Nanoassemblies with Gd-chelating lipids (GMO@DTPA-BSA-Gd) as a potential new type of high molecular weight contrast agents.

Karolina Dydak, Tomasz Zalewski, Marek Kempka, Patryk Florczak, Grzegorz Nowaczyk, Łucja Przysiecka, Jakub Jagielski, Benoit Loppinet, Michał Banaszak, Dorota Flak
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Abstract

Self-assembled lipid nanoparticles containing Gd-chelating lipids are a new type of positive magnetic resonance imaging contrast agents (MRI CAs). High molecular weight imposes reduced molecular reorientation (τr) and corresponding longer reorientation correlation times (τc), finally resulting in overall high relaxivity (r1) of such contrast agents. Therefore, we report nanoassemblies based on two types of amphiphile molecules: glyceryl monooleate (GMO) as a matrix embedded with DTPA-bis(stearylamide) and its gadolinium salt (DTPA-BSA-Gd) as a Gd-chelating lipid, stabilized by surfactant Pluronic F127 molecules. The loading of DTPA-BSA-Gd into the GMO matrix was investigated at low (5% w/w) and high (30, 40, 50% w/w) contents. Small angle X-ray scattering (SAXS), cryogenic transmission electron microscopy (cryo-TEM) and dynamic light scattering (DLS) results show that although the nanoassembly of both amphiphile molecules within the nanoparticle is disturbed in terms of the formed phases, this composition ensures their colloidal stability. In nanoparticles with low DTPA-BSA-Gd contents, the assembly results in a cubic diamond phase that is co-existing with a fraction of liposomes. For high DTPA-BSA-Gd contents, swelling of the structure occurs such that the initially formed primitive cubic phase transforms toward a lamellar phase in the nanoassemblies. Results from inductively coupled plasma mass spectrometry (ICP-MS) indicate that for almost all systems, the loading efficiency (LE) of DTPA-BSA-Gd is high (reaching up to approx. 85%), and the nanoassembly provides strong entrapment of Gd3+ ions, which are then efficiently uptaken by cells. Moreover, the higher the surfactant content, the higher the LE. The viability studies demonstrate that the prepared nanoassemblies preserve high biocompatibility towards both cancer (HeLa) and normal cells (MSU 1.1). Nuclear magnetic resonance relaxometry studies (NMR relaxometry) followed by MRI on the prepared nanoassembly dispersions proved that the formation of GMO@DTPA-BSA-Gd nanoassemblies, considered as high molecular weight CAs, results in high relaxivity parameters (e.g., r1 = 19.72 mM-1 s-1 for 2GMO-40DTPA-10F127) that are superior to commercially developed ones (e.g., Magnevist or Gadovist). These comprehensive studies imply that a high degree of internal ordering of nanoassemblies with a higher content of Gd-chelating lipid is not a decisive factor in determining the increase in relaxivity, thus confirming their potential as positive MRI CAs.

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具有钆螯合脂质(GMO@DTPA-BSA-Gd)的纳米组合物,作为一种潜在的新型高分子量造影剂。
含有钆螯合脂质的自组装脂质纳米粒子是一种新型的正磁共振成像造影剂(MRI CAs)。高分子量会降低分子的重新定向(τr),并相应延长重新定向相关时间(τc),最终导致此类造影剂的整体弛豫度(r1)较高。因此,我们报告了基于两种双亲分子的纳米组合:以单油酸甘油酯(GMO)为基质,嵌入 DTPA-双(硬脂酰胺)及其钆盐(DTPA-BSA-Gd)作为钆螯合脂,并由表面活性剂 Pluronic F127 分子稳定。研究了 DTPA-BSA-Gd 在 GMO 基质中的低含量(5% w/w)和高含量(30、40、50% w/w)情况。小角 X 射线散射(SAXS)、低温透射电子显微镜(cryo-TEM)和动态光散射(DLS)结果表明,虽然纳米粒子内两种双亲分子的纳米组装在形成相方面受到干扰,但这种组成确保了它们的胶体稳定性。在 DTPA-BSA-Gd 含量较低的纳米颗粒中,组装形成的立方钻石相与部分脂质体共存。在 DTPA-BSA-Gd 含量较高的情况下,结构会发生膨胀,使最初形成的原始立方相转变为纳米集合体中的片状相。电感耦合等离子体质谱法(ICP-MS)的结果表明,几乎在所有体系中,DTPA-BSA-Gd 的装载效率(LE)都很高(高达约 85%),纳米组合体能强力吸附 Gd3+ 离子,然后被细胞有效吸收。此外,表面活性剂含量越高,LE 值越高。存活率研究表明,制备的纳米组装体对癌细胞(HeLa)和正常细胞(MSU 1.1)都具有很高的生物相容性。核磁共振弛豫测定法(NMR relaxometry)研究以及对制备的纳米组装分散体进行的核磁共振成像(MRI)证明,GMO@DTPA-BSA-Gd 纳米组装体的形成(被认为是高分子量 CAs)导致了高弛豫参数(例如,2GMO-40DTPA-10F127 的 r1 = 19.72 mM-1 s-1),优于商业开发的产品(例如 Magnevist 或 Gadovist)。这些综合研究表明,钆螯合脂含量较高的纳米组合体的高度内部有序性并不是决定弛豫性增加的决定性因素,从而证实了它们作为正磁共振成像 CA 的潜力。
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来源期刊
Journal of materials chemistry. B
Journal of materials chemistry. B 化学科学, 工程与材料, 生命科学, 分析化学, 高分子组装与超分子结构, 高分子科学, 免疫生物学, 免疫学, 生化分析及生物传感, 组织工程学, 生物力学与组织工程学, 资源循环科学, 冶金与矿业, 生物医用高分子材料, 有机高分子材料, 金属材料的制备科学与跨学科应用基础, 金属材料, 样品前处理方法与技术, 有机分子功能材料化学, 有机化学
CiteScore
12.00
自引率
0.00%
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0
审稿时长
1 months
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