Transformation of Nanomaterials and Its Implications in Gut Nanotoxicology

Ingestion of engineered nanomaterials (ENMs) is inevitable due to their widespread utilization in the agrifood industry. Safety evaluation has become pivotal to identify the consequences on human health of exposure to these ingested ENMs. Much of the current understanding of nanotoxicology in the gastrointestinal tract (GIT) is derived from studies utilizing pristine ENMs. In reality, agrifood ENMs interact with their microenvironment, and undergo multiple physicochemical transformations, such as aggregation/agglomeration, dissolution, speciation change, and surface characteristics alteration, across their life cycle from synthesis to consumption. This work sieves out the implications of ENM transformations on their behavior, stability, and reactivity in food and product matrices and through the GIT, in relation to measured toxicological profiles. In particular, a strong emphasis is given to understand the mechanisms through which these transformations can affect ENM induced gut nanotoxicity.     

Peptide Programmed Hydrogels as Safe Sanctuary Microenvironments for Cell Transplantation

Cell transplantation is one of the most promising strategies for the minimally invasive treatment of a raft of injuries and diseases. However, a standing challenge to its efficacy is poor cell survival due to a lack of mechanical protection during administration and an unsupportive milieu thereafter. In response, a shear‐injectable nanoscaffold vector is engineered considering the three equal requirements of protection, support, and survival. Here, the programmed peptide assembly of tissue‐specific epitopes presents a safe sanctuary microenvironment for the transplantation of cells. For the first time, a mechanistic understanding of the multifactorial role of the nanoscaffold in promoting cell survival is presented, where initial cell survival is dependent on the fluid mechanic process of droplet formation rather than on shear rate. However, provided is the first report of the most critical component of a transplantation vector, distinguishing feigned biological support from mechanical properties from true ongoing biological support post transplantation. This is achieved via the presentation of amino acid constituents that significantly improve the efficacy of the vector compared to a biocompatible, yet inert analogue. Together, the peptide‐programmed hydrogels enable fundamental rules for the engineering of advanced treatment strategies with wide reaching implications for tissue repair and biofabrication.     

Development of medical cotton fabrics with Punica granatum L extract finishing for nosocomial infections control

Transmission of pathogenic microorganisms on textile in the hospital settings may contribute to nosocomial infection. This study was aimed to develop a natural antimicrobial finishing on textile that can prevent transmission of pathogenic microorganisms that meets American Association of Textiles Chemists and Colorists (AATCC) standard. Punica granatum L ethanolic extract was shown to have broad spectrum antimicrobial efficacy with bis(6-methylheptyl)-benzene-1,2-dicarboxylate and ethyl-pentadecanoate as the main bioactive constituents. Textile samples developed with the extract finishing exhibited excellent antimicrobial efficacy with a growth reduction of 99.9% on Hoheinstein Challenge Test. The wash durability of the finished textile was found good even after 30 washes with commercial detergent.     

Inflammation Increases Susceptibility of Human Small Airway Epithelial Cells to Pneumonic Nanotoxicity

Exposure to inhaled anthropogenic nanomaterials (NM) with dimension <100 nm has been implicated in numerous adverse respiratory outcomes. Although studies have identified key NM physiochemical determinants of pneumonic nanotoxicity, the complex interactive and cumulative effects of NM exposure, especially in individuals with preexisting inflammatory respiratory diseases, remain unclear. Herein, the susceptibility of primary human small airway epithelial cells (SAEC) exposed to a panel of reference NM, namely, CuO, ZnO, mild steel welding fume (MSWF), and nanofractions of copier center particles (Nano‐CCP), is examined in normal and tumor necrosis factor alpha (TNF‐α)‐induced inflamed SAEC. Compared to normal SAEC, inflamed cells display an increased susceptibility to NM‐induced cytotoxicity by 15–70% due to a higher basal level of intracellular reactive oxygen species (ROS). Among the NM screened, ZnO, CuO, and Nano‐CCP are observed to trigger an overcompensatory response in normal SAEC, resulting in an increased tolerance against subsequent oxidative insults. However, the inflamed SAEC fails to adapt to the NM exposure due to an impaired nuclear factor erythroid 2‐related factor 2 (Nrf2)‐mediated cytoprotective response. The findings reveal that susceptibility to pulmonary nanotoxicity is highly dependent on the interplay between NM properties and inflammation of the alveolar milieu.     

