The detection of aflatoxins is essential for the food industry to ensure the safety and quality of food products before their release to the market. The lateral-flow immunochromatography assay (LFIA) is a simple technique that allows the rapid on-site detection of aflatoxins. The purpose of this review is to evaluate and compare the limits of detection reported in the most recent research articles, published between the years of 2015 and 2023. The limits of detection (LODs) were compared against the particle type and particle size, as well as other variables, to identify trends and correlations among the parameters. A growing interest in the use of different metal and non-metal nanoparticles was observed over the years of 2015–2023. The diameters of the nanoparticles used were reportedly between 1 nm and 100 nm. Most of these particles displayed lower LODs in the range of 0.01 to 1.0 ng/mL. Furthermore, there was a significant level of interest in detecting aflatoxin B1, perhaps due to its high level of toxicity and common appearance in food products. This study also compares the use of metallic and non-metallic nanoparticles in detecting aflatoxins and the dependence of nanoparticles’ sizes on the detection range. Overall, the type of particle and particle size used in the development of LFIA strips can affect the sensitivity and LOD; hence, the optimization of these parameters and their modulation with respect to certain requirements can enhance the overall assay performance in terms of the reproducibility of results and commercialization.
{"title":"Overview of Various Components of Lateral-Flow Immunochromatography Assay for the Monitoring of Aflatoxin and Limit of Detection in Food Products: A Systematic Review","authors":"Thasmin Shahjahan, Bilal Javed, Vinayak Sharma, Furong Tian","doi":"10.3390/chemosensors11100520","DOIUrl":"https://doi.org/10.3390/chemosensors11100520","url":null,"abstract":"The detection of aflatoxins is essential for the food industry to ensure the safety and quality of food products before their release to the market. The lateral-flow immunochromatography assay (LFIA) is a simple technique that allows the rapid on-site detection of aflatoxins. The purpose of this review is to evaluate and compare the limits of detection reported in the most recent research articles, published between the years of 2015 and 2023. The limits of detection (LODs) were compared against the particle type and particle size, as well as other variables, to identify trends and correlations among the parameters. A growing interest in the use of different metal and non-metal nanoparticles was observed over the years of 2015–2023. The diameters of the nanoparticles used were reportedly between 1 nm and 100 nm. Most of these particles displayed lower LODs in the range of 0.01 to 1.0 ng/mL. Furthermore, there was a significant level of interest in detecting aflatoxin B1, perhaps due to its high level of toxicity and common appearance in food products. This study also compares the use of metallic and non-metallic nanoparticles in detecting aflatoxins and the dependence of nanoparticles’ sizes on the detection range. Overall, the type of particle and particle size used in the development of LFIA strips can affect the sensitivity and LOD; hence, the optimization of these parameters and their modulation with respect to certain requirements can enhance the overall assay performance in terms of the reproducibility of results and commercialization.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"25 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135697026","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-02DOI: 10.3390/chemosensors11100519
Giulia Zonta, Giorgio Rispoli, Cesare Malagù, Michele Astolfi
The necessity of detecting and recognizing gases is crucial in many research and application fields, boosting, in the last years, their continuously evolving technology. The basic detection principle of gas sensors relies on the conversion of gas concentration changes into a readable signal that can be analyzed to calibrate sensors to detect specific gases or mixtures. The large variety of gas sensor types is here examined in detail, along with an accurate description of their fundamental characteristics and functioning principles, classified based on their working mechanisms (electrochemical, resonant, optical, chemoresistive, capacitive, and catalytic). This review is particularly focused on chemoresistive sensors, whose electrical resistance changes because of chemical reactions between the gas and the sensor surface, and, in particular, we focus on the ones developed by us and their applications in the medical field as an example of the technological transfer of this technology to medicine. Nowadays, chemoresistive sensors are, in fact, strong candidates for the implementation of devices for the screening and monitoring of tumors (the second worldwide cause of death, with ~9 million deaths) and other pathologies, with promising future perspectives that are briefly discussed as well.
