2012
DOI: 10.4103/2229-5186.103097
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Development and validation of stability indicating UPLC assay method for ziprasidone active pharma ingredient

Abstract: Aim: The analytical method has been developed to evaluate the efficacy of the cleaning procedure of all the equipment involved in the production of final active ingredients. The choice of the methodology is based on the production method and on the intrinsic properties of the products. For this validation, high-performance liquid chromatography (HPLC) method has been chosen. Materials and Methods: The HPLC chromatographic separations were achieved on (100 mm × 4.6 mm), 3.5 µm make: Phenomenex column employing … Show more

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Cited by 2 publications
(1 citation statement)
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“…13,14 However, chromatographic methods have some disadvantages such as the length of time required for sample identification, the high cost, the need for sample pretreatment, the need for trained technicians, and in some cases, the low sensitivity. [15][16][17][18] Instead, electrochemical sensors have features such as high selectivity and sensitive, cost-effective, low limit of detection (LOD), wide linear range, appropriate stability, and in-situ analysis. [19][20][21] These sensors are also used widely for the identification and analysis of drug materials.…”
Section: Introductionmentioning
confidence: 99%
“…13,14 However, chromatographic methods have some disadvantages such as the length of time required for sample identification, the high cost, the need for sample pretreatment, the need for trained technicians, and in some cases, the low sensitivity. [15][16][17][18] Instead, electrochemical sensors have features such as high selectivity and sensitive, cost-effective, low limit of detection (LOD), wide linear range, appropriate stability, and in-situ analysis. [19][20][21] These sensors are also used widely for the identification and analysis of drug materials.…”
Section: Introductionmentioning
confidence: 99%