Chemometrics and digital image colorimetry approaches applied to paper-based analytical devices: A review.

Colorimetric paper-based analytical devices (CPADs) are cost-efficient and high-throughput technologies that use readily available materials for point-of-need (PON) applications by leveraging color changes in response to target analytes. However, the complexity of samples can limit the precision and accuracy of CPAD applications. Therefore, CPADs have been combined with chemometric approaches to enhance analytical performance and provide simple solutions to complex systems.

Microscale titration of acetic acid using digital colorimetry and paper-based analytical devices.

A quantitative method for acid-base titrations in paper-based devices (PADs) is described to analyze acetic acid in vinegar samples. In this work, two different types of PADs were developed: a device for individual spot testing and a microfluidic device. Digital colorimetry was used as the detection method, and the images were acquired using a smartphone and a homemade box with LED lights for controlled image acquisition.

Determination of food colorants in a wide variety of food matrices by microemulsion electrokinetic capillary chromatography. Considerations on the found concentrations and regulated consumption limits.

Color additives are used widely by the food industry to confer a desirable appearance. Some of the most used colorants (Tartrazine (E102), Sunset Yellow (E110), Red Allure (E129) and Blue Brilliant (E133)) were determined in this study using microemulsion electrokinetic capillary chromatography (MEEKC). Regression coefficients were greater than 0.

Simultaneous determination of color additives tartrazine and allura red in food products by digital image analysis.

A method based on digital image is described to quantify tartrazine (E102), yellow, and allura red (E129) colorants in food samples. HPLC is the habitual method of reference used for colorant separation and quantification, but it is expensive, time-consuming and it uses solvents, sometimes toxic. By a flatbed scanner, which can be found in most laboratories, images of mixtures of colorants can be taken in microtitration plates.

Fluorescence of the Flavin group in choline oxidase. Insights and analytical applications for the determination of choline and betaine aldehyde.

Choline oxidase (ChOx) is a flavoenzyme catalysing the oxidation of choline (Ch) to betaine aldehyde (BA) and glycine betaine (GB). In this paper a fundamental study of the intrinsic fluorescence properties of ChOx due to Flavin Adenine Dinucleotide (FAD) is presented and some analytical applications are studied in detail. Firstly, an unusual alteration in the excitation spectra, in comparison with the absorption spectra, has been observed as a function of the pH.

Polyphenolic profile in cider and antioxidant power.

Background: The aim of this work was to find the effect of polyphenolic compounds in Basque ciders on the following parameters: antioxidant activity, browning, protein-precipitating capacity, turbidity and reduction potential. These five parameters are highly important, as they affect the taste, the visual aspect and the preservation of cider, and are mainly related to polyphenolic compounds.

Results: Procyanidin B1 and procyanidin B2 showed a significant positive effect on antioxidant activity.

Gas chromatography with flame ionization detection for determination of additives in an electrolytic Zn bath.

The monitoring of additives in electrolytic baths is a fundamental task for proper coatings. Among the additives used in zinc baths, benzylideneacetone (BDA), benzoic acid (BA) and polyethylene glycol 400 (PEG400) are easily found. This paper deals with the possibilities of handling the bath sample before it is taken to a gas chromatograph (GC) in order to follow the additives concentration along the bath life.

Optimization and validation of a nonaqueous micellar electrokinetic chromatography method for determination of polycyclic musks in perfumes.

A nonaqueous micellar electrokinetic chromatography method was developed for determination of Tonalide®, Galaxolide®, and Traseolide® polycyclic musks (PCMs). These compounds are widely used as fragrance ingredients in cosmetics. The method was optimized by using a three variable Box-Behnken experimental design and response surface methodology.

Image analysis for maintenance of coating quality in nickel electroplating baths--real time control.

The aim of this paper is to show how it is possible to extract analytical information from images acquired with a flatbed scanner and make use of this information for real time control of a nickel plating process. Digital images of plated steel sheets in a nickel bath are used to follow the process under degradation of specific additives. Dedicated software has been developed for making the obtained results accessible to process operators.

Flatbed scanners as a source of imaging. Brightness assessment and additives determination in a nickel electroplating bath.

