Harr: Clinical Chemistry PQ 9

Lakukan tugas rumah & ujian kamu dengan baik sekarang menggunakan Quizwiz!

The purpose of the nebulizer in an atomic absorption spectrophotometer that uses a flame is to: A. Convert ions to atoms B. Cause ejection of an outer shell electron C. Reduce evaporation of the sample D. Burn off organic impurities

A. Convert ions to atoms A The atomizer of the atomic absorption spectrophotometer consists of either a nebulizer and flame or a graphite furnace. The nebulizer disperses the sample into a fine aerosol, distributing it evenly into the flame. Heat from the flame is used to evaporate water and break the ionic bonds of salts, forming ground state atoms. The flame also excites a small percentage of the atoms, which release a characteristic emission line.

Which wavelength would be absorbed strongly by a red-colored solution? A. 450 nm B. 585 nm C. 600 nm D. 650 nm

A. 450 nm A A solution transmits light corresponding in wavelength to its color, and usually absorbs light of wavelengths complementary to its color. A red solution transmits light of 600-650 nm and strongly absorbs 400-500 nm light.

Which of the following best represents the reference (normal) range for arterial pH? A. 7.35-7.45 B. 7.42-7.52 C. 7.38-7.68 D. 6.85-7.56

A. 7.35-7.45 A The reference range for arterial blood pH is 7.35-7.45 and is only 0.03 pH units lower for venous blood owing to the buffering effects of hemoglobin (Hgb) known as the chloride isohydric shift. Most laboratories consider less than 7.20 and greater than 7.60 the critical values for pH.

A flameless atomic absorption spectrophotometer dehydrates and atomizes a sample using: A. A graphite capillary furnace B. An electron gun C. A thermoelectric semiconductor D. A thermospray platform

A. A graphite capillary furnace A Flameless atomic absorption uses a hollow tube of graphite with quartz ends. The tube is heated in stages by an electric current to successively dry, ash, and atomize the sample. During the ash and atomization steps, argon is injected into the tube to distribute the atoms. The furnace is more sensitive than a flame atomizer and more efficient in atomizing thermostable salts. However, it is prone to greater matrix interference and is slower than the flame atomizer because it must cool down before introduction of the next sample.

In real-time PCR, what value is needed in order to determine the threshold? A. Background signal B. Melt temperature C. Maximum fluorescence D. Treshold cycle

A. Background signal A In real-time PCR, the fluorescence of the reporter probe is proportional to the concentration of PCR products. For quantitation of PCR products, a well factor and background fluorescence must be determined. Well-factor values are analogous to cuvette blanks. They are used to correct the measurements from each well so that the same concentration of fluorescent dye gives the same signal intensity regardless of the well. The threshold is the lowest signal that indicates the presence of product. It can be calculated manually from a real-time amplification curve by finding the average standard deviation of the fluorescent signal (RFU) from cycles 2-10. This is multiplied by 10 to give the threshold value in RFUs.

In gas chromatography, the elution order of volatiles is usually based upon the: A. Boiling point B. Molecular size C. Carbon content D. Polarity

A. Boiling point A The order of elution is dependent upon the velocity of the analyte. Usually, the lower the boiling point of the compound, the greater its velocity or solubility in carrier gas.

Which of the following compounds can interfere with the coulometric chloride assay? A. Bromide B. Ascorbate C. Acetoacetate D. Nitrate

A. Bromide A Chloride assays based upon either coulometric or chemical titration are subject to positive interference from other anions and electronegative radicals that may be titrated instead of chloride ions. These include other halogens such as bromide, cyanide, and cysteine.

Which of the electrodes below is a currentproducing (amperometric) rather than a voltage-producing (potentiometric) electrode? A. Clark electrode B. Severinghaus electrode C. pH electrode D. Ionized calcium electrode

A. Clark electrode A The Clark electrode is composed of two half cells that generate current, not voltage. It is used to measure partial pressure of oxygen (PO2), and is based upon an amperometric method called polarography. When -0.8 V is applied to the cathode, O2 is reduced, causing current to flow. Current is proportional to the PO2 of the sample.

The reference potential of a silver-silver chloride electrode is determined by the: A. Concentration of the potassium chloride filling solution B. Surface area of the electrode C. Activity of total anion in the paste covering the electrode D. The concentration of silver in the paste covering the electrode

A. Concentration of the potassium chloride filling solution A The activity of any solid or ion in a saturated solution is unity. For a silver electrode covered with silver chloride paste, the Nernst equation is E = E° - RT/nF x 2.3 log10 [Ag° × Cl-]/[AgCl]. Because silver and silver chloride have an activity of 1.0, and all components except chloride are constants, the potential of the reference electrode is determined by the chloride concentration of the filling solution. E = Eo - RT/nF × 2.3 log10[Cl-] = E° - 59.2 mV × log[Cl-] (at room temperature)

What component is used in a GC-MS but not used in an LC-MS? A. Electron source B. Mass filter C. Detector D. Vacuum

A. Electron source A The mass spectrometer requires a sample that is suspended in a gas phase, and therefore, the sample from a GC can be directly injected into the mass spectrometer. While chemical ionization of the sample is possible, most GC-MS instruments utilize electron ionization. Electrons are produced by applying 70 electron volts to a filament of tungsten or rhenium under vacuum. The electrons collide with the neutral molecules coming from the GC, splitting them into fragments. The array of fragments is a unique identifier of each molecule

What process is most often used in LC-MS to introduce the sample into the mass filter? A. Electrospray ionization B. Chemical ionization C. Electron impact ionization D. Fast atom bombardment

A. Electrospray ionization A HPLC instruments use solvent rather than gas to separate molecules. The sample is converted into a gaseous state by electrospray ionization before it enters the mass filter. Electrospray ionization uses a small-bore tube that forms a 1-4 μ nozzle at the mass filter inlet and which is charged by several kilovolts. The sample enters the tube along with inert drying gas. The tube is heated to help evaporate solvent, but unlike electron impact used in GC-MS, the ionizer is not under vacuum. When a droplet of the sample reaches the nozzle, it becomes highly charged. The size of the droplet is decreased owing to evaporation. This causes the charge density to become excessive, and the droplets break apart. The tiny charged droplets repel each other and break apart again, forming a plume. These particles are drawn into the mass filter by "ion optics" (a system of repeller plates, counter electrode, and magnets). ESI does not result in extensive fragmentation, producing mostly the parent or "molecular" ion, a process called soft ionization.

In addition to velocity, what variable is also needed to calculate the relative centrifugal force (g force) of a centrifuge? A. Head radius B. Angular velocity coefficient C. Diameter of the centrifuge tube D. Ambient temperature in degrees Centigrade

A. Head radius A The relative centrifugal force (number times the force of gravity) is proportional to the square of the rotor speed in revolutions per minute and the radius in centimeters of the head (distance from the shaft to the end of the tube). RCF = s2 x r x 1.118 x 10-5 where s is the speed in RPM, r is the radius in cM, and 1.118 x 10-5 is a conversion constant.

In addition to sodium bicarbonate, what other substance contributes most to the amount of base in the blood? A. Hemoglobin concentration B. Dissolved O2 concentration C. Inorganic phosphorus D. Organic phosphate

A. Hemoglobin concentration A The primary blood buffer bases preventing acidosis in order of concentration are bicarbonate, deoxyhemoglobin, albumin, and monohydrogen phosphate. At physiological pH, there is significantly more H2PO4 -1 than HPO4 -2, and phosphate is a more efficient buffer system at preventing alkalosis than acidosis. Since all of the blood buffer systems are in equilibrium, the pH can be calculated accurately from the concentration of bicarbonate and dissolved CO2 using the Henderson-Hasselbalch equation.

