2000 (Her2- DMPE-PEG2000);

[0053] (2) dissolving Her2-DMPE-PEG2000 prepared in step (1), soybean lecithin and cholesterol in a molar ratio of 2:78:20 in a composite solvent obtained by mixing chloroform and methanol in a volume ratio of 3:1 to obtain a mixed solution, Composite solvent consumption is 10mmol / L meter with the concentration of soybean lecithin and cholesterol in the obtain...

Embodiment 3

[0057] (1) Her2-cys and dipalmitoylphosphatidylethanolamine-polyethylene glycol 2000-maleamide (DPPE-PEG2000-Mal) are dissolved in methanol at a molar ratio of 1:1 to obtain a mixed solution, and the amount of methanol is as described The concentration of DPPE-PEG2000-Mal in the mixed solution is 5mmol / L. The resulting mixed solution was magnetically stirred at room temperature for 16 hours to react, and after the reaction was completed, the solvent in the reaction solution was removed by rotary evaporation under reduced pressure to obtain Her2-coupled dipalmitoylphosphatidylethanolamine-polyethylene glycol 2000 (Her2-DPPE -PEG2000);

[0058] (2) dissolving Her2-DMPE-PEG2000 prepared in step (1), soybean lecithin and cholesterol in a molar ratio of 8:42:50 in a composite solvent obtained by mixing chloroform and methanol in a volume ratio of 3:1 to obtain a mixed solution, Composite solvent consumption is 5mmol / L with the concentration of soybean lecithin and cholesterol in t...

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Abstract

The invention relates to an ATP (adenosine triphosphate) sensitive fluorescent probe lipidosome, which is characterized in that ATP sensitive nucleotide double chains are encapsulated in a lipid bimolecular layer membrane coupled with tumor targeting polypeptide to form a nanometer vesicle; the ATP sensitive nucleotide double chains are formed by self assembly of an ATP sensitive nucleotide single chain coupled with fluorescent dye and an ATP sensitive nucleotide complementary single chain coupled with a fluorescent quenching agent according to the base complementation and pairing principle; the lipid bimolecular layer membrane coupled with the tumor targeting polypeptide consists of tumor targeting polypeptide coupled pegylation phosphatidyl ethanolamine, phospholipid and cholesterol according to a mole ratio being (2-8):(42-78):(20-50). The invention also provides a preparation method of the lipidosome. The fluorescent probe lipidosome has the tumor active targeting, ATP sensitive intelligent fluorescent light opening and in vivo long circulation functions; the preparation process is simple.

Description

technical field [0001] The invention belongs to the field of imaging reagents, in particular to a fluorescent probe liposome. Background technique [0002] Tumor has become a major disease that threatens human health. At present, when the tumor is diagnosed, the vast majority of cancer patients are in the middle and advanced stages, and the treatment methods mainly include surgery, radiotherapy, and chemotherapy. However, patients with advanced tumors are prone to recurrence, drug resistance, metastasis and complications after treatment, which are the main reasons for treatment failure and patient death. Therefore, it is of great significance to carry out early diagnosis of tumors to improve the treatment effect and reduce the mortality of cancer patients. Fluorescent tracer technology refers to the introduction of fluorescent substances into the cells or tissues to be tracked or developed, and the use of fluorescent properties to provide information about the researched o...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K49/00A61K9/127A61K47/60A61K31/704A61P35/00
CPCA61K9/127A61K9/1273A61K9/1277A61K31/704A61K49/0021A61K49/0056A61K49/0086
Inventor 李莉林艺顾忠伟
Owner SICHUAN UNIV
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