Volatile compounds, antioxidants, and anticancer activities of Cape gooseberry fruit (Physalis peruviana L.): An in-vitro study

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Date: July-December 2015
Publisher: Medknow Publications and Media Pvt. Ltd.
Document Type: Report
Length: 5,983 words
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Byline: Manal. Ramadan, Ahmed. El-Ghorab, Kadry. Ghanem

Background/aim Cape gooseberry is golden-colored spherical fruit commercially produced in Egypt. It is primarily used in folk medicine for treating some diseases. To identify the aroma compounds in Cape gooseberry and to evaluate its antioxidant activities as well as its anticancer (for colon and breast cancers) effects in human cell lines. Materials and methods The volatile compounds were identified using gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). Polyphenols (phenolics and flavonoids) were also determined. Antioxidant activity was determined by three different methods: 2,2?-diphenyl-1-picrylhydrazyl (DPPH), 2,2-azinobis(3-ethyl-benzothiazoline-6-sulfonic acid) (ABTS), and ferric reducing antioxidant power (FRAP) assays. Anticancer (for colon or breast cancer) activity was determined in cancer cell lines using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. Results A total of 34 components of the essential oil were identified by GC and GC-MS. The volatile compounds were grouped in classes of substances, including 11 terpene compounds (six monoterpenoids and five sesquiterpene), 11 esters, five alcohols, two phenolic compounds, two aldehydes, two ketones, and one lactone. Terpenes (monoterpenes and sesquiterpenes) were the most abundant volatile constituents, accounting for the largest portion of the total volatiles (36.09%). The next most abundant compounds were esters, comprising 17.17% of the total volatile components identified. Phenolic compounds were the next most abundant compounds, comprising 16.04% of the total volatiles. Alcohols and aldehydes represented 6.37 and 1.88% of the total volatile compounds, respectively. Ketones and lactones are less abundant in the profile of volatile compounds in Cape gooseberry. Ethanol extract had higher phenolic and flavonoid contents than did hexane extract. As ethanol extract of Cape gooseberry achieved higher antioxidant activity than did hexane extract, it tested as an anticancer (for colon or breast cancer) agent. Cape gooseberry extract was more potent in inhibiting colon cell lines (IC [sub]50 : 142 [micro]g/ml) compared with breast cell line (IC [sub]50 : 371 [micro]g/ml). Conclusion Egyptian Cape gooseberry fruits may be suggested as a potential source of natural antioxidants and anticancer agents.


Functional foods represent an emerging market of growing economic importance. International markets exist for many exotic fruits, and recently the processing of tropical fruits started in many countries [sup][1] . In 2005, there were more than 1.8 million acres of berry crops worldwide including 966 acres of gooseberries [sup][2] .

Cape gooseberries are annuals or short-lived perennials, and are flavor and appearance, though the taste (sweet and sour) is much richer with a hint of tropical luxuriance. The plant is fairly adaptable to wide variety of soils and good crops are obtained on poor sandy ground [sup][1],[3] .

Cape gooseberry ( Physalis peruviana Linn., Solanaceae) has been grown in Egypt, South Africa, India, New Zealand, Australia, and Great Britain [sup][4],[5] . Cape gooseberry ( P. peruviana L.) is a cherry-sized, yellow-fleshed intriguing berry, which was originally cultivated in the Andes. The round orange fruit is loosely enclosed in a papery husk, which provides a natural wrapper for storing the fruit, as long as it is kept dry. Cape gooseberry is used in folk medicine for treating diseases such as malaria, asthma, hepatitis, dermatitis, diuretic, and rheumatism [sup][6],[7] .

Many medicinal properties have been attributed to Cape gooseberry, including antiasthmatic, antiseptic, and strengthener for the optic nerve, and it is used in the treatment of throat affections and elimination of intestinal parasites, amoebas as well as albumin from kidneys. It has an antiulcer activity and it is effective in reducing cholesterol level [sup][8],[9] . Berries have been shown to provide significant health benefits because of their high antioxidant content [sup][2] .

In addition to having a future as a fresh fruit, the fruit can be consumed in many ways as an ingredient in salads, cooked dishes, dessert, jam, natural snack, and preservers. Its extract can also be used for preparing a health drink [sup][5] . This will be important as an indication of the potentially nutraceutical and economical utility of Cape gooseberry as a new source of bioactive phytochemicals and functional foods. The extracts can provide a cheap and sustainable method toward disease reduction and can eventually improve the quality of life of the rural and periurban poor in developing countries [sup][10] .

