|Year : 2019 | Volume
| Issue : 4 | Page : 333-338
Pharmacognostic evaluation of Carapa guianensis Aubl. leaves: A medicinal plant native from Brazilian Amazon
Tássio Rômulo Silva Araújo Luz1, José Antonio Costa Leite1, Samara Araújo Bezerra1, Ludmilla Santos Silva de Mesquita1, Edilene Carvalho Gomes Ribeiro2, José Wilson Carvalho De Mesquita1, Daniella Patrícia Brandão Silveira1, Maria Cristiane Aranha Brito2, Crisálida Machado Vilanova3, Flavia Maria Mendonça do Amaral4, Denise Fernandes Coutinho5
1 Biological and Health Sciences Center, Program in Health Sciences, Federal University of Maranhão, São Luís, MA, Brazil
2 Biological and Health Sciences Center, Program in Biotechnology, Federal University of Maranhão, São Luís, MA, Brazil
3 Department of Pharmacy, Biological and Health Sciences Center, Federal University of Maranhão, São Luís, MA, Brazil
4 Biological and Health Sciences Center, Program in Health Sciences; Department of Pharmacy, Biological and Health Sciences Center, Federal University of Maranhão, São Luís, MA, Brazil
5 Biological and Health Sciences Center, Program in Health Sciences; Biological and Health Sciences Center, Program in Biotechnology; Department of Pharmacy, Biological and Health Sciences Center, Federal University of Maranhão, São Luís, MA, Brazil
|Date of Web Publication||22-Nov-2019|
Prof. Tássio Rômulo Silva Araújo Luz
Av. Dos Portugueses, 1966, Vila Bacanga, Federal University of Maranhão, Laboratory of Pharmacognosy II, São Luís, MA, 65080-805
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: Carapa guianensis Aubl., known as crabwood, has been used in folk medicine as anti-inflammatory, wound healing, and for the treatment of flu and colds. Objective: The present study aimed to establish the pharmacognostic features of C. guianensis leaves. Materials and Methods: The leaves were investigated according to the World Health Organization guideline on the pharmacognostic specification, which comprised macroscopic and microscopic assessment, phytochemical screening, and physicochemical characterization of the leaves, besides the microscopic analysis of the powder. Results: Leaves were characterized as a compound, coriaceous with elliptic shape, entire margin, acuminate apex, obtuse base, and opposite phyllotaxis. The epidermis has straight periclinal and anticlinal walls. Calcium oxalate crystals were observed in druses, anomocytic stomata just on a lower side (hypostomatic), and dorsiventral mesophyll. Phytochemical screening revealed the presence of flavonoids, saponins, triterpenes, and steroids in the crude extract. The values of the physicochemical parameters such as total ash, acid-insoluble ash, and loss on drying are 7.16%, 1.03% and 7.93%, respectively; the ethanol and water-soluble extractive values are 19.47% and 15.97%, respectively. Conclusions: The information obtained with botanical, physicochemical, and phytochemical studies could be used to identify C. guianensis and to certify the authenticity of commercial samples.
Keywords: Andiroba, morphoanatomy, phytochemical screening, quality control, rutin
|How to cite this article:|
Luz TR, Leite JA, Bezerra SA, de Mesquita LS, Ribeiro EC, De Mesquita JW, Silveira DP, Brito MC, Vilanova CM, do Amaral FM, Coutinho DF. Pharmacognostic evaluation of Carapa guianensis Aubl. leaves: A medicinal plant native from Brazilian Amazon. Phcog Res 2019;11:333-8
|How to cite this URL:|
Luz TR, Leite JA, Bezerra SA, de Mesquita LS, Ribeiro EC, De Mesquita JW, Silveira DP, Brito MC, Vilanova CM, do Amaral FM, Coutinho DF. Pharmacognostic evaluation of Carapa guianensis Aubl. leaves: A medicinal plant native from Brazilian Amazon. Phcog Res [serial online] 2019 [cited 2020 Sep 27];11:333-8. Available from: http://www.phcogres.com/text.asp?2019/11/4/333/271438
- Rutin can be used as chemical marker for quality control of C. guianensis.