{"title":"Overview of Gas Sensors Focusing on Chemoresistive Ones for Cancer Detection","authors":"Giulia Zonta, Giorgio Rispoli, Cesare Malagù, Michele Astolfi","doi":"10.3390/chemosensors11100519","DOIUrl":"https://doi.org/10.3390/chemosensors11100519","url":null,"abstract":"The necessity of detecting and recognizing gases is crucial in many research and application fields, boosting, in the last years, their continuously evolving technology. The basic detection principle of gas sensors relies on the conversion of gas concentration changes into a readable signal that can be analyzed to calibrate sensors to detect specific gases or mixtures. The large variety of gas sensor types is here examined in detail, along with an accurate description of their fundamental characteristics and functioning principles, classified based on their working mechanisms (electrochemical, resonant, optical, chemoresistive, capacitive, and catalytic). This review is particularly focused on chemoresistive sensors, whose electrical resistance changes because of chemical reactions between the gas and the sensor surface, and, in particular, we focus on the ones developed by us and their applications in the medical field as an example of the technological transfer of this technology to medicine. Nowadays, chemoresistive sensors are, in fact, strong candidates for the implementation of devices for the screening and monitoring of tumors (the second worldwide cause of death, with ~9 million deaths) and other pathologies, with promising future perspectives that are briefly discussed as well.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"51 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135898612","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-01DOI: 10.3390/chemosensors11100517
Salma Umme, Giulia Siciliano, Elisabetta Primiceri, Antonio Turco, Iolena Tarantini, Francesco Ferrara, Maria Serena Chiriacò
The screening and early diagnosis of diseases are crucial for a patient’s treatment to be successful and to improve their survival rate, especially for cancer. The development of non-invasive analytical methods able to detect the biomarkers of pathologies is a critical point to define a successful treatment and a good outcome. This study extensively reviews the electrochemical methods used for the development of biosensors in a liquid biopsy, owing to their ability to provide a rapid response, precise detection, and low detection limits. We also discuss new developments in electrochemical biosensors, which can improve the specificity and sensitivity of standard analytical procedures. Electrochemical biosensors demonstrate remarkable sensitivity in detecting minute quantities of analytes, encompassing proteins, nucleic acids, and circulating tumor cells, even within challenging matrices such as urine, serum, blood, and various other body fluids. Among the various detection techniques used for the detection of cancer biomarkers, even in the picogram range, voltammetric sensors are deeply discussed in this review because of their advantages and technical characteristics. This widespread utilization stems from their ability to facilitate the quantitative detection of ions and molecules with exceptional precision. A comparison of each electrochemical technique is discussed to assist with the selection of appropriate analytical methods.
{"title":"Electrochemical Sensors for Liquid Biopsy and Their Integration into Lab-on-Chip Platforms: Revolutionizing the Approach to Diseases","authors":"Salma Umme, Giulia Siciliano, Elisabetta Primiceri, Antonio Turco, Iolena Tarantini, Francesco Ferrara, Maria Serena Chiriacò","doi":"10.3390/chemosensors11100517","DOIUrl":"https://doi.org/10.3390/chemosensors11100517","url":null,"abstract":"The screening and early diagnosis of diseases are crucial for a patient’s treatment to be successful and to improve their survival rate, especially for cancer. The development of non-invasive analytical methods able to detect the biomarkers of pathologies is a critical point to define a successful treatment and a good outcome. This study extensively reviews the electrochemical methods used for the development of biosensors in a liquid biopsy, owing to their ability to provide a rapid response, precise detection, and low detection limits. We also discuss new developments in electrochemical biosensors, which can improve the specificity and sensitivity of standard analytical procedures. Electrochemical biosensors demonstrate remarkable sensitivity in detecting minute quantities of analytes, encompassing proteins, nucleic acids, and circulating tumor cells, even within challenging matrices such as urine, serum, blood, and various other body fluids. Among the various detection techniques used for the detection of cancer biomarkers, even in the picogram range, voltammetric sensors are deeply discussed in this review because of their advantages and technical characteristics. This widespread utilization stems from their ability to facilitate the quantitative detection of ions and molecules with exceptional precision. A comparison of each electrochemical technique is discussed to assist with the selection of appropriate analytical methods.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"121 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135459022","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-01DOI: 10.3390/chemosensors11100518
Luca Burratti, Michele Sisani, Irene Di Guida, Fabio De Matteis, Roberto Francini, Paolo Prosposito
In this study, an innovative approach for the integration of silver nanoparticles (AgNPs) into poly(ethylene glycol) diacrylate (PEGDA) hydrogels is described. The composite material is the first in the literature where AgNPs were doped into PEGDA using photo-polymerization technique for a double function: detection and elimination of Hg(II) ions from water. The doping of AgNPs into PEGDA-based matrices was performed using a photo-polymerizable process. The Hg(II) sensing properties were explored in a concentration range from 0 to 20 mg/L. Notably, a linear dependence was observed up to 1 mg/L, accompanied by a limit of detection of 0.3 mg/L. Beyond sensing, the efficiency of the doped hydrogel in removing Hg(II) ions was also investigated and compared with an undoped PEGDA matrix. The outcome highlighted an enhanced removal efficiency of the doped material of approximately 23%. Finally, the experimental data suggested that the interaction between Hg(II) ions and the modified hydrogel adhered to the Langmuir isotherm model, which suggested that chemisorption was the driving mechanism of the adsorption of Hg(II) onto the modified hydrogel matrix.
