Saturday, November 14, 2015

A Consensus Review on Hepatoprotective Potential of Herbal Drugs.


A Consensus Review on Hepatoprotective Potential of Herbal Drugs


Liver injury is major health problems about more than 900 drugs implicated in case of liver injury. Hepatotoxicity is caused by the alcoholic consumption, toxic substances and certain drugs which produce injury to liver such as thioacetamide, paracetamol, anti-tubercular drugs, chemotherapeutic agents and some of organic and inorganic compounds. Medicinal plants are the significant source of hepatoprotective drugs. Mono and poly-herbal preparations have been used in various liver disorders since ages. Clinical research has also shown that herbals have genuine utility in the treatment of liver diseases. The current article deals with phyto pharmacological investigation on some herbs used in liver and gall bladder ailments.

INTRODUCTION
The liver is the largest glandular organ in the body, and has more functions than any other human organ. A person's entire blood supply passes through the liver several times a day; the liver is the key organ of metabolism, secretion and excretion which is continuously and widely exposed to xenobiotics, environmental pollutants and chemo therapeutic agents because of its strategic location in the body.
Liver disease is a worldwide problem. Liver has a pivotal role in human metabolism.Liver produces and secretes bile. It also produces prothrombin and fibrinogen, both blood clotting factors, and heparin, a mucopolysaccharide sulfuric acid ester that helps keep blood from clotting within the circulatory system. The liver converts sugar into glycogen. Conventional drugs used in the treatment of liver diseases are sometimes inadequate and can have serious adverse effects. It is, therefore, necessary to search for alternative drugs for the treatment of liver disease to replace currently used drugs of doubtful efficacy and safety. The liver plays an astonishing array of vital functions in the
maintenance, performance and regulating homeostasis of the body. Liver is considered to be one of the most vital organs that functions as a centre of metabolism for nutrients such as carbohydrates, proteins and lipids and excretion of waste metabolites.

Liver diseases have become one of the major causes of morbidity and mortality in man and animals all over the globe and hepatotoxicity due to drugs appears to be the most common contributing factor. Among the many diseases that can affect the liver the most common is 'viral hepatitis' (Inflammation of liver caused by viral infection). Hepatitis can be caused by drugs, viruses, bacteria, mushrooms, parasites like amoebas or giardiasis. About 20,000 deaths found every year due to liver disorders. The use of natural remedies for the treatment of liver diseases has a long history and medicinal plants and their derivatives are still used all over the world in one form or the other for this purpose. Scientific evaluation of plants has often shown that active principles in these are responsible for therapeutic success. A large number of medicinal plants have been tested and found to contain active principles with curative properties against a variety of diseases. Liver protective plants contain a variety of chemical constituents like phenols, coumarins, lignans, essential oil, monoterpenes, carotinoids, glycosides, flavanoids, organic acids, lipids, alkaloids and xanthenes. Recent experience has shown that plant drugs are relatively non-toxic, safe and even free from serious side effects.

Additionally, it is also handling the metabolism the biochemical pathways to growth, fight against disease, nutrient supply, energy provision and reproduction and excretion of drugs and other xenobiotics from the body thereby providing protection against foreign substances by detoxifying and eliminating them. The bile secreted by the liver has, among other things, plays an important role in digestion. Enhanced lipid per oxidation during metabolism of ethanol may result in development of hepatitis leading to cirrhosis. Since time immemorial, mankind has made the use of plants in the treatment of various ailments. The Indian traditional medicine like Ayurvedic, Siddha and Unani is predominantly based on the use of plant materials. Herbal drugs have gained importance and popularity in recent years because of their safety, efficacy and cost effectiveness.The association of medical plants with other plants in their habitat also influences their medicinal values in some cases. One of the important and welldocumented uses of plant products is their use as hepatoprotective agents. Hence, there is an ever increasing need for safe hepatoprotective agent.

Silymarin is a potent hepatoprotective drug having established place in hepatology practice. Silymarin is flavono-lignan mixture obtained from seeds of Silybum marianum. Silymarin is a mixture of silybin, isosilybin, silychristin and silydianin. Research on Indian medicinal herbs like Picrorhiza kurroa (Kutaki) and Andrographis paniculata (Kalmegh) has thrown light on hepatoptotective activity and it is more promising than silymarin.

Treatment of Liver Disease

Each liver disease will have its own specific treatment regimen. For example, hepatitis A requires supportive care to maintain hydration while the body's immune system fights and resolves the infection. Patients with gallstones may require surgery to remove the gallbladder. Other diseases may need long-term medical care to control and minimize the consequences of their disease. In patients with cirrhosis and end-stage liver disease, medications may be required to control the amount of protein absorbed in the diet. The liver affected by cirrhosis may not be able to metabolize the waste products, resulting in elevated blood ammonia levels and hepatic encephalopathy. Low sodium diet and water pills (diuretics) may be required to minimize water retention.In those with large amounts of ascites fluid, the excess fluid may have to be occasionally removed with a needle and syringe (paracentesis). Using local anesthetic, a needle is inserted through the abdominal wall and the fluid withdrawn. Operations may be required to treat portal hypertension and minimize the risk of bleeding. Liver is the final option for patients whose liver has failed.

