Carafa M, Di Marzio L, Marianecci C, Cinque B, Lucania G, Kajiwara K, Cifone M G, Santucci E
Dip. di Scienze del Farmaco, Faculty of Pharmacy, University G. D'Annunzio, Via dei Vestini, 66100 Chieti, Italy.
Eur J Pharm Sci. 2006 Aug;28(5):385-93. doi: 10.1016/j.ejps.2006.04.009. Epub 2006 Apr 29.
In this work, we report the preparation, the characterization and interaction with cells of novel pH-sensitive non-phospholipid vesicle formulations, from a non-ionic surfactant mixed with cholesterol (CHOL) and his derivative cholesteryl hemisuccinate (CHEMS), as pH-sensitive molecule. This molecule, can destabilize the vesicle lipid bilayer when exposed to an acidic environment, with a subsequent release of vesicular content, enhancing the cytoplasmatic delivery of drugs to target cells. Vesicles were characterized by static and dynamic light scattering, in order to evaluate their dimensions, bilayer thickness and vesicle stability. Membrane permeability changes were determined by the release of entrapped hydroxypyrene-1,3,6-trisulfonic acid (HPTS). Also diphenylhesatriene (DPH) fluorescence anisotropy and zeta potential measurements were used to evidence the pH sensitivity. Furthermore vesicles were characterized by means of electronic microscopy after freeze-fracture. The interaction of non-lipid vesicles containing different fluorescent dyes with Raw 264.7, mouse monocite macrophage, were analyzed by flow cytometric analysis. The obtained results indicate that the pH-sensitive vesicular structures show good plasma stability and relevant pH-sensitivity. Moreover this formulation was able to interact with target membranes (i.e. plasma or endosomal membrane) and to release the encapsulated material into the cytoplasm.
在本研究中,我们报道了新型pH敏感型非磷脂囊泡制剂的制备、表征及其与细胞的相互作用。该制剂由一种非离子表面活性剂与胆固醇(CHOL)及其衍生物胆固醇半琥珀酸酯(CHEMS)混合而成,CHEMS作为pH敏感分子。当暴露于酸性环境时,该分子会破坏囊泡脂质双层的稳定性,随后释放囊泡内容物,从而增强药物向靶细胞的细胞质递送。通过静态和动态光散射对囊泡进行表征,以评估其尺寸、双层厚度和囊泡稳定性。通过包封的羟基芘-1,3,6-三磺酸(HPTS)的释放来测定膜通透性的变化。还使用二苯基己三烯(DPH)荧光各向异性和zeta电位测量来证明pH敏感性。此外,通过冷冻断裂后的电子显微镜对囊泡进行表征。通过流式细胞术分析含有不同荧光染料的非脂质囊泡与小鼠单核巨噬细胞Raw 264.7的相互作用。所得结果表明,pH敏感型囊泡结构具有良好的血浆稳定性和相关的pH敏感性。此外,该制剂能够与靶膜(即质膜或内体膜)相互作用,并将包封的物质释放到细胞质中。