This document discusses tetracycline antibiotics. It covers their classification, mechanism of action, spectrum of activity, mechanisms of resistance, pharmacokinetics, administration, adverse drug reactions, uses, drug interactions, and storage. Tetracyclines are broad-spectrum antibiotics derived from Streptomyces coelicolor bacteria. They work by inhibiting bacterial protein synthesis and include short, intermediate, and long-acting drugs like tetracycline, doxycycline, and minocycline. Resistance can develop through enzymatic inactivation, efflux pumps, or ribosomal protection mechanisms.
Tetracyclines are a class of antibiotics derived from Streptomyces coelicolor bacteria. They were discovered in 1940 and include tetracycline, oxytetracycline, chlortetracycline, doxycycline, and minocycline. Tetracyclines are broad spectrum antibiotics that work by inhibiting bacterial protein synthesis and preventing aminoacyl tRNA from binding to the bacterial ribosome. They are used to treat various infections like acne, atypical pneumonia, cholera, and relapsing fever. Common adverse effects include tooth discoloration, nausea, and photosensitivity.
This document provides information about the antibiotic tetracycline. It discusses tetracycline's structure, classification, mechanisms of action and resistance, pharmacokinetics, administration, uses, adverse effects, drug interactions, and storage requirements. Tetracycline is a broad-spectrum antibiotic derived from bacteria that inhibits bacterial protein synthesis. It is classified based on duration of action and absorbed variably depending on the specific drug. Adverse effects include gastrointestinal issues and toxicity with long-term use.
What is Tetracycline ?
Tetracycline is an antibiotic that fights against infection caused by
bacteria.
Tetracycline is used to treat many different bacterial infections of the
skin, intestines, respiratory tract, urinary tract, genitals, lymph nodes,
and other body systems.
It is often used in treating severe acne, or
sexually transmitted diseases such as syphilis, gonorrhea.
Isolated directly from several species of Streptomyces bacteria or
produced semi-synthetically from those isolated compounds.
Tetracyclines are a class of broad-spectrum antibiotic derived from Streptomyces coelicolor bacteria. They work by inhibiting bacterial protein synthesis by binding to the 30S ribosomal subunit. Common tetracyclines include tetracycline, doxycycline, and minocycline. They are effective against both gram-positive and gram-negative bacteria, as well as other microorganisms. Tetracyclines are administered orally and work best when taken on an empty stomach. Side effects can include diarrhea, nausea, and photosensitivity. They interact with various other drugs and supplements. Tetracyclines must be stored properly at room temperature, away from heat, moisture, and light.
Tetracyclines are a class of broad-spectrum antibiotic drugs obtained from Streptomyces bacteria. They work by inhibiting protein synthesis in bacteria. Tetracyclines bind to the 30S subunit of bacterial ribosomes to prevent aminoacyl-tRNA from attaching, thereby terminating translation. They are effective against both gram-positive and gram-negative bacteria and are used to treat various infections. However, they can cause side effects like nausea, vomiting, diarrhea, and tooth discoloration.
Antibiotics aminoglycoside and tetracyclinerajendranrvs
油
Aminoglycosides and tetracycline antibiotics are discussed. Aminoglycosides work by binding to bacterial ribosomes and interfering with protein synthesis. Tetracyclines also bind to bacterial ribosomes but prevent the introduction of new amino acids during protein synthesis. Early tetracycline antibiotics were unstable in acidic or basic pH, but research led to developing more stable and longer-acting tetracycline compounds like doxycycline and minocycline. The document provides an overview of the mechanisms of aminoglycoside and tetracycline antibiotics.
This document discusses Tetracycline, including its biosynthesis, clinical uses, adverse effects, and contraindications. It notes that Tetracycline is isolated from Streptomyces bacteria and inhibits protein biosynthesis. It is effective against both gram-positive and gram-negative bacteria. Common uses include treating Mycoplasma pneumonia, Chlamydia trachomatis, cholera, and periodontal disease. Adverse effects can include gastrointestinal irritation, hepatotoxicity, and phototoxicity. Tetracycline is contraindicated in breastfeeding women, pregnant females, and children under 8 years old.
