Therapeutic efficacy of DNA-Loaded PLGA microspheres in tumor-bearing mice

2007 ◽  
Vol 30 (8) ◽  
pp. 1047-1050 ◽  
Author(s):  
Hye-Jung Son ◽  
Jin-Seok Kim
2011 ◽  
Vol 2011 ◽  
pp. 1-10 ◽  
Author(s):  
Ying Wang ◽  
Ke-Chun Wu ◽  
Bing-Xiang Zhao ◽  
Xin Zhao ◽  
Xin Wang ◽  
...  

The purpose of this study was to prepare a novel paclitaxel (PTX) microemulsion containing a reduced amount of Cremophor EL (CrEL) which had similar pharmacokinetics and antitumor efficacy as the commercially available PTX injection, but a significantly reduced allergic effect due to the CrEL. The pharmacokinetics, biodistribution,in vivoantitumor activity and safety of PTX microemulsion was evaluated. The results of pharmacokinetic and distribution properties of PTX in the microemulsion were similar to those of the PTX injection. The antitumor efficacy of the PTX microemulsion in OVCRA-3 and A 549 tumor-bearing animals was similar to that of PTX injection. The PTX microemulsion did not cause haemolysis, erythrocyte agglutination or simulative reaction. The incidence and degree of allergic reactions exhibited by the PTX microemulsion group, with or without premedication, were significantly lower than those in the PTX injection group (P<.01). In conclusion, the PTX microemulsion had similar pharmacokinetics and anti-tumor efficacy to the PTX injection, but a significantly reduced allergic effect due to CrEL, indicating that the PTX microemulsion overcomes the disadvantages of the conventional PTX injection and is one way of avoiding the limitations of current injection product while providing suitable therapeutic efficacy.


Theranostics ◽  
2017 ◽  
Vol 7 (7) ◽  
pp. 1928-1939 ◽  
Author(s):  
Cindy J. Choy ◽  
Xiaoxi Ling ◽  
Jonathan J. Geruntho ◽  
Sophia K. Beyer ◽  
Joseph D. Latoche ◽  
...  

2015 ◽  
Vol 3 (39) ◽  
pp. 7707-7717 ◽  
Author(s):  
Jinyan Lin ◽  
Yanxiu Li ◽  
Yang Li ◽  
Fei Cui ◽  
Fei Yu ◽  
...  

Self-targeted, bacillus-shaped, and controlled-release methotrexate prodrug polymeric nanoparticles for highly efficient cancer chemotherapy: more elongated is better.


2012 ◽  
Vol 28 (5) ◽  
pp. 1736-1742 ◽  
Author(s):  
YA-JEN CHANG ◽  
CHIA-YU YU ◽  
CHIN-WEI HSU ◽  
WAN-CHI LEE ◽  
SU-JUNG CHEN ◽  
...  

2018 ◽  
Vol 58 (3) ◽  
pp. 495-536 ◽  
Author(s):  
Soo-Ling Bee ◽  
Z. A. Abdul Hamid ◽  
M. Mariatti ◽  
B. H. Yahaya ◽  
Keemi Lim ◽  
...  

Biomaterials ◽  
2009 ◽  
Vol 30 (15) ◽  
pp. 2929-2939 ◽  
Author(s):  
So Jin Lee ◽  
Kyeongsoon Park ◽  
Yu-Kyoung Oh ◽  
Seung-Hae Kwon ◽  
Songwook Her ◽  
...  

2019 ◽  
Vol 39 (10) ◽  
pp. 5495-5504
Author(s):  
YI-HSUAN HUNG ◽  
YU-CHUAN LIN ◽  
YU-TING LIN ◽  
GUAN-WEN SHIH ◽  
JIUNN-WANG LIAO ◽  
...  

Pharmaceutics ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 617 ◽  
Author(s):  
Po-Chun Peng ◽  
Ruey-Long Hong ◽  
Tsuimin Tsai ◽  
Chin-Tin Chen

Long-circulating PEG-modified liposome has been shown to improve pharmacokinetic properties and reduce systemic toxicity in cancer treatment. However, drug bioavailability from liposome remains a major challenge to the improvement of its therapeutic efficacy. Previously, we designed a PEGylated dual-effect liposome (named as PL-Dox-Ce6) with chlorin e6 incorporated in the lipid bilayer and Doxorubicin encapsulated in the interior. In this study, another dual-effect liposome with cisplatin encapsulated in the interior was further developed. The pharmacokinetics of these two dual-effect liposomes were studied in tumor-bearing mice. Based on the kinetic data of tumor and plasma, light irradiation was applied onto the tumors at different time points after drug administration to compare the therapeutic efficacy. We demonstrated that a single dose of the dual-effect liposomes combined with two doses of light irradiation can completely eradicate over 90% of the tumor in mice alone with significant survival rate and no toxicity. Thus, this study established a platform that utilizes the dual-effect liposome which combines photodynamic therapy and chemotherapy to improve the therapeutic outcomes of tumors.


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