- The crude extract of the leaves has phenolic compounds, saponins, triterpenes and steroids.
- The leaves are characterized by the presence of cells with straight anticlinal walls and polyhedral shape, calcium oxalate crystals in the form of rosette in secondary ribs and anomocytic stomata.
Abbreviations Used: TLC: Thin-layer chromatography.
| Introduction|| |
Medicinal plants are a rich source of secondary metabolites with interesting biological activities, and since the beginning of civilization, plants have been used for man to heal, cure, or prevent diseases; they have great potential for producing new drugs of great benefit to humankind.,
Carapa guianensis Aubl. (Meliaceae), commonly known as andiroba and crabwood, is a tree distributed in the Amazon basin, Central America, and the Caribbean. In Brazil, it was included in a national list of medicinal plants with the potential to advance in the production chain and generate products of interest to the public health system.
Ethnopharmacological studies have reported the therapeutic use of C. guianensis. Leaves and bark are used to prepare the tea for treating fever, worms, and skin illness. The seed oil is largely utilized to treat diseases of the respiratory system, inflammation, and as an insect repellent.,,, Owing to its traditional use for therapeutic purposes for centuries, this species, mainly the oil has been investigated for its pharmacological properties. However, studies with the C. guianensis leaves are lacking. Therefore, it is required studies to validate the popular use of this plant species, in a real perspective of the development of products derived from C. guianensis.,
However, the legislation emphasizes that for the development of herbal medicines, it is necessary to define parameters of efficacy, safety, and quality (authenticity, integrity, and purity) of both the raw material and the finished product, which also allows the inclusion in pharmacopoeias and official codes.
The integrity tests aimed at qualitative and quantitative evaluation of markers of plant material, assays based on characterization and chemical constituents of plant species, which can be started with the phytochemical analysis to identify the relevant secondary metabolites groups.,
As explained above and considering that despite the widespread popular therapeutic use of C. guianensis leaves, studies to define the parameters of quality, efficacy, and safety of that plant species are scarce. In this regard, the present work reports the pharmacobotany, phytochemical, and physicochemical parameters of C. guianensis leaves, with the aim to effectively contribute to quality control of that vegetable raw material.
| Materials and Methods|| |
Plant material collection and identification
The leaves of C. guianensis were collected in São Luís, Maranhão, Brazil (2°33'13.3”S 44°18'20.2”W) in February 2017. The plant material was identified, and a voucher specimen deposited in the Ático Seabra Herbarium of the Federal University of Maranhão with registration code SLS-01253.
The pharmacobotanical study was conducted from the morphological and anatomical characterization of adult leaves of C. guianensis. To perform this study, the adult leaves were collected in three replicates. The morphological descriptions were evaluated using fresh leaves with naked eye and stereomicroscope as per observations described in the literature. For the anatomical description of C. guianensis, transversal sections were cut using stainless steel blades. The sections were bleached in 10% sodium hypochlorite solution, washed in distilled water, and then stained in astra blue and basic fuchsin. Sections were then mounted between slide and coverslip using hydrated glycerin and analyzed by light microscopy. The pictures were taken using a digital camera attached to the microscope. The stomata were classified as method followed by Metcalfe and Chalk. The characterization of cell walls and mesophyll was performed based on Appezzato-da-Glória and Carmello-Guerreiro.
Obtaining crude extract
The leaves of C. guianensis were dried at room temperature under the shade for 7 days, and then cut with knife mill using 2-mm diameter mesh to obtain a coarse powder. The leaf powder was subjected to a percolation extraction process with 70% ethanol, using drug solvent ratio 1:12 (w/v) under cover of light. It was then filtered and concentrated using rotary evaporator.
Total ash, acid-insoluble ash, loss on drying, and extractive matter parameters of C. guianensis leaves were analyzed according to the World Health Organization guideline for quality control methods for medicinal plant materials. All samples were analyzed in triplicate. Grand mean and the pooled standard deviation was calculated.
The crude extract and the fractions were subjected to phytochemical screening tests to detect the secondary metabolites groups. All tests were performed in triplicate.
