Scale-up of a low-temperature spray-drying process for a tuberculosis vaccine candidate using lab-scale equipment

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2025-04-15 Epub Date: 2025-03-10 DOI:10.1016/j.ijpharm.2025.125456
Maximilian Aisenstat , Joseph McCollum , Mani Ordoubadi , Hui Wang , Zahra Minootan , Alana Gerhardt , Andrew R. Martin , Christopher B. Fox , Reinhard Vehring
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Abstract

Laboratory-scale spray drying can be a useful tool in developing new dry powder formulations for the delivery of biologics such as therapeutic proteins or vaccines. Low-temperature drying is often used in these processes to prevent the exposure of biologics to harsh conditions that could potentially lead to degradation or instability of the final product. However, low-temperature drying on small-scale equipment can result in very low production rates that may not be practical for generating sufficient material for studies requiring larger sample quantities, such as key preclinical or toxicology studies. This study demonstrates a scale-up effort for a spray dried adjuvanted protein tuberculosis (TB) vaccine candidate using a custom lab-scale spray dryer. To achieve higher throughput without compromising the stability of the powder and biologic material, a process model for the spray dryer was used to determine optimal processing parameters and establish general vaccine powder manufacturing guidelines, such as minimizing exposure to high temperatures and relative humidity during drying. Maximizing dryer throughput and increasing overall feed concentration resulted in a tenfold increase in production rate using lab-scale equipment, such that 97.6 g of powder (the equivalent of about 5,000 human doses) could be produced using a lab-scale spray dryer in a single 6-hour spray drying run.

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使用实验室规模的设备对一种结核病候选疫苗的低温喷雾干燥工艺进行放大。
实验室规模的喷雾干燥可以成为开发用于递送生物制剂(如治疗性蛋白质或疫苗)的新干粉配方的有用工具。低温干燥通常用于这些工艺中,以防止生物制品暴露在可能导致最终产品降解或不稳定的恶劣条件下。然而,在小型设备上的低温干燥可能导致非常低的生产率,这可能不适合为需要大量样品的研究生产足够的材料,例如关键的临床前或毒理学研究。本研究展示了使用定制的实验室规模喷雾干燥机喷雾干燥佐剂蛋白结核(TB)候选疫苗的规模扩大努力。为了在不影响粉末和生物材料稳定性的情况下实现更高的吞吐量,使用喷雾干燥机的过程模型来确定最佳加工参数并建立一般疫苗粉末生产指南,例如在干燥过程中尽量减少暴露在高温和相对湿度下。最大限度地提高烘干机吞吐量和提高总体饲料浓度导致使用实验室规模设备的生产率提高了十倍,因此,使用实验室规模的喷雾烘干机在单个6小时的喷雾干燥运行中可以生产97.6 g粉末(相当于约5,000人剂量)。
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来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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