2005
DOI: 10.1002/jssc.200301739
|View full text |Cite
|
Sign up to set email alerts
|

Simultaneous determination of metformin and glimepride in pharmaceutical dosage form by reverse‐phase liquid chromatography

Abstract: A simple, rapid, and precise reversed-phase liquid chromatographic method has been developed for the simultaneous determination of metformin in combination with glimepride. Under the developed conditions, good separation of the analytes was achieved in short analysis time. Several parameters affecting the separation of the analytes were studied, including pH and the concentration of SDS. The method is validated and shown to be linear in the range of 25 microg/mL to 150 microg/mL for metformin and 0.1 microg/mL… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
8
0

Year Published

2007
2007
2020
2020

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 18 publications
(8 citation statements)
references
References 7 publications
0
8
0
Order By: Relevance
“…Methods for pharmaceutical determination in water have been described previously (Kolte et al, 2005). In short, filtrated water samples (0.45 lm) were injected into the HPLC (Varian ProStar 210, Germany) by an auto sampler (Varian ProStar 410, Germany) with an injection volume of 25 lL.…”
Section: High-performance Liquid Chromatography (Hplc) Analysismentioning
confidence: 99%
“…Methods for pharmaceutical determination in water have been described previously (Kolte et al, 2005). In short, filtrated water samples (0.45 lm) were injected into the HPLC (Varian ProStar 210, Germany) by an auto sampler (Varian ProStar 410, Germany) with an injection volume of 25 lL.…”
Section: High-performance Liquid Chromatography (Hplc) Analysismentioning
confidence: 99%
“…8 There are two polymorphs of this molecule reported in the literature, form I and form II, of which form II has about 3.5-fold higher solubility than that of form I. 9 There is a growing number of studies describing the determination of glimepiride concentration in biological fluids [10][11][12][13][14][15][16][17][18] and pharmaceutical formulations [19][20][21][22][23][24][25][26][27][28][29][30] using a variety of methods. However, there is no dissolution method for glimepiride tablets in the literature.…”
Section: Introductionmentioning
confidence: 99%
“…The reported methods are applicable to analysis of human plasma, equine plasma and urine, and tablet formulations [23][24][25][26][27][28]. Methods include LC procedures for metformin and glipizide with a lower limit of quantitation (LLQ) of 5.0 and 22.5 ng/mL [23], or metformin and glimepride with a LLQ of 22 and 39 ng/mL, respectively [24]. Methods based on LC/MS/MS have been reported for metformin and gliclazide (LLQ range of 7.8-10.0 ng/mL) [25].…”
Section: Introductionmentioning
confidence: 99%