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研究不同冷却速率对无定形吲哚美辛稳定性的影响。

Investigations on the effect of different cooling rates on the stability of amorphous indomethacin.

机构信息

School of Pharmacy, University of Otago, 18 Frederick Street, Dunedin 9054, New Zealand.

出版信息

Eur J Pharm Sci. 2011 Oct 9;44(3):341-50. doi: 10.1016/j.ejps.2011.08.010. Epub 2011 Aug 23.

Abstract

Amorphous forms of indomethacin have previously been prepared using various preparation techniques and it could be demonstrated that the way the material was prepared influenced the physicochemical properties of the amorphous form of the drug. The aim of this study was to use one preparation technique (transformation via the melt) to prepare amorphous indomethacin and to investigate the influence of the cooling rate (as a processing parameter) on the physical stability of the resulting amorphous form. The amorphous materials obtained were analysed for their structural characteristics using Raman spectroscopy in combination with multivariate data analysis. The onset of crystallisation was determined as an indicator of the physical stability of the materials using differential scanning calorimetry (DSC) and polarising light microscopy. The Johnson-Mehl-Avrami (JMA) model and Sestak-Berggren (SB) model were used in this study to describe the non-isothermal crystallisation behaviour. All differently cooled samples were completely X-ray amorphous. Principal component analysis of the Raman spectra of the various amorphous forms revealed that the samples clustered in the scores plot according to the cooling rate, suggesting structural differences between the differently cooled samples. The minimum cooling rate required to obtain amorphous indomethacin was 1.2 K min(-1), as assessed from the time-temperature-transformation (TTT) diagram. The physical stability of the samples was found to increase as a function of cooling rate in the order of 30 K min(-1) > 20 K min(-1) > 10 K min(-1) > 5 K min(-1) > 3 K min(-1) ≈ 1.2 K min(-1) and was in agreement with calculated descriptors for the glass forming ability (GFA), including the reduced glass transition temperature (T(rg)) and the reduced temperature (T(red)). The JMA model could not be applied to describe the crystallisation process for the differently cooled melts of indomethacin in this study. The kinetic exponent M from the autocatalytic SB model however, showed a positive correlation with glass stability.

摘要

先前已经使用各种制备技术制备了吲哚美辛的无定形形式,可以证明材料的制备方式影响了药物无定形形式的物理化学性质。本研究的目的是使用一种制备技术(通过熔融转化)来制备无定形吲哚美辛,并研究冷却速率(作为加工参数)对所得无定形形式物理稳定性的影响。使用拉曼光谱结合多元数据分析来分析获得的无定形材料的结构特征。使用差示扫描量热法(DSC)和偏光显微镜作为起始结晶的指标来确定材料的物理稳定性。本研究中使用 Johnson-Mehl-Avrami (JMA) 模型和 Sestak-Berggren (SB) 模型来描述非等温结晶行为。所有不同冷却的样品均完全为 X 射线非晶态。各种无定形形式的拉曼光谱的主成分分析表明,根据冷却速率,样品在得分图中聚类,表明不同冷却的样品之间存在结构差异。从时间-温度-转变(TTT)图评估,获得无定形吲哚美辛所需的最小冷却速率为 1.2 K min(-1)。发现样品的物理稳定性随冷却速率的增加而增加,顺序为 30 K min(-1) > 20 K min(-1) > 10 K min(-1) > 5 K min(-1) > 3 K min(-1) ≈ 1.2 K min(-1),与玻璃形成能力(GFA)的计算描述符一致,包括降低的玻璃化转变温度(T(rg)) 和降低的温度(T(red))。在本研究中,JMA 模型不能用于描述不同冷却的吲哚美辛熔体的结晶过程。然而,自催化 SB 模型的动力学指数 M 与玻璃稳定性呈正相关。

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