All of the following compounds contribute to the osmolality of plasma except: A. Lipids B. Creatinine C. Drug metabolites D. Glucose

A. Lipids A Osmolality is the concentration (in moles) of dissolved solute per kilogram solvent. Proteins and lipids are not in solution, and do not contribute to osmolality. The nonionized solutes such as glucose and urea contribute 1 osmole per mole per kilogram water, whereas dissociated salts contribute 1 osmole per mole of each dissociated ion or radical.

The term reverse phase is used in HPLC to indicate that the mobile phase is: A. More polar than the stationary phase B. Liquid and the stationary phase is solid C. Organic and the stationary phase is aqueous D. A stronger solvent than the stationary phase

A. More polar than the stationary phase A In reverse-phase HPLC, the separation takes place using a nonpolar sorbent (stationary phase) such as octadecylsilane (C18). Solutes that are nonpolar are retained longer than polar solutes. Most clinical separations of drugs, hormones, and metabolites use reverse phase because aqueous mobile phases are far less toxic and flammable.

Which of the following formulas for O2 content is correct? A. O2 content = %O2 saturation/100 × Hgb g/dL × 1.39 mL/g + (0.0031 × PO2) B. O2 content = PO2 × 0.0306 mmol/L/mm C. O2 content = O2 saturation × Hgb g/dL × 0.003 mL/g D. O2 content = O2 capacity × 0.003 mL/g

A. O2 content = %O2 saturation/100 × Hgb g/dL × 1.39 mL/g + (0.0031 × PO2) A Oxygen content is the sum of O2 bound to Hgb and O2 dissolved in the plasma. It is dependent upon the Hgb concentration and the percentage of Hgb bound to O2 (O2 saturation). Each gram of Hgb binds 1.39 mL of O2. The dissolved O2 is determined from the solubility coefficient of O2 (0.0031 mL per dL/mm Hg) and the PO2. O2 content = % Sat/100 × Hgb in g/dL × 1.39 mL/g + (0.0031 × PO2).

Which of the following effects results from exposure of a normal arterial blood sample to room air? A. PO2 increased PCO2 decreased pH increased B. PO2 decreased PCO2 increased pH decreased C. PO2 increased PCO2 decreased pH decreased D. PO2 decreased PCO2 decreased pH decreased

A. PO2 increased PCO2 decreased pH increased A The PO2 of air at sea level (21% O2) is about 150 mm Hg. The PCO2 of air is only about 0.3 mm Hg. Consequently, blood releases CO2 gas and gains O2 when exposed to air. Loss of CO2 shifts the equilibrium of the bicarbonate buffer system to the right, decreasing hydrogen ion concentration and blood becomes more alkaline.

The determination of the oxygen saturation of hemoglobin is best accomplished by: A. Polychromatic absorbance measurements of a whole-blood hemolysate B. Near infrared transcutaneous absorbance measurement C. Treatment of whole blood with alkaline dithionite prior to measuring absorbance D. Calculation using PO2 and total hemoglobin by direct spectrophotometry

A. Polychromatic absorbance measurements of a whole-blood hemolysate A Measurement of oxyhemoglobin, deoxyhemoglobin (reduced hemoglobin), carboxyhemoglobin, methemoglobin, and sulfhemoglobin can be accomplished by direct spectrophotometry at multiple wavelengths and analysis of the absorptivity coefficients of each pigment at various wavelengths. The O2 saturation is determined by dividing the fraction of oxyhemoglobin by the sum of all pigments. This eliminates much of the error that occurs in the other methods when the quantity of an abnormal hemoglobin pigment is increased.

A green-colored solution would show highest transmittance at: A. 475 nm B. 525 nm C. 585 nm D. 620 nm

B. 525 nm B Green light consists of wavelengths from 500-550 nm. A green-colored solution with a transmittance maximum of 525 nm and a 50-nm bandpass transmits light of 525 nm and absorbs light below 475 nm and above 575 nm. A solution that is green would be quantitated using a wavelength that it absorbs strongly, such as 450 nm.

Which component is needed for a thermal cycler to amplify DNA? A. Programmable heating and cooling unit B. Vacuum chamber with zero head space C. Sealed airtight constant-temperature chamber D. Temperature-controlled ionization chamber

A. Programmable heating and cooling unit A The polymerase chain reaction for DNA amplification consists of three phases. Denaturation requires a temperature of 90°C 94°C and separates the double-stranded DNA. Annealing requires a temperature between 40°C-65°C and allows the primers to bind to the target base sequence. Extension requires a temperature of 72°C and allows the heat-stable polymerase to add complementary bases to the primer in the 5' to 3' direction. A cycle consists of each temperature stage for a specific number of minutes and most procedures require 30 or more cycles to generate a detectable quantity of target DNA. Rapid heating and cooling is usually achieved using a thermoelectric block that is cooled by forced air flow.

Light scattering when the wavelength is greater than 10 times the particle diameter is described by: A. Rayleigh's law B. Te Beer-Lambert law C. Mie's law D. Te Rayleigh-Debye law

A. Rayleigh's law A Rayleigh's law states that when the incident wavelength is much longer than the particle diameter, there is maximum backscatter and minimum right-angle scatter. The Rayleigh-Debye law predicts maximum right-angle scatter when wavelength and particle diameter approach equality. In nephelometry, the relationship between wavelength and diameter determines the angle at which the detector is located

SITUATION: A technologist is performing an enzyme assay at 340 nm using a visible-range spectrophotometer. After setting the wavelength and adjusting the readout to zero %T with the light path blocked, a cuvette with deionized water is inserted. With the light path fully open and the 100%T control at maximum, the instrument readout will not rise above 90%T. What is the most appropriate first course of action? A. Replace the source lamp B. Insert a wider cuvette into the light path C. Measure the voltage across the lamp terminals D. Replace the instrument fuse

A. Replace the source lamp A Visible spectrophotometers are usually supplied with a tungsten or quartz halogen source lamp. Tungsten lamps produce a continuous range of wavelengths from about 320-2,000 nm. Output increases as wavelength becomes longer peaking at around 1,000 nm, and is poor below 400 nm. As the lamp envelope darkens with age, the amount of light reaching the photodetector at 340 nm becomes insufficient to set the blank reading to 100%T. Quartz halogen lamps produce light from 300 nm through the infrared region. Deuterium or hydrogen lamps produce ultraviolet-rich spectra optimal for ultraviolet (UV) work. Mercury vapor lamps produce a discontinuous spectrum that includes a high output at around 365 nm that is useful for fluorescent applications. Xenon lamps generate a continuous spectrum of fairly uniform intensity from 300-2,000 nm, making them useful for both visible and UV applications.

Which measurement principle is employed in a vapor pressure osmometer? A. Seebeck B. Peltier C. Hayden D. Darlington

A. Seebeck A The Seebeck effect refers to the increase in voltage across the two junctions of a thermocouple caused by a difference in the temperature at the junctions. Increasing osmolality lowers the dew point of a sample. When sample is cooled to its dew point, the voltage change across the thermocouple is directly proportional to osmolality.

Which of the following components is not needed in a chemiluminescent immunoassay analyzer? A. Source lamp B. Monochromator C. Photodetector D. Wash station

A. Source lamp A Chemiluminescence is the production of light following a chemical reaction. Immunoassays based upon chemiluminescence generate light when the chemiluminescent molecule becomes excited; therefore, a light source is not used. In immunoassay platforms, chemiluminescent molecules such as acridinium can be used to label antigens or antibodies. Alternatively, chemiluminescent substrates such as luminol or dioxetane phosphate may be used. Light will be emitted when the enzyme-labeled molecule reacts with the substrate. In such assays, free and bound antigen separation is required and is usually accomplished using paramagnetic particles bound to either antibody or reagent antigen

Correction of pH for a patient with a body temperature of 38°C would require: A. Subtraction of 0.015 B. Subtraction of 0.01% C. Addition of 0.020 D. Subtraction of 0.020

A. Subtraction of 0.015 A The pH decreases by 0.015 for each degree Celsius above the 37°C. Because the blood gas analyzer measures pH at 37°C, the in vivo pH would be 0.015 pH units below the measured pH.

