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MORITA KentaGraduate School of Engineering / Department of Chemical Science and EngineeringAssistant Professor
Research activity information
■ Award- Jun. 2024 13th International Colloids Conference, Best Poster Prize, Molecular aggregation strategy for inhibiting DNases
- May 2022 高分子学会, The society of polymer science, publicity awards, がん細胞の内部をゲル化してアポトーシス死を導くペプチド型抗がん剤の開発
- Aug. 2021 株式会社ストラテジック, IRMAIL science grant, がん細胞を"内側から固めて"殺す自己組織化ペプチド薬の抗がん作用機序の実証
- Oct. 2024, ACS Applied Nano Materials[Refereed]Scientific journal
- A tumor microenvironment (TME)-responsive nanoprobe composed of a fluorescent dye-decorated silicon (Si) nanosphere core and a thin MnO2 shell is proposed for simple and intelligent detection of cancer cells. The Si nanosphere core with diameters of 100-200 nm provides environment-independent Mie scattering imaging, while, simultaneously, the MnO2 shell provides the capability to switch the on/off state of the dye fluorescence reacted to the glutathione (GSH) and/or H2O2 levels in a cancer cell. Si-MnO2 core-shell nanosphere probes are fabricated in a solution-based process from crystalline Si nanosphere cores. The fluorescence switching under exposure to GSH is demonstrated, and the mechanism is discussed based on detailed optical characterizations including single-particle spectroscopy. Different types of human cells are incubated with the nanoprobes, and a proof of concept experiment is performed. From the combination of the robust scattering images and GSH- and H2O2-sensitive fluorescence images, the feasibility of cancer cell detection by the multimodal nanoprobes is demonstrated.Jul. 2024, ACS applied materials & interfaces, 16(26) (26), 33963 - 33970, English, International magazine[Refereed]Scientific journal
- This study highlights the novel potential of molecular aggregates as inhibitors of a disease-related protein. Enzyme inhibitors have been studied and developed as molecularly targeted drugs and have been applied for cancer, autoimmune diseases, and infections. In many cases, enzyme inhibitors that are used for therapeutic applications interact directly with enzymes in a molecule-to-molecule manner. We found that the aggregates of a small compound, Mn007, inhibited bovine pancreatic DNase I. Once Mn007 molecules formed aggregates, they exhibited inhibitory effects specific to DNases that require divalent metal ions. A DNase secreted by Streptococcus pyogenes causes streptococcal toxic shock syndrome (STSS). STSS is a severe infectious disease with a fatality rate exceeding 30% in patients, even in this century. S. pyogenes disrupts the human barrier system against microbial infections through the secreted DNase. Until now, the discovery/development of a DNase inhibitor has been challenging. Mn007 aggregates were found to inhibit the DNase secreted by S. pyogenes, which led to the successful suppression of S. pyogenes growth in human whole blood. To date, molecular aggregation has been outside the scope of drug discovery. The present study suggests that molecular aggregation is a vast area to be explored for drug discovery and development because aggregates of small-molecule compounds can inhibit disease-related enzymes.Lead, Jun. 2024, JACS Au, 4(6) (6), 2262 - 2266, English, International magazine[Refereed]Scientific journal
