Ammonium chloride is an inorganic compound that occurs as a white crystalline powder. It is highly soluble in water and solutions are mildly acidic. Ammonium chloride is prepared commercially by reacting ammonia with hydrogen chloride gas or hydrochloric acid. It has several applications, including use as an expectorant in cough medicines due to its irritating effect on the bronchial mucosa. Ammonium chloride is also used to acidify the urine and as a systemic acidifying agent to treat metabolic alkalosis. It is available in formulations like cough syrups and injections.
The document describes three methods (A, B, and C) for performing a limit test for heavy metals according to the Indian Pharmacopoeia. The test involves reacting heavy metal ions in the sample with hydrogen sulfide or sodium sulfide to form colored heavy metal sulfides. The color produced is compared to that of a standard lead solution to determine whether the sample meets the limit of 20 parts per million for heavy metals. Method A is for clear, colorless solutions, Method B is for solutions that are not clear or colorless, and Method C uses sodium hydroxide for solutions that give a clear colorless solution in sodium hydroxide.
This document describes the procedure for performing a limit test for sulphate according to the Indian Pharmacopoeia. A barium sulphate reagent is prepared containing barium chloride, potassium sulphate, alcohol and water. Standard sulphate solutions are also prepared. The test involves adding nitric acid and the reagent to samples and standards, observing any turbidity formed, and comparing the sample to the standard. If the sample turbidity is less than the standard, it passes the limit test, and if greater, it fails the test.
Anatacid || B pharmacy First Year || Presentation || kkwagh ||
This presentation is helpful for your study
This Presentation Contain
• Introduction
• characteristics of ideal antacid
• classification of antacid
• Some common use antacid
MAKAUT/SEM 1/ PHARMACEUTICAL INORGANIC CHEMISTRY/ UNIT 3/GASTROINTESTINAL AGENTS_CATHARTICS
BY
KUNAL DATTA
ASSISTANT PROFESSOR
B.PHARM , M.PHARM
NETAJI SUBHAS CHANDRA BOSE INSTITUTE OF PHARMACY
Arsenic is well known under desirable hand harmful due to its toxic nature, it poses the serious health hazard, which is present in medical substance, many qualitative and quantitative test for arsenic known, however Pharmacopoeia method is based on ‘Gutzeit Method’.
Concentration of arsenic beyond 0.01 mg/L in pollutant by the World Health Organization (WHO).
Reasons:
• Stannous chloride is used for complete evolution of arsine.
• Zinc, potassium iodide and stannous chloride is used as a reducing agent.
• Hydrochloride acid is used to make the solution acidic.
• Lead acetate pledger or papers are used to trap any hydrogen sulphide, which may be evolved along with arsine.
This document discusses various inorganic pharmaceutical agents including expectorants, terpin hydrate, ammonium chloride, potassium iodide, and emetics such as antimony potassium tartrate. Expectorants are drugs that stimulate respiratory tract secretions to loosen mucus. Terpin hydrate, ammonium chloride, and potassium iodide are expectorants. Emetics induce vomiting and were formerly used but are limited now due to their depression effects. Antimony potassium tartrate is an emetic with a slow onset of vomiting followed by marked depression.
Ammonium chloride is an inorganic compound that occurs as a white crystalline powder. It is highly soluble in water and solutions are mildly acidic. Ammonium chloride is prepared commercially by reacting ammonia with hydrogen chloride gas or hydrochloric acid. It has several applications, including use as an expectorant in cough medicines due to its irritating effect on the bronchial mucosa. Ammonium chloride is also used to acidify the urine and as a systemic acidifying agent to treat metabolic alkalosis. It is available in formulations like cough syrups and injections.
The document describes three methods (A, B, and C) for performing a limit test for heavy metals according to the Indian Pharmacopoeia. The test involves reacting heavy metal ions in the sample with hydrogen sulfide or sodium sulfide to form colored heavy metal sulfides. The color produced is compared to that of a standard lead solution to determine whether the sample meets the limit of 20 parts per million for heavy metals. Method A is for clear, colorless solutions, Method B is for solutions that are not clear or colorless, and Method C uses sodium hydroxide for solutions that give a clear colorless solution in sodium hydroxide.
This document describes the procedure for performing a limit test for sulphate according to the Indian Pharmacopoeia. A barium sulphate reagent is prepared containing barium chloride, potassium sulphate, alcohol and water. Standard sulphate solutions are also prepared. The test involves adding nitric acid and the reagent to samples and standards, observing any turbidity formed, and comparing the sample to the standard. If the sample turbidity is less than the standard, it passes the limit test, and if greater, it fails the test.
