Elephantorrhiza elephantina: Traditional Uses, Phytochemistry, and Pharmacology of an Important Medicinal Plant Species in Southern Africa.
Elephantorrhiza elephantina (Burch.) Skeels is a member of a small and purely African genus represented by nine species on the continent . Elephantorrhiza elephantina is the type species of the genus, where the generic name "Elephantorrhiza" means "elephant root" and is based, most descriptively, on the large underground stem common to most members of the genus . Four species in this genus, namely, E. burkei Benth., E. elephantina, E. goetzei (Harms) Harms, and E. suffruticosa Schinz, are highly regarded as medicinal plants in southern Africa [3-5]. Elephantorrhiza elephantina is an important plant resource in southern Africa, where it provides food and medicine for the indigenous people and the bark of its tuberous rhizome is a popular source of tanning and dyeing materials . The underground rhizomes, often referred to as roots, are one of the primary herbal medicines in southern Africa. Due to its popularity as herbal medicine, E. elephantina is sold as herbal medicine in the herbal medicine (muthi) markets in Botswana and Zimbabwe , the Eastern Cape province of South Africa [8, 9], Gauteng province , Limpopo province , and the Northern Cape province . According to Dold and Cocks , the average price of E. elephantina per kg in the Eastern Cape province is R30.80 (US$3.60) and 108.80 kg is the mean quantity sold per trader per year. Due to high demand of the species as herbal medicine and also because harvesters mainly target the rhizomes, E. elephantina is recorded in the Red Data List of Lesotho as data deficient by Talukdar  based on the utilization of the species as herbal medicine for stopping bleeding, treating syphilis and intestinal disorders. van Wyk  listed E. elephantina as a plant species of high importance with its roots having potential in the formulation of commercial herbal medicines as antioxidant, skin ailments, diarrhoea, perforated ulcers, prostrate hypertrophy, and male pattern baldness in South Africa. In South Africa, E. elephantina is used as a traditional remedy for a wide range of ailments, including diarrhoea and dysentery, stomach disorders, skin diseases and acne, haemorrhoids, and perforated peptic ulcers and as emetics . Rhizomes or bark of E. elephantina is crushed with some water added; the resulting paste is applied to hides to tan and dye them a reddish colour . The young shoots of E. elephantina are eaten by livestock and its seeds have a sweetish taste followed by a burning sensation and are often roasted in southern Africa as a coffee substitute .
With the increasing realization worldwide that traditional medicines based on indigenous medical systems are potential sources of natural products that can be developed into pharmaceutical drugs and health products , substantial efforts have been made to investigate ethnomedicinal uses, chemical constituents, and biological activities of E. elephantina during the last three decades. Unfortunately, no comprehensive review on this important plant species in southern Africa has been published, documenting the species' biology, traditional uses, phytochemistry, and pharmacological properties. Therefore, in this study, the advances in traditional utilization, botany, phytochemistry, pharmacology, and safety aspects of E. elephantina are systematically reviewed. In addition to this, the perspectives for the future research on E. elephantina are also discussed in the hope that the article will provide a better understanding of the plant species.
2. Methodology of the Review
The literature search was performed from March 2016 to January 2017 using electronic search engines such as Google and Google Scholar and publishing sites such as Elsevier, Science Direct, BioMed Central (BMC), and PubMed. The databases and literature sources were chosen based on the topics covered (i.e., biological activities, ethnobotany, ethnomedicinal uses, ethnopharmacology, pharmacology, phytochemistry, and therapeutic value) and geographical coverage (i.e., southern Africa). The following keywords were used to search literature sources: Acacia elephantina, Elephantorrhiza burchellii and Elephantorrhiza elephantina, dwarf elephant's root, eland's bean, eland's wattle, and elephant's foot. Other literature sources included papers published in international journals, reports from international, regional, and national organizations, conference papers, books, theses, websites, and other grey literature. References were also identified by searching the library collections of the National Herbarium and Botanic Gardens (SRGH), Harare, Zimbabwe, and the University of Fort Hare, South Africa.
3. Species Description
Elephantorrhiza elephantina has been recorded in southern Africa, that is, Namibia, Botswana, Zimbabwe, Mozambique, Swaziland, Lesotho, and South Africa. Elephantorrhiza elephantina is usually widespread, often gregarious and forming huge patches in hot and dry areas in grasslands and open scrub . Synonyms of E. elephantina are Acacia elephantina Burch. and Elephantorrhiza burchellii Benth. Elephantorrhiza elephantina is a perennial suffrutex or low shrub, producing annual stems up to 90 cm tall at ground level, from the woody end of an elongate, with often thickened rhizome up to 8 m long . Its leaves are alternate, bipinnately compound, almost glabrous with a petiole up to 8 cm long . The leaves consist of 2-4 pairs of pinnae in lower leaves and 7-17 pairs in upper ones, where the axis is up to 10 cm long. The leaflets are up to 55 pairs per pinna, linear to oblong in shape, 4-15 mm long and 0.50-2.50 mm wide with an asymmetric base, apex acute, and usually mucronate . Elephantorrhiza elephantina inflorescence is an axillary raceme, usually confined to the lower part of the stem usually solitary or clustered. The flowers are bisexual with red-brown glands at the base and free petals which are slightly connate at the base. The petals are linear-oblong, 2-4 mm long and about 1mm wide, and yellow-white in colour . The stamens are 10 which are free, with filaments up to 6.50 mm long . The fruit is a compressed-oblong, straight or slightly curved pod 5-21 cm long and 3-6 cm wide, red-brown in colour, prominently transversely veined, and often swollen over the seeds .
4. Vernacular Names of Elephantorrhiza elephantina
Elephantorrhiza elephantina is known by several vernacular names in its geographical areas of occurrence (Table 1). Literature survey showed no fewer than 41 common or vernacular names for E. elephantina in the seven countries where it is indigenous (Table 1). Local people rarely name plant species that they do not use . This list of common or vernacular names implies that local people in southern Africa have an active interest in E. elephantina. South Africa has the highest number of common or vernacular names (21 in total) followed by Botswana (seven), Namibia (five), and Zimbabwe with four names and the rest of the countries have either one or two names (Table 1). A vernacular name often describes some characteristic feature of the plant species or the plant parts, for example, "eland's bean" (an eland is an indigenous gazelle species); "elandsboontjie"; "eland's wattle"; "elephant's foot"; "elephant-root"; or "dwarf elephant's root" (Table 1). Elephantorrhiza elephantina is commonly referred to as "elandsboontjie" in Afrikaans in South Africa and "eland's bean' and "eland's wattle" in English in Namibia and South Africa because elands feed on the species foliage and pods . The other English common names, "elephant's foot" and "elephant-root," are in reference to large and long rhizomes or roots of the species measuring up to 8 m long . The common name "dwarf elephant's root" is in reference to the height of E. elephantina, which rarely exceeds one metre in height [17, 20] in comparison to a closely related species E. goetzei also known as "elephant's root" but averaging seven metres in height [5, 6].
