Farmakodinamik and farmakokinetik are subdisciplines of pharmacology that study the effects and mechanisms of drug action on the body and the handling of drugs by the body respectively. Farmakodinamik explains the interactions between drugs and the body, while farmakokinetik examines the absorption, distribution, biotransformation and elimination of drugs from the body. Together, these processes determine the effects of drugs over time within the body.
This document discusses the pharmacokinetics of drug absorption and distribution. It covers several key topics in 3 paragraphs:
Membrane transporters, including passive diffusion, carrier-mediated transport processes like facilitated diffusion and active transport, allow drugs to be absorbed into the bloodstream. Factors like a drug's solubility, size and lipid solubility determine which transport mechanisms are used.
Absorption refers to the movement of drugs from the site of administration into circulation. The rate and extent of absorption depends on factors like solubility, concentration, administering area, vascularity and route. Oral drugs are affected by things like acidity, particle size and food. Injection routes see faster absorption.
Distribution
Pharmacology is the study of drug action on living organisms. Pharmacokinetics describes the processes of absorption, distribution, metabolism, and excretion of drugs in the body. Pharmacodynamics examines how drugs act on the body at a biochemical and physiological level, often by binding to receptors. Drugs are administered through various routes including oral, parenteral, topical, inhalation, and others. Factors like dosage form, route of administration, lipid solubility, protein binding, blood supply impact the pharmacokinetic profile of a drug. Adverse effects are also an important aspect of pharmacology studied through toxicology.
This document discusses the pharmacokinetics of drug absorption and distribution. It begins by defining pharmacokinetics as the quantitative study of how the body acts on drugs. It then discusses the different mechanisms of drug transportation across cell membranes, including passive diffusion, filtration, and carrier-mediated transport like facilitated diffusion and active transport. It describes factors that affect drug absorption like solubility, concentration, and route of administration. It also discusses concepts like bioavailability, bioequivalence, distribution, redistribution, barriers to drug movement, and plasma protein binding. In summary, it provides an overview of how drugs move into, through, and out of the body after administration.
Pharmacology is the study of how drugs act on the body. It includes pharmacokinetics, which is what the body does to the drug, and pharmacodynamics, which is what the drug does to the body. Key aspects of pharmacokinetics include absorption, distribution, metabolism and excretion of drugs in the body. Drugs can have intended therapeutic effects as well as unintended adverse effects. Understanding the mechanisms of drug action and factors affecting drug response are important aspects of pharmacology.
This document provides an overview of basic biopharmaceutics and how drugs work in the body. It discusses the processes of absorption, distribution, metabolism, and excretion (ADME) that determine a drug's concentration at its site of action over time. Key concepts covered include drug receptors and sites of action, concentration-effect relationships, ionization and protein binding, first-pass metabolism, and factors that influence bioavailability and bioequivalence between drug products.
The document discusses the process of excretion in the human body. Medications are eliminated from the body through excretion, which primarily occurs through the kidneys. The kidneys filter waste from the blood through glomerular filtration and either reabsorb or actively secrete drugs and other molecules into the urine through tubular transport processes for excretion from the body.
This document discusses the pharmacokinetics of drug absorption and distribution. It covers several key topics in 3 paragraphs:
Membrane transporters, including passive diffusion, carrier-mediated transport processes like facilitated diffusion and active transport, allow drugs to be absorbed into the bloodstream. Factors like a drug's solubility, size and lipid solubility determine which transport mechanisms are used.
Absorption refers to the movement of drugs from the site of administration into circulation. The rate and extent of absorption depends on factors like solubility, concentration, administering area, vascularity and route. Oral drugs are affected by things like acidity, particle size and food. Injection routes see faster absorption.
Distribution
Pharmacology is the study of drug action on living organisms. Pharmacokinetics describes the processes of absorption, distribution, metabolism, and excretion of drugs in the body. Pharmacodynamics examines how drugs act on the body at a biochemical and physiological level, often by binding to receptors. Drugs are administered through various routes including oral, parenteral, topical, inhalation, and others. Factors like dosage form, route of administration, lipid solubility, protein binding, blood supply impact the pharmacokinetic profile of a drug. Adverse effects are also an important aspect of pharmacology studied through toxicology.
This document discusses the pharmacokinetics of drug absorption and distribution. It begins by defining pharmacokinetics as the quantitative study of how the body acts on drugs. It then discusses the different mechanisms of drug transportation across cell membranes, including passive diffusion, filtration, and carrier-mediated transport like facilitated diffusion and active transport. It describes factors that affect drug absorption like solubility, concentration, and route of administration. It also discusses concepts like bioavailability, bioequivalence, distribution, redistribution, barriers to drug movement, and plasma protein binding. In summary, it provides an overview of how drugs move into, through, and out of the body after administration.
