This document discusses different classes of diuretic drugs. It begins with an overview of diuretics and their uses for fluid retention and hypertension. It then covers the sites of action and pharmacology of different classes, including high efficacy loop diuretics, medium efficacy thiazide diuretics, weak potassium-sparing diuretics, carbonic anhydrase inhibitors, and osmotic diuretics. Specific drugs like furosemide, hydrochlorothiazide, and spironolactone are discussed in depth. The document concludes with a short quiz reviewing the material.
Hematinics are substances used to treat and prevent anemia. Megaloblastic anemias are caused by vitamin B12 or folate deficiencies and are characterized by large, abnormal red blood cells. Vitamin B12 is essential for two metabolic reactions and acts as a coenzyme. It is absorbed in the ileum with intrinsic factor and stored in the liver. Deficiencies can be detected using the Schilling test which evaluates vitamin B12 absorption. Treatment involves cyanocobalamin injections or oral methylcobalamin supplements.
This document discusses various haematinics including iron, vitamin B12, and folic acid. It provides information on their dietary sources, daily requirements, absorption, transport, storage, and roles in treating anaemia. Iron is mainly stored in hemoglobin and myoglobin. Vitamin B12 and folic acid are important for cellular growth and the conversion of homocysteine to methionine. Deficiencies can result from inadequate intake, malabsorption, increased demands, or impaired release/circulation. Oral supplements are usually sufficient but injections may be needed for malabsorption.
This document provides information on the pharmacology of diuretics. It begins by explaining that diuretics cause a net loss of sodium and water in urine but sodium balance is restored through homeostatic mechanisms. It then classifies diuretics and describes various classes in detail, including their mechanisms and sites of action, uses, and adverse effects. The classes discussed include high efficacy loop diuretics like furosemide, medium efficacy thiazides, weak carbonic anhydrase inhibitors, potassium sparing aldosterone antagonists, and renal sodium channel inhibitors.
The document discusses proton pump inhibitors (PPIs) which inhibit gastric acid secretion by blocking the hydrogen-potassium ATPase pump in the stomach. PPIs are converted to sulfoxide derivatives that covalently bind to cysteine residues on the pump, preventing it from pumping protons into the stomach lumen. Common PPIs mentioned are omeprazole, pantoprazole, rabeprazole, and lansoprazole. Each drug is used to treat various acid-related gastrointestinal conditions such as heartburn, GERD, and ulcers. The mechanism of action involves the covalent inhibition of the proton pump through binding of activated PPIs to the pump.
this will give brief about the peptic ulcer and give information about the drug used for peptic ulcer and classification of drugs including drugs and there use adverse effect.
This document discusses two categories of drugs - carminatives and digestants.
Carminatives are drugs that promote the expulsion of gases from the gastrointestinal tract and provide a feeling of warmth and comfort in the epigastrium. Commonly used carminatives include sodium bicarbonate, peppermint oil, cardamom tincture, dill oil, and ginger tincture.
Digestants are substances intended to promote digestion by supplying digestive enzymes. Examples include hydrochloric acid, pepsin, papain, pancreatin, and diastase. They may be beneficial in conditions where enzyme production is deficient but their routine use is generally not recommended. Side effects of digestants can
This document discusses haematinics, which are substances required for blood formation and used to treat anaemias. It defines anaemia and lists common causes such as blood loss, increased red blood cell destruction, and deficiencies in iron, vitamin B12, or folic acid. The document categorizes and describes common haematinics including oral and parenteral iron preparations, vitamin B12, folic acid, and erythropoietin. It provides details on absorption, transport, storage and excretion of iron as well as clinical uses of various haematinics to treat different types of anaemia.
This document discusses different classes of diuretic drugs. It begins with an overview of diuretics and their uses for fluid retention and hypertension. It then covers the sites of action and pharmacology of different classes, including high efficacy loop diuretics, medium efficacy thiazide diuretics, weak potassium-sparing diuretics, carbonic anhydrase inhibitors, and osmotic diuretics. Specific drugs like furosemide, hydrochlorothiazide, and spironolactone are discussed in depth. The document concludes with a short quiz reviewing the material.
Hematinics are substances used to treat and prevent anemia. Megaloblastic anemias are caused by vitamin B12 or folate deficiencies and are characterized by large, abnormal red blood cells. Vitamin B12 is essential for two metabolic reactions and acts as a coenzyme. It is absorbed in the ileum with intrinsic factor and stored in the liver. Deficiencies can be detected using the Schilling test which evaluates vitamin B12 absorption. Treatment involves cyanocobalamin injections or oral methylcobalamin supplements.
This document discusses various haematinics including iron, vitamin B12, and folic acid. It provides information on their dietary sources, daily requirements, absorption, transport, storage, and roles in treating anaemia. Iron is mainly stored in hemoglobin and myoglobin. Vitamin B12 and folic acid are important for cellular growth and the conversion of homocysteine to methionine. Deficiencies can result from inadequate intake, malabsorption, increased demands, or impaired release/circulation. Oral supplements are usually sufficient but injections may be needed for malabsorption.
This document provides information on the pharmacology of diuretics. It begins by explaining that diuretics cause a net loss of sodium and water in urine but sodium balance is restored through homeostatic mechanisms. It then classifies diuretics and describes various classes in detail, including their mechanisms and sites of action, uses, and adverse effects. The classes discussed include high efficacy loop diuretics like furosemide, medium efficacy thiazides, weak carbonic anhydrase inhibitors, potassium sparing aldosterone antagonists, and renal sodium channel inhibitors.
