Antibiotic titer determination method based on ink-jet printing principle
An inkjet printing and potency measurement technology, applied in printing, testing pharmaceutical preparations, material inspection products, etc., can solve problems such as droplet rupture, test failure, and cumbersome operation, and achieve error reduction, accuracy and repeatability. Good, simple and fast effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] 1) Select a Canon PIXMA ip1880 thermal jet color inkjet printer with a resolution of 1200×4800d.p.i. as a tool for dropping antibiotics, firstly modify the main body of the printer: remove the shell of the main body of the printer, and remove the roll located under the ink cartridge Paper device and waste ink removal device, and the plastic base below it is sawed off, and the agar glass double dish coated with bacteria layer can be placed in the vacant position. Afterwards, modify the ink cartridge: pry off the outer cover, use tweezers to clamp out the sponge full of ink, and rinse the ink at the bottom of the ink cartridge with clean water until there is no residue. Finally, take out the filter screen located above the nozzle, and rinse it repeatedly with clean water. Before loading antibiotics, wash it with 70% ethanol for 3-5 times. After air-drying, place it under a UV lamp to sterilize for about 1 hour;
[0025] 2) In this example, according to the two-dose method...
Embodiment 2
[0036] 1) step 1 is the same as step 1 in embodiment 1;
[0037] 2) step 2 is the same as step 2 in embodiment 1;
[0038] 3) Except that the experimental bacteria used were changed to Bacillus pumilus, all the other steps were the same as step 3 in Example 1;
[0039] 4) Preparation and printing of standard gentamicin and gentamicin to be tested: use phosphate buffer (0.2% dipotassium hydrogen phosphate, 0.8% potassium dihydrogen phosphate, pH6.0, sterilize at 115°C for 30min) Fully dissolve the standard gentamicin and the gentamicin powder to be tested respectively, prepare the standard gentamicin and the gentamicin to be tested at a concentration of 4 mg / ml, and take out 100 μl of the prepared gentamicin standard Add the sample to the black ink cartridge, take out 100 μl of prepared gentamicin to be tested and drop it into the magenta ink cartridge as the "ink" for printing; place the agar glass double dish containing Bacillus pumilus in step 3) on the 1mm below the nozzl...
Embodiment 3
[0048] 1) step 1 is the same as step 1 in embodiment 1;
[0049] 2) step 2 is the same as step 2 in embodiment 1;
[0050] 3) Except that the experimental bacteria used were changed to Staphylococcus aureus, all the other steps were the same as step 3 in Example 1;
[0051] 4) Preparation and printing of standard streptomycin and streptomycin to be tested: use phosphate buffer (dipotassium hydrogen phosphate 0.2%, potassium dihydrogen phosphate 0.8%, pH 6.0, sterilize at 115°C for 30 minutes) Dissolve the streptomycin standard substance and the streptomycin powder to be tested, prepare the streptomycin standard substance and the streptomycin to be tested at a concentration of 5 mg / ml, take out 100 μl of the prepared streptomycin standard substance and add it dropwise to the black ink cartridge, take out Add 100 μl of the prepared streptomycin to be tested dropwise into the magenta ink cartridge as the "ink" for printing; place the agar glass double dish containing Staphylococ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com