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Application of Crizotinib in the Preparation of Anti-Gram-positive Bacteria Drugs

An anti-Gram-positive, Gram-positive technology, applied in the preparation of anti-Gram-positive bacteria drugs, in the field of crizotinib, can solve the problem of no crizotinib inhibiting bacteria and other problems, and achieve pharmacological safety Reliable, effective, broad antibacterial spectrum

Active Publication Date: 2021-11-19
JINAN UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] But so far, there is no relevant report on the research on the inhibition of bacteria by crizotinib

Method used

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  • Application of Crizotinib in the Preparation of Anti-Gram-positive Bacteria Drugs
  • Application of Crizotinib in the Preparation of Anti-Gram-positive Bacteria Drugs
  • Application of Crizotinib in the Preparation of Anti-Gram-positive Bacteria Drugs

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] The antibacterial spectrum research of embodiment 1 crizotinib

[0040] This example studies the antibacterial spectrum of crizotinib.

[0041]Tested strains: Streptococcus pneumoniae (S.pneumoniae D39) was purchased from China Type Culture Collection; Streptococcus suis (S.suis BM407), Staphylococcus aureus (S.aureus 29213), MRSA (S.aureus ATCC43300) Bacillus subtilis (B.subtilis 2508) was purchased from the Microbial Culture Collection Center of China; Bacillus subtilis (B.subtilis 2508) was purchased from the Guangdong Provincial Microbial Culture Collection Center; The bacterium (P.aeruginosa ATCC9027) was obtained from the American Type Culture Collection, and the minimum inhibitory concentration (MIC) of the model was determined (three single clones of each strain).

[0042] 1. Experimental steps

[0043] Streptococcus pneumoniae was inoculated into 0.5% THYE liquid medium for overnight activation according to the inoculum amount of 5%, and then transferred to f...

Embodiment 2

[0051] Embodiment 2 crizotinib is measured to Staphylococcus aureus minimum inhibitory concentration (MIC)

[0052] The tested strains of this embodiment: Staphylococcus aureus methicillin-resistant strain MRSA (ATCC43300) and the sensitive strain of Staphylococcus aureus (29213) are from the General Microbiology Center of China Committee for Culture Collection of Microorganisms; Staphylococcus aureus single Nike Linmycin strain (29213-K), Staphylococcus aureus single-resistant gentamicin strain (29213-G), Staphylococcus aureus single-resistant ciprofloxacin strain (29213-C), Staphylococcus aureus single-resistant Amoxicillin (29213-A), Staphylococcus aureus single-resistant levofloxacin strain (29213-L) is domesticated from a sensitive strain of Staphylococcus aureus (29213).

[0053] Among them, Staphylococcus aureus single-resistant clindamycin strain (29213-K), Staphylococcus aureus single-resistant gentamycin strain (29213-G), Staphylococcus aureus single-resistant ciprof...

Embodiment 3

[0063] The minimum inhibitory concentration (MIC) determination of embodiment 3 crizotinib to clinically isolated multidrug-resistant Staphylococcus aureus, Enterococcus faecalis, Staphylococcus hemolyticus

[0064] The tested bacterial strain of this embodiment is clinically isolated multi-drug resistant Staphylococcus aureus (168272, 168023, 166471, 166534, 166138, 168293, 900624, 168205, 179634, 179148, 179475, 179459, 178425, 178524, 178360) , Enterococcus faecalis (179521), and Staphylococcus hemolyticus (179595), from the Laboratory Department of Southern Medical University. The above numbers are the system numbers of the corresponding strains in the Laboratory Department of Southern Medical University. The drug resistance of related strains is shown in Table 3.

[0065] Table 3 Drug resistance of related strains (MIC unit: μg / mL)

[0066]

[0067]

[0068] 1. Experimental steps

[0069] The clinically isolated multi-drug-resistant Staphylococcus aureus, Enterococ...

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Abstract

The invention provides the application of crizotinib in the preparation of anti-Gram-positive bacterial drugs, and proposes for the first time that the anti-tumor drug crizotinib can effectively inhibit Gram-positive bacteria, especially can significantly inhibit single drug-resistant strains and The growth of clinical multidrug-resistant strains has a broad antibacterial spectrum, which expands the application range of crizotinib and has the potential to be developed into an antibacterial drug. Crizotinib has been approved for marketing by the drug regulatory authorities of many countries around the world. Its pharmacological safety is more reliable, and it does not need to carry out experiments such as toxicology. It has a good prospect for development and utilization. The treatment of positive bacterial infections (especially drug-resistant bacterial infections) has important practical significance, and provides a new drug option for the clinical treatment of Gram-positive bacterial infections.

Description

technical field [0001] The invention belongs to the field of biomedicine, and in particular relates to the application of crizotinib in the preparation of anti-gram-positive bacteria drugs. Background technique [0002] For a long time, infectious diseases caused by pathogenic microorganisms have been an important factor that endangers human health. Pathogenic bacterial infection is an acute systemic infection caused by pathogenic bacteria or opportunistic pathogenic bacteria invading the blood circulation to grow and reproduce, producing toxins and other metabolites, especially for the elderly, children, those with chronic diseases or low immune function, and those who are not treated in time And those with complications may develop sepsis or sepsis and die. At present, antibiotics are commonly used clinically to inhibit bacteria, and antibiotics have also brought great changes to the treatment of infectious diseases. Due to the overuse and inappropriate application of ant...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K31/4545A61P31/04
CPCA61K31/4545A61P31/04
Inventor 孙雪松郑云丹
Owner JINAN UNIVERSITY
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