Laksee Sakchai, Supachettapun Chamaiporn, Muangsin Nongnuj, Lertsarawut Pattra, Rattanawongwiboon Thitirat, Sricharoen Phitchan, Limchoowong Nunticha, Chutimasakul Threeraphat, Kwamman Tanagorn, Hemvichian Kasinee
Nuclear Technology Research and Development Center, Thailand Institute of Nuclear Technology (Public Organization), Nakhon Nayok 26120, Thailand.
Program in Petrochemistry and Polymer Science, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.
Polymers (Basel). 2021 Aug 10;13(16):2670. doi: 10.3390/polym13162670.
This study presented a green, facile and efficient approach for a new combination of targeted gold nanohybrids functionalized with folate-hydrophobic-quaternized pullulan delivering hydrophobic camptothecin (CPT-GNHs@FHQ-PUL) to enhance the efficacy, selectivity, and safety of these systems. New formulations of spherical CPT-GNHs@FHQ-PUL obtained by bio-inspired strategy were fully characterized by TEM, EDS, DLS, zeta-potential, UV-vis, XRD, and ATR-FTIR analyses, showing a homogeneous particles size with an average size of approximately 10.97 ± 2.29 nm. CPT was successfully loaded on multifunctional GNHs@FHQ-PUL via intermolecular interactions. Moreover, pH-responsive CPT release from newly formulated-CPT-GNHs@FHQ-PUL exhibited a faster release rate under acidic conditions. The intelligent CPT-GNHs@FHQ-PUL (IC = 6.2 μM) displayed a 2.82-time higher cytotoxicity against human lung cancer cells (Chago-k1) than CPT alone (IC = 2.2 μM), while simultaneously exhibiting less toxicity toward normal human lung cells (Wi-38). These systems also showed specific uptake by folate receptor-mediated endocytosis, exhibited excellent anticancer activity, induced the death of cells by increasing apoptosis pathway (13.97%), and arrested the cell cycle at the G0-G1 phase. The results of this study showed that the delivery of CPT by smart GNHs@FHQ-PUL systems proved to be a promising strategy for increasing its chemotherapeutic effects.
本研究提出了一种绿色、简便且高效的方法,用于构建一种新型组合的靶向金纳米杂化物,该杂化物用叶酸-疏水-季铵化普鲁兰糖功能化,用于递送疏水性喜树碱(CPT-GNHs@FHQ-PUL),以提高这些系统的疗效、选择性和安全性。通过仿生策略获得的球形CPT-GNHs@FHQ-PUL新制剂通过透射电子显微镜(TEM)、能谱分析(EDS)、动态光散射(DLS)、zeta电位、紫外可见光谱(UV-vis)、X射线衍射(XRD)和衰减全反射傅里叶变换红外光谱(ATR-FTIR)分析进行了全面表征,显示出均匀的颗粒尺寸,平均尺寸约为10.97±2.29纳米。喜树碱通过分子间相互作用成功负载在多功能GNHs@FHQ-PUL上。此外,新配制的CPT-GNHs@FHQ-PUL在酸性条件下表现出更快的pH响应性喜树碱释放速率。智能CPT-GNHs@FHQ-PUL(半数抑制浓度[IC]=6.2μM)对人肺癌细胞(Chago-k1)的细胞毒性比单独的喜树碱(IC=2.2μM)高2.82倍,同时对正常人肺细胞(Wi-38)的毒性较小。这些系统还通过叶酸受体介导的内吞作用表现出特异性摄取,具有优异的抗癌活性,通过增加凋亡途径(13.97%)诱导细胞死亡,并使细胞周期停滞在G0-G1期。本研究结果表明,通过智能GNHs@FHQ-PUL系统递送喜树碱被证明是提高其化疗效果的一种有前景的策略。