Department of Pharmaceutics and Biopharmaceutics, Johannes Gutenberg University Mainz, D-55099, Mainz, Germany.
BioNTech RNA Pharmaceuticals GmbH, D-55131, Mainz, Germany.
Biomaterials. 2019 Feb;192:612-620. doi: 10.1016/j.biomaterials.2018.10.020. Epub 2018 Nov 17.
mRNA pharmaceuticals represent a new class of therapeutics, with applications, in cancer vaccination, tumour therapy and protein substitution. Formulations are required to deliver messenger RNA (mRNA) to the target sites where induction of genetic transfection following receptor mediated cell uptake & translation is required. In the current study, the cationic polysaccharide diethylaminoethylen (DEAE) - Dextran was selected as a model system carrier for the investigation of polyplex nanoparticle formation together with mRNA as a function of the molar ratio of the components. The structure of the mRNA/Dextran colloids was investigated as a function of the polymer-to-mRNA ratio and correlated with the biological activity determined by cellular transfection with luciferase coding mRNA. Dynamic light scattering (DLS), small angle x-ray scattering (SAXS), and small angle neutron scattering (SANS) with deuterium contrast variation were used to achieve structural insight into the systems. Similarly to previously investigated lipid based systems, colloidally stable particles with confined size were obtained with either excess of positive or negative charge. Highest activity was obtained with positive charge excess. From the scattering experiments information on the internal organization inside the polymer/mRNA systems was derived. Indication for the presence of structural elements in the length scale of ten to 20 nm were found in the excess of dextran, which could be due to either excess or particulate polymer. Information on the molecular organization of the mRNA nanoparticle products may provide a valuable basis for defining critical quality attributes of drug products for pharmaceutical application.
mRNA 药物代表了一类新的治疗药物,可应用于癌症疫苗、肿瘤治疗和蛋白质替代。需要制剂将信使 RNA(mRNA)递送至靶位,在那里需要通过受体介导的细胞摄取和翻译来诱导基因转染。在当前的研究中,选择阳离子多糖二乙氨基乙基(DEAE)-葡聚糖作为模型系统载体,用于研究多聚物纳米颗粒的形成以及作为组分摩尔比函数的 mRNA。研究了 mRNA/葡聚糖胶体的结构作为聚合物与 mRNA 比的函数,并与用编码荧光素酶的 mRNA 进行细胞转染确定的生物活性相关联。动态光散射(DLS)、小角 X 射线散射(SAXS)和小角中子散射(SANS)与氘对比度变化一起用于深入了解系统的结构。与之前研究的脂质基系统类似,用过量的正电荷或负电荷获得了胶体稳定的受限尺寸颗粒。带正电荷过量时获得最高的活性。从散射实验中,获得了关于聚合物/mRNA 系统内部组织的信息。在葡聚糖过量的情况下,发现了在十到二十纳米长度尺度上存在结构元素的迹象,这可能是由于聚合物过量或颗粒状聚合物的存在。有关 mRNA 纳米颗粒产品的分子组织的信息可能为确定用于药物应用的药物产品的关键质量属性提供有价值的基础。