The University of Osaka · 물리·천문학
미호코 마루야마 교수의 연구실은 결정화 과정에서의 분자 구조, 특히 입체화학적 비대칭성(오래된 분자)이 결정 성장에 미치는 영향을 중심으로 연구를 전개하고 있습니다. 특히 생체 분자와 무기 결정의 상호작용, 고체상 전이, 다이내믹한 결정 성장 메커니즘을 실시간으로 관찰하는 고해상도 비파괴 측정 기법을 응용하여, 불안정한 다형체의 선택적 결정화 및 단백질 결정화의 품질 제어를 목표로 하고 있습니다. 이는 신약 개발, 신장결석의 병태생리학 해명, 고성능 소재 설계 등 응용 분야로 이어집니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
The regulation of calcite mineralization by chiral biological molecules is one of the fundamental unresolved issues at the interface between biological, geological, and physical sciences. Here we address the role of chirality of l-aspartic acid (l-Asp), a model additive, in the regulation of the growth of calcite crystals. We apply phase-shift interferometry to nonintrusively monitor in-situ the morphology of the surface and quantify the velocity of propagation of the edges of the unfinished cry
A new method for selective crystallization of the metastable phase (form II) of acetaminophen is described. To obtain form II, we prepared a highly supersaturated solution (σI = 3.7) and then applied ultrasonic irradiation at different frequencies. Without ultrasonic irradiation, spontaneous crystallization did not occur within one month in the highly supersaturated condition (σI = 3.7). When ultrasonic irradiation at 28 kHz was applied, form II preferentially crystallized. Therefore, we conclud
We describe a new method for the selective crystallization of the metastable phase (α-form) of indomethacin. To obtain the α-form, we prepared a highly supersaturated solution and then introduced forcible nucleation techniques, namely, laser irradiation and magnetic stirring. When the laser irradiated near the side wall, the α-form crystallized within 24 h. The α-form crystals showed temporal stability for at least 8 months in air ambient at room temperature. We conclude that control of the lase
The pathogenesis of kidney stone formation includes multi-step processes involving complex interactions between mineral components and protein matrix. Calcium-binding proteins in kidney stones have great influences on the stone formation. The spatial distributions of these proteins in kidney stones are essential for evaluating the in vivo effects of proteins on the stone formation, although the actual distribution of these proteins is still unclear. We reveal micro-scale distributions of three d
The selective crystallization of aspirin form II is exceedingly difficult, because the similarity of the crystal structures of form I and form II enable them to intergrow. We succeeded in crystallizing a pure form II crystal by laser irradiation with a precise condition control. The crystal was identified by Raman spectroscopy and in situ observation of the phase transformation from form II into form I. Accordingly, we conclude that this laser-induced crystallization would be applicable to a var
To grow protein crystals of better quality, there still exists an open question whether a solution flow should be suppressed or intentionally introduced. To obtain a comprehensive understanding of the effects of a solution flow, we directly measured the velocities of individual elementary steps (on {110} faces of tetragonal lysozyme crystals) under a forced solution flow, for the first time, by laser confocal microscopy combined with differential interference contrast microscopy. When we used cr
Abstract We report a new method of obtaining the metastable phase form II crystals of acetaminophen. Solution-mediated phase transformation (SMPT) from trihydrate into form II is utilized to obtain form II crystals. SMPT is triggered by seeding form II crystals into a saturated solution including trihydrate crystals, which are less stable than form II crystals. Form II seed crystals gradually grew at the expense of the dissolving trihydrate crystals, and finally, all the trihydrate crystals in s
We report a novel method for crystallizing the metastable polymorph form II of acetaminophen by using a plastic ball during ultrasonic irradiation. The presence of a plastic ball during ultrasonic irradiation of aqueous acetaminophen solution effectively increased the probability and reduced the induction time of form II crystallization. This method facilitated both laboratory- and large-scale production of form II crystals. Our method has significant advantages for practical application of form