Hashimoto Takuya, Hirai Yuji, Yuba Eiji, Harada Atsushi, Kono Kenji
Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Naka-ku, Sakai, Osaka 599-8531, Japan.
J Funct Biomater. 2020 Mar 13;11(1):16. doi: 10.3390/jfb11010016.
Temperature-responsive nanocarrier systems using external stimuli are one of the most widely investigated stimuli-responsive strategies because heat is easy and safe to use for hyperthermia and controlled drug delivery. Polyamidoamine dendron lipids (PAMAM-DLs) composed of PAMAM dendron as head group and two alkyl chains can exhibit temperature-responsive morphological change through the attachment of suitable moieties to terminal of PAMAM dendron. In this study, oligo(ethylene glycol)s including ethoxy- or methoxy-diethylene glycols were attached to the terminals of PAMAM-DL, and temperature-responsive properties of their self-assemblies were evaluated by calorimetric and turbidity measurements. In the evaluation of temperature-responsive properties, ethoxy diethylene glycol (EDEG)-attached PAMAM-DL composed of two saturated alkyl chains and PAMAM dendron with 1st generation had lipid bilayer structure and suitable cloud point for the application as drug carrier. performances of the assemblies combining EDEG-attached PAMAM-DLs with cholesteryl-oxy-poly(ethylene glycol) (PEG-Chol) was evaluated using doxorubicin (DOX) as an anticancer drug. Cellular uptake of DOX-loaded EDEG-attached PAMAM-DL/PEG-Chol assemblies was promoted at 42 °C rather than 37 °C, resulting in an effective decrease in cell viability.
利用外部刺激的温度响应性纳米载体系统是研究最为广泛的刺激响应策略之一,因为热用于热疗和可控药物递送既简便又安全。由聚酰胺 - 胺(PAMAM)树枝状大分子作为头基和两条烷基链组成的聚酰胺 - 胺树枝状脂质(PAMAM - DLs),通过在PAMAM树枝状大分子末端连接合适的基团,可呈现温度响应性形态变化。在本研究中;将包括乙氧基 - 或甲氧基 - 二甘醇的低聚乙二醇连接到PAMAM - DL的末端,并通过量热法和浊度测量评估其自组装体的温度响应特性。在温度响应特性评估中,由两条饱和烷基链和第一代PAMAM树枝状大分子组成的连接乙氧基二甘醇(EDEG)的PAMAM - DL具有脂质双层结构,且浊点适合用作药物载体。以阿霉素(DOX)作为抗癌药物,评估了连接EDEG的PAMAM - DL与胆固醇氧基聚乙二醇(PEG - Chol)组合的组装体的性能。负载DOX的连接EDEG的PAMAM - DL/PEG - Chol组装体在42℃时比在37℃时的细胞摄取量更高,从而有效降低细胞活力。