1984
DOI: 10.1002/jps.2600730212
|View full text |Cite
|
Sign up to set email alerts
|

Stabilized Normal-Phase High-Performance Liquid Chromatographic Analysis of Aspirin and Salicylic Acid in Solid Pharmaceutical Dosage Forms

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
3
0

Year Published

1984
1984
2011
2011

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 18 publications
(3 citation statements)
references
References 18 publications
0
3
0
Order By: Relevance
“…Both normal phase [3] as reversed phase [4][5][6][7][8][9][10][11][12][13] methods can be found. Further methods can be found using LC-MS [14,15], capillary electrophoresis [16][17][18][19][20][21] and micellar electrokinetic chromatography [17,20,22].…”
Section: Introductionmentioning
confidence: 99%
“…Both normal phase [3] as reversed phase [4][5][6][7][8][9][10][11][12][13] methods can be found. Further methods can be found using LC-MS [14,15], capillary electrophoresis [16][17][18][19][20][21] and micellar electrokinetic chromatography [17,20,22].…”
Section: Introductionmentioning
confidence: 99%
“…extrapolation of results back to time zero,l0 and selection of solvents to minimize salicylic acid formati0n.~. 9,15 The aim of the present work is to make use of t h e chemical reactivity of the acetyl group of aspirin as a pre-column reaction in a direct approach to its determination. It has been found that aspirin quickly transacetylates 3-aminophenol producing 3-hydroxyacetanilide, which is a stable compound and can be determined by reversed-phase HPLC without any interference from salicylic acid and other ingredients of drug formulation.…”
mentioning
confidence: 99%
“…Conversion of aspirin into salicylic acid during sample preparation is a vexing problem and it can limit the accuracy of determination. Attempts to obviate or minimize errors from this source include injection of sample within a few minutes of its preparation (21), extrapolation of results back to time zero (5), preparation of calibrated standards with matching amounts of aspirin (7), selection of solvents to minimize salicylic acid formation (4,20,22), and separation of aspirin from product ingredients that accelerate its degradation (22). Complex formulations have been analyzed by ultraviolet absorption after separation of their constituents by partition chromatography (23)(24)(25).…”
mentioning
confidence: 99%