Anatacid || B pharmacy First Year || Presentation || kkwagh ||
This presentation is helpful for your study
This Presentation Contain
• Introduction
• characteristics of ideal antacid
• classification of antacid
• Some common use antacid
MAKAUT/SEM 1/ PHARMACEUTICAL INORGANIC CHEMISTRY/ UNIT 3/GASTROINTESTINAL AGENTS_CATHARTICS
BY
KUNAL DATTA
ASSISTANT PROFESSOR
B.PHARM , M.PHARM
NETAJI SUBHAS CHANDRA BOSE INSTITUTE OF PHARMACY
Arsenic is well known under desirable hand harmful due to its toxic nature, it poses the serious health hazard, which is present in medical substance, many qualitative and quantitative test for arsenic known, however Pharmacopoeia method is based on ‘Gutzeit Method’.
Concentration of arsenic beyond 0.01 mg/L in pollutant by the World Health Organization (WHO).
Reasons:
• Stannous chloride is used for complete evolution of arsine.
• Zinc, potassium iodide and stannous chloride is used as a reducing agent.
• Hydrochloride acid is used to make the solution acidic.
• Lead acetate pledger or papers are used to trap any hydrogen sulphide, which may be evolved along with arsine.
This document discusses various inorganic pharmaceutical agents including expectorants, terpin hydrate, ammonium chloride, potassium iodide, and emetics such as antimony potassium tartrate. Expectorants are drugs that stimulate respiratory tract secretions to loosen mucus. Terpin hydrate, ammonium chloride, and potassium iodide are expectorants. Emetics induce vomiting and were formerly used but are limited now due to their depression effects. Antimony potassium tartrate is an emetic with a slow onset of vomiting followed by marked depression.
Introduction of Inorganic Chemistry, History of Pharmacopoeia.pptxMs. Pooja Bhandare
This document provides an overview of pharmaceutical inorganic chemistry and the history of pharmacopoeias. It discusses how pharmaceutical inorganic chemistry studies inorganic substances used as drugs, and how pharmacopoeias set quality standards for drugs. The document outlines the contents of pharmacopoeias including monographs describing drugs' names, properties, purity standards, and approved tests. It provides a brief history of major pharmacopoeias like the USP and IP, and describes the development and editions of the Indian Pharmacopoeia since 1944.
This document discusses various types of saline cathartics (laxatives) including their definitions, mechanisms of action, preparations, and uses. The main types discussed are bulk forming laxatives, osmotic laxatives, lubricant laxatives, surfactant laxatives, and purgatives. Specific saline cathartics described in detail include magnesium hydroxide, magnesium sulfate (Epsom salt), and magnesium carbonate. Their preparations, assays, uses as laxatives or other purposes, and dosages are provided.
This document describes the limit test for iron according to the Indian Pharmacopoeia. The test involves comparing the color produced by reacting a sample with thioglycolic acid in an ammonical citrate buffer to the color produced by a standard iron solution under the same conditions. If the color produced by the sample is less than the standard, it passes the limit test for iron. If the color is greater than the standard, it fails the limit test. The test is sensitive and uses citric acid to eliminate interference from other metal cations.
This document describes the limit test for arsenic using the Gutzeit method. Arsenic in a sample is converted to arsine gas, which reacts with mercuric chloride paper to produce a stain that is compared to a standard stain. The test uses an apparatus with two glass tubes, where the sample is placed below zinc and hydrochloric acid to produce arsine gas, which passes through mercuric chloride paper to produce a stain after 40 minutes. By comparing the intensity of this test stain to the standard stain produced in the same way from a solution of known arsenic concentration, the document determines if the sample passes or fails the limit test for arsenic.
Emetics are drugs that induce vomiting by causing the contents of the stomach to be expelled through the mouth. They are important for treating poisoning cases. Copper sulfate is a common emetic that is blue crystalline powder. It can be assayed through an oxidation-reduction titration with iodine and sodium thiosulfate. Sodium potassium tartrate, also known as Rochelle salt, is a crystalline powder that is soluble in water. It has uses as a laxative, diuretic, and food additive.
Limit test of sulphate is based on the reaction of soluble sulphate with barium chloride in presence of dilute hydrochloric acid to form barium sulphate which appears as solid particles (turbidity) in the solution.
This document describes the limit test for sulfate. The test is based on the reaction between barium chloride and soluble sulfates in the presence of hydrochloric acid. This results in the precipitation of barium sulfate. The turbidity produced by the test solution is compared to that of a standard sulfate solution. If the turbidity of the test solution is less than the standard, then the sample passes the limit test for sulfate.
This document provides information about gastrointestinal agents (GI agents), which are drugs used to treat GI disorders. It discusses the classifications of GI agents including acidifying agents, antacids, protectives, adsorbents, and cathartics. It then describes common antacids including aluminum hydroxide gel, calcium carbonate, and magnesium salts. The ideal characteristics of antacids are outlined. Common calcium-containing and magnesium-containing antacids are also discussed in more detail.
