Engineering extracellular vesicles mimetics for targeted chemotherapy of drug-resistant ovary cancer

Aim: To develop nanocarriers for targeting the delivery of chemotherapeutics to overcome multidrug-resistant ovarian cancer. Materials & methods: Doxorubicin-loaded nanovesicles were obtained through serial extrusion, followed by loading of P-glycoprotein siRNA and folic acid. The targeting ability and anticancer efficacy of the nanovesicles were evaluated. Results: The doxorubicin-loaded nanovesicles showed a high production yield. The presence of P-glycoprotein siRNA and folic acid resulted in reversed drug resistance and tumor targeting. This nanoplatform tremendously inhibited the viability of multidrug-resistant ovarian cancer cells, which was able to target tumor tissue and suppress tumor growth without adverse effects. Conclusion: These bioengineered nanovesicles could serve as novel extracellular vesicles mimetics for chemotherapeutics delivery to overcome multidrug resistance.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:19

Enthalten in:

Nanomedicine (London, England) - 19(2024), 1 vom: 19. Jan., Seite 25-41

Sprache:

Englisch

Beteiligte Personen:

Liu, Xiaoguang [VerfasserIn]
Liu, Guangquan [VerfasserIn]
Mao, Yinghua [VerfasserIn]
Luo, Jie [VerfasserIn]
Cao, Yongping [VerfasserIn]
Tan, Weilong [VerfasserIn]
Li, Wenhao [VerfasserIn]
Yu, Huanhuan [VerfasserIn]
Jia, Xuemei [VerfasserIn]
Li, Hong [VerfasserIn]

Links:

Volltext

Themen:

80168379AG
935E97BOY8
ATP Binding Cassette Transporter, Subfamily B
ATP Binding Cassette Transporter, Subfamily B, Member 1
Doxorubicin
Drug Carriers
Drug-delivery system
Engineering nanovesicles
Extracellular vesicles-mimetics
Folic Acid
Journal Article
Multidrug resistance
RNA, Small Interfering
RNAi
Research Support, Non-U.S. Gov't
Targeting therapy

Anmerkungen:

Date Completed 22.01.2024

Date Revised 19.04.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.2217/nnm-2023-0289

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM365503681