The reagent blank corrects for absorbance caused by: A. The color of reagents B. Sample turbidity C. Bilirubin and hemolysis D. All of these options

A. The color of reagents A When a spectrophotometer is set to 100%T with the reagent blank instead of water, the absorbance of reagents is automatically subtracted from each unknown reading. The reagent blank does not correct for absorbance caused by interfering chromogens in the sample such as bilirubin, hemolysis, or turbidity.

In the Henderson-Hasselbalch expression pH = 6.1 + log HCO3 - /dCO2, the 6.1 represents: A. The combined hydration and dissociation constants for CO2 in blood at 37°C B. The solubility constant for CO2 gas C. The dissociation constant of H2O D. The ionization constant of sodium bicarbonate (NaHCO3)

A. The combined hydration and dissociation constants for CO2 in blood at 37°C A The equilibrium constant, Kh, for the hydration of CO2 (dCO2 + H2O → H2CO3) is only about 2.3 × 10-3M, making dCO2 far more prevalent than carbonic acid. The dissociation constant, Kd, for the reaction H2CO3 →H+ + HCO3 - is about 2 × 10-4 M. The product of these constants is the combined equilibrium constant, K´. The negative logarithm of K´ is the pK´, which is 6.103 in blood at 37°C.

Bichromatic measurement of absorbance can correct for interfering substances if: A. The contribution of the interferent to absorbance is the same at both wavelengths B. Both wavelengths pass through the sample simultaneously C. The side band is a harmonic of the primary wavelength D. The chromogen has the same absorbance at both wavelengths

A. The contribution of the interferent to absorbance is the same at both wavelengths A In bichromatic photometry, the absorbance of sample is measured at two different wavelengths. The primary wavelength is at or near the absorbance maximum. An interfering substance having the same absorbance at both primary and secondary (side band) wavelengths does not affect the absorbance difference (Ad).

The half-band width of a monochromator is defined by: A. The range of wavelengths passed at 50% maximum transmittance B. One-half the lowest wavelength of optical purity C. The wavelength of peak transmittance D. One-half the wavelength of peak absorbance

A. The range of wavelengths passed at 50% maximum transmittance A Half-band width is a measure of bandpass made using a solution or filter having a narrow natural bandpass (transmittance peak). The wavelength giving maximum transmittance is set to 100%T (or 0 A). Then, the wavelength dial is adjusted downward, until a readout of 50%T (0.301 A) is obtained. Next, the wavelength is adjusted upward until 50%T is obtained. The wavelength difference is the half-band width. The narrower the half-band width, the better the photometric resolution of the instrument.

What component of a freezing point osmometer measures the sample temperature? A. Thermistor B. Thermocouple C. Capacitor D. Electrode

A. Thermistor A A thermistor is a temperature sensitive resistor. The resistance to current flow increases as temperature falls. The temperature at which a solution freezes can be determined by measuring the resistance of the thermistor. Resistance is directly proportional to the osmolality of the sample.

What is the purpose of an internal standard in HPLC and GC methods? A. To compensate for variation in extraction and injection B. To correct for background absorbance C. To compensate for changes in flow rate D. To correct for coelution of solutes

A. To compensate for variation in extraction and injection A Internal standards should have the same affinity as the analyte for the extraction reagents. Dividing peak height (or area) of all samples (standards and unknowns) by the peak height (or area) of the internal standard reduces error caused by variation in extraction recovery and injection volume.

What is the normal ratio of bicarbonate to dissolved carbon dioxide (HCO3 - :dCO2) in arterial blood? A. 1:10 B. 10:1 C. 20:1 D. 30:1

C. 20:1 C When the ratio of HCO3 -:dCO2 is 20:1, the log of salt/acid becomes 1.3. Substituting this in the Henderson-Hasselbalch equation and solving for pH gives pH = 6.1 + log 20; pH = 6.1 + 1.3 = 7.4. Acidosis results when this ratio is decreased, and alkalosis when it is increased.

The normal difference between alveolar and arterial PO2 (PAO2-PaO2 difference) is: A. 3 mm Hg B. 10 mm Hg C. 40 mm Hg D. 50 mm Hg

B. 10 mm Hg B The PAO2-PaO2 difference results from the low ratio of ventilation to perfusion in the base of the lungs. The hemoglobin in the blood coming from the base of the lung has a lower O2 saturation. This blood will take up O2 from the plasma of blood leaving well-ventilated areas of the lung, thus lowering the mixed arterial PO2.

A solution that has a transmittance of 1.0 %T would have an absorbance of: A. 1.0 B. 2.0 C. 1% D. 99%

B. 2.0 B A = 2.0 - log %T A = 2.0 - log 1.0 The log of 1.0 = 0 A = 2.0

Which reagent is used in thin-layer chromatography (TLC) to extract cocaine metabolites from urine? A. Acid and sodium chloride B. Alkali and organic solvent C. Chloroform and sodium acetate D. Neutral solution of ethyl acetate

B. Alkali and organic solvent B Alkaline drugs such as cocaine, amphetamine, and morphine are extracted at alkaline pH. Ideally, the pH for extracting alkaline drugs into an organic solvent should be 2 pH units greater than the negative log of dissociation constant (pKa) of the drug. More than 90% of the drug will be nonionized and will extract in ethyl acetate or another organic solvent.

The response of a sodium electrode to a 10-fold increase in sodium concentration should be: A. A 10-fold drop in potential B. An increase in potential of approximately 60 mV C. An increase in potential of approximately 10 mV D. A decrease in potential of approximately 10 mV

B. An increase in potential of approximately 60 mV B The Nernst equation predicts an increase of approximately 60 mV per 10-fold increase in sodium activity. For sodium: E = E° + RT/nF × 2.3 log10[Na+] RT/nF × 2.3 = 60 mV at 37°C. Therefore: E = E° + 60 mV × log10[Na+]. If sodium concentration is 10 mmol/L, then: E = E° + 60 mV × log10[10] = E° + 60 mV. If sodium concentration increases from 10 mmol/L to 100 mmol/L, then: E = E° + 60 mV × log10[100] = E° + 60 mV × 2 = E° + 120 mV.

Ion selective analyzers using undiluted samples have what advantage over analyzers that use a diluted sample? A. Can measure over a wider range of concentration B. Are not subject to pseudohyponatremia caused by high lipids C. Do not require temperature equilibration D. Require less maintenance

B. Are not subject to pseudohyponatremia caused by high lipids B Ion-selective analyzers measure the electrolyte dissolved in the fluid phase of the sample in millimoles per liter of plasma water. When undiluted blood is assayed, the measurement is independent of colloids such as protein and lipid. Hyperlipemic samples cause falsely low sodium measurements when assayed by flame photometry and ion-selective analyzers requiring dilution because lipids displace plasma water containing the electrolytes. One drawback to undiluted or direct measuring systems is that the electrodes require more frequent deproteinization and usually have a shorter duty cycle.

Persistent noise from an ion selective electrode is most often caused by: A. Contamination of sample B. Blocked junction at the salt bridge C. Overrange from high concentration D. Improper calibration

B. Blocked junction at the salt bridge B Electrode noise most often results from an unstable junction potential. Most reference electrodes contain a high concentration of KCl internal solution used to produce the reference potential. This forms a salt bridge with the measuring half cell by contacting sample, but is kept from equilibrating via a barrier called a junction. When this junction becomes blocked by salt crystals, the reference potential will be unstable, resulting in fluctuation in the analyzer readout.

