The human environment and life are at constant risk of various complications [1]. Every individual on earth is in search of clean and healthy time. For the management of these major obstacles, a constant utilization of synthetic resources is the common inspiration [2]. Synthetic resources, being the most helpful tools to get rid of many complications are also a great cause of severe side effects [35]. So it is obvious that exploring the natural sources will be a great step toward the solution.

According to a survey, medicinal plants cover 34% of the total plant species found in Pakistan [6]. In Pakistan at least six thousand flowering plants have been reported currently, among which 400–600 are of great medicinal importance [7]. Herbs have been employed in variety of medicinal and non-medicinal purposes, like flavoring, nutrition, spices, beverages, dyeing, repellents, cosmetics, perfumery, fuels and in many other industrial uses. Worldwide about 85% of primary health care medications are depend on natural sources [8]. Till the nineteenth century, man has discovered the great contribution of herbs in the management of almost every pharmacological disorder [9]. According to an estimation, up to 70,000 plant species are used ethno-medicinally worldwide [10]. Sidewise, there are several factors which influence the plant production, such as pest and weeds [11, 12].

Plants in the same family exhibit almost a similar pharmacological profile due to the same genome [13]. The plants in family labiateae or lamiaceae are explored for various pharmacological purposes, like analgesic, anthelmintic and antibacterial [14]. I. rugosus is used ethno-medicinally in the diseases of skin, ear, nose, throat and intestine [15]. Basically the Phytochemicals are broadly classified into two main categories, namely, primary constituents and secondary metabolites. Primary constituents includes proteins, amino acids,, common sugars and chlorophyll, whereas, secondary constituents include glycosides, alkaloids, phenolic compounds, flavonoids, saponins, essential oils, tannins and terpenoids [16]. Majority of phytochemicals contain important therapeutic activities and the plants thus find their medicinal importance due to presence of the respective phytochmical constituents. Furthermore, each pharmacological action demonstrated by a plant sample is attributed to the presence of secondary metabolites in it. In this regard possibly interesting class of molecules are the saponins, secondary plant metabolites composed of steroids or triterpenoid aglycone linked by glycosidic bonds with divergent biological activities [17]. Saponins having the ability to treat different disease conditions and have been used as antimicrobial, antidiabetic, cytotoxic, phytotoxic, antitumor, antioxidant, antispasmodic and as anthelmintic [1821]. The crude saponins have been studied for their anticancer [22], anthelmintic [23] and insecticidal potentials [24].

Keeping in view the published importance of saponins and exploring the medicinal importance of I. rugosus, we have achieved its phytochemical studies along with phytotoxic and cytotoxic potentials.


Phytochemical analysis

Ir.Cr was found to contain glycosides, alkaloids, tannins, terpenoids, flavonoids, saponins, anthraquinones and oils, while tested negative for the presence of sterols (Table 1).

