用于皮下递送的单克隆抗体和蛋白质治疗制剂:高浓度,低容量vs低浓度,高容量。

IF 5.6 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
mAbs Pub Date : 2023-01-01 Epub Date: 2023-11-27 DOI:10.1080/19420862.2023.2285277
M Desai, A Kundu, M Hageman, H Lou, D Boisvert
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引用次数: 0

摘要

生物药物用于治疗各种癌症和慢性疾病。虽然大多数这些治疗都是由训练有素的医疗保健专业人员静脉注射,但皮下(SC)给药的明显趋势已经出现。生物制剂的SC管理提出了几个挑战。生物药物通常需要更高的剂量才能达到最佳效果,这超过了传统的皮下注射方法(如自体注射器)的低体积容量。因此,需要高浓度的活性成分,造成耗时的配方障碍。因此,需要传统SC输送系统的替代方案来支持更大容量的生物制剂,并减少与高浓度生物制剂相关的开发时间和其他风险。在这里,我们概述了SC生物药物制剂和递送的关键考虑因素,并探讨了一种范式转变:低至中等浓度的药物在大批量制剂中提供的灵活性,作为传统的高浓度、小批量SC制剂递送方法的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Monoclonal antibody and protein therapeutic formulations for subcutaneous delivery: high-concentration, low-volume vs. low-concentration, high-volume.

Biologic drugs are used to treat a variety of cancers and chronic diseases. While most of these treatments are administered intravenously by trained healthcare professionals, a noticeable trend has emerged favoring subcutaneous (SC) administration. SC administration of biologics poses several challenges. Biologic drugs often require higher doses for optimal efficacy, surpassing the low volume capacity of traditional SC delivery methods like autoinjectors. Consequently, high concentrations of active ingredients are needed, creating time-consuming formulation obstacles. Alternatives to traditional SC delivery systems are therefore needed to support higher-volume biologic formulations and to reduce development time and other risks associated with high-concentration biologic formulations. Here, we outline key considerations for SC biologic drug formulations and delivery and explore a paradigm shift: the flexibility afforded by low-to-moderate-concentration drugs in high-volume formulations as an alternative to the traditionally difficult approach of high-concentration, low-volume SC formulation delivery.

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来源期刊
mAbs
mAbs 工程技术-仪器仪表
CiteScore
10.70
自引率
11.30%
发文量
77
审稿时长
6-12 weeks
期刊介绍: mAbs is a multi-disciplinary journal dedicated to the art and science of antibody research and development. The journal has a strong scientific and medical focus, but also strives to serve a broader readership. The articles are thus of interest to scientists, clinical researchers, and physicians, as well as the wider mAb community, including our readers involved in technology transfer, legal issues, investment, strategic planning and the regulation of therapeutics.
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