The fragments typically produced and analyzed in methods employing mass spectroscopy are typically: A. Of low molecular size ranging from 10-100 daltons B. Cations caused by electron loss or proton attachment C. Anions caused by bombarding the molecule with an electron source D. Neutral species formed after excited molecules form a stable resonance structure

B. Cations caused by electron loss or proton attachment B In almost all MS applications, cations of the molecule are measured. Cations can be formed by various methods, the most common of which is electron bombardment (electron ionization). The energy transferred to the molecule causes ejection of an outer shell electron. MS can analyze sizes from trace metals through macromolecules. Proteins are measured following conversion to cations by ionization procedures such as matrix-assisted laser desorption ionization (MALDI) in which energy from a nitrogen laser causes transfer of a proton from the matrix (an acid) to the protein.

Which of the following statements accurately characterizes the coulometric titration of chloride? A. The indicator electrodes generate voltage B. Constant current must be present across the generator electrodes C. Silver ions are formed at the generator cathode D. Chloride concentration is inversely proportional to titration time

B. Constant current must be present across the generator electrodes B The Cotlove chloridometer is based upon the principle of coulometric titration with amperometric detection. Charge in the form of silver ions is generated by oxidation of silver wire at the generator anode. Silver ions react with chloride ions, forming insoluble silver chloride (AgCl). When all of the chloride is titrated, free silver ions are detected by reduction back to elemental silver, which causes an increase in current across the indicator electrodes (a pair of silver electrodes with a voltage difference of about 1.0 V DC). Charge or titration time is directly proportional to chloride concentration as long as the rate of oxidation remains constant at the generator anode.

Which of the following situations is likely to cause an error when weighing with an electronic analytical balance? A. Failure to keep the knife edge clean B. Failure to close the doors of the balance before reading the weight C. Oxidation on the surface of the substitution weights D. Using the balance without allowing it to warm up for at least 10 minutes

B. Failure to close the doors of the balance before reading the weight B Electronic balances do not use substitution weights or knife edges to balance the weight on the pan. Instead, they measure the displacement of the pan by the weight on it using electromagnetic force to return it to its reference position. Regardless of the type of balance used, all need to be located on a firm weighing table free of vibration. Doors must be closed to prevent air currents from influencing the weighing, and the pan and platform must be clean and free of dust and chemical residue

The most commonly used detector for clinical gas-liquid chromatography (GLC) is based upon: A. Ultraviolet light absorbance at 254 nm B. Flame ionization C. Refractive index D. Thermal conductance

B. Flame ionization B Volatile solutes can be detected in GLC using flame ionization, thermal conductivity, electron capture, and mass spectroscopy. In flame ionization, energy from a flame is used to excite the analytes as they elute from the column. The flame is made by igniting a mixture of hydrogen, carrier gas, and air. Current is produced when an outer shell electron is ejected from the excited analyte

The freezing point osmometer differs from the vapor pressure osmometer in that only the freezing point osmometer: A. Cools the sample B. Is sensitive to ethanol C. Requires a thermoelectric module D. Requires calibration with aqueous standards

B. Is sensitive to ethanol B Alcohol enters the vapor phase so rapidly that it evaporates before the dew point of the sample is reached. Therefore, ethanol does not contribute to osmolality as measured using the vapor pressure osmometer. Freezing-point osmometers measure alcohol and can be used in emergency department settings to estimate ethanol toxicity.

Why is vacuum necessary in the mass filter of a mass spectrometer? A. Ionization does not occur at atmospheric pressure B. It prevents collision between fragments C. It removes electrons from the ion source D. It prevents contamination

B. It prevents collision between fragments B Vacuum is needed in the mass filter of the MS to prevent random collisions between ions that would alter their trajectory or time of flight. It is also needed in CG-MS instruments that use electron ionization. The vacuum prevents collision between the carrier gas molecules and the ions. In spectrometers that use electrospray ionization, chemical ionization, and laser desorption ionization (MALDI and SELDI TOF), the ion source is not under vacuum.

Select the anticoagulant of choice for blood gas studies. A. Sodium citrate 3.2% B. Lithium heparin 100 U/mL blood C. Sodium citrate 3.8% D. Ammonium oxalate 5.0%

B. Lithium heparin 100 U/mL blood B Heparin is the only anticoagulant that does not alter the pH of blood; heparin salts must be used for pH and blood gases. Solutions of heparin are air equilibrated and must be used sparingly to prevent contamination of the sample by gas in the solution.

Interference in atomic absorption spectrophotometry caused by differences in viscosity is called: A. Absorption interference B. Matrix effect C. Ionization interference D. Quenching

B. Matrix effect B Significant differences in aspiration and atomization result when the matrix of sample and unknowns differ. Differences in viscosity and protein content are major causes of matrix error. Matrix effects can be reduced by using protein-based calibrators and diluting both standards and samples prior to assay.

A patient's blood gas results are: pH = 7.50 PCO2 = 55 mm Hg HCO3 - = 40 mmol/L These results indicate: A. Respiratory acidosis B. Metabolic alkalosis C. Respiratory alkalosis D. Metabolic acidosis

B. Metabolic alkalosis B A pH above 7.45 corresponds with alkalosis. Both bicarbonate and PCO2 are elevated. Bicarbonate is the conjugate base and is under metabolic (renal) control, while PCO2 is an acid and is under respiratory control. Increased bicarbonate (but not increased CO2) results in alkalosis; therefore, the classification is metabolic alkalosis, partially compensated by increased PCO2.

Which element is reduced at the cathode of a Clark polarographic electrode? A. Silver B. Oxygen C. Chloride D. Potassium

B. Oxygen B The Clark electrode is designed to measure oxygen. O2 diffuses through a gas-permeable membrane covering the electrode. It is reduced at the cathode, which is made of platinum or other inert metal. Electrons are supplied by the anode, which is made of silver. The net reaction is: 4 KCl + 2 H2O + O2 + 4 Ag° →4 AgCl + 4 KOH

Which of the following would cause a "response" error from an ion-selective electrode for sodium when measuring serum but not the calibrator? A. Interference from other electrolytes B. Protein coating the ion-selective membrane C. An overrange in sodium concentration D. Protein binding to sodium ions

B. Protein coating the ion-selective membrane B Response is the time required for an electrode to reach maximum potential. Ion-selective analyzers use a microprocessor to monitor electrode response, slope, drift, and noise. When an electrode gives an acceptable response time when measuring an aqueous calibrator, but not when measuring serum, the cause is often protein buildup on the membrane.

One mole per kilogram H2O of any solute will cause all of the following except: A. Lower the freezing point by 1.86°C B. Raise vapor pressure by 0.3 mm Hg C. Raise the boiling point by 0.52°C D. Raise osmotic pressure by 22.4 atm

B. Raise vapor pressure by 0.3 mm Hg B Both freezing point and vapor pressure are lowered by increasing solute concentration. Boiling point and osmotic pressure are raised. Increasing solute concentration of a solution opposes a change in its physical state and lowers the concentration of H2O molecules.

The term RT/nF in the Nernst equation defines the: A. Potential at the ion-selective membrane B. Slope of the electrode C. Decomposition potential D. Isopotential point of the electrode

B. Slope of the electrode B In the term RT/nF, R = the molar gas constant, T = temperature in degrees Kelvin, F = Faraday's constant, and n = the number of electrons donated per atom of reductant. The slope depends upon the temperature of the solution and the valence of the reductant. At room temperature, the slope is 59.2 mV for a univalent ion and 29.6 mV for a divalent ion.

SITUATION: A GC-MS analysis using nitrogen as the carrier gas shows an extensively noisy baseline. A sample of the solvent used for the extraction procedure, ethyl acetate, was injected and showed the same noise. Results of an Autotune test showed the appearance of a base peak at 16 with two smaller peaks at 17 and 18. Tese results indicate: A. The solvent is contaminated B. The carrier gas is contaminated C. There is electrical noise in the detector D. The ion source is dirty

B. The carrier gas is contaminated B All of these situations are sources of baseline noise in GC-MS. However, the peak at 16 indicates the presence of oxygen in the carrier gas. Oxygen in the atmosphere also contains small quantities of two isotopes with molecular weights of 17 and 18 owing to one and two extra neutrons, respectively.

