Submit Manuscript  

Article Details


A Novel Long-circulating DOX Liposome: Formulation and Pharmacokinetics Studies

[ Vol. 8 , Issue. 5 ]

Author(s):

Peihong Xiao, Juan Zhao, Yi Huang, Rongrong Jin, Zhonglan Tang, Ping Wang, Xu Song*, Hongfei Zhu *, Zibin Yang and Nie Yu   Pages 391 - 398 ( 8 )

Abstract:


Background: Doxorubicin (DOX) is a leading chemotherapeutic in cancer treatment because of its high potency and broad spectrum. Liposomal doxorubicin (Doxil®) is the first FDA-approved PEG-liposomes of DOX for the treatment of over 600,000 cancer patients, and it can overcome doxorubicin-induced cardiomyopathy and other side effects and prolong life span. The addition of MPEG2000-DSPE could elevate the total cost of cancer treatment.

Objective: We intended to prepare a novel DOX liposome that was prepared with inexpensive materials egg yolk lecithin and Kolliphor HS15, thus allowing it to be much cheaper for clinical application.

Methods: DOX liposomes were prepared using the combination of thin-film dispersion ultrasonic method and ammonium sulfate gradient method and the factors that influenced formulation quality were optimized. After formulation, particle size, entrapment efficiency, drug loading, stability, and pharmacokinetics were determined.

Results: DOX liposomes were near-spherical morphology with the average size of 90 nm and polydispersity index (PDI) of less than 0.30. The drug loading was up to 7.5%, and the entrapment efficiency was over 80%. The pharmacokinetic studies showed that free DOX could be easily removed and the blood concentration of free DOX group was significantly lower than that of DOX liposomes, which indicated that the novel DOX liposome had a certain sustainedrelease effect.

Conclusion: In summary, DOX liposome is economical and easy-prepared with prolonged circulation time.

Lay Summary: Doxorubicin (DOX) is a leading chemotherapeutic in cancer treatment because of its high potency and broad spectrum. Liposomal doxorubicin (Doxil®) is the first FDAapproved PEG-liposomes of DOX to treat over 600.000 cancer patients, overcoming doxorubicin- induced cardiomyopathy and other side effects and prolonging life span. The addition of MPEG2000-DSPE could elevate the total cost of cancer treatment. We intend to prepare a novel DOX liposome prepared with inexpensive materials egg yolk lecithin and Kolliphor HS15, thus allowing it to be much cheaper for clinical use. The novel DOX liposome is economical and easy-prepared with prolonged circulation time.

Keywords:

DOX liposome, drug loading, entrapment efficiency, Kolliphor HS15, particle size, pharmacokinetics.

Affiliation:

College of Pharmacy and Chemistry, Dali University, Dali 671000, Yunnan Province, Institute of Regulatory Science for Medical Devices, National Engineering Research Center for Bio-materials, Sichuan University, No. 29 Wangjiang Road, Chengdu 610064, Institute of Regulatory Science for Medical Devices, National Engineering Research Center for Bio-materials, Sichuan University, No. 29 Wangjiang Road, Chengdu 610064, Institute of Regulatory Science for Medical Devices, National Engineering Research Center for Bio-materials, Sichuan University, No. 29 Wangjiang Road, Chengdu 610064, Institute of Regulatory Science for Medical Devices, National Engineering Research Center for Bio-materials, Sichuan University, No. 29 Wangjiang Road, Chengdu 610064, Institute of Regulatory Science for Medical Devices, National Engineering Research Center for Bio-materials, Sichuan University, No. 29 Wangjiang Road, Chengdu 610064, Institute of Regulatory Science for Medical Devices, National Engineering Research Center for Bio-materials, Sichuan University, No. 29 Wangjiang Road, Chengdu 610064, Beibei Traditional Chinese Medical Hospital, No. 380 Jiangjun Road, Chongqing 400700, College of Pharmacy and Chemistry, Dali University, Dali 671000, Yunnan Province, Institute of Regulatory Science for Medical Devices, National Engineering Research Center for Bio-materials, Sichuan University, No. 29 Wangjiang Road, Chengdu 610064

Graphical Abstract:



Read Full-Text article