scholarly journals Acute Toxicity Study and Determination of Median Lethal Dose of Catharanthus roseus in Wistar Albino Rats

2019 ◽  
Vol 19 (3) ◽  
pp. 217-222 ◽  
Author(s):  
M.G. Ajuru ◽  
G. Ajuru ◽  
F.W. Nmom ◽  
C.W. Worlu ◽  
P.G. Igoma
Keyword(s):  
Acute Toxicity ◽  
Catharanthus Roseus ◽  
Lethal Dose ◽  
Toxicity Study ◽  
Albino Rats ◽  
Median Lethal Dose ◽  
Acute Toxicity Study ◽  
Wistar Albino Rats

scholarly journals ANTI ARTHRITIC ACTIVITY OF HERBO MINERAL SIDDHA PREPARATION ARUMUGA CHENDURAM AGAINST TYPE II COLLAGEN INDUCED ARTHRITIS IN EXPERIMENTAL RATS

2020 ◽  
pp. 28-36
Author(s):  
M. Ramamurthy ◽  
V. Thanigavelan ◽  
S. Elansekaran ◽  
V. Srinivasan ◽  
P. Shanmugapriya ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Type Ii Collagen ◽  
Toxicity Study ◽  
Albino Rats ◽  
Type Ii ◽  
Collagen Induced Arthritis ◽  
Immune Disorder ◽  
Animal Products ◽  
Acute Toxicity Study ◽  
Wistar Albino Rats

Siddha system of medicine is the eternal science of life. It is a system that has its extensive bonding with Dravidian culture, language and beliefs. The system of medicine mostly prevailed and prospered in the regions of Dravidian cultures by the great Siddhars. It’s unique as one only than other AYUSH traditional systems of medicine across India with its distinctive abundant usage of medicinal plants, metals, minerals and animal products. Siddhars used the steps of Alchemy to prepare various medicines from metallic and mineral origin for attainment elixir and various rare diseases. Siddha medicine is classified into 32 types of internal and external medicine each. Among the 32 types of internal medicine Chendhuram is a medicine shelf life of 75 years usually from herbo-mineral combinations. Arumuga Chendhuram (ARC) is a herbo-mineral formulation cited in Siddha literature ‘Siddha Vaithiya Thirattu’. ARC was orally administered at higher dose 2gm/kg to the Wistar Albino rats in acute toxicity study and during 28 days of repeated (sub acute) toxicity study, at daily doses of 12, 24 & 48mg/kg of body weight to the Wistar Albino rats. Type II collagen arthritis is another model for developing autoimmune arthritis. The immune pathogenesis mediated by T cell and B cell response to collagen. By this model, nearly 100% arthritis can be achieved. In our study, ARC after 42 days treatment reduced the arthritic swelling significantly and degree of inflammation evident to act against auto immune disorder.

Acute Toxicity study of Synthesized drug and Herbal Product

2021 ◽  
pp. 251-256
Author(s):  
Tanuja Yadav ◽  
Sachin Rohane
Keyword(s):  
Acute Toxicity ◽  
Lethal Dose ◽  
Herbal Product ◽  
Therapeutic Index ◽  
Chemical Substance ◽  
Toxicity Study ◽  
Multiple Exposures ◽  
Acute Toxicity Study ◽  
Short Period

Acute toxicity study describes the adverse effects of a substance that result either from a single exposure or from multiple exposures in a short period of time. Whenever an investigator administered a chemical substance or herbal drug to a biological system different types of interactions can occur and a series of dose-related responses result. In most cases these responses are desired and useful, but there are a number of other effects which are not advantageous. These may or may not be harmful to the patient. Acute toxicity study is involved in estimation of LD50. Also it determines the therapeutic index i.e ratio between the lethal dose and the pharmacologically effective dose in the same strain and species. This article Review the methods so for utilized for the determination of acute toxicity.

scholarly journals Acute and Repeated Dose Toxicity Study of Clevira Syrup – A Polyherbal Formulation

2021 ◽  
Vol 14 (3) ◽  
pp. 1459-1467
Author(s):  
Uma Narayanamurthy ◽  
Mirunalini .R ◽  
Subha. V ◽  
K. Manimekalai ◽  
Sakthibalan K ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Toxicity Study ◽  
Tinospora Cordifolia ◽  
Repeated Dose ◽  
Piper Nigrum ◽  
Albino Rats ◽  
Polyherbal Formulation ◽  
Acute Toxicity Study ◽  
Repeated Dose Toxicity ◽  
Wistar Albino Rats

