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在常规和反向Tetronics®中基于添加剂的热响应性纳米级自组装生成

Additive-anchored thermoresponsive nanoscale self-assembly generation in normal and reverse Tetronics®.

作者信息

Patel Dhruvi, Vaswani Payal, Ray Debes, Bhatia Dhiraj, Aswal Vinod K, Kuperkar Ketan, Bahadur Pratap

机构信息

Department of Chemistry, Sardar Vallabhbhai National Institute of Technology (SVNIT), Ichchhanath, Surat-395 007, Gujarat, India.

School of Civil and Environmental Engineering, Cornell University, Ithaca, 14850, NY, USA.

出版信息

Phys Chem Chem Phys. 2024 Feb 14;26(7):6372-6385. doi: 10.1039/d3cp06329a.

Abstract

Self-assembly of ethylene oxide (EO)-propylene oxide (PO)-based star-shaped block copolymers (BCPs) in the presence of different kinds of additives is investigated in an aqueous solution environment. Commercially available four-armed BCPs, namely Tetronics® (normal: T904 with EO as the terminal end block; and reverse: T90R4 with PO as the terminal end block), each with 40%EO, are used. The effect of various additives such as electrolytes (NaCl and NaSO), nonelectrolyte polyols (glucose and sorbitol), and ionic surfactants ( anionic-sodium dodecyl sulfate (SDS), cationic-dodecyltrimethylammonium bromide (DTAB) and zwitterionic dodecyldimethylammonium propane sulfonate (CPS)) on these BCPs is examined to observe their influence on micellization behaviour. The presence of salts and polyols displayed interesting phase behaviour, , the cloud point (CP) was decreased, the water structure was affected and the micelles were dehydrated by expelling water molecules, and thus they were likely to promote micelle formation/growth. In contrast, ionic surfactants in small amounts interacted with the BCPs and showed an increase in CPs thereby forming mixed micelles with increasing charges and decreasing micellar sizes, finally transforming to small surfactant-rich mixed micelles. Molecular interactions such as electrostatic and hydrogen bonding involved within the examined entities are put forth employing a computational simulation approach using the Gaussian 09 window for calculation along with the GaussView 5.0.9 programming software using the (DFT)/B3LYP method and 3-21G basis set. The hydrodynamic diameter () of the micelles is examined using dynamic light scattering (DLS), while the various micellar parameters inferring the shape/geometry are obtained using small-angle neutron scattering (SANS) by the best fitting of the structure factors. It is observed that 10 w/v% T904 remains as spherical micelles with some micellar growth under physiological conditions (37 °C), while 10 w/v% T90R4 remains as unimers and forms spherical micelles in the presence of additives at 37 °C. Furthermore, the additive-induced micellar systems are tested as developing nanovehicles for anticancer (curcumin, Cur) drug solubilization using UV-vis spectroscopy, which shows a prominent increase in absorbance with enhanced solubilization capacity. Additionally, the cytotoxic effect of Cur loaded on the BCP micelles in HeLa cells is studied through confocal microscopy by capturing fluorescence images that depict HeLa cell growth inhibition under the influence of additive-induced micellar systems.

摘要

在水溶液环境中研究了环氧乙烷(EO)-环氧丙烷(PO)基星形嵌段共聚物(BCP)在不同种类添加剂存在下的自组装行为。使用市售的四臂BCP,即Tetronics®(普通型:以EO为末端嵌段的T904;和反向型:以PO为末端嵌段的T90R4),每种都含有40%的EO。研究了各种添加剂,如电解质(NaCl和NaSO)、非电解质多元醇(葡萄糖和山梨醇)以及离子表面活性剂(阴离子型 - 十二烷基硫酸钠(SDS)、阳离子型 - 十二烷基三甲基溴化铵(DTAB)和两性离子型 - 十二烷基二甲基丙烷磺酸钠(CPS))对这些BCP的影响,以观察它们对胶束化行为的影响。盐和多元醇的存在表现出有趣的相行为,浊点(CP)降低,水结构受到影响,胶束通过排出水分子而脱水,因此它们可能促进胶束的形成/生长。相反,少量的离子表面活性剂与BCP相互作用,导致CP升高,从而形成电荷增加且胶束尺寸减小的混合胶束,最终转变为富含表面活性剂的小混合胶束。使用高斯09窗口进行计算,并结合使用高斯视图5.0.9编程软件,采用(DFT)/B3LYP方法和3 - 21G基组,通过计算模拟方法提出了所研究实体中涉及的静电和氢键等分子相互作用。使用动态光散射(DLS)检测胶束的流体动力学直径( ),同时通过对结构因子进行最佳拟合,使用小角中子散射(SANS)获得推断形状/几何结构的各种胶束参数。观察到10 w/v%的T904在生理条件(37°C)下保持为球形胶束并伴有一些胶束生长,而10 w/v%的T90R4在37°C下在添加剂存在下保持为单分子并形成球形胶束。此外,使用紫外 - 可见光谱测试了添加剂诱导的胶束系统作为开发用于抗癌(姜黄素,Cur)药物增溶的纳米载体,结果表明随着增溶能力的增强吸光度显著增加。此外,通过共聚焦显微镜捕获荧光图像,研究了负载在BCP胶束上的Cur对HeLa细胞的细胞毒性作用,这些图像描绘了添加剂诱导的胶束系统影响下HeLa细胞的生长抑制情况。

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