5. Ethnomedicinal Uses of Elephantorrhiza elephantina
The rhizome, roots, leaves, and stems of E. elephantina are reported to possess diverse medicinal properties and are used to treat or manage various human and animal ailments and diseases throughout its distributional range in southern Africa (Table 2). A total of 42 and 14 human and animal ailments and diseases, respectively, are treated by herbal medicines prepared from E. elephantina (Table 2). These reports are from all the countries where E. elephantina is indigenous. The country with the highest ethnomedicinal uses is South Africa (45) based on 25 literature records, followed by Lesotho with ten uses and two literature records, Botswana with nine uses and four literature records, Mozambique and Zimbabwe with five uses and two literature records each, and Namibia and Swaziland with a single use and literature record each. Elephantorrhiza elephantina is mainly used to treat disorders of the gastrointestinal tract (21 citations in six countries), followed by veterinary medicine (14 citations in two countries), skin diseases (six citations from South Africa only), pain (five citations in five countries), and infertility and impotence (five citations in four countries). These records show high degree of consensus for the major diseases and ailments (Table 2) and imply high cross-cultural agreement among ethnomedicinal uses of E. elephantina throughout its distributional range.
The rhizome or root decoction of E. elephantina is used to relieve abdominal pains in Lesotho and Zimbabwe [3, 24] and chest pains in South Africa  and applied to open wounds to stop bleeding . In South Africa, roots and rhizomes of E. elephantina are boiled in water for external use to treat acne and other skin diseases [36-38] while roots and rhizomes of E. elephantina in combination with Pentanisia prunelloides (Klotzsch & Eckl. & Zeyh.) Walp. are used to treat eczema [36, 37]. Roots or rhizome decoction of E. elephantina is taken orally as remedy for various ailments and diseases including anemia in Mozambique , blood pressure, clearing air canal, erectile dysfunction, haemorrhoids, itching, kidney failure, intestinal disorders, menstrual disorders, peptic ulcers, rheumatic conditions, shingles, sores, syphilis, and tonsillitis in South Africa [4, 12, 15, 31, 38, 44, 47, 48, 50]. In Botswana, rhizome or root powder of E. elephantina is used to wipe the anus of children with bloody diarrhoea, to clean the womb after abortion, as remedy for early menstruating children, earache, erectile dysfunction, and sexually transmitted infections [21, 40, 41]. In Lesotho, rhizome decoction of E. elephantina is used to cleanse blood, as remedy for breast cancer, herpes, infertility, intestinal disorders, stomach problems, syphilis, and tuberculosis [24, 39]. Leaf, rhizome, and root decoction of E. elephantina are used as remedy for diarrhoea and dysentery in Mozambique  and South Africa [15, 28, 29, 32, 38, 44,46]. In some cases in South Africa, the rhizome of E. elephantina is mixed with Acokanthera oblongifolia Benth. & Hookf. ex B.D. Jacks root as remedy for diarrhoea and stomach ailments in South Africa . In Mozambique, root decoction of E. elephantina is taken orally as a pain killer  and for sexually transmitted infections .
Elephantorrhiza elephantina root decoction is taken orally as emetics for fever in Mozambique  and South Africa . The rhizome of E. elephantina is mixed with roots of Pentanisia prunelloides and taken orally as remedy for fever and stomach ailments in Zimbabwe . Elephantorrhiza elephantina is an ingredient of a herbal mixture known as "Sejeso" (Ingwe[R] brand) made up of Alepidea amatymbica Eckl. & Zeyh., Hypoxis obtusa Burch. ex Ker Gawl., Pentanisia prunelloides, deionized water, and potassium sorbate as preservative used as remedy for constipation, heartburn, indigestion, loss of appetite, stomach ailments, and vomiting . According to Semenya et al. , the rhizome of E. elephantina is mixed with roots of Boscia albitrunca (Burch.) Gilg & Gilg-Ben., Peltophorum africanum Sond., and Plectranthus ciliatus E. Mey. as remedy for HIV/AIDS opportunistic infections. Research by de Wet et al.  revealed that E. elephantina root decoction is taken orally in combination with Cladostemon kirkii (Oliv.) Pax & Gilg (roots), Drimia delagoensis (Baker) Jessop (bulb), Sarcophyte sanguinea Sparm. ssp. piriei (Hutch.) B. Hansen (bark), and Ranunculus multifidus Forssk (whole plant) as remedy for shingles. Research by de Wet et al.  also revealed that E. elephantina root decoction is taken orally in combination with Cladostemon kirkii (root), Drimia delagoensis (bulb), Ficus sur Forssk. (bark), Ranunculus multifidus (whole plant), Sarcophyte sanguinea ssp. piriei, and Senecio serratuloides DC. (leaves) as remedy for sores.
Rhizome decoction of E. elephantina is widely used by small-scale farmers in Botswana and South Africa as ethnoveterinary medicine for poultry and retained placenta in cattle and as ethnoveterinary medicine for other animals such as goats, horses, pigs, and sheep and for diseases such as black quarter, appetite stimulant, coughing, diarrhoea, gastrointestinal parasites, gall sickness, heartwater, mange, pneumonia, and ectoparasites [22, 23, 27, 30, 33, 48, 52, 53]. The young shoots of E. elephantina are eaten by livestock and wild animals in southern Africa . In Namibia, the pods of E. elephantina are eaten by both people and animals .
