Podcast
Questions and Answers
Which of the following statements best describes the relationship between temperature and heat?
Which of the following statements best describes the relationship between temperature and heat?
- Temperature is a measure of the average kinetic energy of the particles in a system. (correct)
- Temperature is a measure of the rate at which heat flows from one body to another.
- Temperature is a measure of the potential energy of a system due to its position or state.
- Temperature is a measure of the total amount of heat energy in a system.
Which of the following units is used to measure the transfer of energy due to random molecular motion, as described in the content?
Which of the following units is used to measure the transfer of energy due to random molecular motion, as described in the content?
- Joule (J) (correct)
- Fahrenheit (°F)
- Celsius (°C)
- Kelvin (K)
Which temperature scale assigns the freezing point of water as 0°C and the boiling point as 100°C?
Which temperature scale assigns the freezing point of water as 0°C and the boiling point as 100°C?
- Fahrenheit
- Newton
- Kelvin
- Celsius (correct)
Based on the text, which of the following statements accurately describes the zero of the thermodynamic temperature scale (Kelvin scale)?
Based on the text, which of the following statements accurately describes the zero of the thermodynamic temperature scale (Kelvin scale)?
According to the content, what is the key difference between work and heat?
According to the content, what is the key difference between work and heat?
Which of the following scenarios BEST exemplifies the transfer of energy as heat?
Which of the following scenarios BEST exemplifies the transfer of energy as heat?
Based on the provided information, what is the difference between a closed system and an open system?
Based on the provided information, what is the difference between a closed system and an open system?
Which of the following is NOT an example of an energy transfer that can be described as work?
Which of the following is NOT an example of an energy transfer that can be described as work?
Which of the following is NOT a crucial consideration in the successful delivery of drugs to the front of the eye?
Which of the following is NOT a crucial consideration in the successful delivery of drugs to the front of the eye?
Based on the provided information, which of the following is the MOST LIKELY fate of a drug particle greater than 10 µm delivered to the human eye?
Based on the provided information, which of the following is the MOST LIKELY fate of a drug particle greater than 10 µm delivered to the human eye?
The text highlights that the transcellular pathway for drug absorption is particularly relevant for what type of drugs?
The text highlights that the transcellular pathway for drug absorption is particularly relevant for what type of drugs?
Which of the following is TRUE regarding the absorption of drugs into the corneal or conjunctival tissue?
Which of the following is TRUE regarding the absorption of drugs into the corneal or conjunctival tissue?
Based on the provided information, large drug particles are more likely to be found in which location?
Based on the provided information, large drug particles are more likely to be found in which location?
What is the primary purpose of understanding the pharmacokinetics of a drug?
What is the primary purpose of understanding the pharmacokinetics of a drug?
Which term refers to the other components of a formulation aside from the active pharmaceutical ingredient?
Which term refers to the other components of a formulation aside from the active pharmaceutical ingredient?
What is the difference between branded drugs and generic drugs primarily based on?
What is the difference between branded drugs and generic drugs primarily based on?
What is described as the process of combining active pharmaceutical ingredients with excipients?
What is described as the process of combining active pharmaceutical ingredients with excipients?
Why are medicines legally protected under intellectual property rights?
Why are medicines legally protected under intellectual property rights?
What does the term bioavailability refer to in the context of pharmaceuticals?
What does the term bioavailability refer to in the context of pharmaceuticals?
What does the term 'pharmacodynamics' primarily study?
What does the term 'pharmacodynamics' primarily study?
What is a significant advantage of using generic medicines?
What is a significant advantage of using generic medicines?
What is the percentage saving that generic medicines can offer compared to their branded counterparts?
What is the percentage saving that generic medicines can offer compared to their branded counterparts?
Which of the following statements about prescribing by generic name is true?
Which of the following statements about prescribing by generic name is true?
Which condition may require a patient to stay on a branded medicine due to absorption differences?
Which condition may require a patient to stay on a branded medicine due to absorption differences?
What is one of the roles of pharmacists when dispensing generic medicines?
What is one of the roles of pharmacists when dispensing generic medicines?
What might be a consequence of substituting biological medicines with their generic equivalents?
What might be a consequence of substituting biological medicines with their generic equivalents?
What is a potential drawback of modifying a medication's preparation into a generic form?
What is a potential drawback of modifying a medication's preparation into a generic form?
Which of the following resources can provide further information about the guidelines for prescribing generic medicines?
Which of the following resources can provide further information about the guidelines for prescribing generic medicines?
What is the median percentage of generic prescriptions in UK GP practices?
What is the median percentage of generic prescriptions in UK GP practices?
Which of the following factors directly influences the rate of drug liberation from oral dosage forms?
Which of the following factors directly influences the rate of drug liberation from oral dosage forms?
What is the correct sequence of steps for drug dissolution and absorption from oral dosage forms?
