Examples of Tumor Growth Inhibition Properties of Liposomal Formulations of pH-Sensitive Histidinylated Cationic Amphiphiles

被引:10
|
作者
Garu, Arup [1 ]
Moku, Gopikrishna [1 ,3 ]
Gulla, Suresh Kumar [1 ,3 ]
Pramanik, Dipankar [1 ]
Majeti, Bharat K. [1 ]
Karmali, Priya P. [1 ]
Shaik, Haseena [1 ]
Sreedhar, Bojja [2 ]
Chaudhuri, Arabinda [1 ,3 ]
机构
[1] CSIR Indian Inst Chem Technol, Biomat Grp, Hyderabad 500007, Andhra Pradesh, India
[2] CSIR Indian Inst Chem Technol, Inorgan & Phys Chem Div, Hyderabad 500007, Andhra Pradesh, India
[3] Acad Sci & Innovat Res, Madras 600113, Tamil Nadu, India
来源
关键词
endosomal pH-sensitive lipids; histidinylated cationic amphiphiles; cancer cell selective cytoxicity; anti-cancer liposomes; mitochondrial membrane depolarization; IN-VIVO; DELIVERY-SYSTEM; MEMBRANE-FUSION; SIRNA DELIVERY; GENE DELIVERY; LIVING CELLS; LIPIDS; NANOPARTICLES; DOXORUBICIN; INTERFERENCE;
D O I
10.1021/acsbiomaterials.5b00025
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Herein we report on the unexpected cancer cell selective cytotoxicities of the liposomal formulations of aspartic and glutamic acid backbone-based four novel lipids with endosomal pH-sensitive head-groups and aliphatic n-hexadecyl & n-octadecyl hydrophobic tails. Surprisingly, although the formulations killed cancer cells efficiently, they were significantly less cytotoxic in non-cancerous healthy cells. Importantly, intratumoral administration of the liposomal formulations efficiently inhibited growth of melanoma in a syngeneic C57BL/6J mouse tumor model. Western Blotting experiments with the lysates of liposomes treated cancer cells revealed that liposomes of lipids 1-4 induce apoptosis selectively in cancer cells presumably by releasing cytochrome c from depolarized mitochondria and subsequent activation of caspases 3 & 9, upregulation of Box and down regulation of Bcl-2. In summary, the present report describes for the first time tumor growth inhibition properties of the liposomal formulations of endosomal pH-sensitive histidinylated cationic lipids under both in vitro and systemic settings.
引用
收藏
页码:646 / 655
页数:10
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