Research Article - Biomedical Research (2019) Volume 30, Issue 5

Phytochemical analysis, antioxidant and cytotoxic activities of Dryopteris ramosa.

Baloch R^*, Uzair M, Chauhdary BA, Hayat MM, Alamgir M

Pharmaceutical Chemistry, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan

*Corresponding Author:

Baloch R
Department of Pharmaceutical Chemistry
Bahauddin Zakariya University
Multan
Pakistan

Accepted Date: January 30, 2017

Abstract

Objective: The aim of present study was to evaluate phytochemical, cytotoxic and antioxidant potential of dichloromethane and methanol extracts of Dryopteris ramosa (Hope) C. Chr. belongs to family Dryopteridaceae. The plant is traditionally used as anthelminthic, diuretic, antibacterial, astringent and as tonic for various stomach and intestinal problems. Method: The phytochemical potential, total phenol, flavonoid and alkaloid contents of Dryopteris ramosa were determined for the first time. Plant was subjected to Brine shrimp lethality and DPPH inhibition assay was done. Identification and quantification of various phenolic content by was done HPLC. Results: Phytochemical analysis revealed that flavonoids, terpenoids, cardiac glycosides, alkaloids and saponins were present in the plant while tannins were absent. The results depicted high in vitro cytotoxic effect by dichloromethane extract with a LD50 0.6903 μl/ml as standardized with Etoposide with LD50 of 7.4625 μl/ml. The methanol extract showed the strong DPPH scavenging activity with 72.76 ± 1.52% inhibition as compared to the dichloromethane extract with 55.37 ± 3.055% inhibition. The high phenol content was found in methanol extract having 199.2 ± 4.50(mg of GA/g of extract). HPLC analysis showed the presence of various phenol compounds (Gallic acid, quercetin, caffeic aid, vanillic acid, cinnamic acid etc.) with their relevant concentration, in the plant. The dichloromethane extract exhibited high flavonoid content 73.02 ± 1.00 (mg of RE/g of extract). Alkaloidal content was highest in dichloromethane extract with 29.73 ± 4.04 (mg of AE/g of extract).

Keywords

Antioxidant, Cytotoxic, Dryopteris ramosa, HPLC, Phytochemical analysis.

Introduction

Oxidative stress caused by free radicals can cause serious damage to the important cellular macromolecules like DNA and protein [1]. These toxic effects of free radicals have drawn the researcher’s attention to the significance of antioxidants in the prevention and treatment of various ailments [2]. Many studies have been done on the natural sources to produce natural antioxidants with lower cytotoxic profiles [3].

Cancer, a genetic disease, is mainly caused due to genetic instability involving variations in tumor suppressor genes and in oncogenes which causes expression of abnormal proteins engaged in the stimulation of cell proliferation and its survival [4]. Previous studies have proved that free radicals have the key role in the development of cancer [5].

Secondary metabolites, like phenols, alkaloids, flavonoids and tannins, widely distributed in plants, possess multiple biological effects including free radical scavenging activities, anti-inflammatory, antioxidant and anti-carcinogenic effects [6]. Various studies have been done on herbal plants, fruits and vegetables which indicated the presence of antioxidants in the form of phenolic compounds, flavonoids, proanthocyanidins and tannins [7].

Contrariwise, to the best of our understanding, various medicinal plants used as vernacular medicine still require scientific attention and D. ramosa is one of them. Plant is traditionally known as “Pakha”. D. ramosa is used as diuretic, astringent and febrifuge [8]. Plant is also used as tonic for various stomach and intestinal problems [9]. Young leaves are collected in March-May as a vegetable and are used as spinach against gastric ulcer, constipation and as aphrodisiac [10]. Rhizome has anti-bacterial and anthelminthic potential [11]. In the present research dichloromethane and methanol extracts of D. ramosa were evaluated for their phytochemical potential, cytotoxic and antibacterial capacities.

Method

Plant collection and extraction

The plant D. ramosa was collected from place Nathia gali, District Abbottabad, Khyber Pakhtunkhwa province, Pakistan. Plant was identified by Assistant Professor Dr. Zafarullah Zafar, Institute of Pure Applied Biology, Bahauddin Zakariya University, Multan. In order to obtain effective extracts plant was dried in shade for about 15 days. Dried plant was ground and weighed. Extraction of plant done was by the process of maceration. The weighed amount of ground plant was kept in extraction bottle and then pre-determined volume of dichloromethane was added to it. For the purpose of maximum extraction bottle was placed on ultrasonic bath. After 24 hours, filtration was carried out. Same process was done thrice with dichloromethane. Further, marc of plant was extracted with methanol in the same manner. The dichloromethane and methanol extracts were prepared using rotary evaporator. The dichloromethane (100.2 g) and methanol (120.9 g) extracts were collected in separate sample bottles and designated with codes as DRD and DRM respectively.

