Enhanced antitumor efficacy of folate targeted nanoparticles co-loaded with docetaxel and curcumin

被引:15
作者
Hu, Liandong [1 ,2 ]
Pang, Saixi [1 ,2 ]
Hu, Qiaofeng [3 ]
Gu, Deliang [1 ,2 ]
Kong, Dongqian [1 ,2 ]
Xiong, Xiaoyun [4 ]
Su, Jianying [4 ]
机构
[1] Hebei Univ, Sch Pharmaceut Sci, Baoding 071002, Peoples R China
[2] Hebei Univ, Key Lab Pharmaceut Qual Control Hebei Prov, Baoding 071002, Peoples R China
[3] CSPC Pharmaceut Grp NBP Pharmaceut Co Ltd, Shijiazhuang, Peoples R China
[4] Xian Lijun Pharmaceut Ltd Liabil Co, Xian 710000, Peoples R China
关键词
Folate; Docetaxel; Curcumin; Encapsulation; Antitumor activity; SOLID DISPERSION; FOLIC-ACID; DELIVERY; PLGA; CANCER; BIOAVAILABILITY; CHEMOTHERAPY; DENDRIMERS; SILICA; AGENTS;
D O I
10.1016/j.biopha.2015.08.036
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: The current study aimed to investigate whether the novel folate (FT) modified nanoparticles (NPs) co-loaded with docetaxel (DT) and curcumin (CU) (named as FT-NPs) could enhance the delivery efficiency to tumor compared with the NPs without FT (non-targeted NPs). Methods: FT-NPs were successfully formulated in this article. In vitro cytotoxic activity against A549 cells and in vivo antitumor activity of FT-NPs in S180 cell bearing mice were conducted. Cellular uptake test was used to evaluate uptake efficiency of FT-NPs. Histological observation was used to determine the lung security. Besides, the physical chemical properties such as stability, particle size, zeta potential, drug encapsulation efficiency, transmission electron microscopy (TEM) were also conducted. Results: FT-NPs exhibited stronger growth inhibition effects on A549 cells compared with non-targeted NPs, moreover, the novel FT-NPs indicated more effective antitumor efficacy in inhibiting tumor growth. Confocal laser scanning microscopy indicated that the uptake of FT-NPs was facilitated and effective. Histological observation meant that FT-NPs were biocompatible and appropriate for pulmonary administration. Conclusion: These results confirmed that FT-NPs with relatively high drug loading capacity could effectively inhibit tumor growth and reduce toxicity. The novel FT-NPs could produce as an outstanding nanocarrier for the targeted treatment of cancers. (C) 2015 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:26 / 32
页数:7
相关论文
共 22 条
[1]   DOCETAXEL (TAXOTERE(TM)) IS ACTIVE IN NON-SMALL-CELL LUNG-CANCER - A PHASE-II TRIAL OF THE EORTC EARLY CLINICAL-TRIALS GROUP (ECTG) [J].
CERNY, T ;
KAPLAN, S ;
PAVLIDIS, N ;
SCHOFFSKI, P ;
EPELBAUM, R ;
VANMEERBEEK, J ;
WANDERS, J ;
FRANKLIN, HR ;
KAYE, S .
BRITISH JOURNAL OF CANCER, 1994, 70 (02) :384-387
[2]   Folic acid and cell-penetrating peptide conjugated PLGA-PEG bifunctional nanoparticles for vincristine sulfate delivery [J].
Chen, Jianian ;
Li, Shaoshun ;
Shen, Qi .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2012, 47 (02) :430-443
[3]   Multifunctional nanocarrier mediated co-delivery of doxorubicin and siRNA for synergistic enhancement of glioma apoptosis in rat [J].
Cheng, Du ;
Cao, Nuo ;
Chen, Jifeng ;
Yu, Xingsu ;
Shuai, Xintao .
BIOMATERIALS, 2012, 33 (04) :1170-1179
[4]  
Esmaeili F, 2008, J DRUG TARGET, V16, P415, DOI [10.1080/10611860802088630, 10.1080/10611860802088630 ]
[5]   Docetaxel - Review of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy in the management of metastatic breast cancer [J].
Fulton, B ;
Spencer, CM .
DRUGS, 1996, 51 (06) :1075-1092
[6]   Encapsulation of teniposide into albumin nanoparticles with greatly lowered toxicity and enhanced antitumor activity [J].
He, Xinyi ;
Xiang, Nanxi ;
Zhang, Jinjie ;
Zhou, Jing ;
Fu, Yao ;
Gong, Tao ;
Zhang, Zhirong .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2015, 487 (1-2) :250-259
[7]   Improved bioavailability and antiasthmatic efficacy of poorly soluble curcumin-solid dispersion granules obtained using fluid bed granulation [J].
Jang, Dong-Jin ;
Kim, Sung Tae ;
Lee, Kooyeon ;
Oh, Euichaul .
BIO-MEDICAL MATERIALS AND ENGINEERING, 2014, 24 (01) :413-429
[8]   Pharmacokinetics of curcumin-loaded PLGA and PLGA-PEG blend nanoparticles after oral administration in rats [J].
Khalil, Najeh Maissar ;
Frabel do Nascimento, Thuane Castro ;
Casa, Diani Meza ;
Dalmolin, Luciana Facco ;
de Mattos, Ana Cristina ;
Hoss, Ivonete ;
Romano, Marco Aurelio ;
Mainardes, Rubiana Mara .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2013, 101 :353-360
[9]   Enhanced systemic exposure of saquinavir via the concomitant use of curcumin-loaded solid dispersion in rats [J].
Kim, Su-A ;
Kim, Sung-Whan ;
Choi, Hoo-Kyun ;
Han, Hyo-Kyung .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 49 (05) :800-804
[10]   Synthesis, characterization, and in vitro testing of superparamagnetic iron oxide nanoparticles targeted using folic acid-conjugated dendrimers [J].
Landmark, Kevin J. ;
DiMaggio, Stassi ;
Ward, Jesse ;
Kelly, Christopher V. ;
Vogt, Stefan ;
Hong, Seungpyo ;
Kotlyar, Alina ;
Myc, Andrzej ;
Thomas, Thommey P. ;
Penner-Hahn, James E. ;
Baker, James R., Jr. ;
Holl, Mark M. Banaszak ;
Orr, Bradford G. .
ACS NANO, 2008, 2 (04) :773-783