The document discusses proton pump inhibitors (PPIs) which inhibit gastric acid secretion by blocking the hydrogen-potassium ATPase pump in the stomach. PPIs are converted to sulfoxide derivatives that covalently bind to cysteine residues on the pump, preventing it from pumping protons into the stomach lumen. Common PPIs mentioned are omeprazole, pantoprazole, rabeprazole, and lansoprazole. Each drug is used to treat various acid-related gastrointestinal conditions such as heartburn, GERD, and ulcers. The mechanism of action involves the covalent inhibition of the proton pump through binding of activated PPIs to the pump.
this will give brief about the peptic ulcer and give information about the drug used for peptic ulcer and classification of drugs including drugs and there use adverse effect.
This document discusses two categories of drugs - carminatives and digestants.
Carminatives are drugs that promote the expulsion of gases from the gastrointestinal tract and provide a feeling of warmth and comfort in the epigastrium. Commonly used carminatives include sodium bicarbonate, peppermint oil, cardamom tincture, dill oil, and ginger tincture.
Digestants are substances intended to promote digestion by supplying digestive enzymes. Examples include hydrochloric acid, pepsin, papain, pancreatin, and diastase. They may be beneficial in conditions where enzyme production is deficient but their routine use is generally not recommended. Side effects of digestants can
This document discusses haematinics, which are substances required for blood formation and used to treat anaemias. It defines anaemia and lists common causes such as blood loss, increased red blood cell destruction, and deficiencies in iron, vitamin B12, or folic acid. The document categorizes and describes common haematinics including oral and parenteral iron preparations, vitamin B12, folic acid, and erythropoietin. It provides details on absorption, transport, storage and excretion of iron as well as clinical uses of various haematinics to treat different types of anaemia.
Expt. 7 Bioassay of acetylcholine using rat ileum by four point bioassayVISHALJADHAV100
Objective
Principle
Requirements
Experimental specifications (conditions)
Preparation of ACh stock and standard solutions
Preparation of frog ringer solution (PSS)
Procedure
Kymograph recording of contractions
Observation table
Calculation
Result and interpretation
Expt. 1 Introduction to in vitro pharmacology and physiological salt solutionsVISHALJADHAV100
This document provides an overview of in-vitro pharmacology experiments using isolated tissues and physiological salt solutions (PSS). It defines pharmacology and drugs, describes the aims of experimental pharmacology as finding therapeutic agents, studying toxicity and mechanisms of action. It also discusses types of experiments, equipment like organ baths and levers for recording tissue responses, and PSS compositions and roles. PSS are artificial solutions that maintain isolated tissues by resembling extracellular fluid composition. Selection of the appropriate PSS depends on the tissue being studied.
Histamine, meaning ‘tissue amine’ (histos—tissue) is almost ubiquitously present in animal tissues and in certain plants, e.g. stinging nettle. Its pharmacology was studied in detail by Dale in the beginning of the 20th century when close parallelism was noted between its actions and the manifestations of certain allergic reactions. It was implicated as a mediator of hypersensitivity phenomena and tissue injury reactions. It is now known to play important physiological roles.
Anti-arrhythmic drugs are used to treat abnormal heart rhythms by modifying the heart's impulse generation and conduction. They are classified according to their effects on the cardiac action potential, with Class I drugs blocking sodium channels, Class II drugs blocking beta receptors, Class III drugs prolonging repolarization by blocking potassium channels, and Class IV drugs blocking calcium channels. Examples of anti-arrhythmic drugs from each class are provided.
This document summarizes various classes of analgesic drugs including narcotics/opioids, non-narcotics, and specific drugs within each class. It describes the mechanism of action, uses, and side effects of common opioid analgesics like morphine, methadone, fentanyl, and non-opioid analgesics like acetaminophen. It also discusses opioid receptor types and how different drugs can act as agonists, antagonists, or mixed agonist-antagonists at these receptors.
Introduction to Anticoagulants
Coagulants, Local agents, Systemic agents, Anticoagulants, Heparin, Low molecular weight heparins, Heparinoids, Oral anticoagulants (Warfarin), Therapeutic uses
Presented by
N. Ramya
Department of Pharmacology
Histamine is a biogenic amine present in many tissues that functions as a neurotransmitter and is involved in inflammatory and hypersensitivity reactions. It is synthesized from the amino acid histidine. Histamine acts through multiple receptor subtypes and is involved in various physiological processes like gastric acid secretion, smooth muscle contraction, and allergic responses. Antihistamines competitively inhibit histamine receptors, with first generation antihistamines having sedative effects and second generation ones having minimal side effects. They are used to treat allergic disorders, as antiemetics, and for gastric acid reduction with H2 blockers. Concerns have been raised about impurities in the H2 blocker ranitidine. While H3
Drugs acting on the uterus can affect the endometrium or myometrium. Uterine stimulants like oxytocin, ergot alkaloids, and prostaglandins increase uterine motility and are used to induce labor or treat postpartum hemorrhage. Uterine relaxants like beta-adrenergic agonists, calcium channel blockers, and magnesium sulfate decrease uterine motility and are used to suppress premature labor. While tocolytics can postpone delivery, they also increase maternal and fetal risks.
The document discusses expectorants and antitussives. It defines expectorants as drugs that increase bronchial secretion or reduce viscosity, facilitating removal by coughing. Only guaiphenesin is approved as an expectorant in the U.S. Expectorants are classified as bronchial secretion enhancers or mucolytics. Antitussives act in the CNS to suppress cough or act peripherally in the respiratory tract. Antitussives are classified as opioids, nonopioids, antihistamines, or peripherally acting drugs. The document provides examples and doses of expectorants and antitussives and discusses some combination antitussive-expectorant formulations.