Preliminary phytochemical analysis

Chemical tests for identification of secondary metabolites: The dry powder of whole plant D. ramosa was evaluated for the presence of secondary metabolites (like alkaloids, saponins, cardiac glycosides, etc.) according to the standard protocol methods. In these tests formation of turbidity or development of color is generally involved. An authentic specimen is always used to compare the obtained color. While in case of precipitation reaction turbidity formation is compared with the control. Control is always without drug merely containing reagent. These tests can be applied to the extracts as well as isolated constituents [12].

Determination of total phenol content: Total phenolic content was determined using Folin – Ciocalteu colorimetric method. Gallic acid was used as the standard and the results were expressed in terms of equivalent (GAE) per gram of sample. Various concentrations of gallic acid (0.01-0.1 mg/ml) were prepared using methanol as solvent. Fractions of 0.5 ml of the sample and the standard were taken. Two ml of Folin– Ciocalteu reagent was added to these fractions and the reaction was initiated by the addition of (7.5% w/v) sodium carbonate solution. The tubes were then covered with silver foils and were allowed to incubate for about thirty minutes at room temperature. Absorbance was measured at 765 nm while using methanol as blank. All the samples were processed in three repetitions. The total phenolic content of the extract was determined by the help of standard curve of Gallic Acid. Folin- Ciocalteu is a sensitive reagent that reduces compounds including polyphenols, hence producing a blue color upon reaction. This blue color was measured [13].

Determination of total flavonoid content: Aluminum chloride colorimetric assay was used to determine the flavonoid content of the plant extract in this study. Fractions of 0.5 ml of the sample and the standard, Rutin, (0.01-1.0 mg/ml) of were taken. Two ml of distilled water and 0.15 ml of sodium nitrite (5% NaNO2, w/v) solution was added to the fractions and then mixed. To this, 10% solution of AlCl3 w/v, was added after six minutes. The prepared solution was allowed to stand for more six minutes and then 2 ml of (4% NaOH w/v) sodium hydroxide solution was added to it. Dist. water was added immediately to make the final volume 5 ml. This mixture was allowed to stand for 15 min. Absorbance of prepared mixtures was taken at 510 nm. Calibration curve of Rutin was used to determine total flavonoid content and then TFC was expressed in terms of mg Rutin equivalent per gram of sample. Same procedure was performed thrice [14].

Determination of total alkaloid content: 1 mg of plant extract was taken and dissolved in Dimethyl Sulfoxide (DMSO). 1.0 ml of 2 N HCl was added to it and was then filtered. After filtration, filtrate was transferred to separating funnel. 5 ml of bromocresol green solution and 5 ml of phosphate buffer, was added to the separating funnel. This mixture was vigorously shaken by adding 1,2,3 and 4 ml chloroform. Later, it was collected in 10 ml volumetric flask and was diluted with chloroform to make the volume. Reference standard solutions of atropine (20, 40, 60, 80 and 100 μg/ml) were prepared likewise. The absorbance of test and standard solutions was measured at 470 nm in UVSpectrophotometer and the total alkaloid content was expressed as mg of AE/g of extract [15].

Identification and quantification of phenol contents by HPLC: Samples (10 μl) were analyzed by HPLC (Shimadzu Model 10A) pump equipped with a UV-Visible detector, 280 nm using a Shim-Pack CLC-ODS (C-18) column, 25 cm × 4.6 cm × 5 μm. Solvents used were A water-AA (94:6, pH=2.27) and B acetonitrile 100% at a flow rate of 1 ml/min. All the solvents used were of HPLC grade. The phenolic compounds were identified by chromatographic comparison with authentic markers using standards including quercitin, gallic acid, vitamin C, vanillic acid, m-coumaric acid, sinapic acid, ferulic acid, caffeic acid, syringic acid, 4-OH-3 methoxy benzoic acid, trans-4-OH-3-methoxy cinamic acid, chlorogenic acid and chromatotropic acid. Phenolic compounds were quantified by peak area using authentic standards.