- Abstract Polymer composites with thermal conductivity are attractive for heat dissipation in electronic devices. We prepared epoxy resin‐based composite films filled with polythiophene [poly(3‐hexylthiophene‐2,5‐diyl)] (P3HT)/graphene complex or aluminum nitride (AlN). The composite films were characterized by electron microscopic observation, thermogravimetric analysis, and thermal conductivity measurements. The addition of a small content of P3HT/graphene complex (<1 wt%) increased both the out‐of‐plane and in‐plane thermal conductivities of the epoxy resin. The addition of AlN also increased thermal conductivity, but ≥40 wt% was required to obtain thermal conductivity comparable with that of an epoxy resin film doped with 0.9 wt% P3HT/graphene complex. The present results illustrate the potential of P3HT/graphene complexes as fillers for improving the thermal conductivity of epoxy resins without affecting their insulating properties. Highlights Polythiophene/graphene fillers increased epoxy resin films' thermal conductivity. To raise the thermal conductivity of epoxy resin films high AlN content was needed. In‐plane/out‐of‐plane epoxy resin films' thermal conductivities were evaluated.Wiley, May 2024, Polymer Composites, 45(12) (12), 11104 - 11111[Refereed]Scientific journal
- With the progression of regenerative medicine and cell therapy, the importance of cryopreservation techniques for cultured cells continues to rise. Traditional cryoprotectants, such as dimethyl sulfoxide and glycerol, are effective in cryopreserving suspended cells, but they do not demonstrate sufficient efficacy for two-dimensional (2D)-cultured cells. In the past decade, small molecules and polymers have been studied as cryoprotectants. Some L-amino acids have been reported to be natural and biocompatible cryoprotectants. However, the cryoprotective effects of D-amino acids have not been investigated for such organized cells. In the present study, the cryoprotective effects of D- and L-amino acids and previously reported cryoprotectants were assessed using HepG2 cells cultured on a microplate without suspending the cells. d-Proline had the highest cryoprotective effect on 2D-cultured cells. The composition of the cell-freezing solution and freezing conditions were then optimized. The d-proline-containing cell-freezing solution also effectively worked for other cell lines. To minimize the amount of animal-derived components, fetal bovine serum in the cell freezing solution was substituted with bovine serum albumin and StemFit (a commercial supplement for stem cell induction). Further investigations on the mechanism of cryopreservation suggested that d-proline protected enzymes essential for cell survival from freeze-induced damage. In conclusion, an effective and xeno-free cell-freezing solution was produced using d-proline combined with dimethyl sulfoxide and StemFit for 2D-cultured cells.Lead, American Chemical Society (ACS), Mar. 2024, ACS Biomaterials Science & Engineering, 10(4) (4), 2442 - 2450, English, International magazine[Refereed]Scientific journal
- Abstract Cellulose has been developed as an alternative to petrochemical materials. By comparison with refined nanofibers (RCNFs), lignocellulose nanofibers (LCNFs) show particular promise because it is produced from biomass using only mild pretreatment. The mechanical properties of LCNFs depend on the contained lignin. However, the microscopic location of the lignin contained in LCNFs has not been determined. Thus, we developed two methods to detect and visualize lignin. One uses a scanning transmission electron microscope (STEM) equipped with an energy dispersive X-ray spectroscopy detector. The other method uses an atomic force microscope (AFM) equipped with a cantilever coated with an aromatic molecule. Both methods revealed that the lignin in LCNFs covers a thin cellulose fiber and is precipitated in a grained structure. In particular, the AFM system was able to determine the nanoscopic location of lignin-rich areas. The present study establishes a strong tool for analyzing the characteristics of lignin-containing materials. Graphical abstractLead, Springer Science and Business Media LLC, Nov. 2023, Cellulose, 30(18) (18), 11357 - 11367[Refereed]Scientific journal