Expt. 1 Bioassay of serotonin using rat fundus strip by three point bioassayVISHALJADHAV100
This document describes an experiment to determine the unknown concentration of serotonin using a three-point bioassay with an isolated rat fundus strip preparation. The experiment involves constructing dose-response curves for a serotonin standard and test sample, selecting doses that elicit submaximal responses in a 1:2 ratio, and determining the test concentration using the measured responses. Rat fundus tissue is sensitive to serotonin and contracts in a concentration-dependent manner when exposed to increasing doses of the drug. The experiment aims to precisely and reliably estimate the concentration of an unknown serotonin sample through this validated bioassay method.
Diuretics work by preventing the body from absorbing too much salt and increasing the excretion of water and salt in urine. Furosemide is a common diuretic ("water pill") that is prescribed to treat high blood pressure and reduce excess fluid in the body from conditions like heart failure or kidney disease. It works by inhibiting sodium reabsorption in the ascending loop of the kidney, which leads to increased water excretion in urine. Potential side effects include headaches, dizziness, thirst, and electrolyte imbalances.
This document discusses different classes of diuretic drugs, including their mechanisms of action, structures, and uses. It focuses on loop diuretics, describing how they work by inhibiting sodium reabsorption in the ascending limb of the loop of Henle. Adverse effects of loop diuretics include electrolyte abnormalities like hypokalemia. The structure-activity relationships of loop diuretics are also covered, noting features like the carbonyl group and sulfamoyl substituents that contribute to diuretic potency. Loop diuretics are used to treat various conditions involving edema.
Bradykinin and substance P are neuropeptides that act as neurotransmitters and neuromodulators. Bradykinin is generated from kininogens by the enzyme kallikrein and acts through B1 and B2 receptors. It causes vasodilation, increased vascular permeability, and pain sensation. Substance P is an undecapeptide related to neurokinin A that is synthesized in the nervous system and distributed throughout the brain and peripheral tissues. It acts through neurokinin 1 receptors and is involved in nociception and inflammation. Antagonists of bradykinin and substance P receptors have potential therapeutic applications.
This document discusses various haematinics including iron, vitamin B12, folic acid, and erythropoietin. It covers their roles in red blood cell formation, daily requirements, dietary sources, absorption and transport, deficiency states, preparations used to treat deficiencies, and therapeutic uses to treat conditions like iron deficiency anemia and megaloblastic anemia. It provides details on the pharmacokinetics and pharmacology of administering these substances.
The document discusses anti-diabetic agents and provides details about sulfonylureas. It describes the mechanism of action of sulfonylureas, which involves binding to sulfonylurea receptors on pancreatic beta cells and extrapancreatic cells to stimulate insulin secretion and inhibit gluconeogenesis. Adverse effects include hypoglycemia and weight gain. Tolbutamide is provided as an example sulfonylurea drug, with its structure, synthesis, mechanism of action, pharmacokinetics, adverse effects, and therapeutic uses summarized.
Expt. 4 DRC of acetylcholine using frog rectus abdominis muscleVISHALJADHAV100
Objective
Principle
Requirements
Experimental specifications (conditions)
Preparation of ACh stock and standard solutions
Preparation of frog ringer solution (PSS)
Procedure
Kymograph recording of contractions
Observation table
Calculation of magnification value (Mf)
Graphical presentation of CRC/ DRC
Result and interpretation
This document summarizes immunostimulant drugs and immunotherapy. It describes the innate and adaptive immune response and lists immunostimulant microbial products like BCG that boost immune function. Immunostimulant drugs include cytokines, thalidomide, and levamisole. Immunotherapy methods covered are active and passive vaccination, adoptive cell transfer, and cell-based vaccination. The document provides details on specific immunostimulant drugs and their uses and side effects.
Biosynthesis of Histamine,Storage and release,Histamine H1-Receptor ,Histamine H1-Receptor Antagonists,Differences between first generation & second generation antihistamines,H2 receptor blockers
This document discusses antihypertensive drugs used to treat hypertension. It classifies these drugs into 10 categories including diuretics, ACE inhibitors, angiotensin receptor blockers, calcium channel blockers, beta blockers, alpha-beta blockers, alpha blockers, central sympatholytics, vasodilators, and renin inhibitors. For each drug class, it describes the mechanism of action how each lowers blood pressure by relaxing blood vessels or reducing cardiac output and peripheral resistance. Adverse effects like hypotension and cough are also mentioned.
The document describes changes that occur to carbohydrates during food processing, digestion, absorption, and metabolism. It discusses how carbohydrates are broken down during cooking and storage through leaching and the Maillard reaction. It then outlines the multi-step digestion of carbohydrates by salivary and pancreatic enzymes in the mouth, stomach, and small intestine. Absorption of monosaccharides occurs actively in the intestine, and carbohydrates are further metabolized through pathways like glycolysis and the citric acid cycle to generate energy.
In this slide contains introduction, principle, precautions, solution and assay method for vitamin B series.
Presented by: P. VENKATESH (Department of pharmaceutical analysis),
RIPER, anantapur
Expt. 7 Bioassay of acetylcholine using rat ileum by four point bioassayVISHALJADHAV100
Objective
Principle
Requirements
Experimental specifications (conditions)
Preparation of ACh stock and standard solutions
Preparation of frog ringer solution (PSS)
Procedure
Kymograph recording of contractions
Observation table
Calculation
Result and interpretation
Expt. 1 Introduction to in vitro pharmacology and physiological salt solutionsVISHALJADHAV100
This document provides an overview of in-vitro pharmacology experiments using isolated tissues and physiological salt solutions (PSS). It defines pharmacology and drugs, describes the aims of experimental pharmacology as finding therapeutic agents, studying toxicity and mechanisms of action. It also discusses types of experiments, equipment like organ baths and levers for recording tissue responses, and PSS compositions and roles. PSS are artificial solutions that maintain isolated tissues by resembling extracellular fluid composition. Selection of the appropriate PSS depends on the tissue being studied.