Unit 1 PHARMACEUTICAL INORGANIC CHEMISTRYSayali Powar
The document discusses various limit tests performed as per the Indian Pharmacopoeia to determine the presence of impurities below specified limits. It describes the principles, procedures and observations for limit tests of chloride, sulphate, iron, arsenic, heavy metals and lead. Limit tests involve comparing the color or turbidity developed in a test sample to a standard under defined reaction conditions. They provide a semi-quantitative analysis to check if impurity levels pass specified limits in the pharmacopoeia.
This document discusses monophasic liquid dosage forms, which contain components dissolved in a single phase. It provides examples of internal monophasic liquids like syrups and elixirs, and external liquids like gargles and enemas. The advantages of liquids include ease of administration, rapid drug absorption, and uniform dosing. Disadvantages include bulkiness, potential for microbial growth, and reduced drug stability compared to solids. A variety of oral, ocular, nasal and rectal liquids are also described.
This document provides information on various pharmaceutical compounds including expectorants, potassium iodide, copper sulfate, iron sulfate, zinc sulfate, and methods for their analysis. It discusses the definition, chemical and physical properties, preparation, uses and assays of these compounds by redox titration, gravimetric analysis, and complexometric titration. The document also covers emetics, astringents, antidotes and poisons including sodium nitrite, sodium thiosulfate and activated charcoal.
This document describes the limit test for lead using diphenylthiocarbazone (dithizone) which forms a violet colored lead-dithizonate complex in an alkaline medium. The method separates any lead impurity in a substance by extracting an alkaline solution with dithizone chloroform solution. The intensity of the violet color complex is then compared to a standard lead solution to determine the amount of lead present.
The document discusses the limit test for chloride. It defines a limit test as a quantitative or semi-quantitative test to identify and control small amounts of impurities likely to be present in a substance. The limit test for chloride determines the allowable limit of chloride in a sample. It involves dissolving the sample and standard sodium chloride solution, adding nitric acid and silver nitrate, and observing any opalescence or turbidity after 3 minutes. The sample passes the limit test for chloride if the opalescence is less than or equal to the standard solution.
This document describes the Gutzeit test for detecting arsenic. The test works by first converting any arsenic in a sample into arsenious acid, then reducing it to arsine gas. Mercuric chloride paper placed in the apparatus will turn yellow if arsine gas is present, indicating the presence of arsenic in the original sample. The document provides details of the test apparatus, reagents used, procedure, and precautions to get accurate results and avoid contamination.
Limt test Pharmaceutical Inorganic chemistry UNIT-I (Part-III) Limit Test.
Limit tests:- Factors affecting limit tests:
Specificity of the tests
Sensitivity
Control of personal errors (Analyst errors)
Test in which there is no visible reaction
Comparison methods
Quantitative determination
Limit test for Chloride: Principle, Procedure, observation and result.
Limit test for Sulphate: Principle, Procedure, observation and result
Limit test for Iron: Principle, Procedure, observation and result.
Limit test for Heavy metal: Principle, Procedure, observation and result.
Limit test for Lead: Principle, Procedure, observation and result.
Limit test for Arsenic: Principle, Gutzet test Procedure, detail in Gutzet Apparatus. observation and result.
Modifies Limit test for Chloride: Principle, Procedure, observation and result.
Modified Limit test for sulphate: Principle, Procedure, observation and result.
Acids, Bases And Buffers Pharmaceutical Inorganic chemistry UNIT-II (Part-I)
Acids, Bases are defined by Four main theories,
1.Traditional theory / concept
2.Arrhenius theory
3.Bronsted and Lowry theory
4.Lewis theory
Importance of acids and bases in pharmacy
Buffers: Buffer action
Buffer capacity Buffers system
Types of Buffers : Generally buffers are of two types:
1. Acidic buffers
2. Basic buffers
There are some other buffer system:
3. Two salts acts as acid-base pair. Ex- Potassium hydrogen phosphate and potassium dihydrogen phosphate.
4. Amphoteric electrolyte. Ex- Solution of glycine.
5. Solution of strong acid and solution of strong base. Ex- Strong HCl with KCl Mechanism of Buffer action: Mechanism of Action of acidic buffers: Buffer equation-Henderson-Hasselbalch equation:
Standard Buffer Solutions Preparation of Buffer Solutions: Buffers in pharmaceutical systems or Application of buffer: Stability of buffers Buffered isotonic solution Types of Buffer Isotonic solution
1. Isotonic Solutions:
2. Hypertonic Solutions:
3. Hypotonic Solution:
Measurement of Tonicity: 1. Hemolytic method: 2. Cryoscopic method or depression of freezing point:
Methods of adjusting the tonicity:
Class I methods:
In this type, sodium chloride or other substances are added to the solution in sufficient quantity to make it isotonic. Then the preparation is brought to its final volume withan isotonic or a buffered isotonic diluting solution.
