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DOI10.1016/j.jpba.2016.11.032
Development and validation of a simple and robust HPLC method with UV detection for quantification of the hepatitis C virus inhibitor daclatasvir in human plasma
Nannetti, Giulio1; Messa, Lorenzo1; Celegato, Marta1; Pagni, Silvana1,2; Basso, Monica1,2; Parisi, Saverio G.1,2; Palu, Giorgio1,2; Loregian, Arianna1,2
通讯作者Loregian, Arianna
来源期刊JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
ISSN0731-7085
EISSN1873-264X
出版年2017
卷号134页码:275-281
英文摘要

Daclatasvir is an inhibitor of hepatitis C virus NS5A protein that is used for the therapy of chronic hepatitis. So far, published methods for analysis of daclatasvir in plasma are exclusively based on mass spectrometry, which is not always available in standard clinical laboratories. Thus, we wished to develop and validate a simple, but still reliable and sensitive high-performance liquid chromatography (HPLC) assay with UV detection for the quantification of daclatasvir, feasible for a wide-spread clinical routine use. The method consisted of solid-phase extraction of daclatasvir using Waters Oasis HLB 1cc cartridges, reversed-phase liquid chromatography with a Waters XTerra RP18 (150 mm x 4.6 mm, 3.5 mu m) column and a mobile phase of ammonium acetate buffer (pH 5.0, 10 mM) and acetonitrile (56:44, v/v), and UV detection at 318 nm. This assay proved to be sensitive (lower limit of quantification of 0.05 mu g/mL), linear (correlation coefficients >= 0.997), specific (no interference with various potentially co-administrated drugs), reproducible (both intra-day and inter-day coefficients of variation <8.9%), and accurate (deviations ranged from -2.2 to 8.0% and from -6.5 to 9.2% for intra-day and inter-day assays, respectively). The method was applied to therapeutic monitoring of patients undergoing daclatasvir therapy for hepatitis C and showed to be reliable and robust. Thus, this method provides a simple, sensitive, precise, and reproducible assay for dosing daclatasvir that can be readily adaptable to routine use by clinical laboratories with standard equipment. In addition, the stability of daclatasvir in plasma was evaluated under various conditions, including after the heating procedure required for inactivation of infectious viruses and in different light exposure conditions. These studies evidenced photo-instability of the compound under sunlight exposure over time. Thus, blood sampling and the whole handling procedure have to be performed quickly and with minimal light exposure. (C) 2016 Elsevier B.V. All rights reserved.


英文关键词Daclatasvir BMS-790052 HCV NS5A inhibitor Solid-phase extraction HPLC-UV Therapeutic drug monitoring
类型Article
语种英语
国家Italy
收录类别SCI-E
WOS记录号WOS:000392909900035
WOS关键词REPLICATION COMPLEX INHIBITOR ; PERFORMANCE LIQUID-CHROMATOGRAPHY ; MASS-SPECTROMETRY METHOD ; QUANTITATIVE-DETERMINATION ; MS/MS METHOD ; BMS-790052 ; RIBAVIRIN ; HIV ; ANTIVIRALS ; ATAZANAVIR
WOS类目Chemistry, Analytical ; Pharmacology & Pharmacy
WOS研究方向Chemistry ; Pharmacology & Pharmacy
资源类型期刊论文
条目标识符http://119.78.100.177/qdio/handle/2XILL650/200722
作者单位1.Univ Padua, Dept Mol Med, Via Gabelli 63, I-35121 Padua, Italy;
2.Padua Univ Hosp, Clin Microbiol & Virol Unit, Padua, Italy
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Nannetti, Giulio,Messa, Lorenzo,Celegato, Marta,et al. Development and validation of a simple and robust HPLC method with UV detection for quantification of the hepatitis C virus inhibitor daclatasvir in human plasma[J],2017,134:275-281.
APA Nannetti, Giulio.,Messa, Lorenzo.,Celegato, Marta.,Pagni, Silvana.,Basso, Monica.,...&Loregian, Arianna.(2017).Development and validation of a simple and robust HPLC method with UV detection for quantification of the hepatitis C virus inhibitor daclatasvir in human plasma.JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,134,275-281.
MLA Nannetti, Giulio,et al."Development and validation of a simple and robust HPLC method with UV detection for quantification of the hepatitis C virus inhibitor daclatasvir in human plasma".JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS 134(2017):275-281.
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