Multiple classes of phytochemicals including anthocyanidins, anthraquinones, esters, fatty acids, phenolic compounds, flavonoids, glycosides, polysterols, saponins, sugars, tannins, and triterpenoids have been isolated from rhizome extracts of E. elephantina [41, 54-57]. Considerable pharmacological potential of E. elephantina has been documented through detection, isolation and purification of its natural products via advances in spectrometric techniques such as attenuated total reflection (ATR), Fourier transform infrared (FTIR) spectroscopy, liquid chromatography electron spray ionization mass spectroscopy (LC-ESI-MS), gas chromatographymass spectrometry (GC-MS), and nuclear magnetic resonance (NMR) for structural elucidation of new and complex compounds (Table 3). Advanced research through ATR, LCESI-MS, FTIR, GC-MS, and NMR spectroscopy enabled researchers to have a better understanding of the correlations between molecular conformation and biological activities of the natural compounds of E. elephantina and its importance as herbal medicine. The compounds isolated from E. elephantina are documented and listed in Table 3 and their structures are displayed in Figure 1. Aaku et al.  isolated the following compounds from n-butanol rhizome extracts of E. elephantina: dihydrokaempferol 1, kaempferol 2, (-)-catechin 3, ethyl gallate 4, gallic acid 5, 2-(3,4-dihydroxyphenyl) ethanol 6, 4-hydroxybenzoic acid 7, ethyl-1-O-[beta]-D-galactopyranoside 8, and quercetin 3-O-[beta]-D- glucopyranoside 9. Phytochemical study of E. elephantina rhizomes by Mthembu  showed the presence of several phenolic compounds including catechin 3, gallic acid 5, quercetin 3-O-[beta]-D-glucopyranoside 9, methyl gallate 10, [beta]-sitosterol 11, 3-O-galloyl-3,3',5,5',7-pentahydroxyflavone 12, taxifolin-3'-O-[beta]-D-glucoside 13, and epicatechin 14. Recently, Msimanga et al.  isolated the following compounds from hexane root extracts of E. elephantina: hexadecanoic 15, 9,12-octadecadienoic 16, 9-octadecenoic 17, octadecanoic acid 18, butanedioic acid 19, benzoic acid 20, 3phenyl-2-propenoic acid 21, nonanedioic acid 22, tridecanoic acid 23, methyl pentadecanoate 24, methyl hexadec-9-enoate 25, methyl hexadecanoate 26, methyl 3-(3,5-di-tert-butyl4-hydroxy- phenyl)propionate 27, cis-10-Heptadecenoic acid 28, methyl heptadecanoate 29, methyl octadecanoate 30, cis-5,8,11,14,17-eicosapenta-enoic acid 31, eicosanoic acid 32, methyl tetracosanoate 33, pentacosanoic acid 34, hexacosanoic acid 35, methyl octacosanoate 36, and tetradecanedioic acid 37. The phytochemical studies of the rhizome extracts of E. elephantina carried out by Mpofu et al.  showed the presence of anthraquinone 38, triterpenoids oleanolic acid 39, diosgenin 40, rhamnose 41, glucuronic acid 42, and arabinose 43. In another phytochemical evaluation of E. elephantina rhizome extracts, Mpofu et al.  isolated kaempferol 2, epicatechin 14, glucuronic acid 42, arabinose 43, epigallocatechin gallate 44, quercetin 45, and epicatechin gallate 46. The major phytochemical compounds isolated from E. elephantina are mainly fatty acids (39.13% of all known compounds isolated from the species), followed by phenolic compounds (26.09%) and esters (13.04%) and the contribution of the rest of the compounds is less than 10% each; see Table 3.
7. Pharmacological Activities
A number of pharmacological activities of E. elephantina have been reported in literature corroborating some of the ethnomedicinal uses listed in Table 2. Some of the pharmacological activities of E. elephantina listed in literature include anthelmintic [58-60], antibacterial [21, 28, 41, 43, 50, 61], antifungal [21, 41, 50, 61], anti-inflammatory and antinociceptive , antiplasmodial , antioxidant , and antibabesial and antirickettsial [64, 65] activities.
7.1. Anthelmintic Activity. Maphosa et al.  evaluated in vitro anthelmintic activities of crude aqueous extracts of E. elephantina roots on the eggs and larvae of the nematode parasite Haemonchus contortus using Valbazen[R] (11.36% albendazole) at 10 mg/kg and 0.5 mL/kg distilled water as positive and negative controls, respectively. Elephantorrhiza elephantina had 100% egg hatch inhibition at a concentration as low as 2.5 mg/mL. At the lowest concentration of 0.63 mg/mL tested, E. elephantina inhibited egg hatching by >96% and this was comparable to albendazole at the same concentration . Elephantorrhiza elephantina had complete inhibition of larval development at a concentration of 1.25 mg/mL . This study by Maphosa et al.  demonstrated that inhibition of egg hatching and larval development increased significantly with increasing concentration of E. elephantina root extract. In another study, Maphosa and Masika  evaluated efficacy of E. elephantina aqueous root extracts in naturally mixed infections of gastrointestinal worms and Coccidia species in goats that had not been dosed for a period of two months, using Valbazen (11.36% albendazole) at 10 mg/kg and 0.5 mL/kg distilled water as positive and negative controls, respectively. In this study, E. elephantina caused reduction of Trichuris eggs on days 3 and 6 at 250 mg/kg dose. This study also revealed efficacy of E. elephantina against strongyle and Eimeria spp. at 500 mg/kg. The reduction in faecal egg counts in dosed extracts with E. elephantina against mixed gastrointestinal parasite infections shows that this species possess anthelmintic properties and there is credence in its ethnoveterinary use against gastrointestinal parasites in goats. In another study, Maphosa and Masika  evaluated anthelmintic activity of aqueous, hexane, and ethyl root extract of E. elephantina against adult Haemonchus contortus using a bioactivity-guided assay with albendazole and distilled water as positive and negative controls, respectively. The aqueous and ethyl acetate fractions showed high motility inhibition at concentrations of 2.50 mg/mL and above after 6-hour exposure, while the hexane fraction showed motility inhibition at concentrations of 5 mg/mL and above. After 30-hour exposure, all the fractions, that is, aqueous, hexane, and ethyl acetate fractions, and albendazole (commercial drug) showed inhibition of motility and the mortality indexes were not significantly different from each other . All the anthelmintic evaluations carried out so far [58-60] confirmed the anthelmintic activities of the root of E. elephantina, a plant species widely used as anthelmintic remedy by small-scale farmers in South Africa.
7.2. Antibacterial Activity. Aaku et al.  evaluated the antibacterial activity of 70% ethanol and n-butanol rhizome extracts of E. elephantina using the thin-layer chromatography (TLC) bioautography technique with chloramphenicol and miconazole as positive and negative controls, respectively. Both extracts showed activity against Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus at loadings lower than 15 [micro]g. Among the purified compounds, only ethyl gallate 4 and gallic acid 5 showed activity against Bacillus subtilis and Staphylococcus aureus at loadings lower than 50 [micro]g. Similar results were obtained by Cueva et al.  who assessed the influence of pure phenolic compounds such as catechin 3, ethyl gallate 4, gallic acid 5, and epicatechin 14 on the inhibition of the growth of potential respiratory pathogens. These authors found that nonflavonoid compounds such as ethyl gallate 4 and gallic acid 5 were more active than flavonoids such as catechin 3 and epicatechin 14.
Mathabe et al.  evaluated the antibacterial activities of aqueous, acetone, ethanol, and methanol root extracts of E. elephantina against bacteria that cause gastrointestinal infections, namely, Staphylococcus aureus, Vibrio cholerae, Shigella dysentery, Shigella sonnei, Shigellaflexneri, and Shigella boydii, and the minimum inhibitory concentration (MIC) of active extracts was determined by the microplate dilution assay. Mathabe et al.  used ten microliters of dimethyl sulfoxide (DMSO) per well as negative control while discs (5 mm in diameter) of nalidixic acid (30 mg), erythromycin (15 mg), and cotrimoxazole (25 mg) were used as positive controls. MIC activities against the pathogens ranged between 0.08 and 0.63 mg/mL, and the highest inhibition was exhibited against Shigella flexneri with MIC values ranging from 0.08 to 0.16mg/mL , and these findings somehow confirm the species' antibacterial potential and its usefulness in the treatment and management of gastrointestinal infections. Mukanganyama et al.  evaluated antibacterial activities of ethanol root extracts of E. elephantina against Bacillus cereus, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus using the agar diffusion assay. The species exhibited antibacterial properties against all microorganisms tested and the authors assessed the minimal inhibitory concentrations (MICs) against Mycobacterium aurum, where E. elephantina showed some activity with MIC value of 1.25 mg/mL .
