Kim Yun Kyoung, Kim Eun-Joong, Lim Jae Hyun, Cho Heui Kyoung, Hong Woo Jin, Jeon Hyang Hwa, Chung Bong Geun
Department of Biomedical Engineering, Sogang University, Seoul, 04107, South Korea.
Research Center, Sogang University, Seoul, 04107, South Korea.
Nanoscale Res Lett. 2019 Mar 4;14(1):77. doi: 10.1186/s11671-019-2909-y.
Poly-N-isopropyl acrylamide (PNIPAM) nanogels have been modified with different acrylic acid (AAc) contents for the efficient control of lower critical solution temperature (LCST). In this study, PNIPAM-co-AAc nanogels nanogels showed two volume phase transitions in comparison with PNIPAM. The transition temperature of PNIPAM nanogels was increased with AAc contents. The controlled drug release performance of PNIPAM-co-AAc nanogels loaded with β-lapachone was attributed to the AAc content ratio and was efficiently triggered in response to temperature and pH. Moreover, a colorimetric cell proliferation assay and direct fluorescence-based live/dead staining were used to confirm the concurrence on drug release profiles. Finally, PNIPAM-co-AAc20 showed a relatively low level of drug release in the range of acidic to neutral pH at body temperature, while maximizing drug release at basic pH. Therefore, we demonstrated that the PNIPAM-based nanogel with the temperature- and pH-responsive features could be a promising nanocarrier for potential intestine-specific drug delivery.
聚N-异丙基丙烯酰胺(PNIPAM)纳米凝胶已通过不同丙烯酸(AAc)含量进行改性,以有效控制低临界溶液温度(LCST)。在本研究中,与PNIPAM相比,PNIPAM-共-AAc纳米凝胶显示出两个体积相转变。PNIPAM纳米凝胶的转变温度随AAc含量的增加而升高。负载β-拉帕醌的PNIPAM-共-AAc纳米凝胶的可控药物释放性能归因于AAc含量比,并能响应温度和pH有效地触发释放。此外,采用比色法细胞增殖测定和基于直接荧光的活/死染色来确认药物释放曲线的一致性。最后,PNIPAM-共-AAc20在体温下的酸性至中性pH范围内显示出相对较低的药物释放水平,而在碱性pH下药物释放最大化。因此,我们证明了具有温度和pH响应特性的基于PNIPAM的纳米凝胶可能是一种有前景的纳米载体,用于潜在的肠道特异性药物递送。