An analytical “quality by design” approach in RP-HPLC method development and validation for reliable and rapid estimation of irinotecan in an injectable formulation

N Ajitkumar Bhaskaran, L Kumar, MS Reddy… - Acta …, 2021 - hrcak.srce.hr
Sažetak The objective of the present study was to develop a robust, simple, economical and
sensitive HPLC-UV method using the “quality-by-design” approach for the estimation of …

Validated reverse phase HPLC method for the determination of irinotecan in pharmaceutical dosage forms

M Balaram V, V Rao J, RSS Ganesh G… - Journal of …, 2007 - Wiley Online Library
A simple and rapid reverse phase high performance liquid chromatography (RP‐HPLC)
method was developed and validated for quantitative determination of irinotecan in bulk …

Determination of irinotecan and its metabolite SN-38 in dried blood spots using high-performance liquid-chromatography with fluorescence detection

RZ Hahn, PC Arnhold, NB Andriguetti… - … of Pharmaceutical and …, 2018 - Elsevier
Irinotecan (IRI) is an antineoplastic drug widely used for the treatment of colorectal and
advanced pancreatic cancer. Despite its clinical utility, the clinical use of IRI is associated …

Development and validation of a High-Performance Liquid Chromatography–Tandem Mass Spectrometry method for the simultaneous determination of irinotecan and …

E Marangon, B Posocco, E Mazzega, G Toffoli - PLoS One, 2015 - journals.plos.org
Irinotecan is currently used in several cancer regimens mainly in colorectal cancer (CRC).
This drug has a narrow therapeutic range and treatment can lead to side effects, mainly …

Development and validation of reversed phase liquid chromatographic method utilizing ultraviolet detection for quantification of irinotecan (CPT-11) and its active …

T Bansal, A Awasthi, M Jaggi, RK Khar, S Talegaonkar - Talanta, 2008 - Elsevier
A new, simple, sensitive and specific reversed-phase high performance liquid
chromatographic (HPLC) method using ultraviolet detection was developed and validated …

Fast liquid chromatography-tandem mass spectrometry method for routine assessment of irinotecan metabolic phenotype

G Corona, C Elia, B Casetta… - Therapeutic drug …, 2010 - journals.lww.com
Abstract Irinotecan (CPT-11) is an anticancer drug with a complex in vivo metabolism widely
used in the treatment of colon cancer. The assessment of the CPT-11 metabolic phenotype …

Sensitive HPLC-fluorescence method for irinotecan and four major metabolites in human plasma and saliva: application to pharmacokinetic studies

S Poujol, F Pinguet, F Malosse, C Astre… - Clinical …, 2003 - academic.oup.com
Background: We developed gradient HPLC methods for quantification of the antimitotic drug
irinotecan (CPT-11) and its four metabolites, SN-38, SN-38 G, 7-ethyl-10-[4-N-(5 …

Limited sampling models for simultaneous estimation of the pharmacokinetics of irinotecan and its active metabolite SN-38

GG Chabot - Cancer chemotherapy and pharmacology, 1995 - Springer
Abstract Irinotecan (CPT-11) is a novel topoisomerase I inhibitor with clinical activity in
human malignancies. The objective of this study was to develop efficient limited sampling …

Development and validation of an UPLC–MS/MS method for the quantification of irinotecan, SN-38 and SN-38 glucuronide in plasma, urine, feces, liver and kidney …

S Basu, M Zeng, T Yin, S Gao, M Hu - Journal of Chromatography B, 2016 - Elsevier
The objective of this research is to develop and validate a sensitive and reproducible UPLC–
MS/MS method to quantify irinotecan, its active metabolite SN-38 and SN-38 glucuronide …

Clinical pharmacokinetics of irinotecan and its metabolites in relation with diarrhea

R Xie, RHJ Mathijssen, A Sparreboom… - Clinical …, 2002 - Wiley Online Library
Objectives Our objective was to build population pharmacokinetic models that describe
plasma concentrations of irinotecan (CPT‐11) and its metabolites 7‐ethyl‐10 …