In tandem-mass spectroscopy, the first mass filter performs the same function as: A. The ion source B. The chromatography column C. Extraction D. The vacuum system

B. The chromatography column B A tandem mass spectrometer uses two or more mass filters in sequence. The first filter functions as an ion trap. Once the sample is ionized, the filter selects molecular or parent ions of interest by excluding ions outside a specified size range. Therefore, it effectively separates the analyte(s) of interest from unwanted compounds. Tandem MS uses ESI to introduce the sample into the first mass filter, usually a quadrapole. The RF and DC voltages of the quadrapole are set to optimize the trajectory of the parent ions of interest and cause ejection of unwanted ions. The parent ions are drawn into a second mass filter where they are bombarded by argon atoms. The collisions result in the formation of mass fragments called daughter ions. This process is called collision-induced dissociation and the second filter is called a collision chamber. The process can be repeated in a third mass filter that generates granddaughter ions. A total-ion chromatogram is produced from these, enabling the compound of interest to be identified and quantified. Tandem MS is used to screen for inborn errors of fatty acid, amino acid, and organic acid metabolism.

In the coulometric chloride titration: A. Acetic acid in the titrating solution furnishes the counter ion for reduction B. The endpoint is detected by amperometry C. The titrating reagent contains a phosphate buffer to keep pH constant D. Nitric acid (HNO3) is used to lower the solubility of AgCl

B. The endpoint is detected by amperometry B Reduction of Ag+ back to Ag° generates the current, which signals the endpoint. The titrating reagent contains HNO3, acetic acid, H2O, and either gelatin or polyvinyl alcohol. The HNO3 furnishes nitrate, which is reduced at the generator cathode, forming ammonium ions. The ammonium becomes oxidized back to nitrate at the indicator anode. Gelatin or polyvinyl alcohol is needed to prevent pitting of the generator anode. Acetic acid lowers the solubility of AgCl, preventing dissociation back to Ag+

In mass spectroscopy, the term base peak typically refers to: A. The peak with the lowest mass B. The peak with the most abundance C. A natural isotope of the molecular ion D. The first peak to reach the mass detector

B. The peak with the most abundance B The base peak is typically the "molecular ion" or parent ion, meaning that it is the initial fragment made by releasing an electron. The cation thus formed has a charge of +1, and therefore, its m/z ratio is equal to its mass. The base peak is used for selective ion monitoring (SIM). It is the most abundant and most stable ion, and gives the best sensitivity for quantitative analysis.

Why do many optical systems in chemistry analyzers utilize a reference light path? A. To increase the sensitivity of the measurement B. To minimize error caused by source lamp fluctuation C. To obviate the need for wavelength adjustment D. To reduce stray light effects

B. To minimize error caused by source lamp fluctuation B A reference beam is used to produce an electrical signal at the detector to which the measurement of light absorption by the sample is compared. This safeguards against measurement errors caused power fluctuations that change the source lamp intensity. Although reference beams increase the accuracy of measurements, they do so at the expense of optical sensitivity since some of the incident light must be used to produce the reference beam

Which set of results is consistent with uncompensated respiratory alkalosis? A. pH 7.70 HCO3 30 mmol/L PCO2 25 mm Hg B. pH 7.66 HCO3 22 mmol/L PCO2 20 mm Hg C. pH 7.46 HCO3 38 mmol/L PCO2 55 mm Hg D. pH 7.36 HCO3 22 mmol/L PCO2 38 mm Hg

B. pH 7.66 HCO3 22 mmol/L PCO2 20 mm Hg B Respiratory alkalosis is caused by hyperventilation, inducing low PCO2. Very often, in the early phase of an acute respiratory disturbance, the kidneys have not had time to compensate, and the bicarbonate is within normal limits. In answer A, the bicarbonate is high and PCO2 low; thus, both are contributing to alkalosis and this would be classified as a combined acid-base disturbance. In answer C, the pH is almost normal, and both bicarbonate and PCO2 are increased. This can occur in the early stage of a metabolic acid base disturbance when full respiratory compensation occurs or in a combined acid-base disorder. In answer D, both bicarbonate and PCO2 are within normal limits (22-26 mmol/L, 35-45 mm Hg, respectively) as is the pH.

Which of the following represents the Henderson Hasselbalch equation as applied to blood pH? A. pH = 6.1 + log HCO3-/PCO2 B. pH = 6.1 + log HCO3-/ (0.03 × PCO2) C. pH = 6.1 + log dCO2/HCO3- D.pH=6.1 + log (0.03×PCO2) / HCO3-

B. pH = 6.1 + log HCO3-/ (0.03 × PCO2) B The Henderson-Hasselbalch equation describes the pH of a buffer comprised of a weak acid and its salt. pH = pKa + log salt/acid, where pKa is the negative logarithm of the dissociation constant of the acid. In this case, the salt is sodium bicarbonate and the acid is the dissolved CO2, which is equal to 0.03 (mmol/L per mm Hg) x PCO2. The pKa includes both the hydration and dissociation constant for dissolved CO2 in blood, 6.1 and is termed pK´.

In thin-layer chromatography (TLC), the distance the solute migrates divided by the distance the solvent migrates is the: A. tR B. Kd C Rf D. pK

C Rf C Rf is the distance migrated by the solute divided by the distance migrated by the solvent. The tR refers to the retention time of the solute in HPLC or gas chromatography (GC). The Kd is the partition coefficient, and is a measure of the relative affinity of solutes for the stationary phase. The solute with the greater Kd will be retained longer. The pK is the negative logarithm of K, the ionization constant, and is a measure of ionization.

What is the PO2 of calibration gas containing 20.0% O2, when the barometric pressure is 30 in.? A. 60 mm Hg B. 86 mm Hg C. 143 mm Hg D. 152 mm Hg

C. 143 mm Hg C Convert barometric pressure in inches to mm Hg by multiplying by 25.4 (mm/in.). Next, subtract the vapor pressure of H2O at 37°C, 47 mm Hg, to give dry gas pressure. Multiply dry gas pressure by the %O2: 25.4 mm/in. × 30 in. = 762 mm Hg 762 mm Hg - 47 mm Hg (vapor pressure) = 715 mm Hg (dry gas pressure) 0.20 × 715 mm Hg = 143 mm Hg PO2

Which statement regarding reflectometry is true? A. The relation between reflectance density and concentration is linear B. Single-point calibration can be used to determine concentration C. 100% reflectance is set with an opaque film called a white reference D. The diode array is the photodetector of choice

C. 100% reflectance is set with an opaque film called a white reference C Reflectometry does not follow Beer's law, but the relationship between concentration and reflectance can be described by a logistic formula or algorithm that can be solved for concentration. For example, K/S = (1 - R) 2/2R, where K = Kubelka-Munk absorptivity constant, S = scattering coefficient, R = reflectance density. K/S is proportional to concentration. The white reference is analogous to the 100%T setting in spectrophotometry and serves as a reference signal. Dr = log R0/R1, where Dr is the reflectance density, R0 is the white reference signal, and R1 is the photodetector signal for the test sample.

Given the following real-time PCR amplification curve, what is the threshold cycle? A. 15 B. 20 C. 25 D. 30

C. 25 C The maximum curvature of the plot approximates the threshold cycle. A line is drawn from the threshold value on the y-axis through the curve, and a perpendicular dropped to the x-axis. The Ct is determined by the intersection point on the x-axis. The threshold is usually determined by an algorithm but can be calculated manually as 10 times the average standard deviation of the RFUs for cycles 2-10.

