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Visualisation of doxorubicin in human and animal tissues and in cell cultures by immunogold-silver staining.
In previous pharmacologic studies, the native fluorescent properties of doxorubicin (DOX) have been utilised to visualise tissue and cellular drug distribution. Such distribution studies provide valuable additional information to that obtained by measuring tissue drug concentration alone. An alterna...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1992
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977343/ https://www.ncbi.nlm.nih.gov/pubmed/1733446 |
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author | Henneberry, H. P. Aherne, G. W. |
author_facet | Henneberry, H. P. Aherne, G. W. |
author_sort | Henneberry, H. P. |
collection | PubMed |
description | In previous pharmacologic studies, the native fluorescent properties of doxorubicin (DOX) have been utilised to visualise tissue and cellular drug distribution. Such distribution studies provide valuable additional information to that obtained by measuring tissue drug concentration alone. An alternative immunocytochemical method of drug localisation using a rabbit immunoadsorbed antiserum to DOX and silver-enhanced gold-labelled second antibodies has been used to achieve visualisation of DOX in normal and malignant tissues from drug-treated animals and patients, and in human tumour cell lines treated in vitro. Non-specific staining in untreated tissues or in controls stained without primary antibody was minimal. Widespread dark brown to black specific immunostaining was observed in the normal tissues of drug-treated animals and in rat sarcoma and in the mouse EMT6 mammary tumour. In human breast tumour biopsy samples obtained at surgery 1 h following a 25 mg intravenous dose of DOX, considerable variation in drug distribution was observed which appeared to be related to drug concentration. Both nuclear and membrane staining was apparent; the latter was especially noticeable in human tumour cells grown in the presence of DOX at concentrations greater than 0.92 microM. Immunolocalisation using silver enhanced gold-labelled reagents provides an additional technique to study cell and organ specific differences in drug uptake and distribution. IMAGES: |
format | Text |
id | pubmed-1977343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19773432009-09-10 Visualisation of doxorubicin in human and animal tissues and in cell cultures by immunogold-silver staining. Henneberry, H. P. Aherne, G. W. Br J Cancer Research Article In previous pharmacologic studies, the native fluorescent properties of doxorubicin (DOX) have been utilised to visualise tissue and cellular drug distribution. Such distribution studies provide valuable additional information to that obtained by measuring tissue drug concentration alone. An alternative immunocytochemical method of drug localisation using a rabbit immunoadsorbed antiserum to DOX and silver-enhanced gold-labelled second antibodies has been used to achieve visualisation of DOX in normal and malignant tissues from drug-treated animals and patients, and in human tumour cell lines treated in vitro. Non-specific staining in untreated tissues or in controls stained without primary antibody was minimal. Widespread dark brown to black specific immunostaining was observed in the normal tissues of drug-treated animals and in rat sarcoma and in the mouse EMT6 mammary tumour. In human breast tumour biopsy samples obtained at surgery 1 h following a 25 mg intravenous dose of DOX, considerable variation in drug distribution was observed which appeared to be related to drug concentration. Both nuclear and membrane staining was apparent; the latter was especially noticeable in human tumour cells grown in the presence of DOX at concentrations greater than 0.92 microM. Immunolocalisation using silver enhanced gold-labelled reagents provides an additional technique to study cell and organ specific differences in drug uptake and distribution. IMAGES: Nature Publishing Group 1992-01 /pmc/articles/PMC1977343/ /pubmed/1733446 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 Henneberry, H. P. Aherne, G. W. Visualisation of doxorubicin in human and animal tissues and in cell cultures by immunogold-silver staining. |
title | Visualisation of doxorubicin in human and animal tissues and in cell cultures by immunogold-silver staining. |
title_full | Visualisation of doxorubicin in human and animal tissues and in cell cultures by immunogold-silver staining. |
title_fullStr | Visualisation of doxorubicin in human and animal tissues and in cell cultures by immunogold-silver staining. |
title_full_unstemmed | Visualisation of doxorubicin in human and animal tissues and in cell cultures by immunogold-silver staining. |
title_short | Visualisation of doxorubicin in human and animal tissues and in cell cultures by immunogold-silver staining. |
title_sort | visualisation of doxorubicin in human and animal tissues and in cell cultures by immunogold-silver staining. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977343/ https://www.ncbi.nlm.nih.gov/pubmed/1733446 |
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