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Analytical Chemistry May 2022High-throughput surface-enhanced Raman scattering (SERS) reader, especially for liquid sample testing, is of great significance and huge demand in biology, environment,...
High-throughput surface-enhanced Raman scattering (SERS) reader, especially for liquid sample testing, is of great significance and huge demand in biology, environment, and other analytical fields. Inspired by the principle of microplate reader, herein, we developed a microplate-SERS reader for semiautomatic and high-throughput assays by virtue of three-dimensional liquid interfacial arrays (LIAs). For the first time, the formation of LIA in oil-in-water state, water-in-oil state, and two-dimensional plane state is realized by operating the hydrophilicity (contact angle) of the container. Through the force analysis of LIA, the effect of organic (O) phase density on the relative position of LIA was quantified. In addition, the optimized reader offers fast and continuous semiautomatic detection of 12 samples below 10 min with great signal reproducibility (calibration with the characteristic peak of O phase as the internal standard). The isolated wells in the microplate prevent analyte cross talk, allowing accurate quantification of each sample. Multiplex analysis capability highlights that this reader has the ability of rapid identification and quantification of samples containing various analytes and concentrations. The results demonstrate high-resolution dual and triple analyte detection with fully preserved signal and Raman features of individual analytes in a mixture, which implies that it also has excellent anticounterfeiting applications. This microplate-SERS reader combines the superior advantages of the LIA, microplate, and SERS techniques to retrieve the molecular vibrational fingerprints of various chemicals in complex media.
Topics: Hydrophobic and Hydrophilic Interactions; Reproducibility of Results; Spectrum Analysis, Raman; Water
PubMed: 35581026
DOI: 10.1021/acs.analchem.2c00252 -
Journal of Pharmaceutical and... Oct 2023The release of metabolites from their bound to free forms is the main regulatory path in living species. Therefore, the ability to determine the free concentrations of... (Review)
Review
The release of metabolites from their bound to free forms is the main regulatory path in living species. Therefore, the ability to determine the free concentrations of small molecules is highly critical in many biological samples. The main challenges in achieving this task are the interferences inherent to complex matrices and the ability to distinguish between the free and total concentrations. This paper presents a non-invasive microextraction method that enables the determination of endocannabinoids in brain tissue. The proposed method is based on two key principles: the availability of the free concentration of endocannabinoids for partitioning to the solid-phase microextraction (SPME) fiber; and negligible depletion enabled by the small volume of extraction phase on the fiber. These features allow the presented SPME method to provide information about the free concentration of analytes without disturbing the binding equilibrium between the analytes and the matrix. The determination of spiked samples with known concentrations enables the percentage of analyte bound to the tissue to be calculated, which can then be applied to calculate the total concentration from the determined free concentration. This manuscript focuses on the determination of the free concentration and tissue binding percentages of endocannabinoids in brain tissue. Significantly, SPME's small size and potential for non-invasive sampling enable its application in live animal subjects with minimal tissue damage.
Topics: Animals; Endocannabinoids; Brain; Solid Phase Microextraction
PubMed: 37595355
DOI: 10.1016/j.jpba.2023.115624 -
Critical Reviews in Biotechnology Nov 2021Low-cost paper-based analytical devices are the latest generation of portable lab-on-chip designs that offers an innovative platform for the on/off-site analysis... (Review)
Review
Low-cost paper-based analytical devices are the latest generation of portable lab-on-chip designs that offers an innovative platform for the on/off-site analysis (biosensing) of target analytes, especially in rural and remote areas. Recently, microfluidic paper-based analytical devices (μPADs) have attained significant recognition owing to their exciting fundamental features such as: ease of fabrication, rapid operation, and precise interpretations. The incorporation of enzymes with paper-based analytical devices significantly improves analytical performance while exhibiting excellent chemical and storage stability. In addition to that, these devices are highly compact, portable, easy-to-use, and do not require any additional sophisticated equipment for the detection and quantification of target analytes. This review provides a holistic insight into design, fabrication, and enzyme immobilization strategies for the development of enzyme-μPADs, which enables them to be widely implemented for in-field analysis. It also highlights the recent application of enzyme-μPADs in the area of: biomedical, food safety, and environmental monitoring while exploring the mechanisms of detection involved. Further, in order to improve the accuracy of analysis, researchers have designed a smartphone-based scanning tool for multi-variant point-of-care devices, which is summarized in the latter part of the review. Finally, the future perspectives and outlook of major challenges associated with enzyme-μPADs are discussed with their possible solutions. The development of enzyme integrated μPADs will open a new avenue as an exceptional analytical tool to explore various applications.HIGHLIGHTSEnzyme embedded paper-based analytical devices are a revolution in the field of biosensing.The design, fabrication, and enzyme immobilization on μPADs have been comprehensively discussed.The application of enzyme-μPADs food safety, environmental monitoring, and clinical diagnostic have been reviewed.Smartphones can be used as an on-site, user-friendly, and compact next-gen scanning tool for biosensing.
