Quantification (w/w) of betulinic acid present in ethanol extracts from leaves
1. Introduction
The betulinic acid (Figure 1) is a known triterpenoid isolated from various organs and species of plants, including flowering
Despite all of betulinic acid pharmacological potential, it is obtained by extraction of barks or core of some plant species or by synthetic processes, e.g. using the betulin (alcohol triterpene) as a synthetic intermediate isolated from the bark of
As part of a program conducted in our laboratory involving search for new sources of bioactive metabolites from Brazilian plants, we investigated the leaves of
1.1. Seasonal variation
Since the fourth century B.C. there are reports of procedures for the collection of medicinal plants. The executioners Greeks, e.g., they collected their samples of poison hemlock (
Several factors that can coordinate or alter the rate of production of secondary metabolites, genetic factors, physical environment, collection method (date, time, etc.), drying conditions and transport, storage, pH of the soil, growing conditions, nutrient soil, plant part used, interactions between plants, the presence of microorganisms, can directly affect the concentration of the chemical components of each species [Silva, 1996]. Some factors have correlations with each other and not act alone, and may jointly affect the secondary metabolism, e.g. development and seasonality, rainfall and seasonality, temperature and altitude, among others [Gobbo, Lopes, 2007]. It should also be noted that, often, the changes may result from leaf development and / or appearance of new organs concomitant with constancy in the total content of secondary metabolites. This may cause decrease in the concentration of these metabolites by dilution may, however, result in a higher total amount due to the increase of biomass. [Hendriks et al., 1997; Spring, Bienert, Klemt 1987]
The seasonal variation (collection of plants at different times or seasons), is a very significant factor in the percentage and production of secondary metabolites [Mitscher, Pillai, Shankel, 2000; Navarro et al., 2002]. Due to its importance, it is necessary a study of seasonality, when working with medicinal plants [Mitscher, Pillai, Shankel, 2000; Navarro et al., 2002].
This work had as main objectives to develop a protocol for the quantification of betulinic acid present in the leaves of
2. Material and methods
2.1. General experimental procedures
1H and 13C NMR spectra were recorded on a Brucker AM-200 and 500MHz) chemical shifts are given in d values referred to internal tetramethlysilane (TMS), EIMS (MS Agilent 5973; 70eV) and Infrared (IV) spectra were recorded on a Nicolet spectrophotometer with Fourier transform Model Magna–IR 760 wavelengths are expressed in reciprocal centimeter (cm-1).
HPLC analysis were performed at room temperature using the following system: second pump system (Shimadzu LC10AD model, Japan) a photodiode array detector (Shimadzu, SPD10ADVP model), an auto injector (Shimadzu SIL10ADVP model) an oven (Shimadzu, CTO 8-A model) and under the following conditions: Shimpack C-8 (1cm x 4.6mm i.d.) guard column and C-18 column (25cmx4.6mm i.d.; 5μm particle size) was from Zorba Zx provided by Agilent Technologies (USA). The system was controlled by Class Vp (Shimadzu, Japan) software 5.16. The gradient mobile phase was carried acetonitrile (Tedia, Brazil) and water HPLC grade. The mobile phase was degassed with helium and the flow rate adjusted to 1mL. min-1. The water was acidified with TFA (0.05% v/v). All samples were injected automatically (10μ L) in triplicate.
In GC/FID experiments, 1mg each extracts [August 2009 to July 2010] and standard (Carl Roth – Karlsruhe, Germany) were transferred into glass vial and submitted methlylation with CH2N2 with 100% yield. Those samples were dissolved in CH2Cl2 in concentrations 1.4mg/mL and injected for GC-FID and GC-MS analysis. The identification of methylated betulinic acid in extracts was done with use Wiley and NBS peak matching library search system. Authentic standard of the betulinic acid and data reported in the literature were also used for further identification as described.
2.2. Plant material
Healthy leaves of
2.3. Methylation
A solution of diazomethane (CH2N2) in ether was prepared and added (excess) in drops of the solutions of extracts, EF-1 and standard (1mg) CHCl3 or MeOH. The resulting solutions were allowed to stand for 12 hours and the ether removed by passing a stream of N2 [Leonard, Lygo, Procter, 1995].
2.4. Betulinic acid quantification
GC analysis was performed on 6890N (Agilents Technologies, Network series) equipped whit a HP-5 column (30 x 0,25mm; 0,25μm liquid phase). Oven temperature program of 70oC - 300oC at 5oC/min; carrier gas: helium 11,3L/min; split mode of (20:1) and finally held for 30min. The mass spectrometer unit was performed with the same conditions the GC analysis. The calibration curve of the GC / FID was made in triplicate from different concentrations of esterified betulinic acid standard (0.1 to 1μg.mL-1) and the curve was constructed using the average values of the detector response. The detector response was linear to the concentration internal of 0.1 to 1μg.mL-1 (r2 = 0.999, Figure 2a).
