Mohsin Mohammed E Ali, Siddiqa Akhtar Jahan, Mousa Suleiman, Shrivastava Nilesh Kumar
Department of Chemical Engineering, College of Engineering, King Faisal University, P.O. Box 400, Al Ahsa 31982, Saudi Arabia.
Materials Science Centre, Indian Institute of Technology, Kharagpur 721302, West Bengal, India.
Polymers (Basel). 2025 Apr 8;17(8):999. doi: 10.3390/polym17080999.
This study presents a hybrid hydrogel system designed for the targeted delivery of letrozole, a key therapeutic agent in breast cancer treatment. Letrozole-loaded poly(lactic-co-glycolic acid) (PLGA) microparticles were embedded within a poly(2-hydroxyethyl methacrylate) (pHEMA) matrix coated onto acrylamide-grafted low-density polyethylene (AAm-g-LDPE), yielding a mechanically stable system with tunable drug release. Field emission scanning electron microscopy (FE-SEM) and confocal microscopy confirmed uniform microparticle distribution. In vitro release studies in simulated uterine fluid (SUF) at 37 °C demonstrated a sustained release profile over 32 days, with a reduced initial burst effect (~15% lower than conventional PLGA systems). The system's release kinetics followed the Higuchi model ( = 0.803-0.996), indicating Fickian diffusion. This hybrid hydrogel offers enhanced drug stability, reduced dosing frequency, and potential for personalized hormone therapy, improving patient compliance, particularly for individuals with physical or cognitive impairments.
本研究提出了一种用于靶向递送来曲唑的混合水凝胶系统,来曲唑是乳腺癌治疗中的一种关键治疗药物。负载来曲唑的聚(乳酸 - 乙醇酸)(PLGA)微粒被嵌入涂覆在丙烯酰胺接枝的低密度聚乙烯(AAm - g - LDPE)上的聚(甲基丙烯酸2 - 羟乙酯)(pHEMA)基质中,从而产生一种具有可调药物释放的机械稳定系统。场发射扫描电子显微镜(FE - SEM)和共聚焦显微镜证实了微粒分布均匀。在37°C的模拟子宫液(SUF)中进行的体外释放研究表明,在32天内呈现持续释放曲线,初始突释效应降低(比传统PLGA系统低约15%)。该系统的释放动力学遵循Higuchi模型( = 0.803 - 0.996),表明为菲克扩散。这种混合水凝胶提高了药物稳定性,减少了给药频率,并具有个性化激素治疗的潜力,改善了患者的依从性,特别是对于有身体或认知障碍的个体。