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Revista Brasileira de Ciências Farmacêuticas

Print version ISSN 1516-9332

Rev. Bras. Cienc. Farm. vol.44 no.3 São Paulo July/Sept. 2008

http://dx.doi.org/10.1590/S1516-93322008000300008 

ORIGINAL PAPERS

 

Analysis of the essential oils from Calendula officinalis growing in Brazil using three different extraction procedures

 

Análise por CG-EM do óleo essencial de Calendula officinalis cultivado no Brasil utilizando-se três diferentes processos de extração

 

 

Zilda Cristina GazimI; Claudia Moraes RezendeII; Sandra Regina FragaII; Benedito Prado Dias FilhoIII; Celso Vataru NakamuraIII; Diógenes Aparicio Garcia CortezIII, *

IDepartamento de Farmácia, Universidade Paranaense
IIInstituto de Química Universidade Federal do Rio de Janeiro
IIIDepartamento de Farmácia e Farmacologia, Universidade Estadual de Maringá

 

 


ABSTRACT

Terpenes and aroma volatiles from flowers of Calendula officinalis cultivated in southeastern Brazil were obtained by steam distillation (SD), headspace-cold finger (HS-CF) extraction and headspace solid-phase microextraction (HS-SPME) coupled with gas chromatography and mass spectrometric analysis. The dried flowers contained 0.1% oil. Kovats indices and mass spectra were used to identify 27 individual components in the various volatile fractions. The main components present in the volatile fractions of the C. officinalis flowers, obtained by SD, HS-SPME, and HS-CF, were δ-cadinene (22.5, 22.1, and 18.4 %) and γ-cadinene (8.9, 25.4, and 24.9 %) while 20.4 % of α-cadinol was seen only after SD extraction.

Uniterms: Calendula officinalis L; Gas chromatography-mass spectroscopy; Steam distillation; Headspace solid-phase microextraction; Headspace-cold finger


RESUMO

Terpenos e aromas voláteis das flores de Calendula officinalis cultivados no sudoeste do Brasil foram isolados por arraste a vapor (SD), dedo frio (HS-CF) e micro extração em fase sólida (HS-SPME) acoplada à espectrometria de massas. As flores secas da C. officinalis contêm 0,1% de óleo essencial e foram identificadas 27 substâncias químicas através do cálculo do índice de Kováts e interpretação dos espectros de massas. As substâncias majoritárias presentes no óleo essencial das flores de C. officinalis, obtido por SD, HS-SPME e HS-CF foram δ-cadinene (22,5; 22,1 e 18,4 %) γ-cadinene (8,9, 25,4 e 24,9 %) e 20.4 % de α-cadinol foi observado apenas na extração por arraste a vapor.

Unitermos: Calendula officinalis L. Cromatografia a gás acoplada a espectrometria de massas. Destilação por arraste a vapor. Dedo frio "cold finger". Microextração em fase sólida.


 

 

INTRODUCTION

Calendula officinalis (Asteraceae) is an annual herb with yellow to orange flowers, native to Mediterranean region. It is also known as pot marigold, a name historically associated with its use in soups and stews to combat illnesses (Ramos et al., 1988). Nowadays, C. officinalis is approved for food use in U.S.A. and appears in the Food and Drug Administration's list of GRAS (Generally Recognized as Safe) substances. Because of its long history of safety as a medicine for the treatment of inflammations and skin wounds (Della Loggia et al., 1994), a number of reports describe its use for innumerable ailments. As a bonus, the beautiful calendula flowers are frequently seen and easily grown in home gardens all over the world (Ramos et al., 1988).

Sesquiterpene glycosides, saponins, xanthophylls, triol triterpenes, flavonoids, and volatiles are observed in its composition. Chalchat et al. (1991) studied the essential oil of C. officinalis flowers cultivated in the Massif Central, France, and obtained sesquiterpene alcohol and, mainly, α-cadinol using steam distillation. Radulescu et al. (2000) analyzed flowers from Romania by headspace and steam distillation, where δ-cadinene plus 1,3,5-cadinatriene and α-muurolol were found as major compounds.