Pharmacology is the study of how drugs act on the body. It includes pharmacokinetics, which is what the body does to the drug, and pharmacodynamics, which is what the drug does to the body. Key aspects of pharmacokinetics include absorption, distribution, metabolism and excretion of drugs in the body. Drugs can have intended therapeutic effects as well as unintended adverse effects. Understanding the mechanisms of drug action and factors affecting drug response are important aspects of pharmacology.
This document provides an overview of basic biopharmaceutics and how drugs work in the body. It discusses the processes of absorption, distribution, metabolism, and excretion (ADME) that determine a drug's concentration at its site of action over time. Key concepts covered include drug receptors and sites of action, concentration-effect relationships, ionization and protein binding, first-pass metabolism, and factors that influence bioavailability and bioequivalence between drug products.
The document discusses the process of excretion in the human body. Medications are eliminated from the body through excretion, which primarily occurs through the kidneys. The kidneys filter waste from the blood through glomerular filtration and either reabsorb or actively secrete drugs and other molecules into the urine through tubular transport processes for excretion from the body.
Pharmacokinetics and pharmacodynamics.pptxShelly Nayyar
Pharmacokinetics and pharmacodynamics are the two major branches of pharmacology. Pharmacokinetics refers to what the body does to a drug, including absorption, distribution, metabolism, and excretion. Pharmacodynamics refers to what the drug does to the body and its physiological effects. Key concepts in pharmacokinetics include the first-pass effect whereby drugs are metabolized as they pass through the liver, affecting their bioavailability, as well as half-life which determines how long it takes for a drug concentration in the body to reduce by half. Pharmacodynamics examines how drugs act on receptors and enzymes to produce their effects in a selective manner when possible.
LS 1.2- Introduction to Pharmacokinetics & Pharmacodynamics.pptxDorenceSimuntala
This document provides an introduction to pharmacokinetics and pharmacodynamics. It defines key terms like absorption, distribution, metabolism, and excretion which describe how the body processes a drug over time (pharmacokinetics). It also defines mechanisms of drug action, effects, and how drug concentration at the site of action relates to observed responses (pharmacodynamics). The relationship between these concepts and how pharmacokinetics determines drug levels over time to produce pharmacodynamic drug effects is also summarized.
This document provides an overview of principles of pharmacokinetics, pharmacodynamics, and pharmacogenetics. It discusses key topics including absorption, distribution, metabolism, and excretion of drugs. Absorption involves drugs being taken up into systemic circulation and is influenced by route of administration, drug properties, and gastrointestinal factors. Distribution of drugs to tissues depends on blood flow, permeability, protein binding, lipophilicity, and tissue storage. Metabolism transforms drugs via phase I and phase II reactions, mainly in the liver, and can activate or inactivate compounds.
This document provides an overview of the key concepts in medicinal chemistry that will be covered in the class. It discusses the history and evolution of medicinal chemistry, defining drugs and their properties, drug discovery and design processes, and the pharmacokinetic and pharmacodynamic phases of drug action. The goal of medicinal chemistry is to design and synthesize new drug molecules through understanding their interactions with biological targets and structure-activity relationships.
Introduction to Medicinal Chemistry, History and development of medicinal chemistry, Physicochemical properties in relation to biological action Ionization, Solubility, Partition Coefficient, Hydrogen bonding, Protein binding, Chelation, Bioisosterism, Optical and Geometrical isomerism, Drug metabolism Drug metabolism principles- Phase I and Phase II. Factors affecting drug metabolism including stereo chemical aspects
This document discusses dental pharmacology. It begins by defining pharmacology as the study of drugs and their interactions with living systems. It then discusses the history and development of pharmacology. The rest of the document covers various topics in dental pharmacology including local anesthetics, vasoconstrictors, antiseptics, and sources of drugs. It provides details on specific drugs used in dentistry as well as their mechanisms of action, uses, and important considerations.
1. The document discusses the processes involved in a drug molecule traveling through the human body from administration to reaching its target site, known as pharmacokinetics.
2. Pharmacokinetics involves absorption of the drug into systemic circulation, distribution of the drug via blood plasma to tissues and organs, and elimination of the drug from the body through biotransformation or excretion.
3. For a drug to have an effect, it must reach the biophase, or site of action, at an appropriate concentration by passing through biological barriers in the body via processes like passive diffusion, carrier-mediated transport, vesicular transport, or paracellular transport between cells.
Photosynthesis involves two main stages - the light-dependent reactions and the light-independent Calvin cycle. In the light-dependent reactions, chlorophyll uses light energy to convert water and carbon dioxide into oxygen and energy carriers (ATP and NADPH). In the Calvin cycle, the energy carriers are used to convert the energy from the light reactions into glucose through a series of reduction reactions.