Topics: Lab-On-A-Chip Devices; Microfluidic Analytical Techniques; Microfluidics; Paper; Point-of-Care Systems
PubMed: 33730940
DOI: 10.1080/07388551.2021.1898327 -
Advances in Colloid and Interface... Jul 2022Achievements in polymer chemistry enables to design artificial phase boundaries modified by imprints of selected molecules and some larger structures. These structures... (Review)
Review
Achievements in polymer chemistry enables to design artificial phase boundaries modified by imprints of selected molecules and some larger structures. These structures seem very useful for the design of new materials suitable for affinity chromatography and sensors. In this review, we are overviewing the synthesis of molecularly imprinted polymers (MIPs) and the applicability of these MIPs in the design of affinity sensors. Such MIP-based layers or particles can be used as analyte-recognizing parts for sensors and in some cases they can replace very expensive compounds (e.g.: antibodies, receptors etc.), which are recognizing analyte. Many different polymers can be used for the formation of MIPs, but conducing polymers shows the most attractive capabilities for molecular-imprinting by various chemical compounds. Therefore, the application of conducting polymers (e.g.: polypyrrole, polyaniline, polythiophene, poly(3,4-ethylenedioxythiophene), and ortho-phenylenediamine) seems very promising. Polypyrrole is one of the most suitable for the development of MIP-based structures with molecular imprints by analytes of various molecular weights. Overoxiation of polypyrrole enables to increase the selectivity of polypyrrole-based MIPs. Methods used for the synthesis of conducting polymer based MIPs are overviewed. Some methods, which are applied for the transduction of analytical signal, are discussed, and challenges and new trends in MIP-technology are foreseen.
Topics: Molecular Imprinting; Molecularly Imprinted Polymers; Polymers; Pyrroles
PubMed: 35609398
DOI: 10.1016/j.cis.2022.102693 -
Journal of Chromatography. A Aug 2023Retention and separation of enantiomers of amine derivatives of indane and tetralin (rasagiline and its analogues) on chiral stationary phases (CSPs) Chiral-T and... (Review)
Review
Retention and separation of enantiomers of amine derivatives of indane and tetralin (rasagiline and its analogues) on chiral stationary phases (CSPs) Chiral-T and Chiral-V with teicoplanin and vancomycin antibiotics grafted onto superficially porous silica particles under conditions of reversed-phase and polar organic chromatography were studied. The mobile phases (MP) were water-methanol and acetonitrile-methanol solvents modified with triethylamine-acetic acid buffer. The effects of molecular structure and physical properties of the analytes on enantioselective retention are discussed. The retention mechanism is hypothesized to involve the ion-ion attraction between the positively charged amino group of an analyte and the carboxylate anion of either antibiotic. The binding occurs outside of the antibiotic's aglycon basket that accounts for relatively low enantioselectivity observed. The presence of a large substitute at the analyte's amino group complicates enantiorecognition. The effect of the MP solvent composition on retention and enantioseparation was investigated. It is a complex phenomenon combined of different oppositely directed influences that resulted in different shapes, increasing, decreasing, or U-shaped, of the retention factor vs. composition dependences. A model taking into account the interaction of both solvents of a binary MP with both an analyte and an adsorption site was successfully applied to approximate a majority of the studied systems. Pros and cons of the model are discussed.
Topics: Vancomycin; Teicoplanin; Porosity; Methanol; Anti-Bacterial Agents; Solvents; Stereoisomerism; Indicators and Reagents; Chromatography, High Pressure Liquid
PubMed: 37315444
DOI: 10.1016/j.chroma.2023.464120 -
Veterinary Clinical Pathology Sep 2023Biological variation (BV) of urinary (U) biochemical analytes has not been described in absolute terms, let alone as a ratio of the U-creatinine or fractional excretion...
