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Local Structural Effects Due to Micronization and Amorphization on an HIV Treatment Active Pharmaceutical Ingredient

机译:艾滋病毒治疗活性药物成分的微粉化和杂散引起的局部结构效应

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摘要

Processing procedures for inducing domain size reduction and/or amorphous phase generation can be crucial for enhancing the bioavailability of active pharmaceutical ingredients (APIs). It is important to quantify these reduced coherence phases and to detect and characterize associated structural changes, to ensure that no deleterious effects on safety, function, or stability occur. Here, X-ray powder diffraction (XRPD), total scattering pair distribution function (TSPDF) analysis, and solid-state nuclear magnetic resonance spectroscopy (SSNMR) have been performed on samples of GSK2838232B, an investigational drug for the treatment of human immunodeficiency virus (HIV). Preparations were obtained through different mechanical treatments resulting in varying extents of domain size reduction and amorphous phase generation. Completely amorphous formulations could be prepared by milling and microfluidic injection processes. Microfluidic injection was shown to result in a different local structure due to dispersion with dichloromethane (DCM). Implications of combined TSPDF and SSNMR studies to characterize molecular compounds are also discussed, in particular, the possibility to obtain a thorough structural understanding of disordered samples from different processes.
机译:用于诱导域尺寸减少和/或非晶相产生的处理程序对于提高活性药物成分(API)的生物利用度至关重要。重要的是量化这些减少的相干阶段并检测和表征相关的结构变化,以确保不会对安全,功能或稳定性产生有害影响。这里,已经对GSK2838232B的样品,用于治疗人免疫缺陷病毒的研究(艾滋病病毒)。通过不同的机械处理获得制剂,导致域尺寸还原的变化范围和非晶相产生。可以通过研磨和微流体注射过程来制备完全无定形的制剂。显示微流体注射剂由于与二氯甲烷(DCM)分散而导致不同的局部结构。还讨论了组合TSPDF和SSNMR研究表征分子化合物的影响,特别是获得来自不同过程的无序样品的彻底结构理解。

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