enzymes are biological molecules.it is protein produces by living cells.which help a chemical changes to happen more quickly,without being changed itself.more knowledge about enzymes in therapy in this slide.
Antifungal drugs can be classified based on their structure, mechanism of action, or site of action. The major classes include azoles, polyene macrolides, and others. Azoles like fluconazole and itraconazole inhibit fungal ergosterol synthesis. Amphotericin B binds to ergosterol in fungal membranes. These drugs treat superficial and systemic fungal infections. Common side effects of antifungals include liver toxicity, nausea, and hypokalemia.
This document provides information about the drug Aladin, which contains fexofenadine hydrochloride as an active ingredient. Fexofenadine is a non-sedating antihistamine that works by antagonizing the H1 receptor. Aladin is indicated for seasonal allergic rhinitis and chronic idiopathic urticaria. It has fewer side effects than first generation antihistamines like drowsiness since it does not readily cross the blood-brain barrier. The document reviews the pharmacokinetics, dosage, adverse effects, drug interactions, and precautions of Aladin. It also presents the market size and competitors of Aladin formulations containing 120mg and 180mg of fexof
The skin is the largest organ of the body, with a total area of about 20 square feet. The skin protects us from microbes and the elements, helps regulate body temperature, and permits the sensations of touch, heat, and cold
This document discusses plant teratogens, which are substances found in plants that can cause abnormalities in developing fetuses when ingested by the mother. Some examples of plant constituents that are teratogenic include alkaloids, coumarins, lignans, and terpenoids. Specific plants and their teratogenic effects are outlined, such as indigofera spicata containing indospicine which can cause cleft palate and embryo lethality in rats. The document analyzes several other plants and their toxic phytochemicals that have teratogenic properties in livestock and laboratory animals.
Any chemical compounds that have potential of either killing or damaging unwanted plants or weeds for elimination such plant , that depend on biochemical difference in plants, that act selectively for some plants. In early old days (sulfuric acide , aresenic tetroxide and petroleum oil etc ) used but not selective activity.
Pulsatilla is a plant with the botanical name Pulsatilla Vulgaris that contains chemical constituents such as anemonin and pentadecane. It has various traditional medicinal uses such as being antimicrobial by increasing membrane permeability and inhibiting bacterial cell wall synthesis. Pulsatilla is used as an herbal infusion or tincture to treat infections, inflammation, and allergies but can cause irritation and should not be used during pregnancy or in excessive amounts.
Systemic fungal infections can be life-threatening, especially in immunocompromised patients. Anti-fungal drugs target the fungal cell membrane and include polyenes like amphotericin B, azoles, and antimetabolites like flucytosine. Amphotericin B has a broad spectrum of activity but significant toxicity, while azoles like itraconazole are better tolerated and used for both superficial and systemic fungal infections. These drugs differ in their mechanisms of action, pharmacokinetics, spectra of activity, and adverse effect profiles.
This document provides an overview of common drug and plant poisonings. It discusses acetaminophen, iron, and anticonvulsant poisonings in detail, outlining their pathophysiology, clinical features, investigations, and management including use of antidotes like N-acetylcysteine and desferoxamine. It also briefly mentions other common drug poisonings and plant toxins like oleander, datura, and jatropha. The goal is to educate about identifying and treating accidental or intentional overdoses of commonly ingested substances.
Antifungal drugs can be classified based on their structure, mechanism of action, or site of action. The major classes include azoles, polyene macrolides, and others. Azoles like fluconazole and itraconazole inhibit fungal ergosterol synthesis. Amphotericin B binds to ergosterol in fungal membranes. These drugs treat superficial and systemic fungal infections. Common side effects of antifungals include liver toxicity, nausea, and hypokalemia.
This document provides information about the drug Aladin, which contains fexofenadine hydrochloride as an active ingredient. Fexofenadine is a non-sedating antihistamine that works by antagonizing the H1 receptor. Aladin is indicated for seasonal allergic rhinitis and chronic idiopathic urticaria. It has fewer side effects than first generation antihistamines like drowsiness since it does not readily cross the blood-brain barrier. The document reviews the pharmacokinetics, dosage, adverse effects, drug interactions, and precautions of Aladin. It also presents the market size and competitors of Aladin formulations containing 120mg and 180mg of fexof
The skin is the largest organ of the body, with a total area of about 20 square feet. The skin protects us from microbes and the elements, helps regulate body temperature, and permits the sensations of touch, heat, and cold
This document discusses plant teratogens, which are substances found in plants that can cause abnormalities in developing fetuses when ingested by the mother. Some examples of plant constituents that are teratogenic include alkaloids, coumarins, lignans, and terpenoids. Specific plants and their teratogenic effects are outlined, such as indigofera spicata containing indospicine which can cause cleft palate and embryo lethality in rats. The document analyzes several other plants and their toxic phytochemicals that have teratogenic properties in livestock and laboratory animals.