Treatment by herbal drugs

Medicinal herbs are significant source of hepatoprotective drugs. Mono and poly-herbal preparations have been used in various liver disorders. According to one estimate, more than 700 mono and poly-herbal preparations in the form of decoction, tincture, tablets and capsules from more than 100 plants are in clinical use. A drug having beneficial effect on the liver is known as hepatoprotective drug.On the other hand, drugs having toxic affect on the liver are better known as hepatotoxic drugs. Clinical research has also shown that herbals have genuine utility in the treatment of liver diseases. The article deals with investigative work done on herbals beneficial in liver and gall bladder ailments.

Classification of Hepatoprotective Agents

These are generally classified into 3 categories without any strict delineation amongst them. Anti Hepatotoxic agents: These generally antagonize the effects of any hepatotoxins causing hepatitis or any liver disease.

  1. Hepatotropic agents: These generally support or promote the healing process of the liver. In practice these two activities cannot be easily distinguished from each other.
  2. Hepatoprotective agents: These generally prevent various types of liver affections prophilactically. In general any hepatoprotective agent can act as an anti hepatotoxic or hepatotropic agent but the vice versa is always not true.

Hepatoprotective Herbs

Herbal-based therapeutics for liver disorders has been in use in India for a long time and has been popularized world over by leading pharmaceuticals. Despite the significant popularity of several herbal medicines in general, and for liver diseases in particular, they are still unacceptable treatment modalities for liver diseases. The limiting factors that contribute to this eventuality are:

(i) Lack of standardization of herbal drugs.
(ii) Lack of identification of active ingredients(s)/principles(s).
(iii) Lack of randomized controlled clinical trials (RCTs).
(iv) Lack of toxicological evaluation.

The use of natural remedies for the treatment of liver diseases has a long history, starting with the Ayurvedic treatment, and extending to the Chinese, European and other systems of traditional medicines. The 21st century has seen a paradigm shift towards therapeutic evaluation of herbal products in liver disease models by carefully synergizing the strengths of the traditional systems of medicine with that of the modern concept of evidence-based medicinal evaluation, standardization and randomized placebo controlled clinical trials to support clinical efficacy. 

A large number of plants and formulations have been claimed to have hepatoprotective activity. Nearly 160 phytoconstituents from 101 plants have been claimed by Pharmacopeia Foundation to possess liver protecting activity. In India, more than 87 plants are used in 33 patented and proprietary multi-ingredient plant formulations. In spite of the tremendous advances made, no significant and safe hepatoprotective agent is available in modern therapeutics. Therefore, due importance has been given globally to develop plant-based hepatoprotective drugs, effective against a variety of liver disorders. The present review is aimed at compiling data based on reported works on promising phytochemical from medicinal plants that have been tested in hepatotoxicity models.

Abutilon Indicum
Hepatoprotective activity of Abutilon indicum on experimental liver damage in rats was studied by Porchezhian and Ansari.They used carbon tetrachloride and paracetamol induced hepatotoxicity in rats. A. indicum exhibited significant hepatoprotective activity by reducing carbon tetrachloride and
paracetamol induced change in bio-chemical parameters that was evident by enzymatic examination. The plant extract may interfere with freeradical formation, which may conclude in hepatoprotective action. Acute toxicity studies revealed that the LD50 value is more than the dose of 4 g/kg body wt. They attributed the hepatoprotective activity to the inhibitory effects of drug on cytochrome P450 or/and promotion of its glucuronidation. Β-Sitosterol is present in A. indicum and a petroleum ether extract has larvicidal properties against the mosquito larvae Culex quinquefasciatus. A methanol extract of A. indicum has some antimicrobial properties.


Figure 1: Abutilon Indicum


Borreria Articularis
The hepatoprotective activity of methanolic extract of Borreria articularis (L.F) F.N. Willams: (Rubiaceae) at doses of 250 mg/kg and 500 mg/kg were evaluated by carbon tetrachloride (CCl4) intoxication in rats. The toxic group which received 25% CCl4 in olive oil (1 ml/kg) per oral (p.o), alone exhibited significant increase in serum ALT, AST, ALP, and TB levels. It also exhibited significant (P<0.001) decrease in TP and ALB levels. The groups received pretreatment of Borreria articularis at a dose of 250 and 500 mg/kg b.w. p.o. had reduced the AST, ALT, ALP and TB levels and the effects were compared with standard drug (Silymarin100mg/kg b.w. p.o).The total protein
(TP) and albumin (ALB) levels were significantly increased in the animals received pretreatment of the extract at the moderate and higher dose levels and the histo-pathological studies also supported the protective effect of the extract. Plants contain ß-sitosterol and ursolic acid; and d-mannitol. Seeds contain isorhamnetin.


Figure 2: Borreria Articularis

Citrus Microcarpa
The Philippine Department of Health stated that liver cancer is the third common forms of cancer for both males and females, hence the need for more hepatoprotective agents. Silymarin, from milk thistle is the most well known hepatoprotective agent but due to availability and economic concerns with the use of milk thistle other sources were explored. Fruit peels constitute a bulk in Philippine wastes. If such wastes can be used as hepatoprotective agents, then wastes will be decreased and new sources of important products may be discovered.