Aroma and flavor are among the most important attributes and quality criteria that affect the consumption of fruits, and both qualitative and quantitative information is desired for characterizing aroma-producing compounds [sup][11] . However, many synthetic antioxidants used in foods, such as butylated hydroxyanisole and butylated hydroxytoluene, may accumulate in the body, resulting in liver damage and carcinogenesis [sup][12] . For this reason, more attention has been paid to natural nontoxic antioxidants in an effort to protect the human body from free radicals and retard the progress of many chronic diseases, especially cancer. Recently, it was found that many natural extracts from plant sources posses high antioxidant activity and play an excellent role as free radical scavengers in human body [sup][13],[14],[15] .

Natural extracts from different plants growing in Egypt posses high antioxidant activity and high content of phytochemicals [sup][16],[17],[18] . According to our knowledge, very little information exists regarding the chemical composition of volatiles and antioxidant activity as well as bioactive effects of Egyptian Cape gooseberry extracts. Thus, this study has four main objectives:

*To identify the volatile compounds of Egyptian Cape gooseberry fruits by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS); *To determine phenolic and flavonoid content of the Cape gooseberry fruit extracts; *To evaluate the antioxidant capacity of its extracts by three different methods; and *To evaluate the anticancer (breast and colon) cell lines of its extract.Methods


Egyptian Cape gooseberries ( P. peruviana L.), widely cultivated in Nil Valley, were obtained from a local market of Cairo (Egypt). Completely healthy fruits were selected and analyzed as a whole.

Extraction of volatile components

Cape gooseberry fruits were cut to small pieces with a knife and blended for 3 min with a blender (Moulinex, France). Tissues of Cape gooseberry fruits were rapidly juiced and the volatiles were isolated using a dynamic headspace system. The sample was purged for 3 h with nitrogen gas at a flow rate 100 ml/min. The headspace volatiles were swept into cold traps containing diethyl ether and held at −10[degrees]C. The volatile extracts were dried over anhydrous sodium sulfate for 1 h, and then reduced to 1 ml by using rotary evaporator (Heidolph, Germany) [sup][19] .

Identification of volatile compounds

Gas chromatography analysis About 2 [micro]l of each pure volatile oil was used. GC analysis was performed by using Hewlett-Packard model 5890 (Hewlett-Packard, Perkin elmer Co., USA) equipped with a flame ionization detector. A fused silica capillary column DB-5 (Zebron Co., USA) (60 m x 0.32 mm, internal diameter) was used. The oven temperature was maintained initially at 50[degrees]C for 5 min, and then programmed from 50 to 250[degrees]C at a rate of 4[degrees]C/min. Helium was used as the carrier gas, at a flow rate of 1.1 ml/min. The injector and detector temperatures were 220 and 250[degrees]C, respectively. The retention indices (Kovats index) of the separated volatile components were calculated using hydrocarbons (C7-C21; Sigma-Aldrich Co.) as references [sup][20] .

Gas chromatographic-mass spectrometric analysis

The analysis was carried out by using a coupled GC Hewlett-Packard model 5890/MS Hewlett-Packard MS 5970 (Hewlett-Packard). The ionization voltage was 70 eV, and the mass range m / z was 39-400 a.m.u. The isolated peaks were identified by matching with data from the library of mass spectra (National Institute of Standard and Technology), and compared with those of authentic compounds and published data. The quantitative determination was carried out on the basis of peak area integration. Identification of the GC components was also confirmed with the help of National Institute of Standard and Technology mass spectra library data, as well as on comparison of their retention indices with those of authentic compounds [sup][20] .

Preparation of extracts of Cape gooseberry fruits

Nonvolatile (phenolics and flavonoids) compounds were extracted from Cape gooseberry fruits with a modification, as reported by Rajeswari et al . [sup][21] . Two different solvents (hexane and ethanol) were used for preparation of two different extracts. Briefly, 100 g fresh fruits were cut into small pieces and extracted using 500 ml hexane. In another flask, the same amount (100 g) of fresh fruits were extracted with the same volume (500 ml) of 95% ethanol. Two flasks were shaken every hour for the first 6 h and then were kept aside, and again shaken after 24 h. The solvent layer was separated from the solid residue by centrifuging at 2000 g for 10 min. The clear supernatant was transferred to a clean rounded flask and evaporated using a vacuum evaporator at less than 50[degrees]C. The extract concentrated to 2 ml was stored at −20[degrees]C until samples were subjected to the following:

Determination of phenolic and flavonoid content

The phenolic content was determined according to the Folin-Ciocalteu procedure [sup][22] . It was determined by means of a calibration curve prepared with gallic acid, and expressed as mg of gallic acid equivalent/ml of sample. The total flavonoid content was determined as reported by Thaipong et al . [sup][22] , and was expressed as mg of catechin equivalent/ml of sample.

