Efficient HPTLC-dual wavelength spectrodensitometric method for simultaneous determination of sofosbuvir and daclatasvir: Biological and pharmaceutical analysis

被引:21
作者
Abo-Zeid, Mohammad Nabil [1 ]
El-Gizawy, Samia M. [1 ]
Atia, Noha N. [1 ]
El-Shaboury, Salwa R. [1 ]
机构
[1] Assiut Univ, Fac Pharm, Dept Pharmaceut Analyt Chem, Assiut 71526, Egypt
关键词
Sofosbuvir; Daclatasvir; HPTLC-dual wavelength spectrodensitometry; Simultaneous determination; Real human plasma; Pharmaceutical formulations; UPLC-MS/MS METHOD; HUMAN PLASMA APPLICATION; CHRONIC HEPATITIS-C; ANTIVIRAL AGENTS; QUANTIFICATION; BIOEQUIVALENCE; VALIDATION; LEDIPASVIR; INFECTION;
D O I
10.1016/j.jpba.2018.04.049
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Sofosbuvir (SOF) and daclatasvir (DCS) are newly discovered anti-hepatitis C drugs that have direct antiviral activity. A novel and simple high-performance thin-layer chromatography (HPTLC) method was designed for simultaneous determination of SOF and DCS in miscellaneous matrices. The method adopts coupling HPTLC with dual wavelength spectrodensitometry. Consequently, this enabled sensitive, specific and cost-effective determination of the SOF-DCS mixture. The developed HPTLC procedure is based on a simple liquid-liquid extraction, enrichment of the analytes and subsequent chromatographic separation with UV detection. Separations were performed on HPTLC silica gel 60 F254 aluminum plates with a mobile phase consisting of ethyl acetate-isopropanol (85:15, v/v). Dual wavelength scanning was carried out in the absorbance mode at 265 and 311 nm for SOF and DCS, respectively. The linear ranges were 40-640 and 20-320 ng band(-1) for SOF and DCS, respectively with correlation coefficients of >= 0.9997. The detection limits were 11.3 and 6.5 ng band(-1) for SOF and DCS, respectively indicating high sensitivity of the proposed method. Consequently, this permits in vitro and in vivo application of the proposed method in human plasma with good percentage recovery (94.1-103.5%). Validation parameters were assessed according to ICH guidelines and US-FDA guidelines. Furthermore, the application was extended to analysis of SOF and DCS in their pharmaceutical formulations. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:358 / 365
页数:8
相关论文
共 21 条
[1]   Development and validation of LC-MS/MS method for simultaneous determination of sofosbuvir and daclatasvir in human Plasma: Application to pharmacokinetic study [J].
Abdallah, Ola M. ;
Abdel-Megied, Ahmed M. ;
Gouda, Amira S. .
BIOMEDICAL CHROMATOGRAPHY, 2018, 32 (06)
[2]   Ultrasensitive spectrofluorimetric method for rapid determination of daclatasvir and ledipasvir in human plasma and pharmaceutical formulations [J].
Abo-Zeid, Mohammad Nabil ;
Atia, Noha N. ;
El-Gizawy, M. ;
El-Shaboury, Salwa R. .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2018, 152 :155-164
[3]  
[Anonymous], 2001, GUID IND BIOAN METH
[4]  
[Anonymous], 2005, TOP Q2 R1 VAL AN PRO
[5]   A UHPLC-MS/MS method for the quantification of direct antiviral agents simeprevir, daclatasvir, ledipasvir, sofosbuvir/GS-331007, dasabuvir, ombitasvir and paritaprevir, together with ritonavir, in human plasma [J].
Ariaudo, Alessandra ;
Favata, Fabio ;
De Nicolo, Amedeo ;
Simiele, Marco ;
Paglietti, Luca ;
Boglione, Lucio ;
Cardellino, Chiara Simona ;
Carcieri, Chiara ;
Di Perri, Giovanni ;
D'Avolio, Antonio .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2016, 125 :369-375
[6]  
B.-M. S. Company, 2017, DAKLINZATM DACL TABL
[7]  
Chow JH., 2006, The Encyclopedia of Hepatitis and Other Liver Diseases
[8]   Impact of different sofosbuvir based treatment regimens on the biochemical profile of chronic hepatitis C genotype 4 patients [J].
Elsharkawy, Aisha ;
Eletreby, Rasha ;
Fouad, Rabab ;
Soliman, Zeinab ;
Abdallah, Mohamed ;
Negm, Mohamed ;
Mohey, Mohammad ;
Esmat, Gamal .
EXPERT REVIEW OF GASTROENTEROLOGY & HEPATOLOGY, 2017, 11 (08) :773-778
[9]  
European Medicines Agency, 2014, SOV SOF SUMM PROD CH
[10]  
Food and Drug Administration, 2003, GUID IND BIOAV BIOEQ