Abstract
Neural stem cells (NSCs) present attractive natural drug delivery systems (DDSs). Their migratory potential enables crossing of the blood-brain barrier and efficient and selective accumulation near malignant cells. Here, we present the potential of NSCs as DDSs for nucleoside analogue conjugated nanogels (NGs). Two different approaches were investigated: the intracellular loading and extracellular cell surface decoration with NGs. For both designs, the tumor-specific migratory potentials of NSCs remained unchanged; however, the intracellular loading showed a shorter NG retention. The cell surface decoration protocol yielded a high loading capacity of 100% after 1 h and a prolonged drug retention. A redox-sensitive linker between NGs and the nucleoside analogue 5-ethynyl-2 '-deoxycytidine (EdC) allowed a tumor environment-specific drug release and its efficient and preferential incorporation into the DNA of the tumor cells. Interestingly, the tumor-trafficking potentials of NSCs were significantly potentiated by irradiation of tumor cells. In conclusion, this study indicates the potentials of cell surface-decorated NSCs as DDSs for tumor specific release, cellular uptake, and incorporation of EdC into DNA.
| Original language | English |
|---|---|
| Pages (from-to) | 21792-21803 |
| Number of pages | 12 |
| Journal | ACS Applied Materials & Interfaces |
| Volume | 15 |
| Issue number | 18 |
| DOIs | |
| Publication status | Published - 10 May 2023 |
Keywords
- neural stem cells
- drug delivery
- nanogels
- nucleoside
- glioblastoma
- GLIOBLASTOMA
- BRAIN
- NANOPARTICLES
- EXPRESSION
- TRACKING
- THERAPY
- ANALOGS
- TROPISM
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