What is the correct sequence of steps for drug dissolution and absorption from oral dosage forms?
Which law can be applied to describe the passive diffusion of drugs across biological membranes?
Which law can be applied to describe the passive diffusion of drugs across biological membranes?
How does lipophilicity affect drug absorption and diffusion?
How does lipophilicity affect drug absorption and diffusion?
According to the Noyes-Whitney equation, which factor is NOT directly affecting the rate of drug dissolution?
According to the Noyes-Whitney equation, which factor is NOT directly affecting the rate of drug dissolution?
What step is considered to control the overall rate of drug release from a dosage form?
What step is considered to control the overall rate of drug release from a dosage form?
In the context of drug diffusion, what does the Stokes-Einstein equation primarily relate to?
In the context of drug diffusion, what does the Stokes-Einstein equation primarily relate to?
Which of the following describes the term 'bioavailability' in pharmacology?
Which of the following describes the term 'bioavailability' in pharmacology?
Which of the following physiochemical properties are NOT directly relevant to the pre-formulation of solid dosage forms?
Which of the following physiochemical properties are NOT directly relevant to the pre-formulation of solid dosage forms?
What is the primary role of excipients in solid dosage forms?
What is the primary role of excipients in solid dosage forms?
Which of these is NOT a factor influencing drug absorption via different routes?
Which of these is NOT a factor influencing drug absorption via different routes?
How does the concept of 'pH and pKa' affect drug absorption in the gastrointestinal (GI) tract?
How does the concept of 'pH and pKa' affect drug absorption in the gastrointestinal (GI) tract?
Why is the concept of bioavailability crucial in drug development?
Why is the concept of bioavailability crucial in drug development?
Which of the following organs plays the most significant role in drug elimination from the body?
Which of the following organs plays the most significant role in drug elimination from the body?
What is the primary difference between a generic drug and a brand-name drug?
What is the primary difference between a generic drug and a brand-name drug?
Which of the following factors does NOT directly influence the rate of drug dissolution?
Which of the following factors does NOT directly influence the rate of drug dissolution?
Flashcards
ADME
ADME
The journey of a drug from when it enters your body until it leaves. This includes how the drug gets absorbed, distributed, metabolized, and eliminated.
Pharmacokinetics
Pharmacokinetics
The study of how the body affects a drug over time.
Absorption
Absorption
The process where a drug moves from the site of administration into the bloodstream.
Distribution
Distribution
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Metabolism
Metabolism
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Elimination
Elimination
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What is a medicine?
What is a medicine?
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Medicinal Product
Medicinal Product
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Drug/API (Active Pharmaceutical Ingredient)
Drug/API (Active Pharmaceutical Ingredient)
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Excipient
Excipient
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Formulation
Formulation
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Brand Name
Brand Name
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Chemical Name
Chemical Name
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Innovator
Innovator
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Generic Medicines
Generic Medicines
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Generic Prescribing
Generic Prescribing
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Generic Penetration
Generic Penetration
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Biological Medicines
Biological Medicines
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Dosage Forms
Dosage Forms
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Drug absorption
Drug absorption
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Work
Work
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Heat
Heat
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Internal Energy (U)
Internal Energy (U)
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Isolated System
Isolated System
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Closed System
Closed System
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Open System
Open System
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Temperature
Temperature
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Joule (J)
Joule (J)
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Drug Dissolution
Drug Dissolution
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Noyes-Whitney Equation
Noyes-Whitney Equation
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Passive Diffusion
Passive Diffusion
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Fick's First Law
Fick's First Law
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Diffusion Coefficient
Diffusion Coefficient
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Stokes-Einstein Equation
Stokes-Einstein Equation
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Lipophilicity
Lipophilicity
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Drug Release
Drug Release
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Study Notes
Fundamentals of Pharmacy/Pharmacology: The Science of Medicines
- This unit introduces the fundamentals of pharmacy and pharmacology, focusing on the science of medicines.
- The course is designed around lectures, problem-based learning, and workshops.
- Assessment is a combination of examinations and a problem-based learning assignment.
Lecture 1 - Unit Introduction
- Course content includes reasons to study the science of medicines, an overview of pharmacology and pharmaceutics, methods of teaching, and assessment.
- Year one units in pharmacy and pharmacology are presented
- Topics include chemistry of drugs, science of medicines, health and disease, and preparation for professional practice.
Lecture 2 - What is a Medicine?
- Learning objectives include drug delivery and absorption, the medicines development pipeline and the role of the science of medicines, bioavailability, pharmacokinetics and pharmacodynamics, as well as plasma concentration versus time profiles.
- Drug delivery and absorption routes are discussed.
- Pharmaceutics is presented as a very important aspect in the process
Lecture 3 - Concept of medicine and dosage forms, brands and generics.