Thin-layer chromatography of Carapa guianensis
The extract was dissolved in methanol and then plated on silica gel GF254 (Merck) analytical thin-layer chromatography (TLC) plate. For analysis, the AcOEt: H2O: CH2O2(80:10:10) mixture was used as the mobile phase, the plates were then nebulized with ethanolamine diphenylborate, followed by 5% (w/v) polyethylene glycol 4000 in methanol (reagent Natural A, NA) and examined under ultraviolet light (365 nm). As an analytical standard, the rutin (99%) was used for comparison with the compounds present in the extract.
| Results|| |
The leaves of C. guianensis are paripinnate, elliptic shape with an entire margin, leathery texture, smooth surface, acuminate apex, obtuse base with opposite phyllotaxis, and veining pinnate camptodrome type, measuring 25–60 cm in length. Leaves are concolor dark green observed with the naked eye in both sides [Figure 1].
The epidermis (in front view) has cells with straight anticlinal walls and polyhedral shape on both sides [Figure 2]a. The secondary ribs presented the elongated cells with a rectangular shape and showed the presence of calcium oxalate crystals in the form of drusen [Figure 2]b. The anomocytic stomata were found restricted to the abaxial surface [Figure 2]b and [Figure 2]c of the leaf. Extrafloral nectary are observed in both sides of the leaves [Figure 2]d.
|Figure 2: Carapa guianensis Aubl. vertical cross sections of epidermis. (a) Adaxial surface. (b) Abaxial epidermis. (c) Anomocytic stomata. (d) Abaxial epidermis, especially the nectaries. NS: Secondary vein; Dr: Druses; Est: Stomata; CE: Epidermal cells; NE: Extrafloral nectaries|
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The leaf has dorsiventral mesophyll, having two layers of palisade and eight to ten layers of spongy and loosely packed parenchyma. The vascular bundles observed in leaf blades are the collateral type, with xylem facing the adaxial and phloem toward the abaxial epidermis [Figure 3].
|Figure 3: Carapa guianensis Aubl. cross-section of mesophyll. Epab: Lower epidermis; Epad: Upper epidermis; Pp: Palisade parenchyma; Pl: Spongy parenchyma; FV: Vascular bundles|
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The midrib has a biconvex shape with quietly convexity in upper layers as observed in cross section image. The epidermal cells are like the rest of the blade, internally having a layer of cells with sclerified walls. There are three to four layers of chlorenchyma ring and common parenchyma. The central vascular bundle has a triangular shape and is surrounded by sclerenchyma fibers, xylem having the central region being surrounded by the phloem [Figure 4].
|Figure 4: Cross-section showing midrib of Carapa guianensis Aubl. Epab: Lower epidermis; Epad: Upper epidermis; X: Xylem; F: Phloem; FV: Vascular strand (a) Midrib (b) Midrib - focus on epidermis details|
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Microscopy of Carapa guianensis powders
The microscopic observation of C. guianensis powder demonstrates characteristics that identify the species such as cells with straight anticlinal walls and polyhedral shape [Figure 5]a, elongated cells with rectangular shape and showed the presence of calcium oxalate crystals in the form of rosette [Figure 5]b, [Figure 5]d and e], in secondary ribs as well as anomocytic stomata [Figure 5]c, [Figure 5]d and [Figure 5]f.
|Figure 5: Microscopy of Carapa guianensis Aubl. leaf powder. (a and b) epidermis cells (c and d) anomocytic stomata (e) calcium oxalate crystals in the form of drusen (f) secondary ribs with elongated cells|
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The yield of the crude extract was 19.47%, and the phytochemical studies of leaves of this species revealed the presence of phenols, flavonoids in prominent; in addition to saponins, triterpenes, and steroids. The results of the phytochemical screening are described in [Table 1].
|Table 1: Phytochemical screening of Carapa guianensis Aubl. leaves crude extract|
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Chemical profile of thin-layer chromatography of Carapa guianensis Aubl. crude extract
TLC of the hydroethanolic extract shows a profile of five spots, the results are shown in [Figure 6] and [Table 2].
|Figure 6: Thin-layer chromatography of Carapa guianensis Aubl. EA: Crude extract of Carapa guianensis; R: Rutin|
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|Table 2: Profile of thin-layer chromatography of Carapa guianensis Aubl.|
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When comparing the analytical profile obtained by the application of the crude extract with the rutin standard in the TLC, it was possible to confirm the presence of this flavonoid, a comparison made through the retention factor. Rutin, a flavonoid known for its antioxidant activity, is widely used in the world.
