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 …
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 …
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
A simple, precise, linear, robust, accurate, and stability‐indicating liquid chromatography
method was developed and validated to determine Ibrutinib in finished solid dosage forms …
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 …
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
Chiral high performance liquid chromatographic technique usually employs polysaccharide‐
based stationary phases in a normal phase mode. This frequently generates large waste of …
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 …
The present work describes a novel stability-indicating method development and validation
for separation and identification of degradation products, known and genotoxic impurities in …
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 …
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 …
performance liquid chromatography (RP‐HPLC) method is a novel tool. Three factors and …
[HTML][HTML] Green and sensitive analysis of the antihistaminic drug pheniramine maleate and its main toxic impurity using UPLC and TLC methods, blueness assessment …
For the first time, two direct and eco-friendly chromatographic approaches were adapted for
the simultaneous estimation of pheniramine maleate (PAM) and its major toxic impurity, 2 …
the simultaneous estimation of pheniramine maleate (PAM) and its major toxic impurity, 2 …
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 …
caused by infection such as the common cold and flu. Here we were reporting a simple and …