Method for determining content of azithromycin in azithromycin sustained-release eye drops
A technology of slow-release eye drops and azithromycin, which is applied in the field of content determination of azithromycin in Chinese medicine, can solve the problems of low recovery rate, determination of drug content, leakage of main drug, etc., to reduce time and cost, and ensure accurate detection data. high effect
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Embodiment 1
[0044] Mobile phase: methanol-acetonitrile-0.02mol dipotassium hydrogen phosphate buffer (adjust pH=7.2 with phosphoric acid)=50:10:40;
[0045] Determination steps:
[0046]Weigh 5g of azithromycin sustained-release eye drops sample, place it in a 25ml volumetric flask, add mobile phase to half of the volumetric flask, shake gently, and set the volume to the mark. Weigh 50 mg of azithromycin reference substance, place it in a 25ml volumetric flask, add mobile phase to dissolve the reference substance and dilute to the mark with mobile phase. Take the reference substance solution and the sample solution respectively and pass through a 0.22 μm filter membrane, carry out high-performance liquid chromatography analysis according to the above conditions, and record the chromatogram. The obtained chromatogram shows that under this condition, the main peak of azithromycin can be completely separated from the auxiliary material peak. According to reference substance concentration / s...
Embodiment 2
[0048] Mobile phase: methanol-acetonitrile-0.02mol disodium hydrogen phosphate buffer volume ratio (adjust pH=7.2 with phosphoric acid)=20:50:30;
[0049] Determination steps:
[0050] Quantitatively weigh 5g of azithromycin sustained-release eye drops sample, place it in a 25ml volumetric flask, add mobile phase to half of the volumetric flask, shake gently, and set the volume to the mark. Weigh 50mg of azithromycin reference substance, place it in a 25ml volumetric flask, add mobile phase to dissolve and dilute to the mark. Take the reference substance solution and the sample solution respectively and pass through a 0.22 μm filter membrane to carry out high-performance liquid chromatography analysis according to the above conditions, and record the chromatograms. The obtained chromatograms are shown in the attached figure 1 As shown, it can be seen that the azithromycin main peak 1 can be completely separated from the auxiliary material peak under this condition, and the az...
Embodiment 3
[0053] Mobile phase: methanol-acetonitrile-0.02mol dipotassium hydrogen phosphate buffer volume ratio (adjust pH=6.8 with phosphoric acid)=60:20:20;
[0054] Determination steps:
[0055] Quantitatively weigh 5g of azithromycin sustained-release eye drops sample, place it in a 25ml volumetric flask, add mobile phase to half of the volumetric flask, shake gently, and set the volume to the mark. Weigh 50mg of azithromycin reference substance, place it in a 25ml volumetric flask, add mobile phase to dissolve and dilute to the mark. The reference substance solution and the sample solution were respectively passed through a 0.22 μm filter membrane and analyzed by high performance liquid chromatography according to the above conditions, and the obtained spectrum showed that the main peak of azithromycin could be completely separated from the peak of the auxiliary material under this condition. According to reference substance concentration / sample concentration=contrast peak area / sa...
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