BACKGROUND
Biological variation (BV) of urinary (U) biochemical analytes has not been described in absolute terms, let alone as a ratio of the U-creatinine or fractional excretion in healthy dogs. These analytes are potential diagnostic tools for different types of kidney damage and electrolyte disorders in dogs.
OBJECTIVES
We aimed to investigate the BV of specific gravity, osmolality, creatinine, urea, protein, glucose, chloride, sodium, potassium, calcium, and phosphate in urine from healthy pet dogs.
METHODS
Blood and urine samples from 13 dogs were collected once weekly for 8 weeks. Samples were analyzed in duplicate and in randomized order. For each sample, U-analyte and serum concentrations were measured, and U-analyte/U-creatinine and fractional excretion (FE) were calculated. Components of variance, estimated by restricted maximum likelihood, were used to determine within-subject variation (CV ), between-subject variation (CV ), and analytical variation (CV ). Index of individuality (II) and reference change values were calculated.
RESULTS
CV for all urine analytes varied between 12.6% and 35.9%, except for U-sodium, U-sodium/U-Cr, and FE-sodium, which had higher CV s (59.5%-60.7%). For U-protein, U-sodium, U-potassium, U-sodium/U-creatinine, FE-urea, FE-glucose, FE-sodium, FE-potassium, and FE-phosphate II were low, indicating that population-based RIs were appropriate. The remaining analytes had an intermediate II, suggesting that population-based RIs should be used with caution.
CONCLUSION
This study presents information on the biological variation of urinary and serum biochemical analytes from healthy dogs. These data are important for an appropriate interpretation of laboratory results.
Topics: Dogs; Animals; Creatinine; Sodium; Potassium; Glucose; Urea; Phosphates; Reference Values
PubMed: 37316471
DOI: 10.1111/vcp.13225 -
Analytical and Bioanalytical Chemistry Aug 2022A common method to quantify chronic stress is the analysis of stress markers in keratinized matrices such as hair or nail. In this study, we aimed to validate a...
A common method to quantify chronic stress is the analysis of stress markers in keratinized matrices such as hair or nail. In this study, we aimed to validate a sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the combined quantification of steroid hormones and endocannabinoids (eCBs) in the keratinized matrix nail. Furthermore, we aimed to investigate the suitability of the nail matrix for the detection of these stress markers in a pilot study. An LC-MS/MS method was used for the simultaneous identification and quantification of four eCBs (2-arachidonoylglycerol (2-AG), anandamide (AEA), oleoylethanolamide (OEA), palmitoylethanolamide (PEA)) and five steroid hormones (cortisol, cortisone, androstenedione, progesterone, testosterone) in human nails using a surrogate analyte method for each analyte. The method was validated in terms of selectivity, response factor, linearity, limit of quantification (LOQ), precision, accuracy, matrix effect, recovery, robustness, and autosampler stability. Nail samples were extracted for 1 h with methanol following a clean-up with a fully automated supported liquid extraction (SLE). The influence of nail weight on the quantification was investigated by using 0.5-20 mg of nail sample. As a proof of concept, nail samples (N = 57) were analyzed from a cohort representing newborns (1 month old), children (between 1 and 10 years), and adults (up to 43 years). It could be shown that the established workflow using a 1 hour extraction and clean-up by SLE was very robust and resulted in a short sample preparation time. The LC-MS/MS method was successfully validated. Matrix effects with ion enhancement occurred mainly for 2-AG. Sample weights below 5 mg showed variations in quantification for some analytes. Certain analytes such as PEA and progesterone could be accurately quantified at a sample weight lower than 5 mg. This is the first study where steroids and eCBs could be simultaneously detected and quantified in infant and adult nails. These results show that nails may serve as an alternative keratinized matrix (compared to hair) for the retrospective monitoring of cumulative eCB and steroid hormone levels. The combined assessment of eCBs and steroids from nails could provide a new approach to gain new insights into stress exposure in newborns and adults.
