1 - Introduction Flashcards

1
Q

What does analytical chemistry deal w/?

A
  • Physical properties
  • Chemical properties
  • Purity
  • Content
  • Stability
  • And quality of a chemical compound
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2
Q

Pharmaceutical analysis is analytical chemistry w/ focus on ____

A

Pharmaceutical products

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3
Q

Accuracy definition

A
  • Degree of conformity w/ a standard

- Commonly expressed as mean (accuracy) +/- SD (precision)

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4
Q

Precision definition

A

Degree of perfection in an instrument and/or method that is used to obtain a result

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5
Q

Repeatability definition

A
  • Precision under the same operating conditions over a short period of time
  • Sometimes also called intra-assay precision
  • Could indicate either within-day precision or between-day precision of a method or an operator
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6
Q

Reproducibility definition

A
  • Precision among different labs, from using the standard operating procedures (SOPs)
  • Can be within-lab or between-lab reproducibility
  • Pharmacopeial monographs (ex: USP) are regarded as official quality control SOPs
  • Pharmaceutical manufactures often create their own SOPs for internal quality control purposes during the production of a dosage form
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7
Q

Analytical blank definition and example

A
  • Composed of all reagents or solvents used in an assay w/o any analyte being present
  • True analytical blank should reflect all the operations to which the analyte in a real sample is subjected
  • Ex: a chromatographic mobile phase can be used to reconstitute an analyte to minimize interference from other components
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8
Q

Calibration definition and example

A
  • Involves comparison of the value/values of a particular parameter measured by the system under strictly defined conditions w/ preset standard values
  • Most assay methods or instruments require regular calibration
  • Ex: a calibration curve is constructed for an HPLC assay to calculate concentrations of the analyte
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9
Q

Detection limit definition

A
  • The lowest amount of analyte in a sample that can be detected but not necessarily quantitated as an exact value
  • Done for an individual analytical procedure
  • Signal of detection limit of an analyte is normally defined as 3x larger than that of the analytical blank
  • True limit detection should reflect all the processes to which the analyte in a real assay is subjected & not be a simple dilution of a pure standard for the analyte until it can no longer be detected
  • Chromatographic assays normally have lower detection limits than spectrophotometric assays
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10
Q

Quantitation limit defition

A
  • Lowest amount of analyte in a sample that can be quantitatively determined w/ suitable precision & accuracy
  • Done for an individual analytical procedure
  • Signal quantitation limit of an analyte is normally defined at 10x larger than that of the analytical blank or 3x larger than that of the detection limit
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11
Q

Linearity and correlation coefficient definition

A
  • Ability of an analytical procedure to obtain test results w/in a given range that are directly proportional to the concentration (or amount) of analyte in the sample
  • Equation of linearity is normally obtained by linear regression of a series of plots & takes the form of y = mx + b
  • Correlation coefficient indicated how close the calculated values are to the actual values used in a calibration (in general, R > 0.99 is considered satisfactory for assay calibration)
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12
Q

Range definition

A
  • For an analytical procedure, is the interval between the upper and lower concentration (or amount) of analyte in the sample
  • Sample concentrations must be adjusted appropriately beforehand by dilution or concentration so that they fall into the range of the equipment used to make the measurement
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13
Q

Robustness definition and example

A
  • Ability of an analytical procedure to remain unaffected by small, but deliberate variations in experimental parameters
  • Provides indication of reliability during normal application
  • Ex: changes of instrumentation, slight variations in extraction procedures, sensitivity to minor impurities in reagents
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14
Q

Selectivity definition

A
  • How capable a method is of measuring the analyte alone in the presence of other compounds contained in the sample
  • Fluorescence spectrophotometry is more selective than UV/visible spectrophotometry b/c fewer compounds exhibit fluorescence
  • Fluorescence assays may be less robust than UV/visible assays b/c they use more complex principles & therefore more prone to method variations
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15
Q

Sensitivity definition

A

How responsive it is to a small change in the concentration of an analyte

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