Biological activities

Brine shrimp lethality assay: Artificial sea water was prepared by mixing 3.8 g of sea salt/1000 ml of water. It was then filtered and poured in an unevenly divided large tank, eggs of the shrimp were then kept in bigger part of the tank and was later covered with aluminium foil. Eggs then hatched in the tank and larvae started to move in compartment. Temperature of the larvae’s tank was adjusted at 37°C for the maturity and growth of the larvae. Concentration of 1000, 100, 10 micrograms per milliliters were prepared in the vials for testing and in three replicates from every dilution to make total of nine vials, to the 20 mg of sample. After that 2 ml of organic solvent was taken and from the solution 500, 50, 5 μl was used in same order. Solvents were allowed to evaporate under nitrogen by applying high vaccum for about thirty minutes. After the two days 10 shrimps were added to the 5 ml of sea water in each vial. These vials were then placed under light. After about on day number of survived shrimps were counted by the use of 3X magnifying glass. Data, thus obtained, was analyzed by probity analysis by the use of 95% confidence interval [16].

DPPH inhibition assay: A 10 μl of test solution was added in 96-wells plate followed by the addition of 90 μl of 100 μM methanol DPPH solution to make total volume up to 100 μl. The contents were mixed and incubated at 37°C for 30 min. The reduction in the absorbance was measured at 517 nm using Synergy HT BioTek® USA microplate reader. Quercetin was used as standard antioxidant. All experiments were carried out in triplicates. For the determination of IC50 values, test solutions were assayed at various dilutions i.e. 0.5, 0.25, 0.125, 0.0625, 0.0313, 0.015 mM. Data obtained was computed on Ezi-fit software [17]. The decrease in absorbance indicates increased radical scavenging activity which was determined by the following formula.

Where: Absorbance of control=Total enzyme activity without inhibitor, Absorbance of test=Activity in the presence of test compound

Results and Discussion

The shade dried whole plant of D. ramosa was carried for extraction process through the mechanism of maceration with dichloromethane and methanol sequentially. The extraction results, along with their assigned codes used are given in Table 1.

Table 1: Results of extraction of D. ramosa with dichloromethane and methanol.

For the purpose of detection of alkaloids, tests were done by using Mayer s reagents, Wagner s reagents, Hager’s reagents and Dragendroff’s reagents. Keller kiliani test was done for detection of cardiac glycosides. The chemical test for detection of saponins was performed. The obtained results are given in Table 2.

Table 2: Results of detection of secondary metabolites from the whole plants of D. ramosa.

Results of total phenolic, flavonoid and alkaloid content are summarized in Table 3. Methanol extract exhibited higher phenolic content as compared to the dichloromethane extract. While dichloromethane extract showed high flavonoid and alkaloid contents. Values are expressed as mean ± SEM of triplicate measurements.

Table 3: Total phenol, flavonoid and alkaloid content of dichloromethane and methanol extracts of D. ramosa.

Results of identification and quantification of phenolic contents by HPLC showed the presence of chlorogenic acid, benzoic acid, ferulic acid, quercetin, syringic acid and vanillic acid in dichloromethane extract. Whereas caffeic acid, chlorogenic acid, cinnamic acid, gallic acid, p-coumaric acid, m-coumaric acid, quercetin, syringic acid and vanillic acid was present in methanol extract. Tables 4 and 5 show the retention time, area (mV.s), area (%) and concentration of the various phenolic compounds found in methanol and dicholoromehane extracts respectively.

Table 4: Identification and quantification of methanol extract of D. ramosa.

Table 5: Identification and quantification of dichloromethane extract of D. ramosa.

Brine shrimp (Artemiasalina) lethality bioassay was carried out against both dichloromethane and methanol extracts of D. ramosa for cytotoxic evaluation. Dichloromethane extract exhibited a very significant cytotoxic activity with “ LD50 0.6903 μg/ml”. No cytotoxic activity was showed by methanol extract. Results are given in Table 6.

Table 6: Results of Brine shrimp (Artemiasalina) Lethality bioassay of dichloromethane and methanol extract of whole plant of D. ramosa.

Table 7 represent the antioxidant activity of dichloromethane and methanol extracts of D. ramosa. Dichloromethane extract showed 55.37s ± 3.055 DPPH (%) inhibition ± SEM while methanol extract showed 72.76 ± 1.52 DPPH (%) inhibition ± SEM.

