TY - JOUR
T1 - Albumin-Encapsulated Liposomes
T2 - A Novel Drug Delivery Carrier With Hydrophobic Drugs Encapsulated in the Inner Aqueous Core
AU - Okamoto, Yuko
AU - Taguchi, Kazuaki
AU - Yamasaki, Keishi
AU - Sakuragi, Mina
AU - Kuroda, Shun'ichi
AU - Otagiri, Masaki
N1 - Funding Information:
This work was supported in part by a Grant-in-Aid for Challenging Exploratory Research from the Japan Society for the Promotion of Science (JSPS) (KAKENHI 25670085). The synchrotron radiation experiments were conducted at SPring-8 BL40B2 (No. 2015B1708). We wish to thank Dr. Noboru Ohta for his assistance with the experiments at SPring-8.
Funding Information:
This work was supported in part by a Grant-in-Aid for Challenging Exploratory Research from the Japan Society for the Promotion of Science (JSPS) (KAKENHI 25670085 ). The synchrotron radiation experiments were conducted at SPring-8 BL40B2 (No. 2015B1708). We wish to thank Dr. Noboru Ohta for his assistance with the experiments at SPring-8.
Publisher Copyright:
© 2018 American Pharmacists Association®
PY - 2018/1
Y1 - 2018/1
N2 - Liposomes are clinically used in drug delivery, but loading hydrophobic substances is limited to the hydrophobic space of a lipid membrane, despite the fact that it is favorable to encapsulate substances into the inner aqueous core of liposome, from a drug stability of view. We report herein on the preparation of a liposome with bovine serum albumin encapsulated (BSA-liposome). Using this system, it is possible to encapsulate hydrophobic drugs in the inner aqueous core of the liposome based on the hypothesis that the water solubility of hydrophobic drugs is increased when bound to albumin. The physicochemical properties of the prepared BSA-liposomes could be easily regulated and the loading of hydrophobic drugs in the inner aqueous core of the liposome was dramatically improved by virtue of the drug-binding properties of albumin. An in vivo safety and pharmacokinetic study showed that BSA-liposomes possess favorable properties as a drug carrier, including biocompatibility and a stealth effect. This new type of hydrophobic drug carrier, an albumin-liposome, has the potential for use in delivering numerous hydrophobic drugs that typically bind to albumin.
AB - Liposomes are clinically used in drug delivery, but loading hydrophobic substances is limited to the hydrophobic space of a lipid membrane, despite the fact that it is favorable to encapsulate substances into the inner aqueous core of liposome, from a drug stability of view. We report herein on the preparation of a liposome with bovine serum albumin encapsulated (BSA-liposome). Using this system, it is possible to encapsulate hydrophobic drugs in the inner aqueous core of the liposome based on the hypothesis that the water solubility of hydrophobic drugs is increased when bound to albumin. The physicochemical properties of the prepared BSA-liposomes could be easily regulated and the loading of hydrophobic drugs in the inner aqueous core of the liposome was dramatically improved by virtue of the drug-binding properties of albumin. An in vivo safety and pharmacokinetic study showed that BSA-liposomes possess favorable properties as a drug carrier, including biocompatibility and a stealth effect. This new type of hydrophobic drug carrier, an albumin-liposome, has the potential for use in delivering numerous hydrophobic drugs that typically bind to albumin.
KW - albumin
KW - biocompatibility
KW - liposomes
KW - protein binding
KW - solubility
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U2 - 10.1016/j.xphs.2017.08.003
DO - 10.1016/j.xphs.2017.08.003
M3 - Article
C2 - 28826882
AN - SCOPUS:85028922322
SN - 0022-3549
VL - 107
SP - 436
EP - 445
JO - Journal of Pharmaceutical Sciences
JF - Journal of Pharmaceutical Sciences
IS - 1
ER -