These methods are of two types:
Cryoscopic method
Sodium chloride equivalent method.
Class II methods:
In this type, water is added in sufficient quantity make the preparation isotonic. Then the preparation is brought to its volume with an isotonic or a buffered isotonic diluting solution.
These methods are of two types:
White-Vincent method
Sprowls method.
Gastrointestinal agents are drugs used to treat gastrointestinal disorders like achlorhydria, hyperacidity, constipation, and diarrhea. Acidifiers increase acid concentration in the GI tract and are used to treat achlorhydria. Dilute hydrochloric acid maintains or increases stomach acid levels and pH. Antacids neutralize excess stomach acid in hyperacidity. Common acidifiers and antacids include ammonium chloride, dilute hydrochloric acid, and sodium bicarbonate.
This document provides information on flavor enhancers and stabilizers used in foods. It discusses flavor, common flavor enhancers like monosodium glutamate, and techniques for analyzing flavors like gas chromatography. It also defines food stabilizers, provides examples like alginates and agar, describes general confirmatory tests, and discusses applications such as preventing emulsions from separating.
Introduction of Inorganic Chemistry, History of Pharmacopoeia.pptxMs. Pooja Bhandare
This document provides an overview of pharmaceutical inorganic chemistry and the history of pharmacopoeias. It discusses how pharmaceutical inorganic chemistry studies inorganic substances used as drugs, and how pharmacopoeias set quality standards for drugs. The document outlines the contents of pharmacopoeias including monographs describing drugs' names, properties, purity standards, and approved tests. It provides a brief history of major pharmacopoeias like the USP and IP, and describes the development and editions of the Indian Pharmacopoeia since 1944.
This document discusses various types of saline cathartics (laxatives) including their definitions, mechanisms of action, preparations, and uses. The main types discussed are bulk forming laxatives, osmotic laxatives, lubricant laxatives, surfactant laxatives, and purgatives. Specific saline cathartics described in detail include magnesium hydroxide, magnesium sulfate (Epsom salt), and magnesium carbonate. Their preparations, assays, uses as laxatives or other purposes, and dosages are provided.
This document describes the limit test for iron according to the Indian Pharmacopoeia. The test involves comparing the color produced by reacting a sample with thioglycolic acid in an ammonical citrate buffer to the color produced by a standard iron solution under the same conditions. If the color produced by the sample is less than the standard, it passes the limit test for iron. If the color is greater than the standard, it fails the limit test. The test is sensitive and uses citric acid to eliminate interference from other metal cations.
This document describes the limit test for arsenic using the Gutzeit method. Arsenic in a sample is converted to arsine gas, which reacts with mercuric chloride paper to produce a stain that is compared to a standard stain. The test uses an apparatus with two glass tubes, where the sample is placed below zinc and hydrochloric acid to produce arsine gas, which passes through mercuric chloride paper to produce a stain after 40 minutes. By comparing the intensity of this test stain to the standard stain produced in the same way from a solution of known arsenic concentration, the document determines if the sample passes or fails the limit test for arsenic.
Emetics are drugs that induce vomiting by causing the contents of the stomach to be expelled through the mouth. They are important for treating poisoning cases. Copper sulfate is a common emetic that is blue crystalline powder. It can be assayed through an oxidation-reduction titration with iodine and sodium thiosulfate. Sodium potassium tartrate, also known as Rochelle salt, is a crystalline powder that is soluble in water. It has uses as a laxative, diuretic, and food additive.
Limit test of sulphate is based on the reaction of soluble sulphate with barium chloride in presence of dilute hydrochloric acid to form barium sulphate which appears as solid particles (turbidity) in the solution.
This document describes the limit test for sulfate. The test is based on the reaction between barium chloride and soluble sulfates in the presence of hydrochloric acid. This results in the precipitation of barium sulfate. The turbidity produced by the test solution is compared to that of a standard sulfate solution. If the turbidity of the test solution is less than the standard, then the sample passes the limit test for sulfate.
This document provides information about gastrointestinal agents (GI agents), which are drugs used to treat GI disorders. It discusses the classifications of GI agents including acidifying agents, antacids, protectives, adsorbents, and cathartics. It then describes common antacids including aluminum hydroxide gel, calcium carbonate, and magnesium salts. The ideal characteristics of antacids are outlined. Common calcium-containing and magnesium-containing antacids are also discussed in more detail.
