用于直肠生物递送的3D打印英夫利昔单抗栓剂

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Atheer Awad , Alvaro Goyanes , Mine Orlu , Simon Gaisford , Abdul W. Basit
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引用次数: 5

摘要

英夫利昔单抗是一种单克隆抗体,在慢性炎症性肠病(IBD)的管理和治疗中发挥着重要作用。由于其大分子结构,其通过口服途径的递送具有挑战性,限制了其只能通过胃肠外途径给药。直肠途径为英夫利昔单抗的给药提供了一种替代方法,使其能够定位在疾病部位,绕过其穿过消化道的通道,从而保持其完整性和生物活性。三维(3D)打印是一种先进的生产技术,可以通过数字设计创建剂量灵活的药物产品。目前的研究评估了利用半固态挤压3D打印制造用于局部治疗IBD的英夫利昔单抗栓剂的可行性。研究了由Gelucire®(48/16或44/14)与椰子油和/或纯化水混合组成的各种印刷油墨。研究表明,在水中重建后,英夫利昔单抗溶液可以直接掺入Gelucire®48/16的印刷油墨中,并且可以承受挤压过程,从而产生明确的栓剂。由于水含量和温度对于保护英夫利昔单抗的效力至关重要,因此通过测量其结合能力(即主动结合其抗原以发挥作用的英夫利单抗的量)来评估改变印刷油墨的组成和印刷参数对英夫利利昔单抗生物效率的影响。尽管载药分析显示英夫利昔单抗在印刷后保持完整,但发现在分离中掺入水仅导致约65%的结合能力。然而,当将油添加到混合物中时,英夫利昔单抗的结合能力可提高至~85%。这些有希望的结果表明,3D打印有潜力作为一种新的平台来制造含有生物药物的剂型,避免患者对注射剂的依从性问题,并解决他们未满足的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
3D printed infliximab suppositories for rectal biologic delivery

Infliximab is a monoclonal antibody that plays an important role in the management and treatment of chronic inflammatory bowel diseases (IBD). Due to its macromolecular structure, its delivery through the oral route is challenging, limiting its administration to only via the parenteral route. The rectal route offers an alternative way for administering infliximab, allowing it to be localised at the disease site and circumventing its passage across the alimentary canal and thus, maintaining its integrity and bioactivity. Three-dimensional (3D) printing is an advanced production technology that permits the creation of dose-flexible drug products from digital designs. The current study assessed the feasibility of utilising semi-solid extrusion 3D printing for the fabrication of infliximab-loaded suppositories for the local treatment of IBD. Various printing inks composed of Gelucire® (48/16 or 44/14) mixed with coconut oil and/or purified water were investigated. It was shown that following reconstitution in water, the infliximab solution can be directly incorporated into the printing ink of Gelucire® 48/16 and can withstand the extrusion process, resulting in well-defined suppositories. Since water content and temperature are critical for safeguarding infliximab's potency, the effect of changing the composition of the printing inks and printing parameters on infliximab's biologic efficiency was evaluated by measuring its binding capacity (i.e., the amount of infliximab that actively binds to its antigen to exert an effect). Despite drug loading assays showing that infliximab remains intact following printing, it was found that the incorporation of water in isolation results in only ∼65% binding capacity. However, when oil is added to the mixture, infliximab's binding capacity increases up to ∼85%. These promising results demonstrate that 3D printing has the potential to be exploited as a novel platform for fabricating dosage forms containing biopharmaceuticals, avoiding patients' compliance issues observed with injectables and addressing their unmet needs.

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来源期刊
International Journal of Pharmaceutics: X
International Journal of Pharmaceutics: X Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.60
自引率
0.00%
发文量
32
审稿时长
24 days
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