Results 111 to 120 of about 833 (196)

Analytical quality by design (AQbD) approach for the simultaneous quantification of FDC in a cardiovascular drug by RP-HPLC method

open access: yesFuture Journal of Pharmaceutical Sciences
Background A sustainable and stability-indicating reversed-phase high-pressure liquid chromatography (RP-HPLC) method has been developed for the simultaneous estimation of chlorthalidone (CHL), Amlodipine (AML), and olmesartan medoxomil (OLM) in a ...
Varsha Thorat   +2 more
doaj   +1 more source

Stability-Indicating UPLC-PDA-QDa Methodology for Carvedilol and Felodipine in Fixed-Dose Combinations Using AQbD Principles

open access: yesScientia Pharmaceutica
The development of analytical procedures, in line with the recent regulatory requirements ICH Q2 (R2) and ICH Q14, is progressing, and it must be able to manage the entire life cycle of the methodology.
Jesús Alberto Afonso Urich   +6 more
doaj   +1 more source

AQbD-based development of a stability-indicating UHPLC-PDA-QDa method for triptorelin in parenteral formulations

open access: yesAnalytical Methods
A stability-indicating RP-UHPLC method was developed using AQbD principles for quantifying triptorelin in injectable suspensions as a pharmaceutical dosage form.
Jesús Alberto Afonso Urich   +3 more
openaire   +2 more sources

Development of eco-friendly and sustainable analytical methods for Ritonavir through white analytical chemistry and AQbD approach

open access: yesDiscover Chemistry
The present research study outlines the development and validation of a cost-effective, eco-sustainable, and robust analytical procedure for the quantitative estimation of Ritonavir in bulk and tablet dosage form using UV Spectrophotometry and Reverse ...
Vaibhav Sawale   +3 more
doaj   +1 more source

Advancing relugolix analysis: A comparative study and AQbD-driven method optimization with stability testing

open access: yesJournal of Applied Pharmaceutical Science
The current study aimed to develop a novel liquid chromatographic method based on analytical quality by design to analyze relugolix and its related substances. This study builds upon a comparative review of existing analytical methods, highlighting the absence of a pharmacopoeial standard for relugolix determination.
Priyanka Nagar   +5 more
openaire   +1 more source

AQBD BASED LC-UV METHOD FOR ASSESSMENT OF ANTIVIRAL DRUGS IN TERNARY MIXTURE

open access: yesRasayan Journal of Chemistry, 2021
J. R. Tulasi   +2 more
openaire   +1 more source

Development of Analytical Quality by Design Compliant Chaotropic Chromatography Method for Ziprasidone and Its Five Impurities Determination. [PDF]

open access: yesPharmaceuticals (Basel), 2023
Rmandić M   +6 more
europepmc   +1 more source

Design Approach in RP-HPLC Method Development and Validation of Nirogacestat in its Pure and Pharmaceutical Dosage Form [PDF]

open access: yes
Aim: Nirogacestat is a selective γ-secretase inhibitor approved by the USFDA for the treatment of Desmoid Tumour. Objective: In this study, a reversed-phase high performance liquid chromatography (RP-HPLC) method was designed to analyze the concentration
Chandrasekar R, Sivagami B, Roshini M, Kumanan R, Sudha S, Sai Koteswar Sharma
core   +1 more source

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