Thermodynamics and Energy Transfer Quiz
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Questions and Answers

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?

  • 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?

  • 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)?

<p>It represents the absence of any molecular motion. (C)</p> Signup and view all the answers

According to the content, what is the key difference between work and heat?

<p>Work is the transfer of energy in an ordered fashion, while heat is the transfer of energy due to random molecular motion. (A)</p> Signup and view all the answers

Which of the following scenarios BEST exemplifies the transfer of energy as heat?

<p>A hot cup of coffee cooling down in a room. (D)</p> Signup and view all the answers

Based on the provided information, what is the difference between a closed system and an open system?

<p>A closed system cannot exchange matter with its surroundings, while an open system can exchange both matter and energy. (B)</p> Signup and view all the answers

Which of the following is NOT an example of an energy transfer that can be described as work?

<p>A pot of water being heated on a stove. (D)</p> Signup and view all the answers

Which of the following is NOT a crucial consideration in the successful delivery of drugs to the front of the eye?

<p>The rate of drug absorption into the retina must be maximized. (C)</p> Signup and view all the answers

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?

<p>It will be cleared from the eye quickly due to the natural defense mechanisms. (E)</p> Signup and view all the answers

The text highlights that the transcellular pathway for drug absorption is particularly relevant for what type of drugs?

<p>Small, hydrophobic drugs. (D)</p> Signup and view all the answers

Which of the following is TRUE regarding the absorption of drugs into the corneal or conjunctival tissue?

<p>The absorption process is primarily governed by the diffusion of drugs down a concentration gradient. (D)</p> Signup and view all the answers

Based on the provided information, large drug particles are more likely to be found in which location?

<p>The upper airways. (D)</p> Signup and view all the answers

What is the primary purpose of understanding the pharmacokinetics of a drug?

<p>To ensure the drug reaches the correct site at the right dose and rate (B)</p> Signup and view all the answers

Which term refers to the other components of a formulation aside from the active pharmaceutical ingredient?

<p>Excipient (C)</p> Signup and view all the answers

What is the difference between branded drugs and generic drugs primarily based on?

<p>The length of the patent protection period (A)</p> Signup and view all the answers

What is described as the process of combining active pharmaceutical ingredients with excipients?

<p>Drug formulation (B)</p> Signup and view all the answers

Why are medicines legally protected under intellectual property rights?

<p>To facilitate innovation and recover R&amp;D costs (B)</p> Signup and view all the answers

What does the term bioavailability refer to in the context of pharmaceuticals?

<p>The proportion of a drug that enters systemic circulation (B)</p> Signup and view all the answers

What does the term 'pharmacodynamics' primarily study?

<p>The effects and mechanisms of action of drugs on the body (D)</p> Signup and view all the answers

What is a significant advantage of using generic medicines?

<p>They are typically less expensive for consumers (B)</p> Signup and view all the answers

What is the percentage saving that generic medicines can offer compared to their branded counterparts?

<p>Up to 80% (B)</p> Signup and view all the answers

Which of the following statements about prescribing by generic name is true?

<p>Prescribing generic medicines can lead to significant cost savings. (A)</p> Signup and view all the answers

Which condition may require a patient to stay on a branded medicine due to absorption differences?

<p>Epilepsy (D)</p> Signup and view all the answers

What is one of the roles of pharmacists when dispensing generic medicines?

<p>To have the widest choice of products to dispense. (A)</p> Signup and view all the answers

What might be a consequence of substituting biological medicines with their generic equivalents?

<p>Greater variation in absorption rates. (B)</p> Signup and view all the answers

What is a potential drawback of modifying a medication's preparation into a generic form?

<p>Changed therapeutic effect due to absorption rates. (A)</p> Signup and view all the answers

Which of the following resources can provide further information about the guidelines for prescribing generic medicines?

<p>NHS guidance documents. (B)</p> Signup and view all the answers

What is the median percentage of generic prescriptions in UK GP practices?

<p>83% (B)</p> Signup and view all the answers

Which of the following factors directly influences the rate of drug liberation from oral dosage forms?

<p>The dosage form and excipients used (C)</p> Signup and view all the answers

What is the correct sequence of steps for drug dissolution and absorption from oral dosage forms?

<p>Dissolution, diffusion, absorption (C)</p> Signup and view all the answers

Which law can be applied to describe the passive diffusion of drugs across biological membranes?

<p>Fick’s First Law (A)</p> Signup and view all the answers

How does lipophilicity affect drug absorption and diffusion?

<p>Enhances the rate of drug diffusion across membranes (D)</p> Signup and view all the answers

According to the Noyes-Whitney equation, which factor is NOT directly affecting the rate of drug dissolution?

<p>The color of the dosage form (B)</p> Signup and view all the answers

What step is considered to control the overall rate of drug release from a dosage form?

<p>Disintegration of the dosage form (C)</p> Signup and view all the answers

In the context of drug diffusion, what does the Stokes-Einstein equation primarily relate to?

<p>The diffusivity of small drug molecules in a solvent (A)</p> Signup and view all the answers

Which of the following describes the term 'bioavailability' in pharmacology?

