Drug delivery by red blood cells: vascular carriers designed by mother nature

被引:328
作者
Muzykantov, Vladimir R. [1 ,2 ]
机构
[1] Univ Penn, Med Ctr, Dept Pharmacol, Philadelphia, PA 19104 USA
[2] IFEM, Program Targeted Therapeut, Inst Translat Med & Therapeut, Philadelphia, PA 19104 USA
关键词
ERYTHROCYTE COMPLEMENT RECEPTOR; TISSUE-PLASMINOGEN ACTIVATOR; BISPECIFIC MONOCLONAL-ANTIBODIES; HUMAN-IMMUNODEFICIENCY-VIRUS; IN-VIVO SURVIVAL; HETEROPOLYMER-MEDIATED BINDING; REGULATORY PROTEIN-DEFICIENCY; ANTIGEN-BASED HETEROPOLYMERS; PEG-UREASE/PEG-ALADH; POLYETHYLENE-GLYCOL;
D O I
10.1517/17425241003610633
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Areas covered by this review: Two strategies for RBC drug delivery are discussed: encapsulation into isolated RBC ex vivo followed by infusion in compatible recipients and coupling therapeutics to the surface of RBC. Studies of pharmacokinetics and effects in animal models and in human studies of diverse therapeutic enzymes, antibiotics and other drugs encapsulated in RBC are described and critically analyzed. Coupling to RBC surface of compounds regulating immune response and complement, affinity ligands, polyethylene glycol alleviating immune response to donor RBC and fibrinolytic plasminogen activators are described. Also described is a new, translation-prone approach for RBC drug delivery by injection of therapeutics conjugated with fragments of antibodies providing safe anchoring of cargoes to circulating RBC, without need for ex vivo modification and infusion of RBC. What the reader will gain: Readers will gain historical perspective, current status, challenges and perspectives of medical applications of RBC for drug delivery. Take home message: RBC represent naturally designed carriers for intravascular drug delivery, characterized by unique longevity in the bloodstream, biocompatibility and safe physiological mechanisms for metabolism. New approaches for encapsulating drugs into RBC and coupling to RBC surface provide promising avenues for safe and widely useful improvement of drug delivery in the vascular system.
引用
收藏
页码:403 / 427
页数:25
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