Development and validation of a RP-HPLC method for determination of citicoline monosodium in human plasma

A sensitive and specific high performance reversed phase liquid chromatographic method was developed for quantification of citicoline monosodium (CTM) in human plasma. The active drug was isocratically eluted at a flow rate of 1 ml/min at ambient temperature in a nucleosil C18 analytical column with...

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Autores principales: Bindaiya, Shailendra K., Sahu, Kapendra, Bhaisare, Mukesh, Karthikeyan, Chandrabose, Moorthy, N.S.H.N., Mehta, Farhad F., Trivedi, Piyush
Formato: Articulo Comunicacion
Lenguaje:Inglés
Publicado: 2011
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8217
http://www.latamjpharm.org/resumenes/30/4/LAJOP_30_4_2_4.pdf
Aporte de:
id I19-R120-10915-8217
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
Plasma
Cromatografía líquida
human plasma; HPLC; validation; citicoline monosodium
Agentes del Sistema Nervioso Central
spellingShingle Farmacia
Plasma
Cromatografía líquida
human plasma; HPLC; validation; citicoline monosodium
Agentes del Sistema Nervioso Central
Bindaiya, Shailendra K.
Sahu, Kapendra
Bhaisare, Mukesh
Karthikeyan, Chandrabose
Moorthy, N.S.H.N.
Mehta, Farhad F.
Trivedi, Piyush
Development and validation of a RP-HPLC method for determination of citicoline monosodium in human plasma
topic_facet Farmacia
Plasma
Cromatografía líquida
human plasma; HPLC; validation; citicoline monosodium
Agentes del Sistema Nervioso Central
description A sensitive and specific high performance reversed phase liquid chromatographic method was developed for quantification of citicoline monosodium (CTM) in human plasma. The active drug was isocratically eluted at a flow rate of 1 ml/min at ambient temperature in a nucleosil C18 analytical column with a mobile phase composed of tetrabutyl ammonium hydro gen sulfate buffer (0.005 M, pH5.0): methanol (95:05, v/v). Photodiode array (PDA) was performed at 270 nm and the retention time of the drug was found to be 6.64 min. The lowest limit of quantification (LLOQ) and of detection (LOD) were found to be 30 and 10 ng/ml, respectively. The method was validated and the response was found to be linear in the drug (CTM in spiked plasma) concentration range 150-900 ng/ml. The method was found to be accurate, with ranging from 96.38 to 98.65 % and precise, with intra-day, inter-day as well as analyst-toanalyst precision. The total recoveries of the method ranged between 95.69 and 97.89 %. Stability data revealed that the drug is stable in human plasma under various test conditions and the method can be successfully used for analysis of CTM in human plasma and in pharmacokinetic studies.
format Articulo
Comunicacion
author Bindaiya, Shailendra K.
Sahu, Kapendra
Bhaisare, Mukesh
Karthikeyan, Chandrabose
Moorthy, N.S.H.N.
Mehta, Farhad F.
Trivedi, Piyush
author_facet Bindaiya, Shailendra K.
Sahu, Kapendra
Bhaisare, Mukesh
Karthikeyan, Chandrabose
Moorthy, N.S.H.N.
Mehta, Farhad F.
Trivedi, Piyush
author_sort Bindaiya, Shailendra K.
title Development and validation of a RP-HPLC method for determination of citicoline monosodium in human plasma
title_short Development and validation of a RP-HPLC method for determination of citicoline monosodium in human plasma
title_full Development and validation of a RP-HPLC method for determination of citicoline monosodium in human plasma
title_fullStr Development and validation of a RP-HPLC method for determination of citicoline monosodium in human plasma
title_full_unstemmed Development and validation of a RP-HPLC method for determination of citicoline monosodium in human plasma
title_sort development and validation of a rp-hplc method for determination of citicoline monosodium in human plasma
publishDate 2011
url http://sedici.unlp.edu.ar/handle/10915/8217
http://www.latamjpharm.org/resumenes/30/4/LAJOP_30_4_2_4.pdf
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