This study was aimed to evaluate the hepatoprotective activity of Citrus microcarpa Bunge fruit peel extract relative to the commercially available Silymarin preparations. The chemical components of the fruit peels were analyzed to ascertain pharmacologic value. The study used an experimental research design using BFAD- Sprague Dawley rats as subjects. The hepatoprotective activity was evaluated based on changes in the liver morphology- gross examination and differences in serum liver enzyme levels- bilirubin, aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (AP) within and among the groups of rats. There was a significant decrease in ALT, AST and AP levels among rats administered with the fruit peel extract. Silymarin significantly decreased bilirubin levels. These suggest a comparable hepatoprotective activity between Silymarin and the fruit peel extract tested. Phytochemical analysis showed that the fruit peel extract contained flavonoids, tannins, and glycosides. Quantitative analysis on the chemical components of the fruit peel extract is suggested to facilitate the study of its exact mechanism of action. Research on the protective ability of the fruit peel extract on other organ systems is recommended. It is also suggested that other chemical liver toxicity inducers be used to observe the range of hepatoprotective activity of the fruit peel extract studied .


                                                             Figure 3: Citrus Microcarpa

Andrographis Paniculata
King of Bitters botanically known as Andrographis paniculata is an ancient Indian medicinal herb, which has been used for centuries in Asia for its effects on various bodily functions and ailments, ranging from degenerative diseases to the common cold. It is known as Kalmegh and is used as a bitter ingredient in the Indian indigenous system of medicine. The leaves contain andrographolide, most active component of Andrographis paniculata is very bitter in taste .
One the most common therapeutic potential of Andrographis paniculata is its liver protective property, which is well established experimentally. Alcoholic extract of the leaves of Andrographis paniculata was found to be effective in prevention of liver damage. In another study administration of Andrographis paniculata exhibited liver protective effects by enhancing activity of antioxidant enzymes like superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase along with the level of glutathione and decreasing the activity of lipid peroxidase which leads to generation of free radicals damaging the liver cells. Thus by means of its synergistic effects Andrographis paniculata exerts its well-known hepatoprotective action .
Andrographolide, an active ingredient in Andrographis, has been shown to be responsible for the herb's inflammatory modulating actions, including the reduction of cytokine and peritoneal deposition of neutrophils, and modulation of lung inflammation in vivo.

Andrographolide is the major constituent extracted from the leaves of the plant which is a bicyclic diterpenoid lactone. This bitter principle was isolated in pure form by Gorter (1911). Such other activities as liver protection under various experimental conditions of treatment with galactosamine (Saraswat et al., 1995), paracetamol (Visen et al., 1993) etc. are also attributed to andrographolide. The hepatoprotective action of andrographolide is related to the activity of certain metabolic enzymes (Choudhury and Poddar, 1984, 1985; Choudhury et al., 1987). Systematic studies on chemistry of A. paniculata have been carried out.

 Figure 4: Andrographis Paniculata

Cichorium Intybus
Cichorium intybus commonly known as Chicory is an indigenous perennial herb well reputed ancient Indian medicine as a liver tonic. Accordingly it has been used as ayurvedic medicine for gall and liver disturbances. It forms an important component of several important liver preparations in India. In preclinical studies an alcoholic extract of the Cichorium intybus was found to be effective against chlorpromazine - induced hepatic damage in adult albino rats.
Extracts of Cichorium intybus were screened for their ability to protect the CCl4 and paracetamol
intoxicated liver in rats and were found to possess significant anti-hepatotoxic properties. Study done by using ethanol extract of Cichorium intybus in dose of 300 mg/kg showed significant increase in circulating leukocytes and relative weights of liver, as compared with alcohol alone which provides the evidence for liver protective effects of the herb .


 Figure 5: Cichorium Intybus

Wedelia Calendulacea
Bhangra scientifically known as Wedelia calendulacea, belonging to Compositae family is a perennial herb, with light camphor-like odor. The plant is traditionally used as a tonic, for hepatic and spleen enlargement, and in skin diseases. Historical use of Wedelia calendulacea as liver tonic is scientifically confirmed.
Preclinical Studies demonstrate its protective action in paracetamol induced liver damage by increasing serum enzyme levels (lactate dehydrogenase, alanine and aspartate transaminase and alkaline phophatase). The alcoholic extract of whole plant Wedelia calendulacea exhibited protective activity against carbon tetrachloride-induced liver injury in vivo. The extract also increased the bile flow in rats suggesting a stimulation of liver secretory capacity. The minimum lethal dose was greater than 200 mg/kg p.o. in mice.


 Figure 6: Wedelia Calendulacea

Boerhavia Diffusa
The roots of Boerhavia diffusa, commonly known as 'Punarnava', are used by a large number of tribes in India for the treatment of various hepatic disorders and for internal inflammation. Anodectal data has also reported effectiveness of Boerhavia diffusa in cases of oedema and ascites resulting from early cirrhosis of the liver and chronic peritonitis. In scientific studies the chloroform and methanolic extracts of the roots and aerial parts of Boerhavia diffusa exhibited hepatoprotective activity against carbon tetrachloride . A proprietary hepato-tonic herbal formulation containing Boerhavia diffusa as one of the major ingredient offered significant protection against decrease in haemoglobin percentage R.B.C. and W.B.C counts and the various liver microsomal enzymes. Boeravinones G and H are two rotenoids isolated from B. diffusa.


 Figure 7: Boerhavia Diffusa

Salacia Reticulata
Salacia reticulata is a member of Hippocrateaceae family climbing shrub with blackish branches. The roots are traditionally used in treatment of gonorrhea, itches, swelling, diabetes and liver tonic. The Hepatoprotective effects extracts from the roots and stems of Salacia reticulata were examined using an oxidative stress-induced liver injury model. Both extracts significantly suppressed the increase in glutamic oxaloacetic transaminase and glutamic pyruvic transaminase activities in carbon tetrachloride (CCl4)-treated mice. These extracts also inhibited CCl4-induced thiobarbituric acid-reactive substance formation, which indicates increased lipid peroxidation in the liver. These results suggest that the antioxidative activity is involved in the hepatoprotective activity of S. reticulate.