The physicochemical evaluation (% by weight) of C. guianensis leaves was demonstrated in [Table 3].
|Table 3: Physicochemical specification (percentage by weight) of Carapa guianensis Aubl.|
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| Discussion|| |
The quality control of herbal medicines is important to ensure the efficiency and quality of these products. This analysis includes many botanical and chemical methods. Botanical analysis, which includes macroscopic and microscopic parameters, is the simplest and cheapest way of attesting the authenticity of the plant drug; and because most herbals are commercialized in the powder form, the analysis of pulverized plant is essential to assess the quality.
The leaf morphology is consistent with results as described earlier. However, it differs as reported by Pantoja which describes phyllotaxis as an alternate.
The presence of anomocytic stomata in C. guianensis leaves and occurs in other species of the family Meliaceae. The presence of extrafloral nectary in the leaflets of C. guianensis has also been reported by Ferraz et al.
The characteristics found on mesophyll highlight the presence of bi-stratified palisade parenchyma as observed in trees that grow in places with high light intensity. In general, the anatomical patterns described in this study for C. guianensis corroborate the attributes proposed by Metcalfe and Chalk; for species of the family Meliaceae, with the exception of trichomes which are absent and mesophyll that not presents secretory cells.
Phytochemical screening indicates the groups of secondary metabolites present in plants, being of great relevance when there are no data regarding the chemical composition of the plant species of interest.,
Phenolic compounds stand out because of their reducing property and provide a structural variety, which can be simple or more complex. Phenols present hydroxyls act in neutralizing or scavenging-free radicals and, presenting itself as an alternative to prevent oxidative deterioration of food and minimize oxidative damage in living beings.
Saponins are secondary metabolites produced by the plants, and these present surface-active property, which may complex with proteins and cell membrane phospholipids, altering the permeability of membranes, assisting in the uptake of substances or possess toxic action in destroying the membrane. Saponins have also been highlighted due to their biological activities such as wound healing and anti-inflammatory.
The triterpenes and steroids have anti-inflammatory activity, which exploited the traditional use of this plant species. The evidence of this activity in this plant species has been described by testing the isolates of C. guianensis triterpenes.
In this way, the phytochemical prospection indicates an enormous potential of the vegetal species for diverse biological activities such as anti-inflammatory, antioxidant, and antimicrobial, mainly by the presence of compound of rutin, a natural compound belonging to the class of flavonoids, which have various biological activities described in the literature as antifungal,, anticancer, hepatoprotective, neuroprotective, antioxidant;, and the ability to inhibit the activity of lipoxygenase, cyclooxygenase, and phospholipase A.,,,
In therapy, this compound is widely used because of its thrombolytic and antioxidant capacity, being able to bind to the platelet membrane and eliminate free radicals, by blocking the enzymatic protein disulfide isomerase found in all cells involved in blood coagulation. It can also be used as an anticoagulant,, has been sold as an herbal supplement approved by the US Food and Drugs Administration.
The phytochemical analysis by Silva and Almeida in the crude hydroethanolic extract of C. guianensis bark showed the presence of phenols, tannins, and anthraquinones as major metabolites; while the analysis of the ethanol extract of the leaves demonstrated the presence of alkaloids, tannins, saponins, and essential oils, and no flavonoids and triterpenes. In the present study, it is noteworthy to mention that crude extract did not show the presence of alkaloids and tannins. This can be explained by the fact that metabolites vary in composition and proportion depending on several factors, mainly the place of collection and time of year when the plant material has been collected.
The physicochemical evaluation of plants is important for detecting adulteration and testify the quality of the drug.,,, For instance, the total ash is used to indicate the presence of foreign inorganic matter and the purity of the drug. A high value can be due problems in manipulation or even addition of sand.
