Evidence-Based Complementary and Alternative Medicine
Volume 2018 (2018), Article ID 6743862, 5 pages
https://doi.org/10.1155/2018/6743862

Research Article

Evaluation of the In Vitro and In Vivo Antioxidant Potentials of Sudarshana Powder

Weerakoon Achchige Selvi Saroja Weerakoon,¹ Pathirage Kamal Perera,² Dulani Gunasekera,³ and Thusharie Sugandhika Suresh⁴

¹Department of Ayurveda Paediatrics, Institute of Indigenous Medicine, University of Colombo, Colombo, Sri Lanka
²Department of Ayurveda Pharmacology and Pharmaceutics, Institute of Indigenous Medicine, University of Colombo, Colombo, Sri Lanka
³Department of Paediatrics, Faculty of Medical Sciences, University of Sri Jayewardenepura, Nugegoda, Sri Lanka
⁴Department of Biochemistry, Faculty of Medical Sciences, University of Sri Jayewardenepura, Nugegoda, Sri Lanka

Correspondence should be addressed to Pathirage Kamal Perera; drkamalperera@yahoo.com

Received 1 December 2017; Revised 7 February 2018; Accepted 4 March 2018; Published 10 April 2018

Academic Editor: Gianni Sacchetti

Copyright © 2018 Weerakoon Achchige Selvi Saroja Weerakoon et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Sudarshana powder (SP) is one of the most effective Ayurveda powder preparations for paediatric febrile conditions. The objective of the present study was to evaluate the in vitro and in vivo antioxidant potentials of SP. The in vitro antioxidant effects were evaluated using ABTS radical cation decolourization assay where the TROLOX equivalent antioxidant capacity (TEAC) was determined. The in vivo antioxidant activity of SP was determined in Wistar rats using the Lipid Peroxidation (LPO) assay in serum. The in vitro assay was referred to as the TROLOX equivalent antioxidant capacity (TEAC) assay. For the in vivo assay, animals were dosed for 21 consecutive days and blood was drawn to evaluate the MDA level. The in vitro antioxidant activity of 0.5 μg of SP was equivalent to 14.45 μg of standard TROLOX. The percentage inhibition against the radical formation was %. The SP showed a statistically significant () decrease in the serum level of thiobarbituric acid-reactive substance in the test rats when compared with the control group. These findings suggest that the SP possesses potent antioxidant activity which may be responsible for some of its reported bioactivities.

1. Introduction

Sudarshana powder (SP) is the most effective antipyretic Ayurvedic preparation, widely used in Sri Lanka as well as in India from the inception of Ayurveda treatment. SP is mentioned in the Sri Lankan Ayurvedic Pharmacopeia [1] complied under Sec. 41(2) (c) of the Ayurveda Act no. 31 of 1961. The powder is prepared using different parts of plant materials and therefore is a 100% herbal product.

SP contains 53 [1] bitter ingredients and has the capability to treat fever associated symptoms such as dyspepsia, anorexia, fatigue, and nausea. It does not cause constipation and produces a mild laxative effect. It promotes the flow of bile and in gastrointestinal disorders it is used as a digestive.

Initially the main ingredient of the SP in Sri Lanka was Swertia chirata (Roxb. ex Fleming) which was later replaced by Andrographis paniculata (Burm. f.) Wall. ex Nees. Presently the SP contains Andrographis paniculata (Burm. f.) Wall. ex Nees. (50%) along with 52 other ingredients (50%). The other constituents too have different therapeutic uses [2].

Although literature suggests that SP is the most effective and popular Ayurvedic medicine, no scientific evidence is available for its antioxidant potential. Antipyretic effect [3–6], anti- inflammatory effect [7], analgesic effect [8–10], antihistamine effect [11], and long term administration effect [12–15] of the SP were established in Wistar rats in our recent experimental studies. Thus, in the present study, in vitro and in vivo antioxidant potentials of SP were evaluated.

2. Materials and Methods

2.1. Preparation of Sudarshana Powder

SP (Table 1) was prepared according to Ayurveda Pharmacopeia at the Pharmacy of the Institute of Indigenous Medicine, University of Colombo [2].

Table 1: Ingredients of Sudarshana powder.

