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Optimization and validation of a SPE-HPLC-PDA-fluorescence method for the simultaneous determination of drugs used in combined cardiovascular therapy in human plasma
Rapid Resolution RP-HPLC-DAD Method for Simultaneous Determination of Sildenafil, Vardenafil, and Tadalafil in Pharmaceutical Preparations and Counterfeit Drugs
Factorial Design Assisted Rp-Hplc Method for Sımultaneous Estimatıon of Luliconazole and Salicylic Acid: Analytical Quality by Design (AQbD) Approach in Method Development
Design and optimization of a reversed‐phase HPLC with diode array detection method for the determination of acemetacin and its toxic impurities using experimental design
Development and Validation of RP-UHPLC Method for Quantification of Gliclazide in Bulk and Pharmaceutical Dosage Form Using Quality-by-Design (QbD) Approach: A Shifting Paradigm
Response Surface Methodology Optimization of Mono-dispersed MgO Nanoparticles Fabricated by Ultrasonic-Assisted Sol–Gel Method for Outstanding Antimicrobial and Antibiofilm Activities
Box-Behnken Design–Directed Optimization of Wickerhamomyces anomalus–Mediated Biotransformation Process to Enhance the Flavonoid Profile of Polyherbal Extract
Physicochemical and morphological characterization of pharmaceutical nanocarriers and mathematical modeling of drug encapsulation/release mass transfer processes
Novel and sustainable valorization of biogenic waste into microbial protein based fish dietary ingredient in bioreactor: Process optimization and sustainable utilization
Integrative chemometric and intelligent modeling approaches for pollutant adsorption: Synergistic insights from experimental design, artificial intelligence (AI), and DFT applied to bisphenol A, β-naphthol, and eriochrome black
Propitious maneuvering for delivery of the phytopharmaceutical “apocynin” to induced fulminant hepatitis in BALB/c mice: In vitro and in vivo assessments
Catalytic performance of MgO /Fe2O3-SiO2 core-shell magnetic nanocatalyst for biodiesel production of Camelina sativa seed oil: Optimization by RSM-CCD method
The effect of binder concentration and dry mixing time on granules, tablet characteristics and content uniformity of low dose drug in high shear wet granulation
Optimizing derivatization conditions using an experimental design and simultaneous estimation of artemether and lumefantrine by ratio first order derivative spectrophotometric method
Quality-by-design driven analytical method (AQbD) development and validation of HPLC–UV technique to quantify rivastigmine hydrogen tartrate in lipidic nanocarriers: Forced degradation, and assessment of drug content and in vitro release studies
Analytical ‘Quality-by-Design’ paradigm in development of a RP-HPLC method for the estimation of cilnidipine in nanoformulations: Forced degradation studies and mathematical modelling of in-vitro release studies
Quality-by-Design-based development of an eco-friendly HPLC method for the estimation of nisoldipine in nanoformulations: Forced degradation studies and in-vitro release studies
Formulation, optimization and characterization of allantoin-loaded chitosan nanoparticles to alleviate ethanol-induced gastric ulcer: in-vitro and in-vivo studies
Development of RP-HPLC based analytical method for determination of cariprazine hydrochloride in bulk drug and pharmaceutical dosage form using box-behnken statistical design
Quantification and Validation of Stability-Indicating RP-HPLC Method for Efavirenz in Bulk and Tablet Dosage Form using Quality by Design (QbD): A Shifting Paradigm
Full Factorial Design for Development and Validation of a Stability-Indicating RP-HPLC Method for the Estimation of Timolol Maleate in Surfactant-Based Elastic Nano-Vesicular Systems
Development and Validation of Novel RP-HPLC Method for the Simultaneous Estimation of Capecitabine and Thymoquinone in the Biodegradable Nanoparticles using Full Factorial Design
Development and Validation of a Stability-Indicating RP-HPLC Method by a Statistical Optimization Process for the Quantification of Asenapine Maleate in Lipidic Nanoformulations
Development of an Analytical Quality by Design RP-HPLC Method and Its Validation for Estimation of Gefitinib From Bulk, Tablet Dosage Form, and Complex Nanoformulation
Effect of cross-linked enzyme aggregates in hierarchically mesocellular mesoporous magnetic silica preparation conditions towards enzyme activity retention
Combinação dose fixa de hidroclorotiazida (12,5 mg) e valsartana (160 mg): Desenvolvimento de metodologia de dissolução >i /i< e >i /i< para avaliar os perfis de dissolução dos produtos comercializados no Brasil e Peru
Development and validation of high-performance liquid chromatography method for the simultaneous monitoring of pantoprazole sodium sesquihydrate and domperidone maleate in plasma and its application to pharmacokinetic study
Quality by Design-driven Analytical Method: A Quality Risk Management-Based Liquid Chromatography Method for Daclatasvir and Characterization of its Putative Degradants by LC-MS/MS
An LC-MS/MS Method for Determination of Triple Drugs Combination of Valsartan, Amlodipine and Hydrochlorothiazide in Human Plasma for Bioequivalence Study
Retracted: Analytical Method Development and Validation for Determination of Assay of Antibacterial Drugs Besifloxacin Hydrochloride and Phenoxyethanol in Gel Formulation
An analytical “quality by design” approach in RP-HPLC method development and validation for reliable and rapid estimation of irinotecan in an injectable formulation
Formulation and investigation of crushed puffed rice-chitosan-HPMC based polymeric blends as carrier for sustained stomach specific drug delivery of piroxicam using 3(2) Taguchi mathematical design studies
Analytical quality by design-based LC-MS/MS method for the determination of Riociguat in its formulations
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