Analysis of H2 Antagonists Using an HPLC method
Method: | HPLC | ||||||||||||||||||||||||||||||
Matrix: | Medicine | ||||||||||||||||||||||||||||||
Application No.: | 101943 | ||||||||||||||||||||||||||||||
Componds: | Nizatidine, Famotidine, Cimetidine, Ranitidine hydrochloride |
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Columns: | Spursil C18 3 μm 250 x 4.6 mm | ||||||||||||||||||||||||||||||
Cat No.: | 82020 | ||||||||||||||||||||||||||||||
Sample Pretreatment: | Standards: Each single stock solution was prepared at a concentration of 1mg/mL using amixed solution of methanol and acetonitrile (1:5 v/v). | ||||||||||||||||||||||||||||||
Conditions: | Mobile Phase: A: 40mMPotassium phosphate monobasicbuffer (pH2.8) B: Acetonitrile/methanol=60:40 Gradient: 5%B hold 1 min, 5 to 12%B in 14min, hold 2min, 12 to 5%B in 1min,equilibrate at 5%B for 7min Flow Rate: 1.0 mL/min; Injection: 10µL; Temperature: 30℃; Wavelength: 230nm |
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Publisher: | Dikma Technologies Inc. | ||||||||||||||||||||||||||||||
Keyword: | Nizatidine, Famotidine, Cimetidine, Ranitidine hydrochloride, HPLC, H2 Antagonists | ||||||||||||||||||||||||||||||
Abstract: | These four H2 antagonistscould be well separated on a DIKMA SpursilC18 column with good peak shapeand efficient elution out of the column within 16 minutes. | ||||||||||||||||||||||||||||||
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