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ORIGINAL ARTICLE
Year : 2020  |  Volume : 41  |  Issue : 1  |  Page : 24-28  

Shodhana (processing) of Rakta-Snuhi (Euphorbia caducifolia Haines.) latex with Chincha-patra Swarasa (Tamarindus indica L. leaf juice): A pharmaceutical analysis.


1 PhD Scholar, Department of Dravyaguna, Institute of Teaching and Research in Ayurveda, Gujarat Ayurved University, Jamnagar, Gujarat, India
2 Professor and Head, Department of Dravyaguna, Institute of Teaching & Research in Ayurveda, Jamnagar, Gujarat, India
3 Head, Pharmaceutical Laboratory, Institute of Teaching & Research in Ayurveda, Jamnagar, Gujarat, India

Date of Submission27-Apr-2017
Date of Decision07-Apr-2018
Date of Acceptance06-Jan-2021
Date of Web Publication30-Jul-2021

Correspondence Address:
Shashi Gupta
Institute of Teaching and Research in Ayurveda, Jamnagar-361008, Gujarat
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ayu.AYU_90_17

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   Abstract 


Background: Latex of Euphorbia caducifolia Haines. (Euphorbiaceae), botanical source of Rakta Snuhi, a caustic irritant, is being used in different Ayurvedic therapeutics, after proper processing (Shodhana) in some specific media. Shodhana of Snuhi latex with Chincha-Patra Swarasa (juice of tamarind leaves) using Raudra Yantra (instrument/pot kept under sunlight for drying) has been recommended in Ayurveda texts. Snuhi is one of the Upavisha (sub toxic group of herbal drugs) and a well-known plant in the Indian system of medicine. It is used in pharmaceutical procedures like preparation and processing of drugs. Aim: The aim of the study was to carry out Shodhana of E. caducifolia latex with Chincha-Patra Swarasa. Material and methods: Fresh latex of Snuhi was collected from the Sapada area of Jamnagar, Gujarat and fresh leaves of Tamarindus indica L. were collected from the herbal garden of the university and Swarasa was extracted by traditional expression technique. Shodhana of Snuhi Kshira was done under sunlight dried and shade dried method by mixing it with leaf juice of Tamarindus indica L. in a glass bowl in different ratio i.e. Kshira: leaf juice was 8:4, 8:2, 8:1 respectively. Results: This study reveals certain changes in physico-chemical parameters (pH) and organoleptic characters of processed E. caducifolia latex by Tamarind leaf juice both in shade-dried and sunlight-dried samples. Under HPTLC, Shodhana of E. caducifolia latex with Tamarind leaf juice alters the number of spots both sunlight-dried and shade-dried samples. In sun-dried sample, the number of spots increased when the concentration of Tamarind leaf juice is decreased in HPTLC study. The study reveals that in case of shade-dried Shodhita (processed) Snuhi latex sample, the concentration of lupeol increases with the increasing quantity of Tamarind leaf juice. Conclusion: Shodhana with Tamarind leaf juice changes both qualitative and quantitative property of Snuhi latex.

Keywords: Euphorbia caducifolia Haines, latex, purification, Rakta Snuhi, Shodhana, Tamarindus indica L.


How to cite this article:
Gupta S, Acharya R, Shukla VJ. Shodhana (processing) of Rakta-Snuhi (Euphorbia caducifolia Haines.) latex with Chincha-patra Swarasa (Tamarindus indica L. leaf juice): A pharmaceutical analysis. AYU 2020;41:24-8

How to cite this URL:
Gupta S, Acharya R, Shukla VJ. Shodhana (processing) of Rakta-Snuhi (Euphorbia caducifolia Haines.) latex with Chincha-patra Swarasa (Tamarindus indica L. leaf juice): A pharmaceutical analysis. AYU [serial online] 2020 [cited 2021 Dec 5];41:24-8. Available from: https://www.ayujournal.org/text.asp?2020/41/1/24/322838




