Liposaccharide-based nanoparticulate drug delivery system

被引:2
|
作者
Abdelrahim, Adel S. [1 ]
Simerska, Pavla [1 ]
Toth, Istvan [1 ,2 ]
机构
[1] Univ Queensland, SCMB, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Sch Pharm, Woolloongabba, Qld 4102, Australia
基金
澳大利亚研究理事会;
关键词
Charged liposaccharide; Microcalorimetry; Tobramycin; Absorption enhancer; Nanoparticle; Drug delivery; LIPOAMINO ACID; IN-VITRO; LIPIDIC PEPTIDES; DODECYL-SULFATE; AMINO-ACIDS; ABSORPTION; THERMODYNAMICS; MICELLIZATION; AGENTS; ALKYLTRIMETHYLAMMONIUM;
D O I
10.1016/j.tet.2012.04.064
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of anionic liposaccharide derivatives were synthesized in order to develop a system, which would have the capacity to act as an absorption enhancer and to improve oral bioavailability of drugs. The addition of a liposaccharide to a drug enhances drug stability against enzymatic degradation, while the lipophilicity can be controlled by variation of the lipid side chain. All liposaccharide derivatives were purified and fully characterized by nuclear magnetic resonance and high-resolution mass spectrometry. The thermodynamic profiles, critical aggregation concentrations and size of the synthesized liposaccharides were determined by isothermal titration microcalorimetry, transmission electron microscopy and dynamic light scattering. These liposaccharides formed nanoparticles with sizes below 100 nm. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4967 / 4975
页数:9
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