Ana M. López-Estévez, Y. Zhang, María Medel, Iker Arriaga, Lucía Sanjurjo, Cristian Huck-Iriart, Nicola G. A. Abrescia, María J. Vicent, Defang Ouyang, Dolores Torres, María José Alonso
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引用次数: 0
Abstract
The current spotlight of cancer therapeutics is shifting towards personalized medicine with the widespread use of monoclonal antibodies (mAbs). Despite their increasing potential, mAbs have an intrinsic limitation related to their inability to cross cell membranes and reach intracellular targets. Nanotechnology offers promising solutions to overcome this limitation, however, formulation challenges remain. These challenges are the limited loading capacity (often insufficient to achieve clinical dosing), the complex formulation methods, and the insufficient characterization of mAb-loaded nanocarriers. Here, we present a new nanocarrier consisting of hyaluronic acid-based nanoassemblies (HANAs) specifically designed to entrap mAbs with a high efficiency and an outstanding loading capacity (50%, w/w). HANAs composed by an mAb, modified HA and phosphatidylcholine (PC) resulted in sizes of ~ 100 nm and neutral surface charge. Computational modeling identified the principal factors governing the high affinity of mAbs with the amphiphilic HA and PC. HANAs composition and structural configuration were analyzed using the orthogonal techniques cryogenic transmission electron microscopy (cryo-TEM), asymmetrical flow field-flow fractionation (AF4), and small-angle X-ray scattering (SAXS). These techniques provided evidence of the formation of core-shell nanostructures comprising an aqueous core surrounded by a bilayer consisting of phospholipids and amphiphilic HA. In vitro experiments in cancer cell lines and macrophages confirmed HANAs’ low toxicity and ability to transport mAbs to the intracellular space. The reproducibility of this assembling process at industrial-scale batch sizes and the long-term stability was assessed. In conclusion, these results underscore the suitability of HANAs technology to load and deliver biologicals, which holds promise for future clinical translation.
随着单克隆抗体(mAbs)的广泛应用,目前癌症疗法的焦点正转向个性化医疗。尽管 mAbs 的潜力与日俱增,但它们有一个固有的局限性,即无法穿过细胞膜到达细胞内靶点。纳米技术为克服这一局限性提供了前景广阔的解决方案,但制剂方面的挑战依然存在。这些挑战包括有限的负载能力(通常不足以达到临床剂量)、复杂的配制方法以及对载入 mAb 的纳米载体表征不足。在此,我们介绍了一种新型纳米载体,它由透明质酸基纳米组合体(HANAs)组成,专门用于高效吸附 mAb,并具有出色的负载能力(50% w/w)。由 mAb、改性 HA 和磷脂酰胆碱 (PC) 组成的 HANAs 大小约为 100 纳米,表面电荷为中性。计算模型确定了 mAb 与两亲性 HA 和 PC 产生高亲和力的主要因素。利用低温透射电子显微镜(cryo-TEM)、非对称流场-流动分馏(AF4)和小角 X 射线散射(SAXS)等正交技术分析了 HANAs 的组成和结构构造。这些技术为核壳纳米结构的形成提供了证据,核壳纳米结构包括一个由磷脂和两亲性 HA 组成的双分子层所包围的水核。在癌细胞系和巨噬细胞中进行的体外实验证实了 HANAs 的低毒性和将 mAbs 运送到细胞内空间的能力。此外,还评估了这种组装工艺在工业化批量生产中的可重复性和长期稳定性。总之,这些结果强调了 HANAs 技术装载和输送生物制剂的适用性,为未来的临床转化带来了希望。
期刊介绍:
Nano Research is a peer-reviewed, international and interdisciplinary research journal that focuses on all aspects of nanoscience and nanotechnology. It solicits submissions in various topical areas, from basic aspects of nanoscale materials to practical applications. The journal publishes articles on synthesis, characterization, and manipulation of nanomaterials; nanoscale physics, electrical transport, and quantum physics; scanning probe microscopy and spectroscopy; nanofluidics; nanosensors; nanoelectronics and molecular electronics; nano-optics, nano-optoelectronics, and nano-photonics; nanomagnetics; nanobiotechnology and nanomedicine; and nanoscale modeling and simulations. Nano Research offers readers a combination of authoritative and comprehensive Reviews, original cutting-edge research in Communication and Full Paper formats. The journal also prioritizes rapid review to ensure prompt publication.