Behl Chandandeep Kaur, Thakur Archana
Chemistry Department, Chandigarh University, Mohali, Punjab 140413, India.
ACS Omega. 2025 Mar 25;10(13):12856-12871. doi: 10.1021/acsomega.4c04376. eCollection 2025 Apr 8.
This study reports a novel ibuprofen (IBU) drug delivery system using a chromium-trithiocyanuric acid metal-organic framework (Cr-MOF) encapsulated with a biodegradable, nontoxic carboxymethyl cellulose (CMC) for sustained release of ibuprofen (IBU) drug. The chromium metal-organic framework (MOF) was synthesized via the solvothermal method in a mixture of solvents in acidic conditions, followed by loading with the ibuprofen drug (Cr-MOF@IBU). Cr-MOF@IBU was further encapsulated with the CMC polymer and cross-linked with ferric chloride to form CMC/Cr-MOF@IBU hydrogel beads. Different characterization techniques were used, such as FT-IR, field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), BET, and UV-vis spectroscopy, to confirm the successful synthesis and drug loading. pH responsiveness of CMC/Cr-MOF@IBU hydrogel beads demonstrated by the swelling studies confirmed the optimal swelling in a mimicked gastrointestinal environment. The BET analysis further confirmed a significant decrease in surface area after drug loading. An in vitro drug delivery study indicated that controlled and sustained drug delivery was important for better efficacy and reducing the side effects of the drug. The cytotoxicity studies of A549 cell lines revealed the improved biocompatibility and lower toxicity of encapsulated CMC/Cr-MOF@IBU compared to Cr-MOF. This study highlights the potential of CMC/Cr-MOF@IBU as an efficient and effective drug delivery vehicle for the sustained and controlled release of ibuprofen.
本研究报道了一种新型布洛芬(IBU)药物递送系统,该系统使用包裹有可生物降解、无毒羧甲基纤维素(CMC)的三硫氰尿酸铬金属有机框架(Cr-MOF)来实现布洛芬(IBU)药物的缓释。铬金属有机框架(MOF)通过溶剂热法在酸性条件下于混合溶剂中合成,随后负载布洛芬药物(Cr-MOF@IBU)。Cr-MOF@IBU进一步用CMC聚合物包裹,并与氯化铁交联形成CMC/Cr-MOF@IBU水凝胶珠。使用了不同的表征技术,如傅里叶变换红外光谱(FT-IR)、场发射扫描电子显微镜(FE-SEM)、能量色散X射线光谱(EDX)、X射线衍射(XRD)、比表面积分析(BET)和紫外可见光谱,以确认成功合成和药物负载。通过溶胀研究证明的CMC/Cr-MOF@IBU水凝胶珠的pH响应性证实了其在模拟胃肠道环境中的最佳溶胀。BET分析进一步证实了药物负载后表面积显著减小。体外药物递送研究表明,控释和缓释对于提高药物疗效和减少药物副作用很重要。对A549细胞系的细胞毒性研究表明,与Cr-MOF相比,包裹的CMC/Cr-MOF@IBU具有更好的生物相容性和更低的毒性。本研究突出了CMC/Cr-MOF@IBU作为一种高效的药物递送载体用于布洛芬持续和控释的潜力。