Please wait a minute...

中国生物工程杂志

China Biotechnology
China Biotechnology  2013, Vol. 33 Issue (3): 9-14    DOI:
    
Characterization and the Anti-tumor Effect of Doxorubicin Flexible Liposome in vitro
GUO Chun-fang, ZHANG Yang-de, WANG Ji-wei, PAN Yi-feng, LIAO Ming-mei, WANG Ning
Ministry of Health Hepatobiliary & Enteric Surgery Research Center, Central South University, Changsha 410008, China
Download: HTML   PDF(890KB) HTML
Export: BibTeX | EndNote (RIS)      

Abstract  Objective: To evaluate the potential application of flexible nanoliposomes containing membrane softening agent in intravenous administration by comparing doxorubicin (DOX) load capability and tumor cell inhibition of different nanoliposomes. Methods: Traditional liposomes (DOX-CL) and flexible nanoliposomes (DOX-FNL) were prepared by film hydration method with DOX as a model drug. Encapsulation efficiency of liposomes were investigated by Dextran gel chromatography column method. The hydrodynamic size, zeta potential and polydispersity index (PDI) of liposomes in different pH condition and media were characterised by particle size analyzer. The drug release of two liposomes in vitro were detected with membrane dialysis method. The human breast cancer MCF-7cell viability of two liposomes were investigated with MTT assay. The cell cycle changes of MCF-7 cells induced by DOX-CL and DOX-FNL were detected by flow cytometry. Results The encapsulation efficiency of DOX-FNL was higher than DOX-CL, and the DOX-FNL had more excellent suspension stability in neutral pH conditions, water, physiological saline, PBS and RPMI-1640 culture medium with/without 10% FBS. The release rate of two liposomes was no significant difference (P>0.05) in different pH conditions. The cytotoxic detection results showed that the inhibition of MCF-7 cells was hardly different between DOX-CL and DOX-FNL, while tumor cell killing effect of DOX-FNL was more endurable than DOX-CL(P<0.05). The FCM detection results showed that the cell cycle of MCF-7 arrested in G0/G1 phase by DOX-FNL was similar as the DOX-CL, moreover, DOX-FNL is more effective than DOX-CL(P<0.05). Conclusion DOX-FNL has higher drug encapsulation efficiency and stability than DOX-CL. DOX-FNL can affect the cell cycle, and its drug action time is significantly higher than DOX-CL.

Key wordsDoxorubicin hydrochloride      Flexible nanoliposomes      Breast cancer     
Received: 24 January 2013      Published: 25 March 2013
ZTFLH:  Q54  
Cite this article:

GUO Chun-fang, ZHANG Yang-de, WANG Ji-wei, PAN Yi-feng, LIAO Ming-mei, WANG Ning. Characterization and the Anti-tumor Effect of Doxorubicin Flexible Liposome in vitro. China Biotechnology, 2013, 33(3): 9-14.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2013/V33/I3/9

