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首页> 外文期刊>Crystal growth & design >Morphology of Porous Hosts Directs Preferred Polymorph Formation and Influences Kinetics of Solid/Solid Transitions of Confined Pharmaceuticals
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Morphology of Porous Hosts Directs Preferred Polymorph Formation and Influences Kinetics of Solid/Solid Transitions of Confined Pharmaceuticals

机译:多孔宿主的形态指导优选的多晶型物形成,并影响密闭药物的固体/固体转变动力学

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The pore morphology of a porous host may determine which polymorph a crystallizable guest preferentially forms and may influence the kinetics of solid/solid transitions. Slow cooling of the drug acetaminophen (ACE) inside the straight cylindrical pores of anodic aluminum oxide (AAO, tortuosity = 1) in contact with a bulk ACE surface film preferentially yields uniformly oriented form II and/or form III crystals. The occurring orientations of form II and form III crystals are characterized by high structural registry along the AAO pores. The uniformly oriented form III crystals inside the AAO pores were readily converted into likewise uniformly oriented form II crystals by a solid/solid transition. Thus, we obtained uniformly oriented form II crystals in AAO at high yields. We suggest that sporadic heterogeneous nucleation at bulk crystals formed in the bulk surface film on top of the AAO coupled with kinetic selection of crystal orientations results in fast growth of properly oriented crystals along the 100 μm deep AAO pores. This mechanism is suppressed in controlled porous glass (CPG) having isotropic spongelike pores (tortuosity > 1.5) with free growth paths on the order of 100 nm, where form I formed instead. Moreover, the transition from form III to form II is suppressed in CPG. Possible reasons may include impingement of the propagation front of the solid/solid transition on the CPG pore walls after short propagation paths and inevitable formation of form II grains with different orientations separated by energetically disadvantageous grain boundaries. The results reported here are relevant to mesoscopic crystal engineering aimed at controlled drug release from nanoscale delivery systems. Polymorphs not accessible otherwise in nanoscale containers may be produced at high yields. The principles reported here may be transferred to areas such as nanowire-based organic electronics.
机译:多孔主体的孔形态可以确定可结晶客体优先形成的多晶型物,并且可以影响固体/固体转变的动力学。与块状ACE表面膜接触的阳极氧化铝(AAO,曲折度= 1)的直圆柱孔内的药物对乙酰氨基酚(ACE)缓慢冷却,优先产生均匀取向的II型和/或III型晶体。 II型和III型晶体的发生取向的特征是沿AAO孔的高度结构配准。通过固/固转变,在AAO孔内的均匀取向的III型晶体易于转化为同样均匀取向的II型晶体。因此,我们以高收率在AAO中获得了均匀取向的II型晶体。我们建议,在AAO顶部的块状表面膜中形成的块状晶体上的零星异质成核,加上晶体取向的动力学选择,会导致沿100μm深的AAO孔快速生长正确定向的晶体。在具有各向同性的海绵状孔(曲折度> 1.5)且自由生长路径为100 nm数量级的受控多孔玻璃(CPG)中,此机理得到了抑制,而在此处形成了I型。此外,在CPG中抑制了从形式III到形式II的转变。可能的原因可能包括:在短的传播路径之后,固/固相变的传​​播前沿在CPG孔壁上的撞击;不可避免地形成了具有不同方向的II型晶粒,这些晶粒被能量上不利的晶界隔开。此处报道的结果与旨在控制药物从纳米级释放系统释放的介观晶体工程有关。纳米级容器中否则无法获得的多晶型物可以高产率生产。此处报告的原理可能会转移到基于纳米线的有机电子产品等领域。

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