Botanical name
General user name in Sri Lanka
Sanskrit name
Parts used

(1) Andrographis paniculata (burm. f.) Wall. ex Nees.
Heen bincohomba
Chirayetah
Whole plant

(2) Piper longum Linn.
Thippili mul
Chapala
Root

(3) Zingiber officinale Rosc.
Inguru
Ardraka
Rhizome

(4) Piper nigrum Linn.
Gammiris
Katuka
Fruit

(5) Piper longum Linn.
Thippili
Chapala
Fruit

(6) Santalum album Linn.
Suduhandun
Chandana
Stem

(7) Glycyrrhiza glabra Linn.
Valmi
Yashtimadu
Stem

(8) Picrorhiza kurroa Royle ex Benth.
Katukarosana
Katurohini
Herb

(9) Cedrus deodara (Roxb.) Loud.
Devađara
Devodara
Timber

(10) Hedychium spicatum (Ham. ex Smith)
Hingurupiyali
Shati
Rhizome

(11) Embelia ribes Burm F.
Valanghasal
Krimigna
Fruit

(12) Trachyspermum roxburghianum (DC.) Craib.
Asamodagam
Ugragandha
Whole herb

(13) Holarrhena antidysenterica Wall.
Kelinda
Kutaja
Bark and wood

(14) Aconitum heterophyllum Wall.
Athividayan
Athivida
Root

(15) Terminalia chebula Retz.
Aralu
Abaya
Dry fruit

(16) Terminalia bellirica (Gaertner) Roxb.
Bulu
Vibhitaka
Dry fruit

(17) Phyllanthus emblica Linn.
Nelli
Amalakee
Dry fruit

(18) Syzygium aromaticum (L.) Merr. & Perry
Karabunati
Lavanga
Flower

(19) Myristica fragrans Linn.
Vasāvāsi
Jathipala
Fruit cover

(20) Cyperus rotundus Linn.
Kalānduru ala
Granthi
Rhizome

(21) Solanum melongena Linn.
Elabatumul
Vruhathi
Plant

(22) Alysicarpus vaginalis (L.) DC.
Asvanna
-
Plant

(23) Aerva lanata (L.) Juss. ex Schult.
Polpala
-
Whole plant

(24) Solanum xanthocarpum Schrad. & Wendl.
Katuvelbatu
Brihati
Plant

(25) Saussurea lappa Linn.
Suvandakottan
Kushta
Root

(26) Azadirachta indica A. Juss.
Kohambapothu
Nimba
Bark

(27) Tinospora cordifolia (Willd.) Miers ex Hook. f. & Thoms.
Rasakinda
Amurtha
Stem

(28) Curcuma domestica Valet.
Kaha
Haridra
Rhizome

(29) Cinnamomum iners Reinw.
Kollan kola
Thejapatra
Leaves

(30) Trichosanthes cucumerina Linn.
Dummalla
Patola
Leaves

(31) Tragia involucrata Linn.
Val kahabilia
Duralaba
Root

(32) Marsdenia tenacissima (Roxb.) Moon.
Murva
Tejowapi
Stem

(33) Oldenlandia biflora Linn.
Pathpadagam
Parpataka
Whole plant

(34) Bacopa monniera (L.) Wettst.
Lunuvila
Brahmi
Whole plant

(35) Plectranthus zeylanicus Benth.
Irivriya
Valakan
Whole plant

(36) Holarrhena antidysenterica (Linn.) Wall.
Kelinda hal
Kutaja
Seeds

(37) Moringa oleifera Lam.
Murunga eta
Shigruka
Whole plant

(38) Cinnamomum zeylanicum Blume.
Kurundupothu
Bahugandha
Bark

(39) Abies webbiana Lindl.
Thalispatra
Thalispatra
Leaves

(40) Nelumbium speciosum Willd.
Padma kashta
Padmakashta
Rhizome

(41) Vetiveria zizanioides (L.) Nash.
Savandarā
Ushira
Root

(42) Sida cordifolia Linn.
Bavilamul
Bala
Root

(43) Aluminium sulphate
Seenakkaran
Surashtaja

(44) Valeriana wallichii DC.
warala
Tagar
Root

(45) Plumbago indica Linn.
Rathnitol
Chitraka
Root

(46) Coscinium fenestratum (Gaertn.) Colebr.
Wenivalgata
Pitadaru
Wood, stem

(47) Premna herbacea Roxb.
Sirithekku
Bhangi
Root

(48) Asparagus racemosus (Willd.) Oberm.
Kavelu
(Hatavariya)
Shathavari
Rhizome

(49) Bambusa vulgaris Schrad ex Wendl.
Unakapuru
Vamash
Extraction

(50) Withania somnifera Linn.
Rishibaka
(Amukkara)
Ashvagandha
Rhizome

(51) Piper chawya Buch.-Ham.
Siviya
Siviya
Root

(52) Nelumbium speciosum Willd.
Nelum
Pundarika
Lotus stamens

(53) Ipomoea digitata Linn.
KiribaduAla
Jeevaka
Rhizome

All the ingredients were purchased from Ayurveda Drug Corporation, Sri Lanka, and authentication of ingredients was done at the Institute of Indigenous Medicine, University of Colombo, Sri Lanka (Specimen No. 102), and SP was prepared according to Ayurveda Pharmacopeia [1] at the Pharmacy of the Institute of Indigenous Medicine.

