A quality‐by‐design evaluated liquid chromatography method development and validation for the separation and quantification of nitroxoline and its impurities

SP Lankalapalli, KV Rachel, V Chintala… - Journal of …, 2024 - Wiley Online Library
A novel, isocratic, sensitive, stability‐indicating high‐performance liquid chromatography
method was developed for the separation and quantification of related substances in …

Stability‐indicating RP‐HPLC method development and validation for determination of nine impurities in apixaban tablet dosage forms. Robustness study by quality …

VB Subramanian, NK Katari, T Dongala… - Biomedical …, 2020 - Wiley Online Library
A quality by design (QbD) based high‐resolution HPLC method is described for
determination of impurities in apixaban (APX) in the tablet dosage form. Employing a simple …

Development and validation of liquid chromatography method for determination of Ibrutinib in finished dosage forms using quality by design approach

N Konduru, R Gundla, T Dongala… - Separation …, 2022 - Wiley Online Library
A simple, precise, linear, robust, accurate, and stability‐indicating liquid chromatography
method was developed and validated to determine Ibrutinib in finished solid dosage forms …

125 Years of Aspirin: Status of Analytical Methods

NS dos Santos Galvão, A Sinzervinch… - Current …, 2024 - benthamdirect.com
Aspirin, an analgesic, antipyretic and non-steroidal anti-inflammatory drug, was a fascinating
discovery that became the precursor to one of the oldest pharmaceutical success stories. It …

Resolving phenylephrine HCl and guaifenesin enantiomers on cellulose‐based chiral stationary phases: Separation of four enantiomers on 50‐mm column

MA Tantawy, HY Aboul‐Enein, AM Yehia - Chirality, 2023 - Wiley Online Library
Chiral high performance liquid chromatographic technique usually employs polysaccharide‐
based stationary phases in a normal phase mode. This frequently generates large waste of …

Development and validation of a stability-indicating method for ibrutinib: Identification and separation of degradation products, known and genotoxic impurities using …

N Konduru, R Gundla, NK Katari… - Analytical Chemistry …, 2020 - Taylor & Francis
The present work describes a novel stability-indicating method development and validation
for separation and identification of degradation products, known and genotoxic impurities in …

Stability‐indicating ultra performance liquid chromatography method development and validation for simultaneous estimation of metformin, linagliptin, and …

KR Vankalapati, P Alegete… - Biomedical …, 2021 - Wiley Online Library
A rapid stability‐indicating reversed phase‐ultrapure liquid chromatography (RP‐UPLC)
was developed and validated for the estimation of metformin (MET), linagliptin (LIN), and …

Analytical Quality by Design Approach of Reverse‐Phase High‐Performance Liquid Chromatography of Atorvastatin: Method Development, Optimization, Validation …

NK Alruwaili - International Journal of Analytical Chemistry, 2021 - Wiley Online Library
The use of analytical quality by design (AQbD) approach in the optimization of the high‐
performance liquid chromatography (RP‐HPLC) method is a novel tool. Three factors and …

RP-HPLC stability indicating method development and validation of pseudoephedrine sulfate and related organic impurities in tablet dosage forms, robustness by …

T Dongala, LNR Katakam, AK Palakurthi… - Analytical Chemistry …, 2019 - Taylor & Francis
Pseudoephedrine is used for the temporary relief of stuffy nose and sinus pain/pressure
caused by infection such as the common cold and flu. Here we were reporting a simple and …