Cargando…

The use of angiotensin II as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour.

Cytotoxic microspheres have been developed for intra-arterial use in patients with liver metastases. Following injection, the distribution of microspheres reflects the pattern of hepatic arterial blood-flow. Vasoactive agents, such as angiotensin II, by producing vasoconstriction in normal liver, mi...

Descripción completa

Detalles Bibliográficos
Autores principales: Goldberg, J. A., Murray, T., Kerr, D. J., Willmott, N., Bessent, R. G., McKillop, J. H., McArdle, C. S.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1991
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971787/
https://www.ncbi.nlm.nih.gov/pubmed/1997111
_version_ 1782134985222782976
author Goldberg, J. A.
Murray, T.
Kerr, D. J.
Willmott, N.
Bessent, R. G.
McKillop, J. H.
McArdle, C. S.
author_facet Goldberg, J. A.
Murray, T.
Kerr, D. J.
Willmott, N.
Bessent, R. G.
McKillop, J. H.
McArdle, C. S.
author_sort Goldberg, J. A.
collection PubMed
description Cytotoxic microspheres have been developed for intra-arterial use in patients with liver metastases. Following injection, the distribution of microspheres reflects the pattern of hepatic arterial blood-flow. Vasoactive agents, such as angiotensin II, by producing vasoconstriction in normal liver, might divert arterial blood toward tumour and thereby enhance the delivery of drug-loaded particles. Using a double isotope technique, the distribution of radiolabelled microspheres to tumour and normal liver tissue was measured before and after angiotensin II infusion in nine patients with multiple liver metastases. The median increase in tumour: normal ratio following angiotensin II infusion was by a factor of 2.8 (range 0.8-11.7, P less than 0.05). This novel approach to regional chemotherapy, using a combination of angiotensin II infusion and cytotoxic microspheres, increases the exposure of tumour to cytotoxic agents and may, therefore, enhance tumour response rates.
format Text
id pubmed-1971787
institution National Center for Biotechnology Information
language English
publishDate 1991
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-19717872009-09-10 The use of angiotensin II as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour. Goldberg, J. A. Murray, T. Kerr, D. J. Willmott, N. Bessent, R. G. McKillop, J. H. McArdle, C. S. Br J Cancer Research Article Cytotoxic microspheres have been developed for intra-arterial use in patients with liver metastases. Following injection, the distribution of microspheres reflects the pattern of hepatic arterial blood-flow. Vasoactive agents, such as angiotensin II, by producing vasoconstriction in normal liver, might divert arterial blood toward tumour and thereby enhance the delivery of drug-loaded particles. Using a double isotope technique, the distribution of radiolabelled microspheres to tumour and normal liver tissue was measured before and after angiotensin II infusion in nine patients with multiple liver metastases. The median increase in tumour: normal ratio following angiotensin II infusion was by a factor of 2.8 (range 0.8-11.7, P less than 0.05). This novel approach to regional chemotherapy, using a combination of angiotensin II infusion and cytotoxic microspheres, increases the exposure of tumour to cytotoxic agents and may, therefore, enhance tumour response rates. Nature Publishing Group 1991-02 /pmc/articles/PMC1971787/ /pubmed/1997111 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Goldberg, J. A.
Murray, T.
Kerr, D. J.
Willmott, N.
Bessent, R. G.
McKillop, J. H.
McArdle, C. S.
The use of angiotensin II as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour.
title The use of angiotensin II as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour.
title_full The use of angiotensin II as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour.
title_fullStr The use of angiotensin II as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour.
title_full_unstemmed The use of angiotensin II as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour.
title_short The use of angiotensin II as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour.
title_sort use of angiotensin ii as a potential method of targeting cytotoxic microspheres in patients with intrahepatic tumour.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971787/
https://www.ncbi.nlm.nih.gov/pubmed/1997111
work_keys_str_mv AT goldbergja theuseofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT murrayt theuseofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT kerrdj theuseofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT willmottn theuseofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT bessentrg theuseofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT mckillopjh theuseofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT mcardlecs theuseofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT goldbergja useofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT murrayt useofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT kerrdj useofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT willmottn useofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT bessentrg useofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT mckillopjh useofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour
AT mcardlecs useofangiotensiniiasapotentialmethodoftargetingcytotoxicmicrospheresinpatientswithintrahepatictumour