Determination of antioxidant activity

Determination of radical 2,2?-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity

The DPPH assay was carried out as reported by Thaipong et al . [sup][23] . The antioxidant activity was determined by means of a calibration curve prepared with ascorbic acid, and expressed as mg of ascorbic acid equivalent/ml of sample.

2,2-Azinobis(3-ethyl-benzothiazoline-6-sulfonic acid) (ABTS) assay : For ABTS assay, the procedure followed the method described by Arnao et al. [sup][24] . Results were expressed in mmol/l Trolox equivalents (TE)/ml extract. Additional dilution was needed if the ABTS value measured was over the linear range of the standard curve.

Ferric reducing antioxidant power (FRAP) assay : The FRAP assay was carried out according to Benzie and Strain [sup][25] . Results were expressed in mmol/l TE/ml extract. Additional dilution was needed if the FRAP value measured was over the linear range of the standard curve.

Anticancer activity: cell cultures and treatments

Human breast cancer cell line (MCF-7) and colon cancer cell line (Caco-2) were obtained from the American Type Culture Collection (Rockville, Maryland, USA). Cells were grown in RPMI-1640 medium supplemented with 10% fetal bovine serum, 1% nonessential amino acid solution, and 1% penicillin-streptomycin solution (10 000 U of penicillin and 10 mg of streptomycin in 0.9% NaCl) in a humidified atmosphere of 5% CO [sub]2 , 95% air at 35[degrees]C. The passage number range for both cell lines was maintained between 20 and 25. The cells were cultured in 75 cm [sup]2 cell culture flasks. For experimental purposes, cells were cultured in 96-well plates (0.2 ml of cell solution/well). The optimum cell concentration as determined by the growth profile of the cell line was 2 x 10 [sup]5 cells/ml (cells were allowed to attach for 24 h before treatment with tested extracts). The stock solution was filtered with Minisart Filters Merck (Darmstadt, Germany) (0.22 [micro]m). Working two-fold serially diluted test material (1, 2, 5, 10, 20, 40, 80, 162, 325, 750, 1500, and 3000 [micro]g/ml) were prepared. Cell monolayers were washed with PBS and the additional serially diluted materials were dispensed to the precultured plates for the determination of test material's toxicity [sup][26] .

3-(4,5-Dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay : The MTT assay is based on the protocol described for the first time by Mossmann [sup][27] . The assay was optimized for the cell lines used in the experiments. Briefly, for the purposes of the experiments at the end of the incubation time, cells were incubated for 4 h with 0.8 mg/ml of MTT dissolved in serum-free medium (MEM or DMEM for MCF-7 and Caco-2 cells, respectively). Washing with PBS (1 ml) was followed by the addition of DMSO (1 ml), and gentle shaking for 10 min so that complete dissolution was achieved. Aliquots (200 [micro]l) of the resulting solutions were transferred in 96-well plates, and absorbance was recorded at 560 nm using the microplate spectrophotometer system (SpectraMax 190; Molecular Devices, Germany). Results were analyzed with the SoftMax Pro Software, Germany (version 2.2.1) and were presented as percentage of the control value. The relation between surviving fraction and extract concentration was plotted to get the survival curve for the cell line after the specified time. The concentration required for 50% inhibition of cell viability (IC [sub]50 ) was also calculated [sup][27] .

Statistical analysis

The experiments were carried out at least three times, and the results were presented as mean [+ or -] SD. Statistical differences were analyzed by using the one way ANOVA test.