Mabona et al.  evaluated antibacterial activities of aqueous and dichlomethane/methanol (1: 1) leaf, root, and rhizome extracts of E. elephantina using the micro-titre plate dilution technique against dermatologically relevant pathogens such as Brevibacillus agri, Propionibacterium acnes, Pseudomonas aeruginosa, Staphylococcus aureus and Staphylococcus epidermidis with ciprofloxacin as positive control and acetone and dimethyl sulfoxide (DMSO) as negative controls. Mabona et al.  found varied antibacterial activities of the aqueous and dichlomethane/methanol (1: 1) leaf, root and rhizome extracts with minimum inhibition concentration (MIC) ranging from 0.05 to >16.00 mg/mL. Antibacterial activities were displayed by dichlomethane/methanol leaf, root and rhizome extracts against Propionibacterium acnes (MIC values ranging from 0.05 to 1.00 mg/mL), Staphylococcus aureus (0.50 mg/mL) and Staphylococcus epidermis (0.38 to 1.00 mg/mL) as well as aqueous and dichlomethane/methanol root and rhizome extracts against Brevibacillus agri with MIC value of 0.50 mg/mL. The leaf, root and rhizome extracts of E. elephantina are reported to be traditionally used to treat acne vulgaris and pimples and such usage was corroborated by noteworthy activity against Propionibacterium acnes with MIC values between 0.05 and 2.0 mg/mL . Propionibacterium acnes is an important skin pathogen responsible for the chronic inflammatory disease of the sebaceous glands and hair follicles of the skin . The aqueous root extracts of Pentanisia prunelloides combined (1 : 1) with E. elephantina displayed synergistic interactions with sum of the fractional inhibitory concentration (ZFIC) values ranging from 0.31 to 0.38 mg/mL against Staphylococcus aureus and Staphylococcus epidermidis. The synergistic interactions noted for Pentanisia prunelloides and E. elephantina by Mabona et al.  validate their antibacterial effects as these two species are often used in combination as herbal medicines for treating microbial infections in southern Africa. Similarly, Nciki et al.  evaluated antibacterial activities of aqueous and dichlomethane/methanol (1: 1) root extract of E. elephantina using the micro-titre plate dilution technique against dermatologically relevant pathogens such as Brevibacillus agri, Escherichia coli, Propionibacterium acnes, Pseudomonas aeruginosa, Staphylococcus aureus and Staphylococcus epidermidis with ciprofloxacin as positive control. Best antimicrobial results were demonstrated by dichlomethane/methanol extracts against Escherichia coli with MIC value of 130 [micro]g/mL, Brevibacillus agri (MIC value of 250 [micro]g/mL), Propionibacterium acnes (MIC value of 250 [micro]g/mL) and Pseudomonas aeruginosa with MIC value of 250 [micro]g/mL . Nciki et al.  and Mabona et al.  obtained similar results in terms of overall antibacterial activities displayed against Brevibacillus agri, Propionibacterium acnes and Pseudomonas aeruginosa although Nciki et al.  also assessed the antibacterial activities of E. elephantina against Escherichia coli. Nciki et al.  assessed antibacterial activities of aqueous and dichlomethane/methanol (1: 1) root extracts of E. elephantina while Mabona et al.  assessed antibacterial activities of other plant parts which included leaves and rhizomes. Therefore, the results obtained by both Nciki et al.  and Mabona et al.  provide a scientific rational for the traditional use of E. elephantina as herbal medicine against several skin infections in South Africa such as acne [15,36-38], eczema [36,37], itching , sores [50,51] and sunburn [15, 38].
Mpofu et al.  evaluated antibacterial activity of the methanol and aqueous rhizome extracts of E. elephantina using the micro-titre plate dilution technique against Bacillus cereus, Enterococcus faecalis and Escherichia coli with ciprofloxacin as positive control and distilled water and dimethyl sulfoxide (DMSO) as negative controls. The minimum inhibitory concentration (MIC) values for the aqueous (0.50-2.00 mg/mL) and methanol (0.20-4.00 mg/mL) extracts independently demonstrated varied efficacies depending on the pathogen of study. Mpofu et al.  also evaluated the antibacterial activity of E. elephantina with Pentanisia prunelloides combined in 1 : 1 ratios, displaying synergistic interactions with sum of the fractional inhibitory concentration ([SIGMA]FIC) values ranging from 0.19 to 1.00 mg/mL for aqueous extracts and 0.60 to 0.80 mg/mL for methanol extracts against Bacillus cereus, Enterococcus faecalis and Escherichia coli. The antibacterial activity of E. elephantina in combination with Pentanisia prunelloides were determined as a validation of their combined use in southern African traditional medicine. Mpofu et al.  also evaluated the antibacterial activity of epicatechin 14 and hexadecanoic acid 15 isolated from E. elephantina rhizomes using the microtitre plate dilution technique against Bacillus cereus, Enterococcus faecalis and Escherichia coli with ciprofloxacin as positive control and distilled water and dimethyl sulfoxide (DMSO) as negative controls. The efficacy for the two compounds measured via MIC values ranged between 0.13 and 0.63 mg/mL, while synergistic interactions were noted against Escherichia coli and Enterococcus faecalis with ([SIGMA]FIC) values of 0.09 mg/mL and 0.50 mg/mL, respectively . Therefore, the two compounds epicatechin 14 and hexadecanoic acid 15 showed synergistically enhanced activity especially against Escherichia coli and Enterococcus faecalis. Furthermore, previous studies have shown that hexadecanoic acid 15 is active against various bacterial strains  including Escherichia coli  and epicatechin 14 is also active against Escherichia coli and can play an important role in developing pharmaceutical drugs against urinary tract infections . Epicatechin 14 has also been implicated for antibacterial activity against Escherichia coli, Bacillus cereus, Staphylococcus aureus, and Shigella flexneri at minimum inhibition concentration (MIC) values ranging from 12.50 to 100 mg/mL [70,71]. The antibacterial potency of this compound isolated from E. elephantina is noteworthy as the species is administered as a remedy by traditional healers in Botswana [40, 41], Mozambique , South Africa [15, 28, 29, 32, 38, 44, 46], and Swaziland . These results support the traditional use of E. elephantina in treating bacterial infections such as diarrhoea and sexually transmitted infections.
