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Affiliation |
Engineering educational research section Applied Chemistry Program |
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Title |
Professor |
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Related SDGs |
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IZAWA Hironori
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Degree 【 display / non-display 】
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博士（工学） ( 2010.3 鹿児島大学 )
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修士 ( 2005.3 東北大学 )
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学士 ( 2003.3 富山高等専門学校 )
Research Areas 【 display / non-display 】
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Nanotechnology/Materials / Bio chemistry
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Nanotechnology/Materials / Polymer chemistry
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Nanotechnology/Materials / Polymer materials
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Nanotechnology/Materials / Functional solid state chemistry
Papers 【 display / non-display 】
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Cockscomb-Derived Collagen and Hyaluronic Acid as Renewable Precursors for Gel and Film Materials Reviewed
Izawa H., Kihara A., Tagawa S.
Chemistryselect 11 ( 38 ) 2026.10
Publishing type：Research paper (scientific journal) Publisher：Chemistryselect
Although cockscombs are rich in collagen and hyaluronic acid and therefore possess considerable potential as a biomass resource, their use in material applications remains limited. Here we introduce a novel approach for converting cockscombs into useful biomaterial precursors. Cockscomb pieces are subjected to degreasing, crushing, and subsequent acid-extraction processes. The total yield of lyophilized extract obtained from 101.4 ± 7.1 g of cockscombs is 3.6 ± 1.6 g. IR and <sup>1</sup>H NMR analyses reveal that collagen is the main component of the lyophilized extract, with a smaller amount of hyaluronic acid. Colorimetric assays estimate the collagen and hyaluronic acid contents of the extract to be 75.2 ± 3.0% and 6.7 ± 2.0%, respectively. The lyophilized extract forms elastic hydrogels, which we term cockscomb gel. The elastic hydrogels are capable of elongating up to 57.7 ± 2.2%. In addition, the extraction residue still contains substantial amounts of collagen and hyaluronic acid and can be converted into a sticky cast film and adhesive-like paste after papain digestion. These cockscomb-derived gel and digested-residue materials show promise for the development of biomaterials such as wound dressings and bioadhesives.
DOI： 10.1002/slct.74771
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Araki M., Matsumoto J., Kuroda K., Izawa H.
Carbohydrate Polymers 380 2026.5
Publishing type：Research paper (scientific journal) Publisher：Carbohydrate Polymers
We previously reported a low molecular weight water-soluble guanidinylated chitosan (GCS) with a controlled degree of acetylation (DA). However, the effects of DA, degree of guanidinylation (DG), and molecular weight on the solubility, functions, and biocompatibility of GCS remain unclear, even though water-soluble GCSs with varying parameters would contribute to the development of novel biomaterials. Here we show the bio-interface properties of acetylated chitosans (CSs) and GCSs with systematically varied DA, DG, and molecular weight, including their solubility, antibacterial activity, and cytotoxic effects. Solubility tests revealed that guanidinylation generally reduced solubility, particularly in DA-uncontrolled samples and at higher molecular weights, whereas GCSs with DA values of 32–37% specifically exhibited improved solubility. In other words, we revealed that the control of DA represents the critical factor for enhancing the solubility of GCS. The minimum inhibitory concentration assays of representative acetylated CSs and GCSs against Escherichia coli and Staphylococcus epidermidis revealed that reduced acetyl content is more critical for antibacterial activity than positive charge, and that guanidinylation induces antibacterial activity under neutral conditions. The cytotoxicity and cell proliferation results suggest that water-soluble GCSs show low cytotoxicity, comparable to acetylated CSs, while strongly inhibiting cell proliferation, supporting their potential as anticancer agents.
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Watanabe N., Sumita M., Izawa H., Yagi K., Matsui T.
Journal of Physical Chemistry A 130 ( 18 ) 3534 - 3541 2026.5
Publishing type：Research paper (scientific journal) Publisher：Journal of Physical Chemistry A
N-[2-(Trimethylammonium)ethyl]-1,8-naphthalimide (TENI) is a promising, versatile anion sensor that can detect the electronegativity of a target anion depending on the fluorescence intensity. In TENI, an emission from a lower-energy state than the first excited state of a single TENI is observed experimentally, and its character has remained unknown. Here, we have investigated the origin of the lower-energy peaks in the fluorescence spectrum of TENI using molecular dynamics (MD) simulations and time-dependent density functional theory (TD-DFT) calculations with three functionals. The computation reveals that TENIs form a structural ensemble in solution, and that stacked TENI dimers exhibit red-shifted fluorescence compared to a single TENI. The formation of excimer results in the longer-wavelength fluorescence that can be corroborated by changes in frontier orbital energies due to the intermolecular interaction. Our work will provide valuable knowledge for the development of new anion sensors.
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Guanidinylated nanochitins: guanidinylated chitin nanocrystals are dispersible at neutral pH Reviewed
Izawa H., Ando S., Sone K., Tajima W., Zewude D.A., Yamashita Y., Ifuku S.
