Assay of caffeoylquinic acids in Baccharis trimera by reversed-phase liquid chromatography

Baccharis trimera commonly named 'carqueja', is wide-spread in South America and are used as raw material for herbal medicines. A reversed-phase liquid chromatography (RP-LC) method coupled to diode array detector was developed for the analysis of caffeoylquinic acids (CQAs), the main comp...

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Autor principal: Aboy, A.L
Otros Autores: Apel, M.A, Debenedetti, S., Francescato, L., Rosella, M.A, Henriques, A.T
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2012
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Acceso en línea:Registro en Scopus
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024 7 |2 scopus  |a 2-s2.0-84355161820 
024 7 |2 cas  |a alcohol, 64-17-5; water, 7732-18-5; Plant Extracts; Quinic Acid, 77-95-2; caffeoylquinic acid 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a JCRAE 
100 1 |a Aboy, A.L. 
245 1 0 |a Assay of caffeoylquinic acids in Baccharis trimera by reversed-phase liquid chromatography 
260 |c 2012 
270 1 0 |m Henriques, A.T.; Faculdade de Farmácia, UFRGS, Av. Ipiranga, 2752, CEP 90610-000, Porto Alegre, RS, Brazil; email: amelia@farmacia.ufrgs.br 
506 |2 openaire  |e Política editorial 
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504 |a Correa M.P, (1985), 1, p. 74. , Dicionário das plantas úteis do Brasil e das exóticas cultivadas, Rio de Janeiro, Imprensa Nacional, Instituto Brasileiro de Desenvolvimento Florestal; Soicke, H., Leng-Peschlow, E., (1987) Planta Med., 1, p. 37 
504 |a Zdero, C., Bohlmann, F., Solomon, J.C., King, R.M., Robinson, H., (1989) Phytochemistry, 28, p. 531 
504 |a Gene, R.M., Cartana, C., Adzet, T., Marin, E., Parellha, T., Canigueral, S., (1996) Planta Med., 62, p. 232 
504 |a Simões-Pires, C.A., Debenedetti, S., Spegazzini, E., Mentz, L.A., Matzenbacher, N.I., Limberger, R.P., Henriques, A.T., (2005) Plant Syst. Evol., 253, p. 23 
504 |a Simões-Pires, C.A., Queiroz, E.F., Henriques, A.T., Hostettmann, K., (2005) Phytochem. Anal., 16, p. 307 
504 |a Basnet, P., Matsushige, K., Hase, K., Kadota, S., Namba, T., (1996) Biol. Pharm. Bull., 19, p. 1479 
504 |a Azzini, E., Bugianesi, R., Romano, F., Di Venere, D., Miccadei, S., Durazzo, A., Foddai, M.S., Maiani, G., (2007) Br. J. Nutr., 97, p. 963 
504 |a Martino, V.S., Debenedetti, S.L., Coussio, J.D., (1979) Phytochemistry, 18, p. 2052 
504 |a Palacios, P.S., Wilson, E.G., Debenedetti, S.L., (1999) Dominguezia, 15, p. 39 
504 |a Clifford, M.N., Johnston, K.L., Knight, S., Kuhnert, N., (2003) J. Agric. Food Chem., 51, p. 2900 
504 |a Clifford, M.N., Knight, S., Kuhnert, N., (2005) J. Agric. Food Chem., 53, p. 3821 
504 |a International Conference on Harmonization (ICH) Validation of Analytical Procedures: Text and Methodology Q2(R1) (2005) International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, , www.ich.org, Available at (accessed 2011) 
504 |a (2003), 899 (29). , Agência Nacional de Vigilância Sanitária (ANVISA), Resolução RE n° de de maio de; Shabir, G.A., (2003) J. Chromatogr. A, 987, p. 57 
504 |a Clifford, M.N., Kirkpatrick, J., Kuhnert, N., Roozendaal, H., Salgado, P.R., (2008) Food Chem., 106, p. 379 
504 |a Jaiswal, R., Sovdat, T., Vivan, F., Kuhnert, N., (2010) J. Agric. Food Chem., 58, p. 5471 
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520 3 |a Baccharis trimera commonly named 'carqueja', is wide-spread in South America and are used as raw material for herbal medicines. A reversed-phase liquid chromatography (RP-LC) method coupled to diode array detector was developed for the analysis of caffeoylquinic acids (CQAs), the main compounds responsible for its digestive activity. The identity of the quinic acids was established by mass spectrometry and were them: 5-O-[E]-caffeoylquinic acid, 3,4-O-[E]-dicaffeoylquinic acid, 3,5-O-[E]-dicaffeoylquinic acid, 4,5-O-[E]-dicaffeoylquinic acid and a tricaffeoylquinic acid. The RP-LC method for the quantitation of the caffeoylquinic