用玻璃状表面活性剂辅料喷雾干燥实现超高浓度生物治疗

IF 14.6 1区 医学 Q1 CELL BIOLOGY
Carolyn K. Jons, Alexander N. Prossnitz, Noah Eckman, Changxin Dong, Ashley Utz, Eric A. Appel
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引用次数: 0

摘要

多肽和抗体等生物制药已成为医疗保健的关键。尽管它们具有特殊的效力和特异性,但生物制药容易聚集,这可能限制功效。因此,这些疗法通常需要低浓度配方以及冷藏来保持稳定性;然而,治疗许多疾病需要高剂量。大多数批准的蛋白质药物都是静脉给药,给患者带来了过重的负担。需要新的方法来配制高浓度的蛋白质,以减少皮下注射的负担,最好是使用可直接由患者使用的自动注射器。为了解决这一挑战,我们报道了一种皮下注射蛋白质递送平台,该平台由悬浮在非溶剂液体载体中的喷雾干燥蛋白质微粒组成。这些微粒只含有生物药品和高玻璃化转变温度的聚丙烯酰胺衍生共聚物赋形剂,与传统赋形剂相比,它具有重要的优势。首先,该赋形剂通过喷雾干燥过程改善了生物药品的稳定性;其次,它改善了喷雾干燥颗粒的形态和性能,增强了悬浮液的可注射性。我们用白蛋白、人免疫球蛋白G和抗covid单克隆抗体(IDBiologics)证明,该技术可以实现超高浓度蛋白质配方(每毫升超过500毫克),通过标准针头注射,具有临床相关的注射力。此外,对两种临床相关抗体药物的实验表明,这些超高浓度制剂减少了所需的注射量,而不改变小鼠的药代动力学或功效。这种方法可以使适合皮下给药的商业蛋白质药物的数量增加近三倍,从而改善这些关键生物药物的获取途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrahigh-concentration biologic therapeutics enabled by spray drying with a glassy surfactant excipient
Biopharmaceuticals such as peptides and antibodies have become critical to health care. Despite their exceptional potency and specificity, biopharmaceuticals are prone to aggregation, which can limit efficacy. These therapies therefore often require low-concentration formulations as well as cold storage to maintain stability; however, high doses are required to treat many diseases. Most approved protein drug products are administered intravenously, imposing excessive burdens on patients. New approaches are needed to formulate proteins at high concentrations to enable less burdensome subcutaneous injection, preferably with an autoinjector that can be used directly by patients. To address this challenge, we report a subcutaneously injectable protein delivery platform composed of spray-dried protein microparticles suspended in a nonsolvent liquid carrier. These microparticles contain only biopharmaceuticals and a high–glass transition temperature polyacrylamide-derived copolymer excipient that affords key benefits over traditional excipients. First, the excipient improved stabilization of biopharmaceuticals through the spray-drying process, and second, it improved morphology and properties of the spray-dried particles, enhancing suspension injectability. We demonstrated with albumin, human immunoglobulin G, and an anti-COVID monoclonal antibody (IDBiologics) that this technology enables ultrahigh-concentration protein formulations (exceeding 500 milligrams per milliliter) that are injectable through standard needles with clinically relevant injection forces. In addition, experiments with two clinically relevant antibody drugs show that these ultrahigh-concentration formulations reduce required injection volumes without altering pharmacokinetics or efficacy in mice. This approach could nearly triple the number of commercial protein drugs amenable to subcutaneous administration, improving access to these critical biopharmaceuticals.
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来源期刊
Science Translational Medicine
Science Translational Medicine CELL BIOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
26.70
自引率
1.20%
发文量
309
审稿时长
1.7 months
期刊介绍: Science Translational Medicine is an online journal that focuses on publishing research at the intersection of science, engineering, and medicine. The goal of the journal is to promote human health by providing a platform for researchers from various disciplines to communicate their latest advancements in biomedical, translational, and clinical research. The journal aims to address the slow translation of scientific knowledge into effective treatments and health measures. It publishes articles that fill the knowledge gaps between preclinical research and medical applications, with a focus on accelerating the translation of knowledge into new ways of preventing, diagnosing, and treating human diseases. The scope of Science Translational Medicine includes various areas such as cardiovascular disease, immunology/vaccines, metabolism/diabetes/obesity, neuroscience/neurology/psychiatry, cancer, infectious diseases, policy, behavior, bioengineering, chemical genomics/drug discovery, imaging, applied physical sciences, medical nanotechnology, drug delivery, biomarkers, gene therapy/regenerative medicine, toxicology and pharmacokinetics, data mining, cell culture, animal and human studies, medical informatics, and other interdisciplinary approaches to medicine. The target audience of the journal includes researchers and management in academia, government, and the biotechnology and pharmaceutical industries. It is also relevant to physician scientists, regulators, policy makers, investors, business developers, and funding agencies.
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