This document discusses doxycycline, a broad-spectrum antibiotic derived from tetracycline. It inhibits protein synthesis by reversibly binding to the 30S subunit of bacteria to block aminoacyl-tRNA binding. It has activity against many gram-positive and gram-negative bacteria. Doxycycline is used to treat infections caused by Mycoplasma pneumoniae, Rickettsiae, Chlamydia, Vibrio cholerae, Bacillus anthracis, and spirochetes. Adverse effects include gastrointestinal issues, tooth discoloration in children, and photosensitization. It is contraindicated in pregnancy, infants, and those with hypersensitivity.
This document discusses doxycycline, a broad-spectrum antibiotic derived from tetracycline. It inhibits protein synthesis by reversibly binding to the 30S subunit of bacteria to block aminoacyl-tRNA binding. It has activity against many gram-positive and gram-negative bacteria. Doxycycline is used to treat infections caused by Mycoplasma pneumoniae, Rickettsiae, Chlamydia, Vibrio cholerae, Bacillus anthracis, and spirochetes. Adverse effects include gastrointestinal issues, tooth discoloration in children, and liver and photosensitization. It is contraindicated in pregnancy, infants, and those with hypersensitivity.
This document discusses two classes of protein synthesis inhibitors - tetracyclines and chloramphenicol. It provides details on their mechanisms of action, classifications, spectra of activity, pharmacokinetics, clinical uses, resistance, side effects and interactions. Tetracyclines are classified based on source and duration of action. They inhibit bacterial protein synthesis by binding to the 30S ribosomal subunit. Chloramphenicol also inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit. Both classes have broad-spectrum activity and are associated with various side effects.
Tetracyclines are a class of broad-spectrum antibiotics produced by Streptomyces bacteria. They work by inhibiting protein synthesis in bacteria by binding to the 30s subunit of the bacterial ribosome, preventing tRNA from entering the acceptor site. Common examples include oxytetracycline, chlortetracycline, and doxycycline. They are effective against both gram-positive and gram-negative bacteria and are administered orally, though they can cause side effects like discoloring teeth or gastrointestinal upset.
Lecture 6 protein synthesis inhibiting antibioticsana munir
油
This document discusses several classes of antibiotics that inhibit protein synthesis in bacteria. It focuses on chloramphenicol, aminoglycosides, and tetracyclines. Chloramphenicol inhibits peptide bond formation on bacterial ribosomes. Aminoglycosides interfere with protein initiation by causing incorrect mRNA reading. Tetracyclines prevent amino acid attachment to bacterial ribosomes. All three classes bind to different sites on the bacterial ribosome to inhibit protein synthesis and treat various bacterial infections, but have potential toxic side effects when used.
- Tetracyclines are a class of broad spectrum antibiotic drugs derived from bacteria. They work by binding to the bacterial ribosome to inhibit protein synthesis and show bacteriostatic activity.
- Structurally, they contain four cyclic rings. Modifications to the structure can impact their activity. They are classified based on their duration of action as long, intermediate, or short acting.
- Common examples include tetracycline, doxycycline, and minocycline. They are used to treat various bacterial infections but have side effects like nausea, vomiting, and tooth staining when taken.
The document discusses tetracyclines and chloramphenicol antibiotics. It describes that tetracyclines are broad-spectrum antibiotics derived from soil actinomycetes that are bacteriostatic and inhibit protein synthesis. Chloramphenicol also inhibits bacterial protein synthesis. Both have broad antimicrobial spectra but resistance has developed. Adverse effects include bone marrow suppression for chloramphenicol and irritation.
Tetracyclines and Chloramphenicol (Broad-Spectrum Antibiotics).pptxsapnabohra2
油
TYB pharmacy
Pharmacology VI semester
Pharmacology notes
Tetracycline and chloramphenicol notes ppt
broad spectrum antibiotics
Third year B pharmacy pharmacology notes
Pharmacology unit 3 notes
Pharmacology VI semester notes
This document provides an overview of different classes of protein synthesis inhibitors including tetracyclines, glycylcyclines, aminoglycosides, macrolides, ketolides, macrocyclics, lincosamides, oxazolidinones, chloramphenicol, and streptogramins. For each class, it discusses mechanisms of action, antibacterial spectra, resistance, pharmacokinetics, and adverse effects. The classes range from broad spectrum inhibitors like tetracyclines to more narrow spectrum ones such as macrocyclics and oxazolidinones.
