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<p>Glioblastoma multiforme (GBM) remains one of the most lethal primary brain tumors, with limited treatment options and poor patient prognosis. Although temozolomide (TMZ) is the standard chemotherapeutic agent for GBM, its clinical efficacy is severely hindered by rapid systemic clearance, low brain penetration, and non-selective cytotoxicity. In this study, we developed and comparatively evaluated two innovative PLGA-based nanoparticle (NP) systems for oral TMZ delivery, prepared via nanoprecipitation and double emulsion solvent evaporation techniques. Comprehensive physicochemical characterization, including particle size, polydispersity index (PDI), zeta potential (ZP), encapsulation efficiency (EE%), in vitro release kinetics, and solid-state analysis (DSC and FTIR), demonstrated the successful formation of nanosystems with favorable properties. NP1-TMZ (nanoprecipitation) showed superior characteristics, including smaller particle size, narrower size distribution, higher encapsulation efficiency, and more efficient cellular uptake compared to NP2-TMZ (double emulsion). Moreover, cytotoxicity studies in U-87 MG glioblastoma and NIH/3T3 fibroblast cell lines revealed enhanced tumor selectivity and reactive oxygen species (ROS) generation for NP1-TMZ, highlighting its potential for selective tumor targeting. Our results demonstrate that optimized nanoencapsulation significantly improves TMZ delivery, stability, and therapeutic performance, offering a promising strategy for next-generation GBM treatments.</p>

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Preparation and evaluation of temozolomide loaded PLGA nanoparticles for the treatment of glioblastoma multiforme

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年10月16日

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  • Şule Şahin,
  • Elif Kaya-Tilki,
  • Merve Baysal,
  • A. Alper Öztürk

摘要

Glioblastoma multiforme (GBM) remains one of the most lethal primary brain tumors, with limited treatment options and poor patient prognosis. Although temozolomide (TMZ) is the standard chemotherapeutic agent for GBM, its clinical efficacy is severely hindered by rapid systemic clearance, low brain penetration, and non-selective cytotoxicity. In this study, we developed and comparatively evaluated two innovative PLGA-based nanoparticle (NP) systems for oral TMZ delivery, prepared via nanoprecipitation and double emulsion solvent evaporation techniques. Comprehensive physicochemical characterization, including particle size, polydispersity index (PDI), zeta potential (ZP), encapsulation efficiency (EE%), in vitro release kinetics, and solid-state analysis (DSC and FTIR), demonstrated the successful formation of nanosystems with favorable properties. NP1-TMZ (nanoprecipitation) showed superior characteristics, including smaller particle size, narrower size distribution, higher encapsulation efficiency, and more efficient cellular uptake compared to NP2-TMZ (double emulsion). Moreover, cytotoxicity studies in U-87 MG glioblastoma and NIH/3T3 fibroblast cell lines revealed enhanced tumor selectivity and reactive oxygen species (ROS) generation for NP1-TMZ, highlighting its potential for selective tumor targeting. Our results demonstrate that optimized nanoencapsulation significantly improves TMZ delivery, stability, and therapeutic performance, offering a promising strategy for next-generation GBM treatments.