The augmented anticancer potential of AP9-cd loaded solid lipid nanoparticles in human leukemia Molt-4 cells and experimental tumor

被引:16
作者
Bhushan, Shashi [1 ]
Kakkar, Vandita [2 ]
Pal, Harish Chandra [3 ]
Mondhe, D. M. [1 ]
Kaur, Indu Pal [2 ]
机构
[1] Indian Inst Integrat Med, CSIR, Canal Rd, Jammu 180001, India
[2] Panjab Univ, Univ Inst Pharmaceut Sci, Chandigarh 160014, India
[3] Univ Alabama Birmingham, Dept Dermatol, Birmingham, AL 35205 USA
关键词
AP9-cd; Cedrus deodara; SLN; Apoptosis; Ehrlich ascites tumor; DRUG-DELIVERY SYSTEMS; HL-60; CELLS; BOSWELLIA-SERRATA; DOXORUBICIN; APOPTOSIS; CANCER; SLN; TRITERPENEDIOL; CYTOTOXICITY; MECHANISMS;
D O I
10.1016/j.cbi.2015.11.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
AP9-cd, a novel lignan composition from Cedrus deodara has significant anticancer potential, and to further enhance its activity, it was lucratively encumbered into solid lipid nanoparticles (SLNs). These nanoparticles were formulated by micro-emulsion technique with 70% drug trap competence. AP9-cd-SLNs were regular, solid, globular particles in the range of 100-200 nm, which were confirmed by electron microscopic studies. Moreover, AP9-cd-SLNs were found to be stable for up to six months in terms of color, particle size, zeta potential, drug content and entrapment. AP9-cd-SLNs have 30-50% higher cytotoxic and apoptotic potential than the AP9-cd alone. The augmented anticancer potential of AP9-cd-SLNs was observed in cytotoxic IC50 value, apoptosis signaling cascade and in Ehrlich ascites tumor (EAT) model. AP9-cd-SLNs induce apoptosis in Molt-4 cells via both intrinsic and extrinsic pathway. Moreover, the dummy nanoparticles (SLNs without AP9-cd) did not have any cytotoxic effect in cancer as well as in normal cells. Consequently, SLNs of AP9-cd significantly augment the apoptotic and antitumor potential of AP9-cd. The present study provides a podium for ornamental the remedial latent via novel delivery systems like solid lipid nanoparticles. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:84 / 93
页数:10
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