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      Analysis of amide compounds in different parts of Piper ovatum Vahl by high-performance liquid chromatographic

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          Abstract

          Background:

          Piper ovatum (Piperaceae) has been used in traditional medicine for the treatment of inflammations and as an analgesic. Previous studies have showed important biological activities of the extracts and amides from P. ovatum leaves.

          Objective:

          In this study, a high-performance liquid chromatographic (HPLC) method was developed and validated for quantitative determination of the amides in different parts of Piper ovatum.

          Materials and Methods:

          The analysis was carried out on a Metasil ODS column (150 × 4.6 mm, 5μm) at room temperature. HPLC conditions were as follows: acetonitrile (A), and water (B), 1.0% acetic acid. The gradient elution used was 0–30 min, 0-60% A; 30–40 min, 60% A. Flow rate used was 1.0mL/min, and detection at 280nm.

          Results:

          The validation using piperlonguminine, as the standard, demonstrated that the method shows linearity (linear correlation coefficient = 0.998), precision (relative standard deviation <5%) and accuracy (mean recovery = 103.78%) in the concentration range 31.25 – 500μg/mL. The limit of detection and quantification were 1.21 and 4.03μg/mL, respectively. This method allowed the identification and quantification of piperlonguminine and piperovatine in the hydroethanolic extracts of P. ovatum obtained from the leaves, stems and roots. All the extracts showed the same chromatographic profile. The leaves and roots contained the highest concentrations of piperlonguminine and the stems and leaves showed the most concentrations of piperovatine.

          Conclusion:

          This HPLC method is suitable for routine quantitative analysis of amides in extracts of Piper ovatum and phytopharmaceuticals containing this herb.

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          Most cited references26

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          Dicionário das plantas úteis do Brasil e das exóticas cultivada

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            Dicionário das plantas úteis do Brasil e das tóxicas cultivadas

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              Validation in pharmaceutical analysis. Part I: an integrated approach.

              The ICH guidelines achieved a great deal in harmonising the definitions of the required validation characteristics and their basic requirements. However, they provide only a basis for a general discussion of the validation parameters, their calculation and interpretation. It is the responsibility of the analyst to identify parameters which are relevant to the performance of the given analytical procedure as well as to design proper validation protocols including acceptance criteria and to perform an appropriate evaluation. In order to fulfil this responsibility properly, the background of the validation parameters and their consequences must be understood. In this part, the general concept of an integrated validation is discussed. The interdependencies to other ICH guidelines and topics during drug development (e.g. impurities and degradants, stability and specification design) must be taken into account to define the required acceptance criteria. Evaluation of the results in order to prove the suitability of the analytical procedure must be based on the specification limits. Important parameters and aspects are discussed for the individual validation characteristics. In the following parts, these parameters will be discussed in detail. Examples will be given for their interpretation in order to facilitate the selection of parameters which are relevant to the performance and suitability of the given analytical procedure.
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                Author and article information

                Journal
                Pharmacognosy Res
                Pharmacognosy Res
                PR
                Pharmacognosy Research
                Medknow Publications & Media Pvt Ltd (India )
                0976-4836
                0974-8490
                Oct-Dec 2013
                : 5
                : 4
                : 254-259
                Affiliations
                [1] Graduate Program in Pharmaceutical Sciences, State University of Maringa, Parana, Brazil
                [1 ] Department of Chemical Engineering, State University of Maringa, Parana, Brazil
                [2 ] Department of Pharmacy, State University of Maringa, Parana, Brazil
                [3 ] CESUMAR, Paraná, Brazil
                Author notes
                Address for correspondence: Prof. Dr. Diógenes Aparício Garcia Cortez, Universidade Estadual de Maringá, Av. Colombo, 5790, Campus Universitário, 87020-900 Maringá-PR, Brazil. E-mail: dagcortez@ 123456uem.br
                Article
                PR-5-254
                10.4103/0974-8490.118812
                3807989
                24174818
                e3f177a7-ef83-44a8-9950-7a52c7da70d3
                Copyright: © Pharmacognosy Research

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 04 December 2012
                : 07 February 2013
                : 24 September 2013
                Categories
                Original Article

                Pharmacology & Pharmaceutical medicine
                high-performance liquid chromatographic,piper ovatum,piperlonguminine,piperovatine,validation

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