Because of the economic value of C. officinalis as an herbal medicine and its use in cosmetics, perfumery, pharmaceutical preparations, and food, we decided to study the composition of essential oil of C. officinalis growing in southeastern Brazil. Three different extraction techniques were used to investigate the volatiles, including steam distillation (SD), headspace solid-phase micro extraction (HS-SPME), and headspace-cold finger (HS-CF) extraction, in association with gas chromatography-mass spectrometry (GC-MS and GC-FID).

 

MATERIAL AND METHODS

Experimental

Plant material

The flowers of Calendula officinalis were collected from an experimental plot in the medicinal botanical garden of the Universidade Paranaense in Umuarama, Brazil, at S23º 46.225' and W53º 16.730', and an altitude of 391 m. A voucher specimen, 1311, was deposited at the educational herbarium of the Universidade Paranaense (HEUP). Seeds were planted on 30 April 2004 (during autumn), and collection began on 20 July (winter), three months after planting.

The flowers were dried on mats in the shade and at room temperature, spread into thin layers that were not mixed over the 10-day drying period. After this interval, water loss by both drying and desiccation, according to techniques described in the pharmacopoeia, was determined (Farmacopéia Brasileira, 1988).

Three samples each were used for extraction by steam distillation, HS-SPME, and HS-C, respectively.

Instrumentation

  • GC-MS

Oil qualitative analyses and volatile fractions were carried out using an Agilent 6890 Series II gas chromatograph (Palo Alto, U.S.A.) coupled to an Agilent 5973 quadrupole mass spectrometer with electron ionization mode (EI) generated at 70 eV (ion source at 230 ºC and transfer line at 280 ºC). The GC was performed using a J&W DB-5 (5% diphenyl- 95% dimethyl silicone) capillary column (30 m x 0.25 mm i.d. x 0.25 µm film), and helium was used as a carrier gas (1 mL min-1). The initial temperature was programmed from 35 ºC to 60 ºC (at 1 ºC min-1), to 170 ºC (3 ºC min-1), to 200 ºC (8 ºC min-1), and to 280 ºC (15 ºC min-1), and maintained at 280 ºC for 5 min. The injector port (splitless mode, 0.5 min) was at 250 ºC. Retention indexes were calculated with reference to n-alkanes. All compounds were identified by comparison of both the mass spectra (Wiley 275 library) and the retention index data found in the literature (Adams, 1995).

  • GC-FID

The qualitative analyses of essential oil from C. officinalis flowers was carried out using an Agilent 5890 Series II gas chromatograph coupled to an Agilent 3396A integrator equipped with a HP-1 capillary column (12 m X 0.20 mm I.D., 0.33 µm film thickness). Hydrogen was used as the carrier gas (1 mL min-1). Chromatographic conditions were identical to those used for GC-MS.

  • Steam distillation (SD)

Plant material (150 g C. officinalis flowers) was hydrodistilled in a Clevenger-type apparatus for 3 h. The oil layers obtained were dried over anhydrous Na2SO4. The yields (0.1% w/w) were averaged over three experiments, and calculated on the basis of the dry weight of the material. For CG studies, 47 mg of oil dissolved in 1.5 ml of dichloromethane and 1 ml of solution was injected into the GC-MS and the GC-FID spectrometer.

  • Headspace solid-phase microextraction (HS-SPME)

The floral scent of C. officinalis was trapped on a 100 mm polydimethylsiloxane HS-SPME (PDMS) fiber from flower powder (Lee et al., 1988; Jirovets et al., 2002; Kin et al., 2002). 22 g of finely powdered C. officinalis flowers was placed in a 250 ml Erlenmeyer flask at 20 ºC and equilibrated for 30 min. Next, the SPME fiber was exposed to this atmosphere for 30 min, and then removed and placed in the GC injector for 5 min at 250 ºC.

