Preparation of transferrin-targeted temozolomide nano-micelles and their anti-glioma effect.


Journal

PeerJ
ISSN: 2167-8359
Titre abrégé: PeerJ
Pays: United States
ID NLM: 101603425

Informations de publication

Date de publication:
2024
Historique:
received: 20 06 2024
accepted: 06 08 2024
medline: 17 9 2024
pubmed: 17 9 2024
entrez: 17 9 2024
Statut: epublish

Résumé

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, 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. 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. 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.

Identifiants

pubmed: 39285923
doi: 10.7717/peerj.17979
pii: 17979
pmc: PMC11404485
doi:

Substances chimiques

Temozolomide YF1K15M17Y
Micelles 0
Polyethylene Glycols 3WJQ0SDW1A
Antineoplastic Agents, Alkylating 0
Transferrin 0
Drug Carriers 0
Reactive Oxygen Species 0
monomethoxypolyethyleneglycol-polylactide block copolymer 0
Polyesters 0

Banques de données

figshare
['10.6084/m9.figshare.26064226.v1']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e17979

Informations de copyright

© 2024 Yu and Xue.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

Auteurs

Jun Yu (J)

Department of Neurosurgery, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Yonghua Xue (Y)

Department of Neurosurgery, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

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Classifications MeSH