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Multi shape memory polymers (multi-SMPs) exhibit many potential applications such as aerospace, soft robotics, and biomedical devices because of their unique abilities. Although many works are done to broaden the preparations of multi-SMPs, the desire to a simple and versatile strategy as well as more complex shapes still exists. Moreover, a light-induced SMP shows more advantages than a thermal-induced one in many practical working circumstances. Herein, inspired by strong adhesion and efficient photothermal conversion of polydopamine (PDA) coating, we report a more simple and facile approach to prepare light-induced multi-SMPs by introducing a gradient PDA coating on a dual-SMP through time-controlled dipping. The photothermal converting properties with varying thicknesses of PDA under the tunable near-infrared light source are investigated. Then, light-induced multishape memory effects based on gradient PDA coatings are illustrated, where three designs of multi-SMPs - rectangle, triangle, and cross are prepared and demonstrated. Also, the evolutions of coating morphology during shape shifting are carefully studied. Finally, we present few complex designs of patterns and shapes as well as a design of potential application for the highly controllable smart devices. This strategy demonstrates a very simple and general strategy to design and prepare the light-induced multi-SMPs with complex shapes based on any thermal-responsive dual-SMPs.

This study was designed to explore the effects and mechanism of isoliensinine (isolie) from embryos of Nelumbo nucifera on type 2 diabetes and dyslipidemia in vivo and in vitro. The in vitro study showed that isolie increased the GLUT4 translocation by 2.5-fold in L6 cells. Furthermore, after 4 weeks of treatment, the in vivo biochemical study indexes revealed that isolie had a positive effect on decreasing serum insulin level (42.2 ± 5.10 vs 55.7 ± 6.33 mU/L, P < 0.05) and reducing fast blood glucose (9.4 ± 1.5 vs 18.7 ± 2.3 mmol/L, P < 0.001) and body weight (37.8 ± 2.9 vs 46.9 ± 5.4 g, P < 0.05) compared with the KK-Ay model mice. Isolie treatment led to significant increases in GLUT4 proteins (∼2.7-fold in skeletal muscle and ∼2.4-fold in WAT) and phosphorylated AMP-activated protein kinase (∼1.4-fold in skeletal muscle, ∼3.1-fold in WAT, and ∼2.3-fold in liver). However, isolie caused a significant decrease in lipogenesis protein expressions of PPARγ and SREBP-1c, and decreased the activity of ACC by increasing the phospho-ACC level. Our findings showed that isolie has the potential to alleviate type 2 diabetes associated with hyperlipidemia in KK-Ay mice. Regulation of GLUT4, SREBP-1c, PPARγ, AMPK phosphorylation, and ACC phosphorylation is implicated in the antidiabetic effects of isolie.