Photosynthesis involves two main stages - the light-dependent reactions and the light-independent Calvin cycle. In the light-dependent reactions, chlorophyll uses light energy to convert water and carbon dioxide into oxygen and energy carriers (ATP and NADPH). In the Calvin cycle, the energy carriers are used to convert the energy from the light reactions into glucose through a series of reduction reactions.
Biopharmaceutics is the study of the relationship between the physicochemical properties of drugs and drug products and their pharmacological effects. Absorption is the process by which drugs enter systemic circulation from the site of administration, and occurs primarily via passive diffusion, facilitated transport, active transport, or vesicular transport across cell membranes and barriers in the gastrointestinal tract. The rate and extent of drug absorption determines the bioavailability and is influenced by factors such as the drug's physicochemical properties, dosage form characteristics, and gastrointestinal physiology.
ARKIA Official White Paper And Roadmap.pdfaidanshati
1. The document discusses seven pillars that define the principles of life as proposed by Daniel E. Koshland. The seven pillars are program, improvisation, compartmentalization, energy, regeneration, adaptability, and seclusion.
2. The first pillar, program, refers to an organized plan encoded in DNA that describes the interactions among components to allow living systems to persist over time. The second pillar, improvisation, allows living systems to change their program to adapt to environmental changes.
3. The third pillar is compartmentalization, which is the confinement of living things to a limited volume surrounded by a membrane. This maintains concentrations of components needed for reactions.
Introduction of Veterinary pharmacologyQaline Giigii
This document provides an introduction to veterinary pharmacology. It discusses how pharmacology can be defined as the study of substances that interact with living systems, and how veterinary pharmacology specifically focuses on preventing, diagnosing and treating disease in animals. The document then summarizes that veterinary pharmacology has two main subdivisions: pharmacokinetics, which is what the body does to a drug, and pharmacodynamics, which is what the drug does to the body. Several key pharmacokinetic and pharmacodynamic concepts are then defined, including absorption, distribution, metabolism, excretion, drug receptors, and drug effects.
Introduction of Veterinary pharmacology Somaliland Dr.Osman Abdulahi FarahQaline Giigii
This course was prepared by Dr.Osman Abdulahi Farah
Cismaan shiine Lecturer of Gollis University Faculty of Agriculture and Veterinary Medicine 2014
The main content of this course including introduction of Veterinary Pharmacology, division of pharmacology and list of terms of terminology about veterinay pharmacology
Pharmacokinetics is the study of how the body affects drugs. It involves absorption, distribution, metabolism, and excretion of drugs. Absorption is how drugs enter the bloodstream and distribution is how drugs spread to tissues. Metabolism converts drugs to inactive forms through phase I (oxidation) and phase II (conjugation) reactions. Excretion eliminates drugs from the body. Together, these processes determine the effects of drugs over time.
This document provides an introduction to veterinary pharmacology. It discusses key topics including:
1. Veterinary pharmacology is divided into pharmacokinetics, which is what the body does to a drug, and pharmacodynamics, which is what a drug does to the body.
2. Pharmacokinetics includes absorption, distribution, metabolism and excretion of drugs in the body. Pharmacodynamics involves drug receptors, effects, and toxicity.
3. Drugs can be classified by their chemical, generic or brand names. The chemical name provides the exact composition while the generic name is established when first manufactured.
This document discusses pharmacokinetics, specifically absorption and distribution of drugs. It covers several key topics:
1. Modes of permeation and transport across cell membranes including passive diffusion, carrier-mediated transport, pinocytosis, and filtration.
2. Factors that influence absorption including drug properties like size, ionization, and lipid solubility as well as routes of administration.
3. Distribution of drugs in the body and factors that affect it like lipid solubility, ionization, and drug-drug interactions.
The document discusses pharmacokinetics and pharmacodynamics. Pharmacokinetics refers to what the body does to a drug, including absorption, distribution, metabolism, and excretion. Pharmacodynamics refers to what the drug does to the body, including therapeutic and adverse effects. The document provides detailed information on various pharmacokinetic processes like absorption, distribution, metabolism, elimination, and clearance. It describes factors influencing these processes and defines related terms like volume of distribution, half-life, and steady state.
Transgenic animals are created by inserting foreign genes into the animal's genome. The first successful transgenic animal was a "Supermouse" created in 1982. The process involves constructing a transgene with a promoter, gene of interest, and termination sequence. This transgene is then introduced into an animal embryo, usually via microinjection or stem cells. The transgenic progeny are screened for integration of the gene. Transgenic animals are useful models but can have issues like multiple insertions, gene silencing, or affecting normal gene regulation. Examples include glowing fish, Alzheimer's mouse models, and animals altered for agricultural purposes.