   Introduction Top


Rakta-Snuhi (E. caducifolia), botanically identified as Euphorbia caducifolia Haines., is a member of Upavisha group (sub-toxic herbal group)[1] and is being used extensively in different formulations of therapeutic significance, being advocated, in diseases such as Gulma (abdominal lump), Arsha (piles), Grahani (sprue), Pandu (anemia), Kushtha (skin diseases) and Shotha (edema).[2] It's latex is used as Bhavana Dravya (lavigation) in the preparation of Vati (tablets), Varti (suppositories) and herbo-mineral compound formulation.[3] The latex is used in the management of Arsha (piles) and Bhagandara (fistula) and in the preparation of Ksharasutra (alkaline thread).[4] Euphorbia caducifolia latex contains number of chemical constituents such as flavonoids, terpenoids, reducing sugar, carbohydrates and amino acids, among which terpenoids is considered as the main responsible constituent for the poisonous effect.[5] The latex or sap of many Euphorbia plants is toxic and may cause inflammation of the skin[6] and eye[7],[8] on contact. Euphorbia caducifolia has also been reported to cause ocular injury.[9] The latex of E. caducifolia is acrid and liable to cause dermatitis.[10] To minimize or to prevent the poisonous effect of Rakta-Snuhi latex and to enhance the potency and efficacy of the drug, Shodhana is recommended.[11] According to Ayurvedic literature, Snuhi latex should be mixed with leaf juice of Tamarindus indica and then the mixture should be kept under sunlight, in Raudra Yantra (drying in sunlight keeping the contents in a saucer), till it is dried properly.[12],[13]

Lupeol is a pentacyclic triterpene which has a wide therapeutic usage, has been reported in euphorbia species, and possesses anti-inflammatory and antioxidant activity[14] and thus was chosen as a marker in this study. Impact of Shodhana on E. caducifolia latex has not been reported till date. Hence, the present study was carried out to evaluate the impact of purification of E. caducifolia latex by tamarind leaf juice and to develop physicochemical and high-performance thin-layer chromatographic (HPTLC) profile.


   Materials and methods Top


Collection and selection of drug

The plant Rakta-Snuhi was identified by a local plant taxonomist and the botanical name, i.e., Euphorbia caducifolia Haines, was confirmed by studying the morphological characters, as described in Flora of Orissa and Trease and Evans, Pharmacognosy.[15],[16] Sample specimen was authenticated by an expert of Pharmacognosy laboratory of IPGT and RA, Gujarat Ayurved University, Jamnagar, and herbarium of the sample has been deposited to Institute's pharmacognosy museum which consisted of Euphorbia caducifolia Haines (Phm/6213) and its latex that was collected by the scholar from its natural habitat of surrounding place of Jamnagar, during February 2016, early in the morning (7 am). The latex has been stored in a glass jar. Chincha (T. indica) leaves were collected from the campus of Gujarat Ayurved University, Jamnagar.

Procedure

Method of purification of Rakta-Snuhi latex was carried out in two groups. In one group drying latex was mixed with T. indica leaves juice, in a Raudra Yantra and was kept mixed in the sunlight in the ratio of 8:4, 8:2, and 8:1 in a glass bowl. In the other group each of these content were kept in shade (in the absence of direct sunlight). Each procedure was repeated three times to validate the pharmaceutical procedure.[12] Final samples were stored in a airtight glass container and labeled as samples 1 (8:4 shade processed sample), sample 2 (8:2 shade processed sample), sample 3 (8:1 shade processed sample), sample 4 (8:4 sunlight processed sample), sample 5 (8:2 sunlight processed sample) and sample 6 (8:1 sunlight processed sample) [Table 1].
Table 1: pH of different processed samples of Rakta Snuhi (in shade dried and sunlight dried)

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Tamarind leaf juice was prepared by adding 20 ml of water to 100 g of, T. indica leaves and this mixture was titrated and processed in an electronic mixer. Later, tamarind leaves juice was extracted using a muslin cloth.

Organoleptic character and pH

pH and organoleptic characters of these samples were evaluated following standard procedures recommended by Ayurvedic Pharmacopoeia of India.[17]

High-performance thin-layer chromatographic study

Chemicals percolated silica gel 60 F254 thin-layer chromatography (TLC) aluminum plates (10 cm × 10 cm, 0.2 mm thick), analar reagent (AR) grade toluene, ethyl acetate, 5% alcoholic potassium hydroxide, chloroform and vanillin-H2SO4 reagent were obtained from M/S Merck Ltd. Mumbai, India. Lupeol (purity 95% by gas chromatography), the reference standard, was procured from Natural Remedies Pvt. Limited, Bangalore, India.[18]

Samples for high-performance thin-layer chromatography (HPTLC)

The extracts of all samples for HPTLC were made in the same process as mentioned below:

  1. Methanolic extract 2.5 g of sample was macerated with 50 ml of methanol for 24 h and filtered. The filtrate was concentrated to 30 mg and used for spotting
  2. One ml of the sample of latex was mixed in an equal quantity of 5% alcoholic potassium hydroxide and subjected to heat and then an unsaponified layer was obtained by adding the mixture with 3 ml of chloroform. The filtrate was concentrated to 30 mg and used for spotting.


