Occurrence of curcuminoids in Curcuma longa: A quality standardization by HPTLC

Abstract

A simple high performance thin layer chromatographic (HPTLC) method has been developed for the simultaneous determination of the pharmacologically important active curcuminoids viz. curcumin, demethoxycurcumin and bisdemethoxycurcumin in Curcuma longa L. The assay combines the separation and quantification of the analytes on silica gel 60 GF₂₅₄ HPTLC plates with visualization under UV and scanning at 425 nm. Using this technique, the alkaloidal content of different parts of the title plant has been determined.

Introduction

Curcuma longa (Zingiberaceae), commonly called Haldi, is a well known plant drug in Ayurvedic and Unani medicine (Chopra et al., 1956; Kapoor, 2001). It has been used for the treatment of various diseases and disorders particularly for urticaria, skin allergy, viral hepatitis, inflammatory conditions of joints, sore throat, and for wounds (Chattopadhyay et al., 2004).

Curcumin, demethoxycurcumin and bisdemethoxycurcumin, three major pharmacologically important curcuminoids, have been isolated from C. longa (Gupta et al., 1999) and has been shown to possess anti oxidant, anti inflammatory, anticarcinogenic, antimutagenic, antifungal, antiviral and anticancer activity (Chattopadhyay et al., 2004; Ahsan et al., 1999). Methods, so far available for the determination of these alkaloids, are very cumbersome and time consuming and also not economically viable (Khurana and Ho, 1988; Taylor and McDowell, 1992; Schieffer, 2002).

Therefore it was thought worthwhile to develop a simple and high precision HPTLC method for simultaneous analysis of curcumin, demethoxy curcumin and bisdemethoxycurcumin occurring in roots of C. longa.

Materials and Methods

Rhizomes of C. longa were collected from the Experimental Farm for the Development of Medicinal and Aromatic Plants (BCKV, Mohanpur, India). The plant specimens were authenticated and a voucher specimen is deposited in the herbarium.

Reagents used were from Merck (Darmstadt, Germany). Analytical standards of curcuminoids were obtained from Ms. ChromaDex, Santa Ana, CA, USA. Solvents used in entire study were from Merck, India. The identities of curcumin, demethoxycurcumin and bisdemethoxycurcumin were confirmed by comparison of their spectral data with those previously reported (Govindarajan et al., 1980).

Air dried (35-50°C) rhizomes of seven germplasm of C. longa and market turmeric powder samples (1 g each) were ultrasonically extracted separately in 20 mL HPLC grade methanol for 15 min (3 times) and filtered through Whatman No. 42 filter paper after each extraction. Extracts were concentrated under vacuum and finally made up to 20 mL with HPLC grade methanol and ready for HPTLC analysis.

Chromatography was performed on glass backed silica gel 60 GF₂₅₄ HPTLC layers (20 x 20 cm, 300 µm layer thickness) prepared using a Camag (Multenz, Switzerland) TLC plate autocoater. Methanolic solutions of samples and standard compounds curcumin, demethoxycurcumin and bisdemethoxycurcumin of known concentrations were applied to the layers as 7 mm wide bands positioned 15 mm from the bottom and 20 mm from the side of the plate, using a Camag Linomat 5 automated TLC applicator with the nitrogen flow providing a delivery speed of 150 nL/s from the syringe. These parameters were kept constant throughout the analysis of samples.

After sample application plates were developed in a Camag twin trough glass tank presaturated with the mobile phase chloroform:methanol (48:2, v/v) for one hour. It was then poured in twin trough glass solvent development chamber well in advance to allow complete saturation which was further enhanced by keeping one filter paper along one wall of the twin trough chamber. The plate was then kept in a chamber and solvent front was allowed to develop at the height of 7 cm on the plate. The TLC runs were made under laboratory conditions of 25 ± 5°C and 50% relative humidity. After drying, the spots were visualized under Camag UV cabinet (254 and 366 nm). Quantitative analysis of the compounds was done by scanning the plates using Camag TLC scanner model 3 equipped with Wincats software (Camag) applying the following conditions: slit width 6 x 0.45 mm, wavelength (λ_max) 425 nm, absorption reflection scan mode.The identifycation of curcumin, demethoxycurcumin and bisdemethoxycurcumin in rhizomes were confirmed by superimposing the UV spectra of samples and standards within the same R_f window. In order to prepare calibration curves, stock solutions of curcumin, demethoxycurcumin and bisdemethoxycurcumin (1 mg/5 mL each) were prepared and various volumes of these solutions were analyzed by HPTLC exactly as described above. Then calibration curves of peak area vs. concentration were prepared.

Results an Discussion

Different compositions of the mobile phase for HPTLC analysis were tested in order to obtain high resolution and reproducible peaks. The desired aim was achieved using chloroform:methanol (48:2, v/v) as the mobile phase. The wavelength of 425 nm was found to be optimal for the highest sensitivity (Figure 1). The calibration curves for the alkaloids curcumin, demethoxycurcumin and bisdemethoxycurcumin were linear in the range 100-1,000 ng (Table I).

For the quantitative determination of curcumin, demethoxycurcumin and bisdemethoxycurcumin, the analyses of turmeric rhizome specimens of C. longa were repeated three times. The average content of curcumin, demethoxycurcumin and bisdemethoxycurcumin in the rhizomes are given in Table II.

Conclusion

The HPTLC method for the simultaneous analysis of curcumin, demethoxycurcumin and bisdemethoxycurcumin from C. longa reported here is very simple, sensitive, economic and suitable for rapid screening of large number of plant samples. Moreover, this analysis can be performed without any special sample pretreatment and 15 samples can be analyzed on a single TLC laver (20 x 20 cm).

References

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