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Correction: Chemical analysis in saliva and the search for salivary biomarkers – a tutorial review

Kamonwad Ngamchuea , Korbua Chaisiwamongkhol , Christopher Batchelor-McAuley and Richard G. Compton *
Department of Chemistry, Physical & Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QZ, UK. E-mail: richard.compton@chem.ox.ac.uk; Fax: +44 (0)1865275410; Tel: +44 (0)1865275957

Received 22nd December 2017 , Accepted 22nd December 2017

First published on 15th January 2018


Abstract

Correction for ‘Chemical analysis in saliva and the search for salivary biomarkers – a tutorial review’ by Kamonwad Ngamchuea, et al., Analyst, 2018, 143, 81–99.


In the published article some errors were present in Tables 1, 2 and 4.
Table 1 Components of authentic human saliva and a comparison of the normal range of the concentrations between saliva and other biological fluids
Real saliva composition Normal range Ref.
Saliva Other biological fluids
a U mL−1: enzymatic activity per unit (mL) of saliva.
1. Inorganic compounds Na+ 20–80 mmol L−1 Plasma 145 mmol L−1 11
K+ 20 mmol L−1 4 mmol L−1
Ca2+ 1–4 mmol L−1 2.2 mmol L−1
Cl 30–100 mmol L−1 120 mmol L−1
HCO3 15–80 mmol L−1 25 mmol L−1
Phosphate 4 mmol L−1 1.2 mmol L−1
Mg2+ 0.2 mmol L−1 1.2 mmol L−1
SCN 2 mmol L−1 <0.2 mmol L−1
NH3 3 mmol L−1 0.05 mmol L−1
2. Organic compounds (non-protein and lipids) Uric acid 3.38 ± 0.21 mg dL−1 Serum 6.31 ± 0.24 mg dL−1 21–23
217.2 ± 110.3 mol L−1
0.1–7.5 mg dL−1
Bilirubin 0.5–5.0 μmol L−1 Serum 0.2–1.2 mg dL−1 24
Creatinine 0.12 ± 0.06 mg dL−1 Serum 0.89 ± 0.17 mg dL−1 25
0.05–0.2 mg dL−1 Serum 0.6–1.5 mg dL−1
Glucose 4–13 mg dL−1 Blood 80–120 mg dL−1 22 and 26
Blood 88.6 ± 8.0 mg dL−1
Cholesterol 0.02–5.46 μmol L−1 Serum <5 mmol L−1 27
Lactate 0.3–1.8 mM Serum 0.5–1.0 mM 28 and 29
0.1 to 2.5 mmol L−1
3. Protein/polypeptide compounds α-Amylase 19–308 U mL−1[thin space (1/6-em)]a Serum 0.05–0.125 U mL−1[thin space (1/6-em)]a 23 and 30
93 ± 62 U L−1[thin space (1/6-em)]a
2.64 ± 1.8 mg mL−1
Albumin 0.2 ± 0.1 mg mL−1 Serum 3.5–5.5 g dL−1 31
Secretory-IgA 80–717 mg dL−1 Serum 70–400 mg dL−1 23 and 32
124.3–333.5 μg mL−1
Mucin group MUC5B: 2.4 ± 1.7 U mL−1 Serum 9.9 ± 0.8 ng ml−1 31 and 33
1.19 ± 0.17 mg mL−1
Lysozyme 3–50 μg mL−1 Serum 7.4 ± 1.8 mg mL−1 23, 32 and 34
59.7 to 1062.3 μg ml−1 Serum 4–9 μg mL−1
Total proteins 7.1–223.2 mg dL−1 Serum 6–8 g dL−1 23 and 31
0.9 ± 0.2 mg mL−1
4. Hormones Cortisol 3.5–27.0 mg dL−1 Serum 2–25 mg dL−1 35
Testosterone 32–55 pg mL−1 Serum 320–600 ng dL−1 36
Progesterone Luteal phase 436 ± 34 pmol L−1 Serum male: <1 ng mL−1 37
Follicular phase 22.1 ± 2.7 pmol L−1 Serum female: 0.1–20 ng mL−1
Estrogen (Estradiol) Luteal phase 20.6 ± 0.4 pmol L−1 Serum male: 15–60 pg mL−1 37
Serum female: 15–370 pg mL−1


