Cui Xueqing, Wang Xiaoli, Xu Xiaohuan, Xu Bang, Sun Jihong, Bai Shiyang
Beijing Key Laboratory for Green Catalysis and Separation, Beijing University of Technology, Beijing 100124, China.
Polymers (Basel). 2023 Jan 24;15(3):596. doi: 10.3390/polym15030596.
The pH-responsive fluorescent P(1,8-naphthalic anhydride (NA)-acrylic acid (AA)) matrix was successfully prepared by a doping method using poly(acrylic acid) (PAA) as a pH-sensitive polymer and NA as a fluorescent tracer. The fluorescent behaviors of the used NA dispersed in PAA frameworks were demonstrated based on fractal features combined with various characterizations, such as small-angle X-ray scattering (SAXS) patterns, photoluminescence (PL) spectra, scanning electron microscope (SEM) images, thermogravimetry (TG) profiles, Fourier transform infrared (FT-IR) spectroscopy, and time-resolved decays. The effects of NA-doping on the representative fluorescent P(NA-AA) were investigated, in which the fluorescent performance of the doped NA was emphasized. The results indicated that aggregated clusters of the doped NA were gradually serious with an increase in NA doping amount or extension of NA doping time, accompanied by an increase in mass fractal dimension () values. Meanwhile, the doped NA presented stable fluorescent properties during the swelling-shrinking process of PAA. Ibuprofen (IBU) was used as a model drug, and fractal evolutions of the obtained P(NA-AA) along with the drug loading and releasing behaviors were evaluated via SAXS patterns, in which the drug-loaded P(NA-AA) presented surface fractal ( characteristics, while the value varied from 2.94 to 2.58 during sustained drug-release in pH 2.0, indicating occurrences of its structural transformation from dense to loose with extension of IBU-releasing time. Finally, the cytotoxicity and cellular uptake behaviors of the obtained P(NA-AA) were preliminarily explored. These demonstrations revealed that the resultant P(NA-AA) should be a potential intelligent-responsive drug carrier for targeted delivery.
通过掺杂法,以聚丙烯酸(PAA)作为pH敏感聚合物、1,8-萘二甲酸酐(NA)作为荧光示踪剂,成功制备了pH响应型荧光P(1,8-萘二甲酸酐(NA)-丙烯酸(AA))基质。基于分形特征并结合各种表征手段,如小角X射线散射(SAXS)图谱、光致发光(PL)光谱、扫描电子显微镜(SEM)图像、热重分析(TG)曲线、傅里叶变换红外(FT-IR)光谱和时间分辨衰减,证明了分散在PAA骨架中的所用NA的荧光行为。研究了NA掺杂对代表性荧光P(NA-AA)的影响,其中强调了掺杂NA的荧光性能。结果表明,随着NA掺杂量的增加或NA掺杂时间的延长,掺杂NA的聚集簇逐渐严重,同时质量分形维数()值增加。同时,掺杂NA在PAA的溶胀-收缩过程中表现出稳定的荧光特性。以布洛芬(IBU)为模型药物,通过SAXS图谱评估了所得P(NA-AA)的分形演化以及药物负载和释放行为,其中载药P(NA-AA)呈现表面分形(特征,而在pH 2.0的持续药物释放过程中,值从2.94变化到2.58,表明随着IBU释放时间的延长,其结构从致密转变为疏松。最后,初步探索了所得P(NA-AA)的细胞毒性和细胞摄取行为。这些证明表明,所得P(NA-AA)应该是一种潜在的用于靶向递送的智能响应型药物载体。