(Clinical Chemistry. 1998;44:1371-1375.)
© 1998 American Association for Clinical Chemistry, Inc.
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AACC 50th Anniversary Retrospective |
Citation Classics in Intermediary Metabolism
Theodore Peters, Jr.
Research Institute, The Mary Imogene Bassett Hospital, Cooperstown, NY 13326, Fax 607-547-3061, E-mail tedp{at}usa.net
Among the list of 37 Citation Classics in Clinical
Chemistry published in the March issue of this Journal
(1) were 7 dealing with analytes of intermediary metabolism
(2)(3)(4)(5)(6)(7)(8). Two each covered measurement of urea, glucose, and
calcium, whereas one described the combined assay of lactate and
pyruvate. All were published in the period 19621968, when
modifications to methods for these commonly measured substances were
welcome even as automation slowly took over much of their routine
testing.
Chaney and Marbach (2), in their paper from the Chaney
Chemical Laboratory in Glendale, CA, "Modified reagents for
determination of urea and ammonia" (Fig. 1
), simplified the catalyzed indophenol reaction for the
determination of ammonia by combining four reagents into two, each
stable for 60 days or more; urea was determined after conversion to
ammonia and carbon dioxide by incubation with urease for 20 min at room
temperature or 5 min at 60 °C (now there's a stable enzyme!).
Although this is a labor-intensive manual procedure, most readers will
probably not recall the diacetyl monoxime method it largely replaced,
which required heating a serum filtrate in strong sulfuric acid in a
boiling water bath for 20 min. The 1554 citations received by this
paper through 1995 were well deserved.

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Figure 1. The first paper in which Chaney and Marbach describe a
simplified indophenol reaction for the measurement of ammonia,
Clinical Chemistry 1962;8:1302.
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Marsh et al. (3) in 1965 published modifications of the
direct assay of urea with diacetyl monoxime, applicable to both manual
and automated (AutoAnalyzer®, Technicon Corp.) procedures
(Fig. 2
). By including ferric chloride and thiosemicarbazide to
intensify the color development, they were able to reduce the acid
concentration from 67% (v/v) sulfuric acid to 8% (v/v) sulfuric acid
and 1% (v/v) phosphoric acid. Heating in a boiling water bath for 20
min was still needed in the manual procedure; the automated method used
the Technicon 95 °C heating bath. Their paper received 889
citations.

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Figure 2. The first description by Marsh et al. of improved methods
for the measurement of blood urea, Clinical Chemistry
1965;11:6247.
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Dubowski (4) while at the University of Florida was seeking
a single-reagent manual procedure for glucose as a standby procedure
for the automated methods by then in widespread use. Previous color
reagents, benzidine and aminobiphenyl, were unstable or carcinogenic;
Dr. Dubowski adapted o-toluidine (2-aminotoluene) in glacial
acetic acid on the suggestion of Scandinavian chemist O.M. Forsell
(Fig. 3
). This reagent is stable for many months at room temperature.
In the test, it can be added directly to various types of protein-free
filtrates of body fluids and the absorbance read after 20 min in a
boiling water bath. Kurt Dubowski, now at the University of Oklahoma,
is well known to many members as a former secretary and president of
AACC. This detailed and well-documented paper is a good example of his
thorough scientific style.

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Figure 3. Dubowski's paper describing a single-reagent manual
method for measurement of glucose, Clinical Chemistry
1962;8:21535.
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In 1968, Kadish et al. (5) introduced a more specific assay
for glucose, using glucose oxidase with polarographic detection of the
oxygen consumed (Fig. 4
). Co-author James Sternberg, well known for his work with
instrumentation at Beckman Instruments, Inc., was doubtless the
provider of the polarographic analyzer. Measurement of oxygen
consumption directly rather than of hydrogen peroxide production by
reaction with peroxidase greatly improved the specificity of the
method, because peroxide could be lost by action of catalase in the
specimen. In this procedure, any peroxide was destroyed by reduction by
iodide in the presence of ammonium molybdate before it could regenerate
oxygen. The procedure measured the maximum rate of oxygen
loss rather than overall oxygen consumption, which allowed for rapid
readouts with fewer concerns of back-diffusion. It was designed for the
small laboratory or for emergency use.

