Overcoming the polyethylene glycol dilemma via pathological environment-sensitive change of the surface property of nanoparticles for cellular entry

被引:92
作者
Hama, Susumu [1 ]
Itakura, Shoko [1 ]
Nakai, Mayumi [1 ]
Nakayama, Kayoko [1 ]
Morimoto, Satoshi [1 ]
Suzuki, Satoko [1 ]
Kogure, Kentaro [1 ]
机构
[1] Kyoto Pharmaceut Univ, Dept Biophys Chem, Yamashina Ku, Kyoto 6078414, Japan
关键词
Pathological environment-sensitivity; Intratumoral pH; Nanoparticles; Charge-inversion; Cancer therapy; GENE DELIVERY; CATIONIC LIPOSOMES; INTRACELLULAR TRAFFICKING; MEMBRANE-FUSION; SYSTEM; MECHANISM; PEPTIDES; POLYMERS; VECTORS; THERAPY;
D O I
10.1016/j.jconrel.2015.03.011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Modification with polyethylene glycol (PEG) is currently considered an important strategy for anti-cancer drug delivery, because PEGylated-nanoparticles would be effectively delivered to tumor tissue by enhanced permeation and retention effects. However, PEGylation suppresses the cellular uptake of nanoparticles (NPs) to target cells (known as the PEG dilemma). Here, we propose a novel strategy, namely conferring a pathological environment-sensitive property of nanoparticles for overcoming the PEG dilemma. Specifically, although nanoparticles have an overall negative surface charge to avoid interactions with biogenic substances in blood circulation, inversion of surface charge (to positive) at the pH of the tumor microenvironment may allow the nanoparticles to be taken up by cancer cells. To prove this concept, charge-invertible nanoparticles modified with novel slightly acidic pH-sensitive peptide (SAPSP-NPs) were developed. The negatively-charged SAPSP-NPs were delivered to tumor tissue, and were successfully taken up by cancer cells upon inversion of the surface charge to positive at intratumoral pH. SAPSP-NPs may serve as an alternative carrier to the PEGylated NP for anticancer drug delivery. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:67 / 74
页数:8
相关论文
共 29 条
[1]   Targeting Anticancer Drugs to Tumor Vasculature Using Cationic Liposomes [J].
Abu Lila, Amr S. ;
Ishida, Tatsuhiro ;
Kiwada, Hiroshi .
PHARMACEUTICAL RESEARCH, 2010, 27 (07) :1171-1183
[2]   Multi-layered nanoparticles for penetrating the endosome and nuclear membrane via a step-wise membrane fusion process [J].
Akita, Hidetaka ;
Kudo, Asako ;
Minoura, Arisa ;
Yamaguti, Masaya ;
Khalil, Ikrarny A. ;
Moriguchi, Rumiko ;
Masuda, Tomoya ;
Danev, Radostin ;
Nagayama, Kuniaki ;
Kogure, Kentaro ;
Harashima, Hideyoshi .
BIOMATERIALS, 2009, 30 (15) :2940-2949
[3]   EXTRACELLULAR PH DISTRIBUTION IN HUMAN TUMORS [J].
ENGIN, K ;
LEEPER, DB ;
CATER, JR ;
THISTLETHWAITE, AJ ;
TUPCHONG, L ;
MCFARLANE, JD .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 1995, 11 (02) :211-216
[4]   Quantitative comparison of intracellular trafficking and nuclear transcription between adenoviral and lipoplex systems [J].
Hama, S ;
Akita, H ;
Ito, R ;
Mizuguchi, H ;
Hayakawa, T ;
Harashima, H .
MOLECULAR THERAPY, 2006, 13 (04) :786-794
[5]   Development of a novel drug delivery system consisting of an antitumor agent tocopheryl succinate [J].
Hama, Susumu ;
Utsumi, Satoru ;
Fukuda, Yuki ;
Nakayama, Kayoko ;
Okamura, Yuriko ;
Tsuchiya, Hiroyuki ;
Fukuzawa, Kenji ;
Harashima, Hedeyoshi ;
Kogure, Kentaro .
JOURNAL OF CONTROLLED RELEASE, 2012, 161 (03) :843-851
[6]   Development of a novel systemic gene delivery system for cancer therapy with a tumor-specific cleavable PEG-lipid [J].
Hatakeyama, H. ;
Akita, H. ;
Kogure, K. ;
Oishi, M. ;
Nagasaki, Y. ;
Kihira, Y. ;
Ueno, M. ;
Kobayashi, H. ;
Kikuchi, H. ;
Harashima, H. .
GENE THERAPY, 2007, 14 (01) :68-77
[7]  
Hauser H., 1987, CHEM PHYS LIPIDS, V43, P43283
[8]   Effects of particle size and surface charge on cellular uptake and biodistribution of polymeric nanoparticles [J].
He, Chunbai ;
Hu, Yiping ;
Yin, Lichen ;
Tang, Cui ;
Yin, Chunhua .
BIOMATERIALS, 2010, 31 (13) :3657-3666
[9]   Characteristics and biodistribution of cationic liposomes and their DNA complexes [J].
Ishiwata, H ;
Suzuki, N ;
Ando, S ;
Kikuchi, H ;
Kitagawa, T .
JOURNAL OF CONTROLLED RELEASE, 2000, 69 (01) :139-148
[10]   AMPHIPATHIC POLYETHYLENEGLYCOLS EFFECTIVELY PROLONG THE CIRCULATION TIME OF LIPOSOMES [J].
KLIBANOV, AL ;
MARUYAMA, K ;
TORCHILIN, VP ;
HUANG, L .
FEBS LETTERS, 1990, 268 (01) :235-237