Table 1 Phytochemical constituents in crude extract of I. rugosus

Phytotoxic assay

The radish seed germination assay is of great importance for the phytotoxic activity of plant extract. The activity involves the measurement of the average root length and number of seeds inhibition in which the water serves as negative control. All the tested samples for phytotoxic potential of I. rugosus are summarized in Table 2. In this study the Ir.Sp revealed significant phytotoxicity i.e., root length inhibition (RLI) (IC50 = 0.1 μg/ml) and seeds germination inhibition (SGI) (IC50 = 0.1 μg/ml). Among the fractions Ir.Chf exhibited highest phytotoxic activity i.e., 88.40 ± 1.36, 71.37 ± 0.74 and 66.51 ± 0.39% (IC50 = 0.1 μg/ml) RLI and 89.32 ± 3.52, 73.59 ± 0.58 and 68.37 ± 0.62% (IC50 = 0.1 μg/ml) SGI at the concentration of 1000, 100 and 10 μg/ml respectively. Ir.EtAc demonstrated 80.40 ± 0.* + -68, 74.55 ± 0.51 and 61.55 ± 0.67% (IC50 = 0.1 μg/ml) RLI and 81.32 ± 5.8, 71.55 ± 0.65 and 59.44 ± 0.58% (IC50 = 0.1 μg/ml) SGI at 1000, 100 and 10 μg/ml respectively. The Ir.Hex showed 80.40 ± 0.68, 77.33 ± 0.64 and 47.26 ± 0.64% (IC50 = 29 μg/ml) RLI and 56.00 ± 4.6, 47.26 ± 0.61 and 41.55 ± 0.61% (IC50 = 410 μg/ml) SGI at 1000, 100 and 10 μg/ml respectively. The Ir.Cr and Ir.Aq revealed moderate phytotoxicity. The order of phytotoxicity for the given fractions were Ir.Chf > Ir.EtAc > Ir.Cr > Ir.Hex > Ir.Aq. From scientific verification it may be inferred that the other plants growing nearby I. rugosus may affected their growth. Majorly the phenolics are responsible for the phytotoxic action of plant [25].

Table 2 Phytotoxic effect of the crude extract of I. rugosus and its fractions against radish seeds

Cytotoxic assay

The cytotoxic effect exhibited by Ir.Cr, Ir.Sp and resultant fractions of I. rugosus is presented in Table 3. Lethality was highest at the concentration of 1000 μg/ml while low at the minimum concentration of each fraction. The Ir.Sp showed highest cytotoxic activity against brine shrimps i.e., 92.23 ± 1.1, 66.67 ± 1.9 and 52.23 ± 1.1% brine shrimps lethality at the concentration of 1000, 100 and 10 μg/ml respectively with the LC50 of 10 μg/ml. Ir.Chf showed (76.67 ± 3.3, 62.23 ± 2.9 and 48.90 ± 1.1)% cytotoxic effect at the concentration of 1000, 100, 10 μg/ml respectively with the LC50 of 12 μg/ml. The Ir.EtAc also showed almost a similar cytotoxicity (74.43 ± 2.2, 57.77 ± 2.2 and 43.33 ± 1.9)% at the concentration of 1000, 100, 10 μg/ml respectively with the LC50 of 315 μg/ml. The Ir.Aq also showed slightly lower cytotoxicity (65.57 ± 1.1, 53.33 ± 1.9 and 42.23 ± 1.1)% at the concentration of 1000, 100, 10 μg/ml respectively with the LC50 of 60 μg/ml. The cytotoxic profile of Ir.Hex and Ir.Cr were lower compared to other fractions. The LC50 calculated were 10, 12, 60, 120, 220 and 315 μg/ml for Ir.Sp, Ir.Chf, Ir.Aq, Ir.Hex, Ir.Cr and Ir.EtAc respectively. The order of cytotoxic activity were Ir.Sp > Ir.Chf > Ir.EtAc > Ir.Aq > Ir.Hex > Ir.Cr.

Table 3 Concentration dependent cytotoxic effect of the Ir.Cr extract of I. rugosus and its fractions against Artemia salina


Cytotoxic activity is one of the prominent assay to develop novel anticancer drug candidates in different plants samples [26]. In the present study, I. rugosus is investigated for the determination of its anticancer potential against Artemia salina. The order of brine shrimps lethality is crude Ir.Sp > Ir.Chf > Ir.EtAc > Ir.Aq > Ir.Hex > Ir.Cr. The cytotoxic effect of Ir.Sp and Ir.Chf were the most prominent. The high lethality of these plant samples showed that substances responsible for the cytotoxic effect are present in high amount in crude Ir.Sp and Ir.Chf fraction. As reported earlier that a positive co-relation exists between the brine shrimp lethality assay and human nasopharyngeal carcinoma (KB cell line) [27], so this method was employed for the determination of possible antineoplastic activity.