All the 53 Ingredients were thoroughly cleaned to remove any contaminated materials using tap water. Washed ingredients were air-dried. Some herbal ingredients (i.e., Plumbago indica Linn.) were purified using purification methods, mentioned in Ayurveda authentic texts, prior to being powdered. All ingredients were powdered at the mesh size of 80 under the Ayurveda concepts. Andrographis paniculata (Burm. f.) Wall. ex Nees. (2600 g) was mixed with 50 g each of the rest of the ingredients (50 × 52) to obtain the Sudarshana powder.

2.2. Animals

Healthy adult male Wistar rats (200–250 g) were used in the in vivo study. The animals were kept in plastic cages (two per cage) under standardized animal house conditions (temperature, 28–31°C; photoperiod, approximately 12 h natural light “per day”; relative humidity, 50–55%) at the Faculty of Medical Sciences, University of Sri Jayewardenepura, with continuous access to pelleted feed and tap water.

All experiments in rats were carried out in accordance with the guidelines for care and use of laboratory animals and the project proposal was approved (No. 591/11) by the Ethics Review Committee of the Faculty of Medical Sciences of the University of Sri Jayewardenepura, Sri Lanka (http://medical.sjp.ac.lk/index.php/ethics-review-committee-introduction).

2.3. In Vitro Antioxidant Activity

The in vitro antioxidant free radical scavenging activity of SP was determined by using ABTS radical cation decolourization assay [16].

In this assay, 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) or ABTS (C₁₈H₁₈N₄O₆S₄) is converted to its radical cation. This radical cation is dark green in colour and absorbs light at 734 nm. [16]. The reaction was monitored spectrophotometrically. This assay is often referred to as the TROLOX equivalent antioxidant capacity (TEAC) assay.

2.3.1. Preparation of Extracts

The SP (5 g) was extracted with 100 ml ultrapure water, at 80°C for 20 min in a water bath shaker. After cooling, the extract was centrifuged at 5000 rpm for 10 min. The solution was filtered using No. 1 Whatman filter paper and used for ABTS analysis. The sample was diluted 1 : 10 (100 μl sample + 900 μl H₂O) [17].

2.3.2. Formation of ABTS Radical Solution

The ABTS solution (7 mmol) stock solution, 2.6 ml, was mixed with 11.5 ml of potassium persulfate (K₂S₂O₈) solution and kept in a dark place at room temperature (23°C) for 16 hours for free radical formation. The generated ABTS radical cations (ABTS⁺) solution was dark green in colour. The stock solution was diluted with ultrapure water until the absorbance reached 0.700 (±0.02) at 734 nm. The prepared sample (10 μl) was added to ABTS⁺ solution (2990 μl) with phosphate saline buffer until total volume was reached (3 ml). The absorbance reading was taken 6 min after initial mixing. All determinations were performed in triplicate.

2.3.3. Standard Curve for ABTS Radical (ABTS⁺) Activity on TROLOX

TROLOX (C₁₄H₁₈O₄) or (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid) is equivalent antioxidant capacity (TEAC) which measures the antioxidant capacity of a given substance, as compared to the standard, TROLOX.

The stock solution of TROLOX was prepared by dissolving 0.0161 g in 50 ml deionized water. From the prepared stock solution, 5 μl (1.56 μg TROLOX), 10 μl (3.12 μg TROLOX), 15 μl (4.68 μg TROLOX), 20 μl (6.24 μg TROLOX), and 25 μl (7.8 μg TROLOX) were taken and reacted with ABTS⁺ solution with initial absorbance of 0.700 at 734 nm against a phosphate saline buffer blank. Absorbance of reaction mixture was taken till the absorbance came to a plateau. The reduction of absorbance was calculated from the initial and final absorbance. The reduction of absorbance relevant to each TROLOX concentration was performed six times. Standard curve was drawn for mean reduction of absorbance versus quantity of TROLOX in μg. The antioxidant activity was expressed as TROLOX equivalent antioxidant capacity (TEAC).

