| Title | [Influence of different doxorubicin-salt aggregates on the leakage of liposomal doxorubicin in vitro and long circulation in vivo] | | Author(s) | Zhang L, Pan H, Liu M, Lu WY | | Institution | School of Pharmacy, Fudan University, Fudan-Pharmaco Targeting Drug Research Center, Shanghai 200032, China. | | Source | Yao Xue Xue Bao 2004 Dec; 39(12):1018-22. | | MeSH | Ammonium Sulfate
Animals
Area Under Curve
Citric Acid
Comparative Study
Doxorubicin
Drug Carriers
Drug Stability
English Abstract
Glycine
Hydrogen-Ion Concentration
Liposomes
Male
Particle Size
Random Allocation
Rats
Rats, Sprague-Dawley
Research Support, Non-U.S. Gov't
| | Abstract | AIM: To develop liposomes containing doxorubicin with different salts and to investigate their influence on the stability of liposomal doxorubicin in vitro and in vivo.
METHODS: Liposomes were prepared by the film method, treated further by extruded through nuclear membrane. The entrapment efficiency was determined by column chromatography. In vitro drug release experiments were carried out with a dialysis bag (Mw cut-off 12000 - 14000). Reverse-phase HPLC was used to study the pharmacokinetics of liposomal doxorubicin.
RESULTS: The particle size of liposomes with glycinate buffer, citrate buffer and ammonium sulfate as the inner water phase were (103 +/- 8), (102 +/- 12) and (97 +/- 8) nm. The zeta potential and the encapsulation ratio were (-21.3 +/- 0.5), (-21.7 +/- 0.4), (-20.9 +/- 0.7) mV and 47.8%, 96.7%, 98.6%, respectively. The leaking rate of doxorubicin from liposomes was related to the pH value of the release medium. The leaking rate increased at lowered pH. Pharmacokinetic study showed that the MRT (mean retention time) of liposomes with glycinate buffer, citrate buffer and ammonium sulfate as the inner water phase were 12.13, 23.31 and 29.79 h, respectively.
CONCLUSION: Doxorubicin showed different stability in liposomes with different inner water phases, the weaker the acid in the inner water phase, the stabler the liposome. | | Language | chi | | Pub Type(s) | Journal Article
| | PubMed ID | 15813033 |
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