- Lead, Jan. 2023, ACS Applied Nano Materials, 6(2) (2), 1432 - 1440[Refereed]Scientific journal
- Wiley, Jan. 2023, Small, 19(14) (14), 2207318 - 2207318, English, International magazine[Refereed]Scientific journal
- Jan. 2023, Colloids and Surfaces A: Physicochemical and Engineering Aspects, 656[Refereed]Scientific journal
- Lead, Sep. 2022, JACS Au, 2(9) (9), 2023 - 2028, English, International magazine[Refereed]Scientific journal
- Aug. 2022, The Journal of Physical Chemistry B, 126(31) (31), 5793 - 5802, English, International magazine[Refereed]Scientific journal
- Apr. 2022, JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 41(1) (1), 146 - 146, English, International magazine[Refereed]Scientific journal
- Jan. 2022, ACS APPLIED MATERIALS & INTERFACES, 14(2) (2), 3255 - 3263, English, International magazine[Refereed]Scientific journal
- Oct. 2021, PHYSICS & IMAGING IN RADIATION ONCOLOGY, 20, 94 - 97, English, International magazine[Refereed]Scientific journal
- Jul. 2021, RSC ADVANCES, 11(38) (38), 23409 - 23417, English, International magazine[Refereed]Scientific journal
- Jun. 2021, BIOMACROMOLECULES, 22(6) (6), 2524 - 2531, English, International magazine[Refereed]Scientific journal
- Apr. 2021, 化學工業, 72(4) (4), 244 - 251, JapaneseMedical Application of Titanium Peroxide Nanoparticles for Cancer Radiotherapy[Refereed][Invited]
- (一社)日本インターベンショナルラジオロジー学会, Apr. 2021, 日本インターベンショナルラジオロジー学会雑誌, 36(Suppl.) (Suppl.), 191 - 191, JapaneseウサギVX2腫瘍モデルを用いた過酸化チタンナノ粒子動注の基礎的研究
- Lead, Feb. 2021, COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 611, English[Refereed]Scientific journal
- Lead, Feb. 2021, COLLOIDS AND SURFACES B-BIOINTERFACES, 198, 111451 - 111451, English, International magazine[Refereed]Scientific journal
- Feb. 2021, BIOTECHNOLOGY AND BIOENGINEERING, 118(2) (2), 863 - 876, English, International magazine[Refereed]Scientific journal
- Nov. 2020, ACS APPLIED BIO MATERIALS, 3(11) (11), 7743 - 7751, English, International magazine[Refereed]Scientific journal
- Nov. 2020, BIOMASS & BIOENERGY, 142, English[Refereed]Scientific journal
- Aug. 2020, APPLIED NANOSCIENCE, 10(8) (8), 3143 - 3148, English[Refereed]Scientific journal
- Jul. 2020, PHYSICA MEDICA-EUROPEAN JOURNAL OF MEDICAL PHYSICS, 75, 69 - 76, English, International magazine[Refereed]Scientific journal
- Jun. 2020, NANOMATERIALS, 10(6) (6), English, International magazine[Refereed]Scientific journal
- Jun. 2020, RADIATION MEASUREMENTS, 134, English[Refereed]Scientific journal
- 2020, MATERIALS TRANSACTIONS, 61(2) (2), 311 - 317, English[Refereed]Scientific journal
- Dec. 2019, POLYMER JOURNAL, 51(12) (12), 1309 - 1310, English[Refereed]
- Sep. 2019, BIOTECHNOLOGY JOURNAL, 14(9) (9), e1800704, English, International magazine[Refereed]Scientific journal
- Jul. 2019, ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 7(13) (13), 11069 - 11079, English[Refereed]Scientific journal
- May 2019, POLYMER JOURNAL, 51(5) (5), 489 - 499, English[Refereed]Scientific journal
- Apr. 2019, GREEN CHEMISTRY, 21(7) (7), 1795 - 1808, English[Refereed]Scientific journal
- Mar. 2019, ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 7(5) (5), 5010 - 5017, English[Refereed]Scientific journal
- Jul. 2018, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 126(1) (1), 119 - 125, English, Domestic magazine[Refereed]Scientific journal
- Jun. 2018, Biotechnology for biofuels, 11, 180[Refereed]
- Elsevier, May 2018, Nanoparticle Technology Handbook, 439 - 443, EnglishIn book
