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HPLC Analysis of Cefixime and Ofloxacin in Tablets on Chromolith® High Resolution RP-18e

HPLC Analysis of Cefixime and Ofloxacin in Tablets on Chromolith® High Resolution RP-18e application for HPLC

CONDITIONS

sample preparation

Crush 20 tablets. Weigh equivalent to one tablet quantity & transfer to 100 mL volumetric flask. Add 50 ml diluent & sonicate for 20 mins. Dilute up to the mark the same. Further dilute with 2.5 mL of this solution to 100 mL. Filter through 0.2 μm filter

mobile phase

[A] 3.4 g of potassium dihydrogen phosphate in 1000 ml MilliQ water. Mix & sonicate it. Filter it with 0.2 μm filter; [B] acetonitrile; 87:13, A:B)

flow rate

1.0 mL/min

pressure

764 psi (53 bar)

column temp.

25 °C

detector

290 nm cell: 10 μL

injection

5 μL

sample

Weigh 5.0 mg of Cefixime & 5.0 mg of Ofloxacin refernce standard in 100 mL volumetric flask. Add about 50 mL diluent & sonicate till it dissolve. Dilute it upto the mark with the same. (Diluent: Dissolve 7.1 g of di-sodium hydrogen phosphate in 500 ml MilliQ water. Adjust pH at 7.0 with ortho-phosphoric acid. Mix & sonicate it. Filter it with 0.2 μm filter.)

column

Chromolith® High Resolution RP-18 endcapped, 100 x 4.6 mm (1.52022.0001)

说明

分析说明

Sample: 50 ppm (0.050 mg/mL) of each cefixime and ofloxacin in diluent.
Diluent: 7.1 g of disodium hydrogen phosphate in 500 mL Milli-Q water. pH 7.0 with orthophosphoric acid.
Method developed in house for tablet analysis.

法律信息

Chromolith is a registered trademark of Merck KGaA, Darmstadt, Germany