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Synthesis of Eudragit® L100-coated chitosan-based nanoparticles for oral enoxaparin delivery
被引:19
|作者:
Patriota, Yuri Basilio Gomes
[1
]
Arruda, Igor Eduardo Silva
[1
]
Oliveira, Antonia Carla de Jesus
[1
]
de Oliveira, Thaisa Cardoso
[1
]
Silva, Eliadna de Lemos Vasconcelos
[1
]
Chaves, Luise Lopes
[1
,3
]
Ribeiro, Fabio de Oliveira Silva
[2
]
da Silva, Durcilene Alves
[2
]
Soares, Monica Felts de la Roca
[1
]
Soares-Sobrinho, Jose Lamartine
[1
]
机构:
[1] Univ Fed Pernambuco, Qual Control Core Med & Correlates, Recife, PE, Brazil
[2] Fed Univ Delta Parnaiba, Res Ctr Biodivers & Biotechnol BIOTEC, Parnaiba, PI, Brazil
[3] Oswaldo Cruz Fdn FIOCRUZ, Aggeu Magalhaes Inst IAM, Dept Immunol, Rio De Janeiro, Brazil
关键词:
Chitosan;
Drug delivery system;
Eudragit (R) L100;
Low-molecular weight heparin;
Biomacromolecule;
Polymer nanoparticles;
MOLECULAR-WEIGHT HEPARIN;
CONTROLLED DRUG-RELEASE;
IN-VITRO;
GASTROINTESTINAL MUCUS;
NANOCOMPLEXES;
DERIVATIVES;
ABSORPTION;
SYSTEMS;
DESIGN;
D O I:
10.1016/j.ijbiomac.2021.10.111
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:
Enoxaparin is an effective biological molecule for prevention and treatment of coagulation disorders. However, it is poorly absorbed in the gastrointestinal tract. In this study, we developed an Eudragit (R) L100 coated chitosan core shell nanoparticles for enoxaparin oral delivery (Eud/CS/Enox NPs) through a completely eco-friendly method without employing any high-energy homogenizer technique and any organic solvents. Spherical nanocarriers were successfully prepared with particle size lower than 300 nm, polydispersity index about 0.12 and zeta potential higher than +25 mV, entrapment efficiency greater than 95% and the in vitro release behavior confirms the good colloidal stability and the successful Eudragit (R) L100 coating process demonstrated by negligible cumulative enoxaparin release (<10%) when the particles are submitted to simulated gastric fluid conditions. Finally, we demonstrated that the core-shell structure of the particle influenced the drug release mechanism of the formulations, indicating the presence of the Eudragit (R) L100 on the surface of the particles. These results suggested that enteric-coating approach and drug delivery nanotechnology can be successfully explored as potential tools for oral delivery of enoxaparin.
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页码:450 / 456
页数:7
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