- 日本DDS学会, May 2018, 日本DDS学会学術集会プログラム予稿集, 34回, 207 - 207, Japanese新規放射線増感剤としての過酸化チタンナノ粒子の物性解析
- Lead, Dec. 2016, FREE RADICAL RESEARCH, 50(12) (12), 1319 - 1328, English, International magazine[Refereed]Scientific journal
- Jul. 2016, RADIATION ONCOLOGY, 11(1) (1), 91 - 91, English, International magazine[Refereed]Scientific journal
- Aug. 2015, CANCER RESEARCH, 75, English[Refereed]
- (一社)日本放射線影響学会, May 2015, 日本放射線影響学会大会講演要旨集, 58回, 3 - 07, English新たな放射線増感剤としての過酸化チタンナノ粒子は膵癌治療における抗腫瘍効果を増強させる(Titanium Peroxide Nanoparticles, as Novel Radiosensitizers, Enhance Antitumor Efficacy in Pancreatic Cancer Therapy)
- Feb. 2015, JOURNAL OF NANOBIOTECHNOLOGY, 13, 15 - 15, English, International magazine[Refereed]Scientific journal
- (公社)日本分析化学会, Sep. 2014, 日本分析化学会講演要旨集, 63年会, 168 - 168, Japaneseラジカルを発生する金属酸化物ナノ粒子のX線を用いた分析
- Lead, May 2024, 豊田研究報告, 77, 142 - 143, JapaneseStaining Probe for an Observation of Cell Organelle by Using Electron Microscope[Invited]Report scientific journal
- Lead, 01 May 2024, 神戸大学大学院工学研究科HP(Research Topics)分子の「塊」が溶連菌の感染を抑制することを発見
- Lead, 09 Apr. 2024, 神戸大学大学院工学研究科HP(Research Topics)安価なアミノ酸を添加するだけでシート状に培養した細胞を凍結保存可能に
- Jan. 2024, 88(2) (2), 53 - 57, Japaneseペプチド界面活性剤(ペプチド脂質)の自己組織化とがん細胞の殺傷[Invited]Introduction scientific journal
- 30 Sep. 2023, 分離技術, 53(5) (5), 280 - 285, Japanese新規機能を担う高分子の創成と活用 合成高分子の単純塗布によるプラスチック材料表面の機能化[Invited]Introduction scientific journal
- 日本DDS学会, May 2018, 日本DDS学会学術集会プログラム予稿集, 34回, 204 - 204, Japanese過酸化チタンナノ粒子の併用による放射線増感治療法の開発
- A bio-nanocapsule (BNC) that is composed of the L protein of the hepatitis B virus (HBV) surface antigen and a lipid bilayer shows high specificity for human hepatocytes. Therefore, we have developed various specificity-altered BNCs for cancer cell types by gene engineering. While at the same time, we have demonstrated that titanium peroxide nanoparticle (TiOx) shows anticancer effect in combination with X-ray irradiation. Therefore, we tried to encapsulate the TiOx in the BNC and deliver this complex particle into the target tumor. As a result, we succeeded in demonstrating antitumor effect against mouse xenograft model with a combination of the complex particle and X-ray irradiation.Hosokawa Micron Corporation, 15 Dec. 2016, THE MICROMERITICS, 60(60) (60), 13 - 19, Japanese[Refereed][Invited]
- 日本生物工学会, 2013, 日本生物工学会大会講演要旨集, 65, 244 - 244, Japanese3P-225 Nanoparticle-mediated cancer therapy with Xray irradiation
- Single work, 博士論文, Sep. 2018, Japaneseポリアクリル酸修飾過酸化チタンナノ粒子を用いた新規放射線増感治療の開発
- Contributor, Application 8 - A Cancer Treatment Strategy That Combines the Use of Inorganic/Biocomplex Nanoparticles With Conventional Radiation Therapy, Elsevier, 2018, 439-443, English, ISBN: 9780444641106Nanoparticle technology handbookScholarly book
- 13th International Colloids Conference, Jun. 2024, EnglishMolecular aggregation strategy for inhibiting DNasesPoster presentation
- Chemical Science symposium 2023: Chemistry of polymers, Oct. 2023, EnglishMolecular Co-Assembly Creates Species Selectivity in a Conventional AntifungalOral presentation
- 第4回先端膜工学研究センター成果発表会, Mar. 2023, Japanese合成ペプチド脂質の自己組織化による選択的細胞死(菌からがん細胞まで)[Invited]Invited oral presentation
- The 17th pacific polymer conference (PPC17), Dec. 2022, EnglishCo-assembly of a peptide amphiphile and a conventional antifungal drug creates selective toxicity to virulent fungiOral presentation
- 4th G’L’owing Polymer Symposium in KANTO (GPS-K2021), Jul. 2021, EnglishFunction Control of Hydrophobic Antimicrobial Molecules by utilizing Self-Assembly of Oligopeptide-Type Low Molecular Weight HydrogelatorOral presentation
- Pacifichem 2015, Dec. 2015, EnglishDevelopment of novel radiosensitizing cancer therapy: Combination of radiotherapy and titanium peroxide nanoparticlePoster presentation