 Figure 8: Salacia Reticulata

Phyllanthus Amarus
Numerous medicinal plants and their formulations are used for liver disorder in Ethno medical practice and in traditional system in India. Indigenous plant Phyllanthus amarus was selected for clinical investigation of hepatoprotective activity. The ability of whole dried drug powder of Phyllanthus amarus (a traditionally used in the treatment of Jaundice) was tested for hepatoprotective activity on 107 patients who suffering from liver disease . The powder of the herb was given thrice a day (morning, noon and night, 3 gm each time) orally with water for 30-45 days depending on the severity of the disease. The patients were evaluated for the changes in biochemical markers like SGPT, Billirubin and Haemoglobin on day zero, seven, fourteen, twenty one, twenty eight and forty two. There was significant decrease in SGPT, Billirubin and increase in hemoglobin.
Phytochemical studies have shown the presence of many valuable compounds such as lignans, flavonoids, hydrolysable tannins (ellagitannins), polyphenols, triterpenes, sterols and alkaloids. The extracts and the compounds isolated from P. amarus show a wide spectrum of pharmacological activities including antiviral, antibacterial, antiplasmodial, anti-inflammatory, antimalarial, antimicrobial, anticancer, antidiabetic, hypolipidemic, antioxidant, hepatoprotective nephroprotective and diurectic properties.


Figure 9: Phyllanthus Amarus

Stachytarpheta Indica
The objective of the present study appraised the hepatoprotective activity of ethanolic extracts of Stachytarpheta indica (whole plant) on winstar rats. Liver damage was induced by intraperitonial administration of carbon tetrachloride (1ml/kg,b.w,p.o) for 7 days. The extent of damage was studied by assessing biochemical parameters. The ethanolic extracts of Stachytarpheta indica (300mg & 600mg/kg,b.w,p.o) were administered respectively to the animals treated with carbon tetrachloride and its effects on biochemical parameters were compared with standard drug solitarian (100mg/kg,b.w p.o). Stachytarpheta indica showed significant reduction of serum enzymes-AST, ALT, ALP, TP & Bilirubin (Aspartate Transminase, Alanine Transminase, Alkaline Phosphatase, Total Protein & Total Billirubin) when compared to control rats. The hepatoprotective effect of Stachytarpheta indica was comparable with the standard drug Silymarin. It was confirmed by histopathological study. The effect of extract 600mg/kg was almost equal to that of standard drug.


Figure 10: Stachytarpheta Indica

Eclipta Alba
Eclipta alba Hassk. (Bhringaraja, Family: Compositae) is a perrenial shrub which grows widely in moist tropical countries.Different uses have been reported for this shrub. It is used as alterative, anthelmintic, expectorant, antipyretic, antiasthmatic, tonic, in hepatic and spleen enlargement, in skin diseases and as a substitute for Taraxacum (a popular liver tonic). Recently Chandra, have observed a significant anti-inflammatory activity of the powder in rats. It has been reported to be useful in liver ailments & has been shown to possess hepatoprotective activity against carbon- tetrachloride induced liver cell damage in animals. The effect of Eclipta alba (EA) extract was studied on paracetamol induced hepatic damage in Mice. Treatment with ethanol extract of E. alba was found to protect the the mice from hepato-toxic action of paracetamol as evidenced by significant reduction. in the elevated serum transaminase levels .
Eclipta contains Coumestans such as wedelolactone and demethylwedelolactone, polypeptides,thiophene derivatives,steroids,triterpenes,polyacetylenes.


Figure 11: Eclipta Alba

Foeniculum Vulgare
Fennel (Foeniculum vulgare Mill., family Umbelliferae) is an annual, biennial or perennial aromatic herb, depending on the variety, which has been known since antiquity in Europe and Asia Minor. The leaves, stalks and seeds (fruits) of the plant are edible. Foeniculum vulgare is an aromatic herb whose fruits are oblong, ellipsoid or cylindrical, straight or slightly curved and greenish or yellowish brown in colour .Volatile components of fennel seed extracts by chromatographic analysis include transanethole, fenchone, methylchavicol, limonene, α- pinene, camphene, β-pinene, β-myrcene, α- phellandrene, 3-carene, camphor, and cisanethole . Hepatoprotective activity of Foeniculum vulgare (fennel) essential oil was studied using a carbon tetrachloride-induced liver fibrosis model in rats. The hepatotoxicity produced by chronic carbon tetrachloride administration was found to be inhibited by Foeniculum vulgare essential oil with evidence of decreased levels of serum aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase and Billirubin.


