Choices of chromatographic methods as stability indicating assays for pharmaceutical products: A review
YL Chew, MA Khor, YY Lim - Heliyon, 2021 - cell.com
Stability indicating assay describes a technique which is used to analyse the stability of drug
substance or active pharmaceutical ingredient (API) in bulk drug and pharmaceutical …
substance or active pharmaceutical ingredient (API) in bulk drug and pharmaceutical …
Stability‐indicating reversed‐phase‐HPLC method development and validation for sacubitril/valsartan complex in the presence of impurities and degradation products …
According to current regulatory guidelines, a stability‐indicating method has been
developed to determine the impurities in sacubitril (SCB) and valsartan (VLS) tablet dosage …
developed to determine the impurities in sacubitril (SCB) and valsartan (VLS) tablet dosage …
Development of hybrid spectrofluorimetric method for simultaneous determination of Valsartan and Sacubitril in LCZ696 tablets
RM Youssef, SA El-Nahass, SA Soliman… - Spectrochimica Acta Part …, 2021 - Elsevier
A hybrid Spectrofluorimetric method was developed for the simultaneous determination of
binary mixtures, without prior separation steps. It coupled synchronous spectrofluorimetry …
binary mixtures, without prior separation steps. It coupled synchronous spectrofluorimetry …
Ecological assessment and development of analytical methods for concurrent quantification of valsartan and sacubitril: whiteness comparative study based on relative …
Sustainable analytical chemistry is gaining great interest in global environmental pollution
control. In addition, valsartan (VAS) and sacubitril (SAB) have been recently approved by the …
control. In addition, valsartan (VAS) and sacubitril (SAB) have been recently approved by the …
Development and validation of a stability‐indicating, single HPLC method for sacubitril–valsartan and their stereoisomers and identification of forced degradation …
C Vijaykumar, YR Kumar, P Aparna… - Biomedical …, 2023 - Wiley Online Library
The aim of this research work was to develop and validate a stability‐indicating, single
reversed‐phase HPLC method for the separation of five impurities, including enantiomers …
reversed‐phase HPLC method for the separation of five impurities, including enantiomers …
Drug Degradation Prediction, In Silico Toxicity Assessment and Development of Stability-Indicating, Quality by Design Enabled UFLC Method for Sacubitril-Valsartan
Stability and impurity profiling of drugs is crucial in fixed-dose drug combinations as safety,
efficacy, and purity depend on an individual drug's stability behaviour. The formation of drug …
efficacy, and purity depend on an individual drug's stability behaviour. The formation of drug …
A comparative review of methods for estimation of some antihypertensive drugs in pharmaceutical production
This review aim was to study and analyze some of the existing quantitative analytical
methods for estimating some antihypertensive drugs in pharmaceutical planning. Several …
methods for estimating some antihypertensive drugs in pharmaceutical planning. Several …
HPTLC Approach for Simultaneous Quantification of Valsartan and Sacubitril in Bulk and Tablet Formulations
BL Deore, AS Patil, BJ Mali, S Patil… - World Journal of …, 2024 - repository-wjarr.com
The article introduces an inventive, eco-friendly, simple, consistent and reproducible NP-
TLC-Densitometry approach to simultaneous pharmaceutical estimation of Valsartan and …
TLC-Densitometry approach to simultaneous pharmaceutical estimation of Valsartan and …
[PDF][PDF] Stability-Indicating RP-HPLC Method Development And Validation For Determination Of Sacubitril Impurities In Sacubitril And Valsartan Microsphere Dosage …
B Sivaram, T Shyam - NeuroQuantology, 2022 - researchgate.net
A rapid and stability-indicating, reversed-phase high-performance liquid chromatography
(RP-HPLC) method was developed for the determination of Sacubitril impurities in Sacubitril …
(RP-HPLC) method was developed for the determination of Sacubitril impurities in Sacubitril …