TY - JOUR
T1 - Therapeutic impact of erythropoietin-encapsulated liposomes targeted to bone marrow on renal anemia
AU - Miyazaki, Yuri
AU - Taguchi, Kazuaki
AU - Sou, Keitaro
AU - Watanabe, Hiroshi
AU - Ishima, Yu
AU - Miyakawa, Toshikazu
AU - Mitsuya, Hiroaki
AU - Fukagawa, Masafumi
AU - Otagiri, Masaki
AU - Maruyama, Toru
N1 - Publisher Copyright:
© 2014 American Chemical Society.
PY - 2014/9/25
Y1 - 2014/9/25
N2 - (Figure Presented). Bone marrow is a key element in the diagnosis of disorders of erythropoiesis, including anemia, and a potential target in their treatment. However, because efficient delivery of diagnostic and therapeutic agents to bone marrow is difficult, such delivery is achieved by administering drugs in large quantities that often have adverse effects. Here, we achieved selective delivery of recombinant human erythropoietin (rHuEPO) to bone marrow, via its encapsulation in liposomes with L-glutamic acid, N-(3-carboxy-1-oxopropyl)-, 1,5-dihexadecyl ester (SA) (liposome-EPO). The result, in a rabbit model of renal anemia, was a beneficial effect on hematopoiesis, better than with rHuEPO alone. Also, we determined that liposome-EPO delivery to bone marrow depended on specific uptake by bone marrow macrophages because of the presence of SA. These results indicate both that liposome-EPO is a new, promising erythropoietin-stimulating agent and that liposomes with SA have potential for diagnostic and therapeutic applications in diseases originating from bone marrow.
AB - (Figure Presented). Bone marrow is a key element in the diagnosis of disorders of erythropoiesis, including anemia, and a potential target in their treatment. However, because efficient delivery of diagnostic and therapeutic agents to bone marrow is difficult, such delivery is achieved by administering drugs in large quantities that often have adverse effects. Here, we achieved selective delivery of recombinant human erythropoietin (rHuEPO) to bone marrow, via its encapsulation in liposomes with L-glutamic acid, N-(3-carboxy-1-oxopropyl)-, 1,5-dihexadecyl ester (SA) (liposome-EPO). The result, in a rabbit model of renal anemia, was a beneficial effect on hematopoiesis, better than with rHuEPO alone. Also, we determined that liposome-EPO delivery to bone marrow depended on specific uptake by bone marrow macrophages because of the presence of SA. These results indicate both that liposome-EPO is a new, promising erythropoietin-stimulating agent and that liposomes with SA have potential for diagnostic and therapeutic applications in diseases originating from bone marrow.
KW - Bone marrow
KW - Erythropoietin
KW - Liposome
KW - Macrophages
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U2 - 10.1021/mp500453a
DO - 10.1021/mp500453a
M3 - Article
C2 - 25255196
AN - SCOPUS:84928384645
SN - 1543-8384
VL - 11
SP - 4238
EP - 4248
JO - Molecular Pharmaceutics
JF - Molecular Pharmaceutics
IS - 11
ER -