Hitomi Shirahama
Nanyang Technological University
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Publication
Featured researches published by Hitomi Shirahama.
Small | 2016
Raghavendra C. Mundargi; Michael G. Potroz; Soohyun Park; Hitomi Shirahama; Jae Ho Lee; Jeongeun Seo; Nam-Joon Cho
In nature, pollen grains play a vital role for encapsulation. Many pollen species exist which are often used as human food supplements. Dynamic image particle analysis, scanning electron microscopy, and confocal microscopy analysis confirmed the size, structural uniformity, and macromolecular encapsulation in sunflower pollen, paving the way to explore natural pollen grains for the encapsulation of therapeutic molecules.
RSC Advances | 2015
Bae Hoon Lee; Hitomi Shirahama; Nam-Joon Cho; Lay Poh Tan
We report an effective and novel method to controllably produce highly substituted gelatin-MA with nearly 100% degree of substitution despite the use of a very low concentration of methacrylic anhydride (MAA). The method is based on sequential time-lapse loading of MAA after pH adjustment in a carbonate–bicarbonate buffer system. Rheological studies indicate that hydrogels formed from more highly substituted gelatin-MA exhibit significantly improved mechanical stiffness.
Scientific Reports | 2016
Hitomi Shirahama; Bae Hoon Lee; Lay Poh Tan; Nam-Joon Cho
Gelatin-methacryloyl (GelMA) is one of the most commonly used photopolymerizable biomaterials in bio-applications. However, GelMA synthesis remains suboptimal, as its reaction parameters have not been fully investigated. The goal of this study is to establish an optimal route for effective and controllable GelMA synthesis by systematically examining reaction parameters including carbonate-bicarbonate (CB) buffer molarity, initial pH adjustment, MAA concentration, gelatin concentration, reaction temperature, and reaction time. We employed several analytical techniques in order to determine the degree of substitution (DS) and conducted detailed structural analysis of the synthesized polymer. The results enabled us to optimize GelMA synthesis, showing the optimal conditions to balance the deprotonation of amino groups with minimizing MAA hydrolysis, which led to nearly complete substitution. The optimized conditions (low feed ratio of MAA to gelatin (0.1 mL/g), 0.25 M CB buffer at pH 9, and a gelatin concentration of 10–20%) enable a simplified reaction scheme that produces GelMA with high substitution with just one-step addition of MAA in one pot. Looking forward, these optimal conditions not only enable facile one-pot GelMA synthesis but can also guide researchers to explore the efficient, high methacrylation of other biomacromolecules.
Macromolecular Bioscience | 2016
Myunghee Kim; Supriya K. Kumar; Hitomi Shirahama; Jeongeun Seo; Jae-Ho Lee; Vladimir P. Zhdanov; Nam-Joon Cho
Development of artificial tissues providing the proper geometrical, mechanical, and environmental cues for cells is highly coveted in the field of tissue engineering. Recently, microfabrication strategies in combination with other chemistries have been utilized to capture the architectural complexity of intricate organs, such as the liver, in in vitro platforms. Here it is shown that a biofunctionalized poly (ethylene glycol) (PEG) hydrogel scaffold, fabricated using a sphere-template, facilitates hepatic sheet formation that follows the microscale patterns of the scaffold surface. The design takes advantage of the excellent diffusion properties of porous, uniform 3D hydrogel platforms, and the enhanced-cell-extracellular matrix interaction with the display of conjugated collagen type I, which in turn elicits favorable Huh-7.5 response. Collectively, the experimental findings and corresponding simulations demonstrate the importance of biofunctionalized porous scaffolds and indicate that the microscaffold shows promise in liver tissue engineering applications and provides distinct advantages over current cell sheet and hepatocyte spheroid technologies.
Scientific Reports | 2016
Yan Wang; Myunghee Kim; Hitomi Shirahama; Jae Ho Lee; Soon Seng Ng; Jeffrey S. Glenn; Nam-Joon Cho
It is well known that a three-dimensional (3D) culture environment and the presence of extracellular matrix (ECM) proteins facilitate hepatocyte viability and maintenance of the liver-specific phenotype in vitro. However, it is not clear whether specific ECM components such as collagen or fibronectin differentially regulate such processes, especially in 3D scaffolds. In this study, a series of ECM-functionalized inverted colloidal crystal (ICC) microporous scaffolds were fabricated and their influence on Huh-7.5 cell proliferation, morphology, hepatic-specific functions, and patterns of gene expression were compared. Both collagen and fibronectin promoted albumin production and liver-specific gene expression of Huh-7.5 cells, compared with the bare ICC scaffold. Interestingly, cells in the fibronectin-functionalized scaffold exhibited different aggregation patterns to those in the collagen-functionalized scaffold, a variation that could be related to the distinct mRNA expression levels of cell adhesion-related genes. Based on these results, we can conclude that different ECM proteins, such as fibronectin and collagen, indeed play distinct roles in the phenotypic regulation of cells cultured in a 3D environment.
Advanced Functional Materials | 2016
Raghavendra C. Mundargi; Michael G. Potroz; Soohyun Park; Jae Hyeon Park; Hitomi Shirahama; Jae Ho Lee; Jeongeun Seo; Nam-Joon Cho
Integrative Biology | 2016
Myunghee Kim; Supriya K. Kumar; Hitomi Shirahama; Jeongeun Seo; Jae Ho Lee; Nam-Joon Cho
Npg Asia Materials | 2017
Bae Hoon Lee; Hitomi Shirahama; Myunghee Kim; Jae Ho Lee; Nam-Joon Cho; Lay Poh Tan
ACS Biomaterials Science & Engineering | 2016
Yan Wang; Jae Ho Lee; Hitomi Shirahama; Jeongeun Seo; Jeffrey S. Glenn; Nam-Joon Cho
Journal of Visualized Experiments | 2016
Hitomi Shirahama; Supriya K. Kumar; Won-Yong Jeon; Myunghee Kim; Jae Ho Lee; Soon Seng Ng; Seyed R. Tabaei; Nam-Joon Cho