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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.
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页码:16 / 28
页数:13
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