Lea Pašalić, Qiqian Liu, Petra Vukosav, Tea Mišić Radić, Aicha Azziz, Marjan Majdinasab, Mathieu Edely, Marc Lamy de la Chapelle, Danijela Bakarić
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引用次数: 0
摘要
如今,由单胶束和多胶束脂质双分子层(LUV 和 MLV)构成的球形结构不仅被认为是各种治疗药物的纳米载体,而且在与金(Au)纳米粒子(NPs)结合后,还可作为一种成像工具,用于鉴别健康组织和病变组织。由于金纳米粒子或其聚集体的存在可能会影响给药载体的特性,我们研究了吸附在 MLV 表面的金纳米粒子聚集体的形状和位置如何影响脂质分子的排列和构象。通过制备由 1,2-二棕榈酰-sn-甘油-3-磷酸胆碱(DPPC)构成的 MLV,在存在未包覆的 Au NP 聚集体的情况下,我们通过显微技术(冷冻-TEM 和原子力显微镜)证明了脂质双分子层完整性的维持。)利用 SERS 和傅立叶变换红外-ATR 技术,我们不仅能够阐明脂质相互作用模式及其与 Au NP 聚集体的取向,还能明确证实 Au NP 聚集体对 DPPC 碳氢链之间范德华相互作用的持续/断裂的影响。
The presence of uncoated gold nanoparticle aggregates may alter the phase of phosphatidylcholine lipid as evidenced by vibrational spectroscopies.
Spherical structures built from uni- and multilamellar lipid bilayers (LUV and MLV) are nowadays considered not just as nanocarriers of various kinds of therapeutics, but also as the vehicles that, when coupled with gold (Au) nanoparticles (NPs), can also serve as a tool for imaging and discriminating healthy and diseased tissues. Since the presence of Au NPs or their aggregates may affect the properties of the drug delivery vehicle, we investigated how the shape and position of Au NP aggregates adsorbed on the surface of MLV affect the arrangement and conformation of lipid molecules. By preparing MLVs constituted from 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) in the presence of uncoated Au NP aggregates found i) both within liposome core and on the surface of the outer lipid bilayer, or ii) adsorbed on the outer lipid bilayer surface only, we demonstrated the maintenance of lipid bilayer integrity by microscopic techniques (cryo-TEM, and AFM). The employment of SERS and FTIR-ATR techniques enabled us not only to elucidate the lipid interaction pattern and their orientation in regards to Au NP aggregates but also unequivocally confirmed the impact of Au NP aggregates on the persistence/breaking of van der Waals interactions between hydrocarbon chains of DPPC.
期刊介绍:
The Journal of Liposome Research aims to publish original, high-quality, peer-reviewed research on the topic of liposomes and related systems, lipid-based delivery systems, lipid biology, and both synthetic and physical lipid chemistry. Reviews and commentaries or editorials are generally solicited and are editorially reviewed. The Journal also publishes abstracts and conference proceedings including those from the International Liposome Society.
The scope of the Journal includes:
Formulation and characterisation of systems
Formulation engineering of systems
Synthetic and physical lipid chemistry
Lipid Biology
Biomembranes
Vaccines
Emerging technologies and systems related to liposomes and vesicle type systems
Developmental methodologies and new analytical techniques pertaining to the general area
Pharmacokinetics, pharmacodynamics and biodistribution of systems
Clinical applications.
The Journal also publishes Special Issues focusing on particular topics and themes within the general scope of the Journal.