| Literature DB >> 31852284 |
Kunho Chung1, Irfan Ullah1,2, Nahyeon Kim1,3, Jaeyeoung Lim1,4, Jungah Shin1,5, Sangah C Lee1,6, Sangmin Jeon7, Sun Hwa Kim7, Priti Kumar2, Sang-Kyung Lee1.
Abstract
Glioblastoma multiforme (GBM) is the most aggressive form of brain tumour and treatment is very challenging. Despite the recent advances in drug delivery systems, various approaches that allow sufficient deposition of anti-cancer drugs within the brain remain unsuccessful due to limited drug delivery throughout the brain. In this study, we utilised an intranasal (IN) approach to allow delivery of anti-cancer drug, encapsulated in PLGA nanoparticles (NPs). PLGA NPs were modified with the RGD ligand to enable Avβ3 expressing tumour-specific delivery. IN delivery of RGD-conjugated-doxorubicin (DOX)-loaded-PLGA-nanoparticles (RGD-DOX-NP) showed cancer-specific delivery of NP and inhibition of brain tumour growth compared to the free-DOX or non-modified DOX-NP in the C6-implanted GBM model. Further, IN treatment with RGD-DOX-NP induces apoptosis in the tumour region without affecting normal brain cells. Our study provides therapeutic evidence to treat GBM using a non-invasive IN approach, which may further be translated to other brain-associated diseases.Entities:
Keywords: Glioblastoma; RGD; intranasal; nanoparticles; targeted delivery
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Year: 2020 PMID: 31852284 DOI: 10.1080/1061186X.2019.1706095
Source DB: PubMed Journal: J Drug Target ISSN: 1026-7158 Impact factor: 5.016