- 日本生物工学会Jan. 2022 - Present
- 高分子学会Jun. 2020 - Present
- 日本化学工学会Apr. 2017 - Present
- 日本DDS学会Jul. 2018 - Aug. 2019
- 日本生物工学会学生会員Jun. 2014 - Mar. 2017
- 日本学術振興会, 科学研究費助成事業, 基盤研究(B), 神戸大学, 01 Apr. 2024 - 31 Mar. 2026分子の細胞内自己組織化によるがん選択的細胞死誘導技術の確立
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Scientific Research (B), Kobe University, 01 Apr. 2023 - 31 Mar. 2026Induction of cancer-selective cell death by intracellular self-assembly of molecules
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Early-Career Scientists, Kobe University, 01 Apr. 2023 - 31 Mar. 2025Selective electron staining probe for cell organelle
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Early-Career Scientists, Grant-in-Aid for Early-Career Scientists, Kobe University, 01 Apr. 2021 - 31 Mar. 2023Design of amphiphilic oligopeptides that induce destructive self-assembly of pathogenic amyloids
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Research Activity Start-up, Grant-in-Aid for Research Activity Start-up, Kobe University, 11 Sep. 2020 - 31 Mar. 2022A function-adjustable medical gel based on co-assembly of peptide-type gelator with various functional agentsThe study demonstrates that the nano-assembly of a short-peptide hydrogelator (P1) imparts novel antifungal selectivity to amphotericin B (AmB), expanding its application range. AmB's limitations of poor solubility and toxicity are addressed by P1, a low-molecular-weight hydrogelator with low cytotoxicity. P1 successfully solubilizes AmB in water as micelle-like nano-complexes (NCs), reducing its toxicity against Saccharomyces cerevisiae. Protease degradation of P1 in the NCs restores AmB's antifungal activity. Moreover, high-concentration P1 forms an AmB-incorporating hydrogel (AmB-P1 gel), effectively suppressing AmB's antifungal activity. Protease-secreting Aspergillus oryzae fails to grow on the AmB-P1 gel, indicating selective fungicidal effects. Co-assembly strategies hold promise for "drug repositioning" in the medical field, particularly against protease-secreting infectious fungi.
- Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research Grant-in-Aid for Scientific Research (C), Grant-in-Aid for Scientific Research (C), Kobe University, 01 Apr. 2016 - 31 Mar. 2019Our previous studies indicated that titanium peroxide nanoparticles (TiOxNPs) induced reactive oxygen species (ROS) when expose to X-rays and enhanced radiation cytotoxic effect. In this study, the type and amount of ROS generated from TiOxNPs were investigated and compared to those generated by gold nanoparticles (GNPs). The results showed that the amount of ROS generated from TiOxNPs under X-ray irradiation was less than that of GNPs, however TiOxNPs had the ability to release H2O2 regardless of X-ray irradiation. The released H2O2 is assumed to be acted as a strong radiosensitising agent of TiOxNPs in vitro and in vivo set up. On the other hand, only 12% of the TiOxNPs dose had accumulated in the tumour 1 hour after an intravenous injection in vivo experiment. The liver had the largest accumulation of the injected nanoparticles. Future studies will be required to develop the strategies to enhance the tumour targeting ability of TiOxNPs.
- Temperature compensated surface acoustic wave device having mass loading strip with buffer layerUS-2023344408-A1, 30 Mar. 2022, SKYWORKS SOLUTIONS INC (US)Patent right
- Acoustic wave device having mass loading strip with buffer layerUS-2023344407-A1, 30 Mar. 2022, SKYWORKS SOLUTIONS INC (US)Patent right
- Acoustic wave device having mass loading strip with thermal expansion compensation buffer layerUS-2023344406-A1, 30 Mar. 2022Patent right