Lipids with negative spontaneous curvature decrease the solubility of the cancer drug paclitaxel in liposomes

IF 1.8 4区 物理与天体物理 Q4 CHEMISTRY, PHYSICAL
Victoria Steffes, Scott MacDonald, John Crowe, Meena Murali, Kai K. Ewert, Youli Li, Cyrus R. Safinya
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Abstract

Paclitaxel (PTX) is a hydrophobic small-molecule cancer drug that loads into the membrane (tail) region of lipid carriers such as liposomes and micelles. The development of improved lipid-based carriers of PTX is an important objective to generate chemotherapeutics with fewer side effects. The lipids 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE) and glyceryl monooleate (GMO) show propensity for fusion with other lipid membranes, which has led to their use in lipid vectors of nucleic acids. We hypothesized that DOPE and GMO could enhance PTX delivery to cells through a similar membrane fusion mechanism. As an important measure of drug carrier performance, we evaluated PTX solubility in cationic liposomes containing GMO or DOPE. Solubility was determined by time-dependent kinetic phase diagrams generated from direct observations of PTX crystal formation using differential-interference-contrast optical microscopy. Remarkably, PTX was much less soluble in these liposomes than in control cationic liposomes containing univalent cationic lipid 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) and 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine (DOPC), which are not fusogenic. In particular, PTX was not substantially soluble in GMO-based cationic liposomes. The fusogenicity of DOPE and GMO is related to the negative spontaneous curvature of membranes containing these lipids, which drives formation of nonlamellar self-assembled phases (inverted hexagonal or gyroid cubic). To determine whether PTX solubility is governed by lipid membrane structure or by local intermolecular interactions, we used synchrotron small-angle X-ray scattering. To increase the signal/noise ratio, we used DNA to condense the lipid formulations into lipoplex pellets. The results suggest that local intermolecular interactions are of greater importance and that the negative spontaneous curvature-inducing lipids DOPE and GMO are not suitable components of liposomal carriers for PTX delivery.

Graphical abstract

Abstract Image

Abstract Image

具有负自发曲率的脂质可降低抗癌药物紫杉醇在脂质体中的溶解度
紫杉醇(PTX)是一种疏水性小分子抗癌药物,可负载于脂质载体(如脂质体和胶束)的膜(尾部)区域。开发改良的 PTX 脂质载体是产生副作用较少的化疗药物的一个重要目标。1,2-二油酰-sn-甘油-3-磷脂乙醇胺(DOPE)和甘油单油酸酯(GMO)这两种脂质具有与其他脂膜融合的倾向,因此被用于核酸的脂质载体。我们推测 DOPE 和 GMO 可通过类似的膜融合机制增强 PTX 向细胞的递送。作为衡量药物载体性能的一个重要指标,我们评估了 PTX 在含有 GMO 或 DOPE 的阳离子脂质体中的溶解度。溶解度是通过使用微分干涉对比光学显微镜直接观察 PTX 晶体形成而生成的随时间变化的动力学相图确定的。值得注意的是,与含有单价阳离子脂质 1,2-二油酰-3-三甲基铵-丙烷(DOTAP)和 1,2-二油酰-sn-甘油-3-磷脂酰胆碱(DOPC)的对照阳离子脂质体相比,PTX 在这些脂质体中的溶解度要低得多,而这些脂质体不产生熔解。特别是,PTX 在基于 GMO 的阳离子脂质体中的溶解度很低。DOPE 和 GMO 的致熔性与含有这些脂质的膜的负自发曲率有关,这种曲率会推动非膜状自组装相(倒六边形或陀螺立方体)的形成。为了确定 PTX 的溶解度是受脂膜结构还是受局部分子间相互作用的影响,我们使用了同步辐射小角 X 射线散射。为了提高信噪比,我们使用 DNA 将脂质配方凝结成脂质颗粒。结果表明,局部分子间的相互作用更为重要,而诱导负自发曲率的脂质 DOPE 和 GMO 并不适合作为输送 PTX 的脂质体载体成分。
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来源期刊
The European Physical Journal E
The European Physical Journal E CHEMISTRY, PHYSICAL-MATERIALS SCIENCE, MULTIDISCIPLINARY
CiteScore
2.60
自引率
5.60%
发文量
92
审稿时长
3 months
期刊介绍: EPJ E publishes papers describing advances in the understanding of physical aspects of Soft, Liquid and Living Systems. Soft matter is a generic term for a large group of condensed, often heterogeneous systems -- often also called complex fluids -- that display a large response to weak external perturbations and that possess properties governed by slow internal dynamics. Flowing matter refers to all systems that can actually flow, from simple to multiphase liquids, from foams to granular matter. Living matter concerns the new physics that emerges from novel insights into the properties and behaviours of living systems. Furthermore, it aims at developing new concepts and quantitative approaches for the study of biological phenomena. Approaches from soft matter physics and statistical physics play a key role in this research. The journal includes reports of experimental, computational and theoretical studies and appeals to the broad interdisciplinary communities including physics, chemistry, biology, mathematics and materials science.
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