Any chemical compounds that have potential of either killing or damaging unwanted plants or weeds for elimination such plant , that depend on biochemical difference in plants, that act selectively for some plants. In early old days (sulfuric acide , aresenic tetroxide and petroleum oil etc ) used but not selective activity.
Pulsatilla is a plant with the botanical name Pulsatilla Vulgaris that contains chemical constituents such as anemonin and pentadecane. It has various traditional medicinal uses such as being antimicrobial by increasing membrane permeability and inhibiting bacterial cell wall synthesis. Pulsatilla is used as an herbal infusion or tincture to treat infections, inflammation, and allergies but can cause irritation and should not be used during pregnancy or in excessive amounts.
Systemic fungal infections can be life-threatening, especially in immunocompromised patients. Anti-fungal drugs target the fungal cell membrane and include polyenes like amphotericin B, azoles, and antimetabolites like flucytosine. Amphotericin B has a broad spectrum of activity but significant toxicity, while azoles like itraconazole are better tolerated and used for both superficial and systemic fungal infections. These drugs differ in their mechanisms of action, pharmacokinetics, spectra of activity, and adverse effect profiles.
This document provides an overview of common drug and plant poisonings. It discusses acetaminophen, iron, and anticonvulsant poisonings in detail, outlining their pathophysiology, clinical features, investigations, and management including use of antidotes like N-acetylcysteine and desferoxamine. It also briefly mentions other common drug poisonings and plant toxins like oleander, datura, and jatropha. The goal is to educate about identifying and treating accidental or intentional overdoses of commonly ingested substances.
This document provides an overview of various classes of antibiotics, including their mechanisms of action, therapeutic uses, adverse effects, and nursing considerations. It discusses penicillins, cephalosporins, aminoglycosides, macrolides, lincosamides, and tetracyclines. For each class, it describes how they work, common drugs in the class, indications, contraindications, side effects, interactions, and the nursing process for safe administration.
I am Dr. Anil. this is my Lecture delivered to 3rd year MBBS for the subject of Pharmacology. These slides cover basics of Antifungal drugs mainly its pharmacology.
Fungal infections of eye cause one of the most dangerious infections. Accurate diagnosis and proper institution of anti-fungal therapy is essential. Here we discuss the various anti-fungal agents available to be used in ophthalmology.
This presentation gives detailed information about antihistamine agents ,immunopharmacology .They also give details about their classification and mechanism of action.
The presentation gives an in-depth review of the Anti-fungal drugs used to treat various acute and chronic fungal infections along with their uses and MOA.
Ketoconazole was the first orally effective broad-spectrum antifungal but has been replaced by newer azoles. It acts by inhibiting ergosterol biosynthesis. Common side effects include nausea and loss of hair/libido. It interacts with many drugs by inhibiting CYP3A4. Fluconazole has a wider spectrum than ketoconazole and good CSF penetration. Itraconazole and voriconazole are broad-spectrum second-generation triazoles. Terbinafine inhibits squalene epoxidase and accumulates in the skin. Topical agents like clotrimazole, miconazole and econazole are used to treat superficial fung
The Aloe vera plant has been known and used for centuries for its, beauty health, medicinal, skin care and other various properties. It has a vast traditional role in the indigenous system of medicine like Ayurveda, Siddha, Unani and homeopathy. Aloe barbadensis miller is the botanical name of Aloe vera. Aloe vera, commonly known as Barbados, considered as a magical plant. The arborescent, perennial, xerophytic, succulent plant mainly grows in subtropical areas. Aloe vera is considered to be a storehouse of phytochemicals. The plant leaves contain lots of chemical constituents such as anthraquinones, carbohydrates, vitamins, steroids, mineral, other inorganic and organics substances. Bioactive compounds from Aloe vera are very effective in various treatments, such as burns, allergic reactions, rheumatoid arthritis, rheumatic fever, acid indigestion, ulcers, skin diseases, diabetes, dysentery, diarrhoea, piles and inflammatory conditions of the digestive system and other internal organs, including the stomach, small intestine, liver, kidney, and pancreas. The active ingredients from Aloe vera have been shown to have analgesic, anti-inflammatory, antioxidant and anticancer agent. The plant also contains a lot of enzymes that regulate different types of reaction in our body. The cosmetics value of the plant is high from other plants.