Tetracyclines are a group of broad-spectrum antibiotics derived from soil actinomycetes. They inhibit bacterial protein synthesis by binding to the bacterial ribosome. While tetracycline use has declined due to resistance, some remain useful for specific infections. Tetracyclines are classified based on duration of action and include short, intermediate, and long-acting drugs. Adverse effects include gastrointestinal upset, tooth staining in children, and hypersensitivity reactions.
36.ppt protein synthesis inhibitors prokaryotesSudha Sudha
油
This document discusses protein synthesis inhibitors and newer antibiotics, focusing on tetracyclines. It provides details on:
1) The history and development of tetracycline antibiotics from the 1940s onward.
2) The mechanism of action of tetracyclines, which involves binding to the 30S bacterial ribosome to inhibit protein synthesis.
3) The spectrum of activity of various tetracyclines against both gram-positive and gram-negative bacteria as well as other microorganisms.
- Tetracyclines are a class of broad-spectrum antibiotic compounds derived from Streptomyces bacteria. They contain a common tetracyclic ring structure and differ by attached functional groups.
- The first tetracyclines discovered in the 1940s were chlortetracycline and oxytetracycline. They exhibited activity against a wide range of microorganisms.
- Tetracyclines work by inhibiting bacterial protein synthesis through binding to the 30S ribosomal subunit. They have therapeutic uses against both gram-positive and gram-negative bacteria.
This document discusses tetracycline and its modifications. It begins with an introduction to tetracyclines as broad spectrum antibiotics discovered in 1948. It then covers the classification, structural activity relationship, and mechanism of action of tetracyclines. The rest of the document discusses the spectrum of activity, uses, side effects, drug interactions, resistance, and local drug delivery of tetracyclines for periodontal applications. It provides examples of commercially available tetracycline-containing local drug delivery products and studies on their effectiveness.
This document summarizes broad spectrum antibiotics tetracyclines and chloramphenicol. It describes the classification, mechanisms of action, antimicrobial spectrum, resistance, pharmacokinetics, adverse effects and therapeutic uses of tetracyclines. It also summarizes the mechanism of action, antimicrobial spectrum, resistance, pharmacokinetics, adverse effects and therapeutic uses of chloramphenicol. Both antibiotics are bacteriostatic, have broad spectra, can cause bone marrow toxicity and are enterohepatically circulated.
This document discusses various classes of antimicrobial agents used to treat bacterial, viral, and fungal infections. It describes the mechanisms of action and examples of drugs that inhibit cell wall synthesis, cell membrane function, protein synthesis, nucleic acid synthesis, and other metabolic processes in bacteria. It also discusses mechanisms of drug resistance in bacteria and summarizes treatment approaches for herpes virus infections and HIV/AIDS.
This document discusses various classes of antimicrobial drugs used for chemotherapy. It explains that antimicrobials work by targeting differences between microbial and human cells, and are either bactericidal or bacteriostatic. The major classes covered are cell wall inhibitors like penicillins; protein synthesis inhibitors like aminoglycosides and macrolides; and nucleic acid inhibitors like fluoroquinolones. Specific examples within each class are provided, along with their mechanisms of action and importance. The document also discusses drug resistance development in bacteria.
Antibiotics aminoglycoside and tetracyclinerajendranrvs
油
Aminoglycosides and tetracycline antibiotics are discussed. Aminoglycosides work by binding to bacterial ribosomes and interfering with protein synthesis. Tetracyclines also bind to bacterial ribosomes but prevent the introduction of new amino acids during protein synthesis. Early tetracycline antibiotics were unstable in acidic or basic pH, but research led to developing more stable and longer-acting tetracycline compounds like doxycycline and minocycline. The document provides an overview of the mechanisms of aminoglycoside and tetracycline antibiotics.
This document discusses Tetracycline, including its biosynthesis, clinical uses, adverse effects, and contraindications. It notes that Tetracycline is isolated from Streptomyces bacteria and inhibits protein biosynthesis. It is effective against both gram-positive and gram-negative bacteria. Common uses include treating Mycoplasma pneumonia, Chlamydia trachomatis, cholera, and periodontal disease. Adverse effects can include gastrointestinal irritation, hepatotoxicity, and phototoxicity. Tetracycline is contraindicated in breastfeeding women, pregnant females, and children under 8 years old.