{"title":"Poly(ethylene glycol) Diacrylate Hydrogels Doped with Silver Nanoparticles for Optical Sensing and Removing Hg(II) Ions from Water","authors":"Luca Burratti, Michele Sisani, Irene Di Guida, Fabio De Matteis, Roberto Francini, Paolo Prosposito","doi":"10.3390/chemosensors11100518","DOIUrl":"https://doi.org/10.3390/chemosensors11100518","url":null,"abstract":"In this study, an innovative approach for the integration of silver nanoparticles (AgNPs) into poly(ethylene glycol) diacrylate (PEGDA) hydrogels is described. The composite material is the first in the literature where AgNPs were doped into PEGDA using photo-polymerization technique for a double function: detection and elimination of Hg(II) ions from water. The doping of AgNPs into PEGDA-based matrices was performed using a photo-polymerizable process. The Hg(II) sensing properties were explored in a concentration range from 0 to 20 mg/L. Notably, a linear dependence was observed up to 1 mg/L, accompanied by a limit of detection of 0.3 mg/L. Beyond sensing, the efficiency of the doped hydrogel in removing Hg(II) ions was also investigated and compared with an undoped PEGDA matrix. The outcome highlighted an enhanced removal efficiency of the doped material of approximately 23%. Finally, the experimental data suggested that the interaction between Hg(II) ions and the modified hydrogel adhered to the Langmuir isotherm model, which suggested that chemisorption was the driving mechanism of the adsorption of Hg(II) onto the modified hydrogel matrix.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"22 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135457891","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-09-30DOI: 10.3390/chemosensors11100516
Paulina De Leon Portilla, Ana L. González, Enrique Sanchez-Mora
Functionalized Au and Ag nanoparticles (NPs) with ascorbic and tannic acid, respectively, were used as SERS substrates (SS). Several SS were fabricated with different loads of metal NPs deposited on silicon wafers. We focused on the thyroxine (T4) band at 1044 cm−1 and tracked its intensity and position at concentrations from 10 pM to 1 mM. For all SS, the band intensity decreased as the T4 concentration decreased. Additionally, the band shifted to larger wavenumbers as the NP loads increased. In the case of Au, the SS with the highest load of NPs, the minimum concentration detected was 1 μM. The same load of the Ag NP SS showed a better performance detecting a concentration of 10 pM, an outcome from a SERS-EF of 109. The NP spatial distribution includes mainly isolated NPs, quasi-spherical clusters, and semi-linear arrays of NPs in random orientations. From the numerical simulations, we conclude that the hot spots at the interparticle gaps in a linear array of three NPs are the most intense. The Ag NP SS demonstrated good sensitivity, to allow the detection of pM concentrations. Therefore, its complementation to any immunoassay technique provides an interesting alternative for point-of-care implementations, such as test strips.
