Sodium deoxycholate-decorated zein nanoparticles for a stable colloidal drug delivery system

被引:96
作者
Gagliardi, Agnese [1 ]
Paolino, Donatella [1 ]
Iannone, Michelangelo [2 ]
Palma, Ernesto [3 ]
Fresta, Massimo [3 ]
Cosco, Donato [3 ]
机构
[1] Magna Graecia Univ Catanzaro, Dept Expt & Clin Med, Catanzaro, Italy
[2] CNR, Inst Neurol Sci, Sect Pharmacol, Roccelletta Di Borgia, Italy
[3] Magna Graecia Univ Catanzaro, Dept Hlth Sci, Campus Univ S Venuta,Viale S Venuta, I-88100 Catanzaro, Italy
关键词
nanoparticles; sodium deoxycholate; stabilizers; zein; ORAL DELIVERY; FABRICATION; ENCAPSULATION; MICROSPHERES; NANOCAPSULES; ANTIOXIDANT; FORMULATION; LIPOSOMES; PROTEIN; CARRIER;
D O I
10.2147/IJN.S156930
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: The use of biopolymers is increasing in drug delivery, thanks to the peculiar properties of these compounds such as their biodegradability, availability, and the possibility of modulating their physico-chemical characteristics. In particular, protein-based systems such as albumin are able to interact with many active compounds, modulating their biopharmaceutical properties. Zein is a protein of 20-40 kDa made up of many hydrophobic amino acids, generally regarded as safe (GRAS) and used as a coating material. Methods: In this investigation, zein was combined with various surfactants in order to obtain stable nanosystems by means of the nanoprecipitation technique. Specific parameters, eg, temperature, pH value, Turbiscan Stability Index, serum stability, in vitro cytotoxicity and entrapment efficiency of various model compounds were investigated, in order to identify the nanoformulation most useful for a systemic drug delivery application. Results: The use of non-ionic and ionic surfactants such as Tween 80, poloxamer 188, and sodium deoxycholate allowed us to obtain nanoparticles characterized by a mean diameter of 100-200 nm when a protein concentration of 2 mg/mL was used. The surface charge was modulated by means of the protein concentration and the nature of the stabilizer. The most suitable nanoparticle formulation to be proposed as a colloidal drug delivery system was obtained using sodium deoxycholate (1.25% w/v) because it was characterized by a narrow size distribution, a good storage stability after freeze-drying and significant feature of retaining lipophilic and hydrophilic compounds. Conclusion: The sodium deoxycholate-coated zein nanoparticles are stable biocompatible colloidal carriers to be used as useful drug delivery systems.
引用
收藏
页码:601 / 614
页数:14
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