7.3. Antifungal Activity. Aaku et al.  evaluated the antifungal activity of 70% ethanol and n-butanol rhizome extracts of E. elephantina using the TLC bioautography technique with chloramphenicol and miconazole as positive and negative controls, respectively. Both extracts showed activity against Candida mycoderma at loadings lower than 15 [micro]g. These results support the traditional use of E. elephantina in treating fungal infections associated with gastrointestinal tract infections. Mukanganyama et al.  evaluated antifungal activities of root ethanol extracts of E. elephantina against Candida albicans and Candida mycoderma using the agar diffusion assay. The species exhibited antifungal properties against both microorganisms tested and the authors assessed the minimal inhibitory concentrations (MICs) against Candida albicans and E. elephantina showed some activity with MIC value of 1.25 mg/mL . Mabona et al.  evaluated antifungal activities of aqueous and dichlomethane/methanol (1 : 1) extracts of E. elephantina using the microtitre plate dilution technique against dermatologically relevant pathogens such as Candida albicans, Microsporum canis, and Trichophyton mentagrophytes with amphotericin B as positive control and acetone and dimethyl sulfoxide (DMSO) as negative controls. Mabona et al.  found varied antifungal activities of the aqueous and dichlomethane/methanol (1:1) leaf, root, and rhizome extracts with minimum inhibition concentration (MIC) 0.05 to >16.00 mg/mL. Noteworthy antifungal activities were displayed by dichlomethane/methanol leaf, root, and rhizome extracts against Microsporum canis (0.50 mg/mL), Candida albicans (1.00 mg/mL), and Trichophyton mentagrophytes (1.00 mg/mL). The aqueous root extracts of Pentanisia prunelloides combined (1 : 1) with E. elephantina displayed synergistic interactions with sum of the fractional inhibitory concentration (ZFIC) values ranging from 0.31 to 0.38 mg/mL against Candida albicans. The synergistic interactions noted for Pentanisia prunelloides and E. elephantina by Mabona et al.  validate their antifungal effects as these two species are often used in combination as herbal medicines to treat skin infections. Similarly, Nciki et al.  evaluated antifungal activities of aqueous and dichlomethane/methanol (1: 1) root extract of E. elephantina using the microtitre plate dilution technique against dermatologically relevant pathogens such as Candida albicans, Microsporum canis, and Trichophyton mentagrophytes with amphotericin B as positive control. Best antifungal results were demonstrated by dichlomethane/methanol extracts against Candida albicans with MIC value of 130 [micro]g/mL, Microsporum canis (MIC value of 250 [micro]g/mL), and Trichophyton mentagrophytes with MIC value of 250 [micro]g/mL . It is important to note that Nciki et al.  assessed antifungal activities of root extracts only while Mabona et al.  evaluated antifungal roots, leaves, and rhizomes of E. elephantina. There are also differences in terms of best antifungal results documented in these two studies. According to Mabona et al.  the best antifungal activities were demonstrated by dichlomethane/methanol leaf, root, and rhizome extracts against Microsporum canis with MIC value of 0.50 mg/mL while best antifungal results obtained by Nciki et al.  were demonstrated by dichlomethane/methanol extracts against Candida albicans with MIC value of 130 [micro]g/mL. Overall, results obtained by Nciki et al.  and Mabona et al.  provide a scientific basis for the traditional use of E. elephantina as herbal medicine against several skin infections in South Africa such as acne [15, 36-38], eczema [36, 37], itching , sores [50, 51], and sunburn [15, 38].
7.4. Anti-Inflammatory and Antinociceptive Activities. Maphosa et al.  evaluated anti-inflammatory and antinociceptive activities of root extract of E. elephantina using Wistar rats. The authors evaluated anti-inflammatory activities using carrageenan and histamine-induced rat paw oedema while antinociceptive activity was evaluated by acetic acid-induced writhing test and formalin test. The aqueous extract of E. elephantina reduced the formation of oedema induced by carrageenan and histamine and caused reduction in writhings in the acetic acid test and licking time in the formalin test . According to Maphosa et al. , the root extract of E. elephantina reduced oedema and pain even better than the control, indomethacin, a potent inhibitor of prostaglandins (PG) synthesis, showing that the plant species has strong anti-inflammatory and antinociceptive activities. The anti-inflammatory activity displayed by root extract of E. elephantina could be due to anthraquinone 38, as previous research by Mishchenko et al.  showed that cell culture composed of anthraquinone 38 isolated from Rubia cordifolia L. exhibited anti-inflammatory activity, which is manifested by an antiexudative effect and antiproliferative action during the rapid development of a model edema. These results support the traditional use of the species in various inflammatory ailments and diseases ranging from microbial infections to sores and wounds that result in cell injury and pain.
7.5. Antiplasmodial Activity. Clarkson et al.  evaluated aqueous, dichloromethane, and dichlomethane/methane (1: 1) leaf and root extracts of E. elephantina for in vitro activity against Plasmodium falciparum using the parasite lactase dehydrogenase (pLDH) assay and chloroquine diphosphate (Sigma) as the positive control. The dichlomethane/methane (1: 1) leaf and root extracts showed weak activity with IC50 values of 26 and 28 [micro]g/mL, respectively, while aqueous extracts for both leaves and roots showed weak activity with [IC.sub.50] values >100 [micro]g/mL . Although E. elephantina is widely used as traditional remedy for fever in Mozambique , South Africa , and Zimbabwe , the species did not display promising in vitro antiplasmodial activity, to support its traditional usage in the management and treatment of fever. A possible explanation could be that E. elephantina act as antipyretics or immune stimulants to relieve the symptoms of the disease, rather than having direct antiparasitic activity . Alternatively, precursors of the active components may be present in E. elephantina extracts but have to be modified, usually in vivo, before activity is exhibited .
7.6. Antioxidant Properties. Mpofu et al.  evaluated antioxidant properties of E. elephantina using DPPH radical scavenging method with the yen and duh percentage inhibition values ranging from 33 to 72% for both methanol and aqueous extracts. This study carried out by Mpofu et al.  revealed that there were more extractable antioxidants using methanol compared to water as the solvent. The antioxidant activities demonstrated by E. elephantina rhizome extracts are probably due to the presence of flavonoids and phenolics . Antioxidant properties displayed by E. elephantina could be due to the compound ethyl gallate 4. Ethyl gallate 4 isolated from ethanol extract of Acacia nilotica Wild ex Del. subsp. indica (Benth.) Brenan leaves demonstrated antioxidant activities in several in vitro assays , revealing that the compound was a hydrogen donor, metal chelator, and free radical scavenger.