- Intended learning outcomes include understanding of nomenclature of medicinal products, reason for protecting medicines, research and development strategies in the pharmaceutical industry, the difference between branded and generic drugs & benefits and potential drawbacks.
- Details of nomenclature, including brand names and chemical names, are provided
- The role of patents in the pharmaceutical industry is also detailed
Lecture 4 - Role of dosage forms and excipients. - Why different dosage forms
- This lecture covers the role of dosage forms and excipients in drug development
- Emphasis on different dosage forms, the importance of factors such as safety, stability, and appropriate taste masking for different delivery methods
- A wide range of examples relating to different types of drug formulations are provided
Lecture 7 - Physicochemical Properties of Small Drugs
- Learning objectives include drug release and dissolution, how dissolution can be described by the Noyes-Whitney equation, drugs absorption pathways passive diffusion of drugs and Fick's First Law, the application of the Stokes-Einstein equation to drug diffusion across membranes, the importance of lipophilicity, and how the physicochemical properties of small drugs affect their dissolution, diffusion, and absorption.
- This lecture details drug release and dissolution from solid oral forms (tablets/capulets)
- Descriptions of drug dissolution steps and their respective rate determining steps are discussed
- The Noyes-Whitney equation and related parameters are covered
Lecture 8 - Acid-Base Theory, pH, pKa, and pKb
- The lecture describes Lowry-Brønsted definitions of acids and bases, conjugate acid-base pairs, the dissociation of weakly acidic and basic drugs, the importance of the pKa and/or pKb values for different drugs, and how these values affect the degree of ionization.
- Focus on how pH affects drug ionization
- Key definitions and examples of various types of acids and bases are presented
Lecture 10 - Electrolytes and buffers
- The lecture covers strong and weak electrolytes, common ion effects, and buffer capacity.
- pH values from different body fluids are listed and studied
- Discussion of different buffer types for drug solubility
- Explanations of why many drugs are either weak acids or bases and how the degree of ionization is highly dependent on pH including the Henderson-Hasselbalch equation
Lecture 11 - Chemical kinetics and stability of dosage forms 1
- Learning outcomes include introduction to reaction kinetics, use of reaction kinetics, to determine the stability of pharmaceuticals, the determination of reaction orders and rate constants, and the use of the Arrhenius equation for determining reaction rate constants.
- Discusses zero and first order reaction kinetics, and their properties
- The concept of shelf life is also explored
Lecture 14 - Pre-formulation of solid dosage forms 1
- Preformulation is the initial stage in developing a dosage form
- The need for certain components such as pharmaceutical salts, crystalline forms and habits to ensure the drugs are administered to patients appropriately is discussed
- Types of solid forms are presented
Lecture 15 - Pre-formulation of solid dosage forms 2
- This covers how physical form impacts product functionality, bioavailability, stability, and formulation design challenges
- Discusses the rational design behind the choice of drug forms
- Understanding of the impact of crystalline solid structures like polymorphs, hydrates, and solvates is covered
Lecture 16 - Drug Solubility and Dissolution Rate 1
- The lecture includes solubility, (semi-quantitative units), solubility (in quantitative units), and the effect on drug absorption.
- Discusses drug dissolution processes, methods of determining solubility and how these parameters affect treatment
- Overview of how the rate of drug dissolving affect the overall impact of drugs in solution
Lecture 17 - Drug Solubility and Dissolution Rate 2
- The lecture covers the concepts of weak acids & bases, the Henderson-Hasselbalch equation, the effect of pH on drug ionization and related examples.
- This provides a framework to predict the outcome of drug behaviour
- Examples of weakly acidic and basic drugs are provided
Lecture 18 - Drug Solubility and Dissolution Rate 3
- This lecture covers understanding solubility and dissolution rates, classification of drugs according to their solubility in different conditions, and use of co-solvents to increase drug solubility.
- Describes methods for determining drug solubility and dissolution rate
Lecture 19 - Drug Solubility and Dissolution Rate 4
- This lecture covers understanding of the use of cyclodextrins to enhance solubility, methods of classification of surfactants, and their surfactant properties
Lecture 30 & 31 - Physiological factors affecting drug absorption after oral administration
- Learning outcomes are presented, detailing the process, and different physiological factors affecting drug absorption following oral administration.
- Details of gastrointestinal transit, active secretion, hepatic first pass effect, enterohepatic recycling, metabolism within the gastro-intestinal tract and types of oral dosage forms are discussed, including rate of absorption and drug effects
Lecture 32 - Absorption: Sublingual, buccal & rectal drug delivery
- This lecture examines the anatomy and physiology that affects drug absorption via sublingual, buccal and rectal routes
- Details of the physical properties and functionality of the drug in each area and the advantages and disadvantages of these routes are discussed
Other lectures
- The lectures and workshop content will likely cover various aspects of chemical and physical properties, dosage forms, drug interactions, and related physiological and anatomical factors.
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