Table 2 Compositions of different artificial saliva recipes
Artificial saliva compositions Concentration (g L−1)
AFNOR14,15 Fusayama-Meyer16 SAGF17,18 Klimek19 Shellis12
a Bacto-Mucin bacteriological. b Somogyi's unit/L is a measure of the level of activity of amylase in blood serum. One Somogyi unit is defined as the amount of amylase required to produce the equivalent of 1 mg of glucose when acting on a standard starch solution under a defined condition.38
1. Inorganic compounds NaCl 6.70 0.40 0.13 0.58
KCl 1.20 0.40 0.96 1.27 1.16
Na2HPO4 0.26 0.34 0.375
KH2PO4 0.20 0.66 0.33 0.35
NaHCO3 1.50 0.10 0.63 0.54
KSCN 0.33 0.19 0.16 (NaSCN) 0.22
CaCl2·2H2O 0.795 0.23 0.17 0.21
Na2S·9H2O 0.005
Urea 1.00 0.20 0.20 0.17
NaH2PO4·H2O 0.69
NH4Cl 0.18 0.16 0.233
Na2SO4·10H2O 0.76
MgCl2·6H2O 0.043
Sodium citrate 0.013
2. Organic compounds Ascorbic acid 0.002
Glucose 0.03
Uric acid 0.0105
Creatinine 0.0001
Choline 0.013
Mixture of vitamins 0.0008
3. Protein/polypeptide compounds Mucin 2.70a
Glycoprotein 2.5
Alpha amylase 3 × 105 Somogyi's unit L−1[thin space (1/6-em)]b
Albumin 0.025
Mixture of amino acids 0.041


The concentrations of blood glucose were misplaced into the ‘Saliva’ column. They are now moved to the correct ‘Other biological fluids’ column. A full, corrected Table 1 is reproduced here.

The concentration of CaCl2·2H2O (ref. Fusayama-Meyer16) was given incorrectly. The concentration of NH4Cl (ref. SAGF17,18) was missing. A full, corrected Table 2 is reproduced here.

Incorrect values were given for linear ranges, LOD and the pH of the buffers for some of the detection methods in Table 4. The specific changes relate to Phosphate (linear range and buffer pH), caffeine (LOD for the molecularly imprinted electrode and linear range for the SWNCT/CC electrode), glutathione (medium for the Prussian blue/SPE electrode and linear range for the caffeic acid/GC electrode) and uric acid (LOD). A full, corrected Table 4 is reproduced here.

Table 3 Examples of methods of electroanalytical detection available for possible salivary biomarkers (listed in Table 3)
The methods highlighted in grey and blue have been validated in artificial saliva and real saliva, respectively. Methods: AMP: amperometry, CA: chronoamperometry, CE: capillary electrophoresis, CV: cyclic voltammetry, DPV: differential pulse voltammetry, EIS: electrochemical impedance spectroscopy, ISE: ion-selective electrode, LSV: linear sweep voltammetry, MPA: multiple-pulse amperometry, SWV: square wave voltammetry. Electrodes: BDD: boron-doped diamond, BPPG: basal plane pyrolytic graphite, CC: carbon ceramic, CIL: carbon ionic liquid, CNF: carbon nanofiber, CP: carbon paste, EPPG: edge plane pyrolytic graphite, GC: glassy carbon electrode, MWCNT: multi-walled carbon nanotube, NP: nanoparticle, SPE: screen-printed electrode, SWCNT: single-walled carbon nanotube, SWCNH: single-walled carbon nanohorn.a Not stated in the text – values are taken from calibration curves present in the papers.
image file: c7an90101a-u1.tif
image file: c7an90101a-u2.tif


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