This document discusses doxycycline, a broad-spectrum antibiotic derived from tetracycline. It inhibits protein synthesis by reversibly binding to the 30S subunit of bacteria to block aminoacyl-tRNA binding. It has activity against many gram-positive and gram-negative bacteria. Doxycycline is used to treat infections caused by Mycoplasma pneumoniae, Rickettsiae, Chlamydia, Vibrio cholerae, Bacillus anthracis, and spirochetes. Adverse effects include gastrointestinal issues, tooth discoloration in children, and photosensitization. It is contraindicated in pregnancy, infants, and those with hypersensitivity.
This document discusses doxycycline, a broad-spectrum antibiotic derived from tetracycline. It inhibits protein synthesis by reversibly binding to the 30S subunit of bacteria to block aminoacyl-tRNA binding. It has activity against many gram-positive and gram-negative bacteria. Doxycycline is used to treat infections caused by Mycoplasma pneumoniae, Rickettsiae, Chlamydia, Vibrio cholerae, Bacillus anthracis, and spirochetes. Adverse effects include gastrointestinal issues, tooth discoloration in children, and liver and photosensitization. It is contraindicated in pregnancy, infants, and those with hypersensitivity.
This document discusses two classes of protein synthesis inhibitors - tetracyclines and chloramphenicol. It provides details on their mechanisms of action, classifications, spectra of activity, pharmacokinetics, clinical uses, resistance, side effects and interactions. Tetracyclines are classified based on source and duration of action. They inhibit bacterial protein synthesis by binding to the 30S ribosomal subunit. Chloramphenicol also inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit. Both classes have broad-spectrum activity and are associated with various side effects.
Tetracyclines are a class of broad-spectrum antibiotics produced by Streptomyces bacteria. They work by inhibiting protein synthesis in bacteria by binding to the 30s subunit of the bacterial ribosome, preventing tRNA from entering the acceptor site. Common examples include oxytetracycline, chlortetracycline, and doxycycline. They are effective against both gram-positive and gram-negative bacteria and are administered orally, though they can cause side effects like discoloring teeth or gastrointestinal upset.
Lecture 6 protein synthesis inhibiting antibioticsana munir
油
This document discusses several classes of antibiotics that inhibit protein synthesis in bacteria. It focuses on chloramphenicol, aminoglycosides, and tetracyclines. Chloramphenicol inhibits peptide bond formation on bacterial ribosomes. Aminoglycosides interfere with protein initiation by causing incorrect mRNA reading. Tetracyclines prevent amino acid attachment to bacterial ribosomes. All three classes bind to different sites on the bacterial ribosome to inhibit protein synthesis and treat various bacterial infections, but have potential toxic side effects when used.
- Tetracyclines are a class of broad spectrum antibiotic drugs derived from bacteria. They work by binding to the bacterial ribosome to inhibit protein synthesis and show bacteriostatic activity.
- Structurally, they contain four cyclic rings. Modifications to the structure can impact their activity. They are classified based on their duration of action as long, intermediate, or short acting.
- Common examples include tetracycline, doxycycline, and minocycline. They are used to treat various bacterial infections but have side effects like nausea, vomiting, and tooth staining when taken.
The document discusses tetracyclines and chloramphenicol antibiotics. It describes that tetracyclines are broad-spectrum antibiotics derived from soil actinomycetes that are bacteriostatic and inhibit protein synthesis. Chloramphenicol also inhibits bacterial protein synthesis. Both have broad antimicrobial spectra but resistance has developed. Adverse effects include bone marrow suppression for chloramphenicol and irritation.