The phytotoxic activity of I. rugosus was carried out by employing radish seeds. The radish root length inhibition and seeds germination inhibition is actually due to phytotoxic effect of I. rugosus. The radish seeds growth inhibitin was highest for Ir.Chf fraction while lowest for the Ir.Aq as shown in the Table 2. Comparatively, the Ir.EtAc fraction showed low phytotoxicity as compared to Ir.Chf fraction. The other fractions also showed moderate phytotoxic effect which was comparatively low from that of Ir.Chf and Ir.EtAc. It is deduced from the results that the Ir.Chf and Ir.EtAc fractions of I. rugosus contain high amount of that constituents which are responsible for phytotoxic effect. Hence, it is deduced that constituents of the plant with herbicidal action are highly concentrated in Ir.Chf fraction.

Weeds play an important role in low production of crops. Huge economic loss in agriculture is reported each year due to harmful effects of weeds. Different techniques and chemicals are used to eliminate the harmful effects of these weed [28]. But there application is limited due to their other health hazard such as food toxicity and economical factors [29]. Hence alternative factors should be considered for removing these unwanted effects, which may be economical and having minimum harmful effects. The natural herbicides are being investigated in plants to get rid of the delayed hazardous effects of synthetic herbicides [30]. The Natural herbicides are preferred over chemical agents due to safety profile and low cost.

The Ir.Sp obtained from I. rugosus are assayed for the cytotoxic activity because saponins are reported to have anticancer action [31]. Saponins are the active constituent verified by many researchers for its anticancer potentials applying antitumor activity using potato model [32]. The brine shrimps lethality assay has also been conducted on Ir.Sp and have been resulted in promising lethality and hence proved to have cytotoxic activity [33]. The results of this activity reveal that constituents responsible for cytotoxic and phytotoxic effect of I. rugosus may be a significant source of natural herbicides for weeds to enhance the crops production rate in the field of agriculture.


This study reveals that I. rugosus contain secondary metabolites like; glycosides, alkaloids, saponins, tannins, flavonoids, terpenoids and anthraquinones. The plant crude extract, its subsequent fractions and crude saponins exhibited concentration dependent phytotoxic and cytotoxic actions which warrant isolation and characterization of novel and cost-effective compounds responsible for such valuable activities.


Collection and extraction

The plant was collected from Dir (KPK), Pakistan in the month of June. The plant name was confirmed at the Department of Botany, Shaheed Benazir Bhuto University Dir (KPK), Pakistan. The plant sample was kept in the herbarium of the same university with voucher number (1016AZ). The fresh aerial parts of plant were cleaned with distilled water and kept at room temperature for drying. After shade drying, the plant was grinded to coarse powder with the help of cutter mill. The powdered material (8 kg) was kept for maceration in 30 liters of 80% methanol with daily base occasional shaking for 22 days. It was then filtered and concentrated under reduced pressure using rotary evaporator at 40°C. Finally, keeping the concentrated sample in water bath a semisolid crude extract was obtained with weight of 300 g [34].


The Ir.Cr extract was suspended in 500 ml of distilled water and transferred into a separating funnel followed by the addition of an equal amount of n-hexane. Shake it vigorously and then kept for a while to separate the two layers. Both the layers were separated. Similarly, the fractionation was carried out by successive solvent-solvent extraction with increasing polarity of the solvent. Each separated fraction was concentrated individually under reduced pressure using rotary evaporator. The fractions obtained were Ir.Hex 22 g, Ir.Chf 35 g, Ir.EtAc 80 g and Ir.Aq fraction of 120 g.

Extraction of crude Saponins

To the pulverized plant sample (20 g) was added 100 ml of 20% ethanol and kept in water bath for 4 h at 55°C. The sample was filtered and extracted again with 200 ml of 20% ethanol. Then by keeping it in water bath for some time, the volume dropped down to 40 ml. The sample was then transferred into a separating funnel and added 20 ml diethyl ether to it with vigorous shaking. Both the diethyl ether and aqueous layers were separated. The aqueous layer was mixed with 60 ml of n-butanol and separated by using a separating funnel. The n-butanol extract was washed with 10 ml of 5% brine solution. The final volume was concentrated in a water bath and then transferred into a beaker. The sample was kept in an oven to get dried Ir.Sp weighing 1.1 g [35].