{"title":"Thyroxine Quantification by Using Plasmonic Nanoparticles as SERS Substrates","authors":"Paulina De Leon Portilla, Ana L. González, Enrique Sanchez-Mora","doi":"10.3390/chemosensors11100516","DOIUrl":"https://doi.org/10.3390/chemosensors11100516","url":null,"abstract":"Functionalized Au and Ag nanoparticles (NPs) with ascorbic and tannic acid, respectively, were used as SERS substrates (SS). Several SS were fabricated with different loads of metal NPs deposited on silicon wafers. We focused on the thyroxine (T4) band at 1044 cm−1 and tracked its intensity and position at concentrations from 10 pM to 1 mM. For all SS, the band intensity decreased as the T4 concentration decreased. Additionally, the band shifted to larger wavenumbers as the NP loads increased. In the case of Au, the SS with the highest load of NPs, the minimum concentration detected was 1 μM. The same load of the Ag NP SS showed a better performance detecting a concentration of 10 pM, an outcome from a SERS-EF of 109. The NP spatial distribution includes mainly isolated NPs, quasi-spherical clusters, and semi-linear arrays of NPs in random orientations. From the numerical simulations, we conclude that the hot spots at the interparticle gaps in a linear array of three NPs are the most intense. The Ag NP SS demonstrated good sensitivity, to allow the detection of pM concentrations. Therefore, its complementation to any immunoassay technique provides an interesting alternative for point-of-care implementations, such as test strips.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"162 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136343910","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-09-30DOI: 10.3390/chemosensors11100515
Xinyi Li, Zezhou Li, Meiping Zhao
Histidine is an essential amino acid with significant implications for human growth and neuromodulation. Its intracellular concentration, whether increased or decreased, can indicate different diseases. While various methods exist for measuring elevated histidine levels, there remains a significant lack of sensors capable of actively responding to histidine deficiency within cells and releasing strong signals. In this study, we exploited the high induction levels of the his operon in S. Typhimurium SL1344, a histidine auxotroph, within a histidine-deficient environment, to develop a specific bacterial sensor with sensitivity towards low histidine concentrations. By employing plasmid vectors with differing copy numbers, we developed two distinct bacterial fluorescence sensors, both capable of actively responding to histidine deficiency and emitting detectable fluorescence signals within either culture mediums or live cells. The SL1344-pGEX sensor, with a high copy number, exhibited remarkable sensitivity and selectivity to histidine in the range of 0 to 50 μM. Notably, even a minimal addition of histidine (approximately 2.5 μM) to the M9 medium led to observable fluorescence reduction, rendering it highly suitable for monitoring histidine-deficient cellular environments. In contrast, the low-copy-number SL1344-pSB3313 sensor exhibits a broader response range, capable of tracking more extensive shifts in histidine concentrations. These sensors allow for sensitive in situ detection of intracellular histidine concentrations in various live cells, particularly responding to real-time changes in cellular histidine levels. This provides a powerful tool for investigating histidine deficiency-related biological processes, the mechanisms of associated diseases, and the assessment and optimization of therapeutic strategies.
{"title":"Illuminating Histidine-Deficient Intracellular Environments: A Novel Whole-Cell Microbial Fluorescence Sensor","authors":"Xinyi Li, Zezhou Li, Meiping Zhao","doi":"10.3390/chemosensors11100515","DOIUrl":"https://doi.org/10.3390/chemosensors11100515","url":null,"abstract":"Histidine is an essential amino acid with significant implications for human growth and neuromodulation. Its intracellular concentration, whether increased or decreased, can indicate different diseases. While various methods exist for measuring elevated histidine levels, there remains a significant lack of sensors capable of actively responding to histidine deficiency within cells and releasing strong signals. In this study, we exploited the high induction levels of the his operon in S. Typhimurium SL1344, a histidine auxotroph, within a histidine-deficient environment, to develop a specific bacterial sensor with sensitivity towards low histidine concentrations. By employing plasmid vectors with differing copy numbers, we developed two distinct bacterial fluorescence sensors, both capable of actively responding to histidine deficiency and emitting detectable fluorescence signals within either culture mediums or live cells. The SL1344-pGEX sensor, with a high copy number, exhibited remarkable sensitivity and selectivity to histidine in the range of 0 to 50 μM. Notably, even a minimal addition of histidine (approximately 2.5 μM) to the M9 medium led to observable fluorescence reduction, rendering it highly suitable for monitoring histidine-deficient cellular environments. In contrast, the low-copy-number SL1344-pSB3313 sensor exhibits a broader response range, capable of tracking more extensive shifts in histidine concentrations. These sensors allow for sensitive in situ detection of intracellular histidine concentrations in various live cells, particularly responding to real-time changes in cellular histidine levels. This provides a powerful tool for investigating histidine deficiency-related biological processes, the mechanisms of associated diseases, and the assessment and optimization of therapeutic strategies.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"22 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136344694","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-09-29DOI: 10.3390/chemosensors11100514
Stefano Robbiani, Beatrice Julia Lotesoriere, Raffaele L. Dellacà, Laura Capelli
Electronic noses (e-noses) are devices based on combining different gas sensors’ responses to a given sample for identifying specific odor fingerprints. In recent years, this technology has been considered a promising novel tool in several fields of application, but several issues still hamper its widespread use. This review paper describes how some physical confounding factors, such as temperature, humidity, and gas flow, in terms of flow direction and flow rate, can drastically influence gas sensors’ responses and, consequently, e-nose results. Among the software and hardware approaches adopted to address such issues, different hardware compensation strategies proposed in the literature were critically analyzed. Solutions related to e-nose sensors’ modification, design and readout, sampling system and/or chamber geometry design were investigated. A trade-off between the loss of volatile compounds of interest, the decrease of sensors’ sensitivity, and the lack of fast responses need to be pointed out. The existing body of knowledge suggests that the e-nose design needs to be highly tailored to the target application to exploit the technology potentialities fully and highlights the need for further studies comparing the several solutions proposed as a starting point for the application-driven design of e-nose-based systems.