Tetracyclines and Chloramphenicol (Broad-Spectrum Antibiotics).pptxsapnabohra2
油
TYB pharmacy
Pharmacology VI semester
Pharmacology notes
Tetracycline and chloramphenicol notes ppt
broad spectrum antibiotics
Third year B pharmacy pharmacology notes
Pharmacology unit 3 notes
Pharmacology VI semester notes
This document provides an overview of different classes of protein synthesis inhibitors including tetracyclines, glycylcyclines, aminoglycosides, macrolides, ketolides, macrocyclics, lincosamides, oxazolidinones, chloramphenicol, and streptogramins. For each class, it discusses mechanisms of action, antibacterial spectra, resistance, pharmacokinetics, and adverse effects. The classes range from broad spectrum inhibitors like tetracyclines to more narrow spectrum ones such as macrocyclics and oxazolidinones.
Tetracyclines are a group of broad-spectrum antibiotics derived from soil actinomycetes. They inhibit bacterial protein synthesis by binding to the bacterial ribosome. While tetracycline use has declined due to resistance, some remain useful for specific infections. Tetracyclines are classified based on duration of action and include short, intermediate, and long-acting drugs. Adverse effects include gastrointestinal upset, tooth staining in children, and hypersensitivity reactions.
36.ppt protein synthesis inhibitors prokaryotesSudha Sudha
油
This document discusses protein synthesis inhibitors and newer antibiotics, focusing on tetracyclines. It provides details on:
1) The history and development of tetracycline antibiotics from the 1940s onward.
2) The mechanism of action of tetracyclines, which involves binding to the 30S bacterial ribosome to inhibit protein synthesis.
3) The spectrum of activity of various tetracyclines against both gram-positive and gram-negative bacteria as well as other microorganisms.
- Tetracyclines are a class of broad-spectrum antibiotic compounds derived from Streptomyces bacteria. They contain a common tetracyclic ring structure and differ by attached functional groups.
- The first tetracyclines discovered in the 1940s were chlortetracycline and oxytetracycline. They exhibited activity against a wide range of microorganisms.
- Tetracyclines work by inhibiting bacterial protein synthesis through binding to the 30S ribosomal subunit. They have therapeutic uses against both gram-positive and gram-negative bacteria.
This document discusses tetracycline and its modifications. It begins with an introduction to tetracyclines as broad spectrum antibiotics discovered in 1948. It then covers the classification, structural activity relationship, and mechanism of action of tetracyclines. The rest of the document discusses the spectrum of activity, uses, side effects, drug interactions, resistance, and local drug delivery of tetracyclines for periodontal applications. It provides examples of commercially available tetracycline-containing local drug delivery products and studies on their effectiveness.
This document summarizes broad spectrum antibiotics tetracyclines and chloramphenicol. It describes the classification, mechanisms of action, antimicrobial spectrum, resistance, pharmacokinetics, adverse effects and therapeutic uses of tetracyclines. It also summarizes the mechanism of action, antimicrobial spectrum, resistance, pharmacokinetics, adverse effects and therapeutic uses of chloramphenicol. Both antibiotics are bacteriostatic, have broad spectra, can cause bone marrow toxicity and are enterohepatically circulated.
This document discusses various classes of antimicrobial agents used to treat bacterial, viral, and fungal infections. It describes the mechanisms of action and examples of drugs that inhibit cell wall synthesis, cell membrane function, protein synthesis, nucleic acid synthesis, and other metabolic processes in bacteria. It also discusses mechanisms of drug resistance in bacteria and summarizes treatment approaches for herpes virus infections and HIV/AIDS.
This document discusses various classes of antimicrobial drugs used for chemotherapy. It explains that antimicrobials work by targeting differences between microbial and human cells, and are either bactericidal or bacteriostatic. The major classes covered are cell wall inhibitors like penicillins; protein synthesis inhibitors like aminoglycosides and macrolides; and nucleic acid inhibitors like fluoroquinolones. Specific examples within each class are provided, along with their mechanisms of action and importance. The document also discusses drug resistance development in bacteria.