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Pharmacokinetics and pharmacodynamics are the two major branches of pharmacology. Pharmacokinetics refers to what the body does to a drug, including absorption, distribution, metabolism, and excretion. Pharmacodynamics refers to what the drug does to the body and its physiological effects. Key concepts in pharmacokinetics include the first-pass effect whereby drugs are metabolized as they pass through the liver, affecting their bioavailability, as well as half-life which determines how long it takes for a drug concentration in the body to reduce by half. Pharmacodynamics examines how drugs act on receptors and enzymes to produce their effects in a selective manner when possible.
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This document provides an overview of the key concepts in medicinal chemistry that will be covered in the class. It discusses the history and evolution of medicinal chemistry, defining drugs and their properties, drug discovery and design processes, and the pharmacokinetic and pharmacodynamic phases of drug action. The goal of medicinal chemistry is to design and synthesize new drug molecules through understanding their interactions with biological targets and structure-activity relationships.
Introduction to Medicinal Chemistry, History and development of medicinal chemistry, Physicochemical properties in relation to biological action Ionization, Solubility, Partition Coefficient, Hydrogen bonding, Protein binding, Chelation, Bioisosterism, Optical and Geometrical isomerism, Drug metabolism Drug metabolism principles- Phase I and Phase II. Factors affecting drug metabolism including stereo chemical aspects
This document discusses dental pharmacology. It begins by defining pharmacology as the study of drugs and their interactions with living systems. It then discusses the history and development of pharmacology. The rest of the document covers various topics in dental pharmacology including local anesthetics, vasoconstrictors, antiseptics, and sources of drugs. It provides details on specific drugs used in dentistry as well as their mechanisms of action, uses, and important considerations.
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2. Pharmacokinetics involves absorption of the drug into systemic circulation, distribution of the drug via blood plasma to tissues and organs, and elimination of the drug from the body through biotransformation or excretion.
3. For a drug to have an effect, it must reach the biophase, or site of action, at an appropriate concentration by passing through biological barriers in the body via processes like passive diffusion, carrier-mediated transport, vesicular transport, or paracellular transport between cells.
Photosynthesis involves two main stages - the light-dependent reactions and the light-independent Calvin cycle. In the light-dependent reactions, chlorophyll uses light energy to convert water and carbon dioxide into oxygen and energy carriers (ATP and NADPH). In the Calvin cycle, the energy carriers are used to convert the energy from the light reactions into glucose through a series of reduction reactions.
Photosynthesis involves two main stages - the light-dependent reactions and the light-independent Calvin cycle. In the light-dependent reactions, chlorophyll uses light energy to convert water and carbon dioxide into oxygen and energy carriers (ATP and NADPH). In the Calvin cycle, the energy carriers are used to convert the energy from the light reactions into glucose through a series of reduction reactions.
Biopharmaceutics is the study of the relationship between the physicochemical properties of drugs and drug products and their pharmacological effects. Absorption is the process by which drugs enter systemic circulation from the site of administration, and occurs primarily via passive diffusion, facilitated transport, active transport, or vesicular transport across cell membranes and barriers in the gastrointestinal tract. The rate and extent of drug absorption determines the bioavailability and is influenced by factors such as the drug's physicochemical properties, dosage form characteristics, and gastrointestinal physiology.
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1. The document discusses seven pillars that define the principles of life as proposed by Daniel E. Koshland. The seven pillars are program, improvisation, compartmentalization, energy, regeneration, adaptability, and seclusion.
2. The first pillar, program, refers to an organized plan encoded in DNA that describes the interactions among components to allow living systems to persist over time. The second pillar, improvisation, allows living systems to change their program to adapt to environmental changes.
3. The third pillar is compartmentalization, which is the confinement of living things to a limited volume surrounded by a membrane. This maintains concentrations of components needed for reactions.
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This document provides an introduction to veterinary pharmacology. It discusses how pharmacology can be defined as the study of substances that interact with living systems, and how veterinary pharmacology specifically focuses on preventing, diagnosing and treating disease in animals. The document then summarizes that veterinary pharmacology has two main subdivisions: pharmacokinetics, which is what the body does to a drug, and pharmacodynamics, which is what the drug does to the body. Several key pharmacokinetic and pharmacodynamic concepts are then defined, including absorption, distribution, metabolism, excretion, drug receptors, and drug effects.
Introduction of Veterinary pharmacology Somaliland Dr.Osman Abdulahi FarahQaline Giigii
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This document provides an introduction to veterinary pharmacology. It discusses key topics including:
1. Veterinary pharmacology is divided into pharmacokinetics, which is what the body does to a drug, and pharmacodynamics, which is what a drug does to the body.
