Thrombolytic therapy based on lyophilized platelet-derived nanocarriers for ischemic stroke

被引:7
|
作者
Migliavacca, Martina [1 ]
Correa-Paz, Clara [2 ]
Perez-Mato, Maria [2 ]
Bielawski, Patrick-Brian [3 ]
Zhang, Issan [3 ]
Marie, Pauline [4 ]
Hervella, Pablo [5 ]
Rubio, Marina [4 ]
Maysinger, Dusica [3 ]
Vivien, Denis [4 ,6 ]
del Pino, Pablo [1 ]
Pelaz, Beatriz [1 ]
Polo, Ester [1 ]
Campos, Francisco [2 ]
机构
[1] Univ Santiago de Compostela, Ctr Res Biol Chem & Mol Mat CIQUS, Santiago De Compostela 15782, Spain
[2] Hlth Res Inst Santiago de Compostela IDIS, Translat Stroke Lab Grp TREAT, Clin Neurosci Res Lab LINC, Santiago De Compostela 15706, Spain
[3] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ H3G 1Y6, Canada
[4] Normandie Univ, Inst Blood & Brain Caen Normandie BB C, Physiopathol & Imaging Neurol Disorders PhIND, UMR S U1237,UNICAEN,INSERM,GIP Cyceron, F-14000 Caen, France
[5] Hlth Res Inst Santiago de Compostela IDIS, Clin Neurosci Res Lab LINC, Neuroimaging & Biotechnol Lab NOBEL, Santiago De Compostela 15706, Spain
[6] Caen Normandie Univ Hosp, Dept Clin Res, Caen, France
关键词
NANOPARTICLES; MODEL;
D O I
10.1186/s12951-023-02206-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
BackgroundIntravenous administration of fibrinolytic drugs, such as recombinant tissue plasminogen activator (rtPA) is the standard treatment of acute thrombotic diseases. However, current fibrinolytics exhibit limited clinical efficacy because of their short plasma half-lives and risk of hemorrhagic transformations. Platelet membrane-based nanocarriers have received increasing attention for ischemic stroke therapies, as they have natural thrombus-targeting activity, can prolong half-life of the fibrinolytic therapy, and reduce side effects. In this study we have gone further in developing platelet-derived nanocarriers (defined as cellsomes) to encapsulate and protect rtPA from degradation. Following lyophilization and characterization, their formulation properties, biocompatibility, therapeutic effect, and risk of hemorrhages were later investigated in a thromboembolic model of stroke in mice.ResultsCellsomes of 200 nm size and loaded with rtPA were generated from membrane fragments of human platelets. The lyophilization process did not influence the nanocarrier size distribution, morphology, and colloidal stability conferring particle preservation and long-term storage. Encapsulated rtPA in cellsomes and administered as a single bolus showed to be as effective as a continuous clinical perfusion of free rtPA at equal concentration, without increasing the risk of hemorrhagic transformations or provoking an inflammatory response.ConclusionsThis study provides evidence for the safe and effective use of lyophilized biomimetic platelet-derived nanomedicine for precise thrombolytic treatment of acute ischemic stroke. In addition, this new nanoformulation could simplify the clinical use of rtPA as a single bolus, being easier and less time-consuming in an emergency setting than a treatment perfusion, particularly in stroke patients. We have successfully addressed one of the main barriers to drug application and commercialization, the long-term storage of nanomedicines, overcoming the potential chemical and physical instabilities of nanomedicines when stored in an aqueous buffer.
引用
收藏
页数:16
相关论文
共 50 条
  • [1] Thrombolytic therapy based on lyophilized platelet-derived nanocarriers for ischemic stroke
    Martina Migliavacca
    Clara Correa-Paz
    María Pérez-Mato
    Patrick-Brian Bielawski
    Issan Zhang
    Pauline Marie
    Pablo Hervella
    Marina Rubio
    Dusica Maysinger
    Denis Vivien
    Pablo del Pino
    Beatriz Pelaz
    Ester Polo
    Francisco Campos
    Journal of Nanobiotechnology, 22
  • [2] THROMBOLYTIC THERAPY - ENHANCEMENT BY PLATELET AND PLATELET-DERIVED MEDIATOR ANTAGONISTS
    WILLERSON, JT
    GOLINO, P
    MCNATT, J
    EIDT, J
    YAO, SK
    BUJA, LM
    MOLECULAR BIOLOGY & MEDICINE, 1991, 8 (02) : 235 - 243
  • [3] Evaluation of a lyophilized platelet-derived hemostatic product
    Bynum, James A.
    Meledeo, Michael A.
    Peltier, Grantham C.
    McIntosh, Colby S.
    Taylor, Ashley S.
    Montgomery, Robbie K.
    Reddoch-Cardenas, Kristin M.
    Getz, Todd M.
    Fitzpatrick, Michael G.
    Cap, Andrew P.
    TRANSFUSION, 2019, 59 : 1490 - 1498
  • [4] Evaluation of a Lyophilized Platelet-Derived Hemostatic Product
    Bynum, James A.
    Meledeo, Michael A.
    Peltier, Grantham C.
    Taylor, Ashley S.
    McIntosh, Colby S.
    Montgomery, Robbie K.
    Getz, Todd M.
    Fitzpatrick, Mike G.
    Cap, Andrew P.
    TRANSFUSION, 2017, 57 : 41A - 41A
  • [5] Platelet-Derived Microparticle as a Marker of Platelet Activation in Patients with Acute Ischemic Stroke
    Uchiyama, S.
    Taomoto, K.
    Nomura, S.
    Ozaki, Y.
    Goto, S.
    Ikeda, Y.
    STROKE, 2009, 40 (04) : E168 - E168
  • [6] Thrombolytic therapy of ischemic stroke
    Lang, W
    Fazekas, F
    Baumhackl, U
    NEUROPSYCHIATRIE, 2000, 14 (01) : 33 - 39
  • [7] Safety evaluation of a lyophilized platelet-derived hemostatic product
    Barroso, Jeffrey
    Osborne, Barbara
    Teramura, Gayle
    Pellham, Esther
    Fitzpatrick, Michael
    Biehl, Ruth
    Yu, Anna
    Pehta, Joan
    Slichter, Sherrill J.
    TRANSFUSION, 2018, 58 (12) : 2969 - 2977
  • [8] Features of Platelet Hemostasis in Patients with Ischemic Stroke after Systemic Thrombolytic Therapy
    Anisimova A.V.
    Kolesnikova T.I.
    Yutskova E.V.
    Kapel’nitskii P.V.
    Galkin S.S.
    Neuroscience and Behavioral Physiology, 2017, 47 (7) : 833 - 835
  • [9] Antithrombotic and thrombolytic therapy for ischemic stroke
    Fisher, M
    JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 1999, 7 (02) : 165 - 169
  • [10] Antithrombotic and thrombolytic therapy for ischemic stroke
    Albers, Gregory W.
    Amarenco, Pierre
    Easton, J. Donald
    Sacco, Ralph L.
    Teal, Philip
    CHEST, 2008, 133 (06) : 630S - 669S