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通过薄膜冷冻干燥法制备的抗SARS-CoV-2病毒单克隆抗体的可吸入干粉。

Inhalable dry powders of a monoclonal antibody against SARS-CoV-2 virus made by thin-film freeze-drying.

作者信息

Xu Haiyue, Sahakijpijarn Sawittree, Moon Chaeho, Emig Christopher J, Mena Marco, Henry Steven J, Vitug Adela, Ventura Christian John, Kuehl Philip J, Revelli David, Owens Donald E, Christensen Dale J, Williams Robert O, Cui Zhengrong

机构信息

The University of Texas at Austin, College of Pharmacy, Division of Molecular Pharmaceutics and Drug Delivery, Austin, TX, 78712, United States.

TFF Pharmaceuticals, Inc., Austin, TX, 78746, United States.

出版信息

Int J Pharm. 2024 Sep 5;662:124511. doi: 10.1016/j.ijpharm.2024.124511. Epub 2024 Jul 25.

Abstract

Monoclonal antibodies (mAbs) represent a promising modality for the prevention and treatment of viral infections. For infections that initiate from the respiratory tract, direct administration of specific neutralizing mAbs into lungs has advantages over systemic injection of the same mAbs. Herein, using AUG-3387, a human-derived mAb with high affinity to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its various variants, as a model mAb, we formulated the mAb into dry powders by thin-film freeze-drying, confirmed that the AUG-3387 mAb reconstituted from the dry powders retained their integrity, high affinity to the SARS-CoV-2 spike protein receptor binding domain (RBD), as well as ability to neutralize RBD-expressing pseudoviruses. Finally, we showed that one of the AUG-3387 mAb dry powders had desirable aerosol properties for pulmonary delivery into the lung. We concluded that thin-film freeze-drying represents a viable method to prepare inhalable powders of virus-neutralizing mAbs for pulmonary delivery into the lung.

摘要

单克隆抗体(mAbs)是预防和治疗病毒感染的一种有前景的方式。对于从呼吸道开始的感染,将特异性中和单克隆抗体直接注入肺部比全身注射相同的单克隆抗体具有优势。在此,我们使用AUG - 3387(一种对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)及其各种变体具有高亲和力的人源单克隆抗体)作为模型单克隆抗体,通过薄膜冷冻干燥将其制成干粉,证实从干粉中重构的AUG - 3387单克隆抗体保持了其完整性、对SARS-CoV-2刺突蛋白受体结合域(RBD)的高亲和力以及中和表达RBD的假病毒的能力。最后,我们表明AUG - 3387单克隆抗体干粉之一具有理想的气溶胶特性,可用于肺部给药。我们得出结论,薄膜冷冻干燥是制备可吸入的病毒中和单克隆抗体制剂用于肺部给药的一种可行方法。

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