Optimizing lornoxicam-loaded poly(lactic-co-glycolic acid) and (polyethylene glycol) nanoparticles for transdermal delivery: ex vivo/in vivo inflammation evaluation.

Rubina Qaiser, Fahad Pervaiz, Sobia Noreen, Hanasul Hanan, Hina Shoukat, Hassan Mahmood, Muhammad Azeem Ashraf
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Abstract

Aim: This study focused on developing a topical gel incorporating lornoxicam-loaded poly(lactic-co-glycolic acid) and polyethylene glycol (PLGA-PEG) blend nanoparticles to mitigate gastrointestinal (GIT) side effects and enhance therapeutic efficacy. Materials & methods: Synthesized nanoparticles were subjected to in vitro characterization, ex vivo permeation studies, and acute oral toxicity analysis post-incorporation into the gel using a S/O/W double emulsion solvent. Results & conclusion: The nanoparticles displayed a smooth, spherical morphology (170-321 nm) with increased entrapment efficiency (96.2%). LOX exhibited a permeation rate of 70-94% from the nanoparticle-infused gel, demonstrating favorable biocompatibility at the cellular level. The formulated gel, enriched with nanoparticles, holds promising prospects for drug-delivery systems and promising improved therapeutic outcomes for LOX.

优化用于透皮给药的洛诺昔康负载聚(乳酸-共-乙醇酸)和(聚乙二醇)纳米颗粒:体内/体外炎症评估。
目的:本研究的重点是开发一种外用凝胶,其中含有洛诺昔康(lornoxicam)负载的聚(乳酸-共-乙醇酸)和聚乙二醇(PLGA-PEG)混合纳米粒子,以减轻胃肠道(GIT)副作用并提高疗效。材料与方法:使用 S/O/W 双乳液溶剂将合成的纳米颗粒加入凝胶后,进行体外表征、体内外渗透研究和急性口服毒性分析。结果与结论:纳米颗粒显示出光滑的球形形态(170-321 nm),并提高了吸附效率(96.2%)。注入纳米颗粒的凝胶中,LOX 的渗透率为 70-94%,显示出良好的细胞生物相容性。富含纳米颗粒的配制凝胶在药物输送系统中具有广阔的前景,有望改善对 LOX 的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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