2. Pharmacokinetics includes absorption, distribution, metabolism and excretion of drugs in the body. Pharmacodynamics involves drug receptors, effects, and toxicity.
3. Drugs can be classified by their chemical, generic or brand names. The chemical name provides the exact composition while the generic name is established when first manufactured.
This document discusses pharmacokinetics, specifically absorption and distribution of drugs. It covers several key topics:
1. Modes of permeation and transport across cell membranes including passive diffusion, carrier-mediated transport, pinocytosis, and filtration.
2. Factors that influence absorption including drug properties like size, ionization, and lipid solubility as well as routes of administration.
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إضغ بين إيديكم من أقوى الملازم التي صممتها
ملزمة تشريح الجهاز الهيكلي (نظري 3)
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تتميز هذهِ الملزمة بعِدة مُميزات :
1- مُترجمة ترجمة تُناسب جميع المستويات
2- تحتوي على 78 رسم توضيحي لكل كلمة موجودة بالملزمة (لكل كلمة !!!!)
#فهم_ماكو_درخ
3- دقة الكتابة والصور عالية جداً جداً جداً
4- هُنالك بعض المعلومات تم توضيحها بشكل تفصيلي جداً (تُعتبر لدى الطالب أو الطالبة بإنها معلومات مُبهمة ومع ذلك تم توضيح هذهِ المعلومات المُبهمة بشكل تفصيلي جداً
5- الملزمة تشرح نفسها ب نفسها بس تكلك تعال اقراني
6- تحتوي الملزمة في اول سلايد على خارطة تتضمن جميع تفرُعات معلومات الجهاز الهيكلي المذكورة في هذهِ الملزمة
واخيراً هذهِ الملزمة حلالٌ عليكم وإتمنى منكم إن تدعولي بالخير والصحة والعافية فقط
كل التوفيق زملائي وزميلاتي ، زميلكم محمد الذهبي 💊💊
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Level 3 NCEA - NZ: A Nation In the Making 1872 - 1900 SML.pptHenry Hollis
The History of NZ 1870-1900.
Making of a Nation.
From the NZ Wars to Liberals,
Richard Seddon, George Grey,
Social Laboratory, New Zealand,
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2. Farmakodinamik
Farmakodinamik adalah subdisiplin farmakologi yang mempelajari efek biokimia,
fisiologo dan mekanisme kerja obat. Farmakodinamik menjelaskan interaksi antara
obat terhadap tubuh dan efek konsentrasinya.
Secara umum obat harus berikatan dengan reseptor untuk memberikan efek (Buku
Ajar Farmakologi (2023), 19)
Fase farmakodinamik, fase pada saat obat telah berinteraksi dengan reseptor
dan siap memberikan efek farmakologi, sampai efek farmakologi diakhiri.
3. Farmakokinetik
Farmakokinetik merupakan ilmu yang mempelajari kinetika absorpsi,
distribusi dan eliminasi ( yakni ekskresi dan metabolisme ) obat pada manusia
atau hewan dan Absorpsi, distribusi, biotransformasi ( metabolisme ) dan
eliminasi suatu obatdari tubuh merupakan proses dinamis yang kontinu dari
saat suatu obat dimakan sampai semua obat tersebut hilang dari tubuh. Laju
terjadinya proses-proses ini mempengaruhi onset, intensitas, dan lamanya
kerja obat di dalam tubuh (Staff pengajar farmakologi, 2006).
Fase farmakokinetik, adalah fase yang meliputi semua proses yang dilakukan
tubuh, setelah obat dilepas dari bentuk sediaannya yang terdiri dari absorbsi,
distribusi, metabolisme dan ekskresi.
4. Pernedaan farmakokinetik dan farmakodinamik
Farmakokinetik Farmakodinamik
Pengaruh organisme hidup
terhadap obat
Pengaruh obat terhadap
organisme hidup
Penanganan obat oleh
organisme hidup
Studi tentang absorpsi,
distribusi, metabolisme dan
Studi tentang tempat dan
mekanisme kerja serta efek
fisiologi dan biokimia obat
pada organisme hidup
ekskresi
5. fase ini merupakan fase penyerapan
obat pada tempat masuknya obat
selain itu faktor absorpsi ini akan
mempengaruhi jumlah obat yang
harus diminum dan kecepatan
perjalanan obat didalam tubuh.
merupakan fase penyebaran atau
distribusi obat didalam jaringan tubuh.
