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Immunochemotherapy pharmaceutical composition and preparation method therefor

A technology for chemoimmune and chemotherapeutic drugs, applied in drug combinations, pharmaceutical formulations, anti-tumor drugs, etc., can solve problems such as damage to normal organs, high toxicity and side effects of chemotherapy, and low clinical response rates.

Active Publication Date: 2020-03-27
SUZHOU INNOVATIVE BIOMATERIALS & PHARM CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, traditional chemotherapy drugs can also damage normal organs, and the commonly used chemotherapy mode in clinic is systemic administration, which is not very selective for the lesion, and the side effects of chemotherapy are very serious
[0003] Although tumor immunotherapy represented by immune checkpoint blockade has made encouraging achievements in recent years, this therapy still has important limitations, including low clinical response rate (about 20%), non-specific immune response side effects, etc.
In particular, the low clinical response rate of current clinical immune checkpoint blockade therapy means that most patients do not respond to this expensive therapy

Method used

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  • Immunochemotherapy pharmaceutical composition and preparation method therefor
  • Immunochemotherapy pharmaceutical composition and preparation method therefor
  • Immunochemotherapy pharmaceutical composition and preparation method therefor

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0135] Example 1: Preparation and use of sodium alginate (the first type of component) and imiquimod (the third type of component) hydrochloride composition freeze-dried powder injection

[0136] Step 1: Preparation of imiquimod (the third component) hydrochloride. Weigh 50-100 mg of imiquimod into a 50 ml glass mixing container, add 1 ml of 1M dilute hydrochloric acid therein, and add deionized water to dilute after the white powdery imiquimod is fully dissolved until it is colorless and transparent, so that The final concentration of imiquimod is 2.5-5 mg / ml. The solution was freeze-dried to obtain freeze-dried powder of imiquimod hydrochloride. The purpose of this step is to convert the water-insoluble imiquimod into the water-soluble hydrochloride form. Sufficient lyophilization time is required to ensure complete removal of hydrochloric acid residues.

[0137] Step 2: The following three methods can be used to prepare the freeze-dried powder injection of the hydrochlor...

Embodiment 2

[0151] Example 2: Sodium alginate (the first type of component) and CpG oligonucleotide (the third type of component) composition freeze-dried powder injection

[0152] Step 1: Preparation of sodium alginate and CpG oligonucleotide composition freeze-dried powder injection

[0153] Weighing 10-80 mg of sodium alginate and 0.1-5 mg of CpG oligonucleotides are dissolved in 1 ml of aqueous phase solution, fully shaken until the solution is clear and transparent, and then freeze-drying the solution to obtain a freeze-dried powder injection of the composition.

[0154] Figure 5 It is a scanning electron microscope picture of the freeze-dried powder injection of the composition after reconstitution into a gel. It can be seen from the figure that the composition still has good gelation ability after freeze-drying and reconstitution, and from the electron microscope pictures, it can be seen that there are many micron-scale pores after gelation, which is of great help to the sustaine...

Embodiment 3

[0163] Embodiment three: Sodium alginate (the first type of component) and doxorubicin hydrochloride (the second type of component) composition freeze-dried powder injection

[0164] Step 1: Preparation of freeze-dried powder injection of sodium alginate and doxorubicin hydrochloride composition:

[0165] Method 1: Weigh 20-80 mg of sodium alginate and 0.1-10 mg of doxorubicin hydrochloride and dissolve them in 1 ml of aqueous phase solution, stir with a stirring paddle at a speed of 50-300 rpm until the solution is clear and transparent, and then dissolve The solution is freeze-dried to obtain the composition freeze-dried powder injection.

[0166] Method 2: Dissolve 0.1-10 mg of doxorubicin hydrochloride in 1 ml of aqueous phase solution, stir with a stirring paddle at a speed of 50-300 rpm until the solution is clear and transparent, and then dissolve 10-80 mg of sodium alginate Into the aqueous phase solution, add the constantly stirring doxorubicin hydrochloride solution...

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PUM

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Abstract

The invention discloses an immunochemotherapy pharmaceutical composition. The immunochemotherapy pharmaceutical composition is formed by mixing a first mixture with a second mixture; the first mixturecontains immunoadjuvant imiquimod R837; the second mixture contains chemotherapeutic drug oxaliplatin which can cause immunogenicity death, and further contains poloxamer 188 and sodium alginate (ALG); the first mixture is an imiquimod emulsion obtained by mixing the imiquimod R837 with the poloxamer 188; imiquimod particles each have a particle size of 0.5-3 mum; the imiquimod emulsion undergoesmoist heat sterilization; and the second mixture is a mixture prepared in a manner that the sodium alginate (ALG) and the oxaliplatin are stirred and mixed with water, and filtration sterilization isperformed with a micrometer filter membrane. The new anti-cancer pharmaceutical composition can exert the synergistic anticancer effect, reduces the side effect, the cancer metastasis probability andthe cancer recurrence probability, and can inhibit the growth of a distant metastatic tumor and reduce the tumor recurrence probability through the immunoreaction while effectively killing a tumor insitu; and meanwhile, the production process is relatively optimal, and the product stability is high.

Description

technical field [0001] The present invention relates to the field of drugs for treating tumors, in particular to a drug composition for combination therapy with chemotherapy and immunity, as well as a preparation method and application. Background technique [0002] Chemotherapy is one of the three main treatment methods for clinical treatment of tumors. Most cancer patients need to receive a certain degree of chemotherapy. For those tumors that have a tendency to metastasize or have metastasized, chemotherapy is the main treatment. However, traditional chemotherapy drugs can also damage normal organs, and the commonly used chemotherapy mode in clinic is systemic administration, which is not very selective for the lesion, and the side effects of chemotherapy are very serious. [0003] Although tumor immunotherapy represented by immune checkpoint blockade has made encouraging achievements in recent years, this therapy still has important limitations, including low clinical re...

Claims

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Application Information

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IPC IPC(8): A61K39/39A61K31/555A61K31/704A61K31/513A61K31/675A61K39/395A61K47/36A61K47/10A61P35/00A61P35/04
CPCA61K39/39A61K31/555A61K31/704A61K31/513A61K31/675A61K47/36A61K47/10A61P35/00A61K2039/55511A61K45/06A61K2300/00Y02A50/30
Inventor 刘庄许欢陶惠泉巢宇赵琪
Owner SUZHOU INNOVATIVE BIOMATERIALS & PHARM CO LTD
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