Development of hematin conjugated PLGA nanoparticle for selective cancer targeting

被引:14
作者
Amin, Md. Lutful [1 ]
Kim, Dami [1 ]
Kim, SeJin [1 ]
机构
[1] Gachon Univ, Dept BioNano Technol, Songnam, Gyeonggi Do, South Korea
关键词
PLGA nanoparticle; Hematin; Drug delivery; Targeted nanoparticle; Surface modification; LOW-DENSITY LIPOPROTEIN; PHOTODYNAMIC THERAPY; PORPHYRIN LOCALIZATION; ERYTHROLEUKEMIA-CELLS; DRUG-DELIVERY; HELA-CELLS; TUMOR; NANOTECHNOLOGY; HEME; TRANSFERRIN;
D O I
10.1016/j.ejps.2016.05.029
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Targeted nanomedicine for cancer therapy has gained widespread popularity and is being extensively explored. Porphyrins have intrinsic tumor localizing ability and have been studied for photodynamic therapy. However, they have not been used as cancer targeting agents for nanomedicines. In this study, PLGA nanoparticles were formulated and an iron-containing blood porphyrin, hematin was conjugated to the surface of the nanoparticles to investigate selectivity towards cancer cell and cellular internalization. Hematin was previously shown to facilitate growth and proliferation of cancer cells. PLGA nanoparticles were characterized by FE-SEM, AFM, DLS, and Zeta potential analyzer. The conjugation of hematin was confirmed by FTIR. HeLa cells were used to study tumor selectivity and uptake. Hematin conjugated particles (zeta potential: - 15.19 mV) showed higher affinity towards the cancer cells than the control particles. The result indicated that the particles were internalized by heme carrier protein-1. Together these data suggest that hematin is a promising cancer targeting material for nanotherapeutics. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 143
页数:6
相关论文
共 39 条
[1]
Cancer nanotechnology: The impact of passive and active targeting in the era of modern cancer biology [J].
Bertrand, Nicolas ;
Wu, Jun ;
Xu, Xiaoyang ;
Kamaly, Nazila ;
Farokhzad, Omid C. .
ADVANCED DRUG DELIVERY REVIEWS, 2014, 66 :2-25
[2]
DISTRIBUTION OF RECEPTORS FOR TRANSFERRIN AND LOW-DENSITY LIPOPROTEIN ON THE SURFACE OF GIANT HELA-CELLS [J].
BRETSCHER, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (02) :454-458
[3]
REGULATION OF ACTIVITY OF LOW-DENSITY LIPOPROTEIN RECEPTOR IN HUMAN FIBROBLASTS [J].
BROWN, MS ;
GOLDSTEIN, JL .
CELL, 1975, 6 (03) :307-316
[4]
CANCER AND PORPHYRINS - PHOTOCHEMOTHERAPY [J].
BROWN, SB ;
KESSEL, D .
MOLECULAR ASPECTS OF MEDICINE, 1990, 11 (1-2) :99-103
[5]
Catalyst-mediated yet catalyst-free hydrogels formed by interfacial chemical activation [J].
Byun, Eunkyoung ;
Ryu, Ji Hyun ;
Lee, Haeshin .
CHEMICAL COMMUNICATIONS, 2014, 50 (22) :2869-2872
[6]
The uptake and intracellular fate of PLGA nanoparticles in epithelial cells [J].
Cartiera, Malgorzata S. ;
Johnson, Katherine M. ;
Rajendran, Vanathy ;
Caplan, Michael J. ;
Saltzman, W. Mark .
BIOMATERIALS, 2009, 30 (14) :2790-2798
[7]
A holistic approach to targeting disease with polymeric nanoparticles [J].
Cheng, Christopher J. ;
Tietjen, Gregory T. ;
Saucier-Sawyer, Jennifer K. ;
Saltzman, W. Mark .
NATURE REVIEWS DRUG DISCOVERY, 2015, 14 (04) :239-247
[8]
EBERT PS, 1983, CANCER BIOCHEM BIOPH, V6, P157
[9]
EBERT PS, 1981, CANCER RES, V41, P937
[10]
THE INTERACTION OF TUMOR-LOCALIZING PORPHYRINS WITH COLLAGEN, ELASTIN, GELATIN, FIBRIN AND FIBRINOGEN [J].
ELFAR, MA ;
PIMSTONE, NR .
CELL BIOCHEMISTRY AND FUNCTION, 1985, 3 (02) :115-119