Radiochemistry/Pharmacy Flashcards

1
Q

A chemical substance that contains radioactive atoms within its structure and is suitable for administration to humans for diagnosis or treatment of disease is known as a (an):

A

Radiopharmaceutical

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2
Q

Allergic reactions to radiopharmaceuticals are very common due to the large amount of active ingredients found in their formulations: (T/F)

A

False

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3
Q

Which of the agency is responsible for regulating and monitoring the manufacture, distribution, safety, and effectiveness of all drugs and medications, including radiopharmaceuticals, in the United States?

A

Food & Drug Administration (FDA)

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4
Q

The atomic mass of an element represents __________.

A

The number of protons and neutrons in one atom of an element. (Electrons are also included but the majority of the time, are excluded from calculations)

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5
Q

Based on manufacturer recommendations, Tc99m elution expires at:

A

12 Hours

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6
Q

A unique characteristic of a pharmaceutical includes __________, whereas a unique characteristic of an isotope includes ______________.

A

Biodistribution, half-life

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7
Q

The half-life of a radionuclide is ____________.

A

The time for any quantity of radionuclide to decrease to half its original value.

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8
Q

A radiopharmaceutical decaying as a (Beta -) emitter would most likely be useful in which of the following applications?

A

Therapy

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9
Q

The amount of radioactivity administered to a patient (dosage) is expressed in:

A

Curies (Ci)

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10
Q

The mechanism of decay for nuclides that have too many protons relative to the numer of neutrons is:

A

(Beta +)

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11
Q

When one of the species in a coordination compound is a metal ion, the resulting entity is known as a metal complex. Electron donor atoms that bond with the metal ion are donated by a species known as a(an) ___________.

A

Ligand

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12
Q

Radiopharmaceutical kits reconstitued with Tc99m Pertechnetate are prepared in nitrogen- or argon- purged vials to prevent:

A

Oxidation

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13
Q

Which of the following is not part of a commercially produced Tc99m radiopharmaceutical reagent vial?

a) Stannous Ion
b) Reducing Agent
c) Lyphilized Compound
d) Preservative-free Saline

A

d) Preservative-free Saline

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14
Q

What effect does hydrolysis have on the desired radiopharmaceutical product?

A

Produces Tc99mO2 complexed with other ingredients.

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15
Q

When labeling Tc99m (VII), in what state is the Tc99m changed to make it more reactive?

A

(IV) (4)

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16
Q

What is the purpose of ITLC (Instant Thin Layer Chromatography)?

A

Separate substances into their components.

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17
Q

A Tc-99m MDP dose is 20 mCi calibrated at 11:00. The patient shows up 3 hours late for their study. How much activity remains in the dose?

A

14.1 mCi

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18
Q

25 mCi is equivalent to how many MBq?

A

925 MBq

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19
Q

Which of the following components in a Tc99m labeled radiopharmaceutical preparation is a radiochemical impurity?

a) Aluminum
b) Mo99
c) 0.9% NaCl
d) Tc99m04-

A

d) Tc99m04-

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20
Q

The test kit used to measure aluminum ion concentration in Tc99m elute contains specially treated indicator paper and an aluminum solution with concentration of approximately:

A

10 ug/mL

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21
Q

On the basis of USP criteria, MAA particle size should be no larger than __________ in size?

A

150 um

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22
Q

What is the purpose of heating some kits during preparation?

A

Supply energy to complete the chemical reaction

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23
Q

Which species is not part of a Tc99m radiopharmaceutical preparation?

a) Tc99m04-
b) Hydrolyzed-Reduced Tc99m
c) Tc99m - Chelate
d) Tc99m - Buffer

A

d) Tc99m - Buffer

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24
Q

Microembolization of particles describes which method of localization?

A

Capillary Blockade

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25
Q

Why should bacteriostatic normal saline not be used in radiopharmaceutical preparation?

A

Causes oxidation of stannous ion

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26
Q

What effect does an elution with a high amount of ground-state Tc99 have on the radiopharmaceutical product?

A

Increase in unreacted free Tc04-

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27
Q

Covalent bonds are characterized by:

A

Sharing of a pair of electrons between atoms

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28
Q

Nuclear configuration determines what property of an atom?

A

Radioactive Decay

29
Q

The type of radioactive decay that is characterized by the emission of a helium nucleus stripped of its two orbital electrons is:

A

Alpha

30
Q

If a ligand coordinating with a metal ion contains two or more donor atoms, forming a ring stucture with the metal, the complex is called a metal ____________ and the complexing agent is called a ___________ agent.

A

Chelate / Chelating

31
Q

Gamma emitters are used primarily for _________ purposes in nuclear medicine?