2.4. In Vivo Antioxidant Activity

In vivo antioxidant activity of SP was analysed using the method of determination of the Lipid Peroxidation (LPO) in serum. The level of thiobarbituric acid-reactive substance (TBARS) and malondialdehyde (MDA) production was measured in serum by the modified method by Draper and Hadly, 1990 [18].

Wistar rats were randomly divided into two groups of six animals each. On Day 0, blood samples were collected to assess the baseline serum malondialdehyde (MDA) level. The control group received distilled water and test group received hot water extraction of SP (0.5 g/kg). The animals were dosed for 21 consecutive days and were observed daily for signs of toxicity and death throughout the period of study. Body weights were recorded. Twenty-four hours after the last treatment, blood was obtained through direct cardiac puncture to evaluate the MDA level.

The serum (200 μL) was deproteinized by adding 1 ml of 14% trichloro acetic acid and 1 ml of 0.6% thiobarbituric acid. The mixture was heated in a water bath for 30 min at 95°C to complete the reaction and then cooled on ice for 5 min. Following centrifugation at 2000 rpm for 10 min, the absorbance of the coloured product (TBARS) was measured at 535 nm with a UV spectrophotometer.

The TBARS concentration was calculated using the following formula:

where

  is absorbance,  is molar coefficient (1.56 × 10⁵ L/mol/cm),  is concentration of sample,  is path length (1 cm).

2.4.1. Statistical Analysis

The results were analysed using “Student’s -test.” Values of were considered statistically significant.

3. Results

3.1. In Vitro Antioxidant Activity

The standard curve equations and = 0.9962 were obtained from the standard curve for TROLOX. The antioxidant activity of SP 0.5 μg was equivalent to 14.45 μg of standard TROLOX. The percentage inhibition against the radical formation was %.

3.2. In Vivo Antioxidant Activity

Each value represents the mean ± SEM of MDA concentration. Values carrying different superscripts are significantly different (, , and ).

The findings of the study in the rats tested: the serum MDA levels of the control and test group (SP), respectively, were  μmol/L and  μmol/L () and significant reduction () of serum MDA level was observed on Day 21 when compared with Day 0 level of the test group; moreover there were no differences observed in the control group’s MDA concentration on Day 0 and Day 21 (Table 2).

Table 2: Effect of drugs on lipid peroxidation in Wistar rats.

Rat group
MDA con. (µmol/L)

Day 0
Day 21

Control
3.8 ± 0.06
3.9 ± 0.21

Test SP
3.7 ± 0.05

Values are expressed as mean ± SEM; per group.

4. Discussion

An antioxidant is a substance that is able to protect a substrate susceptible to oxidation, being itself present at fairly low concentrations in relation to the substrate. The SP possesses significant therapeutic effects but scientific evidence for these benefits is scarce. Therefore the in vitro and in vivo antioxidant activity of SP were evaluated in this study using ABTS and TBARS assays, respectively.

The ABTS radical method is one of the most frequently used assays for the determination of the concentration of free radicals. The method is applicable to the study of both water-soluble and lipid-soluble antioxidants, pure compounds, and food extracts. The results of the ABTS assay done with SP explained without doubt the potent ability to neutralize the radical spontaneously. The antioxidant activity of 0.5 μg of SP was equivalent to 14.45 μg of standard TROLOX. The percentage inhibition against the radical formation was % and confirms the strong antioxidant power of the SP.

The thiobarbituric acid-reactive substances (TBARS) assay is a widely used method to quantify the concentration of MDA in serum, plasma, or tissue homogenates. At low pH and elevated temperature, MDA readily participates in a nucleophilic addition reaction with 2-thiobarbituric acid (TBA), generating a pink and fluorescent 1 : 2 MDA : TBA adduct. It is a simple, reliable, and a reproducible fluorometric method for measuring TBARS in samples [19]. In this study, the SP showed the significant scavenging activity against MDA formation in rats providing evidence for the potent antioxidant activity of the SP.

5. Conclusion

The present investigation suggests that poly herbal preparation of Sudarshana powder possesses good antioxidant potential and it can be a useful therapeutic agent for the diseases associated with oxidative stress.

Conflicts of Interest

The authors declare that they have no conflicts of interest regarding the publication of this manuscript.

Acknowledgments

Financial assistance is provided by a grant from Human Resource Development Program-HETC project. CMB/IIM/N4 is gratefully acknowledged. The 9th International Research Conference at General Sir John Kotelawala Defence University, Sri Lanka, 8-9 September 2016, is acknowledged for the partial presentation of the abstract.

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