Histamine, meaning ‘tissue amine’ (histos—tissue) is almost ubiquitously present in animal tissues and in certain plants, e.g. stinging nettle. Its pharmacology was studied in detail by Dale in the beginning of the 20th century when close parallelism was noted between its actions and the manifestations of certain allergic reactions. It was implicated as a mediator of hypersensitivity phenomena and tissue injury reactions. It is now known to play important physiological roles.
Anti-arrhythmic drugs are used to treat abnormal heart rhythms by modifying the heart's impulse generation and conduction. They are classified according to their effects on the cardiac action potential, with Class I drugs blocking sodium channels, Class II drugs blocking beta receptors, Class III drugs prolonging repolarization by blocking potassium channels, and Class IV drugs blocking calcium channels. Examples of anti-arrhythmic drugs from each class are provided.
This document summarizes various classes of analgesic drugs including narcotics/opioids, non-narcotics, and specific drugs within each class. It describes the mechanism of action, uses, and side effects of common opioid analgesics like morphine, methadone, fentanyl, and non-opioid analgesics like acetaminophen. It also discusses opioid receptor types and how different drugs can act as agonists, antagonists, or mixed agonist-antagonists at these receptors.
Introduction to Anticoagulants
Coagulants, Local agents, Systemic agents, Anticoagulants, Heparin, Low molecular weight heparins, Heparinoids, Oral anticoagulants (Warfarin), Therapeutic uses
Presented by
N. Ramya
Department of Pharmacology
Histamine is a biogenic amine present in many tissues that functions as a neurotransmitter and is involved in inflammatory and hypersensitivity reactions. It is synthesized from the amino acid histidine. Histamine acts through multiple receptor subtypes and is involved in various physiological processes like gastric acid secretion, smooth muscle contraction, and allergic responses. Antihistamines competitively inhibit histamine receptors, with first generation antihistamines having sedative effects and second generation ones having minimal side effects. They are used to treat allergic disorders, as antiemetics, and for gastric acid reduction with H2 blockers. Concerns have been raised about impurities in the H2 blocker ranitidine. While H3
Drugs acting on the uterus can affect the endometrium or myometrium. Uterine stimulants like oxytocin, ergot alkaloids, and prostaglandins increase uterine motility and are used to induce labor or treat postpartum hemorrhage. Uterine relaxants like beta-adrenergic agonists, calcium channel blockers, and magnesium sulfate decrease uterine motility and are used to suppress premature labor. While tocolytics can postpone delivery, they also increase maternal and fetal risks.
The document discusses expectorants and antitussives. It defines expectorants as drugs that increase bronchial secretion or reduce viscosity, facilitating removal by coughing. Only guaiphenesin is approved as an expectorant in the U.S. Expectorants are classified as bronchial secretion enhancers or mucolytics. Antitussives act in the CNS to suppress cough or act peripherally in the respiratory tract. Antitussives are classified as opioids, nonopioids, antihistamines, or peripherally acting drugs. The document provides examples and doses of expectorants and antitussives and discusses some combination antitussive-expectorant formulations.
Expt. 1 Bioassay of serotonin using rat fundus strip by three point bioassayVISHALJADHAV100
This document describes an experiment to determine the unknown concentration of serotonin using a three-point bioassay with an isolated rat fundus strip preparation. The experiment involves constructing dose-response curves for a serotonin standard and test sample, selecting doses that elicit submaximal responses in a 1:2 ratio, and determining the test concentration using the measured responses. Rat fundus tissue is sensitive to serotonin and contracts in a concentration-dependent manner when exposed to increasing doses of the drug. The experiment aims to precisely and reliably estimate the concentration of an unknown serotonin sample through this validated bioassay method.
Diuretics work by preventing the body from absorbing too much salt and increasing the excretion of water and salt in urine. Furosemide is a common diuretic ("water pill") that is prescribed to treat high blood pressure and reduce excess fluid in the body from conditions like heart failure or kidney disease. It works by inhibiting sodium reabsorption in the ascending loop of the kidney, which leads to increased water excretion in urine. Potential side effects include headaches, dizziness, thirst, and electrolyte imbalances.
This document discusses different classes of diuretic drugs, including their mechanisms of action, structures, and uses. It focuses on loop diuretics, describing how they work by inhibiting sodium reabsorption in the ascending limb of the loop of Henle. Adverse effects of loop diuretics include electrolyte abnormalities like hypokalemia. The structure-activity relationships of loop diuretics are also covered, noting features like the carbonyl group and sulfamoyl substituents that contribute to diuretic potency. Loop diuretics are used to treat various conditions involving edema.
Bradykinin and substance P are neuropeptides that act as neurotransmitters and neuromodulators. Bradykinin is generated from kininogens by the enzyme kallikrein and acts through B1 and B2 receptors. It causes vasodilation, increased vascular permeability, and pain sensation. Substance P is an undecapeptide related to neurokinin A that is synthesized in the nervous system and distributed throughout the brain and peripheral tissues. It acts through neurokinin 1 receptors and is involved in nociception and inflammation. Antagonists of bradykinin and substance P receptors have potential therapeutic applications.