Figure 12: Foeniculum Vulgare

Tinispora Cordifolia
Tinospora Cordifolia commonly known as Guduchi is one of the most valuable medicinal plant of ayurveda. According to Ayurvedic lexicons Tinospora cordifolia is referred to as “Amrita”. The term “Amrita”is attributed to this drug in recognition to its ability to impart youthfulness, vitality and longevity to its patron. In modern medicine it is well known for its Hepatoprotective, Adaptogenic and Immunomodulatory activities. Clinical studies in twenty patients of infective hepatitis showed that Guduchi plays an important role in relieving the symptoms as well as normalization of altered liver functions. The majority of cases i.e. 15 cases (75 %) were cured and 5 cases (25%) improved after treatment with Tinospora cordifolia.
Currently along with antibiotics and supportive intensive care management, immunotherapy with Tinospora cordifolia (Tc) is practiced in surgical units. This therapy has shown to boost host defenses and decrease the incidence of epticaemia, resulting in increased survival of patients. In experimental rats Tinospora cordifolia (100mg/kg/d for 5 weeks) was found to decrease the renal damage, improve the fibrinogen level, and reduce lead acetate induced endotoxaemia. Tinospora cordifolia was also found to decrease renal ischemia induced mortality to 36 percent. The prognosis following Tinospora cordifolia (Tc) appears to be due to protection against all the risk factors. Kupffer cells are major determinants of outcome of liver injury. Their activity was therefore studied in a model of chronic liver disease. The effect of Tinospora cordifolia, with proven hepatoprotective activity, was evaluated on Kupffer cell function, using carbon clearance test as a parameter. Anti-hepatotoxic activity of Tinospora cordifolia was studied in albino rats intoxicated with CCl4. Liver function was assessed based on morphological, biochemical (SGPT, SGOT, Serum alkaline phosphatase, Serum bilirubin) and functional (Pentobarbitone sleep time) tests. Efficacy of Tinospora cordifolia as a sole constituent in goat’s liver were studied. Results revealed clinical and hematobiochemical improvement at the later stages in Tinospora cordifolia treated goats, indicating that it has got hepatoprotective action.
The active adaptogenic constituents are diterpene compounds, polyphenols, and polysaccharides, including arabinogalactan polysaccharide.



Figure 13:Tinispora Cordifolia

Picrorrhiza Kurroa 
It contains picrorrhizin, kutkin, picroside, and apocynin. The plant is used for anti-pyretic1, hepatoprotective, cathartic, tonic, laxative, anti-allergic, anti-anaphylactic, anti-epileptic, anti-paralytic, anthelminitic, appetizer, anti-ulcer, skin diseases, antidote for dog bite and as a anti-histaminic.
Himoliv (HV) is a polyherbal ayurvedic product (M/s. Emami Limited, Kolkata, India). HV contains aqueous extracts of 25 indigenous medicinal plants .Some of these plants, viz., Picorrhiza kurroa, Boerrhavia diffusa, Tinospora cordifolia, Andrographis paniculata and Phyllanthus emblica have been individually reported to possess hepatoprotective effect and antioxidant properties. HV is also claimed to be useful in hepatitis, jaundice and biliary dysfunction. However, the pharmacological effects need experimental evidence for their actions.


Figure 14:Picrorrhiza Kurroa 

Tephrosia Purpurea  
It contains lupeol, rutin, semiglabrin, semiglabrinol, tepurindiol, tephroglabrin and karanjin. The plant is used for its hepatoprotective, hematinic, anthelminitic, alexeteric, diuretic, immunomodulatory, anti-inflammatory, anti diarrhoeal and antipyretic.
Many herbal remedies have been employed in various medical systems for the treatment and management of different diseases. The plant Tephrosia purpurea has been used in different system of traditional medication for the treatment of diseases and ailments of human beings. It is reported to contain various flavonoides, alkaloids, steroids, phenolic compounds. It has been reported as antibacterial, anticancer, antioxidant, anti-inflammatory, antiulcer, hepatoprotective, immunomodulatory, antilithiatic, free radical scavenging, antileishmanial, antibiotic, antimicrobial, anyihyperglycemic, antilipidperoxidative and wound healing activities. There are also reports available for the traditional use of this plant for its antipyretic, anticancer, diuretic properties. Many isolated constituents from Tephrosia purpurea lack the reports of pharmacological activities, which support its further pharmacological studies.


Figure 15:Tephrosia Purpurea 

Justicia Adhatoda
It is belonging to family acanthaceae. Justicia paniculata, decoction or infusion of the leaves has been used in sluggish liver.The leaves of Justicia adhatoda showed significant hepatoprotective effect at a dose of 50-100mg/kg on the liver damage induced by d-galactosamine in rats. Several alkaloids are present in the leaves. The most important is vasicine, a quinazoline alkaloid.The vasicine yield of the herbage has been measured as 0.541 to 1.1% by dry weight.
The leaves showed significant hepatoprotective effect at a dose of 50-100 mg/kg on the liver damage induced by D-galactoseamine in rats.


Figure 16:Justicia Adhatoda

Momordica Charantia 
(Linn Family: Cucurbitaceae) whose fruit is known as Karela/corilla, or bittergourd. Unripe fruits of the plant are mainly used for diabetes and extensive investigation has shown that an extract of the fruits has marked hypoglycemic properties both in animals and human. Charantin is one of the hypoglycemic compounds, which can be isolated from Momordica charantia fruit. It is a mixture of two compounds (1:1) sitosteryl glucoside (C35H60O6) and stigmasteryl glucoside (C35H58O6), both of which are steroidal saponins.
Alcoholic extract of whole fruit of Momordica charantia was prepared. Adult healthy albino rats were divided into four groups and received a dose of 6 mg/100 gm. body weight of alloxan monohydrate. Animals of group I served as diabetic control group. The animals of II, III, and IV groups received 25 mg, 50 mg and 75 mg doses of the extract respectively for different durations. 75 mg dose showed increase in body weight. All doses of alcoholic extract of M. charantia were able to decrease the blood sugar level significantly. Extract feeding showed definite improvement in the islets of Langerhans. No toxic effect was observed in the liver. The significant features of the study have been blood glucose once lowered by the treatment with M. charantia fruit extract remained static even after discontinuation of drug for 15 days. Blood sugar never fell below normal values even with a high dose, in pancreatic islets, beta cells showed definite improvement.


