Effect of hydroxypropyl β-cyclodextrin on the self-assembling and thermogelation properties of Poloxamer 407

被引:60
作者
Bonacucina, Giulia
Spina, Michele
Misici-Falzi, Monica
Cespi, Marco
Pucciarelli, Stefania
Angeletti, Mauro
Palmieri, Giovanni F.
机构
[1] Univ Camerino, Dept Chem Sci, I-62032 Camerino, MC, Italy
[2] Univ Camerino, Dept Mol Cellular & Anim Biol, I-62032 Camerino, MC, Italy
[3] Univ Camerino, Dept Comparat Biosci & Morphol Sci, I-62032 Camerino, MC, Italy
关键词
self-assembling; poloxamer; 407; hydroxypropyl beta-cyclodextrin; viscosity; nano-DSC;
D O I
10.1016/j.ejps.2007.06.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This paper deals with the rheological and thermal characterisation of the self-assembling behaviour of different Poloxamer 407 systems (15-30%, w/v), both alone or after the addition of various amounts of hydroxypropyl p-cyclodextrin (5-20%, w/v). The knowledge of the interactions existing between the two kinds of molecules could allow the development of systems for parenteral administration containing also proteins or peptides drugs. A rheology (temperature sweep and frequency sweep test) study has been performed to characterise the thermogelation process while thermal analysis (nanoDSC) allowed the determination of both micellization and sol/gelation transition processes. These two techniques were also utilised to outline the variation in the critical micelle temperature (cmT) or in the sol/gel temperature (sgT,) of the systems containing also hydroxypropyl P-cyclodextrin (HP P-CD). Both the rheology and thermal analysis showed the presence of interesting interactions between the HP P-CD and the Poloxamer 407, which cause a shift of both cmT and sgT. The presence of HP P-CD modified also Poloxamer samples elastic characters and microrheological structure as demonstrated by the G'-G" mechanical spectra. Rheological and thermal results outlined how these new systems could open the possibility to join the thermogelling behaviour offered by Poloxamer 407 with the well-known stabilization and protection ability of HP P-CD, which could make possible the formulation of systems for the parenteral delivery of peptides and proteins. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 122
页数:8
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