结晶
肺表面活性物质
胶束
十二烷基硫酸钠
介观物理学
结晶学
自组装
化学工程
D-甘露醇
甘露醇
多态性(计算机科学)
化学
材料科学
纳米技术
水溶液
色谱法
有机化学
生物化学
基因
物理
量子力学
基因型
工程类
作者
Frederico Marques Penha,A. V. Gopalan,Jochem Christoffel Meijlink,Fatma İbiş,Hüseyin Burak Eral
标识
DOI:10.1021/acs.cgd.1c00243
摘要
Selective crystallization of polymorphs is highly sought after in industrial practice. Yet, state-of-the-art techniques either use laboriously engineered solid surfaces or strenuously prepared heteronucleants. We propose an approach where surfactants in solution self-assemble effortlessly into mesoscopic structures dictating the polymorphic outcome of the target solute. Sodium dodecyl sulfate (SDS) surfactant is used as a tailored additive to crystallize different polymorphic forms of a model active pharmaceutical ingredient, d-mannitol. Different mesoscopic phases of SDS template particular polymorphs: packed monolayers, micelles, and crystals favored the β, α, and δ forms of d-mannitol, respectively. A synergistic effect of topological templating and molecular interactions is proposed as the rationale behind the observed selective crystallization of polymorphs. This crystal engineering technique suggests that surfactant self-assemblies can be used as tailored templates for polymorphic control.
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