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Engineering erythrocytes for the modulation of drugs' and contrasting agents' pharmacokinetics and biodistribution

Journal

ADVANCED DRUG DELIVERY REVIEWS
Volume 106, Issue -, Pages 73-87

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.addr.2016.05.008

Keywords

Drug delivery by red blood cells; Delivery of vascular contrasting agents; Enzyme replacement therapy; Immunophilins; Dexamethasone; Tacrolimus; Erythrocytes

Funding

  1. FIRB [RBFR1299KO]
  2. Consorzio Interuniveristario Biotecnologie (CIB)
  3. FanoAteneo

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Pharmacokinetics, biodistribution, and biological activity are key parameters that determine the success or failure of therapeutics. Many developments intended to improve their in vivo performance, aim at modulating concentration, biodistribution, and targeting to tissues, cells or subcellular compartments. Erythrocyte-based drug delivery systems are especially efficient in maintaining active drugs in circulation, in releasing them for several weeks or in targeting drugs to selected cells. Erythrocytes can also be easily processed to entrap the desired pharmaceutical ingredients before re-infusion into the same or matched donors. These carriers are totally biocompatible, have a large capacity and could accommodate traditional chemical entities (glucocorticoids, immunossuppresants, etc.), biologics (proteins) and/or contrasting agents (dyes, nanoparticles). Carrier erythrocytes have been evaluated in thousands of infusions in humans proving treatment safety and efficacy, hence gaining interest in the management of complex pathologies (particularly in chronic treatments and when side effects become serious issues) and in new diagnostic approaches. (C) 2016 Elsevier B.V. All rights reserved.

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