Faktor distribusi ini dipengaruhi oleh
ukuran dan bentuk obat yang
digunakan, komposisi jaringan tubuh,
distribusi obat dalam cairan atau
jaringan tubuh, ikatan dengan protein
plasma dan jaringan.
Proses yang dialami obat dalam tubuh
Fase distribusi
Fase absorbsi
6. fase ini dikenal juga dengan
metabolisme obat, dimana terjadi
proses perubahan struktur kimia obat
yang dapat terjadi didalam tubuh dan
dikatalisis olen enzim.
merupakan proses pengeluaran
metabolit yang merupakan hasil dari
biotransformasi melalui berbagai organ
ekskresi. Kecepatan ekskresi ini akan
mempengaruhi jecepatan eliminasi
atau pengulangan efek obat dalam
tubuh.
Proses yang dialami obat dalam tubuh
Fase ekskresi
Fase biotransformasi
7. Prinsip-Prinsip Farmakodinamika
Mekanisme Kerja
Obat
Obat menimbulkan efek
melalui interaksi dengan
reseptor pada sel
organisme. Interaksi obat
dengan reseptornya dapat
menimbulkan perubahan
biokimiawi sebagal respon
khas dari obat tersebut.
Interaksi obat
Interaksi obat adalah
pengaruh obat terhadap
obat lain didalam tubuh.
Interaksi obat dapat terjadi
pada farmakokinetik,
farmakodinamik dan
interaksi gabungan.
Reseptor sel
Reseptor adalah molekul yang
menerima sinyal kimia dari luar
sel. Ketika sinyal kimia tersebut
berikatan dengan reseptor,
maka terjadi beberapa bentuk
respon seller, misal perubahan
aktivitas listriksel.Reseptor
berlokasi di membran sel,
sitoplasma dan nukleus
8. Prinsip-Prinsip Farmakodinamika
Intaraksi
obat-resptor
Interaksi obat dengan reseptor adalah
pembentukan komplek obat
reseptor.Komplek obat reseptor terbentuk
dan berapa besar terbentuk bergantung pada
affinitas obat terhadap reseptor. Kemampuan
obat untuk menimbulkan rangsang dan
membentuk komplek dengan reseptor
disebut aktivitas intrinsik.
Efek terapeutik
Tidak semua obat mampu
memberikan efek
menyembuhkan penyakit,
beberapa obat dibuat hanya
untuk meniadakan atau
meringankan gejala penyakit.
10. Absorbsi
Absorpsi adalah perpindahan obat
dari tempat pemberian menuju
sirkulasi sistemik. Untuk memasuki
aliran sistemik, obat harus dapat
melintasi membran sel/barrier (sel
usus halus, pembuluh darah, sel glia di
otak, sel saraf). Membran ini dapat
dilewati dengan mudah oleh zat-zat
tertentu, namun ada juga zat yang
sukar dilewati, sehingga membran ini
seringkali disebut sebagai membran
semipermeable.
11. Bentuk sediaan
Jenis membran
sel
Rute pemberian
total luas
permukaan tempt
absorpsi
Aliran darah
ketempat absorbs
waktu kontak
permukaan
absorpsi
Faktor yang mempengaruhi proses absorbs:
12. Distribusi
Distribusi obat adalah proses obat
dihantarkan dari sirkulasi sistemik ke
jaringan dan cairan tubuh.Distribusi
obat tergantung pada beberapa
faktor, salah satunya aliran darah.
Pada awal distribusi, obat mengikuti
aliran darah menuju jaringan/organ
yang memiliki perfusi tinggi dengan
darah seperti jantung, paru-paru,
ginjal dan hati. selingga cepat terjadi
keseimbangan dengan sirkulasi
sistemik.
13. Pada tahap selanjutnya, obat
akan terdistribusi ke jaringan
lemak, tulang, otot, kulit dan
jaringan ikat lain yang
mempunyai perfusi lebih rendah.
Pada tahapan ini, obat dapat
terakumulasi dalam jaringan
akibat perbedaan pH, ikatan
dengan komponen intraseluler
atau partisi ke dalam lemak. Obat
yang terakumulasi di dalam
jaringan ini dapat digunakan
sebagai cadangan dalam jumlah
bear dan akan mempertahankan
konsentrasi obat dalam plasma,
karena sifatnya yang reversibel.
14. Metabolisme
Metabolisme adalah suatu
biotransformasi obatsecara kimia
menjadi metabolitnya di dalam
tubuh.Organ metabolisme utama
adalah liver. Metabolismeobat
memiliki tujuan dasar yaitu
mengubah zat aktifmenjadi tidak
aktif, dan zat yang tidak larut
airmenjadi lebih larut air, sehingga
Capat dengan mudahdiekskresikan
melalui urine.
