Cover Image

Validated stability-indicating RP-HPLC assay method for fesoterodine fumarate in pharmaceutical products

The goal of the current study was to develop a precise, sensitive and validated reverse phase HPLC method for determination of fesoterodine fumarate (FST). The current investigation was performed for a stability indicating method in order to obtain both assay and impurity profiles of FST. All the ex...

Full description

Saved in:

Bibliographic Details
Main Authors:	Onur PINARBASLI (Author), Tolga OZBAY (Author), Gulistan Pelin GURBETOGLU (Author), Nagehan SARRACOGLU (Author), Asuman DOGANAY (Author)
Format:	Book
Published:	Polskie Towarzystwo Farmaceutyczne, 2023-05-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

RP-HPLC method development and validation for bedaquiline fumarate to evaluate its forced degradation behaviour and stability in official dissolution media
by: Vishwas Pardhi, et al.
Published: (2020)

Physicochemical properties and drug-release mechanisms of dual-release bilayer tablet containing mirabegron and fesoterodine fumarate
by: Lee HG, et al.
Published: (2019)

Development and validation of stability indicating RP-HPLC method for simultaneous estimation of Ibuprofen and Carisoprodol in Pharmaceutical formulation
by: A Lakshmana Rao, et al.
Published: (2019)

Stability indicating RP-HPLC method development and validation of cefepime and amikacin in pure and pharmaceutical dosage forms
by: Lella Kalyani, et al.
Published: (2018)

Stability-indicating RP-HPLC method development and validation for estimation of Mupirocin calcium in bulk and in pharmaceutical formulation
by: Durgeshwari J. Kalal, et al.
Published: (2022)

Development and validation of RP-HPLC assay of chlorhexidine in gingival crevicular fluid
by: Bogdanovska Liljana, et al.
Published: (2014)

Monolithic LC method applied to fesoterodine fumarate low dose extended-release tablets: Dissolution and release kinetics
by: Maximiliano S. Sangoi, et al.
Published: (2015)

Simultaneous RP-HPLC determination of sparfloxacin and dexamethasone in pharmaceutical formulations
by: Syed Naeem Razzaq, et al.
Published: (2013)

Development and validation of a stability-indicating RP-HPLC method for estimation of Lefamulin in pure and pharmaceutical drug products
by: Muhammad Usman, et al.
Published: (2023)

Concurrent estimation of lamivudine, tenofovir disoproxil fumarate, and efavirenz in blended mixture and triple combination tablet formulation by a new stability indicating RP-HPLC method
by: Ramreddy Godela, et al.
Published: (2021)

Development and Validation of a Stability-Indicating RP-HPLC Method for Rapid Determination of Doxycycline in Pharmaceutical Bulk and Dosage Forms
by: Shabnam Pourmoslemi, Soroush Mirfakhraee, Saeid Yaripour, Ali Mohammadi
Published: (2016)

Development And Validation Of Stability Indicating RP-HPLC Method For Determination Of Ceritinib
by: Vaibhav Suresh Adhao, et al.
Published: (2017)

A new stability indicating RP-UPLC method for simultaneous estimation of Doravirine, Lamivudine and Tenofovir disoproxil fumarate in bulk and their combined pharmaceutical formulation
by: Swetha Addanki, et al.
Published: (2021)

A new validated stability-indicating RP-HPLC method for simultaneous quantification of dolutegravir and lamivudine in bulk and pharmaceutical dosage form
by: Khaleel Noorbasha, et al.
Published: (2020)

RP-HPLC method development and validation for estimation of rivaroxaban in pharmaceutical dosage forms
by: Mustafa Çelebier, et al.
Published: (2013)

Validation of Novel RP-HPLC Method for the Estimation of Naloxegol in Pharmaceutical Dosage Forms
by: A Suneetha, et al.
Published: (2021)

Development and validation of a stability indicating RP-HPLC method for the determination of Rufinamide
by: B. Sai Pavan Kumar, et al.
Published: (2013)