This document discusses anti-protozoal drugs used to treat various protozoal infections. It provides details on the treatment of amebiasis, giardiasis, trichomoniasis, toxoplasmosis, cryptosporidiosis, trypanosomiasis, and leishmaniasis. Key drugs discussed include metronidazole, tinidazole, paromomycin, chloroquine, and hydroxychloroquine. It also covers the biology, stages of infection, and chemotherapy of malaria caused by various Plasmodium species.
This document provides an overview of anti-fungal drugs. It defines anti-fungal medications as fungicides or fungistatics used to treat mycosis (fungal infections). It classifies anti-fungal drugs into several categories including polyenes, echinocandins, azoles, allylamines, and others. For each category, it describes the mechanisms of action, examples of drugs, pharmacokinetics, adverse effects, and common uses. Key drugs discussed include amphotericin B, griseofulvin, flucytosine, ketoconazole, fluconazole, and terbinafine. The document explains that anti-fungal drugs work by
Brief information about Tuberculosis, drugs used for its treatment including recent advances and drug regimen for patients of different categories of TB suggested by WHO (DOTS therapy) including national and international programes for preventing TB.
Griseofulvin inhibits fungus cells from infecting new hair, skin or nails, which ais to get rid of the fungal infection. This process is slow, so it may take multiple weeks for a skin or hair infection to clear up, and up to a year for a nail infection to clear up. Griseofulvin is usually given once each day. This can be in the morning or during evening. Provide the medicine at about the same time each day so that this becomes part of your child’s daily routine, which will help you to remember (Cole et al., 1997).
ACTION Microbiology – Griseofulvin is fungistatic with in vitro activity against differing species of Microsporum, Epidermophyton and Trichophyton. It has completely no effect on bacteria or other genera of fungi (Cole et al., 1997). Active Ingredients: griseofulvin ultra microsize …. 250 mg Inactive Ingredients are: colloidal silicon dioxide, magnesium stearate, methylcellulose, methyl paraben, polyethylene glycol 400 and 8000, povidone, sodium lauryl sulfate, and titanium dioxide.
UNIT V - Study of biological source, chemical nature and uses of drugs of natural origin containing the following drugs
Hallucinogens, Teratogens, Natural allergens
This document summarizes various antifungal drugs, including their mechanisms of action, classifications, and uses. It discusses polyene antibiotics like amphotericin B, the echinocandin caspofungin, the heterocyclic benzofuran griseofulvin, azole antifungals like ketoconazole and fluconazole, and the allylamine terbinafine. It also covers their mechanisms of inhibiting fungal cell membranes or biosynthesis, pharmacokinetics, therapeutic uses for systemic and superficial fungal infections, and potential adverse effects.
This document discusses herbal dosage forms and medicinal teas. It describes various oral dosage forms including liquids, tablets, capsules, and powders. It also discusses inhalation forms, topical forms, and herbal baths. It provides examples of medicinal tea combinations and preparation instructions. It notes advantages and disadvantages of different herbal dosage forms. The document also covers side effects of herbal medicines, prerequisites for production and marketing of herbal remedies, and how to interpret product labels.
This document discusses the herbal medicine lavender. It notes that lavender has constituents like linalool and linalyl acetate that have sedative, anxiolytic, anti-depressive, analgesic, and anti-inflammatory effects. Some of lavender's actions include being sedative, anxiolytic, pain relieving, antiseptic, and wound healing. The document outlines lavender's uses for conditions like insomnia, anxiety, pain, infections, and more. It also discusses lavender's mechanisms of action, dosing methods like oral capsules and diffusers, and Egyptian pharmaceutical products containing lavender.
This document discusses various classes of antifungal agents including azoles. It describes the mechanism of action of azoles, which inhibit ergosterol biosynthesis by targeting cytochrome P450 14α-demethylase. Several individual azoles are mentioned such as clotrimazole, econazole, butoconazole, oxiconazole, tioconazole, miconazole, ketoconazole, terconazole, itraconazole and fluconazole. Their structures, uses in treating fungal infections and side effects are summarized.
