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Year : 2011  |  Volume : 2  |  Issue : 1  |  Page : 37-41
Pharmacognostical evaluation of Barringtonia acutangula leaf

Department of Pharmacognosy, Madras Medical College, Chennai, Tamil Nadu, India

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Date of Submission30-Apr-2010
Date of Acceptance30-Apr-2011
Date of Web Publication26-Jul-2011


Barringtonia acutangula (L.) Gaertn. (Family: Lecythidaceae) is an evergreen tree with simple, alternate leaves, long pendulous racemes, dark scarlet flowers, and ellipsoid to ovoid berries containing one ovoid black seed. The present study deals with a detailed pharmacognostical study on the leaf of the crude drug, B. acutangula. Morphoanatomy of the leaf was studied using light and confocal microscopy and World Health Organization (WHO) guidelines on quality control methods for medicinal plant materials. Literature reveals that the phytoconstituents like tanginol, barrinic acid, and barringenic acid are present in the wood and fruits of this plant. Our preliminary phytochemical studies of the powdered leaves revealed the presence of terpenes, flavanoids, carbohydrates, tannins, steroids, and glycosides. The physico-chemical, morphological, histological parameters, and High Performance-Thin Layer Chromatographic (HPTLC) profile presented in this paper may be proposed as parameters to establish the authenticity of B. acutangula and can possibly help to differentiate the drug from its other species and the pharmacognostic profile of the leaves presented here will assist in standardization viz., quality, purity, and sample identification.

Keywords: Barringtonia acutangula , high performance thin layer chromatographic profile, pharmacognosy

How to cite this article:
Padmavathi D, Susheela L, Bharathi RV. Pharmacognostical evaluation of Barringtonia acutangula leaf. Int J Ayurveda Res 2011;2:37-41

How to cite this URL:
Padmavathi D, Susheela L, Bharathi RV. Pharmacognostical evaluation of Barringtonia acutangula leaf. Int J Ayurveda Res [serial online] 2011 [cited 2015 Mar 3];2:37-41. Available from:

   Introduction Top

Barringtonia acutangula (L.) Gaertn. (Family: Lecythidaceae) known as Dhatriphal in Sanskrit, is a medium-sized tree found throughout India, plentifully in the plains of Bengal. [1] B. asiatica and B. racemosa are the other species of Barringtonia. B. asiatica is a native of mangrove habitats on the tropical coasts and islands of the Indian Ocean and used to treat cysts, goiter, tumor, boils, stomach ache, and rheumatism. B. racemosa is found in coastal swamp forests and on the edges of estuaries in the Indian Ocean and its fruits are prescribed in the Ayurvedic literature for the treatment of pain, inflammation, and rheumatic conditions. B. acutangula is an evergreen tree with simple, alternate leaves, pendulous racemes, up to 40 cm long and 1.5 cm across, dark scarlet flowers with 4 lobed ovate calyx and 2 celled ovary. It has ellipsoid to ovoid berries, fibrous, truncate at both ends, crowned by small persistent calyx and each berry bears one ovoid black seed. [2] In Ayurveda, different formulations like Nichuladi lepa, Apachihara lepa, Lakshmivilasa rasa, Taptaraja taila are used for the treatment of various diseases such as jaundice, diseases of head, hemiplegia, joint pain, eye diseases, stomach disorders, diarrhea, cough, dyspnoea, leprosy, spleenic disorders, and poisoning. [3],[4],[5] According to Ayurveda, the properties (guna) of B. acutangula are ruksha (dry), laghu (light), and tikshna (sharp). It has a rasa (taste) of katu (pungent), tikta (bitter), sheeta (cold), and- virya (potency). Despite the numerous medicinal uses attributed to this plant, there are no pharmacognostical reports on the leaf of this plant. Hence, the present investigation deals with the morphological and anatomical evaluation, determination of physicochemical constants, preliminary phytochemical screening, and HPTLC profile of the different extracts. The profile presented in this paper may be proposed as parameters to establish the authenticity of B. acutangula and can possibly help to differentiate the drug from its other species.

   Materials and Methods Top

Plant material

The leaves of B. acutangula were collected from Chennai, Tamil Nadu, India, in the month of June 2008. After authentication by a taxonomist, a voucher specimen number, MMC/2008/07, has been deposited in the museum of the Department of Pharmacognosy, Madras Medical College, Chennai, India.

