Browsing by Author "Khalili, Mohammad Hakim"

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    Additive manufacturing and physicomechanical characteristics of PEGDA hydrogels: recent advances and perspective for tissue engineering
    (MDPI, 2023-05-17) Khalili, Mohammad Hakim; Zhang, Rujing; Wilson, Sandra; Goel, Saurav; Impey, Susan A.; Aria, Adrianus Indrat
    In this brief review, we discuss the recent advancements in using poly(ethylene glycol) diacrylate (PEGDA) hydrogels for tissue engineering applications. PEGDA hydrogels are highly attractive in biomedical and biotechnology fields due to their soft and hydrated properties that can replicate living tissues. These hydrogels can be manipulated using light, heat, and cross-linkers to achieve desirable functionalities. Unlike previous reviews that focused solely on material design and fabrication of bioactive hydrogels and their cell viability and interactions with the extracellular matrix (ECM), we compare the traditional bulk photo-crosslinking method with the latest three-dimensional (3D) printing of PEGDA hydrogels. We present detailed evidence combining the physical, chemical, bulk, and localized mechanical characteristics, including their composition, fabrication methods, experimental conditions, and reported mechanical properties of bulk and 3D printed PEGDA hydrogels. Furthermore, we highlight the current state of biomedical applications of 3D PEGDA hydrogels in tissue engineering and organ-on-chip devices over the last 20 years. Finally, we delve into the current obstacles and future possibilities in the field of engineering 3D layer-by-layer (LbL) PEGDA hydrogels for tissue engineering and organ-on-chip devices.
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    Shaping the structure and properties of HyTemp using polyethylene glycol diglycidyl ether cross-linkers
    (Wiley, 2024-06-03) Dossi, Eleftheria; Mutele-Nkuna, Khuthadzo Lourate; Wilkinson, Peter; Kister, Guillaume; Patrick, Hugh; Khalili, Mohammad Hakim; Hawi, Sara
    Novel elastomers are made by reaction of hydroxyl-terminated polyacrylic ester (HyTemp) with polyethylene glycol (PEG, number of ethylene glycol units 1, 3, 6, 9) based cross-linkers. The influence of the cross-linker length, the HyTemp/cross-linker (w/w) ratio and the cross-linking accelerator trifluoromethanesulfonate scandium salt (ScTFMS) on the structure and the properties of the materials are studied. The cross-linker length has not influence on the glass transition (Tg) of the products because of the presence of the flexible PEG units that cancels out the cross-linking effect associated to a shift to higher Tg. A two-domain structure is seen by the presence of a dual Tg in samples cured with ScTFMS. Mathematical analysis of the modulated differential scanning calorimetry curves offers for the first time the possibility to identify/confirm structural differences in complex three-dimensional polymeric structures. Scanning electron microscopy and swelling experiments in ethyl acetate respectively reveal an increase in the pore size (1.13 to 5.48 nm) and in the absorption ability of the elastomers cured with different types and quantities of PEG cross-linker. The new elastomeric materials are exhibiting a rubbery state over a wide temperature range and absorptivity for the potential recovery of pollutants in soil and/or water.
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    Thermal response of multi-layer UV crosslinked PEGDA hydrogels
    (Elsevier, 2022-01-07) Khalili, Mohammad Hakim; Afsar, Ashfaq; Zhang, Rujing; Wilson, Sandra; Dossi, Eleftheria; Goel, Saurav; Impey, Susan A.; Aria, Adrianus Indrat
    Poly(ethylene glycol) diacrylate (PEGDA) hydrogels are ubiquitously used in a wide variety of applications in tissue engineering. In this study, the thermal response of multi-layered PEGDA hydrogels was investigated under various conditions of the temperature-controlled environments (8, 20, 37, and 45 °C) through gravimetric and volumetric methods. These multi-layered hydrogels were produced using a computer-controlled projection lithography and compared to the monolithic hydrogels fabricated through bulk photo-crosslinking. It was observed that the volume of multi-layered PEGDA hydrogels increased to about 10% at a temperature of 8 °C, while their volume decreased by 8% and 12% when stored at 37 °C and 45 °C, respectively. PEGDA hydrogel also showed an anisotropic characteristic where the axial dimensional change was about 43% higher than the lateral dimension. This finding is critical to inform the design and fabrication of PEGDA hydrogels to compensate for the axial and lateral volume changes during the application at different temperatures.