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Table 10 Comparison between the present method with the reported method

From: Novel stability-indicating RP-UPLC method for simultaneous estimation of sitagliptin and ertugliflozin in bulk and pharmaceutical formulations

Parameter

Present method

Reported method

Sitagliptin

Ertugliflozin

Sitagliptin

Ertugliflozin

Retention time

0.859min

1.570min

4.60 min

2.39min

LOD

0.5μg/ml

0.13μg/ml

12.71μg/ml

42.37μg/ml

LOQ

1.53μg/ml

0.38μg/ml

8.59μg/ml

28.65μg/ml

Mobile composition

Acetonitrile to water (pH 3.5)

(50:50%, v/v)

0.5 mM potassium

dihydrogen ortho phosphate buffer: Methanol (55:45 v/v)

Flow rate

0.2ml/min

1 ml/min

Column

C8(100×2.1mm, 2μm)

C18 (250×4.6 mm, 5 μm)

  1. LOD limit of detection, LOQ limit of quantification, min minute, μg microgram, ml milliliter, v/v volume by volume, mm millimeter, μm micrometer, % percentage