This document discusses various haematinics including iron, vitamin B12, folic acid, and erythropoietin. It covers their roles in red blood cell formation, daily requirements, dietary sources, absorption and transport, deficiency states, preparations used to treat deficiencies, and therapeutic uses to treat conditions like iron deficiency anemia and megaloblastic anemia. It provides details on the pharmacokinetics and pharmacology of administering these substances.
The document discusses anti-diabetic agents and provides details about sulfonylureas. It describes the mechanism of action of sulfonylureas, which involves binding to sulfonylurea receptors on pancreatic beta cells and extrapancreatic cells to stimulate insulin secretion and inhibit gluconeogenesis. Adverse effects include hypoglycemia and weight gain. Tolbutamide is provided as an example sulfonylurea drug, with its structure, synthesis, mechanism of action, pharmacokinetics, adverse effects, and therapeutic uses summarized.
Expt. 4 DRC of acetylcholine using frog rectus abdominis muscleVISHALJADHAV100
Objective
Principle
Requirements
Experimental specifications (conditions)
Preparation of ACh stock and standard solutions
Preparation of frog ringer solution (PSS)
Procedure
Kymograph recording of contractions
Observation table
Calculation of magnification value (Mf)
Graphical presentation of CRC/ DRC
Result and interpretation
This document summarizes immunostimulant drugs and immunotherapy. It describes the innate and adaptive immune response and lists immunostimulant microbial products like BCG that boost immune function. Immunostimulant drugs include cytokines, thalidomide, and levamisole. Immunotherapy methods covered are active and passive vaccination, adoptive cell transfer, and cell-based vaccination. The document provides details on specific immunostimulant drugs and their uses and side effects.
Biosynthesis of Histamine,Storage and release,Histamine H1-Receptor ,Histamine H1-Receptor Antagonists,Differences between first generation & second generation antihistamines,H2 receptor blockers
This document discusses antihypertensive drugs used to treat hypertension. It classifies these drugs into 10 categories including diuretics, ACE inhibitors, angiotensin receptor blockers, calcium channel blockers, beta blockers, alpha-beta blockers, alpha blockers, central sympatholytics, vasodilators, and renin inhibitors. For each drug class, it describes the mechanism of action how each lowers blood pressure by relaxing blood vessels or reducing cardiac output and peripheral resistance. Adverse effects like hypotension and cough are also mentioned.
The document describes changes that occur to carbohydrates during food processing, digestion, absorption, and metabolism. It discusses how carbohydrates are broken down during cooking and storage through leaching and the Maillard reaction. It then outlines the multi-step digestion of carbohydrates by salivary and pancreatic enzymes in the mouth, stomach, and small intestine. Absorption of monosaccharides occurs actively in the intestine, and carbohydrates are further metabolized through pathways like glycolysis and the citric acid cycle to generate energy.
In this slide contains introduction, principle, precautions, solution and assay method for vitamin B series.
Presented by: P. VENKATESH (Department of pharmaceutical analysis),
RIPER, anantapur
Introduction to Screening Models of Anti-Atherosclerosis
Atherosclerosis, Screening models, In vitro models, In vivo models
Presented by
SHAIK FIRDOUS BANU
Department of Pharmacology
Introduction to Histamine and Antihistamine
Role of histamine, Synthesis, Storage, release of histamine
Mechanism of action of histamine
Anti histamine, Therapeutic uses, Adverse effects
Presented by
Shaik Sabeena
Department of Pharmacology
Introduction to Physiological and pathological role of serotonin
Autocoids, Classification, synthesis ,Serotonergic receptors, Physiological actions, Pathophysiological role
Presented by
K.Firdous banu
Department of Pharmacology
Introduction to Screening Models of Hepatoprotective Drugs
Liver toxicity, Drugs causing DILI, Markers of hepatotoxicity
List of hepatoprotectives, Functions of liver
Screening models of hepatoprotective drugs
Presented by
I. Sai Reddemma
Department of Pharmacology
In this slide contains the deep explanation of Methods of Determination for Drug-Excipient Compatibility Studies.
Presented by: G.Aravind Kumar (Department of industrial pharmacy),
RIPER, anantapur.
In this slide contains definition and determination of Iodine value, Rancidity, Peroxide value.
Presented by: K. SANDHYA RANI (Department of pharmaceutical analysis).RIPER, anantapur
Introduction to Crystal Morphology & Variations,
Classification of Chemical Compounds, Amorphous Forms, Polymorphs, Solvates, Clathrates, Crystal Habit, Crystal Habit Modification Methods, Crystallization, Importance of Crystallization in Preformulation
Presented by
A.Siddartha Tharun Teja
Department of Industrial Pharmacy
Introduction to Screening Models Of Anti Cancer Drugs
Need for novel anti cancer drugs, In - vitro methods, In - vivo methods, Advantages and disadvantages
Presented by
T. Niranjan Reddy
Department of Pharmacology
Introduction to General Anaesthetics
Introduction General Anaesthetics, Stages of anaesthesia, Classification of General Anaesthetics, Mechanism of action of General Anaesthetics, Pharmacokinetics, Pharmacodynamics, Uses, Side effects
Presented by
I. Sai Reddemma
Department of Pharmacology
In this slide contains diabetics, classification, symptoms, complication, invivo and invitro screening models of anti diabetics.
Presented by: GEETHANJALI ADAPALA (Department of pharmacology).