HPLC grade acetonitrile was purchased from TEDIA (Brazil); 0,05% TFA (Trifluoroacetic acid) from Vetec (Brazil). Water was purified by Milli-Qplus system from Milipore (Milford, MA, USA). Betulinic acid was purchased from Carl Roth (Karlsruhe, Germany with 99%). The 30mg ethanol extracts were then dissolved in 5mL of mobile phase. The mobile phase consisted of a gradient of 0,05% aqueous trifluoroacetic acid: acetonitrile delivered at a 1.0mL.min-1 as follows initial (t= 0 min) 30:70, linear gradient over 20min to 15:85, linear gradient over 10min to 100:0 and a new linear gradient over 20min (30:70); 40min as total time of analysis. Flow rate was 1mL.min-1. Quantification was performed using the detector set at a wavelength of 210nm. Injection volume was 30μl. The peak of betulinic acid was identified in each chromatogram from of the ethanol extracts monthly (twelve months) with the help of injection of the standard solution of betulinic acid or comparison of the UV spectrum. The calibration curve of the HPLV-UV was made in triplicate from different concentrations of betulinic acid standard (0.1 to 1μg.mL-1) and the curve was constructed using the average values of the detector response. The detector response was linear to the concentration internal of 0.1 to 0,5μg.mL-1 (r2 = 0.9994, Figure 2b).
3. Results and discussion
3.1. Extraction of betulinic acid
The leaves of
EF-1 was analyzed by spectrophotometer 1H and 13C NMR (Bruker AC 200, 200MHz) using as solvent chloroform (CDCl3) and methanol (CD3OD) deuterated at a ratio of 9:1 to tetramethylsilane (TMS) as internal reference standard. An aliquot of EF-1 (5 mg) was methylated with diazomethane and subjected to mass spectrometry (MS; Agilent Technologies). The spectral data obtained were compared with the literature [Oliveira et al., 2006].
The substance showed an EF-1 in the form of white crystals and the IR spectrum showed a broad band at 3450cm-1 by a characteristic of hydroxyl groups and acid, a broad band at 2942cm-1 one of alkyl groups and bands at 1686cm-1 and 1639cm-1 corresponding respectively to the axial deformation of carbonyl acid and alkene.
The information that led to elucidation of the structure was obtained from experiments nuclear magnetic resonance spectra [DEPT, HMQC, 1H-1H COSY (homonuclear correlation spectroscopy) and HMBC experiment] which indicate a known pattern of the terpenes series lupanos (Nick
The methylation EF-1 with diazomethane promoted the removal of hydrogen from the carboxyl acid and incorporation of a methyl group from the diazomethane, leading to formation of an ester, molecular weight 470. The derivatization and the formation of the ester are ideal possible to decrease the molecular interactions between the sample and a chromatographic column and thus decrease the retention time. An aliquot of esterified EF-1 (1.4mg) was subjected to MS electron impact (70 eV). The MS spectrum of esterified EF-1 confirmed the presence of a terpene class of lupanos due to the absence of peaks m/z 218 and m/z 203 characteristic of the series oleanane and ursane (rearrangement retro Diels-Alder ring C). The presence of the methyl ester group at C-28 is confirmed by the ion m/z 262 (10%). Other peaks were obtained m/z 208 (5%), m/z 190 (10%) and m/z 189 (100%) from the break ring C and the molecular ion m/z 470 5% [Budzikiewicz et al., 1964]. The spectral data obtained from the EF-1 and the ester data were similar to those observed in the literature to betulinic acid [Nick
After calibration with standard of betulinic acid, the monthly extracts from leaves of
|
|
|
August (2009) | 7.43 | 8.01 |
September (2009) | 16.83 | 8.57 |
October (2009) | 26.27 | 11.18 |
November (2009) | 17.97 | 8.36 |
December (2009) | 8.24 | 4.83 |
January (2010) | 6.90 | 2.79 |
February (2010) | 7.92 | 5.12 |
March (2010) | 23.03 | 6.12 |
April (2010) | 9.68 | 6.31 |
May (2010) | 14.85 | 9.16 |
June (2010) | 19.33 | 9.99 |
Jully (2010) | 15.23 | 5.62 |
4. Conclusions
Several activities are being attributed to betulinic acid, however, despite all of their potential pharmacological, it is still obtained by extraction of the bark and heartwood of some [Soler, 1996], synthetic processes [Evers et al., 1996] and by biotransformation [Galgon, 2005]. Unlike these traditional species whose income was less than 3%, we found that betulinic acid was present in all extracts analyzed (table 1), with yields well above those found in the literature.
The betulinic acid level in the
These fluctuations observed in the months described in Table 1 may be related to the chemical ecology of
It is possible that the increased concentration of betulinic acid in the month of March is due to the large amount of rainfall characteristic of the Rio de Janeiro, state. However, more research is needed to determine whether other factors may be influencing the concentration of this metabolite, verify that specimens from other regions have the same or different behavior and examine whether the effect of the solvent can affect the increase in the concentration of this metabolite
Acknowledgments
The authors thank the (FAPERJ) for the financial support. We also acknowledge the Fundação Oswaldo Cruz, Farmanguinhos – PMA (Plataforma de Métodos Analíticos) for GC/FID, GC/MS analysis.References
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