<p>The rate and extent to which a drug is absorbed into systemic circulation (C)</p> Signup and view all the answers

Which of the following physiochemical properties are NOT directly relevant to the pre-formulation of solid dosage forms?

<p>Odor (C)</p> Signup and view all the answers

What is the primary role of excipients in solid dosage forms?

<p>To provide structural support and aid in processing the formulation (A)</p> Signup and view all the answers

Which of these is NOT a factor influencing drug absorption via different routes?

<p>Patient's mood and emotional state (C)</p> Signup and view all the answers

How does the concept of 'pH and pKa' affect drug absorption in the gastrointestinal (GI) tract?

<p>It influences the degree of ionization of the drug, affecting its permeability across membranes. (B)</p> Signup and view all the answers

Why is the concept of bioavailability crucial in drug development?

<p>It predicts the therapeutic effectiveness of the drug in a patient. (D)</p> Signup and view all the answers

Which of the following organs plays the most significant role in drug elimination from the body?

<p>Kidney (D)</p> Signup and view all the answers

What is the primary difference between a generic drug and a brand-name drug?

<p>Generic drugs are chemically equivalent to brand-name drugs, but are often manufactured by different companies. (C)</p> Signup and view all the answers

Which of the following factors does NOT directly influence the rate of drug dissolution?

<p>Patient's age and gender (D)</p> Signup and view all the answers

Flashcards

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

The study of how the body affects a drug over time.

Absorption

The process where a drug moves from the site of administration into the bloodstream.

Distribution

The distribution of a drug throughout your body, reaching its target tissues.

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Metabolism

The breakdown of a drug in the body, usually by the liver, making it inactive.

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Elimination

The process by which the body eliminates a drug, typically through urine, feces, or breath.

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What is a medicine?

Any product used to diagnose, cure, mitigate, treat or prevent a disease.

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Medicinal Product

The presentation of a drug in a dosage form suitable for administration to the public.

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Drug/API (Active Pharmaceutical Ingredient)

The active ingredient in a medicine that produces the desired therapeutic effect.

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Excipient

All the other components of a formulation other than the active drug. They help with things like taste, stability, and delivery.

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Formulation

The process of combining APIs and excipients to create a medicinal product that is safe and effective.

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Brand Name

The name given to a medication by the company that developed it. It is a registered trademark.

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Chemical Name

The scientific name for the active ingredient in a medicine, decided by an expert committee.

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Innovator

The company that originally developed a medicine and holds the patent for it.

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Generic Medicines

Medicines that contain the same active ingredients as branded medicines but are not manufactured by the original company. They are generally less expensive.

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Generic Prescribing

Encouraging doctors to prescribe medicines by their generic names instead of brand names to save on costs and offer more choice.

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Generic Penetration

The percentage of generic medicines used in a particular market. High penetration indicates widespread use of generics.

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Biological Medicines

A specialized, complex medicine that cannot be exactly copied and has its own biosimilar versions, requiring specific manufacturer information.

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Dosage Forms

Dosage forms influence how medicines are taken and absorbed by the body. For instance, tablets, capsules, or solutions. They help with targeted delivery.

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Drug absorption

The process by which a drug moves from the site of administration into the bloodstream.

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Work

The transfer of energy in an ordered fashion. It's about overcoming energy barriers.

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Heat

The transfer of energy in a random fashion due to molecular motion. It's associated with temperature differences.

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Internal Energy (U)

The total energy contained within a system. It includes all forms of energy, like kinetic and potential.

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Isolated System

A system that exchanges neither matter nor energy with its surroundings. It's completely isolated.

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Closed System

A system that exchanges energy but not matter with its surroundings. Think of a hot air balloon – it loses heat but not air.

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Open System

A system that exchanges both energy and matter with its surroundings. Think of a cooking pot – you add ingredients and heat.

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Temperature

The propensity of heat to flow from a hotter body to a colder one. It's a measure of the average kinetic energy of molecules.

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Joule (J)

The unit used to measure energy, including both work and heat. One Joule is the amount of energy required to move one Newton of force over one meter.

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Drug Dissolution

The process by which a solid drug dissolves into a liquid solution, making it available for absorption by the body.

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Noyes-Whitney Equation

A mathematical equation that describes the rate of dissolution of a solid drug, taking into account factors like surface area, solubility, and diffusion coefficient.

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Passive Diffusion

The movement of a drug molecule across a membrane, from an area of high concentration to an area of low concentration, driven by the concentration gradient.

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Fick's First Law

A fundamental principle of diffusion, stating that the rate of diffusion is proportional to the concentration gradient.

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Diffusion Coefficient

A measure of how easily a molecule can move through a liquid medium.

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Stokes-Einstein Equation

A formula that relates the diffusion coefficient of a spherical molecule to its size and the viscosity of the medium.

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Lipophilicity

The ability of a drug to dissolve in a lipid (fat-like) environment. This is crucial for drug absorption, as cell membranes are mostly lipid-based.

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Drug Release

The process by which a drug is released from its dosage form, making it available for dissolution and absorption.

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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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