Although the quality standards are fundamental for the validation of the use of plant species in the therapeutics, few plant products have these parameters described in the literature, as is the case of C. guianensis. In this way, the present work contributes significantly, given the scarce information in the quality control of herbal products.
| Conclusion|| |
This study described the morpho-anatomical characteristics that can be used to identify the C. guianensis Aubl. and established physicochemical parameters that allow the evaluation of commercial samples of this vegetal raw material.
Authors would like to thank the Maranhāo Research Foundation (FAPEMA), Coordination for the Improvement of Higher Education Personnel (CAPES), and National Council for Scientific and Technological Development (CNPq) for the financial support and to Federal University of Maranhão for technical support.
Financial support and sponsorship
This study was financially supported by Maranhāo Research Foundation (FAPEMA), Coordination for the Improvement of Higher Education Personnel (CAPES), and National Council for Scientific and Technological Development (CNPq).
Conflicts of interest
There are no conflicts of interest.
| References|| |
Hussien TA, EL-Toumy SA, Hassan HM, Hetta MH. Cytotoxic and antioxidant activities of secondary metabolites from Pulicaria undulata
. Int J Pharm Pharm Sci 2016;8:150-5.
Pulipaka S, Challa RS, Babu R. Pharmacognostic study and phytochemical investigation of Operculina turpethum
(L.) silva manso. Int J Pharm Pharm Sci 2012;4:171-5.
Brito MC, Godinho JW, Ferreira TT, Luz TR, Leite JA, Moraes DC, et al
. Trade and quality control of medicinal plants in Brazil. Int J Pharm Pharm Sci 2016;8:32-9.
Ministry of Health, Direction of Administration and Finance, Secretary of Science, Technology and Strategic Inputs. RENISUS-National Relation of Medicinal Plants of Interest to SUS. Brasília (Brazil); 2009.
Henriques M, Penido C. The therapeutic properties of Carapa guianensis
. Curr Pharm Des 2014;20:850-6.
Almeida LS, Gama JR, Oliveira FA, Ferreira MS, Menezes AJ, Gonçalves DC. Use of plant species in the rural community of Santo Antônio, BR 163 highway, Brazilian Amazon. Floresta Ambient 2013;20:435-46.
Nardi-Santos M. Local Ecological Knowledge about Andirobeiras and the Artisanal Extraction of Andiroba oil in an Area of Environmental Protection, Periurban Lowland Forest. [Theses]. [Macapá] Federal University of Amapá; 2013. p. 107.
Lima PG, Coelho-Ferreira M, Silva-Santos R. The forest at the fair: Medicinal plants of the municipality of Itaituba, Pará, Brazil. Fragmentos Cultura 2014;24:285-301.
Vasquez SP, Mendonca MS, Noda SN. Ethnobotany of medicinal plants in riverine communities of the municipality of Manacapuru, Amazonas, Brasil. Acta Amaz 2014;44:457-72.
Prophiro JS, da Silva MA, Kanis LA, da Rocha LC, Duque-Luna JE, da Silva OS. First report on susceptibility of wild Aedes aegypti
(Diptera: Culicidae) using Carapa guianensis
) and Copaifera
sp. (Leguminosae). Parasitol Res 2012;110:699-705.
Baldissera MD, Da Silva AS, Oliveira CB, Vaucher RA, Santos RC, Giongo JL,et al
. Using of essential oils in the treatment of mice infected with Trypanosoma evansi
. Rev MVZ Cordoba 2014;2:4109-15.
Ministry of Health, National Health Surveillance Agency. Resolution RDC no. 26, May 13, 2014. Provides for the Registration of Herbal Medicines and the Registration and Notification of Traditional Herbal Products. Section 1. Brasília (Brazil): Official Diary of the Union; 2014.
Michelin DC, Finati SC, Sacramento LV, Vilegas W, Salgado HR. The quality control of Operculina macrocarpa
(Linn) Urb. roots (Convolvulaceae
). Braz J Pharmacogn 2010;20:18-22.
Farias RS. Quality of active pharmaceutical raw materials of natural origin. In: Simões CM, Schenkel EP, Mello JC, Mentz LA, Petrovick PR, editors. Pharmacognosy: The Natural Product to the Drug. 6th
ed. Port Alegre: Artmed; 2017. p. 83-105.
