pH-Responsive Nanoparticles for Drug Delivery

被引:864
作者
Gao, Weiwei [3 ]
Chan, Juliana M. [2 ]
Farokhzad, Omid C. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Anesthesiol,Lab Nanomed & Biomat, Boston, MA 02115 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] MIT, Div Hlth Sci & Technol, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
Nanoparticles; drug delivery; responsive; pH; acid; IN-VIVO EFFICACY; INTRACELLULAR DELIVERY; ORAL DELIVERY; BLOCK-COPOLYMER; SIRNA DELIVERY; CANCER-THERAPY; MESOPOROUS SILICA; PEYERS-PATCHES; M-CELLS; ACID;
D O I
10.1021/mp100253e
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
First-generation nanoparticles (NPs) have been clinically translated as pharmaceutical drug delivery carriers for their ability to improve on drug tolerability, circulation half-life, and efficacy. Toward the development of the next-generation NPs, researchers have designed novel multifunctional platforms for sustained release, molecular targeting, and environmental responsiveness. This review focuses on environmentally responsive mechanisms used in NP designs, and highlights the use of pH-responsive NPs in drug delivery. Different organs, tissues, and subcellular compartments, as well as their pathophysiological states, can be characterized by their pH levels and gradients. When exposed to these pH stimuli, pH-responsive NPs respond with physicochemical changes to their material structure and surface characteristics. These include swelling, dissociating or surface charge switching, in a manner that favors drug release at the target site over surrounding tissues. The novel developments described here may revise the classical outlook that NPs are passive delivery vehicles, in favor of responsive, sensing vehicles that use environmental cues to achieve maximal drug potency.
引用
收藏
页码:1913 / 1920
页数:8
相关论文
共 83 条
[1]
Targeted delivery of antigens to the gut-associated lymphoid tissues: 2. Ex vivo evaluation of lectin-labelled albumin microspheres for targeted delivery of antigens to the M-cells of the Peyer's patches [J].
Akande, Janet ;
Yeboah, Kwame G. ;
Addo, Richard T. ;
Siddig, Aladin ;
Oettinger, Carl W. ;
D'Souza, Martin J. .
JOURNAL OF MICROENCAPSULATION, 2010, 27 (04) :325-336
[2]
Intracellular inducible alkylation system that exhibits antisense effects with greater potency and selectivity than the natural oligonucleotide [J].
Ali, Md. Monsur ;
Oishi, Motoi ;
Nagatsugi, Fumi ;
Mori, Kenya ;
Nagasaki, Yukio ;
Kataoka, Kazunori ;
Sasaki, Shigeki .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (19) :3136-3140
[3]
Polymer-Cisplatin Conjugate Nanoparticles for Acid-Responsive Drug Delivery [J].
Aryal, Santosh ;
Hu, Che-Ming Jack ;
Zhang, Liangfang .
ACS NANO, 2010, 4 (01) :251-258
[4]
Exploitation of intracellular pH gradients in the cellular delivery of macromolecules [J].
Asokan, A ;
Cho, MJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (04) :903-913
[5]
Cyclodextrin conjugated magnetic colloidal nanoparticles as a nanocarrier for targeted anticancer drug delivery [J].
Banerjee, Shashwat S. ;
Chen, Dong-Hwang .
NANOTECHNOLOGY, 2008, 19 (26)
[6]
Behr JP, 1997, CHIMIA, V51, P34
[7]
Oxygen, a source of life and stress [J].
Brahimi-Horn, M. Christiane ;
Pouyssegur, Jacques .
FEBS LETTERS, 2007, 581 (19) :3582-3591
[8]
Tuning the pH sensitivities of orthoester based compounds for drug delivery applications by simple chemical modification [J].
Bruyere, Helene ;
Westwell, Andrew D. ;
Jones, Arwyn T. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (07) :2200-2203
[9]
PEG-SS-PPS: Reduction-sensitive disulfide block copolymer vesicles for intracellular drug delivery [J].
Cerritelli, Simona ;
Velluto, Diana ;
Hubbell, Jeffrey A. .
BIOMACROMOLECULES, 2007, 8 (06) :1966-1972
[10]
Effective oral delivery of insulin in animal models using vitamin B12-coated dextran nanoparticles [J].
Chalasani, Kishore B. ;
Russell-Jones, Gregory J. ;
Jain, Akhlesh K. ;
Diwan, Prakash V. ;
Jain, Sanjay K. .
JOURNAL OF CONTROLLED RELEASE, 2007, 122 (02) :141-150