A

Diagnostic

32
Q

the “lock-and-key” binding of a molecule to a specific receptor site referes to which method of localization?

A

Receptor Binding

33
Q

With technetium compounds, the general redox reactions involve the reduction of technetium pertechnetate by ________________ chloride.

A

Stannous (Sn)

34
Q

What is the most common excretion pathway for radipharmaceuticals?

A

Urine

35
Q

A patient is administered I-131 sodium iodide for a thyroid therapy. I-131 has a physical half-life of 8 days. their individual biological half-life for elimination of this drug is 3 days. What is the overall effective half-life or this radiopharmaceutical?

A

2.2 days

36
Q

What is not a route of administration for radipharmaceuticals?

A

Intramuscular

37
Q

Which method of localization provides information about blood flow patterns within the venous system?

A

First Transit

38
Q

A Patient is administered F-18 FDG for a PET scan. The patient ate a full breakfast that morning and did not have the proper fasting blood glucose level at the time of injection. Why will the quality of their scan be compromised?

A

FDG molecules will be competitively inhibited by presence of glucose

39
Q

A syringe of F-18 FDB currently reads 10 mCi at 11:00 am. What was the original amount of radioactivity when it was drawn in the Radiopharmacy at 6:00 am?

A

66.7 mCi

40
Q

Some kit preparations require the use of a buffer to:

A

Neutralize an acid or base

41
Q

Radiolysis generates free radicals and is one of the main factors for degradation of radiolabeled preparations due to:

A

Breakage of chemical bonds between the radionuclide and the molecule.

42
Q

Venting is used during radiopharmaceutical kit preparation in order to:

A

Add oxygen to the reaction vial

43
Q

What is the acceptable radionuclidic purity standards levels of Mo99 used for kit preparation

A

0.15 uCi of Mo99 / 1 mCi of Tc99m

44
Q

In genreal, for diagnostic imaging applications, clearance of a radiopharmaceutical from the blood plasma is desirable because it:

A

Decreases background counts

45
Q

Regadenoson acts on this receptor.

A

A2A

46
Q

Adenosine (Drug Class)

A

Vasodilator

47
Q

Adenosine (Contraindications)

A

-AV nodal issues
- Depresses the SA and AV nodes
-Asthamtic Patients

48
Q

Adenosine (Acts on)

A

A2A, A2B, A1, A3

49
Q

Adenosine (Rate)

A

140 ug/kg/min for 6 min
IV Infusion

50
Q

Adenosine (Reversal Drug)

A

Aminophylline (125-250 mg, IV)

51
Q

Dipyridamole (Contraindications)

A

-AV nodal issues
- Depresses the SA and AV nodes
-Asthamtic Patients

52
Q

Dipyridamole (Rate)

A

0.56 mg/kg over 4 min
IV Infusion

53
Q

Dipyridamole (Reversal)

A

Aminophylline (125-250 mg, IV)

54
Q

Regadenoson (Brand Name)

A

Lexiscan

55
Q

Regadenoson (Acts on)

A

A2A Receptor

56
Q

Regadenoson (Contraindications)

A

-2nd or 3rd degree AV block
- Sinus node dysfunction (unless the patient has an artificial pacemaker)

57
Q

Regadenoson (Drug Interactions)

A

-Caffeine
-Theophylline
-Aminophylline
(all held 12 hours prior)

58
Q

Regadenoson (Dose)

A

0.4 mg in 5mL pre-filled syringe
- IV Injection (over 10 seconds)

59
Q

Regadenoson (Reversal Drug)

A

Aminophylline (125-250mg, IV)

60
Q

Dobutamine (Brand Name)

A

Dobutrex

61
Q

Dobutamine (Acts on)

A

B1 Receptor Agonist

62
Q

Dobutamine (Mechanism of Action)

A

Increases contractility and oxygen demand, indirectly causes coronary dilatation

63
Q

Dobutamine (Precaution, HR Target)

A

If heart rate is < 85% of predicted target rate after maximal dose is reached, IV atropine 0.2 mg to 1 mg may be administered.

64
Q

Dobutamine (Drug Interactions)

A
  • NOt affected by caffeine or xanthine drugs
  • Beta blockers should be discontinued 24 hr prior
65
Q

Dobutamine (Dose Rate)

A
  • Incremental Dosage
    Start (10 uq/kg/min every 3 minutes)
    Max (40 uq/kg/min)
  • Over 12 Minutes
66
Q

Aminophylline

A

Vasodialator Reversal Medication
(Bronchodilator)

67
Q

Atropine

A

Use to treat symptoms of low heart rate (bradycardia)

68
Q

Atropine (Dose Rate)

A

0.5-1.0 mg to increase heart rate by 15 beats per minute.