Endogenous Enzyme-responsive Nanoplatforms for Anti-tumor Therapy

被引:8
作者
Lou, Xue-Fang [1 ]
Du, Yong-Zhong [2 ]
Xu, Xiao-Ling [2 ]
机构
[1] Zhejiang Univ City Coll, Sch Med, 51 Hu Zhou St, Hangzhou 310015, Peoples R China
[2] Zhejiang Univ, Inst Pharmaceut, Coll Pharmaceut Sci, Hangzhou 310058, Peoples R China
关键词
Enzyme-responsive; matrix metalloproteinase; esterase; hyaluronidase; caspase; cathepsin; DRUG-DELIVERY SYSTEM; BREAST-CANCER; DOXORUBICIN DELIVERY; ANTICANCER DRUG; NANOPARTICLES; MICELLES; POLYMER; ANGIOGENESIS; CHEMOTHERAPY; CHALLENGES;
D O I
10.2174/1389450122666210114095614
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The emergency of responsive drug delivery systems has contributed to reduced cyto-toxicity, improved permeability in tissues and extended circulation time of the active drug. In par-ticular, enzyme-responsive nanoplatforms have attracted a lot of attention due to the specificity and efficiency of an enzyme-catalyzed reaction. In this review, enzyme-based mono responsive drug de-livery systems designed in the past 5 years have been summarized. These drug delivery systems were introduced by different tumor-related enzymes such as matrix metalloproteinase, esterase, hyaluronidase, caspase and cathepsin. Moreover, the enzyme-sensitive nanoplatforms activated by dual-stimuli have been also described. Although great progress had been made in the past years, the translation into clinical practice is still difficult. Thus, three obstacles (enzyme heterogeneity, re-action environment, animal model) were also discussed. In short, enzyme-activated drug delivery systems offer great potential in treating cancers.
引用
收藏
页码:845 / 855
页数:11
相关论文
共 76 条
[1]   Analysis of host- and tumor-derived proteinases using a custom dual species microarray reveals a protective role for stromal matrix metal loproteinase-12 in non-small cell lung cancer [J].
Acuff, Heath B. ;
Sinnamon, Mark ;
Fingleton, Barbara ;
Boone, Braden ;
Levy, Shawn E. ;
Chen, Xiwu ;
Pozzi, Ambra ;
Carbone, David P. ;
Schwartz, Donald R. ;
Moin, Kamiar ;
Sloane, Bonnie F. ;
Matrisian, Lynn M. .
CANCER RESEARCH, 2006, 66 (16) :7968-7975
[2]   Stimulus-responsive sequential release systems for drug and gene delivery [J].
Ahmadi, Sepideh ;
Rabiee, Navid ;
Bagherzadeh, Mojtaba ;
Elmi, Faranak ;
Fatahi, Yousef ;
Farjadian, Fatemeh ;
Baheiraei, Nafiseh ;
Nasseri, Behzad ;
Rabiee, Mohammad ;
Dastjerd, Niloufar Tavakoli ;
Valibeik, Ali ;
Karimi, Mahdi ;
Hamblin, Michael R. .
NANO TODAY, 2020, 34
[3]  
Apolinario AC, 2020, EXPLORING BENEFITS N
[4]   β-Cyclodextrin-modified hyaluronic acid-based supramolecular self-assemblies for pH- and esterase-dual-responsive drug delivery [J].
Bai, Yang ;
Liu, Cai-Ping ;
Chen, Di ;
Liu, Cheng-Fei ;
Zhuo, Long-Hai ;
Li, Hui ;
Wang, Chao ;
Bu, Huai-Tian ;
Tian, Wei .
CARBOHYDRATE POLYMERS, 2020, 246
[5]   Nano-Enhanced Cancer Immunotherapy: Immunology Encounters Nanotechnology [J].
Bockamp, Ernesto ;
Rosigkeit, Sebastian ;
Siegl, Dominik ;
Schuppan, Detlef .
CELLS, 2020, 9 (09)
[6]   Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries (vol 68, pg 394, 2018) [J].
Bray, F. ;
Ferlay, J. ;
Soerjomataram, I ;
Siegel, R. L. ;
Torre, L. A. ;
Jemal, A. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2020, 70 (04) :313-313
[7]   Liver cancer: Approaching a personalized care [J].
Bruix, Jordi ;
Han, Kwang-Hyub ;
Gores, Gregory ;
Llovet, Josep Maria ;
Mazzaferro, Vincenzo .
JOURNAL OF HEPATOLOGY, 2015, 62 :S144-S156
[8]   Protocol for Computational Enzymatic Reactivity Based on Geometry Optimisation [J].
Cerqueira, N. M. F. S. A. ;
Fernandes, P. A. ;
Ramos, M. J. .
CHEMPHYSCHEM, 2018, 19 (06) :669-689
[9]   Enzyme-responsive polymer hydrogels for therapeutic delivery [J].
Chandrawati, Rona .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2016, 241 (09) :972-979
[10]   Self-Assembled Polyprodrug Amphiphile for Subcutaneous Xenograft Tumor Inhibition with Prolonged Acting Time In Vivo [J].
Chen, Dong ;
Huang, Yu ;
Xu, Shuting ;
Jiang, Huangyong ;
Wu, Jieli ;
Jin, Xin ;
Zhu, Xinyuan .
MACROMOLECULAR BIOSCIENCE, 2017, 17 (11)