{"title":"Physical Confounding Factors Affecting Gas Sensors Response: A Review on Effects and Compensation Strategies for Electronic Nose Applications","authors":"Stefano Robbiani, Beatrice Julia Lotesoriere, Raffaele L. Dellacà, Laura Capelli","doi":"10.3390/chemosensors11100514","DOIUrl":"https://doi.org/10.3390/chemosensors11100514","url":null,"abstract":"Electronic noses (e-noses) are devices based on combining different gas sensors’ responses to a given sample for identifying specific odor fingerprints. In recent years, this technology has been considered a promising novel tool in several fields of application, but several issues still hamper its widespread use. This review paper describes how some physical confounding factors, such as temperature, humidity, and gas flow, in terms of flow direction and flow rate, can drastically influence gas sensors’ responses and, consequently, e-nose results. Among the software and hardware approaches adopted to address such issues, different hardware compensation strategies proposed in the literature were critically analyzed. Solutions related to e-nose sensors’ modification, design and readout, sampling system and/or chamber geometry design were investigated. A trade-off between the loss of volatile compounds of interest, the decrease of sensors’ sensitivity, and the lack of fast responses need to be pointed out. The existing body of knowledge suggests that the e-nose design needs to be highly tailored to the target application to exploit the technology potentialities fully and highlights the need for further studies comparing the several solutions proposed as a starting point for the application-driven design of e-nose-based systems.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"50 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135132136","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-09-28DOI: 10.3390/chemosensors11100512
Yonathan Asikin, Mutsumi Kawahara, Sora Kochi, Ryota Maekawa, Yuta Omine, Makoto Takeuchi, Kensaku Takara, Koji Wada
The recent increase in demand for Okinawan pineapples has necessitated the development of new varieties with attractive aromas. This study aimed to evaluate the volatile characteristics of five Okinawan pineapple breeding lines, i.e., ‘No. 22’, ‘No. 25’, ‘No. 26’, ‘No. 27’, and ‘No. 28’. The total volatiles in the cryopulverized fruit flesh were examined using headspace gas-chromatography–mass-spectrometry-based electronic nose analysis. The total ion masses of the volatiles were visualized using principal component analysis, and three replicates of each line with comparable volatile characteristics were selected. Furthermore, the composition of the volatile components in these replicates was assessed, and the odor activity values (OAVs) were calculated. The breeding lines varied in the quantity and composition of their volatile compounds, which were predominantly esters, ketones, terpenes, and alcohols. The ‘No. 22’ fruit contained a greater content of volatiles than the other lines. Moreover, 14 volatiles with OAV > 1 were accounted as aroma-active compounds, and their variations were distinguished as follows: the highest OAV (786.96) was recorded for methyl 2-methylbutanoate of the ‘No. 26’ line; 2,5-dimethyl-4-methoxy-3(2H)-furanone was superior in the ‘No. 26’ and ‘No. 27’ lines; and δ-decalactone was only present in the ‘No. 22’ and ‘No. 27’ fruits, suggesting different potent practical uses for these new breeding lines.