Stability-indicating RP-HPLC method for determination of beclomethasone dipropionate in nanocapsule suspensions
by: Janaíne Micheli Chassot, et al.
Published: (2015)

Stability indicating RP-HPLC method for estimation of cariprazine hydrochloride in human plasma
by: Mohini Shelke, et al.
Published: (2024)

A novel stability-indicating method for determination of a new antidepressant effect of vortioxetine in a pharmaceutical formulation by using RP-HPLC
by: Gizem Tiris, et al.
Published: (2020)

Optimization and validation of an RP-HPLC method for the estimation of 6-mercaptopurine in bulk and pharmaceutical formulations
by: Vanita Somasekhar
Published: (2014)

Chromatographic Quantification of Ivermectin and Pranziquantel in the Tablets Using Stability Indicating RP-HPLC Method
by: Naga Venkata Suresh Kumar Devaka, et al.
Published: (2019)

Stability indicating RP-HPLC method for simultaneous determination of gatifloxacin and dexamethasone in binary combination
by: Syed Naeem Razzaq, et al.
Published: (2017)

Method development and validation for multi-component analysis of lamivudine & tenofovir disoproxil fumarate in bulk drug by UV-visible spectrophotometer & RP-HPLC
by: Shweta Sharma, et al.
Published: (2020)

Fesoterodine for the treatment of urinary incontinence and overactive bladder
by: Pamela Ellsworth
Published: (2009)

Development and validation of RP HPLC method for determination of metformin and sitagliptin in bulk and pharmaceutical dosage form
by: Kavitha D., et al.
Published: (2017)

Development of RP-HPLC method for simultaneous determination of docetaxel and curcumin in rat plasma: Validation and stability
by: Dong Wuk Kim, et al.
Published: (2017)

Development and validation of a stability-indicating RP-HPLC method for estimation of atazanavir sulfate in bulk
by: S. Dey, et al.
Published: (2017)

Development and validation of a new and economical stability indicating RP-HPLC method for cefixime trihydrate
by: Ceema Mathew, et al.

New stability indicating RP-HPLC-PDA method for determination of mifepristone in bulk and tablet formulation
by: Mohammad Mojeeb Gulzar Khan, et al.
Published: (2021)

A novel RP - HPLC methodology for method development and validation of aceclofenac and tizanidine pharmaceutical dosage forms
by: Adilakshmi Nenavath, et al.
Published: (2020)

Sensitive and selective method for the analysis of menthol from pharmaceutical products by RP-HPLC with refractive index detector
by: K A Shaikh, et al.
Published: (2010)

Method development and validation of aspirin and clopidogrel pharmaceutical dosage forms by developing new RP HPLC method
by: Nellore Dharani Sai Sreekanth, et al.
Published: (2020)

Development and Validation of an RP-HPLC-PDA Method for Determination of Paracetamol, Caffeine and Tramadol Hydrochloride in Pharmaceutical Formulations
by: Fernando J. Pereira, et al.
Published: (2021)

Development and validation of RP HPLC method for the estimation of Sofosbuvir and related impurity in bulk and pharmaceutical dosage form
by: Shiny Ganji, et al.
Published: (2021)

Development and validation of a stability-indicating RP-HPLC method for determination of aripiprazole and its degradation products
by: Mijatović Vesna, et al.
Published: (2023)

Design of experiment-driven stability-indicating RP-HPLC method for the determination of tofacitinib in nanoparticles and skin matrix
by: Srividya Gorantla, et al.
Published: (2021)

Development and validation of RP-HPLC method for stability evaluation of model hydrazone, containing a pyrrole ring
by: Diana Tzankova, et al.
Published: (2019)

Stability-indicating RP-HPLC method for simultaneous estimation of levosalbutamol sulfate and theophylline in combined dosage form
by: Sagar Suman Panda, et al.
Published: (2013)

Chemometric Classification of Cocoa Bean Shells Based on Their Polyphenolic Profile Determined by RP-HPLC-PDA Analysis and Spectrophotometric Assays
by: Olga Rojo-Poveda, et al.
Published: (2021)