Biochemical composition and antioxidant capacity of extracts from Podophyllum hexandrum rhizome

Background Podophyllum hexandrum Royle (P. hexandrum) is a perennial herb and widely used in clinic. The present study was designed to separate and identify the biochemical composition and antioxidant capacity of extracts from P. hexandrum rhizome. Methods The ethyl acetate and ethanol extracts from P. hexandrum rhizome were analyzed by GC-MS (gas chromatography–mass spectrometry), and the antioxidant capacity of the extracts and the components was tested by using the DPPH (2, 2-diphenylpicrylhydrazyl) and FRAP (Ferric reducing/antioxidant power) assays. Results The rhizome extracts had greater antioxidant capacity than the petiole extracts in DPPH and FRAP assays. About 16 kinds of main reactive oxygen components were identified in the extracts. Components of PADE (Phthalic acid, diisobutyl ester), BADE (1,2-Benzenedicarboxylic acid, diisooctyl ester), Polyneuridine, PODD (Podophyllotoxin, deoxy), β-Sitosterol and POD (Podophyllotoxin) showed the antioxidant capacity in some degree. PODD, POD, and Polyneuridine showed stronger antioxidant capacity with the IC50 and FRAP values of 9.61 ± 0.81 and 2923.98 ± 21.89 μM, 9.98 ± 0.24 and 2847.27 ± 14.82 μM, and 13.37 ± 0.35 and 2404.32 ± 36.88 μM, respectively, than the positive control ASA (Ascorbic acid) with the values of 60.78 ± 1.22 and 1267.5 ± 30.24 μM (P < 0.01). Conclusions PODD, POD, and Polyneuridine are very critical for the antioxidant capacity in the extract of P. hexandrum rhizome. These results provide useful biochemical basis and information for the potential use of this plant.


Background
Podophyllum hexandrum Royle (P. hexandrum), commonly named Himalayan Mayapple, is a perennial herb that grows in the Himalayan region and the southwest of China [1,2]. Since 1940 P. hexandrum resin has been used topically for various skin lesions such as warts and condylomas [3]. POD is a natural product mainly existing in P.hexandrum rhizome. It has been used in the treatment of genital infection to sterilize noncervical human papilloma virus [4]. Penile warts can be safely treated with 0.5-2.0% podophyllin self applied [5]. Goel et al. [6] reported a significant antitumour effect at subtoxic, well-tolerated, sequential doses of aqueous extract of P. hexandrum. POD is also used as starting compound for the chemical synthesis of etoposide (VP16-213) and teniposide (VM- 26), and its congeners and derivatives have pronounced biological activity as anticancer, antineoplastic and anti-HIV drugs [7][8][9]. Researchers have recently paid attention to the antioxidant activity of POD and its derivatives, such as GP7OH, GP7H, GP7 and VP16 [10]. So far, there is no specific study on the biochemical composition and the antioxidant capacity of P.hexandrum rhizome extracts. In our previous study, GC-MS showed that the ethyl ether extract of P. hexandrum seed contained some bioactive components, such as Hexanedioic acid, Oleic acid, and Octadecanoic acid [11].
In the present study, we tested the antioxidant capacity of ethyl acetate and ethanol extracts in the rhizome and petiole of P.hexandrum by the DPPH and FRAP assays, separated and identified the biochemical compositions of the rhizome extracts by GC-MS, and then evaluated antioxidant capacity of some identified compositions with the parameters of IC 50 and FRAP value.

Plant materials
P. hexandrum was collected from a forest (2,

Preparation of extracts
Rhizome and petiole were washed, dried and grinded to powder. Then the powder was weighted (20.00 g) and soaked in ethyl acetate and ethanol (500 mg/mL) for 10 months at room temperature in dark, and was then filtered, evaporated and condensed to dryness under nitrogen to obtain extracts.

Antioxidant assays
Although there are numerous methods for determining the antioxidant capacity of soluble natural extracts and insoluble food components [12], no perfect system is available to help us know the "true" antioxidant capacity of a complex medium [13,14]. The DPPH and FRAP assays, despite their disadvantages, are still used by many researchers for rapid evaluation of antioxidant [15].

DPPH assay
The free radical scavenging activity (FRSA) of DPPH was measured according to Ramadan et al. [16] and Nencini et al. [17]. which is one of the few stable and commercially available organic nitrogen radical assays [18,19]. Foti et al. [20] suggested it is an electron transfer reaction. The initial electron transfer occurs very quickly, while the subsequent hydrogen transfer occurs more slowly and depends on the hydrogen-bond accepting solvent [18,19]. This reaction has been measured by the decoloration assay where DPPH has an absorption band at 515 nm which disappears upon reduction by an antiradical compound [18,21]. The specific steps are as follows.
The extracts were diluted with 15% aqueous ethanol with concentration of 10 mg/mL, and then 50 μL of the diluted extracts was added with 950 μL of 10 −4 M DPPH methanol solution. Then the mixture was shaken and kept in dark for 30 min at room temperature. The decreased absorbance of DPPH solution was evaluated at 515 nm by a spectrophotometer UV-1018, and 500 μM 15% aqueous ethanol ASA was tested as a positive control. The test was carried out in triplicate, and the capability to scavenge the DPPH radicals was calculated as: where A 0 and A were the absorbance of DPPH without and with sample, respectively.

