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克服基于脂质赋形剂的稳定性挑战的新方法。第 2 部分:脂肪酸聚甘油酯作为热熔包衣赋形剂的应用。

Novel approach for overcoming the stability challenges of lipid-based excipients. Part 2: Application of polyglycerol esters of fatty acids as hot melt coating excipients.

机构信息

Research Center for Pharmaceutical Engineering GmbH, Graz, Austria; Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology, University of Graz, Graz, Austria.

Research Center for Pharmaceutical Engineering GmbH, Graz, Austria; Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology, University of Graz, Graz, Austria.

出版信息

Eur J Pharm Biopharm. 2020 Mar;148:107-117. doi: 10.1016/j.ejpb.2020.01.009. Epub 2020 Jan 23.

Abstract

The application of hot melt coating (HMC) as an economic and solvent-free technology is restricted in pharmaceutical development, due to the instable solid-state of HMC excipients resulting in drug release instability. We have previously introduced polyglycerol esters of fatty acids (PGFAs) with stable solid-state (Part 1). In this work we showed a novel application of PGFAs as HMC excipients with stable performance. Three PGFA compounds with a HLB range of 5.1-6.2 were selected for developing immediate-release formulations. The HMC properties were investigated. The viscosity of molten lipids at 100 °C was suitable for atomizing. The DSC data showed the absence of low solidification fractions, thus reduced risk of agglomeration during the coating process. The driving force for crystallization of selected compounds was lower and the heat flow exotherms were broader compared to conventional HMC formulations, indicating a lower energy barrier for nucleation and lower crystallization rate. Lower spray rates and a process temperature close to solidification temperature were desired to provide homogeneous coating. DSC and X-ray diffraction data revealed stable solid state during 6 months storage at 40 °C. API release was directly proportional to HLB and indirectly proportional to crystalline network density and was stable during investigated 3 months. Cytotoxicity was assessed by dehydrogenase activity and no in vitro cytotoxic effect was observed.

摘要

热熔包衣(HMC)作为一种经济且无溶剂的技术,由于 HMC 赋形剂的不稳定性固态导致药物释放不稳定,因此在药物开发中的应用受到限制。我们之前介绍了具有稳定固态的脂肪酸聚甘油酯(PGFA)(第 1 部分)。在这项工作中,我们展示了 PGFAs 作为具有稳定性能的 HMC 赋形剂的新应用。选择了 HLB 范围为 5.1-6.2 的三种 PGFA 化合物来开发即释制剂。研究了 HMC 的性能。在 100°C 下熔融脂质的粘度适合雾化。DSC 数据表明不存在低凝固分数,从而降低了包衣过程中团聚的风险。与常规 HMC 制剂相比,所选化合物的结晶驱动力较低,热流放热较宽,表明成核的能量障碍较低,结晶速率较低。为了提供均匀的涂层,需要较低的喷雾速率和接近固化温度的工艺温度。DSC 和 X 射线衍射数据表明,在 40°C 下储存 6 个月时具有稳定的固态。API 释放与 HLB 直接成正比,与结晶网络密度间接成反比,在研究的 3 个月内稳定。通过脱氢酶活性评估细胞毒性,未观察到体外细胞毒性作用。

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