玻璃表面活性剂实现超高浓度生物疗法

Carolyn K Jons, Alexander N Prossnitz, Noah Eckman, Changxin Dong, Eric Appel
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引用次数: 0

摘要

蛋白质疗法,如肽和抗体,已成为医疗保健的关键。尽管生物制药具有卓越的效力和特异性,但它们很容易发生聚集,通常需要低浓度的制剂以及冷藏和配送来保持稳定性。然而,治疗许多疾病都需要高剂量。为了达到这些剂量,大多数已获批准的蛋白质药物产品都需要静脉注射,这给患者和医疗系统带来了过重的负担。我们需要新的方法来配制高浓度蛋白质,以减轻皮下注射的负担,最好采用自动注射器的形式。为了应对这一挑战,我们报告了一种可皮下注射的生物治疗给药平台,该平台由悬浮在无溶剂液体载体中的喷雾干燥蛋白质微粒组成。这些微颗粒只含有活性生物药剂和一种高玻璃化温度的聚丙烯酰胺衍生共聚物赋形剂,与传统赋形剂相比具有几个主要优点,包括:(i) 通过喷雾干燥过程提高生物药剂的稳定性;(ii) 改善喷雾干燥颗粒的形态和特性,提高悬浮注射性。白蛋白和人类 IgG 的实验表明,该技术可实现超高浓度蛋白质制剂(超过 500 毫克/毫升),可通过标准针头以临床相关注射力进行注射。此外,小鼠实验表明,这些超高浓度制剂可减少所需的注射量,而不会改变药代动力学。这种方法可将适合皮下注射的商业蛋白质药物数量增加一倍,极大地减轻了负担,并改善了获得这些关键生物制药的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glassy Surfactants Enable Ultra-High Concentration Biologic Therapeutics
Protein therapeutics, like peptides and antibodies, have become critical to healthcare. Despite their exceptional potency and specificity, biopharmaceuticals are prone to aggregation, often necessitating low formulation concentrations as well as cold storage and distribution to maintain stability. Yet, high doses are required to treat many diseases. To achieve these doses, most approved protein drug products are administered intravenously, imposing excessive burdens on patients and the healthcare system. New approaches are needed to formulate proteins at high concentrations to enable less burdensome subcutaneous injection, preferably in an autoinjector format. To address this challenge, we report a subcutaneously injectable biotherapeutic delivery platform composed of spray-dried protein microparticles suspended in a non-solvent liquid carrier. These microparticles contain only active biopharmaceutical agent and a high glass transition temperature polyacrylamide-derived copolymer excipient affording several key benefits over traditional excipients, including: (i) improved stabilization of biopharmaceuticals through the spray drying process, and (ii) improved morphology and properties of the spray-dried particles, enhancing suspension injectability. Experiments with albumin and human IgG demonstrate that this technology enables ultra-high-concentration protein formulations (exceeding 500 mg/mL) that are injectable through standard needles with clinically relevant injection forces. Additionally, experiments in mice show these ultra-high-concentration formulations reduce required injection volumes without altering pharmacokinetics. This approach could double the number of commercial protein drugs amenable to subcutaneous administration, dramatically reducing burden and improving access to these critical biopharmaceuticals.
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