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复杂冷冻干燥制剂动力学特性研究 II:基于玻璃化动力学分析密度变化及其与整体流动性、快速动力学和正电子湮没寿命谱(PALS)的比较。

Characterization of dynamics in complex lyophilized formulations: II. Analysis of density variations in terms of glass dynamics and comparisons with global mobility, fast dynamics, and Positron Annihilation Lifetime Spectroscopy (PALS).

机构信息

Department of Pharmaceutical Science, University of Connecticut, Storrs, CT, USA.

出版信息

Eur J Pharm Biopharm. 2013 Oct;85(2):197-206. doi: 10.1016/j.ejpb.2013.03.036. Epub 2013 Apr 25.

Abstract

Amorphous HES/disaccharide (trehalose or sucrose) formulations, with and without added polyols (glycerol and sorbitol) and disaccharide formulations of human growth hormone (hGH), were prepared by freeze drying and characterized with particular interest in methodology for using high precision density measurements to evaluate free volume changes and a focus on comparisons between "free volume" changes obtained from analysis of density data, fast dynamics (local mobility), and PALS characterization of "free volume" hole size. Density measurements were performed using a helium gas pycnometer, and fast dynamics was characterized using incoherent neutron scattering spectrometer. Addition of sucrose and trehalose to hGH decreases free volume in the system with sucrose marginally more effective than trehalose, consistent with superior pharmaceutical stability of sucrose hGH formulations well below Tg relative to trehalose. We find that density data may be analyzed in terms of free volume changes by evaluation of volume changes on mixing and calculation of apparent specific volumes from the densities. Addition of sucrose to HES decreases free volume, but the effect of trehalose is not detectable above experimental error. Addition of sorbitol or glycerol to HES/trehalose base formulations appears to significantly decrease free volume, consistent with the positive impact of such additions on pharmaceutical stability (i.e., degradation) in the glassy state. Free volume changes, evaluated from density data, fast dynamics amplitude of local motion, and PALS hole size data generally are in qualitative agreement for the HES/disaccharide systems studied. All predict decreasing molecular mobility as disaccharides are added to HES. Global mobility as measured by enthalpy relaxation times, increases as disaccharides, particularly sucrose, are added to HES.

摘要

无定形 HES/二糖(海藻糖或蔗糖)制剂,添加或不添加多元醇(甘油和山梨糖醇)和人生长激素(hGH)的二糖制剂,通过冷冻干燥制备,并特别关注使用高精度密度测量来评估自由体积变化的方法,以及关注从密度数据分析、快速动力学(局部流动性)和 PALS 对“自由体积”孔尺寸的表征中获得的“自由体积”变化之间的比较。使用氦气比重瓶进行密度测量,使用非相干中子散射光谱仪对快速动力学进行表征。向 hGH 中添加蔗糖和海藻糖会降低体系中的自由体积,其中蔗糖的效果略优于海藻糖,这与蔗糖 hGH 制剂在低于 Tg 时相对于海藻糖具有更好的药物稳定性一致。我们发现,通过评估混合时的体积变化并从密度计算表观比容,可以根据自由体积变化分析密度数据。向 HES 添加蔗糖会降低自由体积,但在实验误差之上,海藻糖的影响无法检测到。向 HES/海藻糖基础制剂中添加山梨糖醇或甘油似乎会显著降低自由体积,这与这些添加剂对玻璃态药物稳定性(即降解)的积极影响一致。从密度数据、快速动力学局部运动幅度和 PALS 孔尺寸数据评估的自由体积变化通常与研究的 HES/二糖系统一致。所有这些都预测随着二糖的添加,分子流动性会降低。如通过焓弛豫时间测量的整体流动性随着二糖,特别是蔗糖,添加到 HES 中而增加。

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