Instruments and chemicals

Compound microscope, stage micrometer, camera lucida, drawing sheets, glass slides, cover slips, watch glass and other common glassware were the basic apparatus and instruments used for the study. Microphotographs were taken using a Leica (Dissecting Microscope Lighting System-DMLS) microscope attached with Leitz (Magnification Power System- MPS) 32 camera. Solvents viz., 95% Ethanol (EtOH), Petroleum ether (PE), Ethyl acetate (EtOAc) and reagents such as phloroglucinol, glycerin, hydrochloric acid, chloral hydrate, and sodium hydroxide were procured from Ranbaxy Fine Chemicals Ltd., Mumbai, India.

Macroscopic and microscopic analysis

The macroscopy and microscopy of the leaves were studied according to the method of Brain and Turner. [6] For the microscopic studies, cross sections were prepared and stained as per the procedure of Johansen. [7] The micropowder analysis was done according to the method of Brain and Turner [8] and Kokate. [9]

Leaf constants

Leaf constants such as vein islet number, veinlet termination number, palisade ratio, and stomatal index were studied according to the method of Evans. [10]

Physicochemical analysis

Physicochemical analysis such as the percentage of ash values and extractive values were carried out according to the official methods prescribed in Indian Pharmacopoeia [11] and the WHO guidelines on quality control methods for medicinal plant materials [12] Fluorescence analysis was carried out by the method of Chase and Pratt [13] and Kokoski. [14]

Preliminary phytochemical screening

Preliminary screening was carried out by using standard procedures described by Kokate [9] and Harborne. [15]

HPTLC profile

Qualitative densitometric HPTLC analysis was performed for the development of characteristic finger print profile for PE, EtOAc, and EtOH extracts of leaves of B. acutangula. 10 μl of the sample solutions were applied and the plates were developed in PE and EtOAc (8:2) for PE extract, toluene and acetonitrile (3:1) for EtOAc and EtOH extracts. Developed plates were then scanned densitometrically at various wavelengths. Retention factor (R f ) values, peak area, peak height, and spectrum of each peak were determined for these extracts.

   Results Top

Macroscopic characters

The leaves are simple, alternate, 7-14.5 cm in length and 4-8 cm in breadth, obovate to oblong, acute apex, decurrent base, minutely denticulate to crenate margin, reticulate venation with smooth, dark green upper surface and rough, faint green lower surface.

Microscopic characters


The transverse section of the leaf of B. acutangula shows a dorsiventral nature [Figure 1]. The section is broadly divided into lamina and midrib region. The lamina of the leaf shows three distinct regions viz., adaxial epidermis, abaxial epidermis, and mesophyll [Figure 1]a. The adaxial epidermis is single layered with squarish cells covered by a distinct cuticle. The abaxial epidermis is also single layered with rectangular cells having prominent peg like outgrowths. The mesophyll is differentiated into palisade and spongy parenchyma. The palisade parenchyma has two layers of narrow, cylindrical, and compact cells. The spongy parenchyma consists of about 12 layers of small, lobed, loosely arranged cells with wide air-chambers.
Figure 1: T. S of leaf (a) T.S. of lamina, (b) T.S. of midrib, (c) T.S. of petiole, (d) Crystal distribution (AdE- Adaxial epidermis, AbE- Abaxial epidermis, PM- Palisade mesophyll, SM- Spongy mesophyll, CPCuticular papillae, LV- Lateral vein, AdH- Adaxial hump, LB-Lateral bundle, MB- Main bundle, GT- Ground tissue, OB- Outer bundle, Cr- Crystal, Ve- Vein, Ep- Epidermis)

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The lateral veins have prominent vascular strands, but do not project on to the leaf surface. The lateral vein has a small group of xylem elements and few phloem elements. The vascular strand is en-sheathed by thick sclerenchymatous tissue which extends into adaxial and abaxial pillars. The leaf margin is thick and semicircular and has fairly prominent circular vascular strands. The epidermal layer shows anomocytic type of stomata.

The midrib has prominent adaxial hump and wide semicircular abaxial part [Figure 1]b. The epidermal layer of the midrib is thin, comprising of small, thick walled squarish cells with outer papillate walls. The ground tissue is parenchymatous and homocellular. A wide mass of thick walled cells are located in the center of the adaxial hump. The vascular system of the midrib is complex. The vascular bundles are of three types; main bundle-xylem elements are thick walled, circular and it occurs in parallel radial rows with small sclerenchyma cells in between the rows and phloem occurs in thin sheath around the xylem, two circular lateral bundles and a row of six small circular vascular strands. The type of calcium oxalate crystals are druses and found in the vascular strands, veins of leaf, ground tissue of midrib and petiole as well as in phloem parenchyma [Figure 1]d.