Graves' disease is an autoimmune disorder causing hyperthyroidism in 60-80% of cases. Genetic and environmental factors contribute to susceptibility. Smoking increases the risk of ophthalmopathy. Hyperthyroidism is caused by thyroid stimulating immunoglobulins that activate the TSH receptor and cause overproduction of thyroid hormones. Treatment involves antithyroid drugs, radioiodine ablation, or surgery. Ophthalmopathy may cause eye swelling, bulging, and vision issues. Thyroiditis refers to inflammation of the thyroid and can be acute, subacute, or chronic depending on duration and symptoms. Subacute thyroiditis causes thyroid pain and temporary changes in thyroid function. Pregnancy causes changes in
The document discusses food poisoning in children, noting that it is caused by bacteria, viruses, and toxins from contaminated food and water. Common symptoms in children include nausea, vomiting, diarrhea, stomach cramps, and fever. Doctors diagnose food poisoning through symptoms and treat it with hydration and electrolyte replacement or antibiotics if bacterial. The document emphasizes safe food handling, preparation, storage, and avoiding high-risk foods to prevent food poisoning in children.
Motor disorders in children can be caused by genetic, neurological, and environmental factors and affect a child's ability to control their movements. There are two main types: hypokinesia, characterized by decreased movement and muscle tone; and hyperkinesia, characterized by excessive uncontrolled movements. Treatment focuses on improving muscle tone, range of motion, and movement control through therapies like physical therapy and medication. Communication disorders can interfere with everyday interactions and involve deficits in vocabulary, sentence formation, and social skills. They are often accompanied by difficulties in language use, listening, and conversation organization.
There are many tests that can examine the health of the immune system and help diagnose immune disorders. Blood tests can detect typical levels of infection-fighting proteins and immune cells, and determine if the immune system is responding properly to foreign invaders. Prenatal testing of samples like amniotic fluid or placental tissue can check for genetic defects in future pregnancies if a parent has an immune disorder. Treatments involve preventing and treating infections, boosting the immune system, and addressing the underlying cause, which may include long-term antibiotics, immunoglobulin therapy, stem cell transplantation, or gene therapy.
The document discusses key principles for surgery including:
1) Mastering surgical instruments and procedures such as cutting, hemostasis, and suturing.
2) Understanding principles of sterile technique and minimally invasive surgery.
3) Ensuring asepsis throughout the operative phases to prevent infection and tumor dissemination.
Computer Application in Business (commerce)Sudar Sudar
油
The main objectives
1. To introduce the concept of computer and its various parts. 2. To explain the concept of data base management system and Management information system.
3. To provide insight about networking and basics of internet
Recall various terms of computer and its part
Understand the meaning of software, operating system, programming language and its features
Comparing Data Vs Information and its management system Understanding about various concepts of management information system
Explain about networking and elements based on internet
1. Recall the various concepts relating to computer and its various parts
2 Understand the meaning of softwares, operating system etc
3 Understanding the meaning and utility of database management system
4 Evaluate the various aspects of management information system
5 Generating more ideas regarding the use of internet for business purpose
Mate, a short story by Kate Grenvile.pptxLiny Jenifer
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A powerpoint presentation on the short story Mate by Kate Greenville. This presentation provides information on Kate Greenville, a character list, plot summary and critical analysis of the short story.
Digital Tools with AI for e-Content Development.pptxDr. Sarita Anand
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This ppt is useful for not only for B.Ed., M.Ed., M.A. (Education) or any other PG level students or Ph.D. scholars but also for the school, college and university teachers who are interested to prepare an e-content with AI for their students and others.
Useful environment methods in Odoo 18 - Odoo 際際滷sCeline George
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In this slide well discuss on the useful environment methods in Odoo 18. In Odoo 18, environment methods play a crucial role in simplifying model interactions and enhancing data processing within the ORM framework.
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In this slide, well discuss on how to configure flexible working schedule in Odoo 18 Employee module. In Odoo 18, the Employee module offers powerful tools to configure and manage flexible working schedules tailored to your organization's needs.
APM People Interest Network Conference 2025
- Autonomy, Teams and Tension
- Oliver Randall & David Bovis
- Own Your Autonomy
Oliver Randall
Consultant, Tribe365
Oliver is a career project professional since 2011 and started volunteering with APM in 2016 and has since chaired the People Interest Network and the North East Regional Network. Oliver has been consulting in culture, leadership and behaviours since 2019 and co-developed HPTM速an off the shelf high performance framework for teams and organisations and is currently working with SAS (Stellenbosch Academy for Sport) developing the culture, leadership and behaviours framework for future elite sportspeople whilst also holding down work as a project manager in the NHS at North Tees and Hartlepool Foundation Trust.