Aim and Objectives: This study evaluated the acute and repeated dose toxicity effects of Clevira Syrup Polyherbal formulation (CSPHF), which was prepared from ten different herbs, well known and widely used in traditional medicine for the management of viral infections and other inflammatory disease conditions. Individually these herbs (Carica papaya, Melia azedarach, Andrographis paniculata, Vetiveria zizanioides, Trichosanthes dioica, Cyperus rotundus, Zingiber officinale, Piper nigrum, Mollugo Cerviana and Tinospora cordifolia )were completely safe, but the polyherbal formulation effects were not known. Thus, this study was done for the investigation of toxicological profile of CSPHF in Wistar Albino rats. Methods: As per OECD(Organisation for Economic Co-operation and Development) guidelines 423 and 407, Acute and Repeated dose toxicity study were proceeded. In the acute toxicity study a single dose of CSPHF (2000mg/kg) was administered orally to female Wistar rats and in repeated dose toxicity study, CSPHF was administered orally in Control group and three different doses (1000, 500 and 250mg/kg body weight) to both male and female wistar albino rats for 28 days. At the end of the study, the animals were euthanized, observed the external and internal morphology (Acute Toxicity) and assessed the effect of CSPHF on histopathological and biochemical parameters (Repeated Dose toxicity study). Results: In acute toxicity study, there were no visual signs of toxicity of CSPHF (2000mg/kg) observed, whereas in Repeated dose toxicity study Ischaemia, inflammation and hematoma of the internal organs were observed at 1000mg/kg dose, but no such toxic features were seen at 500 and 250mg/kg dose of CSPHF. Conclusion: The results of the Acute and Repeated Dose toxicity study could be authenticated in future studies, which will be more useful and evidence based for the management of Viral infectionsduring pandemics.

Acute Toxicity Study and Faecal Dropping Capability of Ethanolic Extract of Tecoma stans in Albino Rats

Pharmacologia ◽  
2013 ◽  
Vol 4 (7) ◽  
pp. 464-468 ◽  
Author(s):  
S. Kameshwara ◽  
C. Jothimaniv ◽  
R. Senthilkum ◽  
S. Thenmozhi ◽  
R. Sundaragan ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Ethanolic Extract ◽  
Toxicity Study ◽  
Albino Rats ◽  
Acute Toxicity Study

scholarly journals Toxicity assessment of the methanol extract of Jatropha tanjorensis (Euphorbiaceae) leaves

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
C. Christian Chibuogwu ◽  
U. Obioma Njoku ◽  
F. C. Okwesili Nwodo ◽  
E. O. Vincent Ozougwu ◽  
N. Victor Nweze
Keyword(s):  
Acute Toxicity ◽  
Biochemical Parameters ◽  
Lethal Dose ◽  
Toxicity Assessment ◽  
Toxicity Study ◽  
Acute Toxicity Study ◽  
Relative Safety ◽  
Liver And Kidney ◽  
Potential Damage ◽  
Dose Dependent Decrease

Abstract Background The leaves of Jatropha tanjorensis have been found to have important application both in traditional medicine and as an edible vegetable in Nigerian soups. It is popularly employed in Nigeria for the treatment of anemia, diabetes, and malaria. The dearth of information on its toxicity prompted this study. Mice were administered single oral doses of 10, 100, 1000, 1600, 2900, and 5000 mg/kg b.wt (n = 3/group) of the extract and were observed for 24 h for any sign of toxicity and mortality in the acute toxicity study. For the sub-acute toxicity study, doses of 100, 200, and 400 mg/kg b.wt of the extract were administered to experimental rats (n = 6/group) for 28 days after which the assessment of hematological and biochemical parameters, as well as liver and kidney histology was conducted post-treatment. Body weight of the animals was also taken weekly. Results The result showed that percentage weight gain decreased as the dose of extract increased. The haematological and biochemical parameters showed that the extract had no toxic effect on experimental animals, though there was a non-significant dose-dependent decrease in WBC. The extract also showed potential to cause hepatotoxicity at the highest dose. Conclusion Though the median lethal dose of the plant extract suggests relative safety of the plant material, consuming large amounts over a prolonged time may need to be discouraged to avoid potential damage to vital organs such as the liver.

scholarly journals In vivo antiplasmodial potential of aqueous seed extract of Ricinus communis