Cross section of the petiole is circular with slightly flat adaxial side [Figure 1]c. It has a thin epidermal layer consisting of narrowly rectangular thick walled cells and some of them have peg like outgrowths on the tangential walls. The ground tissue consists of thick walled, angular, compact parenchymatous cells. The vascular system is complex, multi-stranded consisting of larger deeply curved main vascular bundle, two circular lateral bundles and eleven small vascular strands arranged in arcs. The main vascular bundle consists of several parallel rows of vessel multiples alternating with narrow intervening sclerenchyma cells. Phloem occurs in thick band all along the outer part of the xylem arc.

Powder characteristics

The organoleptic evaluation of the leaf powder revealed the following characteristics. The leaf powder is pale green in color, with a characteristic odor and bitter taste. On microscopic examination, the powder showed epidermal trichomes which are sparse [Figure 2]a and b. Starch grains are present in minute quantities and are spherical, concentric, and three lobed [Figure 2]c. Fibers of the petiole are wider and straight measuring 660-750 μm long and 20-25 μm wide [Figure 2]d. The trichomes are multicellular, uniseriate, and unbranched. The epidermal cells are small, polygonal thick walled, and straight. Fibers of the lamina are usually bent, narrow measuring 550- 650 μm long and 15-20 μm wide [Figure 2]e.
Figure 2: Powder microscopy (a) Trichomes, (b) Epidermal fragments, (c) Starch grains, (d) Fibers of petiole, (e) Fibers of lamina

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Leaf constants

The leaf constants viz., vein islet number, veinlet termination number, palisade ratio, and stomatal index are presented in [Table 1].
Table 1: Leaf constants of B. acutangula

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Physicochemical constants

Ash values of a drug gave an idea of the earthy matter or the inorganic composition and other impurities present along with the drug. The ash values [Table 2] of the leaf powder of B. acutangula revealed a high concentration of sulphated ash. The extractive values are primarily useful for the determination of exhausted or adulterated drug. The ethanol soluble extractive was high for B. acutangula. The results of fluorescence analysis of leaf powder are presented in the [Table 3].
Table 2: Physicochemical constants of leaf powder of B. acutangula

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Table 3. Preliminary phytochemical screening of leaf powder of B. acutangula

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Preliminary phytochemical screening

Preliminary phytochemical screening mainly revealed the presence of carbohydrates, phytosterols, terpenoids, flavonoids, glycosides, tannins, and saponins [Table 4].
Table 4. Fluorescence analysis of leaf powder of B. acutangula

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HPTLC profile

A densitometric HPTLC analysis was performed for the development of characteristic finger print profile for PE, EtOAc, and EtOH extracts of the leaf powder of B. acutangula [Figure 3], which may be used as markers for quality evaluation and standardization of the drug. Most of the compounds have shown maximum absorbance at 260 nm for PE extract, 366 nm for EtOAc extract, and 550 nm for EtOH extract. Two different mobile phases were selected to carry out the HPTLC profile for three different extracts viz., PE, EtOAc, and EtOH. All the three extracts did not show good separation in the same (single) mobile phase, because, different chemical constituents are present in different extracts. EtOAC and EtOH extracts generally contain moderately polar/polar compounds, while PE extract contains only non-polar compounds. Hence, depending on the polarity of compounds present in the extracts, two different mobile phases i.e., PE and EtOAc (8:2) for PE extract, toluene and acetonitrile (3:1) for EtOAc and EtOH extracts were used. The bands in the sample were obtained at R f , 0.05, 0.08, 0.12, 0.17, 0.21, 0.29, 0.39, 0.54, 0.63, 0.72 [PE extract] and 0.06, 0.09, 0.20, 0.36, 0.40, 0.46, 0.57, 0.63, 0.68, 0.72, 0.79, 0.82 [EtOAC extract] and 0.13, 0.17, 0.24, 0.28, 0.44, 0.56, 0.65, 0.72, 0.80, 0.86 [EtOH extract], which can be used as identifying markers. The above R f values and number of spots are invariable for the various extracts (PE, EtOAC, and EtOH) at particular solvent system studied. Change in R f values and number of spots is an indicative marker of adulteration with this extract. Hence, the HPTLC finger print profile can be used as a marker for identification of adulteration in B. acutangula.
Figure 3: HPTLC chromatogram of PE, EtOAc, and EtOH extracts of B. acutangula leaf, (PE- Petroleum ether extract, EtOAc- Ethyl acetate extract, EtOH- Ethanol extract)

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   Discussion Top

The microscopic characters, leaf constants, quantitative analysis, and physico-chemical constants studied here can be used for judging the adulteration and purity of this drug. Since these parameters studied are constant and any change in these values are indicative of substitution and adulteration with the plant, B. acutangula.

