Polyethylene glycol-complexed cationic liposome for enhanced cellular uptake and anticancer activity

2009 ◽  
Vol 382 (1-2) ◽  
pp. 254-261 ◽  
Author(s):  
Suk Hyun Jung ◽  
Soon Hwa Jung ◽  
Hasoo Seong ◽  
Sun Hang Cho ◽  
Kyu-Sung Jeong ◽  
...  
2021 ◽  
Vol 119 ◽  
pp. 111619
Author(s):  
Paul Jänicke ◽  
Claudia Lennicke ◽  
Annette Meister ◽  
Barbara Seliger ◽  
Ludger A. Wessjohann ◽  
...  

2014 ◽  
Vol 114 ◽  
pp. 349-356 ◽  
Author(s):  
Nattika Saengkrit ◽  
Somsak Saesoo ◽  
Wanwisa Srinuanchai ◽  
Sarunya Phunpee ◽  
Uracha Rungsardthong Ruktanonchai

2014 ◽  
Vol 893 ◽  
pp. 194-197
Author(s):  
Yan Liu ◽  
Jie Ren ◽  
Jun Zhao Leng ◽  
Jian Bo Li ◽  
Li Deng

Nanosized calcium phosphate was prepared by a reverse microemulsion method, with a 20~40 nm diameter, which is pH-responsive, nontoxic and colloidally stable in physiological solution. Polyethylene glycol modified calcium phosphate nanoparticles shifted the zeta potential to a neutral charge, which prolonged the nanoparticle circulation time and increased cellular uptake efficacy to targeted cells. The PEG-functionalized nanoparticles exhibit a great potential for efficaciously delivering hydrophobic anticancer drug, such as paclitaxel, to cells and tumors.


2020 ◽  
Vol 49 (23) ◽  
pp. 7977-7992
Author(s):  
János P. Mészáros ◽  
Jelena M. Poljarević ◽  
István Szatmári ◽  
Oszkár Csuvik ◽  
Ferenc Fülöp ◽  
...  

Synthesis and characterization of an 8-hydroxyquinoline–proline hybrid, and its complex formation with half-sandwich organometallic cations: aqueous chemistry, lipophilicity, cellular uptake and anticancer activity.


Nanomedicine ◽  
2021 ◽  
Vol 16 (5) ◽  
pp. 373-389
Author(s):  
Geetha Maniam ◽  
Chun-Wai Mai ◽  
Mohd Zulkefeli ◽  
Ju-Yen Fu

Aim: To synthesize niosomes co-encapsulating gemcitabine (GEM) and tocotrienols, and physicochemically characterize and evaluate the antipancreatic effects of the nanoformulation on Panc 10.05, SW 1990, AsPC-1 and BxPC-3 cells. Materials & methods: Niosomes-entrapping GEM and tocotrienols composed of Span 60, cholesterol and D-α-tocopheryl polyethylene glycol 1000 succinate were produced by Handjani-Vila and film hydration methods. Results: The film hydration produced vesicles measuring 161.9 ± 0.5 nm, approximately 50% smaller in size than Handjani-Vila method, with maximum entrapment efficiencies of 20.07 ± 0.22% for GEM and 34.52 ± 0.10% for tocotrienols. In Panc 10.05 cells, GEM’s antiproliferative effect was enhanced 2.78-fold in combination with tocotrienols. Niosomes produced a significant ninefold enhancement in cytotoxicity of the combination, supported by significantly higher cellular uptake of GEM in the cells. Conclusion: This study is a proof of concept on the synthesis of dual-drug niosomes and their efficacy on pancreatic cancer cells in vitro.


RSC Advances ◽  
2016 ◽  
Vol 6 (46) ◽  
pp. 39896-39902 ◽  
Author(s):  
Lipeng Qiu ◽  
Mengqin Zhu ◽  
Yan Huang ◽  
Kai Gong ◽  
Jinghua Chen

DOX/HM23, based on appropriate DS and proper particle size, presented enhanced anticancer activity and efficient internalization to achieve the highest intracellular drug concentration.


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