7.7. Antirickettsial and Antibabesial. Antibabesial and antirickettsial in vitro assay systems have been used to evaluate E. elephantina rhizome extracts. Naidoo et al.  used a cell culture-based antibabesial test, exposing Babesia caballi cultures to E. elephantina, and effectivity was established by the degree of inhibition using a colour change method as well as by evaluating percentage of parasitized cells on thin culture smears and calculating the degree of residual infectivity. The antibabesial drugs used as controls, imidocarb and diminazene, demonstrated efficacy, exhibiting [EC.sub.50] values of 0.08 and 0.30 [micro]g/mL, respectively. Similarly, E. elephantina acetone rhizome extract demonstrated activity at 100 [micro]g/mL. Acetone rhizome extracts of E. elephantina demonstrated significant activity against a tick-borne disease that is problematic to the livestock of South African farmers .
Naidoo et al.  evaluated the antirickettsial activity of leaf acetone extracts of E. elephantina in an in vitro Ehrlichia ruminantium culture system. Ehrlichia ruminantium cultures were incubated with acetone extracts of the leaves and results were compared to those obtained with oxytetracycline and untreated controls. Elephantorrhiza elephantina possessed antiehrlichial activity with [EC.sub.50] values of 111.40 [micro]g/mL and [EC.sub.90] values of 228.90 [micro]g/mL. The [EC.sub.50] and [EC.sub.90] values for oxytetracycline were 0.29 and 0.08 [micro]g/mL. These results demonstrate that E. elephantina leaf extracts may be inhibitory against the Ehrlichia parasite by a similar mechanism to each other, which was unrelated to the mechanism of action of the tetracyclines .
7.8. Toxicity. Despite the long use of E. elephantina as herbal medicine in southern Africa to treat numerous human and animal diseases and ailments, the species is known to be harmful when used at an excessive dosage [3, 4, 48]. Root infusions of E. elephantina have been reported to have constipating effects  while seeds are strongly irritant and have been suspected of causing human death when used as herbal medicine . According to Hutchings et al.  an aqueous extract of the seed equivalent to 0,75 g produced extensive necrosis at the point of injection and gastroenteritis and pulmonary oedema when injected subcutaneously in the guinea-pig. Symptoms of poisoning were apathy, loss of appetite, and profuse foetid diarrhoea with death occurring within twenty-four hours with the animal in a state of exhaustion. Postmortem examination revealed acute gastroenteritis with numerous haemorrhages and marked degeneration of the liver . Jansen  reported that the seeds of E. elephantina are toxic to sheep with a lethal dose 250 g and rabbits (lethal dose 5-7.50 g/kg) causing gastroenteritis and pulmonary oedema.
Preliminary acute toxicity evaluation of root extract of E. elephantina using Wistar rats showed no physiological and behavioural changes in the animals and also no mortalities were recorded . In another study, Maphosa et al.  evaluated the acute, subacute, and chronic toxicity of E. elephantina root extracts by oral route in male and female Wistar rats. The authors recorded no mortalities but changes in body weight and haematological and serum biochemical parameters between the control and treated animals were observed. In acute tests, Maphosa et al.  observed decreased respiratory rate at higher doses of 1600 mg/kg, and, in subacute tests, the root extract of E. elephantina caused an increase in white blood cells, monocytes, and serum levels of creatinine at higher doses of 400 and 800 mg/kg. In chronic toxicity, E. elephantina extracts caused increase in lymphocytes and platelets and changes were also noted in the body and organ weights in both subacute and chronic toxicities. Maphosa et al.  observed acute hepatitis, intracrystal deposition (reminiscent of oxalate crystals) with renal crystals and secondary ascending pyelonephritis in animals receiving 800 mg/kg in subacute toxicity tests while pulmonary granulomas were noted in animals which received 400 mg/kg. In chronic toxicity tests, Maphosa et al.  observed mild to moderate splenic siderosis, pulmonary granulomas, refractile crystal deposits, and associated ascending pyelonephritis. Mpofu et al.  evaluated cytotoxicity activity of E. elephantina using the brine shrimp lethality test. Chloroform rhizome extract of E. elephantina exhibited some degree of biological activity with [LC.sub.50] value of 0.80 . Based on toxicity evaluations done so far [54, 62, 76], it can be inferred that E. elephantina has some potential toxicity at certain dose levels and should be taken with caution when used as herbal medicine.
The present review summarizes the ethnomedicinal uses and recent findings on traditional uses, phytochemistry, pharmacology, and toxicity of different extracts and compounds of E. elephantina. Anthocyanidins, anthraquinones, esters, fatty acids, phenolic compounds, flavonoids, glycosides, polysterols, saponins, sugars, tannins, and triterpenoids have been demonstrated to be the main active ingredients of E. elephantina. Recent studies have focused on evaluating anthelmintic, antibacterial, antifungal, anti-inflammatory and antinociceptive, antiplasmodial, antioxidant, antibabesial, and antirickettsial activities of the different extracts and compounds isolated from the species. In the past 30 years, E. elephantina has been the subject of phytochemical and pharmacological research, and some of the traditional uses of this plant particularly against microbial infections and gastrointestinal parasites in animals have been validated by pharmacological studies. But there is not yet enough data on ethnopharmacological evaluation and clinical research on the species and few evaluations of target-organ toxicity have been documented. Most of the phytochemical and pharmacological evaluations have focused on rhizomes and roots of E. elephantina. The most important research gaps identified in this study are as follows:
(1) Since E. elephantina is widely used in combination with other plant species in various herbal concoctions, there is need for extensive research to evaluate synergistic effects of the different extracts or pure isolates to evaluate their ability to enhance the efficiency of the additive mixtures,
(2) Future research should also focus on aerial parts of the species in order to ensure full utilization of the possible medicinal potential of E. elephantina. There is need to investigate the chemical constituents and pharmacological effects of the bark, leaves, flowers, fruits, and seeds of E. elephantina.
(3) Literature studies show that the major phytochemical compounds isolated from E. elephantina so far are mainly fatty acids, phenolic compounds, and esters, but very little attempt has been made to correlate the activities of these compounds with the ethnomedicinal uses of the species. Therefore, there is need for further research on different compounds isolated from E. elephantina; examples include fatty acids and esters. Detailed phytochemical studies of E. elephantina and its pharmacological properties especially the mechanism of action of its bioactive constituents to illustrate the correlation between its ethnomedicinal uses and pharmacological activities should be the focus of future research studies.
(4) Extensive in vivo experiments are required to validate the existing pharmacological activities.
(5) Since E. elephantina contain potentially toxic compounds, future studies should include the identification of toxic compounds, possible side effects caused by taking E. elephantina as herbal medicine, and mechanisms of how potential toxic components of the species can be managed.
Conflicts of Interest
The author declares that there are no conflicts of interest regarding the publication of this paper.
The author would like to express his gratitude to the National Research Foundation (NRF) and Govan Mbeki Research and Development Centre (GMRDC), University of Fort Hare, for financial support to conduct this research.
