Undaria pinnatifida fucoidan nanoparticles loaded with quinacrine attenuate growth and metastasis of pancreatic cancer

被引:22
|
作者
Etman, Samar M. [1 ]
Mehanna, Radwa A. [2 ,3 ]
Bary, Amany Abdel [4 ]
Elnaggar, Yosra S. R. [1 ,5 ]
Abdallah, Ossama Y. [1 ]
机构
[1] Alexandria Univ, Dept Pharmaceut, Fac Pharm, 1 Khartoum Sq,Messalla PO,POB 21521, Alexandria, Egypt
[2] Alexandria Univ, Fac Med, Med Physiol Dept, Alexandria, Egypt
[3] Alexandria Univ, Fac Med, Ctr Excellence Res Regenerat Med & Applicat CERRM, Alexandria, Egypt
[4] Alexandria Univ, Fac Med, Pathol Dept, Alexandria, Egypt
[5] Pharos Univ Alexandria, Dept Pharmaceut, Fac Pharm, Int Publicat & Nanotechnol Ctr INCC, Sidi Gaber, Alexandria Gove, Egypt
关键词
Fucoidan; Undaria pinnatifida; P-selectin; Quinacrine; Pancreatic cancer; Lactoferrin; CELL-LINE; NANOPRECIPITATION METHOD; BIOACTIVE QUINACRINE; BERBERINE CHLORIDE; DRUG-DELIVERY; STEM-CELLS; CYTOTOXICITY; APOPTOSIS; INHIBITION; CA-19-9;
D O I
10.1016/j.ijbiomac.2020.12.109
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pancreatic cancer is a devastating gastrointestinal tumor with limited Chemotherapeutic options. Treatment is restricted by its poor vascularity and dense surrounding stroma. Quinacrine is a repositioned drug with an anticancer activity but suffers a limited ability to reach tumor cells. This could be enhanced using nanotechnology by the preparation of quinacrine-loaded Undaria pinnatifida fucoidan nanopartides. The system exploited fucoidan as both a delivery system of natural origin and active targeting ligand. Lactoferrin was added as a second active targeting ligand. Single and dual-targeted particles prepared through nanoprecipitation and ionic interaction respectively were appraised. Both particles showed a size lower than 200 nm, entrapment efficiency of 80% and a pH-dependent release of the drug in the acidic environment of the tumor. The anticancer activity of quinacrine was enhanced by 5.7 folds in dual targeted particles compared to drug solution with a higher ability to inhibit migration and invasion of cancer. In vivo, these particles showed a 68% reduction in tumor volume compared to only 20% for drug solution. In addition, they showed a higher animals' survival rate with no hepatotoxicity. Hence, these particles could be an effective option for the eradication of pancreatic cancer cells. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:284 / 297
页数:14
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