Journal of Materials Chemistry B 14 ( 1 ) 144 - 152 2026.1
Publishing type：Research paper (scientific journal) Publisher：Journal of Materials Chemistry B
Despite nanochitins showing favorable biological effects, the colloid stability of positively charged nanochitins by virtue of the amino group is limited to acidic pH, which is different from biological conditions. Here, we show that guanidinylated chitin nanocrystals (GChNCs) are dispersible at neutral pH. The GChNCs are prepared by guanidinylation of partially deacetylated chitin nanocrystals (ChNCs) with 1-amidinopyrazole hydrochloride. The degrees of guanidinylation and acetylation of the GChNCs are 4.6% and 75.7%, respectively. A 1.0 wt% GChNC dispersion is prepared with 0.5 wt% acetic acid solution by sonication treatment. Although slight white turbidity is observed due to scattering, no visible macroscopic precipitates are observed. The average diameter of the GChNCs estimated by DLS analysis is 327.2 nm. When the GChNC dispersion is neutralized by adding 0.1 M NaOH solution, the transmittance of the GChNC dispersion is decreased by aggregation. However, the transmittance of the GChNC dispersion is higher than that of the ChNC dispersion, suggesting that the GChNC particles are less aggregated than the ChNC particles due to the positive charge by virtue of the high basicity of the guanidino group. Interestingly, we find that the GChNCs homogeneously disperse in 0.1 M HEPES buffer (pH 7.4) up to 0.5 wt% by sonication treatment, even though the average diameter of the GChNCs in the solution is 3.4-fold higher (1115.1 nm) than that prepared at pH 3.0. We additionally find no observation of this improved dispersibility of guanidinylated chitin nanofibers due to the guanidino group. This result indicates that the guanidinylation is effective in improving the dispersion of nanochitins with smaller aspect ratios, like ChNCs. Furthermore, we demonstrate that the dispersibility of GChNCs at neutral pH can be utilized for material development, where a gelatin–GChNF composite hydrogel displaying enhanced mechanical properties is successfully prepared by adding 10% (w/w) GChNCs.
DOI： 10.1039/d5tb01771h
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Guanidinylated Chitosan as a Multifunctional Enhancer for Improved Flurbiprofen Delivery Reviewed
Khan N.F., Nakamura H., Izawa H., Ikeda T., Ifuku S., Otagiri M., Anraku M.
Biological and Pharmaceutical Bulletin 48 ( 8 ) 1246 - 1254 2025.8
Publishing type：Research paper (scientific journal) Publisher：Biological and Pharmaceutical Bulletin
In this study, we investigated guanidinylated chitosan (GCS), a chemically modified derivative of unmodified low-molecular-weight chitosan (CS), as a multifunctional excipient to enhance the solubility and absorption of poorly water-soluble drugs. Flurbiprofen (FP) was selected as a model drug to compare the performance of kneaded dispersions GCS-based (FP-GCS) and CS-based (FP-CS). Both GCS and CS increased the solubility of FP in a concentration-dependent manner, with no significant differences between them. However, dissolution testing showed that FP-GCS kneaded dispersion significantly enhanced the dissolution rate of FP alone in water and simulated gastric fluid (pH 1.2), but not under simulated intestinal conditions (pH 6.8). In vivo pharmacokinetic studies in rats demonstrated that FP-GCS kneaded dispersion achieved the highest plasma concentration of FP, suggesting enhanced gastrointestinal permeability. Moreover, FP-GCS kneaded dispersion markedly reduced gastric ulceration in a rat ulcer model. These results indicate that GCS is an effective oral drug delivery excipient capable of improving both the bioavailability and gastrointestinal safety of FP.
Presentations 【 display / non-display 】
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酸性pHの制約を受けにくい高機能キトサン誘導体の開発
井澤浩則
令和6年度高分子学会九州支部講演会
Event date： 2024.12.6
Presentation type：Oral presentation (invited, special)
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水溶性グアニジル化キトサン：置換度と分子量が溶解性に与える影響
荒木 美穂、井澤 浩則
2024年 繊維学会秋季研究発表会
Event date： 2024.11.28 - 2024.11.29
Presentation type：Oral presentation (general)
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Solubility of Chitosan-Oligomers Having Different Degrees of Acetylation
Miho Araki, Hironori Izawa
International Symposium on Fiber Science and Technology
Event date： 2024.11.25 - 2024.11.28
Presentation type：Poster presentation
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アセチル化度の異なるキトサンの溶解性とイオンコンプレックス形成挙動
荒木 美穂、井澤 浩則
第14回CSJ化学フェスタ２０２４
Event date： 2024.10.22 - 2024.10.24
Presentation type：Poster presentation
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中性で均一分散するグアニジル化ナノキチンの開発
井澤 浩則、曽根 健聖、田嶋 航
第7３回高分子討論会
Event date： 2024.9.25 - 2024.9.27
Presentation type：Poster presentation
Grant-in-Aid for Scientific Research 【 display / non-display 】
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多機能性キトサンを基盤とした抗酸化型機能食品と製剤特性改善素材に関する包括的研究
Grant number：24K09953 2024.04 - 2027.03
独立行政法人日本学術振興会 科学研究費基金 基盤研究(C)
Authorship：Coinvestigator(s)
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微細構造表面を誘起するスキン層の科学の開拓
Grant number：19K05616 2019.04 - 2022.03
日本学術振興会 科学研究費助成事業 基盤研究(C) 基盤研究(C)
井澤 浩則
Authorship：Principal investigator