This document discusses several plants that can cause food poisoning, including cyanogenic plants containing glycosides that release cyanide. Cassava is highlighted, which if insufficiently processed before eating can liberate cyanide and cause tropical ataxic neuropathy. Sweet pea and prickly poppy are also mentioned. The document then focuses on bitter almond containing amygdalin, which can be toxic in large quantities. Finally, it discusses chickling pea which can cause lathyrism if consumed chronically, and yellow poppy which contains toxic compounds and has been adulterated in oils.
Antifungal drugs, also known as antimycotics, are used to treat and prevent fungal infections like athlete's foot, ringworm, thrush, and more serious systemic infections. There are different types of antifungal agents that work by various mechanisms. Polyene antibiotics like amphotericin B and nystatin bind to ergosterol in the fungal cell membrane, increasing permeability and loss of intracellular contents. Azoles inhibit ergosterol synthesis and have broad antifungal activity. Other classes of antifungals include allylamines, pyrimidines, thiocarbamates, and nonpolyene antibiotics like griseofulvin that inhibit fungal growth.
Bactrim D.S. (Sulfamethoxazole and Trimethoprim Tablets)The Swiss Pharmacy
Bactrim D.S. (Sulfamethoxazole and Trimethoprim Tablets) is indicated in adults and pediatric patients two months of age and older for treatment of infections caused by designated, susceptible bacteria.
The indications include urinary tract infections, acute otitis media in pediatric patients, acute exacerbations of chronic bronchitis, treatment of travelers’ diarrhea, treatment of enteritis, treatment of documented Pneumocystis carinii pneumonia and prophylaxis against Pneumocystis carinii pneumonia in individuals who are immunosuppressed.
Enzymes have many uses in clinical diagnosis and treatment, research, and industry. Clinically, enzymes are used to regulate digestion, diffuse drugs, treat wounds, dissolve blood clots, diagnose hypertension, and treat cancer. Enzymes are also used in recombinant DNA technology and genetic manipulation. Industrially, enzymes have wide applications in the dairy, detergent, starch, brewing, and pharmaceutical industries.
Enzymes have many uses in clinical diagnosis and treatment, research, and industry. Clinically, enzymes are used to regulate digestion, diffuse drugs, treat wounds, dissolve blood clots, diagnose hypertension, and treat cancer. Enzymes are also used in recombinant DNA technology and genetic manipulation. Industrially, enzymes have wide applications in the dairy, detergent, starch, brewing, and pharmaceutical industries.
This document provides an overview of various classes of antibiotics, including their mechanisms of action, therapeutic uses, adverse effects, and nursing considerations. It discusses penicillins, cephalosporins, aminoglycosides, macrolides, lincosamides, and tetracyclines. For each class, it describes how they work, common drugs in the class, indications, contraindications, side effects, interactions, and the nursing process for safe administration.
I am Dr. Anil. this is my Lecture delivered to 3rd year MBBS for the subject of Pharmacology. These slides cover basics of Antifungal drugs mainly its pharmacology.
Fungal infections of eye cause one of the most dangerious infections. Accurate diagnosis and proper institution of anti-fungal therapy is essential. Here we discuss the various anti-fungal agents available to be used in ophthalmology.
This presentation gives detailed information about antihistamine agents ,immunopharmacology .They also give details about their classification and mechanism of action.
The presentation gives an in-depth review of the Anti-fungal drugs used to treat various acute and chronic fungal infections along with their uses and MOA.