Oliveira F, Akisue G. Fundamentals Pharmacobotany and Plant Morphology. 3th
ed. São Paulo: Editora Atheneu; 2009.
Kraus JE, Arduin M. Basic Manual of Plant Morphology Methods. Rio de Janeiro: EDUR; 1997.
Metcalfe CR, Chalk L. Anatomy of the Dicotyledons – Leaves, Stem and Wood in Relation to Taxonomy with Notes on Economic Uses. Oxford: At the Clarendon Press; 1957.
Appezzato-da-Glória B, Carmello-Guerreiro SM. Plant Anatomy. 2nd
ed. Viçosa: UFV; 2006.
World Health Organization. Quality Control Methods for Herbal Materials. Geneva: World Health Organization; 1998.
Matos FJ. Introduction to Experimental Phytochemistry. 3th
ed. Fortaleza: University Press Editions UFC; 2009.
Ferraz ID, Camargo JL, Sampaio PT. Roba-mahogany (Carapa guianensis
Aubl. and Carapa procera
D. C.): Ecological, botanical and technological aspects of its seeds and seedlings. Acta Amaz 2002;32:647-61.
Pantoja TF. Morphological Description and Genetic Variability Analysis for Fruit, Seed and Germination Processes Associated with Oil Yield in Carapa guianensis
Aublet., a Meliaceae
from the Amazon. [Theses]. São Paulo: Paulista State University; 2007. p. 83.
Mourão KS, Dias-Pinto D, Souza LA, Moscheta IS. Morpho-anatomy of the plantlet and threedendron of Trichilia catigua
A. Juss., T. elegans A. Juss. e T. pallida Sw. (Meliaceae
). Acta Sci 2002;24:601-10.
Ferraz ID, Camargo JL, Sampaio PT. Andiroba (Carapa guianensis
Aubl.; Carapa procera
, D.C) Meliaceae. Manual de sementes da Amazônia, 1. Manaus: INPA; 2003. p. 6.
Moraes FK. Physiological and anatomical analysis of leaflets at different stages of development of young plants of andiroba (Carapa guianensis
Aubl.). [Theses]. [Manaus] Federal University of Amazônia; 2010. p. 66.
Metcalfe CR, Chalk L. Anatomy of the Dicotyledon. Vol. 1. Oxford: Clarendon Press; 1979.
Da Silva NL, Miranda FA, Da Conceição GM. Phytochemical screening of Savana plants, from the municipal environmental protection of inhamum, Caxias, Maranhão. Sci Plena 2010;6:1-17.
Simões CM, Schenkel EP, Mello JC, Mentz LA, Petrovick PR. Pharmacognosy: The Natural Product to the Drug. Port Alegre; 2017.
Sousa CM, Silva HR, Vieira GM Jr., Ayres MC, Costa CL, Araújo DS, et al
. Total phenolics and antioxidant activity of five medicinal plants. Quim Nova 2007;30:351-5.
Silva FR, Almeida SS. Phytochemical analysis and microbiological activity of the crude ethanol extract of the Crabwood, Carapa guianensis
Aubl. Amazonian Biota 2014;4:10-4.
Del Re PV, Jorge N. Spices as natural antioxidants: Their application in food and implication for health. Rev Bras Plant Med 2012;14:389-99.
Rodrigues KA, Dias CN, Florêncio JC, Vilanova CM, Gonçalves JR, Moraes DF. Phytochemical prospecction and molluscicidal activity of the leaves of Momordica charantia
L. Cad Pesq 2010;17:69-76.
Janeway Junior CA, Travers P, Walport M, Shlomchik MJ. Immunobiology: The Immune System in Health and Disease. Porto Alegre: Artmed; 2006.
Süleyman H, Mshvildadze V, Gepdiremen A, Elias R. Acute and chronic antiinflammatory profile of the ivy plant, Hedera helix
, in rats. Phytomedicine 2003;10:370-4.
Penido C, Costa KA, Pennaforte RJ, Costa MF, Pereira JF, Siani AC, et al.