What is the PCO2 if the dCO2 is 1.8 mmol/L? A. 24 mm Hg B. 35 mm Hg C. 60 mm Hg D. 72 mm Hg

C. 60 mm Hg C Dissolved CO2 is calculated from the measured PCO2 × 0.0306, the solubility coefficient for CO2 gas in blood at 37°C. dCO2 = PCO2 × 0.03. Therefore, PCO2 = dCO2 /0.03 PCO2 = 1.8 mmol/L ÷ 0.03 mmol/L per mm Hg = 60 mm Hg

What is the blood pH when the partial pressure of carbon dioxide (PCO2) is 60 mm Hg and the bicarbonate concentration is 18 mmol/L? A. 6.89 B. 7.00 C. 7.10 D. 7.30

C. 7.10 C Solve using the Henderson-Hasselbalch equation. pH = pK´ + log HCO3 -/(0.03 × PCO2), where pK´, the negative logarithm of the combined hydration and dissociation constants for dissolved CO2 and carbonic acid, is 6.1 and 0.03 is the solubility coefficient for CO2 gas. pH = 6.1 + log 18/(0.03 × 60) = 6.1 + log 18/1.8 pH = 6.1 + log 10. Because log 10 = 1, pH = 7.10

Which instrument requires a highly regulated DC power supply? A. A spectrophotometer with a barrier layer cell B. A colorimeter with multilayer interference filters C. A spectrophotometer with a photomultiplier tube D. A densitometer with a photodiode detector

C. A spectrophotometer with a photomultiplier tube C When AC voltage regulators are used to isolate source lamp power, light output fluctuates as the voltage changes. Because this occurs at 60 Hz, it is not detected by eyesight or slow-responding detectors. Photomultiplier tubes are sensitive enough to respond to the AC frequency and require a DC-regulated power supply.

The method for measuring iron or lead by plating the metal and then oxidizing it is called: A. Polarography B. Coulometry C. Anodic stripping voltometry D. Amperometry

C. Anodic stripping voltometry C Anodic stripping voltometry is used to measure lead and iron. The cation of the metal is plated onto a mercury cathode by applying a negative charge. The voltage of this electrode is reversed until the plated metal is oxidized back to a cation. Current produced by oxidation of the metal is proportional to concentration.

In polarography, the voltage needed to cause depolarization of the cathode is called the: A. Half-wave potential B. Isopotential point C. Decomposition potential D. Polarization potentia

C. Decomposition potential C In polarography, a minimum negative voltage must be applied to the cathode to cause reduction of metal ions (or O2) in solution. This is called the decomposition potential. It is concentration dependent (dilute solutions require greater negative voltage), and can be determined using the Nernst equation.

Which condition is a common cause of stray light? A. Unstable source lamp voltage B. Improper wavelength calibration C. Dispersion from second-order spectra D. Misaligned source lamp

C. Dispersion from second-order spectra C Stray light is caused by the presence of any light other than the wavelength of measurement reaching the detector. It is most often caused by second-order spectra, deteriorated optics, light dispersed by a darkened lamp envelope, and extraneous room light.

Which method is the most useful when screening for errors of amino and organic acid metabolism? A. Two-dimensional thin-layer chromatography B. Gas chromatography C. Electrospray ionization tandem-mass spectroscopy D. Inductively charged coupled-mass spectroscopy

C. Electrospray ionization tandem-mass spectroscopy C While two-dimensional thin-layer chromatography can separate both amino and organic acids, it is not sufficiently sensitive for newborn screening. Electrospray ionization allows a small alcohol-extracted whole-blood sample to be analyzed by two mass spectrometers without prior separation by liquid or gas chromatography. Disorders of both organic and fatty acid metabolism are identified by the specific pattern of acylcarnitine ions produced. Amino acids are detected as amino species that have lost a carboxyl group during ionization, a process called neutral loss.

Which instrument requires a primary and secondary monochromator? A. Spectrophotometer B. Atomic absorption spectrophotometer C. Fluorometer D. Nephelometer

C. Fluorometer C A fluorometer uses a primary monochromator to isolate the wavelength for excitation, and a secondary monochromator to isolate the wavelength emitted by the fluorochrome.

What is the confirmatory method for measuring drugs of abuse? A. HPLC B. Enzyme-multiplied immunoassay technique (EMIT) C. Gas chromatography with mass spectroscopy (GC-MS) D. TLC

C. Gas chromatography with mass spectroscopy (GC-MS) C GC-MS determines the mass spectrum of the compounds eluting from the analytic column. Each substance has a unique and characteristic spectrum of mass fragments. This spectrum is compared to spectra in a library of standards to determine the percent match. A match of greater than 95% is considered confirmatory.

What type of detector is used in high-performance liquid chromatography with electrochemical detection (HPLC-ECD)? A. Calomel electrode B. Conductivity electrode C. Glassy carbon electrode D. Polarographic electrode

C. Glassy carbon electrode C HPLC-ECD uses a glassy carbon measuring electrode and a silver-silver chloride reference. The analyte is oxidized or reduced by holding the glassy carbon electrode at a positive voltage (oxidization) or negative voltage (reduction). The resulting current flow is directly proportional to concentration. Phenolic groups such as catecholamines can be measured by HPLC-ECD.

Which of the following contributes the most to the serum total CO2? A. PCO2 B. dCO2 C. HCO3- D. Carbonium ion

C. HCO3- C The total CO2 is the sum of the dCO2, H2CO3 (carbonic acid or hydrated CO2), and bicarbonate (as mainly NaHCO3). When serum is used to measure total CO2, the dCO2 is insignificant because all the CO2 gas has escaped into the air. Therefore, serum total CO2 is equivalent to the bicarbonate concentration. Total CO2 is commonly measured by potentiometry. An organic acid is used to release CO2 gas from bicarbonate and pCO2 is measured with a Severinghaus electrode. Alternately, bicarbonate can be measured by an enzymatic reaction using phosphoenol pyruvate carboxylase. The enzyme forms oxaloacetate and phosphate from phosphoenol pyruvate and bicarbonate. The oxaloacetate is reduced to malate by malate dehydrogenase and NADH is oxidized to NAD+. The negative reaction rate is proportional to plasma bicarbonate concentration.

What method is used to introduce the sample into a mass spectrometer for analysis of a trace element? A. Electrospray ionization B. Laser desorption C. Inductively charged plasma (ICP) ionization D. Direct injection

C. Inductively charged plasma (ICP) ionization C Mass spectrometers can be used to measure trace metals, but the atoms need to be vaporized and ionized like molecules before they enter the mass filter. This is done by introducing the sample into a very hot plasma (6,000-10,000°K) called a torch. The torch is made by circulating argon through inner and outer quartz tubes. The tubes are wrapped with a coil of wire that receives a radio frequency. This creates current flow through the wire and a magnetic field at the torch end. Argon atoms are excited by the current and magnetic field and ionize. When the argon is ignited by a spark, it forms the plasma. The sample is mixed with argon at the other end to create an aerosol. When it reaches the torch, the solvent is evaporated and the energy from the torch and collisions with argon ions cause ejection of outershell electrons, forming cations of the element. ICP-MS is used to measure any trace element that readily forms cations.

The term isocratic is used in high-performance liquid chromatography (HPLC) to mean the: A. Mobile phase is at constant temperature B. Stationary phase is equilibrated with the mobile phase C. Mobile phase consists of a constant solvent composition D. Flow rate of the mobile phase is regulated

C. Mobile phase consists of a constant solvent composition C An isocratic separation uses a single mobile phase of constant composition, pH, and polarity, and requires a single pump. Some HPLC separations use a gradient mobile phase to increase distance between peaks. Gradients are made by mixing two or more solvents using a controller to change the proportions of solvent components.

Select the equation describing the potential that develops at the surface of an ion-selective electrode. A. van Deemter equation B. van Slyke equation C. Nernst equation D. Henderson-Hasselbalch equation

C. Nernst equation C The van Deemter equation describes the relation between the velocity of mobile phase to column efficiency in gas chromatography. The Henderson-Hasselbalch equation is used to determine the pH of a solution containing a weak acid and its salt. van Slyke developed an apparatus to measure CO2 and O2 content using a manometer.

