Pharmaceutical Terminology Part 2 Flashcards

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1
Q

Define aqueous

A

Something that is water based; made with or containing water

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2
Q

Define hydro-

A

A prefix that means water

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3
Q

Define in-vitro

A

Medical study or experiment that is done in the laboratory within a test tube or laboratory dish

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4
Q

Define in-vivo

A

Medical test or experiment done in a living organism

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5
Q

Define disintegration

A

The breakdown of solid dosage forms into small particles

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6
Q

Define dissolution

A

The process in which a substance forms a solution

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7
Q

Define adsorption

A

The adhesion of molecules to a surface because of chemical or electrical attraction

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8
Q

Define osmosis

A

A process by which the molecules of a solvent pass from a solution of low concentration to a solution of high concentration through a semi-permeable membrane

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9
Q

Define passive diffusion

A

The movement of molecules down the concentration gradient

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10
Q

Define facilitated diffusion

A

A type of diffusion in which the molecules move from the region of higher concentration to the region of lower concentration assisted by a carrier

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11
Q

Define active transport

A

The movement of molecules from a region of lower concentration to a region of higher concentration with the use of energy

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12
Q

Define endocytosis

A

The process of actively transporting molecules into the cell by engulfing it with its membrane

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13
Q

Define absorption

A

The process of a drug moving from its site of delivery into the bloodstream

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14
Q

Define distribution

A

The movement of a drug to and from the blood and various tissues of the body

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15
Q

Define metabolism

A

Chemical alteration and breakdown of a drug by the body

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16
Q

Define excretion

A

The removal of drugs and their metabolites from the body

17
Q

Define half life

A

The time taken for the plasma concentration of a drug to reduce to half its original value
The half-life is used to estimate how long it takes for a drug to be removed from your body

18
Q

Define bioavailability

A

The rate and extent to which the active constituent of a drug is absorbed from a drug product and reaches the circulation, thereby accessing the site of action

19
Q

Define bioequivalence

A

The property of two things with identical active ingredients, possess similar bioavailability and produce the some effect at the site of physiological activity

20
Q

Define brand drug

A

A brand-name drug product is originally discovered and developed by a pharmaceutical company

21
Q

Define generic drugs

A

Contain the same active ingredients as the brand product, in the same dosage form, at the same dose or concentration, and for the same route of administration.
The drug may differ in color, shape, taste, inactive ingredients, preservatives and packaging

22
Q

Define drug manufacturing

A

The process of industrial scale synthesis of pharmaceutical drugs by pharmaceutical companies

23
Q

Define raw materials

A

Starting materials, reagents, and solvents intended for use in the production of drug products

24
Q

Define intermediate

A

Partly processed material which must undergo further manufacturing steps before it becomes a bulk product

25
Q

Define bulk product

A

Any product that has completed all processing stages up to, but not including, final packaging

26
Q

Define packaging

A

All operations, including filling and labeling, which a bulk product has to undergo in order to become a finished product

27
Q

Define labeling

A

Information on the immediate or outer packaging to identify a pharmaceutical product

28
Q

Define GMP

A

Good manufacturing practice, a system for ensuring that products are consistently produced and controlled according to qualify standards

29
Q

Define quality control

A

The procedures done to check or test that the quality of the drug product is meeting the required specifications

30
Q

Define in-process control

A

Checks performed during production in order to monitor and, if necessary, adjust the process to ensure that the finished product conforms to its specification

31
Q

Define batch

A

A specific amount of pharmaceutical product that is intended to have a uniform character and quality and is manufactured according to a single production order during the same manufacturing cycle

32
Q

Define contamination

A

The undesired introduction of impurities of a chemical or microbiological nature, or of foreign matter

33
Q

Define impurity

A

Any component present in the intermediate or product that is not the desired entity

34
Q

Define sterile

A

Free from the presence of viable microorganisms