Exploration of hydrophobic modification degree of chitosan-based nanocomplexes on the oral delivery of enoxaparin

被引:18
作者
Wang, Linlin [1 ]
Li, Liang [1 ]
Sun, Yujiao [1 ]
Tian, Ye [1 ]
Li, Ying [1 ]
Li, Conghao [1 ]
Junyaprasert, Varaporn B. [2 ]
Mao, Shirui [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China
[2] Mahidol Univ, Fac Pharm, Dept Pharm, Bangkok 10400, Thailand
关键词
Chitosan; Glyceryl monostearate; Oral; Enoxaparin; Polyelectrolyte nanocomplexes; MOLECULAR-WEIGHT HEPARIN; IN-VITRO; DRUG-DELIVERY; MACROMOLECULES; NANOPARTICLES; SHELL; MUCOADHESIVE; ABSORPTION; POLYMERS; BEHAVIOR;
D O I
10.1016/j.ejps.2013.07.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The objective of this paper is to elucidate the influence of lipophilic modification degree of chitosan on the peroral absorption of enoxaparin. A series of novel chitosan grafted glyceryl monostearate (GM) copolymers with different GM substitution degree were synthesized and the successful synthesis was confirmed by H-1 NMR, FTIR and X-ray diffraction. Enoxaparin loaded nanocomplexes with different carriers were prepared by self-assembly process. Influence of GM substitution degree and chitosan molecular weight in the copolymer on the properties of the nanocomplexes was investigated. Morphology of the nanocomplexes was observed by atomic force microscopy. Mucoadhesive properties of the nanocomplexes were characterized using mucin particle method. Initially, mucoadhesion of the nanocomplexes increased with the increase of GM substitution degree and it started to decrease when the substitution degree was up to 18.6%. A good linear relationship between GM substitution degree and in vivo absorption of enoxaparin in fasted rats was established in the substitution degree range of 0-11.1%. In agreement with mucoadhesion data, further increasing GM substitution degree to 18.6% caused a decrease in oral absorption. In conclusion, oral bioavailability of enoxaparin can be enhanced by structure modification of the carriers and the bioavailability is hydrophobic modification degree dependent. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:263 / 271
页数:9
相关论文
共 45 条
[1]   Formulation and Delivery of siRNA by Oleic Acid and Stearic Acid Modified Polyethylenimine [J].
Alshamsan, Aws ;
Haddadi, Azita ;
Incani, Vanessa ;
Samuel, John ;
Lavasanifar, Afsaneh ;
Uludag, Hasan .
MOLECULAR PHARMACEUTICS, 2009, 6 (01) :121-133
[2]   Hydrophobized dextran-spermine conjugate as potential vector for in vitro gene transfection [J].
Azzam, T ;
Eliyahu, H ;
Makovitzki, A ;
Linial, M ;
Domb, AJ .
JOURNAL OF CONTROLLED RELEASE, 2004, 96 (02) :309-323
[3]   Effect of unsaturated lipid chains on dimensions, molecular order and hydration of membranes [J].
Binder, H ;
Gawrisch, K .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (49) :12378-12390
[4]   Tuning of shell and core characteristics of chitosan-decorated acrylic nanoparticles [J].
Bravo-Osuna, I. ;
Ponchel, G. ;
Vauthier, C. .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 30 (02) :143-154
[5]   Mucoadhesion mechanism of chitosan and thiolated chitosan-poly(isobutyl cyanoacrylate) core-shell nanoparticles [J].
Bravo-Osuna, Irene ;
Vauthier, Christine ;
Farabollini, Alessandra ;
Palmieri, Giovanni Filippo ;
Ponchel, Gilles .
BIOMATERIALS, 2007, 28 (13) :2233-2243
[6]   Elaboration and characterization of thiolated chitosan-coated acrylic nanoparticles [J].
Bravo-Osuna, Irene ;
Schmitz, Thierry ;
Bernkop-Schnuerch, Andreas ;
Vauthier, Christine ;
Ponchel, Gilles .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 316 (1-2) :170-175
[7]   A review of the prospects for polymeric nanoparticle platforms in oral insulin delivery [J].
Chen, Mei-Chin ;
Sonaje, Kiran ;
Chen, Ko-Jie ;
Sung, Hsing-Wen .
BIOMATERIALS, 2011, 32 (36) :9826-9838
[8]   The characteristics, biodistribution and bioavailability of a chitosan-based nanoparticulate system for the oral delivery of heparin [J].
Chen, Mei-Chin ;
Wong, Hen-Sheng ;
Lin, Kun-Ju ;
Chen, Hsin-Lung ;
Wey, Shiaw-Pyng ;
Sonaje, Kiran ;
Lin, Yu-Hsin ;
Chu, Che-Yi ;
Sung, Hsing-Wen .
BIOMATERIALS, 2009, 30 (34) :6629-6637
[9]   Reversal of heparin-induced increases in aPTT in the rat by PM102, a novel heparin antagonist [J].
Cushing, Daniel J. ;
Cooper, Warren D. ;
Cohen, Marlene L. ;
McVoy, Julie R. S. ;
Sobel, Michael ;
Harris, Robert B. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2010, 635 (1-3) :165-170
[10]   Linoleic acid-grafted chitosan oligosaccharide micelles for intracellular drug delivery and reverse drug resistance of tumor cells [J].
Du, Yong-Zhong ;
Wang, Ling ;
Yuan, Hong ;
Hu, Fu-Qiang .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2011, 48 (01) :215-222