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Preparation of transferrin-targeted temozolomide nano-micelles and their anti-glioma effect.
- Source :
-
PeerJ [PeerJ] 2024 Sep 13; Vol. 12, pp. e17979. Date of Electronic Publication: 2024 Sep 13 (Print Publication: 2024). - Publication Year :
- 2024
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Abstract
- Objectives: This study aims to develop brain-targeted temozolomide (TMZ) nanograins using the biodegradable polymer material PEG-PLA as a carrier. The model drug TMZ was encapsulated within the polymer using targeted nanotechnology. Key characteristics such as appearance, particle size, size distribution, drug loading capacity, in vitro release rate, stability, and anti-tumor effects were systematically evaluated through in vitro experiments.<br />Methods: Transmission electron microscopy (TEM) and Malvern size analyzer were employed to observe the morphological and particle size features of the TMZ nanospheres at various time points to assess stability. The effects of TMZ nanograins on glioma cell viability and apoptosis were evaluated using MTT assays and flow cytometry.<br />Results: The targeted TMZ nano-micelles were successfully synthesized. After loading and targeted modifications, the particle size increased from 50.7 to 190 nm, indicating successful encapsulation of TMZ. The average particle size of the nano-micelles remained stable around 145 ± 10 nm at 1 day, 15 days, and 30 days post-preparation. The release rate of the nano-micelles was monitored at 2 h, 12 h, 24 h, and 48 h post-dialysis, ultimately reaching 95.8%. Compared to TMZ alone, the TMZ-loaded PEG-PLA nano-micelles exhibited enhanced cytotoxicity and apoptosis in glioma cells. This was accompanied by increased mitochondrial membrane potential and reactive oxygen species (ROS) levels following treatment with the TMZ nano-micelles.<br />Conclusions: TMZ-loaded nano-micelles demonstrated a gradual release profile and significantly enhanced inhibitory effects on human glioma U251 cells compared to TMZ alone. The findings suggest that TMZ-loaded PEG-PLA nano-micelles may offer a more effective therapeutic approach for glioma treatment.<br />Competing Interests: The authors declare that they have no competing interests.<br /> (© 2024 Yu and Xue.)
- Subjects :
- Humans
Cell Line, Tumor
Transferrin chemistry
Drug Carriers chemistry
Cell Survival drug effects
Brain Neoplasms drug therapy
Brain Neoplasms pathology
Brain Neoplasms metabolism
Reactive Oxygen Species metabolism
Nanoparticles chemistry
Polyesters chemistry
Temozolomide pharmacology
Temozolomide chemistry
Glioma drug therapy
Glioma pathology
Glioma metabolism
Micelles
Polyethylene Glycols chemistry
Polyethylene Glycols pharmacology
Apoptosis drug effects
Antineoplastic Agents, Alkylating pharmacology
Antineoplastic Agents, Alkylating chemistry
Particle Size
Subjects
Details
- Language :
- English
- ISSN :
- 2167-8359
- Volume :
- 12
- Database :
- MEDLINE
- Journal :
- PeerJ
- Publication Type :
- Academic Journal
- Accession number :
- 39285923
- Full Text :
- https://doi.org/10.7717/peerj.17979