2019 ◽  
Vol 8 (2) ◽  
pp. 133-138
Author(s):  
Peace ME. Ubulom ◽  
Ette O. Ettebong ◽  
Edidiong J. Udofia ◽  
Rachel S Inyang Etuk
Keyword(s):  
Acute Toxicity ◽  
Ricinus Communis ◽  
Lethal Dose ◽  
Suppressive Effect ◽  
Seed Extract ◽  
Toxicity Study ◽  
Control Group ◽  
Active Principle ◽  
Acute Toxicity Study

Introduction: Ricinus communis is used by the people of Niger-Delta region of Nigeria, for the treatment of various ailments, especially malaria. This study evaluated the antiplasmodial potentials of the aqueous seed extract of R. communis, using Plasmodium berghei berghei. Methods: Acute toxicity study was carried out to determine the median lethal dose (LD50) of the extract. Antiplasmodial effect of the extract was assessed in suppressive, repository/ prophylactic and curative models, using Swiss albino mice (15-29 g). Mice were infected intraperitoneally with 0.2 mL of parasitized blood. Extract doses administered were 54.77, 109.54 and 164.32 mg/kg/d of the seed extract and each dose had 6 replicates. Artesunate (5 mg/kg/d) and pyrimethamine (1.2 mg/kg/d) were used as standard drugs, while distilled water (10 mL/kg/d) served as control. Results: Acute toxicity study produced LD50 of 547.72 mg/kg. The extract demonstrated a dosedependent reduction in parasitaemia in all tests. At the end of 4-day test, suppressive effect of 20.80, 49.00, 75.00 and 88.40% were obtained for doses 54.77, 109.54 and 164.32 mg/kg/d of the seed extract and artesunate, respectively. In the repository test pyrimethamine was more potent (72.26%) than the seed extract (9.47%–51.42%). The extract also exhibited appreciable curative effect. The activity of the seed extract was significant when compared with the control (P < 0.05). Mice treated with the seed extract and drugs survived for longer duration than the control group. Conclusion: The aqueous seed extract of R. communis has antiplasmodial potential and its active principle should be elucidated and further investigated to help in the ongoing fight against malaria.

An experiemental study to evaluate the principle Trini Dravyani Nati Upayunjita w.s.r. to Kshara (Alkali)

2019 ◽  
Vol 4 (04) ◽  
Author(s):  
Amrita Paul ◽  
Umapati C. Baragi ◽  
Kashinath Hadimur ◽  
R. A. Deshmukh
Keyword(s):  
Acute Toxicity ◽  
Adverse Effects ◽  
Dose Level ◽  
Behavioral Changes ◽  
Toxicity Study ◽  
Fixed Dose ◽  
Albino Rats ◽  
Acute Administration ◽  
Acute Toxicity Study ◽  
Acute Study

Background: In Charaka Samhita it has been mentioned that three medicinal substances viz. Pippali (Piper longum), Kshara (alkali) and Lavana (salt) can be used as emergency medicine, but they should not be consumed in excess (Ati Upayunjita). If they are consumed in excess quantity they will cause several adverse effects in the body. Hence in the present study Kshara has been evaluated in experimental animals in two different phases viz. acute administration at graded doses as part of acute toxicity study and sub-acute administration at fixed dose level, as part of sub-acute toxicity study, to assess the possible adverse effects if any. Objectives: To evaluate the acute and sub-acute toxic effect of Kshara in albino rats to establish the principle of Trini Dravyani Nati Upayunjita. Materials and Methods: Wister strain albino rats of either sex weighing between 150 - 200g body weights were used for experimental study. The experiment was carried out as per ‘Ayush Guidelines’ after the IAEC clearance. For Acute Toxicity - 9 Albino rats were used and for Sub-Acute Toxicity - 12 Albino rats were used. The dose calculation was done on the basis of body surface area ratio using the table of ‘Paget and Barnes rule’. Results: In Acute toxicity study no mortality and behavioral changes were observed when the drug Kshara was studied after two dose level i.e. TED X 5 and TED X 10. In Sub-acute study some behavioral changes (including cage side behavior) were observed. No mortality was observed in any of the groups. Discussion: Acute toxicity study of Kshara showed no immediate and evident toxic signs and mortality within 24 hours of observation. In Sub-acute toxicity study in all four groups, no mortality or evident toxic effects were observed, however some mild histopathological changes were observed in sub-acute study.

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