Polymer-lipid hybrid nanoparticles as enhanced indomethacin delivery systems

被引:47
|
作者
Dalmoro, Annalisa [1 ,2 ]
Bochicchio, Sabrina [1 ,2 ]
Nasibullin, Shamil F. [3 ]
Bertoncin, Paolo [4 ]
Lamberti, Gaetano [5 ]
Barba, Anna Angela [1 ,2 ]
Moustafine, Rouslan I. [3 ]
机构
[1] Univ Salerno, Dipartimento Farm, Via Giovanni Paolo 2,132, I-84084 Fisciano, SA, Italy
[2] Eng4Life Srl, Spin Off Acad, Via Fiorentino 32, I-83100 Avellino, Italy
[3] Kazan State Med Univ, Dept Pharmaceut Analyt & Toxicol Chem, Butlerov St 49, Kazan 420012, Russia
[4] Univ Trieste, Dipartimento Sci Vita, Ctr Microscopia Elettron, Via Fleming 31 A-B, I-34127 Trieste, Italy
[5] Univ Salerno, Dipartimento Ingn Ind, Via Giovanni Paolo 2,132, I-84084 Fisciano, SA, Italy
基金
俄罗斯科学基金会;
关键词
Nano-encapsulation; Drug delivery; Indomethacin; Chitosan; Liposome; Simil-microfluidic technique; TEM; HOT-MELT EXTRUSION; CHITOSAN-COATED LIPOSOMES; DRUG-DELIVERY; DISPERSIONS; INSULIN; FORMULATIONS; TEMPERATURE; HYDROLYSIS; TRANSITION; STABILITY;
D O I
10.1016/j.ejps.2018.05.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Non-steroidal anti-inflammatory drugs (NSAIDs), i.e. indomethacin used for rheumatoid arthritis and non-rheumatoid inflammatory diseases, are known for their injurious actions on the gastrointestinal (GI) tract. Mucosal damage can be avoided by using nanoscale systems composed by a combination of liposomes and biodegradable natural polymer, i.e. chitosan, for enhancing drug activity. Aim of this study was to prepare chitosan-lipid hybrid delivery systems for indomethacin dosage through a novel continuous method based on microfluidic principles. The drop-wise conventional method was also applied in order to investigate the effect of the two polymeric coverage processes on the nanostructures features and their interactions with indomethacin. Thermal-physical properties, mucoadhesiveness, drug entrapment efficiency, in vitro release behavior in simulated GI fluids and stability in stocking conditions were assayed and compared, respectively, for the uncoated and chitosan-coated nanoliposomes prepared by the two introduced methods. The prepared chitosan-lipid hybrid structures, with nanometric size, have shown high indomethacin loading (about 10%) and drug encapsulation efficiency up to 99%. TEM investigation has highlighted that the developed novel simil-microfluidic method is able to put a polymeric layer, surrounding indomethacin loaded nanoliposomes, thicker and smoother than that achievable by the drop-wise method, improving their storage stability. Finally, double pH tests have confirmed that the chitosan-lipid hybrid nanostructures have a gastro retentive behavior in simulated gastric and intestinal fluids thus can be used as delivery systems for the oral-controlled release of indomethacin. Based on the present results, the simil-microfluidic method, working with large volumes, in a rapid manner, without the use of drastic conditions and with a precise control over the covering process, seems to be the most promising method for the production of suitable indomethacin delivery system, with a great potential in industrial manufacturing.
引用
收藏
页码:16 / 28
页数:13
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