RIPER, anantapur
Target Validation
Introduction,Drug discovery, Target identification and validation, Target validation and techniques
By
Ms. B. Mary Vishali
Department of Pharmacology
ANTIOXIDANT ACTIVITY AND HEPATOPROTECTIVE EFFECTOF POMEGRANATE PEEL AND WHEY...Anurag Raghuvanshi
The antioxidant activity of pomegranate peel powder (PPP) and whey powder (WP) was evaluated, their hepatoprotective effect of each alone or in combination (PPWP) at equal levels was also evaluated in Wistar rats against carbon tetrachloride (CCL4) induced liver injury.
The hepatoprotective activity was assessed using various biochemical parameters and histopathological studies.
In this slides contains deep introduction about pesticides and analysis of pesticide residue in vegetables.
Presented by: M. Malarvannan (Department of pharmaceutical analysis),
RIPER, anantapur.
The document discusses methods for estimating pesticides in vegetables. It begins with introductions to pesticides and their classification. It then discusses regulations around pesticide residues and terminology used in pesticide analysis. The document outlines the workflow for pesticide residue analysis including sample collection, preparation, extraction, clean up, and analysis. It provides details on sample extraction methods for vegetables, including the QuEChERS method. Finally, it discusses multiresidue analysis methods for pesticides using gas chromatography.
This document discusses various types and classifications of food proteins. It describes proteins as polymers of amino acids linked by amide bonds. It then covers different methods used to determine protein quality, including protein efficiency ratio, biological value, net protein utilization, protein digestibility corrected amino acid score, and digestible indispensable amino acid score. Various protein sources and their protein contents are listed. Recommended dietary allowances for protein by age are provided. The document concludes by classifying proteins based on their composition, function, solubility, shape and size, essential amino acid availability, and biological value.
The document describes the development of a new magnetic solid phase extraction (MSPE) adsorbent called polyDOPA@Ag-MNPs for the analysis of trace beta-blockers in biological samples. PolyDOPA@Ag-MNPs were synthesized by reducing silver ions on the surface of magnetic nanoparticles coated with poly(3,4-dihydroxyphenylalanine). The adsorbent was able to isolate beta-blockers from sample matrices using a magnetic field. Optimization of the MSPE method identified pH 7, 2 minutes adsorption time, 4 mg polyDOPA@Ag-MNPs, methanol containing 1% acetic acid as the eluent, 2 minutes elution
JOURNAL CLUB PRESENTATION (20L81S0402-PA & QA)
Presented by: K VENKATSAI PRASAD (Department of pharmaceutical analysis and quality assurance).RIPER, anantapur
The cost of acquiring information by natural selectionCarl Bergstrom
This is a short talk that I gave at the Banff International Research Station workshop on Modeling and Theory in Population Biology. The idea is to try to understand how the burden of natural selection relates to the amount of information that selection puts into the genome.
It's based on the first part of this research paper:
The cost of information acquisition by natural selection
Ryan Seamus McGee, Olivia Kosterlitz, Artem Kaznatcheev, Benjamin Kerr, Carl T. Bergstrom
bioRxiv 2022.07.02.498577; doi: https://doi.org/10.1101/2022.07.02.498577
Travis Hills of MN is Making Clean Water Accessible to All Through High Flux ...Travis Hills MN
By harnessing the power of High Flux Vacuum Membrane Distillation, Travis Hills from MN envisions a future where clean and safe drinking water is accessible to all, regardless of geographical location or economic status.
The binding of cosmological structures by massless topological defectsSérgio Sacani
Assuming spherical symmetry and weak field, it is shown that if one solves the Poisson equation or the Einstein field
equations sourced by a topological defect, i.e. a singularity of a very specific form, the result is a localized gravitational
field capable of driving flat rotation (i.e. Keplerian circular orbits at a constant speed for all radii) of test masses on a thin
spherical shell without any underlying mass. Moreover, a large-scale structure which exploits this solution by assembling
concentrically a number of such topological defects can establish a flat stellar or galactic rotation curve, and can also deflect
light in the same manner as an equipotential (isothermal) sphere. Thus, the need for dark matter or modified gravity theory is
mitigated, at least in part.
Immersive Learning That Works: Research Grounding and Paths ForwardLeonel Morgado
We will metaverse into the essence of immersive learning, into its three dimensions and conceptual models. This approach encompasses elements from teaching methodologies to social involvement, through organizational concerns and technologies. Challenging the perception of learning as knowledge transfer, we introduce a 'Uses, Practices & Strategies' model operationalized by the 'Immersive Learning Brain' and ‘Immersion Cube’ frameworks. This approach offers a comprehensive guide through the intricacies of immersive educational experiences and spotlighting research frontiers, along the immersion dimensions of system, narrative, and agency. Our discourse extends to stakeholders beyond the academic sphere, addressing the interests of technologists, instructional designers, and policymakers. We span various contexts, from formal education to organizational transformation to the new horizon of an AI-pervasive society. This keynote aims to unite the iLRN community in a collaborative journey towards a future where immersive learning research and practice coalesce, paving the way for innovative educational research and practice landscapes.
Mending Clothing to Support Sustainable Fashion_CIMaR 2024.pdfSelcen Ozturkcan
Ozturkcan, S., Berndt, A., & Angelakis, A. (2024). Mending clothing to support sustainable fashion. Presented at the 31st Annual Conference by the Consortium for International Marketing Research (CIMaR), 10-13 Jun 2024, University of Gävle, Sweden.