15. Ekskressi/eliminasi
Ekskresi adalah pengeluaran obat dari tubuh terutama
melalui ginjal ginjal bersama urine, melaluiempedu ke
dalam usus bersama tinja, melalui keringat, kulit dan air
susu ibu, serta dikeluarkan dalam bentuk metabolit
maupun bentuk asalnya.
17. —Someone Famous
“This is a quote, words
full of wisdom that
someone important
said and can make the
reader get inspired.”
18. The slide title goes here!
Do you know what helps you make your point clear?
Lists like this one:
● They’re simple
● You can organize your ideas clearly
● You’ll never forget to buy milk!
And the most important thing: the audience won’t
miss the point of your presentation
19. General characteristics
Do you know what helps you make your point clear?
Lists like this one:
● They’re simple
● You can organize your ideas clearly
● You’ll never forget to buy milk!
And the most important thing: the audience won’t
miss the point of your presentation
24. Maybe you need to divide the content
Mercury
Mercury is the closest planet to
the Sun and the smallest one in
the Solar System—it’s only a bit
larger than the Moon
Venus
Venus has a beautiful name
and is the second planet from
the Sun. It’s hot and its
atmosphere is poisonous
27. A picture always
reinforces
the concept
Images reveal large amounts
of data, so remember: use an
image instead of long texts
28. Images reveal large amounts of data,
so remember: use an image instead
of a long text. Your audience will
appreciate it
A picture always
reinforces the concept
29. Images reveal large amounts of
data, so remember: use an
image instead of a long text.
Your audience will appreciate it
A picture always
reinforces the concept
34. Mercury is the smallest
planet of them all
Venus is the second
planet from the Sun
35% 65%
Enterprises E-commerce
Areas of expertise
35. Use a graph to show your data
Venus
Mars
Jupiter
To modify this graph, click on it, follow the link, change the data and replace it
