Dextran/poly-L-arginine multi-layered CaCO3-based nanosystem for vascular drug delivery

被引:21
作者
Ferrari, Pier Francesco [1 ]
Zattera, Elena [1 ]
Pastorino, Laura [2 ]
Perego, Patrizia [3 ,4 ]
Palombo, Domenico [1 ,4 ,5 ]
机构
[1] Univ Genoa, Dept Surg & Integrated Diagnost Sci, Viale Benedetto XV, I-16132 Genoa, Italy
[2] Univ Genoa, Dept Informat Bioengn Robot & Syst Engn, Via Opera Pia 13, I-16145 Genoa, Italy
[3] Univ Genoa, Dept Civil Chem & Environm Engn, Via Opera Pia 15, I-16145 Genoa, Italy
[4] Univ Genoa, Res Ctr Biol Inspired Engn Vasc Med & Longev, Via Montallegro 1, I-16145 Genoa, Italy
[5] IRCCS Osped Policlin San Martino, Vasc & Endovasc Surg Unit, Largo Rosanna Benzi 10, I-16132 Genoa, Italy
关键词
Cardiovascular diseases; Targeted therapy; Immuno-nanoparticles; Layer-by-layer; Calcium carbonate; BY-LAYER NANOPARTICLES; ENDOTHELIAL-CELLS; ANTICANCER DRUG; CHITOSAN; HEMOCOMPATIBILITY; EXPRESSION; INFLAMMATION; FABRICATION; STABILITY; PARTICLES;
D O I
10.1016/j.ijbiomac.2021.02.058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of heterogeneous drug delivery systems leads to innovative strategies for targeted therapy of common pathologies, such as cancer, immunological and neurological disorders. Nowadays, it is possible to choose among a great variety of nanoparticles on the basis of the needs they have to satisfy. However, a candidate for the treatment of cardiovascular pathologies is still missing. In this context, a targeted therapy implies the conceptualization of nanoparticles that take active part in the treatment of vascular pathologies. The aim of this work was to provide a method to produce multi-layered calcium carbonate (CaCO3) nanoparticles encapsulating a model protein, bovine serum albumin, with model antibodies on their surface. CaCO3 nanoparticles were produced by the combination of complex coacervation and mineralization and were engineered using layer by-layer technique with a polysaccharide, dextran sulfate, and a homo-poly-amino acid, poly-L-arginine. Morphology, biocompatibility, cellular uptake, influence on cell expression of the inflammatory marker matrix metalloproteinase-9, and hemocompatibility of the nanoparticles were studied. The presence of the dextran/ poly-L-arginine layers did not negatively affect the nanoparticle overall characteristics and they did not trigger proinflammatory response in vitro. Taking together all the obtained results, we consider the proposed CaCO3 nanoparticles as a promising tool in cardiovascular field. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:548 / 558
页数:11
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