Ketoconazole was the first orally effective broad-spectrum antifungal but has been replaced by newer azoles. It acts by inhibiting ergosterol biosynthesis. Common side effects include nausea and loss of hair/libido. It interacts with many drugs by inhibiting CYP3A4. Fluconazole has a wider spectrum than ketoconazole and good CSF penetration. Itraconazole and voriconazole are broad-spectrum second-generation triazoles. Terbinafine inhibits squalene epoxidase and accumulates in the skin. Topical agents like clotrimazole, miconazole and econazole are used to treat superficial fung
The Aloe vera plant has been known and used for centuries for its, beauty health, medicinal, skin care and other various properties. It has a vast traditional role in the indigenous system of medicine like Ayurveda, Siddha, Unani and homeopathy. Aloe barbadensis miller is the botanical name of Aloe vera. Aloe vera, commonly known as Barbados, considered as a magical plant. The arborescent, perennial, xerophytic, succulent plant mainly grows in subtropical areas. Aloe vera is considered to be a storehouse of phytochemicals. The plant leaves contain lots of chemical constituents such as anthraquinones, carbohydrates, vitamins, steroids, mineral, other inorganic and organics substances. Bioactive compounds from Aloe vera are very effective in various treatments, such as burns, allergic reactions, rheumatoid arthritis, rheumatic fever, acid indigestion, ulcers, skin diseases, diabetes, dysentery, diarrhoea, piles and inflammatory conditions of the digestive system and other internal organs, including the stomach, small intestine, liver, kidney, and pancreas. The active ingredients from Aloe vera have been shown to have analgesic, anti-inflammatory, antioxidant and anticancer agent. The plant also contains a lot of enzymes that regulate different types of reaction in our body. The cosmetics value of the plant is high from other plants.
This document discusses anti-protozoal drugs used to treat various protozoal infections. It provides details on the treatment of amebiasis, giardiasis, trichomoniasis, toxoplasmosis, cryptosporidiosis, trypanosomiasis, and leishmaniasis. Key drugs discussed include metronidazole, tinidazole, paromomycin, chloroquine, and hydroxychloroquine. It also covers the biology, stages of infection, and chemotherapy of malaria caused by various Plasmodium species.
This document provides an overview of anti-fungal drugs. It defines anti-fungal medications as fungicides or fungistatics used to treat mycosis (fungal infections). It classifies anti-fungal drugs into several categories including polyenes, echinocandins, azoles, allylamines, and others. For each category, it describes the mechanisms of action, examples of drugs, pharmacokinetics, adverse effects, and common uses. Key drugs discussed include amphotericin B, griseofulvin, flucytosine, ketoconazole, fluconazole, and terbinafine. The document explains that anti-fungal drugs work by
Brief information about Tuberculosis, drugs used for its treatment including recent advances and drug regimen for patients of different categories of TB suggested by WHO (DOTS therapy) including national and international programes for preventing TB.
Griseofulvin inhibits fungus cells from infecting new hair, skin or nails, which ais to get rid of the fungal infection. This process is slow, so it may take multiple weeks for a skin or hair infection to clear up, and up to a year for a nail infection to clear up. Griseofulvin is usually given once each day. This can be in the morning or during evening. Provide the medicine at about the same time each day so that this becomes part of your child’s daily routine, which will help you to remember (Cole et al., 1997).
ACTION Microbiology – Griseofulvin is fungistatic with in vitro activity against differing species of Microsporum, Epidermophyton and Trichophyton. It has completely no effect on bacteria or other genera of fungi (Cole et al., 1997). Active Ingredients: griseofulvin ultra microsize …. 250 mg Inactive Ingredients are: colloidal silicon dioxide, magnesium stearate, methylcellulose, methyl paraben, polyethylene glycol 400 and 8000, povidone, sodium lauryl sulfate, and titanium dioxide.
UNIT V - Study of biological source, chemical nature and uses of drugs of natural origin containing the following drugs
Hallucinogens, Teratogens, Natural allergens
This document summarizes various antifungal drugs, including their mechanisms of action, classifications, and uses. It discusses polyene antibiotics like amphotericin B, the echinocandin caspofungin, the heterocyclic benzofuran griseofulvin, azole antifungals like ketoconazole and fluconazole, and the allylamine terbinafine. It also covers their mechanisms of inhibiting fungal cell membranes or biosynthesis, pharmacokinetics, therapeutic uses for systemic and superficial fungal infections, and potential adverse effects.
This document discusses herbal dosage forms and medicinal teas. It describes various oral dosage forms including liquids, tablets, capsules, and powders. It also discusses inhalation forms, topical forms, and herbal baths. It provides examples of medicinal tea combinations and preparation instructions. It notes advantages and disadvantages of different herbal dosage forms. The document also covers side effects of herbal medicines, prerequisites for production and marketing of herbal remedies, and how to interpret product labels.
This document discusses the herbal medicine lavender. It notes that lavender has constituents like linalool and linalyl acetate that have sedative, anxiolytic, anti-depressive, analgesic, and anti-inflammatory effects. Some of lavender's actions include being sedative, anxiolytic, pain relieving, antiseptic, and wound healing. The document outlines lavender's uses for conditions like insomnia, anxiety, pain, infections, and more. It also discusses lavender's mechanisms of action, dosing methods like oral capsules and diffusers, and Egyptian pharmaceutical products containing lavender.