What is the primary means of solute separation in HPLC using a C18 column? A. Anion exchange B. Size exclusion C. Partitioning D. Cation exchange

C. Partitioning C Stationary phases (column packings) used in HPLC separate solutes by multiple means, but in reverse-phase HPLC the relative solubility between the mobile phase and stationary phase is most important and depends upon solvent polarity, pH, and ionic strength.

Which component is required in a spectrophotometer in order to produce a spectral absorbance curve? A. Multiple monochromators B. A reference optical beam C. Photodiode array D. Laser light source

C. Photodiode array C There are two ways to perform spectral scanning for compound identification. One is to use a stepping motor that continuously turns the monochromator so that the wavelength aligned with the exit slit changes at a constant rate. A more practical method is to use a diode array detector. This consists of a chip embedded with as many as several hundred photodiodes. Each photodiode is aligned with a narrow part of the spectrum produced by a diffraction grating, and produces current proportional to the intensity of the band of light striking it (usually 1-2 nm in range). The diode signals are processed by a computer to create a spectral absorbance or transmittance curve.

A patient's blood gas results are as follows: pH = 7.26 dCO2 = 2.0 mmol/L HCO3 - = 29 mmol/L These results would be classified as: A. Metabolic acidosis B. Metabolic alkalosis C. Respiratory acidosis D. Respiratory alkalosis

C. Respiratory acidosis Imbalances are classified as respiratory when the primary disturbance is with PCO2 because PCO2 is regulated by ventilation. PCO2 = dCO2/0.03 or 60 mm Hg (normal 35-45 mm Hg). Increased dCO2 will increase hydrogen ion concentration, causing acidosis. Bicarbonate is moderately increased, but a primary increase in NaHCO3 causes alkalosis. Thus, the cause of this acidosis is CO2 retention (respiratory acidosis), and it is partially compensated by renal retention of bicarbonate.

Which type of filter is best for measuring stray light? A. Wratten B. Didymium C. Sharp cutoff D. Neutral density

C. Sharp cutoff C Sharp cutoff filters transmit almost all incident light until the cutoff wavelength is reached. At that point, they cease to transmit light. Because they give an "all or none effect," only stray light reaches the detector when the selected wavelength is beyond the cutoff.

A plasma sample is hemolyzed and turbid. What is required to perform a sample blank in order to correct the measurement for the intrinsic absorbance of the sample when performing a spectrophotometric assay? A. Substitute deionized water for the sample B. Dilute the sample 1:2 with a standard of known concentration C. Substitute saline for the reagent D. Use a larger volume of the sample

C. Substitute saline for the reagent C A sample blank is used to subtract the intrinsic absorbance of the sample usually caused by hemolysis, icterus, turbidity, or drug interference. On automated analyzers, this is accomplished by measuring the absorbance after the addition of sample and a first reagent, usually a diluent. For tests using a single reagent, sample blanking can be done prior to the incubation phase before any color develops. Substituting deionized water for sample is done to subtract the absorbance of the reagent (reagent blanking). Diluting the sample with a standard (standard addition) may be done when the absorbance is below the minimum detection limit for the assay. Using a larger volume of sample will make the interference worse.

When measuring lead in whole blood using atomic absorption spectrophotometry, what reagent is required to obtain the needed sensitivity and precision? A. Lanthanum B. Lithium C. Triton X-100 D. Chloride

C. Triton X-100 C A graphite furnace is preferred over a flame for measuring lead because it is sufficiently sensitive to detect levels below 5 μg/dL, the cutoff needed for lead screening of children. The matrix modifier consists of Triton X -100, ammonium phosphate and nitric acid. This allows for release of Pb from the RBCs, and solubilization of cell stroma. The matrix modifier also prevents loss of Pb caused by formation of lead halides and promotes interaction between Pb and the tube wall, preventing its loss during the ashing cycle.

Which of the following statements about fluorometry is accurate? A. Fluorometry is less sensitive than spectrophotometry B. Fluorometry is less specific than spectrophotometry C. Unsaturated cyclic molecules are often fluorescent D. Fluorescence is directly proportional to temperature

C. Unsaturated cyclic molecules are often fluorescent C Increasing temperature results in more random collision between molecules by increasing their motion. This causes energy to be dissipated as heat instead of fluorescence. Temperature is inversely proportional to fluorescence. Fluorescence is more sensitive than spectrophotometry because the detector signal can be amplified when dilute solutions are measured. It is also more specific than spectrophotometry because both the excitation and emission wavelengths are characteristics of the compound being measured.

The ion-selective membrane used to measure potassium is made of: A. High-borosilicate glass membrane B. Polyvinyl chloride dioctylphenyl phosphonate ion exchanger C. Valinomycin gel D. Calomel

C. Valinomycin gel C Valinomycin is an antibiotic with a highly selective reversible-binding affinity for potassium ions. Sodium electrodes are usually composed of a glass membrane with a high content of aluminum silicate. Calcium and lithium ion-selective electrodes are made from organic liquid ion exchangers called neutral carrier ionophores Calomel is made of mercury covered with a paste of mercurous chloride (Hg°/Hg2Cl2) and is used as a reference electrode for pH.

A decreased PAO2-PaO2 difference is found in: A. A/V (arteriovenous) shunting B. V/Q (ventilation/perfusion) inequality C. Ventilation defects D. All of these options

C. Ventilation defects C Patients with A/V shunts, V/Q inequalities, and cardiac failure will have an increased PAO2-PaO2 difference. However, patients with ventilation problems have low alveolar PO2 owing to retention of CO2 in the airway. This reduces the PAO2-PaO2 difference.

What type of measuring circuit is used in a freezing point osmometer? A. Electrometer B. Potentiometer C. Wheatstone bridge D. Thermal conductivity bridge

C. Wheatstone bridge C The resistance of the thermistor is measured using a network of resistors called a Wheatstone bridge. When the sample is frozen, the bridge is balanced using a calibrated variable resistor, so that no current flows to the readout. The resistance required to balance the meter is equal to the resistance of the thermistor.

When calibrating a semiautomatic pipet that has a fixed delivery of 10.0 µL using a gravimetric method, what should be the average weight of deionized water transferred? A. 10.0 µg B. 100.0 µg C. 1.0 mg D. 10.0 mg

D. 10.0 mg D Gravimetric and spectrophotometric analysis are the two methods used to verify pipet volume accuracy and precision. Since spectrophotometric analysis involves dilution, gravimetric analysis is associated with greater certainty. At 20°C, the density of pure water is 0.99821 g/mL. Therefore, each microliter weighs almost exactly 1.0 mg.

What is the maximum recommended storage time and temperature for an arterial blood gas sample drawn in a plastic syringe? Storage Time / Temperature A. 10 min 2°C-8°C B. 20 min 2°C-8°C C. 30 min 2°C-8°C D. 30 min 22°C

D. 30 min 22°C D Arterial blood gas samples collected in plastic syringes should be stored at room temperature because cooling the sample allows oxygen to enter the syringe. Storage time should be no more than 30 minutes because longer storage results in a significant drop in pH and PO2 and increased PCO2.