Figure 17: Momordica Charantia 

Nordostachus Jatamansi
Nardostachys jatamansi DC. or ‘jatamansi’ is a small, perennial, dwarf, rhizomatous, herb and the most primitive  species within the family Valerianaceae. All parts of N. jatamansi are used and are effective antipyretics, antiseptics, anticonvulsants, antispasmodics, antibacterial, antifungals, antiemetic and analgesics.
Pretreatment of rats with 800 mg/kg body wt of the 50% ethanolic extract of N. jatamansi DC demonstrated significant hepatoprotective activity against thioacetamide induced hepatotoxicity. Marked reduction in raised levels of serum transaminase and alkaline phosphatase was observed. Pretreatment of the animals with the extract further resulted in an increase in survival in rats intoxicated with LD90 dose of the hepatotoxic drug.


Figure 18: Nordostachus Jatamansi

CONCLUSION
Considering the enormous biodiversity resources of Indian traditional system and the high incidence of liver complications, the present review extensively focuses on collection of data for different plants, which are available in India. These medicinal plants claimed as liver protective agents are classified according to their biological source, phytoconstituents; part used and plants in formulations. People from India are still dependent on conventional therapies to treat liver complications. Because of their easy availability and low cost. Since large mass of populations used preferable herbal preparation, therefore there is need to be evaluate for their proportion, their dose and rational behind combination in different polyhedral preparation.

LINK- http://www.ijptb.com/issues/archives/vol1_issue1/IJPTB%200006.pdf





Friday, November 13, 2015

Gaurav Kumar Sharma : Training Techniques for the Young Guns of India to...

Gaurav Kumar Sharma : Training Techniques for the Young Guns of India to...: Training Techniques for the Young Guns of India to develop a Job Oriented Workforce Currently, the young generation have overtaken th...

Training Techniques for the Young Guns of India to develop a Job Oriented Workforce


Training Techniques for the Young Guns of India to develop a Job Oriented Workforce


Currently, the young generation have overtaken the largest segment of the Indian workforce. But forget about Today for a moment and look ahead to 2030. By then, the job demographic will look completely different in 15 years.
For now, let’s discuss about presently working generation , This group of workers is unique in how they approach their jobs, how they communicate with their bosses and each other, and what they value both in and away from the workplace. Organizations must adapt their philosophies,views,prospects including effective training to the priorities of this generation. 
Here are few Training Techniques for the Young Guns of India.

1. Use technology that resonates

At a certain point in the 1990's, many industries turned to computers for workplace functions. If you were a young employee at that time, this would have seemed a major innovation and a sign that you worked for a truly cutting-edge company. For today’s professionals, handing them a printed training manual is on par with sitting a teenager in front of a typewriter 20 years ago. Tablets and smartphones are technologies that today’s younger employees are already comfortable with. Adopting solutions that incorporate these devices into training processes not only will impress young professionals, but also will result in increased effectiveness and impact.

2. Don’t bore them

No list of  training tips would be complete without this obvious piece of advice: Make learning interesting. If you bore young employees during training, they will tune out and not be fully prepared to apply the skills they need to be productive. Furthermore, if training creates a negative impression on new hires on their first day, the odds they will stick around to be long-term employees greatly decrease. Mobile learning solutions that incorporate dynamic approaches and are more than just studying written content will keep employees interested.

3. Realize the power of video

Young professionals are accustomed to watching videos on mobile devices. Video has been shown to be more effective in terms of retention and impact as opposed to written content. Combine these two facts and you get a powerful means to teach younger employees and have them eager to learn. Mobile training solutions are perfectly positioned to use video without much hassle. The best platforms compress file size so that videos can reside locally, without streaming and without monopolizing all of a device’s storage. Among training tips, this might be the most important in connecting with young professionals.

4. Engage them immediately

For the most part, young professionals want to be immediately engaged in their new jobs, and also want to be part of the process and have their voices heard and opinions considered. A training environment that discourages this, even unintentionally, can decrease productivity and increase turnover. Today’s mobile training solutions get employees up to speed faster, as well as allow communication if they have questions or comments during the learning process.

Thursday, November 5, 2015

HOW TO BE HEALTHY....

 HOW TO BE HEALTHY....

KYA KHAYE
v  HARI PATTE DAR SABJIYA,GAJAR,MULLI,SABJI KA JUICE,ANKURIT BEEJ
v  APPLE,BANANA,ORANGE,WATER MELLON,FRUIT JUICE
v  DALS JESE MOONG DAL,MASOOR DAL,CHANA DAL,RAJMA
v  ROTI,IDLI,DALIYA,RICE,DOSA,MOONG KI DAL KI KHICHRI.

KYA KUM KHAYE
v  TALI HUE POORI,PARANTHA,SAMOSA,NAMKEEN,CHIPS,PAKORA AND KACHORI.
v  MEETHI CHIJE JESE GUR,HONEY,SUGAR ,JEM,SWEETS,CAKE,ICECREAM.
v  SUKHE MEVE JESE KAJU,DAKH,BAADAM,NARIYAL,MUNGFALI.
v  NON VEG.JESE MEAT,FISH,CHICKEN ,EGG,RED MEAT.
v  VASA YUKT CHEESE JESE EXCESS OIL,GHEE,BUTTER,CHEESE,MALAI.

