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Simultaneous measurement of liposome extravasation and content release in tumors.

Publication ,  Journal Article
Wu, NZ; Braun, RD; Gaber, MH; Lin, GM; Ong, ET; Shan, S; Papahadjopoulos, D; Dewhirst, MW
Published in: Microcirculation
March 1997

OBJECTIVE: The success of liposome-based drug delivery systems for tumor targeting relies on maximum extravasation of liposomes into tumor interstitium, as well as optimal release of contents from the liposomes once within the tumor Liposome extravasation and content release are two separate processes that can be individually or jointly manipulated so a method is needed to monitor these two processes independently and simultaneously. In this report, we describe a method to measure liposome extravasation and content release in tumor tissues growing in a rat skinfold window chamber preparation. METHODS: Mixtures of liposomes containing either doxorubicin or calcein, both of which are fluorescent, and liposomes surface-labeled with rhodamine were injected intravenously. Fluorescent, light intensities in a tumor region in two fluorescent channels were measured using an image-processing system. Light intensities of plasma from blood samples were also measured using this system. These measurements were used to calculate the amounts of liposomes and released contents in both plasma and tumor interstitium. The calculations were based on the fact that the liposome surface labels and contents emit fluorescent light at different wavelengths and when encapsulated, the contents fluorescence is self-quenched. The model included equations to account for fluorescent light "cross-contamination" by the two fluorochromes as well as equations relating the measured fluorescent light intensities to the amounts of liposomes and released contents. This method was applied to three situations in which liposome extravasation and content release were manipulated in different, predictable ways. RESULTS AND CONCLUSION: Our results indicate that this method can perform simultaneous independent and quantitative measurements of liposome extravasation and content release. This method can potentially be used to study drug delivery of other carrier systems in vivo.

Duke Scholars

Published In

Microcirculation

DOI

ISSN

1073-9688

Publication Date

March 1997

Volume

4

Issue

1

Start / End Page

83 / 101

Location

United States

Related Subject Headings

  • Temperature
  • Rhodamines
  • Rats
  • Microcirculation
  • Mammary Neoplasms, Experimental
  • Liposomes
  • Hot Temperature
  • Hematocrit
  • Fluorescent Dyes
  • Fluorescence
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Wu, N. Z., Braun, R. D., Gaber, M. H., Lin, G. M., Ong, E. T., Shan, S., … Dewhirst, M. W. (1997). Simultaneous measurement of liposome extravasation and content release in tumors. Microcirculation, 4(1), 83–101. https://doi.org/10.3109/10739689709148320
Wu, N. Z., R. D. Braun, M. H. Gaber, G. M. Lin, E. T. Ong, S. Shan, D. Papahadjopoulos, and M. W. Dewhirst. “Simultaneous measurement of liposome extravasation and content release in tumors.Microcirculation 4, no. 1 (March 1997): 83–101. https://doi.org/10.3109/10739689709148320.
Wu NZ, Braun RD, Gaber MH, Lin GM, Ong ET, Shan S, et al. Simultaneous measurement of liposome extravasation and content release in tumors. Microcirculation. 1997 Mar;4(1):83–101.
Wu, N. Z., et al. “Simultaneous measurement of liposome extravasation and content release in tumors.Microcirculation, vol. 4, no. 1, Mar. 1997, pp. 83–101. Pubmed, doi:10.3109/10739689709148320.
Wu NZ, Braun RD, Gaber MH, Lin GM, Ong ET, Shan S, Papahadjopoulos D, Dewhirst MW. Simultaneous measurement of liposome extravasation and content release in tumors. Microcirculation. 1997 Mar;4(1):83–101.
Journal cover image

Published In

Microcirculation

DOI

ISSN

1073-9688

Publication Date

March 1997

Volume

4

Issue

1

Start / End Page

83 / 101

Location

United States

Related Subject Headings

  • Temperature
  • Rhodamines
  • Rats
  • Microcirculation
  • Mammary Neoplasms, Experimental
  • Liposomes
  • Hot Temperature
  • Hematocrit
  • Fluorescent Dyes
  • Fluorescence