Ma Hao, Li Wan, Fan Haojun, Xiang Jun
College of Biomass Science and Engineering, Sichuan University, Chengdu 610065, China.
Polymers (Basel). 2023 May 28;15(11):2489. doi: 10.3390/polym15112489.
Photoresponsive polymers hold vast potential in the realm of drug delivery. Currently, most photoresponsive polymers use ultraviolet (UV) light as the excitation source. However, the limited penetration ability of UV light within biological tissues serves as a significant hindrance to their practical applications. Given the strong penetration ability of red light in biological tissues, the design and preparation of a novel red-light-responsive polymer with high water stability, incorporating the reversible photoswitching compound and donor-acceptor Stenhouse adducts (DASA) for controlled drug release is demonstrated. In aqueous solutions, this polymer exhibits self-assembly into micellar nanovectors (~33 nm hydrodynamic diameter), facilitating the encapsulation of the hydrophobic model drug Nile red (NR) within the micellar core. Upon irradiation by a 660 nm LED light source, photons are absorbed by DASA, leading to the disruption of the hydrophilic-hydrophobic balance of the nanovector and thereby resulting in the release of NR. This newly designed nanovector incorporates red light as a responsive switch, successfully avoiding the problems of photodamage and limited penetration of UV light within biological tissues, thereby further promoting the practical applications of photoresponsive polymer nanomedicines.
光响应聚合物在药物递送领域具有巨大潜力。目前,大多数光响应聚合物使用紫外线(UV)作为激发源。然而,紫外线在生物组织中的穿透能力有限,这对其实际应用构成了重大阻碍。鉴于红光在生物组织中具有较强的穿透能力,本文展示了一种新型的具有高水稳定性的红光响应聚合物的设计与制备,该聚合物包含用于可控药物释放的可逆光开关化合物和给体-受体斯滕豪斯加合物(DASA)。在水溶液中,这种聚合物自组装成胶束纳米载体(流体动力学直径约为33 nm),便于将疏水性模型药物尼罗红(NR)包裹在胶束核心内。在660 nm LED光源照射下,光子被DASA吸收,导致纳米载体的亲水-疏水平衡被破坏,从而使NR释放出来。这种新设计的纳米载体将红光作为响应开关,成功避免了紫外线在生物组织中的光损伤和穿透受限问题,进而进一步推动了光响应聚合物纳米药物的实际应用。