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罗替戈汀:具有可预测的整体单向行为的意外多态性。

Rotigotine: Unexpected Polymorphism with Predictable Overall Monotropic Behavior.

作者信息

Rietveld Ivo B, Céolin René

机构信息

Caractérisation des Matériaux Moléculaires à Activité Thérapeutique (CAMMAT), Faculté de Pharmacie de Paris, Université Paris Descartes, Paris 75006, France.

LETIAM, IUT d'Orsay, Université Paris Sud 11, Orsay 91400, France.

出版信息

J Pharm Sci. 2015 Dec;104(12):4117-4122. doi: 10.1002/jps.24626. Epub 2015 Sep 7.

Abstract

Crystallization of polymorphs still has a touch of art, as even prior observations of polymorphs do not guarantee their crystallization. However, once crystals of various polymorphs have been obtained, their relative stabilities can be established with a straightforward thermodynamic approach even if the conclusion will depend on the quality of the experimental data. Rotigotine is an active pharmaceutical ingredient, which has suffered the same setback as Ritonavir: a sudden appearance of a more stable crystalline polymorph than the one used for the formulation. Although the cause of the defect in the formulation was quickly established, the interpretation of the phase behavior of rotigotine has been lacking in clarity. In the present paper, data published in the patents resulting from the discovery of the new polymorph have been used to establish the pressure-temperature phase diagram of the two known solid forms of rotigotine. The analysis clearly demonstrates that form II is the stable solid phase and form I is metastable in the entire pressure-temperature domain: form I is overall monotropic in relation to form II. Thus, it was a sensible decision of European Medicines Agency to ask for a reformulation, as the first formulation was metastable even if crystallization appeared to be very slow.

摘要

多晶型物的结晶仍带有一丝艺术性,因为即便之前已观察到多晶型物,也不能保证它们会结晶。然而,一旦获得了各种多晶型物的晶体,即使结论将取决于实验数据的质量,也可以用一种直接的热力学方法确定它们的相对稳定性。罗替戈汀是一种活性药物成分,它遭遇了与利托那韦相同的挫折:突然出现了一种比用于制剂的晶型更稳定的结晶多晶型物。尽管制剂缺陷的原因很快就被确定了,但罗替戈汀相行为的解释一直不够清晰。在本文中,利用新多晶型物发现过程中专利公布的数据,建立了罗替戈汀两种已知固态形式的压力-温度相图。分析清楚地表明,晶型II是稳定的固相,而晶型I在整个压力-温度范围内是亚稳的:相对于晶型II,晶型I总体上是单向转变的。因此,欧洲药品管理局要求重新配方是一个明智的决定,因为第一种配方即使结晶似乎非常缓慢,也是亚稳的。

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