Volume 6 • Issue 5 • 1000193
J Drug Metab Toxicol
ISSN: 2157-7609 JDMT, an open access journal
Research Article Open Access
Pawar and Lalitha, J Drug Metab Toxicol 2015, 6:5
DOI: 10.4172/2157-7609.1000193
Research Article Open Access
Drug Metabolism & Toxicology
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ISSN: 2157-7609
*Corresponding author: Dr. Harshal Ashok Pawar, Assistant Professor and Head
of Department (Quality Assurance), Dr. L. H. Hiranandani College of Pharmacy,
Smt. CHM Campus, Opp. Ulhasnagar Railway Station, Ulhasnagar-421003,
Maharashtra, India, Tel: +91-8097148638; E-mail: harshal.dlhhcop@gmail.com
Received October 30, 2015; Accepted December 03, 2015; Published December
13, 2015
Citation: Pawar HA, Lalitha KG (2015) Toxicological Evaluation of Gum
(Galactomannans) Isolated from Senna tora Seeds . J Drug Metab Toxicol 6: 193.
doi:10.4172/2157-7609.1000193
Copyright: © 2015 Pawar HA, et al. This is an open-access article distributed under
the terms of the Creative Commons Attribution License, which permits unrestricted
use, distribution, and reproduction in any medium, provided the original author and
source are credited.
Abstract
Seed gums possess excellent emulsifying, suspending, binding, thickening stabilizing and water-holding
properties. Therefore they are used in various pharmaceutical dosage forms like tablets, syrups, suspensions,
lotions, ointments and for sustained drug release systems. Gum derived from the seeds of Senna tora L. is common
herbaceous annual occurring weed throughout the India. The present investigation reports preliminary phytochemical
screening and toxicological evaluation of the isolated seed gum from the Senna tora. The acute toxicity study was
carried out in adult albino rats by “fxed dose” method. The sub-acute toxicity study was carried out for 28 days
in wistar albino rats. All the Animals used were observed for clinical signs, physical abnormalities, changes in
body weight and pre-terminal deaths. Laboratory investigations such as hematology and clinical chemistry were
performed at sacrifce and the data were statistically analyzed. Based on the results of the acute oral toxicity on the
polysaccharide in Wistar rats, it may be concluded that the LD50 of the Senna tora gum is greater than 2000 mg/kg.
In the sub-acute toxicity study, the gum treated groups did not show any sign of toxicity after getting treated at dose
levels of 500, 1000 and 1500 mg/kg daily for 28 days.
Toxicological Evaluation of Gum (Galactomannans) Isolated from Senna
tora Seeds
Harshal A Pawar
1
* and KG Lalitha
2
1
Dr. L. H. Hiranandani College of Pharmacy, Ulhasnagar-421003, Maharashtra, India
2
Ultra College of Pharmacy, 4/235, College Road, Thasildar Nagar,Madurai-625020, Tamil Nadu, India
Keywords: Toxicity; Phytochemical screening; Seed gum; Senna
tora; Galactomannans
Introduction
Seed gums are vital food hydrocolloids used globally in various
food and pharmaceutical industries. Te rising industrial applications
of these gums in the area of paper, textile, petroleum, food and
pharmaceutical industries has resulted in an impetus in India for
intensifed research on new sources of gum and their derived products
[1]. Tese gums are normally stable at a wide pH range and have good
interaction abilities with organic, inorganic and food constituents.
Tey are biocompatible, cheap and easily available. Natural materials
have advantages over synthetic ones since they are chemically inert,
nontoxic, less expensive, biodegradable and widely available [2]. Tey
possesses excellent binding, suspending, emulsifying, thickening
stabilizing and water-holding properties and could be utilized for
the preparation of pharmaceutical dosage forms like tablets, syrups,
suspensions, lotions, ointments and for sustained drug release systems
[3].
Gum isolated from the seeds of Senna tora L. is common herbaceous
annual occurring weed throughout the India. It is also commonly
known as ‘Sickle Pod’ [4]. Literature survey revealed presence of various
phytoconstituents such as anthraquinone glycosides, naphthopyrone
glycosides, favanoids and phenolic compounds in diferent parts of
Senna tora plant [5-7]. Several medicinal properties have been credited
to Senna tora in Indian system of medicine. Te seeds of Senna tora
have been used in Chinese medicine as aperients, antiasthnic, diuretic
agent and also improve the visual activity [8]. Te Senna tora leaves
extract has been found to exhibit signifcant hepatoprotective activity
and anti-infammatory activity [9,10].
It is important to study phytochemistry and toxicity of the
galactomannans isolated from Senna tora seeds to fnd its utility,
suitability and acceptability as a polymer/excipient in formulating
various pharmaceutical dosage forms. Te objective of acute oral
toxicity study was to assess the toxicological profle of the Senna tora
gum when administered to rats by a single oral gavage. Tis study
aimed at providing a rational basis for risk assessment in human being.
Te purpose repeated dose (28-day) oral toxicity study was to assess
the systemic toxic potential of the test item when administered by
gavage to rats. Tis study provides information on the possible health
hazards likely to arise from repeated exposure over a relatively limited
period of time. Te study was performed at Ultra College of Pharmacy
in compliance with OECD (Organization for Economic Co-operation
and Development) guidelines.
Materials and Method
Collection and authentication of plant material
Te pods of Senna tora were collected in the month of September-
October from Maharashtra region. Te seeds were separated manually
and dried under shade. Plant material was authenticated by Dr.
Rajendra D. Shinde, Associate Professor, Blatter Herbarium; St.
Xavier’s College, Mumbai and was identifed as Senna tora (L.) Roxb
(Herbarium Specimen no.8361). Te herbarium specimen of Senna
tora was stored in Ultra College of Pharmacy, Madurai for future
reference.
Isolation and purifcation of gum
Te endosperms of the Senna tora seed were separated mechanically
followed by milling. Te powder of the endosperm obtained was soaked
in benzene–ethanol solution (1:1) overnight to remove lipids and then