Unit 1 PHARMACEUTICAL INORGANIC CHEMISTRYSayali Powar
The document discusses various limit tests performed as per the Indian Pharmacopoeia to determine the presence of impurities below specified limits. It describes the principles, procedures and observations for limit tests of chloride, sulphate, iron, arsenic, heavy metals and lead. Limit tests involve comparing the color or turbidity developed in a test sample to a standard under defined reaction conditions. They provide a semi-quantitative analysis to check if impurity levels pass specified limits in the pharmacopoeia.
This document discusses monophasic liquid dosage forms, which contain components dissolved in a single phase. It provides examples of internal monophasic liquids like syrups and elixirs, and external liquids like gargles and enemas. The advantages of liquids include ease of administration, rapid drug absorption, and uniform dosing. Disadvantages include bulkiness, potential for microbial growth, and reduced drug stability compared to solids. A variety of oral, ocular, nasal and rectal liquids are also described.
This document provides information on various pharmaceutical compounds including expectorants, potassium iodide, copper sulfate, iron sulfate, zinc sulfate, and methods for their analysis. It discusses the definition, chemical and physical properties, preparation, uses and assays of these compounds by redox titration, gravimetric analysis, and complexometric titration. The document also covers emetics, astringents, antidotes and poisons including sodium nitrite, sodium thiosulfate and activated charcoal.
This document describes the limit test for lead using diphenylthiocarbazone (dithizone) which forms a violet colored lead-dithizonate complex in an alkaline medium. The method separates any lead impurity in a substance by extracting an alkaline solution with dithizone chloroform solution. The intensity of the violet color complex is then compared to a standard lead solution to determine the amount of lead present.
The document discusses the limit test for chloride. It defines a limit test as a quantitative or semi-quantitative test to identify and control small amounts of impurities likely to be present in a substance. The limit test for chloride determines the allowable limit of chloride in a sample. It involves dissolving the sample and standard sodium chloride solution, adding nitric acid and silver nitrate, and observing any opalescence or turbidity after 3 minutes. The sample passes the limit test for chloride if the opalescence is less than or equal to the standard solution.
This document describes the Gutzeit test for detecting arsenic. The test works by first converting any arsenic in a sample into arsenious acid, then reducing it to arsine gas. Mercuric chloride paper placed in the apparatus will turn yellow if arsine gas is present, indicating the presence of arsenic in the original sample. The document provides details of the test apparatus, reagents used, procedure, and precautions to get accurate results and avoid contamination.
Limt test Pharmaceutical Inorganic chemistry UNIT-I (Part-III) Limit Test.
Limit tests:- Factors affecting limit tests:
Specificity of the tests
Sensitivity
Control of personal errors (Analyst errors)
Test in which there is no visible reaction
Comparison methods
Quantitative determination
Limit test for Chloride: Principle, Procedure, observation and result.
Limit test for Sulphate: Principle, Procedure, observation and result
Limit test for Iron: Principle, Procedure, observation and result.
Limit test for Heavy metal: Principle, Procedure, observation and result.
Limit test for Lead: Principle, Procedure, observation and result.
Limit test for Arsenic: Principle, Gutzet test Procedure, detail in Gutzet Apparatus. observation and result.
Modifies Limit test for Chloride: Principle, Procedure, observation and result.
Modified Limit test for sulphate: Principle, Procedure, observation and result.
Acids, Bases And Buffers Pharmaceutical Inorganic chemistry UNIT-II (Part-I)
Acids, Bases are defined by Four main theories,
1.Traditional theory / concept
2.Arrhenius theory
3.Bronsted and Lowry theory
4.Lewis theory
Importance of acids and bases in pharmacy
Buffers: Buffer action
Buffer capacity Buffers system
Types of Buffers : Generally buffers are of two types:
1. Acidic buffers
2. Basic buffers
There are some other buffer system:
3. Two salts acts as acid-base pair. Ex- Potassium hydrogen phosphate and potassium dihydrogen phosphate.
4. Amphoteric electrolyte. Ex- Solution of glycine.
5. Solution of strong acid and solution of strong base. Ex- Strong HCl with KCl Mechanism of Buffer action: Mechanism of Action of acidic buffers: Buffer equation-Henderson-Hasselbalch equation:
Standard Buffer Solutions Preparation of Buffer Solutions: Buffers in pharmaceutical systems or Application of buffer: Stability of buffers Buffered isotonic solution Types of Buffer Isotonic solution
1. Isotonic Solutions:
2. Hypertonic Solutions:
3. Hypotonic Solution:
Measurement of Tonicity: 1. Hemolytic method: 2. Cryoscopic method or depression of freezing point:
Methods of adjusting the tonicity:
Class I methods:
In this type, sodium chloride or other substances are added to the solution in sufficient quantity to make it isotonic. Then the preparation is brought to its final volume withan isotonic or a buffered isotonic diluting solution.
These methods are of two types:
Cryoscopic method
Sodium chloride equivalent method.