acids was validated according to ICH guidelines, based on the following parameters: linearity, selectivity, robustness, limits of detection and quantification, precision and recovery. Hydroalcoholic extracts were prepared by the maceration of the plant material with ethanol:water 1:1 (v/v) in a 0.1:25gmL -1 plant:solvent ratio in a water bath at 40°C. Validation data indicated that the HPLC method proposed is suitable for the analysis of caffeoylquinic acids in B. trimera raw material. The results of the LOD and LOQ analyses for the 5-CQA were 4.1μgmL -1 and 12.5μgmL -1, respectively, 1.3μgmL -1, 3.9μgmL -1 for 4,5-diCQA and 1.7μgmL -1, 5.1μgmL -1 for triCQA. The levels of total CQAs ranged from 2.1 to 4.0g% (w/w). The influence of season harvest and site collection was also evaluated and variations were observed in the results and can be related to phonologic phase, different locations, seasons and soil. Long term and photostability of plant material were carried out and was observed a stable behavior during the time of the experiments. © 2011 Elsevier B.V.  |l eng 
536 |a Detalles de la financiación: Conselho Nacional de Desenvolvimento Científico e Tecnológico, CNPq 
536 |a Detalles de la financiación: This work was supported by CNPq . Appendix A 
593 |a Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil 
593 |a Cátedra de Farmacognosia Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina 
593 |a Facultad de Ciencias Exactas y Naturales, Universidad de Belgrano, Capital Federal, Ciudad Autónoma de Buenos Aires, Argentina 
690 1 0 |a BACCHARIS TRIMERA 
690 1 0 |a CAFFEOYLQUINIC ACIDS 
690 1 0 |a DICAFFEOYLQUINIC ACIDS 
690 1 0 |a PHOTOSTABILITY 
690 1 0 |a RP-LC 
690 1 0 |a TRICAFFEOYLQUINIC ACIDS 
690 1 0 |a BACCHARIS TRIMERA 
690 1 0 |a CAFFEOYLQUINIC ACIDS 
690 1 0 |a DIODE ARRAY DETECTORS 
690 1 0 |a HERBAL MEDICINES 
690 1 0 |a HPLC METHOD 
690 1 0 |a LIMITS OF DETECTION 
690 1 0 |a PHOTO-STABILITY 
690 1 0 |a PLANT MATERIAL 
690 1 0 |a QUINIC ACIDS 
690 1 0 |a REVERSED-PHASE LIQUID CHROMATOGRAPHY 
690 1 0 |a RP-LC 
690 1 0 |a VALIDATION DATA 
690 1 0 |a WATER BATHS 
690 1 0 |a ETHANOL 
690 1 0 |a LIQUIDS 
690 1 0 |a MASS SPECTROMETRY 
690 1 0 |a ORGANIC SOLVENTS 
690 1 0 |a PLANT EXTRACTS 
690 1 0 |a LIQUID CHROMATOGRAPHY 
690 1 0 |a 3,4 O DICAFFEOYLQUINIC ACID 
690 1 0 |a 3,5 O DICAFFEOYLQUINIC ACID 
690 1 0 |a 4,5 O DICAFFEOYLQUINIC ACID 
690 1 0 |a 5 O CAFFEOYLQUINIC ACID 
690 1 0 |a ALCOHOL 
690 1 0 |a CAFFEOYLQUINIC ACID DERIVATIVE 
690 1 0 |a PLANT EXTRACT 
690 1 0 |a PLANT MEDICINAL PRODUCT 
690 1 0 |a TRICAFFEOYLQUINIC ACID 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a WATER 
690 1 0 |a ACCURACY 
690 1 0 |a ARTICLE 
690 1 0 |a BACCHARIS 
690 1 0 |a BACCHARIS TRIMERA 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DEVICES 
690 1 0 |a DIODE ARRAY DETECTOR 
690 1 0 |a LIMIT OF DETECTION 
690 1 0 |a LIMIT OF QUANTITATION 
690 1 0 |a LINEAR SYSTEM 
690 1 0 |a MASS SPECTROMETRY 
690 1 0 |a NONHUMAN 
690 1 0 |a PHYSICAL PARAMETERS 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a REVERSED PHASE LIQUID CHROMATOGRAPHY 
690 1 0 |a SEASONAL VARIATION 
690 1 0 |a SOIL 
690 1 0 |a VALIDATION STUDY 
690 1 0 |a BACCHARIS 
690 1 0 |a BRAZIL 
690 1 0 |a CHROMATOGRAPHY, HIGH PRESSURE LIQUID 
690 1 0 |a CHROMATOGRAPHY, REVERSE-PHASE 
690 1 0 |a DRUG STABILITY 
690 1 0 |a LIMIT OF DETECTION 
690 1 0 |a PHOTOCHEMICAL PROCESSES 
690 1 0 |a PLANT EXTRACTS 
690 1 0 |a QUINIC ACID 
690 1 0 |a REPRODUCIBILITY OF RESULTS 
690 1 0 |a TANDEM MASS SPECTROMETRY 
690 1 0 |a BACCHARIS TRIMERA 
651 4 |a SOUTH AMERICA 
651 4 |a ARGENTINA 
700 1 |a Apel, M.A. 
700 1 |a Debenedetti, S. 
700 1 |a Francescato, L. 
700 1 |a Rosella, M.A. 
700 1 |a Henriques, A.T. 
773 0 |d 2012  |g v. 1219  |h pp. 147-153  |p J. Chromatogr. A  |x 00219673  |w (AR-BaUEN)CENRE-1093  |t Journal of Chromatography A 
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856 4 0 |u https://doi.org/10.1016/j.chroma.2011.11.042  |y DOI 
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