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Figure 4. The first description of a polarographic method for the
measurement of glucose, Clinical Chemistry
1968;14:11631.
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Gerald Kessler and Morris Wolfman (6) in 1964 adapted
accepted procedures for calcium and phosphate to the AutoAnalyzer (Fig. 5
). Dialysis obviated preparation of a protein-free filtrate;
addition of 1 mol/L HCl to the specimen assured the release of bound
calcium so that total calcium would be measured. This was one of the
early applications of the colorimetric metal-complexing dye,
cresolphthalein complexone, to detection of calcium; the phosphate
assay used the standard Fiske-SubbaRow chemistry.

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Figure 5. The first AutoAnalyzer method for the simultaneous
measurement of calcium and phosphorus without preliminary sample
treatment, Clinical Chemistry 1964;10:686703.
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In 1967, Trudeau and Freier (7) studied the use of lanthanum
chloride to simplify the assay of calcium by atomic absorption
spectrophotometry (AAS) (Fig. 6
).Following the results of Zettner and Seligson(9)
(Fig. 7
), they found that 0.1% lanthanum (w/v) suppressed the effects
of anions, including protein and phosphate, on the calcium absorbance.
At the same time, the arrival of the more sensitive PerkinElmer 303
spectrophotometer permitted use of a 1:50 dilution of serum, which
avoided clogging of the burner by protein and so eliminated the need
for preparation of a protein-free filtrate. Urine could be analyzed
accurately upon dilution with 0.5% lanthanum. The entire procedure
required only 1 to 2 min.

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Figure 6. The paper in which Trudeau and Freier first describe the
use of lanthanum in the measurement of calcium in biological fluids,
Clinical Chemistry 1967;13:10114.
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Figure 7. The original paper by Zettner and Seligson on the use of
atomic absorption spectrophotometry to measure serum calcium,
Clinical Chemistry 1964;10:86990.
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Marbach and Weil (8) in 1967 simplified the enzymatic assay
of lactate and pyruvate in blood (Fig. 8
), using a single enzyme (lactic dehydrogenase) and a single
protein-free filtrate (in 5% metaphosphoric acid). To measure lactate,
an excess of NAD was added in a glycine-hydrazine buffer at pH 9.0; to
measure pyruvate, an excess of NADH was used in a Tris buffer at pH
7.5. Dr. Marbach, it might be noted, is one of only two authors whose
name appears twice in the list of 37 "Classics" (1) (the
other is G. Szasz). By the time of this paper, Edward Marbach had moved
from the Chaney Laboratory to the University of Southern California; he
appeared in the 1988 ACCC Membership Directory as a bioconsultant in
Los Angeles.

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Figure 8. The first description by Marbach and Weil of a simplified
assay for lactate and pyruvate, Clinical Chemistry
1967;13:31425.
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Why were these seven papers so frequently recognized? We can't be
sure, but they offered sound chemistry in detailed, well-documented
procedures for important metabolic constituents. And I like to think
that their popularity is also a credit to the tradition of careful
editing by the Clinical Chemistry staff.
References
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Bruns DE. Citation classics in Clinical Chemistry. Clin Chem 1998;44:698-699.
[Free Full Text]
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Chaney AL, Marbach EP. Modified reagents for determination of urea and ammonia. Clin Chem 1962;8:130-132.
[Abstract]
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Marsh WH, Fingerhut B, Miller H. Automated and manual direct methods for the determination of blood urea. Clin Chem 1965;11:624-627.
[Abstract]
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Dubowski KM. An o-toluidine method for body-fluid glucose determination. Clin Chem 1962;8:215-235.
[Abstract]
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Kadish AH, Litle RL, Sternberg JC. A new and rapid method for the determination of glucose by measurement of rate of oxygen consumption. Clin Chem 1968;14:116-131.
[Abstract]
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Kessler G, Wolfman M. An automated procedure for the simultaneous determination of calcium and phosphorus. Clin Chem 1964;10:686-703.
[Abstract]
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Trudeau DL, Freier EF. Determination of calcium in urine and serum by atomic absorption spectrophotometry (AAS). Clin Chem 1967;13:101-114.
[Abstract]
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Marbach EP, Weil MH. Rapid enzymatic measurement of blood lactate and pyruvate. Clin Chem 1967;13:314-325.
[Abstract]
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Zettner A, Seligson D. Application of atomic absorption spectrophotometry in the determination of calcium in serum. Clin Chem 1964;10:869-890.
[Abstract]