Multichannel Imaging to Quantify Four Classes of Pharmacokinetic Distribution in Tumors. Issue 10 (21st July 2014)
- Record Type:
- Journal Article
- Title:
- Multichannel Imaging to Quantify Four Classes of Pharmacokinetic Distribution in Tumors. Issue 10 (21st July 2014)
- Main Title:
- Multichannel Imaging to Quantify Four Classes of Pharmacokinetic Distribution in Tumors
- Authors:
- Bhatnagar, Sumit
Deschenes, Emily
Liao, Jianshan
Cilliers, Cornelius
Thurber, Greg M. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Low and heterogeneous delivery of drugs and imaging agents to tumors results in decreased efficacy and poor imaging results. Systemic delivery involves a complex interplay of drug properties and physiological factors, and heterogeneity in the tumor microenvironment makes predicting and overcoming these limitations exceptionally difficult. Theoretical models have indicated that there are four different classes of pharmacokinetic behavior in tissue, depending on the fundamental steps in distribution. In order to study these limiting behaviors, we used multichannel fluorescence microscopy and stitching of high‐resolution images to examine the distribution of four agents in the same tumor microenvironment. A validated generic partial differential equation model with a graphical user interface was used to select fluorescent agents exhibiting these four classes of behavior, and the imaging results agreed with predictions. BODIPY‐FL exhibited higher concentrations in tissue with high blood flow, cetuximab gave perivascular distribution limited by permeability, high plasma protein and target binding resulted in diffusion‐limited distribution for Hoechst 33342, and Integrisense 680 was limited by the number of binding sites in the tissue. Together, the probes and simulations can be used to investigate distribution in other tumor models, predict tumor drug distribution profiles, and design and<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Low and heterogeneous delivery of drugs and imaging agents to tumors results in decreased efficacy and poor imaging results. Systemic delivery involves a complex interplay of drug properties and physiological factors, and heterogeneity in the tumor microenvironment makes predicting and overcoming these limitations exceptionally difficult. Theoretical models have indicated that there are four different classes of pharmacokinetic behavior in tissue, depending on the fundamental steps in distribution. In order to study these limiting behaviors, we used multichannel fluorescence microscopy and stitching of high‐resolution images to examine the distribution of four agents in the same tumor microenvironment. A validated generic partial differential equation model with a graphical user interface was used to select fluorescent agents exhibiting these four classes of behavior, and the imaging results agreed with predictions. BODIPY‐FL exhibited higher concentrations in tissue with high blood flow, cetuximab gave perivascular distribution limited by permeability, high plasma protein and target binding resulted in diffusion‐limited distribution for Hoechst 33342, and Integrisense 680 was limited by the number of binding sites in the tissue. Together, the probes and simulations can be used to investigate distribution in other tumor models, predict tumor drug distribution profiles, and design and interpret <italic>in vivo</italic> experiments. © 2014 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 103:3276–3286, 2014</p> </abstract> … (more)
- Is Part Of:
- Journal of pharmaceutical sciences. Volume 103:Issue 10(2014:Oct.)
- Journal:
- Journal of pharmaceutical sciences
- Issue:
- Volume 103:Issue 10(2014:Oct.)
- Issue Display:
- Volume 103, Issue 10 (2014)
- Year:
- 2014
- Volume:
- 103
- Issue:
- 10
- Issue Sort Value:
- 2014-0103-0010-0000
- Page Start:
- 3276
- Page End:
- 3286
- Publication Date:
- 2014-07-21
- Subjects:
- Pharmacy -- Periodicals
615.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1520-6017 ↗
http://www.jpharmsci.org/issues ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jps.24086 ↗
- Languages:
- English
- ISSNs:
- 0022-3549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5031.900000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3890.xml