FRAP assay
The FRAP test was first introduced by Benzie et al. [22] for measuring the total antioxidant activity, which was initially developed to assay plasma antioxidant capacity but can also be used on other fluids. In the FRAP test, reductants (antioxidants) in the sample reduce ferric-tripyridyltriazine complex (Fe 3+ -TPTZ), in stoichiometric excess, to a blue ferrous form (Fe 2+ ), with an increase in absorbance at 593 nm [17]. The specific steps were described by Tsao et al. [23] as follows.
The working FRAP reagent was prepared ex tempore by mixing 10 volumes of 300 mmol/L acetate buffer, pH 3.6, with 10 mmol/L TPTZ in 40 mmol/L HCl, and 20 mmol/L FeCl 3 · 6H 2 O at 10:1: The 300μL FRAP reagent and the 10μL standard samples (FeSO 4 · 7H 2 O, 500 μM) or test samples (10 mg/mL 15% aqueous ethanol) were added and mixed well. The reaction temperature was 37°C and the absorbance readings were taken at 593 nm immediately and 4 min later using a spectrophotometer UV-1018. And 500 μM 15% aqueous ethanol ASA was tested as a positive control. All tests were carried out in triplicate. The FRAP value of the test samples was calculated on the basis of 500 μM Fe 2+ (FeSO 4 · 7H 2 O) as follows: where ÄA 593nm was the absorbance of the sample minus the absorbance of the blank at the 4th minute.

Evaluation of antioxidant assays
Reagents PADE, BADE, Polyneuridine, PODD, β-Sitosterol, POD, and including the positive control ASA were dissolved in 15% aqueous ethanol and tested at the same concentration of 500 μM. Antioxidant capacity was expressed IC 50 (μM) and FRAP (μM) and the test methods were mentioned above (as the DPPH and FRAP assays).

Statistical analysis
The results were presented as mean ± SD of triplicate determinations. Statistical analysis was performed by SPSS 11.5. One-way analysis of variance (ANOVA) was utilized to evaluate differences.

Antioxidant capacity of rhizome and petiole extracts
FRSAs from the rhizome and petiole extracts of P. hexandrum expressed as I % are showed in Figure 1, and the antioxidant capacity expressed as FRAP value is reported in Figure 2. FRSAs of ethyl acetate and ethanol extracts were higher from the rhizome (90.17 ± 1.11 and 94.52 ± 0.17%, respectively) than from the petiole (68.75 ± 0.52 and 77.23 ± 1.01%, respectively). The FRAP values showed the same trend as FRSAs, and the FRAP values of ethyl acetate and ethanol extracts from the rhizome were 1784.09 ± 52.07 and 2079.55 ± 34.09 μM, and the values of the petiole were 420.45 ± 85.79 and 886.36 ± 68.18 μM. In both DPPH and FRAP assays, 500 μM ASA was tested as a positive control, and the values of I% and FRAP value were 88.25 ± 0.24% and 1267.5 ± 30.24 μM, respectively. The statistical analyses showed that the rhizome extracts had greater antioxidant capacity than the petiole extracts and the ethanol extracts had greater antioxidant capacity than the ethyl acetate extract both in DPPH and FRAP assays (p < 0.01).

Separation and identification of rhizome extracts
In order to further study the biochemical compositions in P. hexandrum rhizome, the extracts of the ethyl acetate and ethanol were separated and identified by GC-MS. In total, About 16 kinds of reactive oxygen were identified. The compound retain time (RT), name, molecular formula, molecular weight, area and percentage of area (POA) were listed in Table 1 (the ethyl acetate extract) and Table 2 (the ethanol extract), and the compound structures were presented in Figure 3

Discussion
Podophyllum contained 4-20% of podophyllum resin, which is the source of POD [24,25]. Giri et al. [3] reported that Podophyllotoxin is commonly extracted from P.hexandrum that contains 6-12% of resin, of which the concentration of podophyllotoxin is around 40%. Chawla et al. [26] reported that polyphenols and lignans were rich in P.hexandrum rhizome, which revealed several bioactivities of direct relevance to radioprotection.
In this work, about 16 kinds of reactive oxygen components were identified by GC-MS, some of which have been preliminarily studied for antioxidant capacity or identified from other plants. Zhang et al. [27] and Jin et al. [28] reported that POD derivatives had strong  Although the POAs of other components in the ethyl acetate and ethanol extracts are relatively small, antioxidant capacity was also reported in other plant extracts, such as D-allose [33], Dibutyl phthalate [34,35], n-Hexadecanoic acid [33][34][35][36], Oleicacid [36,37], Octadecanoic acid [37], Octadec-9-enoic acid [32], Campesterol [38,39], Retinol [40]. So far, both PADE and BADE have not been reported on the antioxidant capacity. Other active components might be present in the extracts and should be under further investigation.

Conclusions
The rhizome extracts had greater antioxidant capacity than the petiole extracts in DPPH and FRAP assays. About 16 kinds of reactive oxygen components were identified by GC-MS in the extracts of P.hexandrum, this was the first to report PADE and BADE from a plant product and further study the antioxidant capacity of the identified components PADE, BADE, Polyneuridine, PODD, β-Sitosterol, and POD. The results of tested data and statistical analysis proved that the extracts from P. hexandrum had strong antioxidant capacity, and the PODD, POD and Polyneuridine played an important role. Based on the above data it can be recommended as