|Home | About | Journals | Submit | Contact Us | Français|
The study was undertaken to develop a simplified procedure for the isolation of bioactive isoflavone from Iris kashmiriana, using a direct method of isolation, avoiding the use of chromatographic techniques. The compound was isolated by commercially viable procedure. The extraction of powdered drug (500 g) was done with petroleum ether (60–80) using a Soxhlet apparatus (24 h run). The petroleum ether extract (gums and resins 2.13 g) was obtained and the marc (400 g) was subjected to extraction with 95% methanol using a Soxhlet apparatus (24 h run). The methanolic extract (5 g) was subjected to successive fractionation with toluene, chloroform and ethyl acetate and n- butanol. On the basis of phytochemical analysis, the glycoside was present in n- butanol fraction. The n-butanol fraction (1.5 g) was taken in dried methanol, passed through activated animal charcoal and subjected to acid hydrolysis. The isoflavone (250 mg), was obtained after the usual process of separation. The purity of the compound was checked by analyzing TLC (Thin Layer chromatography) and melting point. Further, the chemical method was used to characterize the compound by shift reagents using UV spectroscopy. The quantitative estimation of isoflavone was done using RP-HPLC and was found to be 98.9% pure.
Solvent-solvent extraction technique was adopted for the isolation of novel compound. In continuing with this technique the rhizomes of Iris kashmiriana Baker were dried, chopped, and powdered (500 g). The extraction of powdered drug was done with petroleum ether (60–80) using a Soxhlet apparatus (24 h run). The petroleum ether extract (gums and resins 2.13 g) was obtained and the marc (400 g) was subjected to extraction with 95% methanol using a Soxhlet apparatus (24 h run). The methanolic extract (5 g) was subjected to successive fractionation with toluene, chloroform and ethyl acetate and n- butanol . On the basis of phytochemical screening results, the glycoside was present in n- butanol fraction. The n-butanol fraction (1.5 g) was taken in dried methanol (80%), passed through activated animal charcoal. The acid hydrolysis was carried out in the presence of 5% HCl (the reaction mixture was refluxed for 2–3 h at 45–50 °C and kept for night) . Completion of reaction was monitored on TLC (10% Methanol in Toluene). The solution was poured into water and the mixture was separated out by separating funnel. From organic layer, the solvent was removed by distillation and residue was further dried. The identification of compound was confirmed by TLC in chloroform: methanol 9:1 with Rf value 0.65 . The structure of the compound was characterized and established by various spectroscopic techniques viz, UV, IR, 1HNMR, 13CNMR, Mass spectrometry and 2D NMR. Furthermore, the compound was also characterized by chemical methods by shift reagents (AlCl3 and CH3COONa) using UV spectrophotometer . Finally, the compound was considered as an aglycone/isoflavone (250 mg). The aqueous portion of the above was subjected to paper chromatography  using n-butanol, acetone and water in the ratio 4:1:5, where it was clearly observed that the sugar attached was glucose, with Rf value 0.68.
Why this method was adopted in the present work?
10 mg test sample was dissolved in 100 mL of methanol to prepare 100 ppm solution; further dilution was made to prepare 10 ppm solution.
A simple, sensitive and accurate RP- high performance liquid chromatography (RP-HPLC) method has been used for the quantitative estimation ,  of “previously undescribed” isoflavone from Iris kashmiriana Baker. Agilent 1200 series HPLC binary pump system was performed on a C18 column with water: methanol (45:55), as mobile phase. Detection was performed by the DAD detector at 338 nm. This technique has been applied, for the quantitative estimation of new isoflavone. The retention time of the isoflavone was 11.2 min and no other peaks were observed. Injection volume was taken 10 μL. The purity of the compound was found to be 98.9% with single peak, which indicates the compound isolated was substantially pure and single; moreover the present study appears to be first of its kind of approach (Fig. 1).
What is the significance adopted in the present work?
Ultraviolet and visible spectroscopy was one of the basic techniques routinely used for flavonoid/isoflavanoid analysis due to the existence of two characteristic UV/Vis bands in flavonoids, band I in the 300–550 nm range, arising from the B ring, and band II in the 240–285 nm range, arising from the A ring, with some variations.