Anti-allergic effects of natural tetranortriterpenoids isolated from Carapa guianensis
aublet on allergen-induced vascular permeability and hyperalgesia. Inflamm Res 2005;54:295-303.
Arif T, Mandal TK, Dabur R. Natural products: Antifungals agents derived from plants. Oportunity, Challenge and Scope of Natural Products in Medicinal Chemistry. Trivadum, Kerala, India: Research Signpost; 2011. p. 283-311.
Salas PM, Céliz G, Geronazzo H, Daz M, Resnik SL. Antifungal activity and enzimatically-modified flavonoids isolated from citrus species. Food Chem 2011;4:1411-5.
Freitas CR, Freitas NR, Nepomuceno JC. Evaluation of anticancer effect of rutin on a test for the detection of clones of epithelial tumors (warts) in Drosophila melanogaster
. Perquirere 2014;11:247-57.
Janbaz KH, Saeed SA, Gilani AH. Protective effect of rutin on paracetamol- and CCl4-induced hepatotoxicity in rodents. Fitoterapia 2002;73:557-63.
Pu F, Mishima K, Irie K, Motohashi K, Tanaka Y, Orito K, et al.
Neuroprotective effects of quercetin and rutin on spatial memory impairment in an 8-arm radial maze task and neuronal death induced by repeated cerebral ischemia in rats. J Pharmacol Sci 2007;104:329-34.
Azevedo MI, Pereira AF, Nogueira RB, Rolim FE, Brito GA, Wong DV, et al.
The antioxidant effects of the flavonoids rutin and quercetin inhibit oxaliplatin-induced chronic painful peripheral neuropathy. Mol Pain 2013;9:53.
Ratha P, Jhon DY. Increase of rutin, quercetin and antioxidant activity during germinated buckwheat (Fagopyrum esculentum
Moench) Fermentation. Ferment Technol 2017;6:147.
Pathak D, Pathak K, Singla AK. Flavonoids as medicinal agents: Recent advances. Fitoterapia 1991;57:371-89.
Pelzer LE, Guardia T, Osvaldo Juarez A, Guerreiro E. Acute and chronic antiinflammatory effects of plant flavonoids. Farmaco 1998;53:421-4.
Gryglewski JR, Korbut R, Robak J, Swies J. On mechanism of antithrombotic action of flavonoids. Biochem Pharmacol 1987;36:317-22.
Silva RR, Oliveira TT, Nagem TJ, Leão MA. Effect of flavonoids on the arachidonic acid metabolism. Medicina (Ribeirão Preto Online) 2002;35:127-33.
Dar MA, Tabassum N. Rutin- potent natural thrombolytic agent. Int J Curr Pharm Res 2012;1:431-5.
Kuntić V, Filipović I, Vujić Z. Effects of rutin and hesperidin and their al (III) and cu (II) complexes onin vitro
plasma coagulation assays. Molecules 2011;16:1378-88.
Nayak BS, Kanhai J, Milne DM, Pinto Pereira L, Swanston WH. Experimental evaluation of ethanolic extract of Carapa guianensis
L. leaf for its wound healing activity using three wound models. Evid Based Complement Alternat Med 2011;2011:419612.
Gobbo-Neto L, Lopes NP. Medicinal plants: Factors of influence on the content of secondary metabolites. Quim Nova 2007;30:374-81.
Chaowuttikul C, Palanuvej C, Ruangrungsi N. Pharmacognostic specification, chlorogenic acid content, andin vitro
antioxidant activities of Lonicera japonica
flowering bud. Pharmacognosy Res 2017;9:128-32.
Sahoo N, Manchikanti P, Dey S. Herbal drugs: Standards and regulation. Fitoterapia 2010;81:462-71.
Liu W. Traditional Herbal Medicine Research Methods: Identification, Analysis, Bioassay and Pharmaceutical and Clinical Studies. United State: John Wiley and Sons; 2011.
Charoensup R, Duangyod T, Palanuvej C, Ruangrungsi N. Pharmacognostic specifications and lawsone content of Lawsonia inermis
leaves. Pharmacognosy Res 2017;9:60-4.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]
[Table 1], [Table 2], [Table 3]