The samples were titled as Track-1 to 11 and the details are as below:

Track-1: 2.5 μg of standard lupeol

Track-2: 5 μg of standard lupeol (taken as reference standard)

Track-3: 7.5 μg of standard lupeol

Track-4: 10 μg of raw latex

Track-5: 10 μg of raw Chincha leaf juice

Track-6: 10 μg of 8:1 shade processed sample

Track-7: 10 μg of 8:2 shade processed sample

Track-8: 10 μg of 8:4 shade processed sample

Track-9: 10 μg of 8:1 sunlight processed sample

Track-10: 10 μg of 8:2 sunlight processed sample

Track-11: 10 μg of 8:4 sunlight processed sample

Mobile phase: toluene: ethyl acetate (14:6) v/v

Detection: spray with vanillin-H2SO4.

Chromatographic conditions

A Camag Linomat V HPTLC system equipped with an automatic TLC sampler, TLC scanner III and integrated software Win CATS was used for the analysis. Precoated silica gel GF254 plates were used for the study. Development was carried out in Camag Twin Trough Chamber where chamber saturation was 30 min, development time was 30 min, and development distance was 10 cm.


   Results Top


pH

pH of raw Euphorbia caducifolia was 4.35 and T. indica leaf juice was 2.70 and pH of various processed samples are presented in [Table 1]. It took 11 and 7 days for complete drying of samples under shade and in sunlight, respectively.

Odor

The odor of samples was noted at a regular interval of 12 h. Sunlight-dried processed samples became odorless after 12 h, while shade-dried processed samples became odorless after 48 h.

Color

The colors of all the processed samples were noted after 24 h. The color of all shade-dried samples changed from milky white to creamish white on the 3rd day and then changed to light brown after 7th day. While in sun light-dried samples, the milky white color changed to creamish white color on the 2nd day and then creamish light brown on the 4th day.

Estimation of lupeol

The lupeol quantities in different tracks were noted and details are presented in [Table 2].
Table 2: Lupeol quantity in different samples of processed latex of Euphorbia caducifolia

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   Discussion Top


Tamarind leaf juice is highly acidic (2.70) in nature. There was a significant reduction in pH as the amount of tamarind leaf juice proportion increased, i.e., 4.35–3.27 which differs in different processed samples due to differences in the ratio of E. caducifolia latex and T. indica leaf juice. Tamarind leaf juice neutralizes the poisonous effect of E. caducifolia latex by its chemical composition and strong acid nature.

Sun light processed samples became odorless in 12 h and dried in 7 days, while shade dried samples became odorless in 48 h and dried in 11 days. This may be due to the direct effect of heat.

High-performance thin-layer chromatographic findings

The concentration of lupeol in E. caducifolia latex was found to be increased in shade-dried processed sample when the concentration of T. indica leaf juice was increased.

On the other hand, the concentration of lupeol gets decreased when the sample is exposed to sunlight. The concentration of lupeol in ample quantity in T. indica leaf juice provides potency to E. caducifolia latex. It has been reported that the concentration of lupeol depends on temperature and duration;[19] thus, lupeol was in higher concentration in shade sample than sun-dried sample.

Rf value

HPTLC study at 524 nm showed 11 spots in raw latex sample, 11 spots in tamarind leaf juice, 12 spots in 8:4 shade-dried sample, 14 spots in 8:2 shade-dried sample, 12 spots in 8:1 shade-dried sample, 10 spots in 8:4 sun-dried sample, 11 spots in 8:2 sun-dried sample and 12 number of spots in 8:1 sun-dried sample. 2D densitograms shows variation of lupeol during purification methods of E. caducifolia latex [Figure 1]a, [Figure 1]b, [Figure 1]c, [Figure 1]d, [Figure 1]e, [Figure 1]f, [Figure 1]g, [Figure 1]h, [Figure 2]a, [Figure 2]b, [Figure 2]c, [Figure 2]d, [Figure 2]e, [Figure 2]f, [Figure 2]g, [Figure 2]h.
Figure 1: (a) Linearity (two-dimensional densitograms) graph of lupeol (2.5 μl). (b) Linearity (two-dimensional densitograms) graph of lupeol (5 μl). (c) Linearity (two-dimensional densitograms) graph of lupeol (7.5 μl). (d) Densitogram showing lupeol in latex of E. caducifolia. (e) Densitogram showing lupeol in leaf juice of T. indica. (f) Densitogram showing lupeol in 8:4 Latex of E. caducifolia: Leaf juice of T. indica, shade processed sample. (g) Densitogram showing lupeol in 8:2 latex of E. caducifolia: Leaf juice of T. indica, shade processed sample. (h) Densitogram showing lupeol in 8:1 latex of E. caducifolia: Leaf juice of T. indica, shade processed sample

