Ariaudo Daniela, Cavalieri Francesca, Rinaldi Antonio, Aguilera Ana, Lopez Matilde, Perez Hilda Garay, Felipe Ariel, Del Carmen Dominguez Maria, Ruiz Odalys, Martinez Gillian, Venanzi Mariano
Department of Chemical Science and Technologies, University of Rome Tor Vergata, Via della Ricerca Scientifica 1, 00133 Rome, Italy.
PROMAS-MATPRO Laboratory, Sustainability Department, ENEA, 00123 Rome, Italy.
Nanomaterials (Basel). 2023 Oct 5;13(19):2709. doi: 10.3390/nano13192709.
The quest for biocompatible drug-delivery devices that could be able to open new administration routes is at the frontier of biomedical research. In this contribution, porous polysaccharide-based microsponges based on crosslinked alginate polymers were developed and characterized by optical spectroscopy and nanoscopic microscopy techniques. We show that macropores with a size distribution ranging from 50 to 120 nm enabled efficient loading and delivery of a therapeutic peptide (CIGB814), presently under a phase 3 clinical trial for the treatment of rheumatoid arthritis. Alginate microsponges showed 80% loading capacity and sustained peptide release over a few hours through a diffusional mechanism favored by partial erosion of the polymer scaffold. The edible and biocompatible nature of alginate polymers open promising perspectives for developing a new generation of polysaccharide-based carriers for the controlled delivery of peptide drugs, exploiting alternative routes with respect to intravenous administration.
寻求能够开辟新给药途径的生物相容性药物递送装置是生物医学研究的前沿领域。在本研究中,我们制备了基于交联藻酸盐聚合物的多孔多糖微海绵,并通过光谱学和纳米显微镜技术对其进行了表征。我们发现,孔径分布在50至120纳米的大孔能够有效地负载和递送一种治疗性肽(CIGB814),该肽目前正处于治疗类风湿性关节炎的3期临床试验阶段。藻酸盐微海绵显示出80%的负载能力,并通过聚合物支架的部分侵蚀所促进的扩散机制在数小时内持续释放肽。藻酸盐聚合物的可食用和生物相容性为开发新一代基于多糖的载体以实现肽药物的控释开辟了广阔前景,有望开拓静脉给药之外的替代给药途径。