SOLID DOSAGE FORMS Flashcards

(61 cards)

1
Q

Solid dosage form that may contain only the active drug or a mixture with excipients.

A

Powder

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2
Q

Science of small particles, including measurement and behavior.

A

Micromeritics

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3
Q

Process of reducing particle size (e.g., trituration, pulverization by intervention, levigation).

A

Comminution

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4
Q

Mixing powders with a spatula; not suitable for large quantities.

A

Spatulation

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5
Q

Grinding or mixing powders in a mortar and pestle.

A

Trituration

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6
Q

Mixing potent drug with large diluent by proportionate additions.

A

Geometric dilution

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7
Q

Passing powders through sifters for light, fluffy powders.

A

Sifting

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8
Q

Mixing in large rotating containers.

A

Tumbling

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9
Q

Non-potent powders measured by teaspoon/cup.

A

Bulk powders

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10
Q

Fine powders applied to skin, labeled for external use.

A

Dusting powders

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11
Q

Powders dissolved in water for vaginal use.

A

Douche powders

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12
Q

Powders blown into body cavities (e.g., nose, ears).

A

Insufflations

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13
Q

Medicated powders inhaled using a device (particle size 1–6 µm).

A

Aerosol powders

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14
Q

Dry powder inhaler using drug in blister packs.

A

Diskhaler

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15
Q

Device where capsule is split and powder inhaled.

A

Rotahaler

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16
Q

Single doses wrapped in paper/foil.

A

Divided powders (Chartulae)

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17
Q

Larger particles (sieve size 4–12), prepared by moistening and drying powders.

A

Granules

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18
Q

Contain citric acid, tartaric acid, and sodium bicarbonate; release CO₂ in water.

A

Effervescent granules

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19
Q

Solid dosage form with drug enclosed in gelatin shell.

A

Capsule

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20
Q

Derived from collagen; Type A (acid processed) or Type B (alkali processed).

A

Gelatin

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21
Q

Made of gelatin + excipients; contain 13–16% water.

A

Hard gelatin capsules

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22
Q

Numbered 000 (largest) to 5 (smallest).

A

Capsule sizes

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23
Q

Elastic shells with glycerin/sorbitol; contain liquids, pastes, or suspensions.

A

Soft gelatin capsules

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24
Q

Methods of preparing soft gels.

A

Plate process, Rotary die process, Reciprocating die process

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25
Telescoping (caps sliding), Sweating (moisture issues).
Problems in capsules
26
Solid dosage form prepared by compression/molding with excipients.
Tablet
27
Fillers for bulk (e.g., lactose, starch, MCC).
Diluents
28
Promote granulation and cohesion (e.g., starch paste, glucose solution, gums).
Binders/Adhesives
29
Facilitate breakup in GI tract (e.g., starch, cellulose, clays).
Disintegrants
30
Reduce friction during ejection (e.g., magnesium stearate).
Lubricants
31
Prevent sticking to punches (e.g., talc).
Antiadherents
32
Improve powder flow (e.g., colloidal silica).
Glidants
33
Made by single compression.
Compressed tablets
34
Layered or compression-coated for separation or controlled release.
Multiply compressed tablets
35
Coated for taste, stability, or appearance (heavier).
Sugar-coated tablets
36
Coated with thin polymer film; more durable than sugar-coated.
Film-coated tablets
37
Capsule-shaped tablets for easier swallowing.
Gelatin-coated tablets (Gelcaps)
38
Resist stomach acid, release drug in intestines.
Enteric-coated tablets
39
Dissolve in buccal pouch.
Buccal tablets
40
Dissolve under the tongue.
Sublingual tablets
41
Disintegrate when chewed; often flavored.
Chewable tablets
42
Release CO₂ when dissolved in water.
Effervescent tablets
43
Soft, rapidly dissolving tablets.
Molded tablets
44
Small, cylindrical tablets containing potent drugs.
Tablet triturates
45
Old tablets used for parenteral solution prep.
Hypodermic tablets
46
Formerly used by pharmacists for compounding.
Dispensing tablets
47
Disintegrate without delay.
Immediate-release tablets
48
Dissolve within 1 min in mouth.
Rapidly Disintegrating Tablets (RDTs/ODTs)
49
Dissolve slowly in mouth for local effect.
Lozenges/Lollipops
50
Release drug gradually over time.
Extended-release tablets
51
Compressing powders with good flow/cohesion directly into tablets.
Direct compression
52
Precompressing slugs → grinding → compression.
Dry granulation
53
Uses liquid binder to form granules; not suitable for water/heat-sensitive drugs.
Wet granulation
54
Tablet crown separates.
Capping
55
Splitting into layers.
Lamination
56
Tablet material sticks to punch/die.
Picking/Sticking
57
Uneven color.
Mottling
58
Ability to resist breaking/chipping during handling.
Friability
59
Measures crushing strength.
Hardness test
60
Determines drug release rate.
Dissolution test
61