J 2021

Development and Testing of Thrombolytics in Stroke

NIKITIN, Dmitri; Seungbum CHOI; Jan MIČAN; Martin TOUL; Wi-Sun RYU et al.

Základní údaje

Originální název

Development and Testing of Thrombolytics in Stroke

Autoři

NIKITIN, Dmitri; Seungbum CHOI; Jan MIČAN; Martin TOUL; Wi-Sun RYU; Jiří DAMBORSKÝ; Robert MIKULÍK a Dong-Eog KIM

Vydání

JOURNAL OF STROKE, SEOUL, KOREAN STROKE SOC, 2021, 2287-6391

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Stát vydavatele

Korejská republika

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14310/21:00121798

Organizace

Přírodovědecká fakulta – Masarykova univerzita – Repozitář

EID Scopus

Klíčová slova anglicky

Stroke; Thrombolytic therapy; Tissue plasminogen activator; Protein engineering
Změněno: 16. 2. 2023 04:23, RNDr. Daniel Jakubík

Anotace

V originále

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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