This document discusses various classes of antifungal agents including azoles. It describes the mechanism of action of azoles, which inhibit ergosterol biosynthesis by targeting cytochrome P450 14α-demethylase. Several individual azoles are mentioned such as clotrimazole, econazole, butoconazole, oxiconazole, tioconazole, miconazole, ketoconazole, terconazole, itraconazole and fluconazole. Their structures, uses in treating fungal infections and side effects are summarized.
This document discusses several plants that can cause food poisoning, including cyanogenic plants containing glycosides that release cyanide. Cassava is highlighted, which if insufficiently processed before eating can liberate cyanide and cause tropical ataxic neuropathy. Sweet pea and prickly poppy are also mentioned. The document then focuses on bitter almond containing amygdalin, which can be toxic in large quantities. Finally, it discusses chickling pea which can cause lathyrism if consumed chronically, and yellow poppy which contains toxic compounds and has been adulterated in oils.
Antifungal drugs, also known as antimycotics, are used to treat and prevent fungal infections like athlete's foot, ringworm, thrush, and more serious systemic infections. There are different types of antifungal agents that work by various mechanisms. Polyene antibiotics like amphotericin B and nystatin bind to ergosterol in the fungal cell membrane, increasing permeability and loss of intracellular contents. Azoles inhibit ergosterol synthesis and have broad antifungal activity. Other classes of antifungals include allylamines, pyrimidines, thiocarbamates, and nonpolyene antibiotics like griseofulvin that inhibit fungal growth.
Bactrim D.S. (Sulfamethoxazole and Trimethoprim Tablets)The Swiss Pharmacy
Bactrim D.S. (Sulfamethoxazole and Trimethoprim Tablets) is indicated in adults and pediatric patients two months of age and older for treatment of infections caused by designated, susceptible bacteria.
The indications include urinary tract infections, acute otitis media in pediatric patients, acute exacerbations of chronic bronchitis, treatment of travelers’ diarrhea, treatment of enteritis, treatment of documented Pneumocystis carinii pneumonia and prophylaxis against Pneumocystis carinii pneumonia in individuals who are immunosuppressed.
Enzymes have many uses in clinical diagnosis and treatment, research, and industry. Clinically, enzymes are used to regulate digestion, diffuse drugs, treat wounds, dissolve blood clots, diagnose hypertension, and treat cancer. Enzymes are also used in recombinant DNA technology and genetic manipulation. Industrially, enzymes have wide applications in the dairy, detergent, starch, brewing, and pharmaceutical industries.
Enzymes have many uses in clinical diagnosis and treatment, research, and industry. Clinically, enzymes are used to regulate digestion, diffuse drugs, treat wounds, dissolve blood clots, diagnose hypertension, and treat cancer. Enzymes are also used in recombinant DNA technology and genetic manipulation. Industrially, enzymes have wide applications in the dairy, detergent, starch, brewing, and pharmaceutical industries.
Enzymes have many uses in clinical diagnosis and treatment, analysis, manipulation, and industry. Some key uses include:
1. Clinical uses such as regulating digestion, aiding drug diffusion during infections, wound healing, dissolving blood clots, diagnosing hypertension, cancer therapy, and removing parasites or digestive issues.
2. Analytical uses like determining levels of substances in samples.
3. Manipulative uses in biotechnology and genetic engineering with enzymes like DNA polymerase and restriction enzymes.
4. Wide industrial applications in dairy, detergents, starch, brewing, distilling, and pharmaceuticals using enzymes such as rennin, amylase, protease, and cellulase.
This document provides an overview of key concepts in pharmacology. It defines pharmacology and its branches, which include pharmacokinetics and pharmacodynamics. It discusses sources of drugs, routes of drug administration like oral, parenteral, and topical, and factors that determine administration route. It also covers ligands and their types like agonists and antagonists. In summary, the document outlines the fundamental principles of pharmacology including how drugs are developed, distributed in the body, and exert their effects.
introduction to General pharmacology by : Dr Debasish PradhanDr Debasish Pradhan
Introduction to general Pharmacology, Routes of drug administration with their advantages and Disadvantages, Factors affecting routes of drug administration.
