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比较和对比表面活性剂(泊洛沙姆 F-127 和吐温 80)和糖(β-环糊精和菊粉)对喷雾干燥和结晶溶菌酶性质的影响。

Compare and contrast the effects of surfactants (PluronicF-127 and CremophorEL) and sugars (β-cyclodextrin and inulin) on properties of spray dried and crystallised lysozyme.

机构信息

University of Sunderland, Department of Pharmacy, Health and Well-being, Sunderland SR1 3SD, UK.

出版信息

Eur J Pharm Sci. 2013 Jul 16;49(4):519-34. doi: 10.1016/j.ejps.2013.05.004. Epub 2013 May 25.

Abstract

The stabilisation of proteins using different excipients in dried forms for possible therapeutic use is extensively studied. However, the effects of excipients on proteins in crystallised forms are sparsely documented. Therefore, the influences of PluronicF-127 and CremophorEL (as surfactants) and β-cyclodextrin and inulin (as sugars) on stability and biological activity of lysozyme, a model protein, in spray dried and crystallised forms were investigated. Spray dried and crystallised lysozyme were prepared in absence and presence of the mentioned excipients in a concentration of 0.05% w/v. The protein formulations were characterised in both solution state (using biological assay, particle size analysis and protein concentration determination) and solid state (employing yield determination, scanning electron microscopic (SEM) examination, Fourier transform infrared (FT-IR) spectroscopy for secondary structure analysis and Differential Scanning Calorimetry (DSC) for thermal study). Also, protein samples were assayed for their biological activities after exposing to storage stability study for 20 weeks in solid states at 24 °C/76% relative humidity (RH) and in aqueous states at 24 °C. The results showed that lysozyme crystals with CremophorEL, PluronicF-127, β-cyclodextrin and inulin maintained protein thermal stability (as indicated by DSC) to greater extent compared with spray dried protein formulations. Also, PluronicF-127 was competent to recover 100% lysozyme from crystallisation protein solutions (as confirmed by yield determination); this surfactant was able to prevent aggregate formation within spray dried lysozyme (as demonstrated by particle size analysis). The presence of PluronicF-127, β-cyclodextrin and inulin preserved the protein biological activity in freshly prepared spray dried and crystallised samples. PluronicF-127 was competent to protect lysozyme in both spray dried and crystallised forms after storage. PluronicF-127 has proved to be a promising protectant of proteins. The improved stability of the spray dried and crystallised protein containing PluronicF-127 shows promise for delivery of proteins via inhalation (in a spray dried form which has particle size range suitable for inhalation as revealed by particle size analysis and SEM) and injectable routes (in spray dried and crystallised forms). The way excipients react with proteins is different in the case of spray drying and crystallisation techniques, hence the choice of the additives and the processing techniques play a great role in controlling protein properties, activity and stability as shown in this study.

摘要

使用不同辅料将蛋白质制成干粉形式用于可能的治疗用途的稳定性已得到广泛研究。然而,辅料对结晶形式蛋白质的影响却鲜有记录。因此,本研究考察了 PluronicF-127 和 CremophorEL(表面活性剂)以及β-环糊精和菊糖(糖类)对喷雾干燥和结晶形式溶菌酶(模型蛋白)的稳定性和生物活性的影响。在不存在和存在上述辅料的情况下,以 0.05%w/v 的浓度制备喷雾干燥和结晶溶菌酶。通过生物测定、粒度分析和蛋白质浓度测定对蛋白质制剂在溶液状态下进行了表征,并通过产率测定、扫描电子显微镜(SEM)检查、傅里叶变换红外(FT-IR)光谱用于二级结构分析和差示扫描量热法(DSC)用于热研究,对固体状态下进行了表征。此外,在 24°C/76%相对湿度(RH)下的固态和 24°C 下的水溶液中,对暴露于 20 周储存稳定性研究后的蛋白质样品进行了生物活性测定。结果表明,与喷雾干燥蛋白制剂相比,含有 CremophorEL、PluronicF-127、β-环糊精和菊糖的溶菌酶晶体在更大程度上保持了蛋白质的热稳定性(如 DSC 所示)。此外,PluronicF-127 能够从结晶蛋白溶液中回收 100%的溶菌酶(如产率测定所证实);这种表面活性剂能够防止喷雾干燥溶菌酶内的聚集形成(如粒度分析所示)。PluronicF-127、β-环糊精和菊糖的存在在新制备的喷雾干燥和结晶样品中保持了蛋白质的生物活性。PluronicF-127 能够在储存后保护喷雾干燥和结晶形式的溶菌酶。PluronicF-127 已被证明是蛋白质的一种有前途的保护剂。含有 PluronicF-127 的喷雾干燥和结晶蛋白的稳定性提高,有望通过吸入(如粒度分析和 SEM 所示,喷雾干燥形式的粒径范围适合吸入)和注射途径(喷雾干燥和结晶形式)递送蛋白质。在喷雾干燥和结晶技术中,辅料与蛋白质的反应方式不同,因此添加剂的选择和加工技术在控制蛋白质的性质、活性和稳定性方面起着重要作用,正如本研究所示。

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