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Figure 2: (a) Densitogram showing lupeol in 8:4 latex of E. caducifolia: Leaf juice of T. indica, sunlight processed sample. (b) Densitogram showing lupeol in 8:2 latex of E. caducifolia: Leaf juice of T. indica, sunlight processed sample. (c) Densitogram showing lupeol in 8:1 latex of E. caducifolia: Leaf juice of T. indica, sunlight processed sample. (d) Densitogram showing three-dimensional wavelength graph. (e) Densitogram showing multi-wavelength graph. (f) Thin-layer chromatography plate in vanillin-H2SO4. (g) Thin-layer chromatography plate at 254 nm. (h) Thin-layer chromatography plate at 366 nm

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Details of common Rf value having similar spectra in different processed samples are given in [Table 3].
Table 3: Common Rf values in different processed samples of Rakta Snuhi Ksheera

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After purification process, there is a change in concentration at similar Rf, but no new moiety is formed at a similar Rf. At 0.77 Rf, similar spectra were observed both in lupeol and Tamarind leaf juice, whereas dissimilar spectra were observed in E. caducifolia latex and in all processed samples at 0.77 Rf. Spectral comparison graph of different samples during purification methods of E. caducifolia [Figure 3]a, [Figure 3]b, [Figure 3]c, [Figure 3]d, [Figure 3]e, [Figure 3]f, [Figure 3]g, [Figure 3]h.
Figure 3: (a) Spectral comparison at 0.45 Rf. (b) Spectral comparison at 0.41 Rf. (c) Spectral comparison at 0.53 Rf. (d) Spectral comparison at 0.60 Rf. (e) Spectral comparison at 0.68 Rf. (f) Spectral comparison at 0.73 Rf. (g) Spectral comparison at 0.77 Rf. (h) Spectral comparison at 0.89 Rf

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   Conclusion Top


Shodhana (purification process) of Euphorbia caducifolia latex with tamarind leaf juice changes both its qualitative and quantitative properties of Rakta Snuhi latex. Shodhana alters the pH, color, and odor of Euphorbia caducifolia latex. It also alters the number of spots both in sun and shade-dried samples. The study reveals that in case of shade-dried processed latex sample, the concentration of lupeol increases with the increasing quantity of Tamarind indica leaves juice.

Financial support and sponsorship

This study was financially supported by IPGT & RA, Gujarat Ayurved University, Jamnagar, India.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

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Kumar TK, Shweta V, Hitesh B, Patgiri BJ. Exposure to Snuhi Ksheera (Euphorbia caducifolia Haines. latex) resulting in ocular injury: A case report. J Ayurvedic Herb Med 2017;3:1-4.  Back to cited text no. 9
    
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Shashtri A, editor. Bhaishajya Ratnavali of Govindas sen. Shodhana marana adhyaya, Ver. 170. Reprint edition. Varanasi: Chaukhamba Prakashan; 2011. p. 34.  Back to cited text no. 13
    
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Fernandez MA, La Heras B, Dolores García-Gimenez M, Teresa Sáenz, Villar A, et al. New insights into the mechanism of action of the anti-inflammatory triterpene lupeol. J Pharm Pharmacol 2001;53:1533-9.  Back to cited text no. 14
    
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Trease and Evans, Pharmacognosy. Ed. 15th, W.B. Sunders Company Ltd. 1996. p. 521-547.  Back to cited text no. 16
    
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Stahl E. Thin Layer Chromatography – A Laboratory Handbook. Berlin and New York: Springer Verlag and Heidelberg; 1969. p. 52-56.  Back to cited text no. 18
    
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Vithana MD, Stuart SZ. Cold storage temperatures and durations affect the concentrations of lupeol, mangiferin, phenolic acids and other health-promoting compounds in the pulp and peel of ripe mango fruit. Postharvest Biol Technol 2017;139:91-8.  Back to cited text no. 19
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]
 
 
    Tables

  [Table 1], [Table 2], [Table 3]



 

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