Phytochemical investigation

Qualitative phytochemical analysis of the plant extracts was carried out for the existence of glycosides, flavonoids, saponins, alkaloids, anthraquinones, terpenoids, sterols and tannins using the reported procedures [36]. For the detection of glycosides the plant extracts were hydrolyzed with HCl followed by neutralization with NAOH. Few drops of Fehling’s solution were added to the preparation and determined by the presence of red precipitates. The alkaloids were determined by using Dragendorff’s reagent. For the detection of terpenoids and sterols the samples were treated with petroleum ether followed by extraction with chloroform. The appearance of reddish brown color for terpenoids and green to pink color for sterols was noted after treatment of chloroform layer with acetic anhydride and concentrated HCl in series. Anthraquinones were determined by the process of dissolving the extract in 1% of HCl, then benzene and finally mixing with NH4OH. The presence of anthraquinones was observed by appearance of pink, red or violet color.

The Presence of saponins was detected by the formation of froth bubbles in a beaker upon vigorous shaking using diluted samples.

Phytotoxicity (radish seeds) assay

The stock solution of each extract was prepared according the reported procedure [37]. A specific quantity, i.e. 50 mg of each extract was dissolved in 5 ml of methanol and 5 ml of n-hexane respectively in a beaker to obtain concentration of 10,000 μg/ml. Proper size filter papers (Whatman #1) were kept in the petri plates. The solution containing plant extract was added to the petri dishes. By keeping in laminar flow for a while the solvent get evaporated from the petri plates. Each petri dish was diluted with 5 ml of distilled water. Methanol, n-hexane and distilled water were used as control group. The seeds were sterilized with 0.1% mercuric chloride solution. Twenty five radish seeds were placed in each petri plate. All the petri plates containing the seeds were kept in incubator for five days at 25°C. The root length and number of seeds germination inhibition were measured and counted. All the tests were performed in triplicate.

Cytotoxicity (Brine shrimps lethality) assay

The cytotoxic effect against Artemia salina (brine shrimp eggs) of the Ir.Cr and various fractions (Ir.Hex, Ir.Chf, Ir.EtAc, Ir.Aq) and Ir.Sp were carried following the reported procedure [38].

Brine solution was prepared by dissolving 38 g of sodium chloride in double distilled water. The brine solution prepared was simulated sea water. A tray having dimensions of 22 × 32 cm was used in which a partition was created by a perforated plate. One side of the tray was covered by aluminum foil in which 50 mg Artemia salina eggs were sprinkled and the other side was kept as such to be the place for newly hatched brine shrimps larvae. The tray was kept in incubator at 37°C for hatching purpose. After 24 h when the larvae got hatched, it was attracted from dark side using torch and collected using a Pasteur pipette. 30 larvae were put in different vials. Three dilutions of the solution were made by dissolving 20 mg of the test sample in 2 ml of organic solvents and then by transferring 5, 50 and 500 μl of the stock solution into three different vials making 10, 100 and 1000 μg/ml concentrations respectively. To each vial sea water was added to adjust the volume 5 ml. Etoposide was used as positive control while for negative control sea water was used. The brine shrimps were kept in the vials for 24 h under light at 25°C. After 24 h, the number of brine shrimps alive and dead was counted in each vial using magnifying glass. The data was recorded in triplicate with the determination of LC50.

Statistical analysis

Each experiment was performed in replicates and values were expressed as mean ± SEM. Two way ANOVA followed by multiple comparison Bonferroni’s test were used to compare control group with the tested groups. The P values less than 0.05 were considered as statistically significant. IC50 values were calculated by a linear regression analysis among the percent inhibition against the extract concentrations via Microsoft Office Excel 2007 program.