01 Flashcards

1
Q

Systemic Administration (definition)

A

The entire body is exposed to the drug, generally AFTER the drug reaches the circulatory system.

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2
Q

Categories of Systemic administration

A

1- Enteral administration
2- Parenteral Administration

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3
Q

Difference between enteral and parenteral administration?

A

Enteral adm : via GI
BUT
Parenteral: not via GIA

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4
Q

Examples of Enteral administration ?

A

1- Oral
2- Sublingual
3- Buccal
4- Rectal

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5
Q

Examples of parenteral administration ?

A

1- Intravenous (IV)
2- subcutaneous (SC)
3- Intramuscular (IM)
4- Surgical implants
5- Transdermal patches

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6
Q

Pros and cons of Parenteral administration?

A

(+) No hepatic first pass effect

(-) other absorption barriers

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7
Q

How do intravenous (IV), subcutaneous (SC), and intramuscular (IM) routes differ?

A
  • Intravenous (IV): Administers the drug directly into the general circulation.
  • Subcutaneous (SC) and Intramuscular (IM): Create a depot of drug at the iinjection site (under the skin or in the muscle).
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8
Q

What are the considerations for subcutaneous (SC) and intramuscular (IM) routes?

A

_No first pass effect.
_Reduced Absorption (drug degradation before reaching circulation).

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9
Q

What is local administration?

A

Local administration involves delivering the drug directly to its site of action (e.g., lotions, nasal sprays, eye drops, inhalers).

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10
Q

What are the advantages of local administration?

A

Restricts the drug site of action to a specific tissue or organ, minimizing systemic exposure and adverse events.

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11
Q

What is the key consideration for local administration?

A

Even locally administered drugs may reach the systemic circulation to some extent.

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12
Q

What are the key pharmacokinetic parameters associated with drug administration?

A

1- Clearance
2- Volume of distribution
3- Half-life
4- Bioavaibility

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13
Q

What is Clearance (CL)?

A

The rate at which a drug is removed from the body.

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14
Q

What is Volume of Distribution?

A

The extent to which a drug is distributed throughout the body.

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15
Q

What is Half-life?

A

The time it takes for the drug’s plasma concentration to reduce by half. Driven by the drug’s clearance and volume of distribution.

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16
Q

What is Bioavailability?

A

The extent to which a drug reaches the systemic circulation. Important for all non-IV injection routes. IV-administered drugs are 100% bioavailable