Pradines Bénédicte, Djabourov Madeleine, Vauthier Christine, Loiseau Philippe M, Ponchel Gilles, Bouchemal Kawthar
Institut Galien Paris Sud, UMR CNRS 8612, Université Paris-Sud, Faculté de Pharmacie, 5, rue J-B. Clément, 92296, Châtenay-Malabry Cedex, France; BioCis, Biomolécules : conception, isolement, synthèse- Chimiothérapie Antiparasitaire, UMR CNRS 8076, Université Paris-Sud, Faculté de Pharmacie, 5, rue J.B. Clément, 92296 Châtenay-Malabry Cedex, France; Laboratoire de Physique Thermique, ESPCI-ParisTech, PSL Research University, 10 rue Vauquelin, 75231 Paris Cedex 05, France.
Laboratoire de Physique Thermique, ESPCI-ParisTech, PSL Research University, 10 rue Vauquelin, 75231 Paris Cedex 05, France.
Colloids Surf B Biointerfaces. 2015 Nov 1;135:669-676. doi: 10.1016/j.colsurfb.2015.08.021. Epub 2015 Aug 22.
The aim of this investigation is to combine the advantages of pluronic(®) F127 hydrogels and nanoparticles composed of poly(isobutylcyanoacrylate) (PIBCA) core coated with a mixture of chitosan and thiolated chitosan to design novel multifunctional formulation for mucosal application. Nanoparticles offer the advantage of being mucoadhesive while pluronic(®) F127 hydrogel allowed prolonged contact time onto mucosal surfaces. This work highlights an unprecedented comprehensive study on the effect of nanoparticles on gelation and micellization behaviors of pluronic(®) F127 using rheology and micro-calorimetry experiments. Results showed that presence of nanoparticles induced (i) smaller crystal peak of F127, (ii) a decrease of the enthalpy of F127 micellization and (iii) a non-reversibility of micelle formation (during heating ramp) and micelle melting (during cooling ramp). Together, these findings suggest that a part of F127 was not able to associate into micelles and the formation of mixed micelles containing F127 unimers and PIBCA/(chitosan/thiolated chitosan) copolymer and/or PIBCA homopolymer was suspected. The interaction of F127 unimers with nanoparticles resulted from their physical de-structuration as revealed by nanoparticle size measurement. In addition, we found that short polymerization duration of one hour induced more pronounced nanoparticle de-structuration. Twenty-four hour-polymerization of isobutylcyanoacrylate in the presence of chitosan and thiolated chitosan led to more stable nanoparticles when mixed with pluronic(®) F127.
本研究的目的是结合普朗尼克(®)F127水凝胶和由聚(异丁基氰基丙烯酸酯)(PIBCA)核组成、表面包覆壳聚糖和硫醇化壳聚糖混合物的纳米颗粒的优点,设计用于黏膜应用的新型多功能制剂。纳米颗粒具有黏膜黏附性的优点,而普朗尼克(®)F127水凝胶能使在黏膜表面的接触时间延长。这项工作通过流变学和微量量热法实验,对纳米颗粒对普朗尼克(®)F127的凝胶化和胶束化行为的影响进行了前所未有的全面研究。结果表明,纳米颗粒的存在导致:(i)F127的结晶峰变小;(ii)F127胶束化焓降低;(iii)胶束形成(在加热过程中)和胶束熔化(在冷却过程中)的不可逆性。综合这些发现表明,一部分F127无法缔合成胶束,并且怀疑形成了包含F127单体与PIBCA/(壳聚糖/硫醇化壳聚糖)共聚物和/或PIBCA均聚物的混合胶束。如纳米颗粒尺寸测量所揭示的,F127单体与纳米颗粒的相互作用源于它们的物理解构。此外,我们发现一小时的短聚合时间会导致更明显的纳米颗粒解构。在壳聚糖和硫醇化壳聚糖存在下,异丁基氰基丙烯酸酯聚合24小时,当与普朗尼克(®)F127混合时会产生更稳定的纳米颗粒。