[1] Mustafa M E, Ossama Y A, Viviane F N, et al. Lipid vesicles for skin delivery of drugs: reviewing three decades of research. International Journal of Pharmaceutics, 2007, 332: 1-16.
[2] Gillet A, Lecomte F, Hubert P, et al. Skin penetration behaviour of liposomes as a function of their composition. European Journal of Pharmaceutics and Biopharmaceutics, 2011, 79: 43-53.
[3] Honeywell N, Arenja, Bouwstra. Skin penetration and mechanisms of action in the delivery of the D2-agonist rotigotine from surfactant-based elastic vesicle formulations. Pharm. Res, 2003, 20: 1619-1625.
[4] Honeywell N, Bouwstra. The in vitro transport of pergolide from surfactant-based elastic vesicles through human skin: a suggested mechanism of action. J. Control. Release, 2003, 86: 145-156.
[5] Zheng W S, Fang X Q, Wang L L, et al. Preparation and quality assessment of itraconazole transfersomes. International Journal of Pharmaceutics, 2012, 436: 291-298.
[6] Pathomthat S, Phensri T, Uracha R, et al. Physico-chemical characteristics of methotrexate-entrapped oleic acid-containing deformable liposomes for in vitro transepidermal delivery targeting psoriasis treatment. International Journal of Pharmaceutics, 2012, 427: 426-434.
[7] Huang Y B, Tsai M J, Wu P C, et al. Elastic liposomes as carriers for oral delivery and the brain distribution of (+)-catechin. Journal of Drug Targeting, 2011, 19(8): 709-718.
[8] Li W Z, Zhou Y Q, Zhao N, et al. Pharmacokinetic behavior and efficiency of acetylcholinesterase inhibition in rat brain after intranasal administration of galanthamine hydrobromide loaded flexible liposomes. Environmental Toxicology and Pharmacology, 2012, 34: 272-279.
[9] Torchilin V P, Weissig V.脂质体.第二版,北京:化学工业出版社,2005:208. Torchilin V P, Weissig V. Liposomes. 2ed. Beijing: Chemical Industry Press, 2005:208.
[10] Kaur I P, Bhandari R, Bhandari S, et al. Potential of solid lipid nanoparticles in brain targeting. J Control Release, 2008, 127: 97-109.
[11] Xie Y, Ye L, Zhang X, et al. Transport of nerve growth factor encapsulated into liposomes across the blood brain barrier: in vitro and in vivo studies. J Control Release, 2005, 105: 106-119.
[1] LU Yu-xiang,LI Yuan,FANG Dan-dan,WANG Xue-bo,YANG Wan-peng,CHU Yuan-kui,YANG Hua. The Role and Expression Regulation of MiR-5047 in the Proliferation and Migration of Breast Cancer Cells[J]. China Biotechnology, 2021, 41(4): 9-17.
[2] Jie XIAN,Xue QIN,You-de CAO. Numb Inhibits the Ubiquitination Degradation of p53 by HDM2 in Triple-negative Breast Cancer[J]. China Biotechnology, 2019, 39(7): 1-7.
[3] Qun WAN,Meng-yao LIU,Jing XIA,Li-yao GOU,Min TANG,Shi-lei SUN,Yan ZHANG. The Effects of LncRNA SNHG3 on the Proliferation, Migration and Invasion of Human Breast Cancer MCF-7 Cells[J]. China Biotechnology, 2019, 39(1): 13-20.
[4] SONG Li-jie, WANG Li, YANG Chuan-hong, LAI Huang-wen, WANG Jie. Effect of Cas9 Protein on Biological and Ultrastructural Characteristics of the Human Bone-seeking Breast Cancer Cell Line[J]. China Biotechnology, 2016, 36(7): 1-6.
[5] LI Yu-qiang, ZHU Zhi-tu, WANG Wei, LI Chen, XU Na, WANG Yu, LI Nan, SUN Hong-zhi. Effect of Silencing Nup88 Gene by RNA Interference on Growth and Invasion in Human Breast Cancer MCF-7 Cell[J]. China Biotechnology, 2014, 34(9): 31-39.
[6] LI Fei-fei, FANG Jing, MA Qiong, FU Hui, MAO Jian-ping. Natural Borneol Liquid Induced Cancer Cells Apoptosis[J]. China Biotechnology, 2013, 33(5): 22-27.
[7] WU Chen, TIAN Huan-na, WANG Yuan-yuan, LIU Fang-ming, ZHANG Xiao-kang, LI Qin-jian, XIE Yuan-yuan. Effect of GALNT14 on the Migration of Human Breast Cancer Cells MCF-7[J]. China Biotechnology, 2012, 32(07): 8-15.
[8] SUN Xiao-xiao, WANG Ke, FENG Hong-lei, LIU Yue-hong, WAN Shao-heng, LUO Jin-yong, ZHANG Yan. Effects and Possible Mechanism of BMP9 on the Bone Metastasis of Human Breast Cancer Cells MDA-MB-231[J]. China Biotechnology, 2012, 32(03): 7-13.
[9] XIE Qiu-ling, LU Jia, LIU Lan, ZHANG Chuan-yu, GUO Xin-yong, PENG Wen-dan, CHEN Xiao-jia. Study of Human PDGFR β Promoter in Different Human Breast Cancer Cells[J]. China Biotechnology, 2011, 31(04): 18-24.
[10] ZHAO Wei, HAN Hai-bo, ZHANG Zhi-qian. The Effects of Human PEX, a C-terminal Hemopexin-like Domain of MMP-2, on the Growth and Metastasis of Human Breast Cancer BICR-H1 Cells[J]. China Biotechnology, 2011, 31(03): 13-17.
[11] XU Liang, GU Yu-Chao, SHI Han, FU Wen-Xi, XU Wen-Gong. STAT3 Silencing Inhibits Migration of Murine Breast Cancer Cells in vitro[J]. China Biotechnology, 2010, 30(06): 1-7.
[12] LIU Hai-Yan- Gu-Yu-Chao- Fu-Wen-Xi- Xu-Wen-Gong. Akt1 Silencing Inhibits Lung Metastasis of Murine Breast Cancer Cells[J]. China Biotechnology, 2009, 29(03): 14-19.
[13] Yu-chao GU . Regulation of gene expression profile by Twist in murine breast cancer cell[J]. China Biotechnology, 2008, 28(4): 1-6.
[14] . Construction of eIF-4e adenovirus and its effect on metastasis ability of human breast cancer cell line MCF-7[J]. China Biotechnology, 2008, 28(3): 8-12.