KESE KHAYE
v  THIK SE CHABA K KHANA KHAYE
v  KHANA AARAM OR TASALLI SE KHAYE
v  SUBAH ROJ NASHTA JAROOR KARE
v  EK SATH KHANE K BAZAYE THODA THODA TUKDO ME BAAR BAAR KAR K KHAYE.

 KYA NHE KHAYE
v  COLD DRINKS JESE PEPSI,COCACOLA,LIMCA,CAKES AND CHOCHLATES
v  JYADA MAATRA ME GRAPES,PINEPPALE,MANGOES,RAISHE VALE FRUITS NAA KHAYE.
v  NAMAK KUM KHAYE
v  KUM FAT KHAYE  JESE  MEAT FAT AND BUTTER,CREAM,DAIRY PRODUCTS
v  ZYADA TEEKHA OR MASALE DAAR KHANA.

 KAB KHAYE
v  ACHA NASHTA KARE
v  MEDIUM LUNCH KARE
v  LIGHT DINNER KARE
v  KHANE SE PAHLE LEMON JUICE,CHACH,SOUP PIYE
v  KHANA KHANE K 2 GANTE K BAAD ME SOYE.

ACHCHI SEHAT SAB KI CHAHAT..........TO KYA KARE
v  BLOOD DONATE KARE
v  SAAL ME EK BAAR POORA BODY CHECK UP KARAYE.
v  MORNING WALK YA JOGING KARE.
v  KISI TARAH KA NASHA NAA KARE.
v  DOCTOR SE SAMAY SAMAY PAR  APNE SWASTH SAMBANDHIT ZANKARI LE.


                                                                                                                                                                                                                                                                                                                                         

TABLET GRANULATION TECHNIQUES


TABLET GRANULATION TECHNIQUES


GRANULATION PROCESS
Granulation process may be defined as a process wherein small particles adhere together by forming bonds between them , resulting in the formation of large aggregates called granules.

Why we prepare granules when we have powders?

1.To avoid powder segregation,If, the powder is composed of particles with different dimensions & different densities a separation between these particles will occur. 
2.To enhance the flow of powder,
   Higher flowability gives better filling of the dies or containers, during a volumetric dosage
3.Granules have higher porosity than powders,
4.To improve the compressibility of powders.
5.The granulation of toxic materials will reduce the hazard of generation of toxic dust, which may arise during the handling of the powders.
6.Materials, which are slightly hygroscope, may adhere & form a cake if stored as a powder.

Methods of Granulation
Some of the available methods in the industrial field for the preparation of granules:
  A. Direct compression.
  B. Dry granulation methods.
  C. Wet Granulation.
  D. Granulation by Crystallization.

A. Direct compression
Direct compression is a dry process where in the powdered material (tablet formulation) is compressed directly into the tablets without the physical nature of the former being modified.

Ex.- Formulation of Ascorbic Acid Tablets.
        Formulation of Chewable Antacid Tablets.

Step -1 Grinding
Drug is added to the granulator and grinded.

Step -2 Blending or Mixing
The suitable adjuvants (Ex. Directly compressible vehicles and other excipients) are added in a blender and mix thoroughly.

Step -3 Tablet press
The blended powdered material is compressed by machine tooling ( Dies and punches) of a tablet press .


B. Dry Granulation
The process of dry granulation is also called Double Compression or Compression Granulation or Pre-Compression Granulation.
The process involves the formation of tablet by first converting the tablet formulation into slugs or compact masses. These formed masses are screened to form uniform sized fine granules. The technique is suitable for those drugs which are moisture sensitive, degrade at higher temperature and administered in higher doses.
The technique of Dry granulation of powdered material can be accomplished by  two methods.
(a)Slugging (slug formation).
(b)Roller compaction method.



Step -1 Grinding
Drug is added to the granulator and grinded.

Step -2 Blending or Mixing
The suitable adjuvants (Ex. Diluent and other excipients) are added and mixed in a blender .

Step -3 Compaction
After mixing, the powder mixture is slugged or compressed into large flat tablets or pellets about 1 inch diameter . On large scale , Roller compactor is preferred.

Step -4 Crushing
These slugs are broken down by hand or by milling to form granules .

Step -5 Screening or Sifting
The granules undergo dry screening through a desired mesh for sizing.

Step -6 Blending or Mixing
Finally, the lubricating agent is added and mixed thoroughly in a blender.

Step -7 Tablet press
The resultant granules are compressed by machine tooling ( Dies and punches) of a tablet press.
Ex. Of Formulations Prepared by Dry Granulation Method:
Formulation of Acetyl Salicylic Acid tablets.,
Formulation of Vitamin B Complex.

C. Wet Granulation
Wet granulation or Moist granulation is the most conventional , versatile and widely used techniques for the manufacture of compressed tablets, as it imparts all the physical properties to the granules.
This technique differs from the other granulation methods as it involves the usage of liquids to form compact masses.
Ex. Of Formulations Prepared by Wet Granulation Method:
Formulation of Acetaminophen tablets.,
Formulation of Aluminium Hydroxide Chewable tablets.


 
Step -1 Grinding
Drug is added to the granulator and grinded.