1) Histamine plays an important role in human physiology through regulating various body systems like the cardiovascular, respiratory, and immune systems.
2) Histamine is synthesized from the amino acid L-histidine and stored in mast cells and basophils before being released, especially during allergic reactions.
3) There are four types of histamine receptors (H1-H4) located in different tissues that mediate various physiological actions when activated by histamine, such as vasodilation, gastric acid secretion, and inflammation. Antihistamines work by blocking H1 receptors.
This document provides an overview of pharmacology and mechanisms of drug action. It defines pharmacology as the study of drug interaction with living organisms. Key points include: drugs can come from natural, animal, mineral or laboratory sources; various routes of administration depend on factors like physical properties and site of action; pharmacodynamics examines how drugs affect the body by interacting with receptors, ion channels, enzymes or through chemical reactions; and pharmacogenetics considers genetic differences in metabolic pathways that influence drug responses.
- Drugs are classified based on their structure, mechanism of action, and pharmacological effects. Drugs interact with biomolecules like lipids and proteins, called drug targets.
- Enzymes are proteins that catalyze biochemical reactions. Drugs can inhibit enzymes by competing for active sites or binding to allosteric sites.
- Receptors are proteins involved in cell communication. Chemical messengers bind to receptor sites to transmit messages without entering cells.
- Different classes of drugs are used to treat various conditions like pain, infection, inflammation, and more. Drugs are classified based on their therapeutic use and chemical structure.
This document provides an overview of plant metabolites. It defines metabolites as intermediate products produced during plant metabolism. Primary metabolites such as carbohydrates, proteins, and lipids are essential for plant growth and development, while secondary metabolites like alkaloids and flavonoids are not essential for growth but play important roles in plant defense. The document then discusses several primary and secondary metabolites in more detail, including casein, papain, bromelain, serratiopeptidase, and urokinase enzymes.
This document provides an overview of plant metabolites. It defines metabolites as intermediate products produced during plant metabolism. Primary metabolites such as carbohydrates, proteins, and lipids are essential for plant growth and development, while secondary metabolites like alkaloids and flavonoids are not essential for growth but play important roles in plant defense. The document then discusses several primary and secondary metabolites in more detail, including casein, papain, bromelain, serratiopeptidase, and urokinase enzymes.
Group 4 presentation (drug used to treat and prevent).pptxSunitaArslan
The document discusses drugs used to treat and prevent infections. It covers several categories of antiparasitic drugs including antinematodal, anticestodal, antilungworm, antitrematodal, and antiprotozoal. Specific drugs discussed include piperazine, amodiaquine, furazolidone, and mebendazole. Their mechanisms of action, pharmacokinetics, and common side effects are summarized. The document also discusses pyrimethamine, its uses for malaria treatment, mechanism of action by inhibiting dihydrofolate reductase, and potential side effects of antiparasitic agents.
This document discusses antiprotozoal agents used to treat various protozoal diseases. It begins by introducing common protozoal diseases like malaria, amoebiasis, and leishmaniasis that infect humans and animals in tropical countries. The document then classifies antiprotozoal drugs and describes several types and their mechanisms of action. Key drugs discussed include emetine, metronidazole, ornidazole, tinidazole, clioquinol, and iodoquinol. The mechanisms of these drugs involve inhibiting protein synthesis, binding to DNA or metal ions, or undergoing microbial reduction to produce reactive intermediates.
This document discusses various classes of antiviral drugs, including their mechanisms of action, pharmacokinetics, therapeutic uses, and adverse effects. It describes DNA and RNA polymerase inhibitors such as acyclovir, ganciclovir, and ribavirin which work by inhibiting viral replication. It also covers adamantane derivatives amantadine and rimantidine which inhibit influenza virus uncoating, as well as neuraminidase inhibitors oseltamivir and zanamivir which prevent viral spread. Immunomodulators like interferons are also summarized, which activate the immune system against viruses.
Autacoids are naturally occurring substances that act as local hormones near their site of synthesis. The main classes of autacoids are amines, peptides, and lipids. Prostaglandins, histamine, bradykinin, and serotonin are some of the most important autacoids. They have various roles like mediating inflammation, vasodilation, gastric acid secretion, and neurotransmission. Their effects are mediated via receptors and they have therapeutic uses for conditions like inflammation, ulcers, and allergies.