Gas chromatography and gas chromatographic-mass spectrometric analysis

A total of 34 components were identified by GC and GC-MS analysis. The volatile compounds were grouped in classes of substances, including 11 terpene compounds (six monoterpenes and five sesquiterpenes), 11 esters, five alcohols, two phenolic compounds, two aldehydes, two ketones, and one lactone, as shown in [Table 1]. Terpenes (monoterpene: 20.81% and sesquiterpene: 15.28%) were the most abundant volatile constituents, accounting for the largest portion of the total volatiles (36.09%). Citronellyl acetate, followed by d-muurolene, verbenone, and [sz]-bisabolol were the terpenes found in highest concentration. The next most abundant compounds were esters, comprising 17.17% of the total volatile components identified. Methyl butanoate, followed by propyl hexanoate, phenyl ethyl benzoate, neryl acetate, and ethyl benzoate were the esters found in the highest concentration. Phenolic compounds were the next most abundant compounds, comprising 16.04% of the total volatile components determined. Isoeugenol represented 14.76%, whereas 4-propyl guaiacol represented 1.28%. Alcohols represented 6.37%, whereas aldehydes represent 1.88% of the total volatile compounds. 2-Undecenal was the predominant aldehyde. 3,5-Octadienone was the major constituent among the ketones, which accounted for the 0.95% of the identified volatile constituents. Lactones comprised small part (0.76%) of the total volatiles identified.{Table 1}

Total phenolic and flavonoid content

The amounts of total phenols and flavonoids in the hexane and ethanol extracts of the Cape gooseberry fruits are shown in [Table 2]. The total phenolic contents of hexane and ethanol extracts of Cape gooseberries fruits were 30.0 [+ or -] 1.1 and 89.6 [+ or -] 2.1 mg gallic acid equivalent/ml extract. The total flavonoid contents of hexane and ethanol extracts of Cape gooseberries fruits were 21.3 [+ or -] 1.1 and 77.1 [+ or -] 3.1 mg catechin equivalent/ml extract.{Table 2}

Antioxidant activity

This study evaluated the role of gooseberry fruit extracts as antioxidants in vitro by using three different methods: ABTS, ferric reducing antioxidant power (FRAP), and DPPH [Table 3]. Data showed that ethanol extract exhibits stronger antioxidant activity than does hexane extract. Means of the antioxidant activity levels in ethanol extract were 1.785 [+ or -] 0.02 and 1.922 [+ or -] 0.03 mmol TE/ml extract as determined by ABTS and FRAB assays, and 2.016 [+ or -] 0.03 mg ascorbic acid equivalent/ml extract by DPPH assay, whereas means of the antioxidant activity in hexane extract were 0.611 [+ or -] 0.01 and 0.713 [+ or -] 0.02 mmol TE/ml extract by ABTS and FRAB assays and 0.903 [+ or -] 0.01 mg ascorbic acid equivalent/ml extract by DPPH assay, as shown in [Table 3]. Ethanol extract achieved the highest antioxidant activity as well as high total flavonoid and total phenolic content, and thus tested its activity as anticancer.{Table 3}

Anticancer activity of Cape gooseberry fruits

The Cape gooseberry ethanol extract showed growth inhibition as anticancer. The in-vitro cytotoxicity was performed against two different human cancer cell lines, namely breast (MCF-7) and colon (Caco-2). Comparison of the mean MCF-7 and Caco-2 cell viabilities analyzed using the MTT method indicated a significant difference between them ( P < 0.05). Increasing the dose significantly decreased the cell viability in both types of cancer cell lines. In the case of colon Caco-2 cell line, Cape gooseberry fruit extract showed maximum activity [Figure 1]. Cape gooseberry fruit extract was more potent in inhibiting colon cell lines (IC [sub]50 : 142 [micro]g/ml) compared with breast cell lines (IC [sub]50 : 371 [micro]g/ml) [Figure 2].{Figure 1}{Figure 2}


Total Cape gooseberry aroma is the result of the presence of different compounds such as alcohols, esters, terpenes, aldehydes, ketones, and lactones. Among them, esters are the most important group because they are responsible for fruity and fresh flavor [sup][28] . Our results are in agreement with a study conducted by Yilmatekin [sup][28] , which demonstrated the presence of esters, aldehyde, alcohols, terpenes, ketones, and lactones in Turkish Cape gooseberry. Terpenes were the most abundant volatile constituents derived by repetitive fusion of branched five carbon units based on isopentane skeleton. Many of them were volatile, such as monoterpenes (C [sub]10 ), and sesquiterpenes (C [sub]15 ).