As there is no pharmacognostic anatomical work on record for this much valued traditional drug, the present work was taken up with a view to lay down standards which could be useful to detect the authenticity of this medicinally useful plant. Macro and micro morphological standards and HPTLC profile discussed here can be considered as identifying parameters to substantiate and authenticate the drug. In Ayurveda, its preparations include powder and pastes, used in vitiated conditions of kapha and pitta, leprosy, dysmenorrhea, plumbago, skin diseases, diarrhea, inflammation, flatulence, hemorrhoids, and as an anthelmintic. The preliminary phytochemical screening revealed the presence of terpenoids, flavonoids, glycosides, tannins, and saponins. These constituents may be possibly responsible for the above said activity.

   Acknowledgement Top

Madras Medical College, Chennai for providing the facilities to carry out the study.

   References Top

1.Nadkarni KM. Indian Materia Medica. Vol 1. Mumbai, India: Popular Prakashan Ltd.; 1954. p. 176-7.  Back to cited text no. 1
2.Nair NC, Henry HN. Flora of Tamilnadu. Vol 1. Botanical Survey of India; 1983. p. 158.  Back to cited text no. 2
3.Yoganarashimhan. Medicinal Plants of India - Tamil Nadu. Vol 2. Bangalore: Cyber Media; 2000. p. 71.   Back to cited text no. 3
4.Satapathy KB, Brahmam M. Ethnobotanical survey on tribal area plant Barringtonia acutangula. Fourth International Congress Ethnobiology. Lucknow: NBRO; 1994.   Back to cited text no. 4
5.The Wealth of India, A Dictionary of Indian Raw Materials and Industrial Products, 1 st Supplemental Series (Raw Material). Vol 1, A - Ci. New Delhi: National Institute of Science Communication and Information resources: CSIR; 1997. p. 118-21.  Back to cited text no. 5
6.Brain KR, Turner TD. The Practical Evaluation of Phytopharmaceuticals. Bristol: Wright-Scientechnica; 1975. p. 4-9.   Back to cited text no. 6
7.Johansen DA. Plant Microtechnique. NewYork: Mc Graw Hill Book Co; 1940. p. 182-5.   Back to cited text no. 7
8.Brain KR, Turner TD. The Practical Evaluation of Phytopharmaceuticals. Bristol: Wright-Scientechnica; 1975. p. 36-45.  Back to cited text no. 8
9.Kokate CK. Practical Pharmacognosy. 1 st ed. New Delhi: Vallabh Prakashan; 1986. p. 111-20.   Back to cited text no. 9
10.Evans WC. Trease and Evans Pharmacognosy. 15 th edn. London: Saunders; 2003. p. 545-547.  Back to cited text no. 10
11.Indian Pharmacopoeia. 4 th ed, Vol 2. Government of India, Ministry of Health and Welfare. New Delhi: Controller of Publications; 1996. p. A53-4.   Back to cited text no. 11
12.WHO/PHARM/92.559/rev.1. Quality Control Methods for Medicinal Plant Materials. Geneva: Organisation Mondiale De La Sante; 1992. p. 9-34.   Back to cited text no. 12
13.Chase CR, Pratt RS. Fluorescence of powdered vegetable drugs with particular reference to development of a system of identification. J Am Pharmcol Assoc 1949;38:32-5.   Back to cited text no. 13
14.Kokoshi J, Kokoshi R, Sharma FJ. Fluorescence of Powdered vegetable drug under ultraviolet radiation, J Am Pharmcol Assoc 1958;47:715-7.   Back to cited text no. 14
15.Harborne JB. Methods of Extraction and isolation. In: Phytochemical Methods, London: Chapman and Hall; 1998. p. 60-6.  Back to cited text no. 15

Correspondence Address:
Rajkishore Vijaya Bharathi
Department of Pharmacognosy, Madras Medical College, Chennai - 600 003, Tamil Nadu
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DOI: 10.4103/0974-7788.83189

PMID: 21897641

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  [Figure 1], [Figure 2], [Figure 3]

  [Table 1], [Table 2], [Table 3], [Table 4]

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