Back to Search Start Over

Novel Tubeimoside I liposomal drug delivery system in combination with gemcitabine for the treatment of pancreatic cancer.

Authors :
Li, Shuhui
Liu, Yuansheng
Sui, Xiaojun
Zhuo, Yuzhen
Siqi, He
Sijia, Zhang
Hui, Zhang
Dihua, Li
Dapeng, Zhang
Lei, Yang
Source :
Nanomedicine; 2024, Vol. 19 Issue 24, p1977-1993, 17p
Publication Year :
2024

Abstract

Aim: To evaluate the anti-pancreatic cancer effect of novel Tubeimoside I multifunctional liposomes combined with gemcitabine. Methods: Liposomes were prepared through the thin film hydration method, with evaluations conducted on parameters including encapsulation efficiency (EE%), particle size, polydispersity index (PDI), zeta potential (ZP), storage stability, and release over a 7-day period. The cellular uptake rate, therapeutic efficacy in vitro and in vivo and the role of immune microenvironment modulation were evaluated. Results: The novel Tubeimoside I multifunctional liposomal exhibited good stability, significant anti-cancer activity, and immune microenvironment remodeling effects. Furthermore, it showed a safety profile. Conclusion: This study underscores the potential of Novel Tubeimoside I multifunctional liposomal as a promising treatment option for pancreatic cancer. Article highlights Tubeimoside I was used instead of cholesterol as the membrane component of liposomes. Tubeimoside I can not only be used as a membrane stabilizer, but also as a chemotherapy adjuvant. Tubeimoside I and gemcitabine have synergistic anti-cancer effects. Tub I-GEM-LPs can reconstruct the immune microenvironment. Tub I-GEM-LPs can improve the hemolysis of Tub I. Tub I-GEM-LPs efficiently promoted tumor cell apoptosis. Tub I-GEM-LPs has better stability and significantly reduced drug leakage rate. These Tub I-GEM-LPs may aid in the treatment of pancreatic cancer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17435889
Volume :
19
Issue :
24
Database :
Complementary Index
Journal :
Nanomedicine
Publication Type :
Academic Journal
Accession number :
180217712
Full Text :
https://doi.org/10.1080/17435889.2024.2382076