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Food is one of the most necessary needs since human civilization. For Muslims, it is mandatory to consume halal food. From a halal authentication perspective, adulteration of food products is an emerging challenge worldwide. The demand for halal food consumption has resulted in an ever‐increasing need for halal product validity. In the market, there are several food products in which actual ingredients and their source are not mentioned on the label and cannot be observed by the naked eye. Commonly nonhalal items include pig derivatives like lard, pork, and gelatin derivatives, dead meats, alcohol, blood, and prohibited animals. Purposely, various conventional and modern methods offer precise approaches to ensure the halalness and wholesomeness of food products. Conventional methods are physiochemical (dielectric) and electrophoresis. At the same time, modern techniques include high‐pressure liquid chromatography (HPLC), gas chromatography (GC), electronic nose (E‐Nose), polymerase chain reaction (PCR), enzyme‐linked immunosorbent assay (ELISA), differential scanning calorimetry (DSC), nuclear magnetic resonance (NMR), near‐infrared (NIR) spectroscopy, and Fourier transform infrared (FTIR) spectroscopy. This review intends to give an extensive and updated overview of conventional and modern analytical methods for ensuring food halal authenticity. [ABSTRACT FROM AUTHOR]

Background. Monitoring cellular processes across different levels of complexity, from the cellular to the tissue scale, is important for understanding tissue structure and function. However, it is challenging to monitor and estimate these structural and dynamic interactions within three-dimensional (3D) tissue models. Objective. The aim of this study was to design a method for imaging, tracking, and quantifying 3D changes in cell morphology (shape and size) within liver tissue, specifically a precision-cut liver slice (PCLS). A PCLS is a 3D model of the liver that allows the study of the structure and function of liver cells in their native microenvironment. Methods. Here, we present a method for imaging liver tissue during anisosmotic exposure in a multispectral four-dimensional manner. Three metrics of tissue morphology were measured to quantify the effects of osmotic stress on liver tissue. We estimated the changes in the volume of whole precision cut liver slices, quantified the changes in nuclei position, and calculated the changes in volumetric responses of tissue-embedded cells. Results. During equilibration with cell-membrane-permeating and non-permeating solutes, the whole tissue experiences shrinkage and expansion. As nuclei showed a change in position and directional displacement under osmotic stress, we demonstrate that nuclei could be used as a probe to measure local osmotic and mechanical stress. Moreover, we demonstrate that cells change their volume within tissue slices as a result of osmotic perturbation and that this change in volume is dependent on the position of the cell within the tissue and the duration of the exposure. Conclusion. The results of this study have implications for a better understanding of multiscale transport, mechanobiology, and triggered biological responses within complex biological structures. [ABSTRACT FROM AUTHOR]

Cardio-genic disruptions of in utero exposure of a non-fluoridated Cypermethrin (CP) and a fluoridated λ-Cyhalothrin (LC) type 2 pyrethroid insecticide were explored in albino mice. Pregnant dams were divided into three groups (n=10); 1) Vehicle Control Group (VCG) (intra-gastric treatment of 0.1mL corn oil); 2) Cypermethrin Group (CPG) and; 3) λ-Cyhalothrin Group (LPG) (intra-gastric treatment of 5mg/kg Cypermethrin (CP) and λ-Cyhalothrin respectively in corn oil). These treatments were applied on 7--10th days of pregnancy. Embryos were removed from the gravid uteri of the euthanized dams on 18th day of pregnancy and fixed in formyl ethanol for 24hrs to finally remove their hearts for histological and histometric analyses. Both insecticides were found to cause micro-anatomical derangements like decreased ventricular wall thickness, rudimentary appearance or complete absence of inter-ventricular (AV) septa, abnormalities of the cardiac valves, and decreased thickness of the muscular layer of the aortic trunk. However, these disruptions were much more pronounced in LCG. Morphometric results revealed a significant decrease (P>0.05) in the thickness of left ventricular wall in CPG (295.90±12.3µ) and LCG (104.27±5.6µ) as compared to VCG (346.68±9.5µ). The mean thickness of interventricular septum was significantly decreased in CPG (440.03±20.4µ) and LCG (214.3±10.2µ) groups than the VCG (2641.75±186.2µ). The thickness of the aortic intima also showed a significant (P>0.05) decrease in CPG (12.70±0.25µ) and LCG (11.03±0.3µ) than the VCG (18.44±0.37µ). Similarly, the thickness of aortic adventitia remained significantly (P>0.05) lower in CPG (26.96±1.1µ) and LCG (23.97±1.5µ) than the VCG (41.09±2.1µ). The relative abundance of myocardiocytes and cardio-myoblasts (per 5000µ2) also showed significant decrease in both CPG (8.98 ±0.45, 2.50±0.24 respectively) and LCG (4.7 ±0.48, 6.26±0.79) to the VCG (18.19±0.56, 1.02±0.13). The results show that type-2 pyrethroid insecticides inflict a highly toxic impact on the developing heart in mammals and the fluoridated LC is more toxic than the CP in this context. [ABSTRACT FROM AUTHOR]

Toxic effects of heavy metals on grass hopper species, Oxya hyla hyla (Serville) were studied by exposing O.hyla hyla to Cd+2, Pb+2 and Hg+2 at different concentrations of CdCl2, PbCl2 and HgCl for variable exposure time (24h, 50h and 75h) observing changes in the activities of 2 antioxidant enzymes [superoxide dismutase (SOD), catalase (CAT), peroxidase (POD)] and biochemical composition of haemolymph. Significant accumulation of metals was noticed that alarmingly increases with increase in exposure time and dosage. At low metal concentrations, oxidative stress was expressed by SOD and this effect disappeared at high concentrations. Assayed activities of CAT, POD and LPO level were significantly accelerated and correlated positively as metal exposure time increased. A significant decrease in total soluble protein, sugar, lipids and glycogen contents was also observed due to metal exposure throughout the entire test period except after the first 24h of exposure at lower concentrations. The study proved O.hyla hyla (Orthoptera: Acrididae) and its antioxidant enzyme level as bio-indicators and bio-markers of biotic and abiotic stresses. [ABSTRACT FROM AUTHOR]