Class II methods:
In this type, water is added in sufficient quantity make the preparation isotonic. Then the preparation is brought to its volume with an isotonic or a buffered isotonic diluting solution.
These methods are of two types:
White-Vincent method
Sprowls method.
Gastrointestinal agents are drugs used to treat gastrointestinal disorders like achlorhydria, hyperacidity, constipation, and diarrhea. Acidifiers increase acid concentration in the GI tract and are used to treat achlorhydria. Dilute hydrochloric acid maintains or increases stomach acid levels and pH. Antacids neutralize excess stomach acid in hyperacidity. Common acidifiers and antacids include ammonium chloride, dilute hydrochloric acid, and sodium bicarbonate.
This document provides information on flavor enhancers and stabilizers used in foods. It discusses flavor, common flavor enhancers like monosodium glutamate, and techniques for analyzing flavors like gas chromatography. It also defines food stabilizers, provides examples like alginates and agar, describes general confirmatory tests, and discusses applications such as preventing emulsions from separating.
Major intra & extra cellular electrolytes ATTRIRAKESH1
This document discusses various electrolytes used in acid-base therapy and their properties and uses. It describes sodium acetate, potassium acetate, sodium bicarbonate, sodium citrate, potassium citrate, sodium lactate, ammonium chloride, and potassium bicarbonate. It also discusses oral rehydration solutions, their formulations and benefits. The World Health Organization recommends reduced osmolarity oral rehydration solutions containing sodium, potassium, citrate, magnesium, zinc, and glucose to effectively treat diarrhea and dehydration.
The document discusses the gastrointestinal tract and its components and functions. It then discusses various types of acidifying reagents or acidifiers that can increase acidity in the gastrointestinal tract, including gastric, urinary, and systemic acidifiers. It provides ammonium chloride as an example of an acidifier, discussing its preparation, properties, identification tests, purity tests, and uses to produce mild acidosis.
Gastrointestinal agents
Inorganic chemicals used to treat Castro intestinal tract by different class of agents
Acidifying Agents
ANTACID
PROTECTIVE AND ADSORBENTS
SALINE CATHARTICS
This document discusses gastrointestinal agents including acidifying agents, antacids, and cathartics. It provides details on various acidifying agents such as ammonium chloride, hydrochloric acid, and dilute hydrochloric acid. It also discusses antacids including sodium bicarbonate, aluminium hydroxide gel, and magnesium hydroxide mixture. Finally, it covers cathartics such as magnesium sulphate, sodium orthophosphate, and kaolin. The document provides information on the uses, properties, preparations and other details of these various gastrointestinal agents.
This document discusses various gastrointestinal agents including acidifying agents, antacids, cathartics, and anti-microbial agents. It provides details on ammonium chloride, hydrochloric acid, and dilute hydrochloric acid which are used as acidifying agents to treat conditions where there is insufficient stomach acid production such as achlorhydria. It also discusses the uses, properties, methods of analysis and other details of these three acidifying agents.
Unit-III Gastro-intestinal agent for B&D Pharmacy.pptx by Bulet Kumar GuptaChevallaMaheshwari
The document discusses various agents used to treat gastrointestinal conditions. It describes the anatomy and functions of the gastrointestinal tract. It then discusses different types of gastric antacids including their classification, mechanisms of action, and examples like aluminum hydroxide, magnesium hydroxide, and sodium bicarbonate. It also covers acidifiers, cathartics, and their uses to treat conditions like achlorhydria, constipation, and diarrhea.
Food additives are substances added to food to preserve or enhance qualities like flavour, taste, texture and appearance. They help maintain or improve the keeping quality of foods. Additives are classified based on their function and include colours, preservatives, acids, antioxidants, sweeteners, flavours, stabilizers and thickeners. Common preservatives added are benzoic acid, sulphuric acid, nitrates/nitrites and propionates. Tests are used to identify and quantify levels of additives in foods.
The document discusses gastrointestinal agents and provides information about antacids. It defines antacids as alkaline substances used to neutralize hydrochloric acid in the stomach and provides relief from pain caused by excess stomach acid. The summary discusses classification of antacids as systemic or non-systemic based on absorption and criteria for an ideal antacid preparation. It also mentions combination antacid preparations can help avoid side effects of individual compounds.
This document discusses various gastrointestinal agents used to treat gastrointestinal disorders, including acidifiers, antacids, adsorbents, and cathartics. It provides details on specific agents such as ammonium chloride, dilute hydrochloric acid, and aluminum hydroxide gel. It explains that antacids are weak bases that neutralize stomach acid and relieve pain by raising the gastric pH to between 4-7 without causing systemic alkalosis. The document also outlines the ideal characteristics of antacids and categorizes them as either systemic/absorbable or non-systemic.