Table 7: DPPH %inhibition of dichloromethane and methanol extract of D. ramosa.

Herbal plants rich in phenolic compounds are progressively being utilized in food industry due to their retarding effect on oxidative degradation of lipids as well as can improve the nutritional value and quality of food [18].

Higher total phenolic content was found in the methanol extract 199.2 ± 4.50 (mg of GA/g of extract) than that of dichloromethane 184.2 ± 4.04 (mg of GA/g of extract).

Phenolic compounds of plants are categorized into various categories; major among these are flavonoids which have promising antioxidant activities [19]. Flavonoids are naturally present in plants and are known to produce positive effect on human health. Studies have proved that flavonoids have diverse range of antiviral, anti-inflammatory, antibacterial, anti-allergic and anticancer activities [20]. Moreover, flavonoids possess strong scavenging effect on oxidizing molecules like singlet oxygen and various free radicals [21] involved in various diseases. In our study higher flavonoid content was found in dichloromethane extract with 73.02 ± 1.00 (mg of extract) as compared to that of methanol extract having 50.13 ± 3.51 (mg of RE/g of extract) (Figures 1 and 2).

Figure 1: Identification and quantification of phenolic contents of methanol extract of D. ramosa by HPLC.

Figure 2: Identification and quantification of phenolic contents of dichloromethane extract of D. ramosa by HPLC.

The electron donating capacity of herbal plants can be determined 2,20-diphenyl-1- picrylhydrazyl radical (DPPH), purple colored solution bleaching. The method is based on the principle that DPPH solution is scavenged and decolorized on the addition of some radical species or antioxidants. The change in color is directly proportional to the concentration of antioxidants. An enormous decrease is observed in the absorbance of reaction mixture which indicates the significant radical scavenging activity of the compound under test [20]. In the present study methanol extract showed higher free radical scavenging activity with 72.76 ± 1.52% inhibition of DPPH as compared to the dichloromethane extract showing 55.37 ± 3.055% inhibition of DPPH. Studies have proved that methanol extract may possess phenolic and hydroxyl-phenolic compounds with alcohol, sugar, acids and glycosides [22]. Higher antioxidant activity of methanol extract of D. ramosa may be due to the presence of these compounds or flavonoids.

In cytotoxic assay that is carried out through Brine Shrimp (Artemiasalina) Lethality Assay, the DCM extract show very high potential for Cytotoxicity. Results revealed that the LD50 of dichloromethane extract is 0.6903 μl/ml as standardized with Etoposide with LD50 of 7.4625 μl/ml. It is concluded that dichloromethane extract of D. ramosa is 10 time more potent than Etoposide. Previous studies have proved that some flavonoids like quercetin possesses anticancer activity and inhibited the growth of cancer cells [23]. Gallic acid had free radical scavenging effect and induced apoptosis and differentiation in leukemia, lymphocyte cells, colon adenocarcinoma cell lines and lung cancer [24]. It has been proved that gallic acid have key role in the hindrance of cancer development and malignant transformation just like quercetin.

Thus it may be attributed that plant possesses high cytotoxic effect due to the presence of high flavonoid content in the plant.

Alkaloids have diverse range of biological properties involving antibacterial and anticancer activities and thus are responsible for the healing properties of natural medicine [25]. The present study showed the presence of significant level of alkaloids in both extracts. In dichloromethane extract alkaloid content was found to be 29.73 ± 4.04 (mg of AE/g of extract) whereas in methanol extract it was 23.92 ± 1.52 (mg of AE/g of extract).

Conclusion

The present study provides the evidence that the D. ramosa have prominent cytotoxic and antioxidant potential due to the presence of higher phenol, flavonoid and alkaloid content in the plant. Future research may be based on systemic investigation, fractionation, purification and isolation of antioxidants and cytotoxic agents for the development of novel, target oriented, more effective antioxidants and cytotoxic agents with safe therapeutic index. Further, work related to the isolation of the active constituents through bioassay-directed fractionation is in progress in our laboratory.

Acknowledgments

Authors are grateful to Department of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan for providing laboratory facilities to carry out research.

Conflict of Interest

No conflict of interest associated with this study.

Contribution of Authors

It is declared that this work was done by the authors named in this article and all liabilities pertaining to claims relating to the content of this article will be borne by them.

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