Codelivery of nivolumab and galunisertib by EGFR-targeted spherical polymeric nanoparticles for effective treatment of non-small cell lung cancer
International Journal of Pharmaceutics, cilt.703, 2026 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 703
- Basım Tarihi: 2026
- Doi Numarası: 10.1016/j.ijpharm.2026.127338
- Dergi Adı: International Journal of Pharmaceutics
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, Chemical Abstracts Core, EMBASE, MEDLINE, Academic Search Ultimate (EBSCO)
- Anahtar Kelimeler: Drug delivery, Galunisertib, Immunotherapy, Nivolumab, NSCLC, PLGA, Polymeric nanoparticles
- Hacettepe Üniversitesi Adresli: Evet
Özet
The incidence of cancer is among the leading causes of death worldwide, with more than 29 million people expected to be diagnosed by 2040. Despite advancements in cancer therapies, current immunotherapeutic approaches face challenges such as limited efficacy and off-target effects. To address these challenges, this study focuses on enhancing the efficacy of immunotherapeutics in the treatment of non-small cell lung cancer (NSCLC) through combination with a TGF-β inhibitor. A novel nanosystem was developed by co-loading galunisertib, a TGF-β inhibitor, and nivolumab, a PD-1 inhibitor, into spherical nanoparticles composed of PLGA derivatives conjugated with anti-EGFR for targeted delivery. In vitro characterization studies, including the nanoparticle size, zeta potential, morphology, drug release, toxicity evaluation in healthy and tumor cells, and T cell immune responses, demonstrated promising results. Based on these findings, in vivo studies were conducted on humanized mice that developed heterotopic xenograft tumors. In the concept of in vivo studies, biodistribution studies revealed that antibody-conjugated nanoparticles exhibited higher tumor accumulation compared to the control group. The targeted co-loaded nanoparticles maintained antitumor activity comparable to the free-drug combination while enabling tumor-directed delivery and showing a more favorable preliminary tolerability profile.