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Modification of liposomes by addition of HCO60. II. Encapsulation of doxorubicin into liposomes containing HCO60.

作者信息

Kato Y, Hosokawa T, Okubo Y, Hayakawa E, Ito K

机构信息

Pharmaceutical Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., Shizuoka, Japan.

出版信息

Biol Pharm Bull. 1993 Oct;16(10):965-9. doi: 10.1248/bpb.16.965.

DOI:10.1248/bpb.16.965
PMID:8287046
Abstract

The efficiency of encapsulation of doxorubicin (DOX) into liposomes containing HCO60 was studied. Empty egg phosphatidylcholine (PC) liposomes containing various amounts of HCO60 were passed through a polycarbonate membrane filter (0.1 micron). Closed vesicles were formed even with liposomes containing 90 wt% HCO60. DOX was encapsulated efficiently (more than 1 mg DOX/8 mg lipids) using a pH-gradient method. HCO60 accelerated the leakage of DOX from liposomes into phosphate buffer at temperatures above 25 degrees C. HCO60 suppressed the leakage of DOX from egg PC/cholesterol (7/3, w/w) liposomes into phosphate buffer containing 50% fetal bovine serum (FBS). Studies on the interaction between liposomes and serum components using zeta potential and turbidity suggest that HCO60 prevents the liposomes from interacting with serum components.

摘要

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