Evaluating the Efficiency of CBAM-Resnet Using Malaysian Sign Language

The deaf-mutes population is constantly feeling helpless when others do not understand them and vice versa. To fill this gap, this study implements a CNN-based neural network, Convolutional Based Attention Module (CBAM), to recognise Malaysian Sign Language (MSL) in videos recognition. This study has created 2071 videos for 19 dynamic signs. Two different experiments were conducted for dynamic signs, using CBAM-3DResNet implementing ‘Within Blocks’ and ‘Before Classifier’ methods. Various metrics such as the accuracy, loss, precision, recall, F1-score, confusion matrix, and training time were recorded to evaluate the models’ efficiency. Results showed that CBAM-ResNet models had good performances in videos recognition tasks, with recognition rates of over 90% with little variations. CBAM-ResNet ‘Before Classifier’ is more efficient than ‘Within Blocks’ models of CBAM-ResNet. All experiment results indicated the CBAM-ResNet ‘Before Classifier’ efficiency in recognising Malaysian Sign Language and its worth of future research.     

Hydrodynamically Guided Hierarchical Self‐Assembly of Peptide–Protein Bioinks

Effective integration of molecular self‐assembly and additive manufacturing would provide a technological leap in bioprinting. This article reports on a biofabrication system based on the hydrodynamically guided co‐assembly of peptide amphiphiles (PAs) with naturally occurring biomolecules and proteins to generate hierarchical constructs with tuneable molecular composition and structural control. The system takes advantage of droplet‐on‐demand inkjet printing to exploit interfacial fluid forces and guide molecular self‐assembly into aligned or disordered nanofibers, hydrogel structures of different geometries and sizes, surface topographies, and higher‐ordered constructs bound by molecular diffusion. PAs are designed to co‐assemble during printing in cell diluent conditions with a range of extracellular matrix (ECM) proteins and biomolecules including fibronectin, collagen, keratin, elastin‐like proteins, and hyaluronic acid. Using combinations of these molecules, NIH‐3T3 and adipose derived stem cells are bioprinted within complex structures while exhibiting high cell viability (>88%). By integrating self‐assembly with 3D‐bioprinting, the study introduces a novel biofabrication platform capable of encapsulating and spatially distributing multiple cell types within tuneable pericellular environments. In this way, the work demonstrates the potential of the approach to generate complex bioactive scaffolds for applications such as tissue engineering, in vitro models, and drug screening.     

Formation of microporous polymeric materials by microemulsion polymerization of methyl methacrylate and 2-hydroxyethyl methacrylate

The investigated microemulsion system consisted of methyl methacrylate, 2-hydroxyethyl methacrylate and water using sodium dodecyl sulphate as surfactant. Ethylene glycol dimethacrylate acting as a cross-linker was also incorporated to enhance the mechanical strengths of the microporous polymeric materials. The polymerization was carried out at room temperature using a reactive redox initiator comprising ammonium persulphate and N,N,N′,N′-tetramethylethylene diamine. The conductivities of the microemulsion samples were monitored during the course of polymerization. The conductivities for a bicontinuous microemulsion before and after polymerization were found to be very similar. In addition, the transformation of microstructures was also examined using a transmission as well as a field emission scanning electron microscope. It is evidenced from the micrographs that microporous polymeric materials prepared from bicontinuous microemulsion polymerization are attributed to numerous coagulations of spherical particles. A possible mechanism for the microstructural transformation is discussed based on the information of conductivity measurements and electron micrographs. © 1996 John Wiley & Sons, Inc.