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Development of a stable low-dose aglycosylated antibody formulation to minimize protein loss during intravenous administration

机译：稳定的低剂量糖糖化抗体制剂的研制，以最小化静脉内给药过程中的蛋白质损失

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Sorina Morar-Mitrica; Manasi Puri; Alexandra Beumer Sassi; Joshua Fuller; Ping Hu; George Crotts; Douglas Nesta;
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年度 2015
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1. Optimizing flecainide plasma concentration profile for atrial fibrillation conversion while minimizing adverse ventricular effects by rapid, low-dose intratracheal or intravenous administration [J] . Marum Alexandre A., Silva Bruna A., Bortolotto Alexandre L., International Journal of Cardiology . 2019,第期

机译：优化絮凝剂血浆浓度曲线，用于心房颤动转化，同时通过快速，低剂量腹腔内或静脉内给药最小化不良室外效应
2. Three insulation methods to minimize intravenous fluid administration set heat loss. [J] . Richardt Piek, Christopher Stein Prehospital emergency care . 2013,第1期

机译：三种绝缘方法可最大程度地减少静脉输液，从而增加热量散失。
3. Three insulation methods to minimize intravenous fluid administration set heat loss. [J] . Richardt Piek, Christopher Stein Prehospital emergency care . 2013,第1期

机译：三种绝缘方法，以最小化静脉内流体给药设定热量损失。
4. Preparation of an Emulsion Formulation of Clopidogrel for Intravenous Administration [C] . Rajeev A Jain, Olinda Carneiro, Namrata Pandit, Controlled Release Society Annual Meeting and Exposition . 2007

机译：氯吡格雷静脉给药乳剂的制备
5. Understanding physical and chemical stability of proteins in solution: Relevance to therapeutic protein and monoclonal antibody formulations [D] . Thirumangalathu, Renuka 2007

机译：了解溶液中蛋白质的物理和化学稳定性：与治疗性蛋白质和单克隆抗体制剂的相关性
6. Development of a stable low-dose aglycosylated antibody formulation to minimize protein loss during intravenous administration [O] . Sorina Morar-Mitrica, Manasi Puri, Alexandra Beumer Sassi, 2015

机译：开发稳定的低剂量无糖基化抗体制剂以最大程度减少静脉内给药过程中的蛋白质损失
7. Site-Specific Glycosylation of an Aglycosylated Human IgG1-Fc Antibody Protein Generates Neoglycoproteins with Enhanced Function [O] . Watt Gregory M., Lund John, Levens Michaela, 2003

机译：糖基化的人IgG1-Fc抗体蛋白的位点特异性糖基化产生功能增强的新糖蛋白

Development of a stable low-dose aglycosylated antibody formulation to minimize protein loss during intravenous administration

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