Topics: Adult; Child; Humans; Infant; Infant, Newborn; Chromatography, Liquid; Endocannabinoids; Hydrocortisone; Nails; Pilot Projects; Progesterone; Retrospective Studies; Steroids; Tandem Mass Spectrometry
PubMed: 35781588
DOI: 10.1007/s00216-022-04189-y -
Journal of Chromatography. A Jan 2022Pesticides are used extensively in a wide range of applications and due to their high rate of consumption, they are ubiquitous in the different media and samples like... (Review)
Review
Pesticides are used extensively in a wide range of applications and due to their high rate of consumption, they are ubiquitous in the different media and samples like environment, water sources, air, soil, biological materials, wastes (liquids, solids or sludges), vegetables and fruits, where they can persist for long periods. Pesticides often have hazardous side effects and can cause a range of harmful diseases like Parkinson, Alzheimer, asthma, depression and anxiety, cancer, etc, even at low concentrations. To this end, extraction, pre-concentration and determination of pesticides from various samples presents significant challenges caused by sample complexity and the low concentrations of them in many samples. Often, direct extraction and determination of pesticides are impossible due to their low concentrations and the complexity of samples. The main goals of sample preparation are removing interfering species, pre-concentrating target analyte/s and converting the analytes into more stable forms (when needed). The most popular approach is solid-phase extraction due to its simplicity, efficiency, ease of operation and low cost. This method is based on using a wide variety of materials, among which covalent organic frameworks (COFs) can be identified as an emerging class of highly versatile materials exhibiting advantageous properties, such as a porous and crystalline structure, pre-designable structure, high physical and chemical stability, ease of modification, high surface area and high adsorption capacity. The present review will cover recent developments in synthesis and applications of COFs and their composites for extraction of pesticides, different synthesis approaches of COFs, possible mechanisms for interaction of COFs-based adsorbents with pesticides and finally, future prospects and challenges in the fabrication and utilization of COFs and their composites for extraction of pesticides.
Topics: Adsorption; Metal-Organic Frameworks; Pesticides; Solid Phase Extraction; Vegetables
PubMed: 34844738
DOI: 10.1016/j.chroma.2021.462612 -
Chemosphere Apr 2022Plastic particle pollution has been shown to be almost completely ubiquitous within our surrounding environment. This ubiquity in combination with a variety of unique... (Review)
Review
Plastic particle pollution has been shown to be almost completely ubiquitous within our surrounding environment. This ubiquity in combination with a variety of unique properties (e.g. density, hydrophobicity, surface functionalization, particle shape and size, transition temperatures, and mechanical properties) and the ever-increasing levels of plastic production and use has begun to garner heightened levels of interest within the scientific community. However, as a result of these properties, plastic particles are often reported to be challenging to study in complex (i.e. real) environments. Therefore, this review aims to summarize research generated on multiple facets of the micro- and nanoplastics field; ranging from size and shape definitions to detection and characterization techniques to generating reference particles; in order to provide a more complete understanding of the current strategies for the analysis of plastic particles. This information is then used to provide generalized recommendations for researchers to consider as they attempt to study plastics in analytically complex environments; including method validation using reference particles obtained via the presented creation methods, encouraging efforts towards method standardization through the reporting of all technical details utilized in a study, and providing analytical pathway recommendations depending upon the exact knowledge desired and samples being studied.
Topics: Hydrophobic and Hydrophilic Interactions; Microplastics; Plastics; Water Pollutants, Chemical
PubMed: 35016963
DOI: 10.1016/j.chemosphere.2022.133514 -
Lab on a Chip Jun 2021A greener analytical technique for quantifying compounds in dense suspensions is needed for wastewater and environmental analysis, chemical or bio-conversion process...
A greener analytical technique for quantifying compounds in dense suspensions is needed for wastewater and environmental analysis, chemical or bio-conversion process monitoring, biomedical diagnostics, and food quality control, among others. In this work, we introduce a green, fast, one-step method called nanoextraction for extraction and detection of target analytes from sub-milliliter dense suspensions using surface nanodroplets without toxic solvents and pre-removal of the solid contents. With nanoextraction, we achieve a limit of detection (LOD) of 10-9 M for a fluorescent model analyte obtained from a particle suspension sample. The LOD is lower than that in water without particles (10-8 M), potentially due to the interaction of particles and the analyte. The high particle concentration in the suspension sample, thus, does not reduce the extraction efficiency, although the extraction process was slowed down up to 5 min. As a proof of principle, we demonstrate the nanoextraction for the quantification of model compounds in wastewater slurry containing 30 wt% solids and oily components (i.e. heavy oils). The nanoextraction and detection technology developed in this work may be used in fast analytical technologies for complex slurry samples in the environment, industrial waste, or in biomedical diagnostics.
Topics: Limit of Detection; Solid Phase Extraction; Solvents; Suspensions; Wastewater; Water Pollutants, Chemical
PubMed: 34008650
DOI: 10.1039/d1lc00139f