Barbiturates Flashcards

1
Q

From what chemical compound are barbiturates derived?

A

Barbituric acid

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2
Q

Why is barbituric acid not used as an anesthetic?

A

It lacks hypnotic properties

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3
Q

Substitutions at which positions in the barbituric acid molecule make barbiturates thio or oxy barbiturates.

A

Position 2

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4
Q

Substituting a _________ atom at position 2 on a barbituric acid molecule creates a thiobarbiturate

A

Sulfur

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5
Q

Substituting a _____ atom at position 2 in the barbituric acid molecule creates an oxybarbiturate.

A

Oxygen

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6
Q

Is sodium pentothal an oxybarbiturate or thiobarbiturate?

A

Thiobarbiturate

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7
Q

Is methohexital an oxybarbiturate or a thiobarbiturate?

A

Oxybarbiturate

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8
Q

The type and position of substitutions on the barbituric acid molecule affects what properties of the drug?

A
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9
Q

The pH of thiopental and methohexital is alkaline, neutral or acidic

A

Alkaline

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10
Q

The pH of thiopental and methohexital is_____.

A

higher than 10

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11
Q

What are the advantages of the high pH of barbiturates?

A

It prevents bacterial growth and

Increases shelf life

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12
Q

What is the disadvantage of the high pH of barbiturates?

A

It will precipitate when mixed with acidic drugs such as neuromuscular blockers

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13
Q

What is the hazard of preciptation in an IV line?

A

It can irreversibly block intravenous delivery lines

Can form emboli

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14
Q

Are thiopental and methohexital R isomers, D isomers or a racemic mixture of isomers?

A

Racemic mixture their potencies are the summation of the potencies of the individual isomers

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15
Q

How are thiopental and methohexital metabolized?

A
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16
Q

Are metabolites of thiopental and methohexital acitve or inactive?

A

Inactive

17
Q

How are metabolites of thiopental and methohexital excreted?

A

Through the urine and after cojugation thorugh bile

18
Q
A
19
Q

How is pheobarbital metabolized and excreted?

A

It is not metabolized. It is eliminated unchagned thorugh renal excretion.

20
Q

W

A