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Department of Botany, University of Fort Hare, Private BagX1314, Alice 5700, South Africa
Correspondence should be addressed to Alfred Maroyi; firstname.lastname@example.org
Received 11 January 2017; Accepted 12 April 2017; Published 14 May 2017
Academic Editor: Sandy van Vuuren
Caption: Figure 1: Chemical structures of major compounds isolated from rhizomes or roots of Elephantorrhiza elephantina.
Table 1: Vernacular names of Elephantorrhiza elephantina. Vernacular name(s), ethnic group or Country References geographical region in brackets Elephant's foot (English), chizezana, Botswana [21-23] mosibe, mosidi, mositsane, mositsane tjizezana, motshijane (Setswana) Mositsane (Sotho) Lesotho  Xivurayi (Changana), dwarf elephant's Mozambique  root (English) Elandsboontjie (Afrikaans), eland's bean Namibia  (English), gerbwurzel (German), [??]an[??]gab (Khoekhoegowab), omundjoze (Otjiherero) Baswortel, elandsboontjie, leerbossie, South Africa [4, 8,11,17, looiersboontjie, olifantswortel 20, 27-33] (Afrikaans), dwarf elephant's root, eland's bean, eland's wattle, elephant's foot, (English), leshitsana, mosehlana, mositsana, motshitshane (Sepedi), gwejobomvu, mositsane (Sotho, Tswana), ntolwane (Swazi), intolwane, xixuvari (Xhosa), intolwane, intolwanu (-enkulu), ugweje, umdabu (Zulu) Intolwane (Swazi) Swaziland  Elephant-root (English), intolwane Zimbabwe [20, 35] encinyane (Ndebele), chizezepasi, mupangara (Shona) Table 2: Ethnomedicinal uses of Elephantorrhiza elephantina in southern Africa. Use Plant part(s) used and preparation Abdominal pains Rhizome, root decoction taken orally Acne Rhizome, root infusion applied externally Anemia Root decoction taken orally Aphrodisiac Root decoction taken orally Bleeding Root decoction applied on affected body part Bloody Root powder wiped around anus diarrhoea in children Blood pressure Rhizome decoction taken orally Breast cancer Rhizome decoction taken orally Chest pains Roots taken as emetics Cleans blood Rhizome decoction taken orally Cleaning the Rhizome decoction taken womb after orally abortion Clearing air Rhizome decoction taken canal orally Constipation, Ingredient of a herbal heartburn, mixture known as "Sejeso" indigestion, (Ingwe brand) which also loss of includes Alepidea amatymbica Eckl. appetite, & Zeyh., Hypoxis obtusa Burch. ex stomach Ker Gawl., Pentanisia prunelloides ailments, (Klotzsch & Eckl. & Zeyh.) Walp., vomiting deionized water and potassium sorbate as preservative Diarrhoea Leaf, rhizome, root, stem decoction taken orally Diarrhoea Rhizome mixed with root of Acokanthera oblongifolia Benth. & Hook.f. ex B.D. Jacks Dysentery Root decoction taken orally Earache Rhizome decoction taken orally Roots and rhizome used in combination with Eczema Pentanisia prunelloides to treat eczema Erectile Rhizome, root decoction dysfunction taken orally Fever Roots taken as emetics Rhizome decoction taken Fever orally mixed with Pentanisia prunelloides Haemorrhoids Rhizome, root decoction taken orally Herpes Rhizome decoction taken orally HIV/AIDS Rhizome decoction taken opportunistic orally mixed with roots of diseases Boscia albitrunca (Burch.) Gilg & Gilg-Ben., Peltophorum africanum Sond. and Plectranthus ciliatus E. Mey. Itching Rhizome decoction taken orally Infertility in Rhizome, root decoction taken women orally Intestinal Rhizome, root decoction taken disorders orally Kidney failure Rhizome decoction taken orally Love charms Roots taken as emetics Menstrual Root, stem decoction taken problems orally Pain killer Root decoction taken orally Peptic ulcers Root decoction taken orally Rheumatic heart conditions Root decoction taken orally Rheumatic heart conditions Root decoction taken orally Sexually Rhizome decoction taken transmitted orally infections Shingles Rhizome decoction taken orally Root decoction taken orally in combination with Cladostemon kirkii (Oliv.) Pax & Gilg (roots), Drimia delagoensis (Baker) Jessop Shingles (bulb), Sarcophyte sanguinea Sparm. subsp. piriei (Hutch.) B. Hansen (bark)and Ranunculus multifidus Forssk. (whole plant) Sores Rhizome decoction taken orally Root decoction taken orally in combination with Cladostemon kirkii (root), Drimia delagoensis (bulb), Sores Ficus sur Forssk. (bark), Ranunculus multifidus (whole plant), Sarcophyte sanguinea subsp. piriei and Senecio serratuloides DC. (leaves) Stomach Roots taken as emetics ailments Stomach Rhizome decoction taken ailments orally mixed with Acokanthera oblongifolia root or Pentanisia prunelloides Sunburn Underground parts used to treat sunburn Syphilis Root decoction taken orally Tonsillitis Rhizome boiled and extract taken orally Tuberculosis Rhizome decoction taken orally Ethnoveterinary medicine Appetite Rhizome decoction stimulant Black quarter Rhizome decoction Cough Rhizome decoction Diarrhoea Rhizome decoction Dysentery in Root decoction cattle and horses Ectoparasites Root decoction in goats (mites, ticks) Gastrointestinal Rhizome decoction parasites Gall sickness Rhizome decoction Heartwater Rhizome decoction Mange Root decoction given to cows Pneumonia Rhizome decoction Retained Rhizome decoction placenta in cattle Tonic Rhizome decoction Use Country of References practice Abdominal pains Lesotho; [3, 24] Zimbabwe Acne South Africa [15, 36-38] Anemia Mozambique  Aphrodisiac Zimbabwe  Bleeding Lesotho  Bloody Botswana [40, 41] diarrhoea in children Blood pressure South Africa  Breast cancer Lesotho  Chest pains South Africa  Cleans blood Lesotho  Cleaning the Botswana; South [36, 40, 41] womb after Africa abortion Clearing air South Africa  canal Constipation, South Africa  heartburn, indigestion, loss of appetite, stomach ailments, vomiting Diarrhoea Mozambique, [15, 28, 29, 32, South Africa, 34,38,44-46] Swaziland Diarrhoea South Africa  Dysentery South Africa [15, 38, 46] Earache Botswana  Eczema South Africa [36, 37] Erectile Botswana, South [21, 31, 47] dysfunction Africa Fever Mozambique, [25, 42] South Africa Fever Zimbabwe  Haemorrhoids Lesotho, South [15,24,38,48] Africa Herpes Lesotho  HIV/AIDS South Africa  opportunistic diseases Itching South Africa  Infertility in Lesotho, [3, 24] women Zimbabwe Intestinal Lesotho, South [15,24,38,39] disorders Africa Kidney failure South Africa  Love charms South Africa  Menstrual Botswana, South [40, 44] problems Africa Pain killer Mozambique  Peptic ulcers South Africa  Rheumatic heart conditions South Africa  Rheumatic heart conditions South Africa  Sexually Botswana, [41, 45] transmitted Mozambique infections Shingles South Africa  Shingles South Africa  Sores South Africa  Sores South Africa  Stomach Lesotho, South [24, 42] ailments Stomach Africa [43, 44] ailments South Africa; Zimbabwe Sunburn South Africa [15, 38] Syphilis Lesotho, South [15,24,38,39] Africa Tonsillitis South Africa  Tuberculosis Lesotho  Ethnoveterinary medicine Appetite South Africa  stimulant Black quarter South Africa [27, 30] Cough South Africa  Diarrhoea South Africa [30, 48, 52] Dysentery in South Africa  cattle and horses Ectoparasites South Africa  in goats (mites, ticks) Gastrointestinal South Africa  parasites Gall sickness South Africa  Heartwater South Africa [27,52] Mange South Africa  Pneumonia South Africa  Retained Botswana, South [22, 30] placenta in Africa cattle Tonic South Africa  Table 3: Phytochemical compounds isolated from rhizomes or roots of Elephantorrhiza elephantina. Phytochemical Extract compounds Anthraquinone Anthraquinone 38 Chloroform, Ester methanol Ethyl gallate 4 n-butanol Butanedioic acid 19 Hexane Benzoic acid 20 Hexane 3-phenyl-2-propenoic acid 21 Hexane Nonanedioic acid 22 Hexane Methyl 3-(3,5-di-tert- butyl-4-hydroxy- Hexane phenyl)propionate 27 Fatty acid Hexadecanoic acid 15 Hexane 9,12-Octadecadienoic 16 Hexane 9-Octadecenoic 17 Hexane Octadecanoic acid 18 Hexane Tridecanoic acid 23 Hexane Methyl pentadecanoate 24 Hexane Methyl hexadec-9-enoate 25 Hexane Methyl hexadecanoate 26 Hexane Cis-10-Heptadecenoic acid 28 Hexane Methyl heptadecanoate 29 Hexane Methyl octadecanoate 30 Hexane Cis-5,8,11,14,17- eicosapenta-enoic acid 31 Hexane Eicosanoic acid 32 Hexane Methyl tetracosanoate 33 Hexane Pentacosanoic acid 34 Hexane Hexacosanoic acid 35 Hexane Methyl octacosanoate 36 Hexane Tetradecanedioic acid 37 Hexane Flavonoids Dihydrokaempferol 1 n-butanol Kaempferol 2 Ethanol, n-butanol Glycoside Ethyl-1-O-[beta]-D- n-butanol galactopyranoside Phenolic compounds 2-(3,4- Dihydroxyphenyl) n-butanol ethanol 6 Chloroform, Catechin 3 methanol, n-butanol Chloroform, Gallic acid 5 methanol, n-butanol 4-Hydroxybenzoic acid 7 n-butanol Quercetin 3-O-[beta]-D- Chloroform, glucopyranoside methanol, 9 n-butanol Epigallocatechin gallate 44 Ethanol Quercetin 45 Ethanol Epicatechin gallate 46 Ethanol Methyl gallate 10 Chloroform, methanol 3-O-Galloyl-3,3',5,5',7- Chloroform, methanol pentahydroxyflavone 12 Taxifolin-3'-O-[beta]-D- Chloroform, methanol glucoside 13 Epicatechin 14 Chloroform, ethanol, methanol Phytosterols [beta]-Sitosterol 11 Chloroform, methanol Saponin Diosgenin 40 Chloroform, methanol Sugar Rhamnose 41 Chloroform, methanol Chloroform, Glucuronic acid 42 ethanol, methanol Chloroform, Arabinose 43 ethanol, methanol Triterpenoid Oleanolic acid 39 Chloroform, methanol Method of Phytochemical compound References compounds characterization Anthraquinone Anthraquinone 38 LC-ESI-MS  Ester Ethyl gallate 4 GC-MS  Butanedioic acid 19 GC-MS  Benzoic acid 20 GC-MS  3-phenyl-2-propenoic acid 21 GC-MS  Nonanedioic acid 22 GC-MS  Methyl 3-(3,5-di-tert- butyl-4-hydroxy- GC-MS  phenyl)propionate 27 Fatty acid Hexadecanoic acid 15 GC-MS  9,12-Octadecadienoic 16 GC-MS  9-Octadecenoic 17 GC-MS  Octadecanoic acid 18 GC-MS  Tridecanoic acid 23 GC-MS  Methyl pentadecanoate 24 GC-MS  Methyl hexadec-9-enoate 25 GC-MS  Methyl hexadecanoate 26 GC-MS  Cis-10-Heptadecenoic acid 28 GC-MS  Methyl heptadecanoate 29 GC-MS  Methyl octadecanoate 30 GC-MS  Cis-5,8,11,14,17- eicosapenta-enoic acid 31 GC-MS  Eicosanoic acid 32 GC-MS  Methyl tetracosanoate 33 GC-MS  Pentacosanoic acid 34 GC-MS  Hexacosanoic acid 35 GC-MS  Methyl octacosanoate 36 GC-MS  Tetradecanedioic acid 37 GC-MS  Flavonoids Dihydrokaempferol 1 GC-MS  Kaempferol 2 GC-MS, LC-ESI-MS [41, 56] Glycoside Ethyl-1-O-[beta]-D- GC-MS  galactopyranoside Phenolic compounds 2-(3,4- Dihydroxyphenyl) GC-MS  ethanol 6 Catechin 3 GC-MS, NMR [41, 57] Gallic acid 5 GC-MS, NMR [41, 57] 4-Hydroxybenzoic acid 7 GC-MS  Quercetin 3-O-[beta]-D- glucopyranoside GC-MS, NMR [41, 57] 9 Epigallocatechin gallate 44 LC-ESI-MS  Quercetin 45 LC-ESI-MS  Epicatechin gallate 46 LC-ESI-MS  Methyl gallate 10 NMR  3-O-Galloyl-3,3',5,5',7- NMR  pentahydroxyflavone 12 Taxifolin-3'-O-[beta]-D- NMR  glucoside 13 Epicatechin 14 FTIR, LC-ESI-MS, NMR [56, 57] Phytosterols [beta]-Sitosterol 11 NMR  Saponin Diosgenin 40 LC-ESI-MS  Sugar Rhamnose 41 LC-ESI-MS  Glucuronic acid 42 LC-ESI-MS [54, 56] Arabinose 43 LC-ESI-MS [54, 56] Triterpenoid Oleanolic acid 39 LC-ESI-MS
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|Date:||Jan 1, 2017|
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