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      Safety Profile of a Polyherbal Formulation ( Gynocare capsules) in Female Rats by Subchronic Oral Toxicity Study

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          Abstract

          Gynocare capsules, is a polyherbal formulation, are used as uterine tonic and for treating gynaecological ailments like infertility, leucorrhea, and menstrual disorders. The formulation contains ingredients of herbal origin, such as, extracts of Ashoka, Vasaka, Durva, Chandan, Musk, and so on. It was evaluated for its safety at the therapeutic dose level by a repeated dose oral toxicity study in albino Wistar rats. The herbal formulation was administered orally at a therapeutic dose of 100 mg/kg/day, for 90 days. All animals were monitored daily for their health status and signs of abnormalities. The body weight, water consumption, and food intake were measured once weekly. At the end of the experimental period, various hematological and biochemical parameters were estimated and histopathologies of selected organs were conducted. The study resulted from the long-term oral administration of Gynocare capsules (100 mg/kg), did not cause any relevant signs of toxicity nor significant changes in the physical, hematological and biochemical parameters. However, statistically significant differences were seen in the relative organ weights of adrenal gland, ovary, and serum creatinine levels. The reduction in ovary weight revealed the possibility of the drug targeting the ovary. Moreover, no pathological features were identified in the treated group as monitored by the histopathological analysis of the internal organs. The study established that Gynocare capsules at the dose given (100 mg/kg) did not induce any remarkable or significant toxic effects, indicating that it was safe in rats following oral administration for 90 consecutive days.

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          From magic bullets to designed multiple ligands.

          Increasingly, it is being recognised that a balanced modulation of several targets can provide a superior therapeutic effect and side effect profile compared to the action of a selective ligand. Rational approaches in which structural features from selective ligands are combined have produced designed multiple ligands that span a wide variety of targets and target classes. A key challenge in the design of multiple ligands is attaining a balanced activity at each target of interest while simultaneously achieving a wider selectivity and a suitable pharmacokinetic profile. An analysis of literature examples reveals trends and insights that might help medicinal chemists discover the next generation of these types of compounds.
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            Acute and chronic toxicity of the aqueous extract of Artemisia afra in rodents.

            Artemisia afra (Jacq. Ex. Willd), "African Wormwood" is widely used traditionally in South Africa with no literature evidence substantiating its safety. The aim of this study was to investigate the safety of the aqueous extract of Artemisia afra by determining its pharmaco-toxicological effects after acute and chronic administration in mice and rats, respectively. The aqueous extract mimicked the traditional decoction dosage form of Artemisia afra. In mice, single intraperitoneal injections of Artemisia afra-extract (1.5-5.5g/kg) induced a regular dose-dependent increase in the death rate and incidence of general behaviour adverse effects, while with single oral doses (2-24g/kg) the increases in incidence of general behaviour adverse effects and mortality rate were dose-independent. The LD(50s) after acute intraperitoneal and oral doses were 2.45 and 8.96g/kg, respectively. Rats given oral doses of Artemisia afra-extract (0.1 or 1g/kg/day) survived the 3 months of dosing (i.e. LD(50) much higher than 1g/kg), experienced no significant changes in general behaviour and haematological and biochemical parameters, except for transient decrease in AST activity. No significant changes were observed in organ weights, and histopathological results showed normal profile suggesting no morphological alterations. Collectively, the results indicate that Artemisia afra-extract is non-toxic when given acutely, has low chronic toxicity potential and, in high doses, may have a hepatoprotective effect.
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              Acute and sub-chronic oral toxicity profiles of the aqueous extract of Polygala fruticosa in female mice and rats.

              Polygala fruticosa (P.J. Bergius) is one of the most popular medicinal plants in South Africa but to date there is no documented evidence corroborating its safety. This study thus aimed to determine the toxicity profile of the aqueous extract of Polygala fruticosa by determining its effects after acute and sub-chronic oral administration in female mice and rats, respectively. In adult mice, single oral administrations of the aqueous extract of Polygala fruticosa (2-20 g/kg body weight) induced an increase in the incidence of general behavioural adverse effects. The mortality rate also increases with increasing dosage (LD(50)=10.8 g/kg). In rats, daily single oral doses of Polygala fruticosa aqueous extract (0.1 and 1g/kg) were well tolerated behaviourally after 31 days of dosing (LD(50) much higher than 1g/kg) and induced no significant changes in body and organs weights. However, haematological and biochemical parameters showed a significant decrease in platelet count and significant increases in ALT, AST and creatinine levels suggesting disturbances of haemopoiesis, liver and kidney functions. Overall, the findings of this study indicate that Polygala fruticosa is non-toxic and has, at low dose, a low toxicity potential in acute and chronic oral administrations, respectively. However, at high chronic oral doses, Polygala fruticosa has significant anti-haemopoietic, hepatotoxic and nephrotoxic activities. Copyright (c) 2010 Elsevier Ireland Ltd. All rights reserved.
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                Author and article information

                Journal
                Toxicol Int
                Toxicol Int
                TI
                Toxicology International
                Medknow Publications & Media Pvt Ltd (India )
                0971-6580
                0976-5131
                May-Aug 2012
                : 19
                : 2
                : 106-111
                Affiliations
                [1]Department of Pharmaceutical Chemistry, C. U. Shah College of Pharmacy, SNDT Women's University, Santacruz (West), Mumbai, India
                Author notes
                Address for correspondence: Dr. Pratima A. Tatke, C. U. Shah College of Pharmacy, S.N.D.T Women's University, Juhu Campus, Mumbai - 400 049, India. E-mail: patatke@ 123456gmail.com
                Article
                TI-19-106
                10.4103/0971-6580.97196
                3388751
                22778505
                60356ca7-f355-4f78-a79c-102a033f08fd
                Copyright: © Toxicology International

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Categories
                Original Article

                Toxicology
                polyherbal formulation,repeated dose oral toxicity,sub-chronic oral toxicity
                Toxicology
                polyherbal formulation, repeated dose oral toxicity, sub-chronic oral toxicity

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