Step -2 Blending or Mixing
The suitable adjuvants (Ex. Diluent and other excipients) are added and mixed in a blender .

Step -3 Shear Mixing
Granulating liquids (Ex. Alcohols ) are added to form a damp mass of the powdered material which resembles agglomerates.

Step -4 Wet screening
The mass is screened to form pellets or granules.

Step -5 Drying
   The pellets or granules are dried to remove excess of the liquid.

Step -6 Dry screening
Dry screening of granules results in size reduction.

Step -7 Blending
 The lubricating agent is added and the mixture is mixed thoroughly in a blender.

Step -8 Tablet press
The resultant granules are compressed by machine tooling of a tablet press.
D. Granulation by Crystallization
This method exploits the presence of crystallization water in the active material; this method is rarely used..

Wednesday, November 4, 2015

HOW TO BE HEALTHY....


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Introduction to Intellectual Property


We know that the inventor of a machine, the author of a book, or the writer of music
somehow usually ‘own’ their work. From this ownership, certain consequences
flow and you probably have been made aware of the fact that we cannot just
copy or buy a copy of their works without consideration of their rights. Equally,
original industrial designs of furniture, wallpaper and the like seem naturally to
be owned by someone or some organization.
Each time we buy such ‘protected’ items, a part of what we pay goes back
to the owner as recompense for the time, money, effort and thought they put
into the creation of the work. This has resulted over the years in the
development of industries such as the music industry growing worldwide and
encouraging new talent to produce more and more original ideas and articles.

The following  suggests some of the things that are entitled to protection as intellectual property under national intellectual property laws and / or various international treaties:

  1. Discs 
  2. Designs for objects 
  3. Geographical indications of origin for certain types of products
  4. Performances 
  5. Images 
  6. Companies' names
  7. Broadcasts 
  8. Logos
  9.  Industrial processes
  10. Videos 
  11. Trademarks 
  12. Chemical formulas
  13. Computer games
  14.  Integrated circuits 
  15. Materials
  16. Computer programs
  17.  Inventions 
  18. Perfumes

Let’s begin with a more formal definition of intellectual property, so as to build a solid foundation for later explanations of the various types of intellectual property, and then the relevant governing international treaties. The best place to start is with a consideration of the meaning of the word property.
The outstanding features that most types of property share are that the owner of the property is free to use it as she/he wishes, provided the use is not against the law, and to exclude others from so using that owned item of property.
Now the term "intellectual property" is reserved for types of property that result from creations of the human mind, the intellect. Interestingly, the term intellectual property in the Convention Establishing the World Intellectual Property Organization, or "WIPO", does not have a more formal definition.
The States that drafted the Convention chose to offer an inclusive list of the rights as relating to:
“Literary artistic and scientific works; performances of performing artists, phonograms, and broadcasts; inventions in all fields of human endeavor; scientific discoveries; industrial
designs; trademarks, service marks, and commercial names and designations; protection against unfair competition; and "all other rights resulting from intellectual activity in the industrial,
scientific, literary or artistic fields.” (Convention Establishing the World Intellectual Property Organization, Signed at Stockholm on July 14, 1967; Article 2, § viii).

For various administrative and historical reasons, intellectual property is usually dealt with under the following main headings:
1) Literary, artistic and scientific works e.g. books.Protection of this property is governed by laws
concerning Copyright.
2) Performances, broadcasts e.g. concerts. Protection of this property is governed by laws concerning Copyright's Related Rights.
3) Inventions e.g. a new form of jet engine. Protection of inventions is covered by laws concerning Patents.
4) Industrial designs e.g. the shape of a soft drinks bottle. Industrial Designs may be protected by its own specialized laws, or those of Industrial Property or Copyright.
5) Trademarks, service marks and commercial names and designations e.g. logos or names for a product with unique geographical origin, such as Champagne. Protection is normally available under various laws. In this course the laws are covered within the Trademark module.
6) Protection against unfair competition. e.g. false claims against a competitor or imitating a competitor with a view to deceive the customer. This is a theme that occurs in many of the modules in this course and is in fact the subject of a separate module.

Why do Intellectual Property Rights Matter?
The first reason is that it is both just and appropriate that the person putting in the work and effort into an intellectual creation has some benefit as a result of this endeavor. The second reason is that by giving protection to intellectual property many such endeavors are encouraged and industries
based on such work can grow, as people see that such work brings financial return.

An example of this later point is given by the case of the world pharmaceutical industry. An investment of many years, and R&D expenses (lab time for creation, testing, government or agency approval procedures) running into the hundreds of millions of pounds sterling (or yen, rands, lira, dollars) may be necessary before any new medicine reaches the market. Without the IP rights to exclude competitors from also making such a new medicine, the pharmaceutical company creating such a new compound would have no incentive to spend the time and efforts outlined
above to develop their drugs.
Without patent protection, such a company would face economic losses originating from the "free-riding" of their competitors. Without trademark protection, this company, again, could not build "brand loyalty" that, hopefully, would last beyond the years of protection granted by patents.
Without the protections given within IP laws and treaties, such pharmaceutical firms simply would not commit an effort to experiment, in searching for new health products. As you can see from this brief example, without the protections outlined above, the world might well be literally less healthy than it is.
Intellectual property rights may also help to extend protection to such things as the unwritten and unrecorded cultural expression of many developing countries, generally known as folklore. With such protection they may be exploited to the benefit of the country and cultures of origin.