Unveiling the Performance of Co-Assembled Hybrid Nanocarriers: Moving towards the Formation of a Multifunctional Lipid/Random Copolymer Nanoplatform

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmaceutics Pub Date : 2024-09-13 DOI:10.3390/pharmaceutics16091204
Efstathia Triantafyllopoulou, Diego Romano Perinelli, Aleksander Forys, Pavlos Pantelis, Vassilis G. Gorgoulis, Nefeli Lagopati, Barbara Trzebicka, Giulia Bonacucina, Georgia Valsami, Natassa Pippa, Stergios Pispas
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Abstract

Despite the appealing properties of random copolymers, the use of these biomaterials in association with phospholipids is still limited, as several aspects of their performance have not been investigated. The aim of this work is the formulation of lipid/random copolymer platforms and the comprehensive study of their features by multiple advanced characterization techniques. Both biomaterials are amphiphilic, including two phospholipids (1,2-dioctadecanoyl-sn-glycero-3-phosphocholine (DSPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC)) and a statistical copolymer of oligo (ethylene glycol) methyl ether methacrylate (OEGMA) and 2-(diisopropylamino) ethyl methacrylate (DIPAEMA). We examined the design parameters, including the lipid composition, the % comonomer ratio, and the lipid-to-polymer ratio that could be critical for their behavior. The structures were also probed in different conditions. To the best of the authors’ knowledge, this is the first time that P(OEGMA-co-DIPAEMA)/lipid hybrid colloidal dispersions have been investigated from a membrane mechanics, biophysical, and morphological perspective. Among other parameters, the copolymer architecture and the hydrophilic to hydrophobic balance are deemed fundamental parameters for the biomaterial co-assembly, having an impact on the membrane’s fluidity, morphology, and thermodynamics. Exploiting their unique characteristics, the most promising candidates were utilized for methotrexate (MTX) loading to explore their encapsulation capability and potential antitumor efficacy in vitro in various cell lines.
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揭示共组装混合纳米载体的性能:逐步形成多功能脂质/无规共聚物纳米平台
尽管无规共聚物具有吸引人的特性,但这些生物材料与磷脂的结合使用仍然受到限制,因为尚未对其性能的几个方面进行研究。这项工作的目的是配制脂质/无规共聚物平台,并通过多种先进的表征技术对其特性进行全面研究。这两种生物材料都是两亲性的,包括两种磷脂(1,2-双十八酰-sn-甘油-3-磷酸胆碱(DSPC)、1,2-双油酰-sn-甘油-3-磷酸胆碱(DOPC))和一种低聚(乙二醇)甲基醚甲基丙烯酸酯(OEGMA)与 2-(二异丙基氨基)乙基甲基丙烯酸酯(DIPAEMA)的统计共聚物。我们研究了设计参数,包括可能对其行为至关重要的脂质组成、共聚物比例以及脂质与聚合物的比例。我们还在不同条件下对这些结构进行了探测。据作者所知,这是首次从膜力学、生物物理学和形态学角度对 P(OEGMA-co-DIPAEMA)/脂质杂化胶体分散体进行研究。在其他参数中,共聚物结构和亲水与疏水的平衡被认为是生物材料共组装的基本参数,对膜的流动性、形态和热力学都有影响。利用它们的独特特性,最有前途的候选化合物被用于装载甲氨蝶呤(MTX),以探索它们的封装能力和在体外各种细胞系中的潜在抗肿瘤功效。
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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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