32%
78%
45%
36. Mercury is the smallest planet
in the Solar System
Venus is the second planet
from the Sun
Earth is the only planet that
harbors life
Despite being red, Mars is
actually a cold place
Competitor A
Competitor C
Competitor B
Competitor D
Our competitors
37. Jupiter is the biggest
planet of them all
Saturn is a gas giant
and has several rings
Mercury is the smallest
planet of them all
Ceres is located in the
main asteroid belt
Neptune is the farthest
planet from the Sun
Service #1 Service #2 Service #3
Service #4 Service #5
Our services
38. Reviewing concepts is a good idea
Mercury
Mercury is the closest
planet to the Sun
Venus
Venus has a beautiful
name, but it’s terribly hot
Mars
Despite being red, Mars is
a cold place
Jupiter
It’s the biggest planet in
the Solar System
Saturn
Saturn is the ringed
planet and a gas giant
Neptune
Neptune is the farthest
planet from the Sun
39. Saturn is a gas giant
and has several rings
Specialty C
Specialty A Mercury is the closest
planet to the Sun
Specialty B
Venus is the second
planet from the Sun
Earth is the third planet
from the Sun
Specialty D
Despite being red, Mars
is actually a cold place
Our specialties
Specialty E Jupiter is the biggest
planet of them all
Specialty F
40. Use a graph to show your data
To modify this graph, click on it,
follow the link, change the data
and paste the new graph here
Venus
Mars
Jupiter
45.7%
50%
4.3%
41. Our clients
Earth
Earth is the only
planet that has life
Mercury
Mercury is a close
planet to the Sun
Venus
Venus has really
high temperatures
Follow the link in the graph to modify its data and then
paste the new one here. For more info, click here
100
0
25
50
75
Mars Mars Mars
42. Infographics make your idea understandable...
Despite being red, Mars is a cold place
Mercury is the closest planet to the Sun
Jupiter is the biggest planet
Venus is terribly hot
43. How our system works
Pluto
Pluto is now seen as
a dwarf planet
Ceres is in the main
asteroid belt
Ceres
The Moon is Earth’s
only natural satellite
The Moon
44. Business chart
Venus has a
beautiful name
Idea A
Mars is actually
a cold place
Idea B
Saturn has
several rings
Idea C
Ceres is in an
asteroid belt
Idea D
Mercury is the smallest planet in the
entire Solar System
A successful business
Earth is where
we all live on
Earth
Jupiter is the
biggest planet
Jupiter
Neptune is far
away from us
Neptune
The Moon is
Earth’s satellite
The Moon
49. This is a map
Venus has a
beautiful name
Jupiter is the
biggest planet
Mars is a cold
place to live on
50. Our locations
The Moon is Earth’s only
natural satellite
Design office
The Sun is the star at the
center of the Solar System
Headquarters
Ceres is located in the
main asteroid belt
Admin office
51. A timeline always works well
We all live
on Earth
Jupiter is a
big planet
Mars is a
cold place
Venus is
very hot
Day 1 Day 2 Day 3 Day 4
52. Continue your timeline
We all live
on Earth
Jupiter is a
big planet
Mars is a
cold place
Venus is
very hot
Day 5 Day 6 Day 7 Day 8
53. Another slide with three columns
Mercury
Mercury is the closest
planet to the Sun and
the smallest one in the
Solar System
Venus
Venus has a beautiful
name and is the
second planet from the
Sun. It’s terribly hot
Despite being red, Mars
is actually a very cold
place. It’s full of iron
oxide dust
Mars
54. 1981
Mercury is the smallest
planet of them all
1961
Saturn is a gas giant and
has several rings
1969 Jupiter is the biggest
planet of them all
59. Our team
Maria
You can speak a bit
about this person here
Luis
You can speak a bit
about this person here
Ana
You can speak a bit
about this person here
60. Our team
Ana Alvarado
You can speak a bit
about this person here
Adam Williamson
You can speak a bit
about this person here
61. Desktop mockup
You can replace the image on
the screen with your own work.
Just delete this one, add yours
and center it properly
62. Tablet mockup
You can replace the image on
the screen with your own work.
Just delete this one, add yours
and center it properly
63. Phone mockup
You can replace the image on
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Just delete this one, add yours
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64. You can replace the images on the screen with your own work.
Just right-click on them and select “Replace image”
Mockup devices
65. CREDITS: This presentation template was created
by Slidesgo, including icons by Flaticon, and
infographics & images by Freepik
Thanks!
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67. Alternative resources
PHOTOS
● Smart phone with white display screen on white table
● Business executives discussing with their colleagues
● Business people at the office
● Group of young professionals working together
● Portrait of young male enjoying work
● Woman working with laptop
68. Alternative premium resources
Here’s an assortment of alternative resources whose style fits the one of this template:
PHOTOS
● Full shot colleagues working together
● Full shot smiley colleagues posing together
● High angle people working together
● High angle smiley colleagues working
● Business man banner concept with copy space
● Business woman banner concept with copy space I
● Business woman banner concept with copy space II
● Business colleagues banner concept with copy space I
● Business colleagues banner concept with copy space II
● Empowered business woman working in the city I
● Empowered business woman working in the city II
● Empowered business woman working in the city III
● Financial independent woman buying new house
● Three businesspeople looking at business report in the office
● Medium shot man working on laptop
69. Resources
Did you like the resources on this template? Get them for free at our other websites.
PHOTOS
● Man and woman coworking with papers
● Thoughtful man at laptop in office
● Cheerful coworkers with papers
● Cheerful people in office
● Thoughtful people doing paperwork
● Collaborating man and woman with papers
● Lovely woman working in office
● Happy successful female student posing with arms crossed
● Portrait of a smiling young man in eyewear
● Portrait of a smiling casual woman
● Minimalistic working desk with blank monitor screen
● White stationery and tablet on desk
● Top view smartphone template over workspace
70. Premium resources
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Get them for free at our other websites.
PHOTOS
● Smiley woman at work medium shot
● Businessman and a businesswoman
● Young man using laptop with coffee
cup and digital tablet on kitchen
counter
● Industrial designers working on 3d
model
● Empowered business women working
● Medium shot empowered business
woman
● Teamwork concept with business
people
● Low angle womens team meeting
● Group of businesspeople looking at
business plan in the office
● Close-up of a woman examining
document
● Smiling young woman working at
laptop in office
● Ethnic young employee working at
laptop
● Front view women working together
ICONS
● Mentoring and Training | Lineal
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73. Create your Story with our illustrated concepts. Choose the style you like the most, edit its colors, pick
the background and layers you want to show and bring them to life with the animator panel! It will boost
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Storyset
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75.
76.
77. JANUARY FEBRUARY MARCH APRIL
PHASE 1
Task 1
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JANUARY FEBRUARY MARCH APRIL MAY JUNE
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78.
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87. Add the title here
Text 1 Text 2 Text 3
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2016 2017 2018 2019 2020
“Despite being red,
Mars is actually a
very cold place”
“Mercury is the
smallest planet in
the Solar System”
“Neptune is the
farthest planet from
the Sun”
“Saturn is a gas
giant and has
several rings”
“Venus is the
second planet from
the Sun and is
terribly hot”
Premium infographics
88. “Mercury is the
smallest planet in the
Solar System”
TITLE 1
“Despite being red,
Mars is actually a
very cold place”
“Jupiter is the
biggest planet in the
entire Solar System”
“Saturn is a gas
giant and has
several rings”
75%
Premium infographics
75%