Release of liposomal contents by cell-secreted matrix metalloproteinase-9.

TitleRelease of liposomal contents by cell-secreted matrix metalloproteinase-9.
Publication TypeJournal Article
Year of Publication2009
AuthorsBanerjee J, Hanson AJ, Gadam B, Elegbede AI, Tobwala S, Ganguly B, Wagh AV, Muhonen WW, Law B, Shabb JB, Srivastava DK, Mallik S
JournalBioconjug Chem
Volume20
Issue7
Pagination1332-9
Date Published2009 Jul
ISSN1520-4812
KeywordsAdenocarcinoma, Breast Neoplasms, Cell Line, Tumor, Colorectal Neoplasms, Female, Fluoresceins, Humans, Lipopeptides, Liposomes, Matrix Metalloproteinase 9
Abstract

Liposomes have been widely used as a drug delivery vehicle, and currently, more than 10 liposomal formulations are approved by the Food and Drug Administration for clinical use. However, upon targeting, the release of the liposome-encapsulated contents is usually slow. We have recently demonstrated that contents from appropriately formulated liposomes can be rapidly released by the cancer-associated enzyme matrix metalloproteinase-9 (MMP-9). Herein, we report our detailed studies to optimize the liposomal formulations. By properly selecting the lipopeptide, the major lipid component, and their relative amounts, we demonstrate that the contents are rapidly released in the presence of cancer-associated levels of recombinant human MMP-9. We observed that the degree of lipid mismatch between the lipopepides and the major lipid component profoundly affects the release profiles from the liposomes. By utilizing the optimized liposomal formulations, we also demonstrate that cancer cells (HT-29) which secrete low levels of MMP-9 failed to release a significant amount of the liposomal contents. Metastatic cancer cells (MCF7) secreting high levels of the enzyme rapidly release the encapsulated contents from the liposomes.

DOI10.1021/bc9000646
Alternate JournalBioconjug Chem
PubMed ID19601658
PubMed Central IDPMC3247015
Grant ListP20 RR016471 / RR / NCRR NIH HHS / United States
1R01 CA113746 / CA / NCI NIH HHS / United States
R01 CA113746 / CA / NCI NIH HHS / United States
1 R01 CA 132034 / CA / NCI NIH HHS / United States
P20 RR016741 / RR / NCRR NIH HHS / United States
R01 CA132034 / CA / NCI NIH HHS / United States
R01 CA132034-03 / CA / NCI NIH HHS / United States
Related Institute: 
Molecular Imaging Innovations Institute (MI3)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065