This document discusses several types of gastrointestinal agents including acidifiers, antacids, cathartics, and antimicrobials. It provides details on specific agents such as ammonium chloride, dilute hydrochloric acid, aluminum hydroxide gel, milk of magnesia, sodium bicarbonate, and their uses, preparations, and assays. Antacids are discussed in terms of their ideal properties and combinations used. Acidifiers are described as agents that increase acidity in the gastrointestinal tract for various purposes.
Pharmaceutical Inorganic Chemistry -B Pharmacy First Year -First semester -PI...manjusha kareppa
This document provides an overview of gastrointestinal agents used to treat various gastrointestinal disorders. It discusses acidifiers that increase acid in the stomach and are used to treat achlorhydria. It also covers antacids that neutralize excess stomach acid and are used for hyperacidity/hyperchlorhydria. Finally, it discusses cathartics/laxatives that relieve constipation through increasing bowel movements. Specific agents covered include ammonium chloride, dilute hydrochloric acid, sodium bicarbonate, aluminum hydroxide gel, and magnesium hydroxide mixture.
This document discusses several inorganic acids and bases. It provides details on the preparation, properties, uses and titration methods for hydrochloric acid, sodium phosphate, calcium phosphate, ammonium chloride and other compounds. Key points include that inorganic acids produce or become acid in water, are used as systemic acidifiers, and their concentrations can be determined through acid-base titration using various pH indicators.
To Determine which Antacid could Neutralize the most Stomach AcidAnkur Chaturvedi
The document describes an experiment to determine which antacid could neutralize the most stomach acid. Materials used included various antacid samples, hydrochloric acid solution, and sodium carbonate solution. The antacids were tested by adding them to hydrochloric acid and titrating with sodium carbonate. The amount of sodium carbonate solution required indicated how much acid was neutralized. The results showed that Ocid was the most effective antacid, neutralizing the most stomach acid as it required the least amount of sodium carbonate solution at 7 mL.
This document discusses various antacids, including their compositions, mechanisms of action, preparations, and analysis methods. It covers common antacid combinations containing aluminum hydroxide gel, magnesium hydroxide, magnesium trisilicate, and sodium bicarbonate. Individual antacids like milk of magnesia and aluminum hydroxide gel are also described, outlining their chemical properties, uses as antacids, and methods for quantitative analysis. Preparation processes are provided for sodium bicarbonate and analysis methods involve titrimetric techniques.
This document discusses acidifying reagents, including dilute hydrochloric acid and ammonium chloride. It provides details on their preparation, properties, tests for identification and purity, assays, storage, and uses. Dilute hydrochloric acid is a clear, colorless liquid prepared by diluting concentrated hydrochloric acid with water. Ammonium chloride is a white, crystalline powder prepared by neutralizing ammonia with hydrochloric acid. Both are used as acidifiers in pharmaceutical preparations and to treat conditions like metabolic alkalosis.
This document discusses acidifying agents used to treat conditions caused by low stomach acid such as achlorhydria. It describes two main acidifying agents - ammonium chloride and hydrochloric acid. Ammonium chloride is used as a systemic acidifier, expectorant, and diuretic. It is prepared by neutralizing hydrochloric acid with ammonia. Hydrochloric acid is used as an acidifying agent, solvent, and catalyst. It is prepared by reacting sulfuric acid with sodium chloride. Both agents work to increase stomach acid levels and support digestion when acid production is impaired.
This document discusses various types of cathartics/laxatives including bulk forming, stimulant, stool softeners, and osmotic laxatives. It provides examples of specific cathartics that fall into each category such as magnesium sulfate, sodium orthophosphate, kaolin, and bentonite. Details are given on the properties, identification tests, uses and methods of preparation/assay for some of these cathartic agents. Constipation and the role of laxatives in treating it are also briefly covered.
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In Odoo, making a field required can be done through both Python code and XML views. When you set the required attribute to True in Python code, it makes the field required across all views where it's used. Conversely, when you set the required attribute in XML views, it makes the field required only in the context of that particular view.
How to Setup Warehouse & Location in Odoo 17 InventoryCeline George
In this slide, we'll explore how to set up warehouses and locations in Odoo 17 Inventory. This will help us manage our stock effectively, track inventory levels, and streamline warehouse operations.
Gender and Mental Health - Counselling and Family Therapy Applications and In...PsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
This document provides an overview of wound healing, its functions, stages, mechanisms, factors affecting it, and complications.
A wound is a break in the integrity of the skin or tissues, which may be associated with disruption of the structure and function.
Healing is the body’s response to injury in an attempt to restore normal structure and functions.
