Development of Molecular Imprinting Polymer Nanofiber for Aflatoxin B1 Detection Based on Quartz Crystal Microbalance

Aflatoxin B1 (AFB1) is one of the mycotoxins with the most dangerous poisons and poses a threat to living things. Several detection methods for Aflatoxin B1 (AFB1) with high sensitivity (LC-MS technique, HPLC, ELISA, etc.) still require lengthy preparation time and are not real-time and portable. Aflatoxin B1 (AFB1) detection is one of the major challenges in the field of food safety because Aflatoxin B1 (AFB1) attacks the food and agricultural products sector. One of the potential sensors that can be used as a base for Aflatoxin B1 (AFB1) detection is the Quartz Crystal Microbalance (QCM) sensor. This study examines the performance of the Quartz Crystal Microbalance (QCM) sensor as one of the Aflatoxin B1 detection techniques through the physical deposition method. The Quartz Crystal Microbalance (QCM) sensor modified uses polyvinyl acetate (PVAc) material as a container to embed a molecular model that will be detected through a molecular imprinting polymer (MIP) process coated on QCM using the electrospinning method. The response results show that the value of the sensor response using the MIP process is more significant than without the MIP process. The sensor characteristics demonstrated by the PVAc/AFB 50 sample have a limit of detection (LOD) value is 0.63 ppb, and a limit of quantitation (LOQ) is 1.91 ppb with a coefficient correlation is 0.97 for testing with a concentration range of 5.0 – 40.0 ppb. Therefore, the MIP process in QCM provides a favorable response for the detection of AFB1 in the future.

Study on synthesis and adsorption properties of glutathione surface molecular imprinting polymer

Purpose In this study, a novel glutathione (GSH) surface molecular imprinting polymer (SMIP) was successfully prepared by using macroporous adsorption resins (MAR) as substrate, which could separate and purify GSH efficiently. Design/methodology/approach SMIP was synthesized by chloromethylated modified MAR (LX1180-Cl) as the substrate, N, N’-methylenebisacrylamide (NMBA) as a crosslinker, GSH as a template, acrylamide (AM) and N-vinylpyrrolidone (NVP) as functional monomers. The morphology and structure of the polymer were characterized by scanning electron microscope and Fourier transforms infrared spectroscopy. Findings The maximum adsorption capacity toward GSH was 39.0 mg/g and the separation decree had relation to L-cysteine (L-cys) was 4.2. The optimal operation conditions were studied in detail and the got as follows: the molar ratios of NMBA, AM, GSH and NVP, were 7.0, 0.8 and 0.5. The optimal time and temperature were 14 h and 40°C, respectively. The Langmuir and pseudo-first-order model were fitting these adsorption characteristics well. Practical implications GSH has a diversity of medicinal and bioactive functions, so the purpose of this study representing a method in separate and purify technology of GSH, which provided a way for the development of medicine. Originality/value This contribution provided a novel way to separate GSH from L-cys. Under the optimal conditions, the maximum adsorption capacity toward GSH was 39.0 mg/g and the separation decree had relation to L-cys was 4.2.

Molecular Imprinting Polymer-Based QCM Sensor for Detection of α-Pinene

The quartz crystal microbalance (QCM) modified by chitosan/α-pinene, prepared by spin-coating technique has been successfully developed with molecular imprinting polymer (MIP) concept. To remove the template, we carried out two treatments namely heating and vacuum in a desiccator. To find out selectivity of the sensor, the QCM modified with polymer chitosan has been tested with another analyte such as acetone, ethanol, N-amyl alcohol, iso-amyl alcohol. The result shows that chitosan/α-pinene coated QCM sensor can provide a good response as good as sensitivity. The best QCM at heating treatment in a furnace with the decline of frequency is 32 Hz, then the QCM vacuum pumping treatment with decline frequency is 27 Hz.