Authoring a personal GPT for your research and practice: How we created the Q...Leonel Morgado
Thematic analysis in qualitative research is a time-consuming and systematic task, typically done using teams. Team members must ground their activities on common understandings of the major concepts underlying the thematic analysis, and define criteria for its development. However, conceptual misunderstandings, equivocations, and lack of adherence to criteria are challenges to the quality and speed of this process. Given the distributed and uncertain nature of this process, we wondered if the tasks in thematic analysis could be supported by readily available artificial intelligence chatbots. Our early efforts point to potential benefits: not just saving time in the coding process but better adherence to criteria and grounding, by increasing triangulation between humans and artificial intelligence. This tutorial will provide a description and demonstration of the process we followed, as two academic researchers, to develop a custom ChatGPT to assist with qualitative coding in the thematic data analysis process of immersive learning accounts in a survey of the academic literature: QUAL-E Immersive Learning Thematic Analysis Helper. In the hands-on time, participants will try out QUAL-E and develop their ideas for their own qualitative coding ChatGPT. Participants that have the paid ChatGPT Plus subscription can create a draft of their assistants. The organizers will provide course materials and slide deck that participants will be able to utilize to continue development of their custom GPT. The paid subscription to ChatGPT Plus is not required to participate in this workshop, just for trying out personal GPTs during it.
The technology uses reclaimed CO₂ as the dyeing medium in a closed loop process. When pressurized, CO₂ becomes supercritical (SC-CO₂). In this state CO₂ has a very high solvent power, allowing the dye to dissolve easily.
ESA/ACT Science Coffee: Diego Blas - Gravitational wave detection with orbita...Advanced-Concepts-Team
Presentation in the Science Coffee of the Advanced Concepts Team of the European Space Agency on the 07.06.2024.
Speaker: Diego Blas (IFAE/ICREA)
Title: Gravitational wave detection with orbital motion of Moon and artificial
Abstract:
In this talk I will describe some recent ideas to find gravitational waves from supermassive black holes or of primordial origin by studying their secular effect on the orbital motion of the Moon or satellites that are laser ranged.
EWOCS-I: The catalog of X-ray sources in Westerlund 1 from the Extended Weste...Sérgio Sacani
Context. With a mass exceeding several 104 M⊙ and a rich and dense population of massive stars, supermassive young star clusters
represent the most massive star-forming environment that is dominated by the feedback from massive stars and gravitational interactions
among stars.
Aims. In this paper we present the Extended Westerlund 1 and 2 Open Clusters Survey (EWOCS) project, which aims to investigate
the influence of the starburst environment on the formation of stars and planets, and on the evolution of both low and high mass stars.
The primary targets of this project are Westerlund 1 and 2, the closest supermassive star clusters to the Sun.
Methods. The project is based primarily on recent observations conducted with the Chandra and JWST observatories. Specifically,
the Chandra survey of Westerlund 1 consists of 36 new ACIS-I observations, nearly co-pointed, for a total exposure time of 1 Msec.
Additionally, we included 8 archival Chandra/ACIS-S observations. This paper presents the resulting catalog of X-ray sources within
and around Westerlund 1. Sources were detected by combining various existing methods, and photon extraction and source validation
were carried out using the ACIS-Extract software.
Results. The EWOCS X-ray catalog comprises 5963 validated sources out of the 9420 initially provided to ACIS-Extract, reaching a
photon flux threshold of approximately 2 × 10−8 photons cm−2
s
−1
. The X-ray sources exhibit a highly concentrated spatial distribution,
with 1075 sources located within the central 1 arcmin. We have successfully detected X-ray emissions from 126 out of the 166 known
massive stars of the cluster, and we have collected over 71 000 photons from the magnetar CXO J164710.20-455217.
PPT on Direct Seeded Rice presented at the three-day 'Training and Validation Workshop on Modules of Climate Smart Agriculture (CSA) Technologies in South Asia' workshop on April 22, 2024.
Basics of crystallography, crystal systems, classes and different forms
Haematinics
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K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 1
A seminar as a part of curricular requirement
For 1 year M. Pharm. 1 semester
3-6-2021
Presented by
R. Rekha, (20L81S111)
M. Pharmacy
Department of pharmacology
Under the guidance of
Mr. A. Sudheer Kumar.,M. Pharm, Ph.D.
Associate Professor
Dept. Of Pharmacology
Haematinics
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Raghavendra Institute of Pharmaceutical Education and Research - Autonomous
K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 2
Introduction of Haematinics
Iron
Cynacobalamine
Folic acid
Plasma expanders
References
Contents
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K.R.Palli Cross, Chiyyedu, Anantapuramu, A. P- 515721 3
These are the agent required in the formation of blood & used for
treatment of anemia's
Etiology:
Anemia occurs when,
A. Blood loss (acute or chronic)
B. Impaired red formation due to;
a)Deficiency of iron,vit.B12. folic acid.
b)Bone marrow depression
C. Increased destruction of RBCs.
HAEMATINICS
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1. Iron & it’s compound:
eg:-ferrous succinate, ferrous sulfate,
ferrous gluconate etc.
2. Maturation factor:-
eg:-cynacobalamine,
Hydroxy cynocobalamine
3. Miscellaneous:-
eg:-copper,
cobalt
Riboflavin.
Classification:-
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• According to Greek thought MARS is the god of strength & IRON is
dedicated to it
• .Source of iron:-
• Rich:- Liver, egg yolk, dry bean, dry fruit.
• Medium:- Meat, chicken, fish, banana, apple.
• Poor:- Milk & it’s product
Daily requirement:-
• Adult male :- 0.5-1mg(13µg/kg).
• Adult female:-1-2mg(21µg/kg)
• Infant :-60µg/kg.
• Children :-25µg/kg
• Pregnancy :-3-5mg(80µg/kg).
