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通过液相电子显微镜直接观察到药物晶体的非经典结晶途径。

Non-classical crystallisation pathway directly observed for a pharmaceutical crystal via liquid phase electron microscopy.

机构信息

Physics Department & Bernal Institute, University of Limerick, Castletroy, Co. Limerick, Ireland.

School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK.

出版信息

Sci Rep. 2020 Nov 5;10(1):19156. doi: 10.1038/s41598-020-75937-2.

Abstract

Non-classical crystallisation (NCC) pathways are widely accepted, however there is conflicting evidence regarding the intermediate stages of crystallisation, how they manifest and further develop into crystals. Evidence from direct observations is especially lacking for small organic molecules, as distinguishing these low-electron dense entities from their similar liquid-phase surroundings presents signal-to-noise ratio and contrast challenges. Here, Liquid Phase Electron Microscopy (LPEM) captures the intermediate pre-crystalline stages of a small organic molecule, flufenamic acid (FFA), a common pharmaceutical. High temporospatial imaging of FFA in its native environment, an organic solvent, suggests that in this system a Pre-Nucleation Cluster (PNC) pathway is followed by features exhibiting two-step nucleation. This work adds to the growing body of evidence that suggests nucleation pathways are likely an amalgamation of multiple existing non-classical theories and highlights the need for the direct evidence presented by in situ techniques such as LPEM.

摘要

非经典成核(NCC)途径已被广泛接受,但关于成核的中间阶段、它们如何表现以及进一步发展成晶体的证据存在冲突。对于小分子有机分子来说,直接观察的证据尤其缺乏,因为将这些低电子密度的实体与其相似的液相环境区分开来,存在信噪比和对比度方面的挑战。在这里,液相电子显微镜(LPEM)捕捉到了小分子氟芬酸(FFA)的中间预成核阶段,FFA 是一种常见的药物。在其天然环境(有机溶剂)中对 FFA 进行高时空成像表明,在该体系中遵循预成核簇(PNC)途径,然后出现表现出两步成核的特征。这项工作增加了越来越多的证据,表明成核途径可能是多种现有非经典理论的融合,并强调了需要直接证据,而原位技术如 LPEM 就提供了这样的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71e6/7644682/e4fca1278385/41598_2020_75937_Fig1_HTML.jpg

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