Shift reagents, such as aluminium chrolide and sodium acetate, lead to shifts in the maximum wavelength of these bands due to acetate-induced deprotonation of OH groups or Al3+ complexation by OH groups, were also used to study flavonoid/isoflavanoid structure.
The test compound (10 mg) was dissolved in 100 mL methanol and λmax was determined (341 and 238.4 nm). When few drops of AlCl3 was added, a complex was formed between carbonyl group, hydroxyl group (at C-5) and AlCl3, resulting in the shift of λmax from 341 nm to 377.6 nm and 238.4 nm to 264.8 nm, respectively. In continuation with the procedure, few drops of HCl was added in the same mixture, there was no change in the shift of λmax except the optical density. This clearly indicates the vicinity of hydroxyl groups at C5- OH and carbonyl (>CO at C4) in the isoflavone moiety (Table 1, Table 2).
The compound (10 mg) was dissolved in 100 mL methanol and λmax was determined.
Since, no shift in λmax has been observed in UV region (341 nm, 238.4 nm) after the addition of sodium acetate, thereby it clearly indicated, that the absence of free hydroxyl groups at C-3′,C-5′ and C-4′ positions.
Why this method was adopted in the present work?
This technique is inexpensive, reproducible and less time-consuming to study the flavonoids/isoflavonoid structure, though the other methods of characterization are equally important. Nowadays these techniques are not routinely used but still continue to be applied in some cases, in particular to HPLC eluates – a hyphenated LC-UV-MS has been developed using post-column UV shift reagents for the flavonoid/isoflavonoid analysis of crude extracts.
The aglycone was isolated, purified and recrystallized with methanol, the melting points was found to be 225–227 °C (uncorrected) and further analyzed for C14H12O6. The elemental analysis found (%) C;64.00,H;4.03,O;31.97 and calculated; C;63.21,H;3.40, O;30.83. Mass spectrometry analysis by TOF,MS, ES+. (m/z) = 301.26.The structure was further assigned by IR,1H NMR, C13 NMR, Mass spectrometry, together with U.V. RP- HPLC and chemical methods . The structure of isolated isoflavone is given below (Fig. 2).
The IR data indicates the presence of carbonyl group, aromatic ring and hydroxyl groups.
13C- NMR (400 MHz, δ, DMSO, TMS = 0): C-4, 180.50, C-4′ 157.39, C-5 153.22 C-7 153.30, C-2 153.31, C-6 131.22, C-8a 121.92, C-8 132.47, C-3′,5′, 115.01, C-2′,6′ 129.91, C-1′,104.89, C-3 121.14, C-4a 93.71,CH3-59.80
TOF MS ES+ 2.33e.3 m/z (rel. int): 301[M]+ (45.94), 294[M-6H]+2(13.12),285[M-CH3] + (36.79),269[M-CH3-O] + (12.05),253[M-CH3-O-O] + (63.63),237 [M-CH3-O-O-O] + (10.32), 208 [M-CH3-O-O-CO2] + (7.01),201 [M-C6H4CO ring B] + (6.63), Ring B = m/z 100. 187[M-CH3-O-O-O-C4H2] + (61.82),178[M-C6H4CO—CC—] + (28.26),162[M-C6H4CO—CC-O] + (34.94),146[M- C6H4CO—CC-O-O-] + (22.05), 136[M- C6H4CO—CC-O-C2H2] + (7.05), 117[M-CH3-3O-ring A] (4.91). Ring A = m/z116. 107[M- C6H4CO—CC-O-C2H2-CHO](59.13). 85[117-2O](100)
With the help of above methodology, our team isolated more than 10 new molecules from different plant species. For example, karanjin and their new analogues are isolated from seed oils of Pongamia pinnata, Lactone and their analogues are isolated from Inula resemosa (Pushkarmool).The RP-HPLC method developed can also be extrapolated for the standardization of herbal formulation containing isoflavone.
The authors thank to Faculty of Pharmaceutical Sciences Shoolini University India for providing research facilities. We must thank to SAIF, Auvtar Singh and Manish Kumar, Panjab University, Chandigarh, (India) to get spectral data of 1HNMR, C13NMR, and Mass Spectrometry.