Terpenes are derived either from mevalonate pathway, which is active in cytosol and starts from acetyl-CoA, or from methylerythritol-4-phosphate pathway, which is active in the plastids and starts from pyruvate and glyceraldehyde-3-phosphate [sup][29] . In contrast, the biosynthesis of some terpene-derived compounds can be explained by catabolic pathways in fruits. These are primarily oxidative degradation products of the carotenoids. Carotenoid oxidation occurs when the plant tissue is damaged or during ripening [sup][30] . Terpenes and their derivatives have been identified at varying levels in most of the soft fruits [sup][31] and they are responsible for the varietal character of the fruits being present, at least, in part, as glycosides [sup][32] .

They were reported as volatile components responsible for a wide spectrum of aromas (woody, piney, turpentine-like, herbaceous, and terpy), mostly perceived as very pleasant [sup][32],[33] . Esters contribute to the aroma of nearly all fruits and many other foods. Some are also responsible for the smell of a particular flower; however, many of these esters possess a nonspecific fruity odor. As the number of carbon atoms increases, the odor changes to fatty soapy and even metallic. The straight-chain ester constituents are believed to be synthesized through [sz]-oxidation of fatty acid, which may be then reduced to the corresponding alcohols before transesterification [sup][34] .

Alcohol acyltransferases are responsible for the transfer of alcohol to acyl-CoA, resulting in the synthesis of a wide range of esters [sup][32],[35],[36] . Aldehydes are common in fruit flavors and are believed to play an important role in many fruits [sup][37] . Fatty acids and amino acids are precursors of a great number of volatile aldehydes. Linoleic and linolenic acids in fruits and vegetables are subjected to oxidative degradation by lipoxygenase alone or in combination with a hydroperoxide lyase. The oxidative cleavage yields oxoacids, aldehydes, and allyl alcohols [sup][32],[38] . Ketones are less abundant in the profile of volatile compounds in Cape gooseberry. The ketones can be formed by condensation of activated fatty acids [sup][39] .

Lactones are produced in a very low amount by catabolic processes and originate from their corresponding hydroxyl carboxylic acids (4-hydroxy carboxylic acid or 5-hydroxy carboxylic acid) [sup][40] . These compounds, particularly g-lactones, are important in terms of their contribution to the aroma and, in general, present fruity odor descriptors [sup][33] . The odor of these lactones depends on the chemical structure, functional groups, and the length of side chains, and due to their low odor threshold, they have a high flavor value in fruits [sup][40] . Despite its importance, the literature about the flavor compounds of volatiles of Cape gooseberry ( P. peruviana L.) is scarce.

The results of the present study indicated that the ethanol extract has higher total phenolics content than does hexane extract ( P < 0.05). In addition, ethanol extract has higher total flavonoid compounds than does hexane extract. According to these results, there is a relationship between phenolic and flavonoid contents and radical scavenging activity. The differences in the amount of polyphenols may be due to varied efficiency of the solvents to dissolve endogenous compounds. Phenolic compounds, biologically active components, are the main agents that can donate hydrogen to free radicals and thus break the chain reaction of lipid oxidation at the first initiation step. This high potential of phenolic compounds to scavenge radicals may be explained by their phenolic hydroxyl groups [sup][41] . Various bioactive compounds (flavonoids and phenolics) are reported to be present in P. peruviana [sup][42] . Some of these compounds have a strong antioxidant property and prevent peroxidation [sup][43] .

It is very important to point out that there is a positive relationship between antioxidant activity potential and the amount of phenolic compounds of the extracts. From the phenol antioxidant index, a combined measure of the quality and quantity of antioxidants in vegetables has been obtained [sup][44] . Data showed that antioxidant activity of ethanol extract of gooseberry fruits increased ( P < 0.05) 2.921, 2.69, and 2.23 times that of hexane extract by ABTS, FRAB, and DPPH methods, respectively. These results are in agreement with studies conducted by Matkowski and Piotrowska [sup][45] and Li et al . [sup][46] .

Narvaez-Cuenca et al . [sup][47] indicated that gooseberry ( P. peruviana L.) has a high antioxidant activity. The high antioxidant capacity of the fruits is probably due to their richness in oxygenated monoterpene compounds. The stronger antioxidant activity exhibited by Cape gooseberries, in both the DPPH test and ABTS assay, confirms results showing that some of the oxygenated monoterpenes are mostly responsible for protective effects [sup][48] . The antioxidant activity of volatile compounds was variable; this variability is mainly related to their molecular composition.