This document provides information on antibiotics and analgesics used for periodontal diseases. It defines antibiotics as agents that destroy or inhibit the growth of microorganisms. Various antibiotics discussed that are used for periodontal diseases include tetracyclines, metronidazole, penicillins, cephalosporins, clindamycin, ciprofloxacin, and macrolides. It also discusses local delivery methods for antibiotics. Analgesics are defined as drugs that selectively relieve pain. The classes discussed include non-opioid types like aspirin, acetaminophen, ibuprofen and opioid types like morphine, codeine, synthetic opioids, and their mechanisms and side effects.
A prodrug is an inactive or less active pharmacological substance that is converted into an active drug through normal metabolic processes. Prodrugs are designed to improve properties like absorption, distribution, metabolism, and excretion of the intended drug. Prodrugs can be classified as Type I, which are activated intracellularly, or Type II, which are activated extracellularly such as in digestive fluids or circulation. Common examples of prodrugs include enalapril, which is converted to enalaprilate; oseltamivir (Tamiflu), which is converted to oseltamivir carboxylate; and famciclovir, which is converted to penciclovir.
Antiparasitic drugs are a group of medications used in the management and treatment of infections by parasites, including protozoa, helminths, and ectoparasites.
White spots through-out the body-ICH DISEASE
Enzymes are organic catalysts produced by living organisms that perform complex chemical reactions involved in life processes. They are proteins that act as catalysts, remaining unchanged at the end of the reactions. Enzymes function best within a certain temperature and pH range, and their activity can be affected by other substances. They are classified according to the reactions they catalyze and have molecular weights ranging from 13,000 to 840,000. Many enzymes require non-protein cofactors called coenzymes to function and some vitamins serve as coenzymes. Enzymes are used therapeutically as digestants and to dissolve blood clots, and industrially in fermentation and cheese production.
Enzymes are organic catalysts produced by living organisms that perform complex chemical reactions involved in life processes. They are proteins that act as catalysts, remaining unchanged at the end of the reactions. Enzymes function best within a certain temperature and pH range, and their activity can be affected by other substances. They are classified according to the reactions they catalyze and have molecular weights ranging from 13,000 to 840,000. Many enzymes require non-protein cofactors called coenzymes to function and some vitamins serve as coenzymes. Enzymes are used therapeutically as digestants and to dissolve blood clots, and industrially in fermentation and cheese production.
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
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These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
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Does Over-Masturbation Contribute to Chronic Prostatitis.pptxwalterHu5
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2. Introduction
Enzymes are proteins produced by the living
cells.
They catalyze several biochemical reaction.some
substances act with specific enzymes and are
called coenzymes.
4. Mammalian enzymes
1. TRYPSIN
It is obtained from pancreas .it is a proteolytic enzymes which
directly hydrolase natural proteins .it digests dead tissues ,
bacteria and debris .
Trypsin may be used topically ,sublingually or intramuscularly.
•Adverse effects :-allergic reaction can occur.
5. Uses
Trypsin solution used topically for debridement
of necrotic tissues.
Used topically for liquefaction of coagulated
blood and exudates.
Trypsin containing gelatin capsules are inserted
into sinuses and fistulae that can not be
adequately irrigated.
It can also be used for irrigation of nasal cavities.
6. 2. Hyaluronidase
Hyaluronidase is obtained from mammalian testes.
It increase the tissue permeability and enhances the
rate of absorption of subcutaneously, administered fluids
and drugs.
Hyaluronidase can produce allergic reaction .
It should not be injected around an infected an infected
site to avoid the spread of infection.
It is available as dry powder.
7. uses
To hasten resorption of fluids and blood in
hematoma.
Along with local anesthetics – to increase the
effectiveness of local anesthesia.
Radiography – hyaluronidase enhances
absorption of the radiopaque substances.
8. Bacterial enzymes
1. streptodornase – it is liquify viscous and purulent material.
• they have no effect on living cells.they are active in presence
of magnesium ions.
• Adverse effects- allergic reaction may occur.it is contraindicated
in the presence of bleeding .They should not be used around a
local infected area.
9. Uses
•They are used topically to liquify clotted blood, pus and
to clear the debris in chronic ulcers and other wounds.
Plant enzymes
Papain is obtained from the unripe fruit of carica
papaya.it is a proteolytic enzymes used topically for
debriding wound surfaces.
10. This Photo by Unknown Author is licensed under CC BY