Efimova Anna A, Abramova Tatyana A, Yatsenko Igor V, Kazantsev Alexey V, Pozdyshev Denis V, Lukashev Nikolay V, Muronets Vladimir I, Yaroslavov Alexander A
Department of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory 1-3, 119991 Moscow, Russia.
Belozersky Institute of Physico-Chemical Biology, M.V. Lomonosov Moscow State University, Leninskie Gory 1/40, 119992 Moscow, Russia.
Molecules. 2025 Jun 16;30(12):2608. doi: 10.3390/molecules30122608.
A new method of the design of stimuli-sensitive multiliposomal containers for encapsulation and controlled drug release is described. Despite quite a wide choice of pH-sensitive containers, there is still a considerable challenge to synthesize those that respond quickly to small variations in pH and release most of the encapsulated drug in a short time. The suggested AMS-containing multiliposomal complexes demonstrated an excellent rate of encapsulated substance release under altering the pH of the outer solution. To improve the efficiency of the delivery of bioactive compounds to target cells and to increase the therapeutic effect, pH-sensitive liposomes were concentrated on the surface of the carrier- PEG-coated cationic liposomes. A pH-sensitive ampholytic derivative of cholan-24-oic acid embedded into the membrane of anionic liposomes allowed the rapid release of the cargo in the areas of low pH, such as tumors, inflammation sites, etc. The diameter of the complexes was optimized for passive targeting and typically ranged from 250 to 400 nm. The biodegradability of liposomes ensured enzymatic destruction of the multiliposomal containers and their elimination from the body after performing their transport function. The multiliposomal complexes and products of their biodegradation demonstrated low cytotoxicity. The composition of multiliposomal complexes, in particular, the amount of PEGylated lipid in the bilayer, was estimated to provide a high speed of the cargo release upon changing the pH. The novel developed pH-sensitive containers show potential for biomedical applications.
本文描述了一种用于药物包封和控释的刺激敏感型多层脂质体容器的新设计方法。尽管pH敏感型容器的选择范围相当广泛,但合成那些能对pH的微小变化快速响应并在短时间内释放大部分包封药物的容器仍然面临相当大的挑战。所建议的含AMS多层脂质体复合物在改变外部溶液pH时表现出优异的包封物质释放速率。为了提高生物活性化合物向靶细胞的递送效率并增强治疗效果,pH敏感型脂质体被浓缩在载体——聚乙二醇包被的阳离子脂质体表面。嵌入阴离子脂质体膜中的胆烷-24-酸的pH敏感两性衍生物能使货物在低pH区域(如肿瘤、炎症部位等)快速释放。复合物的直径经过优化以实现被动靶向,通常在250至400纳米之间。脂质体的生物可降解性确保了多层脂质体容器的酶促破坏以及它们在完成运输功能后从体内清除。多层脂质体复合物及其生物降解产物表现出低细胞毒性。特别是多层脂质体复合物的组成,尤其是双层中聚乙二醇化脂质的量,经过评估以确保在改变pH时货物能高速释放。新开发的pH敏感型容器在生物医学应用方面具有潜力。