  • Headspace-cold finger (HS-CF) extraction

3620 g of finely powdered C. officinalis flowers was placed in a 4000 ml Erlenmeyer flask, which was then closed with a cold finger containing dry ice (Acree and Teranishi 1993). During a 16-hour period at 20 ºC, the cold finger was removed every 10 minutes, and the material deposited on the cold glass surface was scraped and washed with 2 mL of dichloromethane (spectroscopic quality) into a beaker. The material was dried with anhydrous Na2SO4 and concentrated at 40 ºC in a distillation unit with a Claisen head, and cold-finger-cooled to 3 ºC to a final volume of 10 ml. A volume of 2 ml were injects in HRGC-MS (Rezende et al., 1999; Rezende et al., 2004).

 

RESULTS AND DISCUSSION

The yield of oil was determined from dried flowers, in agreement with the methods described in the Farmacopéia Brasileira (1988), in order to provide information useful in future production of a phytomedicine.

The yield found in the literature for the essential oil of Calendula officinalis is 0.3% (Chalchat et al., 1991) and 0.2% (PDR, 2000). The present experiment yielded an average of 0.1% in each oil extraction. In the experiment by Chalchat et al. (1991), calendula cultures from the region of the Massif Central, France, where this plant is native and grows at low temperatures, were evaluated. The likely explanation for this difference in yield is that Calendula is a plant native to cold climates, and now acclimated in southern Brazil where autumn and winter temperatures are higher.

Analysis of the C. officinalis essential oil extraction techniques by steam distillation, headspace-HS-SPME, or cold-finger analyses and retention indexes, revealed 27 compounds.

Steam-distillation mainly showed sesquiterpene hydrocarbons (68.0 % of total area, compounds 1 to 15 and 22) and sesquiterpenols (27.0 % of total area, compounds 16 to 21) (Figure 1 and Table I). δ-cadinene (22.5%) and α-cadinol (20.4 %) were the main compounds, in agreement with Chalchat et al. (1991), who worked with C. officinalis from the French Central Massif (δ-cadinene at 12.1 % and α-cadinol at 25.5 %). Radulescu et al. (2000) isolated volatile oils of C. officinalis from flowers collected in Bucharest, Romania, by steam distillation and HS; these were analyzed by capillary gas-chromatography-mass spectrometry, and had α-muurolol (41.5 % of total area) as the chief component.

 

 

Only sesquiterpene hydrocarbons were identified by HS-SPME at room temperature using a PDMS fiber and analyzed by GC-MS, as shown in Figure 1 and Table II. The HS-CF extraction showed similar compositions as when using HS-SPME (Figure 1 and Table III).

 

 

 

 

In the present experiment, three different techniques were used, with different conditions of time and temperature, resulting in the identification of more compounds in steam distillation compared with the HS-SPME and HS-CF methods. By analyses of chromatograms (Figure 1), δ-cadinene appeared as one of the major compounds in all three techniques.

The absence of the sesquiterpene alcohols in the HS-SPME product suggests that polar alcohols and low-molecular-mass terpenes are not well adsorbed by the PDMS fiber used.

The experiment demonstrated that the HS-SPMS and HS-CF techniques did not replace the traditional technique of steam distillation in the analytical conditions used, because these techniques have different purposes and applications.

 

ACKNOWLEDGEMENTS

The authors thank the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for the financial support.

 

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REZENDE, C. M.; CORRÊA, V. F. S.; COSTA, A. V. M.; CASTRO, B. C. S. Constituintes químicos voláteis das flores e folhas do pau-brasil (Caesalpinia echinata, Lam.). Quím. Nova, v.27, p.414-416, 2004.         [ Links ]

REZENDE, C. M.; LOPES, O. C.; FRAGA, S. R. Principais substâncias responsáveis pelo aroma de mangas comerciais brasileiras identificadas por cromatografia gasosa de alta resolução/ olfatometria/ espectrometria de massas. Quím. Nova, v.22, p.31-36, 1999.         [ Links ]

 

 

Recebido para publicação em 06 de dezembro de 2006
Aceito para publicação em 06 de julho de 2008

 

 

* Correspondence:
D. A. G. Cortez
Department of Pharmacy and
Pharmacology, Universidade Estadual de Maringá,
Av. Colombo, 5790,
87020-900, Maringá, PR, Brazil
E-mail: dagortez@uem.br