Desktop flatbed scanners are very well-known devices that can provide digitized information of flat surfaces. They are practically present in most laboratories as a part of the computer support. Several quality levels can be found in the market, but all of them can be considered as tools with a high performance and low cost.

Quantitative nuclear magnetic resonance for additives determination in an electrolytic nickel bath.

The use of proton nuclear magnetic resonance (¹H-NMR) for the quantitation of additives in a commercial electrolytic nickel bath (Supreme Plus Brilliant, Atotech formulation) is reported. A simple and quick method is described that needs only the separation of nickel ions by precipitation with NaOH. The four additives in the bath (A-5(2X), leveler; Supreme Plus Brightener (SPB); SA-1, leveler; NPA, wetting agent; all of them are commercial names from Atotech) can be quantified, whereas no other analytical methods have been found in the literature for SA-1 and NPA.

Determination of additives in an electrolytic zinc bath by q1H-NMR spectroscopy.

The use of proton nuclear magnetic resonance ((1)H-NMR) for the quantification of additives in an electrolytic Zn bath is reported. A simple and quick method is described that does not need any prior sample preparation. Contrary to other analytical methods, the three additives in the bath, benzylidene acetone (BDA), benzoic acid (BA) and poly(ethylene glycol) (PE400), can be quantified.

Simultaneous determination of glucose and choline based on the intrinsic fluorescence of the enzymes.

It has been possible to perform the simultaneous determination of choline and glucose using the intrinsic fluorescence of the corresponding enzyme as an analytical signal. This can be done in two ways. First, for low glucose and choline concentrations (about 0.

Multicomponent determinations by partial least-squares regression analysis of fast-reaction multiwavelength profiles obtained by continuous addition of a reagent.

Partial least-squares regression (PLS) analysis of multiwavelength reaction profiles, obtained by continuous addition of a reagent to a binary mixture of analytes, giving fast reactions, is presented. The methodology has proved to be useful for the simultaneous determination of the mixture components. Octacyanomolibdate(V) (Mo(V)) has been used as a reagent for mixtures of hydroquinone (HQ) and pyrogallol (PG) in acidic medium.

Study of a fluorometric-enzymatic method for bilirubin based on chemically modified bilirubin-oxidase and multivariate calibration.

The chemical derivatization of bilirubin oxidase (BOx) with a fluorescein derivative (FS) yields a chemically modified enzyme (BOx-FS), with excitation and emission maxima at 487 and 520 nm, respectively. During the oxygen oxidation reaction of bilirubins, in the presence of the modified enzyme, the change in the fluorescence of the modified enzyme depends on the concentration and type of bilirubin. This effect can be used for analytical purposes.

Detection limit estimator for multivariate calibration by an extension of the IUPAC recommendations for univariate methods.

A methodology is proposed to estimate the limit of detection (LOD) of analytical methods when multivariate calibration is applied. It tries to follow the same premises as the IUPAC methodology for univariate calibration. The mathematical support is given and algorithms such as partial least squares (PLS) regression, PLS2 and principal component regression (PCR) are used.

Interference modelling, experimental design and pre-concentration steps in validation of the Fenton's reagent for pesticides determination.

The determination of atrazine in real samples (commercial pesticide preparations and water matrices) shows how the Fenton's reagent can be used with analytical purposes when kinetic methodology and multivariate calibration methods are applied. Also, binary mixtures of atrazine-alachlor and atrazine-bentazone in pesticide preparations have been resolved. The work shows the way in which interferences and the matrix effect can be modelled.

The acetylsalicylic acid-bromine system for multicomponent kinetic determinations.

When acetylsalicylic acid (ASA) is added to a bromine solution, slow decay of the bromine concentration occurs. Hydrolysis of ASA yields salicylic acid (SA) slowly, and bromine reacts rapidly with SA but not with ASA. Simulated reaction profiles based on a two-step reaction scheme agree closely with the experimental profiles.

The bromination of acetone. application to multicomponent kinetic determinations.

A very simple kinetic method is proposed for the resolution of mixtures of acetone and a second component. It is based on the reaction, at constant temperature, between bromine and acetone. This reaction can be regarded, under certain conditions, as pseudo-zero-order on the bromine concentration.