{"title":"Assessment of Volatile Characteristics of Okinawan Pineapple Breeding Lines by Gas-Chromatography–Mass-Spectrometry-Based Electronic Nose Profiling and Odor Activity Value Calculation","authors":"Yonathan Asikin, Mutsumi Kawahara, Sora Kochi, Ryota Maekawa, Yuta Omine, Makoto Takeuchi, Kensaku Takara, Koji Wada","doi":"10.3390/chemosensors11100512","DOIUrl":"https://doi.org/10.3390/chemosensors11100512","url":null,"abstract":"The recent increase in demand for Okinawan pineapples has necessitated the development of new varieties with attractive aromas. This study aimed to evaluate the volatile characteristics of five Okinawan pineapple breeding lines, i.e., ‘No. 22’, ‘No. 25’, ‘No. 26’, ‘No. 27’, and ‘No. 28’. The total volatiles in the cryopulverized fruit flesh were examined using headspace gas-chromatography–mass-spectrometry-based electronic nose analysis. The total ion masses of the volatiles were visualized using principal component analysis, and three replicates of each line with comparable volatile characteristics were selected. Furthermore, the composition of the volatile components in these replicates was assessed, and the odor activity values (OAVs) were calculated. The breeding lines varied in the quantity and composition of their volatile compounds, which were predominantly esters, ketones, terpenes, and alcohols. The ‘No. 22’ fruit contained a greater content of volatiles than the other lines. Moreover, 14 volatiles with OAV > 1 were accounted as aroma-active compounds, and their variations were distinguished as follows: the highest OAV (786.96) was recorded for methyl 2-methylbutanoate of the ‘No. 26’ line; 2,5-dimethyl-4-methoxy-3(2H)-furanone was superior in the ‘No. 26’ and ‘No. 27’ lines; and δ-decalactone was only present in the ‘No. 22’ and ‘No. 27’ fruits, suggesting different potent practical uses for these new breeding lines.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"78 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135344153","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-09-28DOI: 10.3390/chemosensors11100513
Szymon Wójcik, Jan Wyrwa, Filip Ciepiela, Małgorzata Jakubowska
This work demonstrates the successful application of the picein wax carbon composite electrode (PWCCE) for profiling both commercial and homemade plant milks. Picein wax was utilized as an unconventional binder. The resulting electrode paste exhibited a solidified and hard texture, enabling its use in a manner analogous to that of the glassy carbon electrode. Differential pulse voltammetry (DPV) with an automated measurement and recording procedure was employed to obtain plant-based milk profiles. The utilization of operator-independent measurement procedures yielded high-quality electrochemical fingerprints suitable for subsequent calculations. To interpret the data, unsupervised machine learning methods were implemented, such as principal component analysis (PCA) and cluster analysis. These chemometric techniques confirmed the electrode effectiveness of the construction for this type of research. Moreover, they proved valuable in distinguishing between plant-based milk and cow’s milk, including two different variants: whole milk and lactose-free milk.
{"title":"The Application of Picein Wax Carbon Composite Electrode for Plant-Based Milk Profiling","authors":"Szymon Wójcik, Jan Wyrwa, Filip Ciepiela, Małgorzata Jakubowska","doi":"10.3390/chemosensors11100513","DOIUrl":"https://doi.org/10.3390/chemosensors11100513","url":null,"abstract":"This work demonstrates the successful application of the picein wax carbon composite electrode (PWCCE) for profiling both commercial and homemade plant milks. Picein wax was utilized as an unconventional binder. The resulting electrode paste exhibited a solidified and hard texture, enabling its use in a manner analogous to that of the glassy carbon electrode. Differential pulse voltammetry (DPV) with an automated measurement and recording procedure was employed to obtain plant-based milk profiles. The utilization of operator-independent measurement procedures yielded high-quality electrochemical fingerprints suitable for subsequent calculations. To interpret the data, unsupervised machine learning methods were implemented, such as principal component analysis (PCA) and cluster analysis. These chemometric techniques confirmed the electrode effectiveness of the construction for this type of research. Moreover, they proved valuable in distinguishing between plant-based milk and cow’s milk, including two different variants: whole milk and lactose-free milk.","PeriodicalId":10057,"journal":{"name":"Chemosensors","volume":"18 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135385941","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-09-25DOI: 10.3390/chemosensors11100511
Camille Van Camp, Wannes Hugo R. Van Hassel, Mohamed F. Abdallah, Julien Masquelier
Dairy milk holds a prominent position as a widely consumed food, particularly among infants and children. However, it is crucial to address the presence of multiple natural toxic compounds that may co-occur in dairy milk to ensure its safety prior to consumption. Aflatoxin M1 (AFM1), an emerging mycotoxin of interest, is a potential contaminant in the milk of animals who ingest aflatoxin B1 (AFB1). The toxin is regulated in the European Union under Commission Regulation No 1881/2006. Unfortunately, there is a notable lack of data concerning the transfer of various emerging microbial contaminants into dairy milk and, therefore, their natural occurrences. In this study, a simple and sensitive LC-MS/MS method was developed and validated for the quantification of multiple cyanotoxins (microcystin congeners and nodularin) and AFM1 by the main analytical guidelines. Toxins are extracted with methanol 80%, followed by an SPE clean-up step before LC-MS/MS analysis. The LOQ was fixed at 1 µg/L for the nine cyanotoxins and 0.05 µg/L for AFM1. Recoveries were measured between 82.67% and 102%. To the best of our knowledge, there are no other LC-MS/MS methods available for the simultaneous quantification of cyanotoxins and mycotoxins in milk.
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