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采用聚赖氨酸和聚谷氨酸对脂质体进行层层包裹,以提高其在生物介质中的稳定性。

Development and characterization of layer-by-layer coated liposomes with poly(L-lysine) and poly(L-glutamic acid) to increase their resistance in biological media.

机构信息

3BIO Team, UMR 7199, Université de Strasbourg/CNRS, Faculté de Pharmacie, 74 route du Rhin, 67401 Illkirch Cedex, France.

CNM Team, UMR 7199, Université de Strasbourg/CNRS, Faculté de Pharmacie, 74 route du Rhin, 67401 Illkirch Cedex, France.

出版信息

Int J Pharm. 2020 Aug 30;586:119568. doi: 10.1016/j.ijpharm.2020.119568. Epub 2020 Jun 24.

DOI:10.1016/j.ijpharm.2020.119568
PMID:32592900
Abstract

Multilayered coated liposomes were prepared using the layer-by-layer (LbL) technique in an effort to improve their stability in biological media. The formulation strategy was based on the alternate deposition of two biocompatible and biodegradable polyelectrolytes - poly(L-lysine) (PLL) and poly(L-glutamic acid) (PGA) - on negatively charged small unilamellar vesicles (SUVs). Some parameters of the formulation process were optimized such as the polyelectrolyte concentration and the purification procedure. This optimized procedure has allowed the development of very homogeneous formulations of liposomes coated with up to 6 layers of polymers (so-called layersomes). The coating was characterized by dynamic light scattering (DLS), zeta potential measurements and Förster resonance energy transfer (FRET) between two fluorescently labeled polyelectrolytes. Studies on the stability of the formulations at 4 °C in a buffered solution have shown that most structures are stable over 1 month without impacting their encapsulation capacity. In addition, fluorophore release experiments have demonstrated a better resistance of the layersomes in the presence of a non-ionic detergent (Triton™ X-100) as well as in the presence of phospholipase A and human plasma. In conclusion, new multilayered liposomes have been developed to increase the stability of conventional liposomes in biological environments.

摘要

采用层层(LbL)技术制备了多层包被脂质体,以提高其在生物介质中的稳定性。该制剂策略基于两种生物相容和可生物降解的聚电解质-聚(L-赖氨酸)(PLL)和聚(L-谷氨酸)(PGA)-在带负电荷的小单层囊泡(SUV)上的交替沉积。优化了制剂过程的一些参数,如聚电解质浓度和纯化程序。该优化程序允许开发非常均匀的脂质体制剂,包被多达 6 层聚合物(所谓的层状脂质体)。通过动态光散射(DLS)、zeta 电位测量和两种荧光标记聚电解质之间的Förster 共振能量转移(FRET)对涂层进行了表征。在缓冲溶液中 4°C 下对制剂稳定性的研究表明,大多数结构在 1 个月内稳定,而不会影响其包封能力。此外,荧光团释放实验表明,在存在非离子型洗涤剂(Triton™ X-100)以及磷脂酶 A 和人血浆的情况下,层状脂质体具有更好的稳定性。总之,开发了新型多层脂质体以提高常规脂质体在生物环境中的稳定性。

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