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Pharmacology · Drugs in pregnancy: insulin and the placenta
Sample itemA woman with gestational diabetes not controlled by diet is started on insulin. Which property makes insulin suitable in pregnancy from the point of view of fetal exposure?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
D. It is a large peptide that does not cross the placenta appreciably
Insulin is a large polypeptide of about 5800 daltons and does not cross the placenta in meaningful amounts, so it controls maternal glucose without direct fetal pharmacological effect. Small, lipid-soluble, unionised drugs cross readily.
Option by option
A. It is an unionised weak base that is trapped in the fetus
Insulin is not a weak base, and ion trapping does not apply.
B. It is converted by the placenta into an inactive form
The placenta does not inactivate insulin, and this is not why it is chosen.
C. It is highly lipid soluble and crosses freely
Insulin is a polar peptide and is not lipid soluble.
D. It is a large peptide that does not cross the placenta appreciably (correct)
Correct. Its size prevents significant transplacental passage.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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