Hyaluronic acid-coated chitosan nanoparticles as carrier for the enzyme/ prodrug complex based on horseradish peroxidase/indole-3-acetic acid: Characterization and potential therapeutic for bladder cancer cells

被引:22
|
作者
Pereira, Fernanda Menezes [1 ,2 ]
Melo, Micael Nunes [1 ,2 ]
Mendes Santos, Atali Kayane [1 ,2 ]
Oliveira, Karony Vieira [1 ,2 ]
Diz, Fernando Mendonca [3 ]
Ligabue, Rosane Angelica [3 ]
Morrone, Fernanda Bueno [4 ]
Severino, Patricia [1 ,2 ]
Fricks, Alini Tinoco [1 ,2 ]
机构
[1] Univ Tiradentes, Av Murilo Dantas 300, BR-49032490 Aracaju, SE, Brazil
[2] Inst Technol & Res, Av Murilo Dantas 300, BR-49032490 Aracaju, SE, Brazil
[3] Pontifical Catholic Univ Rio Grande do Sul PUCRS, Sch Technol, Av Ipiranga 6681, BR-90619900 Porto Alegre, RS, Brazil
[4] Pontifical Catholic Univ Rio Grande do Sul PUCRS, Sch Hlth & Life Sci, Av Ipiranga 6681, BR-90619900 Porto Alegre, RS, Brazil
关键词
Hyaluronic acid-coated chitosan nanoparticles; Enzyme; pro-drug therapy; Bladder cancer cells; DRUG-DELIVERY SYSTEM; IN-VITRO EVALUATION; MOLECULAR-WEIGHT; TRIPOLYPHOSPHATE NANOPARTICLES; POLYMERIC NANOPARTICLES; CONTROLLED-RELEASE; PEROXIDASE; IMMOBILIZATION; STABILITY; CYTOTOXICITY;
D O I
10.1016/j.enzmictec.2021.109889
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hybrid nanoparticles composed of different biopolymers for delivery of enzyme/prodrug systems are of interest for cancer therapy. Hyaluronic acid-coated chitosan nanoparticles (CS/HA NP) were prepared to encapsulate individually an enzyme/pro-drug complex based on horseradish peroxidase (HRP) and indole-3-acetic acid (IAA). CS/HA NP showed size around 158 nm and increase to 170 and 200 nm after IAA and HRP encapsulation, respectively. Nanoparticles showed positive zeta potential values (between +20.36 mV and +24.40 mV) and higher encapsulation efficiencies for both nanoparticles (up to 90 %) were obtained. Electron microscopy indicated the formation of spherical particles with smooth surface characteristic. Physicochemical and thermal characterizations suggest the encapsulation of HRP and IAA. Kinetic parameters for encapsulated HRP were similar to those of the free enzyme. IAA-CS/HA NP showed a bimodal release profile of IAA with a high initial release (72 %) followed by a slow-release pattern. The combination of HRP-CS/HA NP and IAA- CS/HA NP reduced by 88 % the cell viability of human bladder carcinoma cell line (T24) in the concentrations 0.5 mM of pro-drug and 1.2 mu g/mL of the enzyme after 24 h.
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页数:12
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