Which monochromator specification is required in order to measure the true absorbance of a compound having a natural absorption bandwidth of 30 nm? A. 50-nm bandpass B. 25-nm bandpass C. 15-nm bandpass D. 5-nm bandpass

D. 5-nm bandpass D Bandpass refers to the range of wavelengths passing through the sample. The narrower the bandpass, the greater the photometric resolution. Bandpass can be made smaller by reducing the width of the exit slit. Accurate absorbance measurements require a bandpass less than one-fifth the natural bandpass of the chromophore

All of the following are required when measuring magnesium by atomic absorption spectrophotometry except: A. A hollow cathode lamp with a magnesium cathode B. A chopper to prevent optical interference from magnesium emission C. A monochromator to isolate the magnesium emission line at 285 nm D. A 285-nm reference beam to correct for background absorption

D. A 285-nm reference beam to correct for background absorption D Atomic absorption requires a lamp with a cathode made from the metal to be assayed. The lamp emits the line spectrum of the metal, providing the wavelength that the atoms can absorb. The chopper pulses the source light, allowing it to be discriminated from light emitted by excited atoms. A monochromator eliminates light emitted by the ideal gas in the lamp. Deuterium (wide bandpass light) or Zeeman correction (splitting the incident light into side bands by a magnetic field) may be used to correct for background absorption.

Which photodetector is most sensitive to low levels of light? A. Barrier layer cell B. Photodiode C. Diode array D. Photomultiplier tube

D. Photomultiplier tube D The photomultiplier tube uses dynodes of increasing voltage to amplify the current produced by the photosensitive cathode. It is 10,000 times as sensitive as a barrier layer cell, which has no amplification. A photomultiplier tube requires a DC-regulated lamp because it responds to light fluctuations caused by the AC cycle.

Which type of monochromator produces the purest monochromatic light in the UV range? A. A diffraction grating and a fixed exit slit B. A sharp cutoff filter and a variable exit slit C. Interference filters and a variable exit slit D. A prism and a variable exit slit

D. A prism and a variable exit slit D Diffraction gratings and prisms both produce a continuous range of wavelengths. A diffraction grating produces a uniform separation of wavelengths. A prism produces much better separation of high-frequency light because refraction is greater for higher-energy wavelengths. Instruments using a prism and a variable exit slit can produce UV light of a very narrow bandpass. The adjustable slit is required in order to allow sufficient light to reach the detector to set 100%T.

In absorption spectrophotometry: A. Absorbance is directly proportional to transmittance B. Percent transmittance is directly proportional to concentration C. Percent transmittance is directly proportional to the light path length D. Absorbance is directly proportional to concentration

D. Absorbance is directly proportional to concentration D Beer's law states that A = a × b × c, where a is the absorptivity coefficient (a constant), b is the path length, and c is concentration. Absorbance is directly proportional to both b and c. Doubling the path length results in incident light contacting twice the number of molecules in solution. This causes absorbance to double, the same effect as doubling the concentration of molecules.

Select the chemical that is used in most HPLC procedures to decrease solvent polarity. A. Hexane B. Nonane C. Chloroform D. Acetonitrile

D. Acetonitrile D All of the compounds mentioned have nonpolar properties. Because most HPLC is reverse phase (a polar solvent is used), hexane and nonane are too nonpolar. Acetonitrile is more polar and less toxic than chloroform and along with methanol is a common polarity modifier for HPLC.

Which formula correctly describes the relationship between absorbance and %T ? A. A = 2 - log %T B. A = log 1/T C. A = -log T D. All of these options

D. All of these options D Absorbance is proportional to the inverse log of transmittance. A = -log T = log 1/T Multiplying the numerator and denominator by 100 gives: A = log (100/100 X T) 100 X T = %T, substituting %T for 100 X T gives: A = log 100/%T A = log 100 - log %T A = 2.0 - log %T For example, if %T = 10.0, then: A = 2.0 - log 10.0 log 10.0 = 1.0 A = 2.0-1.0 = 1.0

Which of the following materials is best suited for verifying the wavelength calibration of a spectrophotometer? A. Neutral density filters B. Potassium dichromate solutions traceable to the National Bureau of Standards reference C. Wratten filters D. Holmium oxide glass

D. Holmium oxide glass D Wavelength accuracy is verified by determining the wavelength reading that gives the highest absorbance (or transmittance) when a substance with a narrow natural bandpass (sharp absorbance or transmittance peak) is scanned. For example, didymium glass has a sharp absorbance peak at 585 nm. Therefore, an instrument should give its highest absorbance reading when the wavelength dial is set at 585 nm. Holmium oxide produces a very narrow absorbance peak at 361 nm; likewise, the hydrogen lamp of a UV spectrophotometer produces a 656-nm emission line that can be used to verify wavelength. Neutral density filters and dichromate solutions are used to verify absorbance accuracy or linearity. A Wratten filter is a widebandpass filter made by placing a thin layer of colored gelatin between two glass plates and is unsuitable for spectrophotometric calibration

When measuring calcium by atomic absorption spectrophotometry, which is required? A. An organic extraction reagent to deconjugate calcium from protein B. An internal standard C. A magnesium chelator D. Lanthanum oxide to chelate phosphates

D. Lanthanum oxide to chelate phosphates D An acidic diluent such as hydrochloric acid (HCl) will displace calcium bound to albumin. However, calcium forms a thermostable bond with phosphate that causes chemical interference in atomic absorption. Lanthanum displaces calcium, forming lanthanum phosphate, and eliminates interference from phosphates. Unlike in some colorimetric methods for calcium (e.g., o-cresolphthalein complexone), magnesium does not interfere because it does not absorb the 422.7 nm emission line from the calcium-hollow cathode lamp.

Which substance is used to generate the light signal in electrochemiluminescence? A. Acridinium B. Luminol C. Dioxetane phosphate D. Ruthenium

D. Ruthenium D All of these substances are chemiluminescent. Dioxetane phosphate is excited by alkaline phosphatase. Acridinium and luminol are excited by hydrogen peroxide. In electrochemiluminesence, ruthenium is used to label antibody or antigen. Antigen-antibody complexes containing the ruthenium label are bound to paramagnetic particles via a strepavidin-biotin reaction. The paramagnetic particles are attracted to an electrode surface. The flowcell is washed with a solution containing tripropylamine (TPA) to remove unbound ruthenium label. At the electrode surface, the TPA is oxidized and the electrons excite the ruthenium, causing production of 620-nm light

A linearity study is performed on a visible spectrophotometer at 650 nm and the following absorbance readings are obtained: Concentration of Standard 10.0 mg/dL 20.0 mg/dL 30.0 mg/dL 40.0 mg/dL 50.0 mg/dL Absorbance 0.20 0.41 0.62 0.79 0.92 The study was repeated using freshly prepared standards and reagents, but results were identical to those shown. What is the most likely cause of these results? A. Wrong wavelength used B. Insufficient chromophore concentration C. Matrix interference D. Stray light

D. Stray light D Stray light is the most common cause of loss of linearity at high-analyte concentrations. Light transmitted through the cuvette is lowest when absorption is highest. Therefore, stray light is a greater percentage of the detector response when sample concentration is high. Stray light is usually most significant when measurements are made at the extremes of the visible spectrum because lamp output and detector response are low.

Which statement regarding nephelometry is true? A. Nephelometry is less sensitive than absorption spectrophotometry B. Nephelometry follows Beer's law C. The optical design is identical to a turbidimeter except that a HeNe laser light source is used D. The detector response is directly proportional to concentration

D. The detector response is directly proportional to concentration D In nephelometry, the detector output is proportional to concentration (as opposed to turbidimetry where the detector is behind the cuvette). The detector(s) is (are) usually placed at an angle between 25° and 90° to the incident light, depending upon the application. Nephelometers, like fluorometers, are calibrated to read zero with the light path blocked, and sensitivity can be increased up to 1,000 times by amplification of the detector output or increasing the photomultiplier tube dynode voltage


Set pelajaran terkait

Entrepreneurial Management Chapter 1-4 Quiz

View Set

Chapter 59 Assessment and Management of Patients w/ male reproductive Disorders

View Set

Pediatric Final: Chapters 25-33, 35, 45-49, 51

View Set

Adv. Bio 1 Keystone Review Packet Questions, Vocab, and Notes

View Set

Chapter 5: Big Data & Marketing Analytics

View Set

PrQ31: Practice Quiz - Ch. 31: Inflation and the Quantity Theory of Money

View Set