单甘油酯中间相及其生物大分子冕的分子间动力学。

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Wye-Khay Fong, Dimitri Vanhecke, Daniel Hauser, Sandor Balog, Philipp Lemal, Shiva Montasseri, Barbara Rothen-Rutishauser, Alke Petri-Fink
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引用次数: 0

摘要

脂质纳米颗粒的发展已经导致了递送系统既保护被封装的药物,又改善了治疗结果。当引入体内时,纳米颗粒迅速被生物分子电晕覆盖,影响其生物学命运,即与细胞的相互作用、摄取和细胞内命运。本研究探讨了非层状脂质药物传递系统与复杂细胞培养基中非脂溶成分之间的相互作用,重点研究了电晕的动态形成及其对脂质纳米颗粒行为的影响。单甘油酯配方监测纳米结构和粒度的变化,并阐明了这些变化的机制。这些生物大分子不仅影响纳米颗粒本身的大小和结构,而且它们可以同时扩散到中间相纳米结构中。该研究强调,脂质纳米颗粒在复杂细胞培养基中受吸附蛋白质和其他非降解成分影响的生理条件下发生动态变化,而不是由脂肪酶或其他酶促因子引起的影响。这些诱导的结构转变可以显著改变纳米颗粒的物理性质和药物释放谱,可能导致其预期治疗性能的偏离。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输送系统的设计和功能至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intermolecular Dynamics of Monoglyceride Mesophases with Their Biomacromolecular Corona.

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.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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