Recent advances in nanomedicines for the treatment of ischemic stroke

被引:127
作者
Li, Chao [1 ,2 ]
Sun, Tao [1 ]
Jiang, Chen [1 ]
机构
[1] Fudan Univ, Key Lab Smart Drug Delivery, Minist Educ, State Key Lab Med Neurobiol, Shanghai 201203, Peoples R China
[2] Fudan Univ, MOE Frontiers Ctr Brain Sci, Dept Pharmaceut, Sch Pharm,Res Ctr Aging & Med, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
Stroke; Ischemic cascade; Reperfusion; Neuroprotectant; Thrombolytics; Nanomedicine; Blood.brain barrier; FOCAL CEREBRAL-ISCHEMIA; BLOOD-BRAIN-BARRIER; TUMOR-NECROSIS-FACTOR; NANOPARTICLE-MEDIATED DELIVERY; TARGET-SENSITIVE LIPOSOMES; HEALTH-CARE PROFESSIONALS; NERVE GROWTH-FACTOR; NF-KAPPA-B; DRUG-DELIVERY; ISCHEMIA/REPERFUSION INJURY;
D O I
10.1016/j.apsb.2020.11.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ischemic stroke is a cerebrovascular disease normally caused by interrupted blood supply to the brain. Ischemia would initiate the cascade reaction consisted of multiple biochemical events in the damaged areas of the brain, where the ischemic cascade eventually leads to cell death and brain infarction. Extensive researches focusing on different stages of the cascade reaction have been conducted with the aim of curing ischemic stroke. However, traditional treatment methods based on antithrombotic therapy and neuroprotective therapy are greatly limited for their poor safety and treatment efficacy. Nanomedicine provides new possibilities for treating stroke as they could improve the pharmacokinetic behavior of drugs in vivo, achieve effective drug accumulation at the target site, enhance the therapeutic effect and meanwhile reduce the side effect. In this review, we comprehensively describe the pathophysiology of stroke, traditional treatment strategies and emerging nanomedicines, summarize the barriers and methods for transporting nanomedicine to the lesions, and illustrate the latest progress of nanomedicine in treating ischemic stroke, with a view to providing a new feasible path for the treatment of cerebral ischemia. (C) 2021 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:1767 / 1788
页数:22
相关论文
共 163 条
[1]   Therapeutic potential of neurotrophic factors and neural stem cells against ischemic brain injury [J].
Abe, K .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (10) :1393-1408
[2]   Selective Liposomal Transport through Blood Brain Barrier Disruption in lschemic Stroke Reveals Two Distinct Therapeutic Opportunities [J].
Al-Ahmady, Zahraa S. ;
Jasim, Dhifaf ;
Ahmad, Sabahuddin Syed ;
Wong, Raymond ;
Haley, Michael ;
Coutts, Graham ;
Schiess, Ingo ;
Allan, Stuart M. ;
Kostarelos, Kostas .
ACS NANO, 2019, 13 (11) :12470-12486
[3]   Oxidative stress and its role in the pathogenesis of ischaemic stroke [J].
Allen, C. L. ;
Bayraktutan, U. .
INTERNATIONAL JOURNAL OF STROKE, 2009, 4 (06) :461-470
[4]   Anti-apoptotic and neuroprotective effects of edaravone following transient focal ischemia in rats [J].
Amemiya, S ;
Kamiya, T ;
Nito, C ;
Inaba, T ;
Kato, K ;
Ueda, M ;
Shimazaki, K ;
Katayama, Y .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2005, 516 (02) :125-130
[5]   THE PROTECTIVE ROLE OF CATALASE AGAINST CEREBRAL ISCHEMIA IN VITRO AND IN VIVO [J].
Armogida, M. ;
Spalloni, A. ;
Amantea, D. ;
Nutini, M. ;
Petrelli, F. ;
Longone, P. ;
Bagetta, G. ;
Nistico, R. ;
Mercuri, N. B. .
INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2011, 24 (03) :735-747
[6]   Simultaneous Blood-Brain Barrier Crossing and Protection for Stroke Treatment Based on Edaravone-Loaded Ceria Nanoparticles [J].
Bao, Qunqun ;
Hu, Ping ;
Xu, Yingying ;
Cheng, Tiansheng ;
Wei, Chenyang ;
Pan, Limin ;
Shi, Jianlin .
ACS NANO, 2018, 12 (07) :6794-6805
[7]   A recombinant polymeric hemoglobin with conformational, functional, and physiological characteristics of an in vivo O2 transporter [J].
Bobofchak, KM ;
Mito, T ;
Texel, SJ ;
Bellelli, A ;
Nemoto, M ;
Traystman, RJ ;
Koehler, RC ;
Brinigar, WS ;
Fronticelli, C .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 285 (02) :H549-H561
[8]   Adenosine 5′-triphosphate and adenosine as endogenous signaling molecules in immunity and inflammation [J].
Bours, M. J. L. ;
Swennen, E. L. R. ;
Di Virgilio, F. ;
Cronstein, B. N. ;
Dagnelie, P. C. .
PHARMACOLOGY & THERAPEUTICS, 2006, 112 (02) :358-404
[9]   Microglial phagocytosis of live neurons [J].
Brown, Guy C. ;
Neher, Jonas J. .
NATURE REVIEWS NEUROSCIENCE, 2014, 15 (04) :209-216
[10]   Tenecteplase versus Alteplase before Thrombectomy for Ischemic Stroke [J].
Campbell, B. C. V. ;
Mitchell, P. J. ;
Churilov, L. ;
Yassi, N. ;
Kleinig, T. J. ;
Dowling, R. J. ;
Yan, B. ;
Bush, S. J. ;
Dewey, H. M. ;
Thijs, V. ;
Scroop, R. ;
Simpson, M. ;
Brooks, M. ;
Asadi, H. ;
Wu, T. Y. ;
Shah, D. G. ;
Wijeratne, T. ;
Ang, T. ;
Miteff, F. ;
Levi, C. R. ;
Rodrigues, E. ;
Zhao, H. ;
Salvaris, P. ;
Garcia-Esperon, C. ;
Bailey, P. ;
Rice, H. ;
de Villiers, L. ;
Brown, H. ;
Redmond, K. ;
Leggett, D. ;
Fink, J. N. ;
Collecutt, W. ;
Wong, A. A. ;
Muller, C. ;
Coulthard, A. ;
Mitchell, K. ;
Clouston, J. ;
Mahady, K. ;
Field, D. ;
Ma, H. ;
Phan, T. G. ;
Chong, W. ;
Chandra, R. V. ;
Slater, L. -A. ;
Krause, M. ;
Harrington, T. J. ;
Faulder, K. C. ;
Steinfort, B. S. ;
Bladin, C. F. ;
Sharma, G. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 378 (17) :1573-1582