Fong Wye-Khay, Vanhecke Dimitri, Hauser Daniel, Balog Sandor, Lemal Philipp, Montasseri Shiva, Rothen-Rutishauser Barbara, Petri-Fink Alke
Adolphe Merkle Institute and National Center of Competence in Research Bio-Inspired Materials, University of Fribourg, Chemin des Verdiers 4, Fribourg 1700, Switzerland.
Discipline of Chemistry, College of Science, Engineering and Environment, University of Newcastle, New South Wales, Callaghan 2308, Australia.
Mol Pharm. 2025 Jul 7;22(7):4221-4229. doi: 10.1021/acs.molpharmaceut.5c00435. Epub 2025 Jun 17.
Advances in the development of lipid nanoparticles have resulted in delivery systems that both protect the encapsulated drug and improve therapeutic outcomes. When introduced in vivo, nanoparticles are rapidly covered by a biomolecular corona, influencing their biological fate, i.e., interaction with cells, uptake, and intracellular fate. This study explores the interactions between nonlamellar lipidic drug delivery systems and non-lipolytic components of complex cell culture media, focusing on the dynamic formation of the corona and its effects on the lipid nanoparticle behavior. Monoglyceride formulations were monitored for changes in nanostructure and particle size, and mechanisms for these changes were elucidated. Not only do these biomacromolecules influence the size and structure of the nanoparticles themselves, but they can simultaneously diffuse into the mesophase nanostructure. The study highlights that lipid nanoparticles undergo dynamic changes in physiological conditions influenced by adsorbed proteins and other nondegradative components in complex cell culture media, separate from effects caused by lipases or other enzymatic factors. These induced structural transformations can significantly alter the nanoparticles' physical properties and drug release profiles, potentially causing deviation from their intended therapeutic performance. Understanding these interactions is thus crucial for optimizing the design and functionality of lipid-based drug delivery systems in biomedical applications.
脂质纳米颗粒的发展进步带来了既能保护被包裹药物又能改善治疗效果的递送系统。当纳米颗粒被引入体内时,它们会迅速被生物分子冠层覆盖,从而影响其生物学命运,即与细胞的相互作用、摄取以及细胞内命运。本研究探讨了非层状脂质药物递送系统与复杂细胞培养基中非脂解成分之间的相互作用,重点关注冠层的动态形成及其对脂质纳米颗粒行为的影响。监测了甘油单酯制剂的纳米结构和粒径变化,并阐明了这些变化的机制。这些生物大分子不仅会影响纳米颗粒本身的大小和结构,还能同时扩散到中间相纳米结构中。该研究强调,脂质纳米颗粒在生理条件下会发生动态变化,这受到复杂细胞培养基中吸附的蛋白质和其他非降解成分的影响,与脂肪酶或其他酶促因素引起的影响无关。这些诱导的结构转变会显著改变纳米颗粒的物理性质和药物释放曲线,可能导致其预期治疗性能出现偏差。因此,了解这些相互作用对于优化生物医学应用中基于脂质的药物递送系统的设计和功能至关重要。