Literature DB >> 16708077

Three catheter-based strategies for cardiac delivery of therapeutic gelatin microspheres.

K Hoshino1, T Kimura, A M De Grand, R Yoneyama, Y Kawase, S Houser, H Q Ly, T Kushibiki, Y Furukawa, K Ono, Y Tabata, J V Frangioni, T Kita, R J Hajjar, M Hayase.   

Abstract

Gelatin hydrogel microspheres (GHMs) have been reported as novel non-viral vectors for gene or protein delivery (GHM therapy). However, the components of an effective catheter-based delivery strategy for GHM therapy are unknown. We evaluated the effectiveness of three catheter-based strategies for cardiac GHM therapy: (1) antegrade injection (AI) via coronary arteries; (2) retrograde injection (RI) via coronary veins; and (3) direct myocardial injection (DI) via the coronary sinus. AI distributed microspheres homogeneously throughout the target area with 73+/-11% retention. RI scattered microspheres non-homogenously with 22+/-8% retention. DI distributed microspheres in the needle-advanced area with 47+/-14% retention. However, despite high efficiency, AI did not show biological effects of inducing angiogenesis from basic fibroblast growth factor bound to GHMs. Furthermore, focal micro-infarctions, owing to micro-embolism of aggregated GHMs into small coronary arterioles, were detected in the AI group. Conversely, only RI and DI groups displayed increased coronary flow reserve. DI groups also demonstrated increased capillary density. These results suggest that RI and DI are effective for cardiac GHM therapy, while AI appears inappropriate owing to the risk of focal infarctions.

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Year:  2006        PMID: 16708077     DOI: 10.1038/sj.gt.3302793

Source DB:  PubMed          Journal:  Gene Ther        ISSN: 0969-7128            Impact factor:   5.250


  15 in total

Review 1.  Delivery of gene and cellular therapies for heart disease.

Authors:  Justin A Mariani; David M Kaye
Journal:  J Cardiovasc Transl Res       Date:  2010-05-11       Impact factor: 4.132

2.  Gelatin microspheres crosslinked with genipin for local delivery of growth factors.

Authors:  Luis Solorio; Christopher Zwolinski; Amanda W Lund; Megan J Farrell; Jan P Stegemann
Journal:  J Tissue Eng Regen Med       Date:  2010-10       Impact factor: 3.963

Review 3.  Cardiac gene therapy with SERCA2a: from bench to bedside.

Authors:  Judith K Gwathmey; Alexan I Yerevanian; Roger J Hajjar
Journal:  J Mol Cell Cardiol       Date:  2010-11-18       Impact factor: 5.000

Review 4.  Nonviral vector gene modification of stem cells for myocardial repair.

Authors:  Husnain K Haider; Ibrahim Elmadbouh; Michel Jean-Baptiste; Muhammad Ashraf
Journal:  Mol Med       Date:  2008 Jan-Feb       Impact factor: 6.354

Review 5.  Percutaneous approaches for efficient cardiac gene delivery.

Authors:  Kiyotake Ishikawa; Jaume Aguero; Charbel Naim; Kenneth Fish; Roger J Hajjar
Journal:  J Cardiovasc Transl Res       Date:  2013-06-08       Impact factor: 4.132

Review 6.  Rescuing the failing heart by targeted gene transfer.

Authors:  Yoshiaki Kawase; Dennis Ladage; Roger J Hajjar
Journal:  J Am Coll Cardiol       Date:  2011-03-08       Impact factor: 24.094

7.  Hydrogel microparticles for biomedical applications.

Authors:  Andrew C Daly; Lindsay Riley; Tatiana Segura; Jason A Burdick
Journal:  Nat Rev Mater       Date:  2019-11-07       Impact factor: 66.308

8.  Micro- and Nanoparticles for Treating Cardiovascular Disease.

Authors:  S Suarez; A Almutairi; K L Christman
Journal:  Biomater Sci       Date:  2015-04       Impact factor: 6.843

9.  pH-Sensitive and Thermosensitive Hydrogels as Stem-Cell Carriers for Cardiac Therapy.

Authors:  Zhenqing Li; Zhaobo Fan; Yanyi Xu; Wilson Lo; Xi Wang; Hong Niu; Xiaofei Li; Xiaoyun Xie; Mahmood Khan; Jianjun Guan
Journal:  ACS Appl Mater Interfaces       Date:  2016-04-22       Impact factor: 9.229

Review 10.  Human studies of angiogenic gene therapy.

Authors:  Rajesh Gupta; Jörn Tongers; Douglas W Losordo
Journal:  Circ Res       Date:  2009-10-09       Impact factor: 17.367

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