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Application of nano-ciprofloxacin particles in inhibiting biofilm formation of Pseudomonas aeruginosa

A technology of ciprofloxacin hydrochloride and nano rings, which is applied in the field of bio-nano, can solve problems such as treatment difficulties, and achieve the effects of low cytotoxicity, high drug loading rate, and stable loading system

Inactive Publication Date: 2020-01-21
NORTHWEST UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Coupled with the inherent and acquired resistance of Pseudomonas aeruginosa to multiple antibiotics, the infectious diseases of Pseudomonas aeruginosa are very difficult to treat clinically

Method used

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  • Application of nano-ciprofloxacin particles in inhibiting biofilm formation of Pseudomonas aeruginosa
  • Application of nano-ciprofloxacin particles in inhibiting biofilm formation of Pseudomonas aeruginosa
  • Application of nano-ciprofloxacin particles in inhibiting biofilm formation of Pseudomonas aeruginosa

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Example 1 Preparation of Nano Ciprofloxacin Particles

[0023] (1) CS is made into an aqueous solution with a concentration of 1.0 mg / ml with sterile double-distilled water, adjusted to pH 5.0 with NaOH, and sterilized by sterile microporous membrane filtration;

[0024] (2) S-β-CD is made into an aqueous solution with a concentration of 1.0 mg / ml with sterile double-distilled water, and is sterilized by microporous membrane filtration;

[0025] (3) Cip is made into an aqueous solution with a concentration of 1 mg / ml with sterile double-distilled water, sterilized by microporous membrane filtration, added to an equal volume of 1 mg / ml S-β-CD solution, and magnetically stirred at room temperature for 1 hour;

[0026] (4) Add an equal volume of 1 mg / ml CS aqueous solution, and continue to stir at room temperature for 4 h to obtain nano antibiotic drug-loaded particle emulsion. Centrifuge at 16000rpm for 30min, take the supernatant, measure the encapsulation efficiency, r...

Embodiment 2

[0028] Example 2 Preparation of empty nanoparticles

[0029] CS and S-β-CD with a concentration of 1.0 mg / ml were mixed according to the volume of 1:1, placed on a magnetic stirrer at room temperature and stirred for 4 hours, and the empty nanoparticle emulsion was obtained. Centrifuge at 16000rpm for 30min, rinse the precipitated particles three times with sterile water, and freeze-dry overnight to obtain empty nanoparticles (NPs).

Embodiment 3

[0030] Example 3 Detection of Ciprofloxacin Hydrochloride Concentration

[0031] (1) Prepare 10µg / ml Cip standard solution.

[0032] (2) According to the method in Table 1, dilute the 10 µg / ml Cip standard solution to obtain different concentrations, use distilled water as the blank control solution, and measure the absorbance value of each concentration of Cip at the maximum absorption wavelength of Cip at 276 nm with a UV-visible spectrophotometer . Draw a standard curve with the concentration as the X axis and the OD value as the Y axis. The regression equation is: y=0.109x-0.012 (R²=0.997), Y is the absorbance value, and X is the drug concentration (µg / ml).

[0033] Table 1 Cip standard curve drawing solution component preparation

[0034] Solution number 1 2 3 4 5 6 7 8 9 Cip standard solution (ml) 0.5 0.75 1.0 1.25 1.5 1.75 2.0 2.25 2.5 Distilled water (ml) 2.5 2.25 2.0 1.75 1.5 1.25 1.0 0.75 0.5 Cip final concentrat...

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Abstract

The invention discloses a preparation method of nanometer ciprofloxacin particles and their application in inhibiting the formation of biofilm of Pseudomonas aeruginosa. Specifically, chitosan hydrochloride and β-cyclodextrin sulfate are used as carriers to wrap Preparation of nanometer ciprofloxacin particles from ciprofloxacin hydrochloride. The encapsulation system composed of CS and S‑β‑CD is stable, has high drug loading rate and low cytotoxicity. Nanosized ciprofloxacin particles can effectively inhibit the formation of Pseudomonas aeruginosa biofilm, which will provide a new and effective way to clinically treat Pseudomonas aeruginosa infectious diseases.

Description

technical field [0001] The invention relates to a method for preparing nanometer ciprofloxacin particles for inhibiting the formation of Pseudomonas aeruginosa biofilm, and belongs to the field of biological nanometers. Background technique [0002] The development of new antibiotics is far behind the emergence of clinical drug-resistant bacteria, and mankind will face the severe challenge of no cure. Improving the antibacterial efficacy of existing antibiotics seems to be a life-saving straw for human beings. At present, an effective way to solve this problem is how to change the delivery mode and release location of antibiotics, so as to play the role of targeting and enrichment, and realize the efficacy of antibiotics in inhibiting pathogenic infection efficiently. Nano-antibiotics (nano-antibiotics) is a new type of antibiotic system currently developed, which can deliver drugs at the nanoscale and evade the drug resistance mechanism of bacteria. It is considered to be ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/19A61K47/61A61K31/496A61P31/04
CPCA61K9/19A61K31/496
Inventor 张亚妮邵小龙
Owner NORTHWEST UNIV