David Bovis
Consultant, Duxinaroe
A Leadership and Culture Change expert, David is the originator of BTFA and The Dux Model.
With a Masters in Applied Neuroscience from the Institute of Organisational Neuroscience, he is widely regarded as the Go-To expert in the field, recognised as an inspiring keynote speaker and change strategist.
He has an industrial engineering background, majoring in TPS / Lean. David worked his way up from his apprenticeship to earn his seat at the C-suite table. His career spans several industries, including Automotive, Aerospace, Defence, Space, Heavy Industries and Elec-Mech / polymer contract manufacture.
Published in Londons Evening Standard quarterly business supplement, James Caans Your business Magazine, Quality World, the Lean Management Journal and Cambridge Universities PMA, he works as comfortably with leaders from FTSE and Fortune 100 companies as he does owner-managers in SMEs. He is passionate about helping leaders understand the neurological root cause of a high-performance culture and sustainable change, in business.
Session | Own Your Autonomy The Importance of Autonomy in Project Management
#OwnYourAutonomy is aiming to be a global APM initiative to position everyone to take a more conscious role in their decision making process leading to increased outcomes for everyone and contribute to a world in which all projects succeed.
We want everyone to join the journey.
#OwnYourAutonomy is the culmination of 3 years of collaborative exploration within the Leadership Focus Group which is part of the APM People Interest Network. The work has been pulled together using the 5 HPTM速 Systems and the BTFA neuroscience leadership programme.
https://www.linkedin.com/showcase/apm-people-network/about/
Prelims of Kaun TALHA : a Travel, Architecture, Lifestyle, Heritage and Activism quiz, organized by Conquiztadors, the Quiz society of Sri Venkateswara College under their annual quizzing fest El Dorado 2025.
The Constitution, Government and Law making bodies .saanidhyapatel09
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This PowerPoint presentation provides an insightful overview of the Constitution, covering its key principles, features, and significance. It explains the fundamental rights, duties, structure of government, and the importance of constitutional law in governance. Ideal for students, educators, and anyone interested in understanding the foundation of a nations legal framework.
Finals of Kaun TALHA : a Travel, Architecture, Lifestyle, Heritage and Activism quiz, organized by Conquiztadors, the Quiz society of Sri Venkateswara College under their annual quizzing fest El Dorado 2025.
How to use Init Hooks in Odoo 18 - Odoo 際際滷sCeline George
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In this slide, well discuss on how to use Init Hooks in Odoo 18. In Odoo, Init Hooks are essential functions specified as strings in the __init__ file of a module.
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This PPT is showing the effect of social changes in human life and it is very understandable to the students with easy language.in this contents are Itroduction, definition,Factors affecting social changes ,Main technological factors, Social change and stress , what is eustress and how social changes give impact of the human's life.
2. INTRODUCTION
Tetracyclines are a class of
antibiotic,which are chemical substances
produced by a microorganism that are
able to kill other microorganisms without
being toxic to the person,animal or plant.
Tetracyclines are derived directly from a
bacterium known as Streptomyces
coelicolor.
4. MECHANISM OF ACTION
Tetracyclines are specific inhibitors of bacterial
protien synthesis.
They bind to the 30s ribosomal subunit and
thereby prevent the binding of aminoacyl tRNA to
the mRNA ribosome complex.
Tetracyclines also inhibit protein synthesis in
the host,but are less likely to reach the
concentration required because eukaryotic cells
do not have a tetracycline uptake mechanism.
7. ADMINISTRATION
Oral capsules is the dosage form in
which tetracyclines are most commonly
administered.
The capsule should be taken 1/2hr before
or 2hr after food.
Not recommended for i.m. route of
administration.
8. USES OF TETRACYCLINE
Tetracycline is used to treat wide
variety of infections, including acne.
It is an antibiotic that works by
stopping the growth of bacteria.
Venerel disease
Atypical pneumonia
Cholera
Relapsing fever
Rickettsial infections,plague
9. DRUG INTERACTION
Tetracycline may interact with other
medicine. Effects of one or both of drugs
may change or rick of side effect may be
greater.
Calcium supplements
Mineral supplements
Multivitamin
Cholesterol lowering drugs
Penicillin compounds