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Cited 20 time in webofscience Cited 24 time in scopus
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Development and Testing of Thrombolytics in Strokeopen access

Authors
Nikitin, DmitriChoi, SeungbumMican, JanToul, MartinRyu, Wi-SunDamborsky, JiriMikulik, RobertKim, Dong-Eog
Issue Date
Jan-2021
Publisher
KOREAN STROKE SOC
Keywords
Stroke; Thrombolytic therapy; Tissue plasminogen activator; Protein engineering
Citation
JOURNAL OF STROKE, v.23, no.1, pp 12 - 36
Pages
25
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF STROKE
Volume
23
Number
1
Start Page
12
End Page
36
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/5544
DOI
10.5853/jos.2020.03349
ISSN
2287-6391
2287-6405
Abstract
Despite recent advances in recanalization therapy, mechanical thrombectomy will never be a treatment for every ischemic stroke because access to mechanical thrombectomy is still limited in many countries. Moreover, many ischemic strokes are caused by occlusion of cerebral arteries that cannot be reached by intra-arterial catheters. Reperfusion using thrombolytic agents will therefore remain an important therapy for hyperacute ischemic stroke. However, thrombolytic drugs have shown limited efficacy and notable hemorrhagic complication rates, leaving room for improvement. A comprehensive understanding of basic and clinical research pipelines as well as the current status of thrombolytic therapy will help facilitate the development of new thrombolytics. Compared with alteplase, an ideal thrombolytic agent is expected to provide faster reperfusion in more patients; prevent re-occlusions; have higher fibrin specificity for selective activation of clot-bound plasminogen to decrease bleeding complications; be retained in the blood for a longer time to minimize dosage and allow administration as a single bolus; be more resistant to inhibitors; and be less antigenic for repetitive usage. Here, we review the currently available thrombolytics, strategies for the development of new clot-dissolving substances, and the assessment of thrombolytic efficacies in vitro and in vivo.
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