Egyptian Cape gooseberry fruit content bisabolol compound is a monocyclic sesquiterpene alcohol. Baraga et al . [sup][49] showed that bisabolol has an antioxidant/anti-inflammatory activity. The antioxidants are an increasingly important ingredient in food processing. The most widely used synthetic antioxidants in food (butylated hydroxytoluene, butylated hydroxyanisole) are very effective in their role as antioxidants. However, their use in food products has been failing off because of their instability, as well as because of a suspected action as promoters of carcinogenesis [sup][50] . Consequently, there has been considerable interest in the use of antioxidant compounds from natural sources to exhibit different biological properties [sup][51] . They protect the human body from free radicals and retard the progress of many chronic diseases, especially cancer. In the present study, ethanol extract of Cape gooseberry fruit achieved higher antioxidant activity than did hexane extract, and thus tested as having anticancer activity.

Up to this day, in spite of the great nutritional value of Cape gooseberry fruit, studies about its effect on colon or breast cancer are scarce. According to WHO, 80% of the people living in rural areas depend on medicinal plants as primary healthcare system. The synthetic anticancer remedies are beyond the reach of common man because of the cost factor. Plant medicines have a vital role to play in the prevention and treatment of cancer, and medicinal plants are commonly available and comparatively economical [sup][52] .

Cape gooseberry fruit preparations can be used as a cheaper alternative to the conventional disinfectants. Cape gooseberry fruit is a storehouse of a good variety of compounds (phenolic, flavonoid, and volatile). Latest and previous studies have concluded the beneficial aspects of plant-derived drugs as good source of anticancer activity agents [sup][10] . Flavonoids are known for their immune-modulatory and anti-inflammatory activities, and inhibiting proinflammatory cytokine production and their receptors [sup][53] . Wu et al . [sup][54] reported that P. peruviana extract has anti-inflammatory activity. Supercritical carbon dioxide extracts of P. peruviana contained high levels of flavonoid and phenol. The extract demonstrated strong xanthine oxidase inhibitory effect. It prevented lipopolysaccharide-induced cell cytotoxicity in murine macrophage cells and remarkably blocked the lipopolysaccharide induction of inducible nitric oxide synthase and cyclooxygenase-2 expression [sup][54] . Cellular generation of free radicals has been associated with human disease states, such as inflammatory diseases, neurodegenerative diseases, cancer, and aging [sup][55] .

The results of the present study showed that citronellyl acetate possesses the highest concentration of terpenes in Cape gooseberry fruit. Citronellyl acetate, a monoterpene product of the secondary metabolism of plants, has been shown in the literature to possess several biological activities [sup][56] . Ethanol extract of P. peruviana inhibits growth and induces apoptotic death of human Hep G2 cells in culture. In addition, it possesses potent antihepatoma activity and its effect on apoptosis is associated with mitochondrial dysfunction [sup][4] .

Our results showed that terpenes (monoterpenes and sesquiterpenes) were in the highest concentration compared with other volatile compounds in Cape gooseberry fruit. Terpenes, one of the most extensive and varied structural compounds occurring in nature, display a wide range of biological and pharmacological activities. Terpenes have been shown to provide relevant protection under oxidative stress conditions in different diseases including liver, renal, neurodegenerative, and cardiovascular diseases, cancer, diabetes as well as in aging [sup][57] . Our results showed that isoeugenol was in the highest concentration of all other alcohols in Cape gooseberry fruit [sup][58] . Many studies have explored isoeugenol as an antiproliferative agent against malignant melanoma cells [sup][58] . The literature showed that eugenol possesses antioxidant, antimutagenic, antigenotoxic, anti-inflammatory, and anticancer properties [sup][59],[60],[61] . Kim et al. [sup][62] and Vidhya and Niramjli [sup][63] demonstrated eugenol-induced apoptosis in human melanoma and breast cancer cells.

In conclusion, Egyptian Cape gooseberry fruits may be suggested as a potential source of natural antioxidant and anticancer agents. This will be important as an indication of the potentially nutraceutical and economical utility of Cape gooseberry as a new source of bioactive phytochemicals and functional food. Future research should be carried out to evaluate its bioactive effects in vivo.


The authors extend appreciations to Dr Sameh Rada Hussein, Department of Phytochemistry and Plant Systemic, for his support.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.


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Gale Document Number: GALE|A443524746