Sonication-assisted Layer-by-Layer self-assembly nanoparticles for resveratrol delivery

被引:10
|
作者
Santos, Ana Claudia [1 ,2 ]
Sequeira, Joana A. D. [1 ,3 ]
Pereira, Irina [1 ,2 ]
Cabral, Celia [4 ,5 ]
Gonzallez, Mar Collado [1 ,6 ]
Fontes-Ribeiro, C. [7 ]
Ribeiro, Antonio J. [1 ,3 ]
Lvov, Yuri M. [8 ,9 ]
Veiga, Francisco J. [1 ,2 ]
机构
[1] Univ Coimbra, Fac Pharm, Dept Pharmaceut Technol, P-3000548 Coimbra, Portugal
[2] Univ Coimbra, Fac Pharm, Grp Pharmaceut Technol, REQUIMTE LAQV, Coimbra, Portugal
[3] Inst Mol & Cell Biol, Grp Genet Cognit Dysfunct, i3S, Rua Campo Alegre 823, P-4150180 Porto, Portugal
[4] Univ Coimbra, Fac Med, CNC IBILI, Polo Ciencias Saude, P-3000548 Coimbra, Portugal
[5] Univ Coimbra, CEIS20, Rua Filipe Simoes 33, P-3000186 Coimbra, Portugal
[6] Univ Murcia, Sch Chem, Dept Phys Chem, Campus Espinardo,Via Perimetral S-N, E-30100 Murcia, Spain
[7] Univ Coimbra, Fac Med, Dept Pharmacol & Expt Therapeut, Polo Ciencias Saude, P-3000548 Coimbra, Portugal
[8] Louisiana Tech Univ, Inst Micromfg, POB 10137, Ruston, LA 71272 USA
[9] Natl Univ Sci & Technol MISiS, Moscow 119049, Russia
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2019年 / 105卷
关键词
Layer-by-Layer self-assembly; Resveratrol; Washless; Colloid; Nanoparticle; Controlled release; Biocompatibility; Oral delivery; VITRO/IN-VIVO CHARACTERIZATION; TRANS-RESVERATROL; DRUG-DELIVERY; LOADED NANOPARTICLES; SOLUBLE DRUGS; BIOAVAILABILITY; POLYELECTROLYTE; INFLAMMATION; COMBINATION; PERFORMANCE;
D O I
10.1016/j.msec.2019.110022
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
This paper advances the development of a novel drug nanodelivery solution to the oral administration of resveratrol (RSV), a low soluble drug whose recognized therapeutic applications are circumscribed when administered in the free compound form. Layer-by-Layer (LbL) self-assembly is an emergent nanotechnology proposed to address this concern with means to afford control over key formulation parameters, which are able to ultimately promote an improved pharmacokinetics. LbL self-assembly consists in the sequential adsorption of oppositely charged polyelectrolytes upon a low soluble drug nanopartide (NP) template, giving rise to onion-like multilayered nanoarchitectures. In this work, RSV nanoprecipitation followed by LbL self-assembly of polyelectrolytes, led by a washless approach, was carried out by using the cationic poly(allylamine hydrochloride) (PAH) and the anionic dextran sulfate (DS) as polyelectrolytes towards the nanoencapsulation of RSV. Each saturated polyelectrolyte layer deposition involved the rigorous polyelectrolyte concentration assessment which was accomplished by tracing titration curves. This way, aqueous RSV nanocores and RSV LbL nanoformulations with a distinct number of PAH/DS bilayers were developed, including 2.5 (RSV-(PAH/DS)(2.5) NPs), 5.5 (RSV-(PAH/DS)(5.5) NPs) and 7.5 (RSV-(PAH/DS)(7.5) NPs) bi-layered nanoformulations. Homogenous particle size distributions at the desired nanoscale interval (ca. 116-220 nm; polydispersity index below 0.15), good colloidal (zeta potential magnitudes ca. +/- 20-30 mV) and chemical stabilizations, high encapsulation efficiency (above 90%) together with an excellent cytocompatibility with Caco-2 cells (cell viability above 90%) were observed for all the nanoformulations. Eventfully, LbL Mos promoted a controlled release of RSV pursuant to the number of polyelectrolyte bilayers under simulated gastrointestinal conditions, particularly in the intestine medium, emphasizing their biopharmaceutical advantage. Our findings manifestly pinpoint that LbL PAH/DS NPs constitute a promising nanodelivery system for the oral delivery of RSV, providing a rational strategy to enlarge the implementation range of this interesting polyphenol, which is possibly the most actively investigated phytochemical worldwide.
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页数:14
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