IRON
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Iron Absorption
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As such, on entering plasma it is immediately converted to the
ferric form and complexed with a glycoprotein transferrin (Tf).
Iron is transported into erythropoietic and other cells through
attachment of transferrin to specific membrane bound
transferrin receptors(T f Rs)
The complex is engulfed by receptor mediated endocytosis.
Iron dissociates from the complex at the acidic pH of the
intracellular vesicles. the released iron is utilized for
haemoglobin synthesis or other purposes
Tf and T f R are returned to the cell surface to carry fresh loads.
Transport,utilization,storage & excretion:
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1. Iron deficiency anaemia.
2. Megaloblastic anaemia.
3. As an astringent :-Ferric chloride is used in throat paint.
Adverse effects :-
1.Epigastric pain.
2. heartburn.
3. nausea, vomiting
4. staining of teeth
5. metallic taste.
6. Constipation.
Therapeutic uses:-
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VITAMIN-B12 (Cyanocobalamine)
1. Vitamin B12 occurs as water soluble, thermostable red
crystals.
2.It is synthesized in nature only by microorganisms; plants
and animals acquire it from them.
Dietary sources :-Liver, kidney, sea fish, egg yolk, meat, cheese.
Daily requirement: 1–3 μg, pregnancy and lactation 3–5 μg.
Cynacobalamine
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Essential for normal erythropoieses maintainance of normal
myelin sheath
Vitamin B12 is essential for the conversion of hom o-cysteine
to methionine.
Now it appears that interference with the reaction:
Vitamin B12 is essential for cell growth and multiplication.
Purine and pyrimidine synthesis .
Metabolic functions:-
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Intrinsic factor secreted by stomach forms a complex with B12
attaches to specific receptors present on intestinal mucosal cells and
is absorbed by active carrier mediated transport.
Vitamin B12 is transported in blood in combination with a specific β
globulin transcobalamine II (TCII).
Vitamin B12 is especially taken up by liver cells and stored about 2/3
to 4/5 of body’s content (2–8 mg) is present in liver.
Vitamin B12 is not degraded in the body. It is excreted mainly in
bile (3–7 μg/day); all but 0.5–1 μg of this is reabsorbed—
considerable entero-hepatic circulation occurs.
pharmacokinetics:
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• Manifestations of vitamin b12:
Glossits
Atropy of tongue&vagina
Neurological:
sub acute comibned degenaration of posterior harm leads to ataxia
Paraesthesia
Peripheral neuropathy
Loss of memory,halogenation
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Therapeutic use:-
Pernicious anaemia.
Malabsorption syndrome
Nutritional deficiency.
Neurological condition.
Psychitric disorder
Adevrse drug reaction:-
Allergic reactions have occurred by injection
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ACID Folic acid(Pteroyl glutamic acid) is a member of the B
complex group of vitamin
Dietary sources:-
Liver, green leafy vegetables (spinach), egg, meat, milk.
Daily requirement:- 0.2 mg/day
FOLIC ACID
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Folic acid is present in food as poly-glutamates
The additional glutamate residues are split off primarily in the upper
intestine before being absorbed.
Small, physiological amounts of folate are absorbed by specific
carrier-mediated active transport in the intestinal mucosa
Folic acid is rapidly extracted by tissues and stored in cells as
polyglutamate.
Liver takes up a large part and secretes methyl-THFA in bile & again
reabsorbed by enterohepatic cycle 50-90% of adose may be
excreated in urine
Absorption,transport& utilization
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1. Conversion of homocysteine to methionine:
2. Generation of thymidylate, an essential constituent of DNA:
3. Conversion of serine to glycine.
4. Purine synthesis.
5. Histidine metabolism.
Metabolic functions of folic acid
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Deficiency & menifestation:-
1. Megaloblastic anaemia.
2. Nutritional deficiency.
3. Malabsorption.
4. Epithelial damage.
5. Weight loss.
Therapeutic use:- 1. Improve absorption. 3. Protect epithelial cell. 4.
Growth factor.
Adverse effects: Hypersensitivity reaction by injection.
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PLASMA EXPANDERS
Ideal properties of a plasma expander are:
1. Should exert oncotic pressure comparable
to plasma.
2. Should remain in circulation and not leak
out in tissues.
3. Should be pharmacodynamically inert.
4. Should not be pyrogenic or antigenic.
5. Should be stable, easily sterilizable.
Dextran It is a polysaccharide obtained from
sugar beat .
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• The more commonly used preparation is dextran- 70.
• It expands plasma volume for nearly 24 hours.
• it is slowly excreted by glomerular filtration as well as oxidized in
the body over weeks.
• Some amount is deposited in RE cells
• Dextran has nearly all the properties of an ideal plasma expander.
Dextran-40
• It acts more rapidly than dextran-70.
• It reduces blood viscosity. Microcirculation may improve.
Dextran-70:
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1. Plasma loss.
2. Burn
3. Hypovolemic & endotoxin shock.
4. Sever trauma & extensive
tissue damage
5. Whole blood loss.
Contraindications 1. severe anaemia. 2. cardiac failure. 3. Pulmonary
edema.
USE OF PLASMA EXPANDERS:-
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1.Agstaff, Adam, Claeson Marian. 2004. The Millennium Development Goals
for Health-Rising to the Challenges. World Bank. Washington, Tripati,
Goodman & Gillman. 2004;6;14.
2.Global Governance Initiative Annual Report 2005, world economic
forum
3.Seshadri S. Nutritional anaemia in south Asia. In Malnutrition in South
Asia. A Regional Profile. Ed. Gillespie S. UNICEF Regional Office.
Reference:
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