4 - Drug Delivery Modalities & The plasma Concentration Curve Flashcards

1
Q

What is the most common enteral route of drug administration

A

Oral — easy to take, can be modified (e.g., enteric-coated, extended-release)

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2
Q

What is the benefit of sublingual administration

A

Rapid absorption and bypasses first-pass metabolism (e.g., glyceryl trinitrate for angina)

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3
Q

When is rectal administration used

A

When oral intake isn’t possible; partial bypass of first-pass metabolism (e.g., diazepam for seizures)

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4
Q

Which parenteral route provides the fastest systemic effect

A

Intravenous (IV) — fast and direct

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5
Q

What is a key feature of intramuscular (IM) administration

A

Moderate absorption; can be sustained with depot formulations

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6
Q

What is the absorption profile of subcutaneous (SC) administratio

A

Slower absorption with sustained release

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7
Q

What is the benefit of intrathecal administration

A

Bypasses the blood–brain barrier (e.g., epidural)

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8
Q

Which route provides rapid systemic absorption of anaesthetics?

A

Inhalation

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9
Q

What is the effect of topical/cutaneous drug administration

A

Localised effect (e.g., steroid creams), with some systemic absorption possible (e.g., nicotine patches)

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10
Q

What does the plasma concentration curve describe

A

Drug concentration in plasma over time after administration

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11
Q

What can we learn from the plasma concentration curve

A

Onset, peak effect, duration, and therapeutic range

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12
Q

What factors affect the plasma concentration curve

A
  1. Route of administration
  2. Drug formulation (e.g., extended-release)
  3. Elimination rate (slow vs. fast clearance)
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13
Q

What percentage of body volume is blood plasma

A

55%

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14
Q

What does blood plasma contain

A

Proteins

Glucose

Clotting factors

Electrolytes

Hormones

CO2

Drugs.

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15
Q

How are drug concentrations in plasma measured

A

By mass spectrometry or HPLC, using plasma samples at different time points

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16
Q

What is the therapeutic window

A

The range between the Minimum Effective Concentration (MEC) and the Maximum Tolerated Concentration (MTC)

17
Q

What is the goal of repeated dosing

A

To maintain drug levels within the therapeutic window

18
Q

What is therapeutic drug monitoring used for

A

Drugs with a narrow therapeutic window (e.g., HIV medications)

19
Q

What is the pharmacokinetic profile of IV morphine for acute pain

A

Rapid peak, short duration

20
Q

How do oral antibiotics behave pharmacokinetically

A

Slower absorption, lower peak, longer duration

21
Q

What is the effect of enteric-coated tablets

A

Delayed release and prolonged peak effect

22
Q

Why is IV morphine used for acute pain

A
  1. Rapid absorption and effect.
  2. High peak concentration quickly relieves pain.
  3. Rapid distribution throughout the body. Ideal when the patient is in agony and needs immediate relief
23
Q

Why use an IV infusion for antibiotics

A

Provides longer-term effect without a high systemic peak

Reduces side effects due to lower peak concentration

Delivers a sustained therapeutic level

Offers moderate distribution and elimination — ideal for controlled treatment of infection

24
Q

What are the benefits of long-term oral antibiotics for infections

A

Convenient — no need for frequent dosing

Slower absorption and lower peak (reduced side effects)

Slower distribution and elimination — provides extended effect over time. Ideal when compliance and convenience are priorities

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DIAGRAMS OF PLASMA CONCENTRATION CURVES ON ONENOTE