Shepard Kimberly B, Pluntze Amanda M, Vodak David T
Small Molecules R&D, Lonza Group AG, Bend, OR 97703, USA.
Pharmaceutics. 2022 May 26;14(6):1130. doi: 10.3390/pharmaceutics14061130.
Spray drying is a particle engineering technique used to manufacture respirable pharmaceutical powders that are suitable for delivery to the deep lung. It is amenable to processing both small molecules and biologic actives, including proteins. In this work, a simultaneous spray-drying process, termed simul-spray, is described; the process involves two different active pharmaceutical ingredient (API) solutions that are simultaneously atomized through separate nozzles into a single-spray dryer. Collected by a single cyclone, simul-spray produces a uniform mixture of two different active particles in a single-unit operation. While combination therapies for dry powder inhalers containing milled small molecule API are commercially approved, limited options exist for preparing combination treatments that contain both small molecule APIs and biotherapeutic molecules. Simul-spray drying is also ideal for actives which cannot withstand a milling-based particle engineering process, or which require a high dose that is incompatible with a carrier-based formulation. Three combination case studies are demonstrated here, in which bevacizumab is paired with erlotinib, cisplatin, or paclitaxel in a dry powder inhaler formulation. These model systems were chosen for their potential relevance to the local treatment of lung cancer. The resulting formulations preserved the biologic activity of the antibody, achieved target drug concentration, and had aerosol properties suitable for pulmonary delivery.
喷雾干燥是一种颗粒工程技术,用于制造适合递送至肺深部的可吸入药物粉末。它适用于处理小分子和生物活性物质,包括蛋白质。在这项工作中,描述了一种同时喷雾干燥工艺,称为同步喷雾;该工艺涉及两种不同的活性药物成分(API)溶液,它们通过单独的喷嘴同时雾化进入单个喷雾干燥器。通过单个旋风分离器收集,同步喷雾在单个单元操作中产生两种不同活性颗粒的均匀混合物。虽然含有研磨小分子API的干粉吸入器的联合疗法已获得商业批准,但制备同时包含小分子API和生物治疗分子的联合治疗方法的选择有限。同步喷雾干燥对于无法承受基于研磨的颗粒工程工艺的活性物质,或需要高剂量且与基于载体的制剂不相容的活性物质也非常理想。这里展示了三个联合案例研究,其中贝伐单抗在干粉吸入器制剂中与厄洛替尼、顺铂或紫杉醇配对。选择这些模型系统是因为它们与肺癌的局部治疗可能相关。所得制剂保留了抗体的生物活性,达到了目标药物浓度,并具有适合肺部递送的气溶胶特性。