I3S, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Portugal; INEB - Instituto de Engenharia Biomédica, Universidade do Porto, Rua Alfredo Allen, 208, 4200-135 Porto, Portugal; CESPU, Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da Saúde, Rua Central de Gandra 1317, 4585-116 Gandra, Portugal; ICBAS - Instituto Ciências Biomédicas Abel Salazar, Universidade do Porto, Rua de Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal; INL - International Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, 4715-330 Braga, Portugal.
INL - International Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga, 4715-330 Braga, Portugal.
Acta Biomater. 2018 Sep 15;78:285-295. doi: 10.1016/j.actbio.2018.07.040. Epub 2018 Jul 21.
Bevacizumab is one of the most common monoclonal antibodies used to treat cancer due to its antiangiogenic role. However, the frequent parenteral administrations are not attractive for the patient adhesion to the therapy. Nanoencapsulation of bevacizumab might be a useful alternative to increase administration intervals, due to controlled release properties. To achieve a long-term bevacizumab stability into PLGA nanoparticles, we developed an optimized and validated lyophilization protocol. The co-encapsulation of trehalose and bevacizumab into PLGA nanoparticles, associated to their lyophilization with external 10% (w/v) of trehalose, allowed maintenance of the physical-chemical characteristics of nanoparticles and bevacizumab secondary and tertiary structure. More relevant, the antiangiogenic activity of bevacizumab was kept over 6 months of storage while formulated with this protocol. No significant differences were found upon 6 months of storage at 4 °C and 25 °C/60% HR, and minor differences were observed for storage at 40 °C/75% HR, bringing to our knowledge, the first successfully report for monoclonal antibody storage at room temperature, without losing its structural and functional features. Our results served as starting point to understand the monoclonal antibody-based nanoparticle behavior over time, creating an innovative approach for a long-term monoclonal antibody stability.
Nanoencapsulation of monoclonal antibodies has boost the interest of researchers as an alternative to the current antibody-based therapy, changing the route of administrations through controlled release of monoclonal antibodies. Despite good results have been achieved with nanoencapsulation process, no strategy has still found concerning a long-term stability of nanoparticles and monoclonal antibodies. In this study, the aim was to find out a validated and optimized method that allows a long-term stability of nanoparticles and antibodies. Over 6 months of storage, an optimized nanosystem was considered stable for both nanoparticles and antibody structure, at 4 °C and 25 °C, resulting the first successfully report for monoclonal antibody storage at room temperature.
贝伐珠单抗因其抗血管生成作用而成为最常用于治疗癌症的单克隆抗体之一。然而,频繁的肠胃外给药方式对患者对治疗的依从性并没有吸引力。由于具有控制释放的特性,将贝伐珠单抗纳米囊化可能是增加给药间隔的一种有用方法。为了实现 PLGA 纳米粒中长期稳定的贝伐珠单抗,我们开发了一种优化和验证的冷冻干燥方案。海藻糖和贝伐珠单抗共包封到 PLGA 纳米粒中,并与外部 10%(w/v)海藻糖一起进行冷冻干燥,保持了纳米粒和贝伐珠单抗二级和三级结构的物理化学特性。更重要的是,通过该方案配制后,贝伐珠单抗的抗血管生成活性可保持 6 个月以上。在 4°C 和 25°C/60%相对湿度下储存 6 个月没有发现明显差异,在 40°C/75%相对湿度下储存时观察到较小差异,这是我们首次成功报道单克隆抗体在室温下储存而不失去其结构和功能特性。我们的结果为了解基于单克隆抗体的纳米粒随时间的行为提供了起点,为单克隆抗体的长期稳定性创造了一种创新方法。
单克隆抗体的纳米囊化作为当前抗体治疗的替代方法,增加了研究人员的兴趣,通过控制单克隆抗体的释放改变了给药途径。尽管纳米囊化过程取得了良好的效果,但仍没有找到一种策略可以长期稳定纳米粒和单克隆抗体。在这项研究中,我们的目标是找到一种经过验证和优化的方法,可以实现纳米粒和抗体的长期稳定性。在 6 个月的储存期内,该优化的纳米系统被认为在 4°C 和 25°C 时对纳米粒和抗体结构都是稳定的,这是首次成功报道单克隆抗体在室温下储存。