Healing can occur in two ways: Regeneration and Repair
There are 4 phases of wound healing: hemostasis, inflammation, proliferation, and remodeling. This document also describes the mechanism of wound healing. Factors that affect healing include infection, uncontrolled diabetes, poor nutrition, age, anemia, the presence of foreign bodies, etc.
Complications of wound healing like infection, hyperpigmentation of scar, contractures, and keloid formation.
This presentation was provided by Racquel Jemison, Ph.D., Christina MacLaughlin, Ph.D., and Paulomi Majumder. Ph.D., all of the American Chemical Society, for the second session of NISO's 2024 Training Series "DEIA in the Scholarly Landscape." Session Two: 'Expanding Pathways to Publishing Careers,' was held June 13, 2024.
Philippine Edukasyong Pantahanan at Pangkabuhayan (EPP) CurriculumMJDuyan
(𝐓𝐋𝐄 𝟏𝟎𝟎) (𝐋𝐞𝐬𝐬𝐨𝐧 𝟏)-𝐏𝐫𝐞𝐥𝐢𝐦𝐬
𝐃𝐢𝐬𝐜𝐮𝐬𝐬 𝐭𝐡𝐞 𝐄𝐏𝐏 𝐂𝐮𝐫𝐫𝐢𝐜𝐮𝐥𝐮𝐦 𝐢𝐧 𝐭𝐡𝐞 𝐏𝐡𝐢𝐥𝐢𝐩𝐩𝐢𝐧𝐞𝐬:
- Understand the goals and objectives of the Edukasyong Pantahanan at Pangkabuhayan (EPP) curriculum, recognizing its importance in fostering practical life skills and values among students. Students will also be able to identify the key components and subjects covered, such as agriculture, home economics, industrial arts, and information and communication technology.
𝐄𝐱𝐩𝐥𝐚𝐢𝐧 𝐭𝐡𝐞 𝐍𝐚𝐭𝐮𝐫𝐞 𝐚𝐧𝐝 𝐒𝐜𝐨𝐩𝐞 𝐨𝐟 𝐚𝐧 𝐄𝐧𝐭𝐫𝐞𝐩𝐫𝐞𝐧𝐞𝐮𝐫:
-Define entrepreneurship, distinguishing it from general business activities by emphasizing its focus on innovation, risk-taking, and value creation. Students will describe the characteristics and traits of successful entrepreneurs, including their roles and responsibilities, and discuss the broader economic and social impacts of entrepreneurial activities on both local and global scales.
3. • Acidifiers or Acidifying Reagents are the
drugs which are able to increase the acidity
temporarily in GIT.
• In another words Acidifiers are inorganic
chemicals that either produce or become
acid.
• These chemicals increase the level of gastric
acid in the stomach when ingested, thus
decreasing the stomach pH.
• Systemic acidifiers given via injection
reduces the alkali accumulation in the body
and useful in reducing metabolic alkalosis.
4. Types Of Acidifiers
Mainly there are three types of acidifiers:
1.Gastric Acidifiers
2.Urinary Acidifiers
3.Systemic Acidifiers
9. Preparation
• It is prepared by adding 274 g of concentrated HCl
slowly into 726 g of purified water.
• Pungent odour
• Colorless liquid
• Fuming
• It reacts with metals and release hydrogen gas.
10. Assay
• Acid base titration reaction.
• An accurate amount about 4 g of HCl dissolved in
40 ml of water and titrated against 1 N NaOH
using methyl orange as an indicator.
• Neutralization reaction takes place.
• Methyl orange is yellow in alkali medium and it
changes to red in acid medium.
15. Preparation
• Ammonium chloride is prepared by commercial
method.
• Neutralization of Ammonia with HCl yields
Ammonium Chloride.
• The purification is done by sublimation process.
16. Properties
• Appearance :White solid, hygroscopic
• Odor: Odourless
• Taste: Cooling saline
• Density: 1.5274 g/cm3
• Melting point: 338 degree C (decomposes, sublimes)
• Solubility: free soluble in water and glycerol,
Sparingly soluble in alcohol.
17. Assay
• Acid base titration reaction.
• Dissolve 1.000 g of Ammonium chloride in 20 ml of
water and add a mixture of 5 ml of formaldehyde
solution, with few drops of phenolphthalein solution.
After 1 min to 2 min, titrate slowly with 1M sodium
hydroxide.
• Neutralization reaction takes place.
• End point is the appearance of pale permanent pink
color.
19. Uses
Ammonium chloride is used as an expectorant in cough
medicine.
Ammonium salts are an irritant to the gastric mucosa and
may induce nausea and vomiting.
Ammonium chloride is used as a systemic acidifying agent
in treatment of severe metabolic alkalosis.
The main application of ammonium chloride is as a
nitrogen source in fertilizers.
Ammonium chloride is used as a flux in preparing metals
to be tin coated, galvanized or soldered.