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Intracellular Hyperthermia for Cancer Using Magnetite Cationic Liposomes: In vitro Study

‘Magnetite cationic liposomes (MCL)’ were developed as a means to generate intracellular hyperthermia. Affinity of the MCL to glioma cells was ten times higher than that of magnetite‘neutral’ liposomes due to the electrostatic interaction based on the positive charge of the MCL. Heat generation of t...

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Detalles Bibliográficos
Autores principales: Shinkai, Masashige, Yanase, Mitsugu, Honda, Hiroyuki, Wakabayashi, Toshihiko, Yoshida, Jun, Kobayashi, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921008/
https://www.ncbi.nlm.nih.gov/pubmed/9045948
http://dx.doi.org/10.1111/j.1349-7006.1996.tb03129.x
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author Shinkai, Masashige
Yanase, Mitsugu
Honda, Hiroyuki
Wakabayashi, Toshihiko
Yoshida, Jun
Kobayashi, Takeshi
author_facet Shinkai, Masashige
Yanase, Mitsugu
Honda, Hiroyuki
Wakabayashi, Toshihiko
Yoshida, Jun
Kobayashi, Takeshi
author_sort Shinkai, Masashige
collection PubMed
description ‘Magnetite cationic liposomes (MCL)’ were developed as a means to generate intracellular hyperthermia. Affinity of the MCL to glioma cells was ten times higher than that of magnetite‘neutral’ liposomes due to the electrostatic interaction based on the positive charge of the MCL. Heat generation of the MCL was studied using agar phantoms and small pellets of rat glioma cells. When a high‐frequency magnetic field, 118 kHz, 384 Oe was applied to glioma cells in the presence of MCL, the glioma cell pellet of 80 μl (5.4 mm in diameter) was heated to over 43°C and all the cells died after 40 min irradiation owing to the hyperthermic effect. The terminal temperature of the cell pellet was proportional to the pellet volume when other parameters were constant. It thus appears that the MCL can heat a tumor of more than 80 μl in volume to above 42°C.
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spelling pubmed-59210082018-05-11 Intracellular Hyperthermia for Cancer Using Magnetite Cationic Liposomes: In vitro Study Shinkai, Masashige Yanase, Mitsugu Honda, Hiroyuki Wakabayashi, Toshihiko Yoshida, Jun Kobayashi, Takeshi Jpn J Cancer Res Article ‘Magnetite cationic liposomes (MCL)’ were developed as a means to generate intracellular hyperthermia. Affinity of the MCL to glioma cells was ten times higher than that of magnetite‘neutral’ liposomes due to the electrostatic interaction based on the positive charge of the MCL. Heat generation of the MCL was studied using agar phantoms and small pellets of rat glioma cells. When a high‐frequency magnetic field, 118 kHz, 384 Oe was applied to glioma cells in the presence of MCL, the glioma cell pellet of 80 μl (5.4 mm in diameter) was heated to over 43°C and all the cells died after 40 min irradiation owing to the hyperthermic effect. The terminal temperature of the cell pellet was proportional to the pellet volume when other parameters were constant. It thus appears that the MCL can heat a tumor of more than 80 μl in volume to above 42°C. Blackwell Publishing Ltd 1996-11 /pmc/articles/PMC5921008/ /pubmed/9045948 http://dx.doi.org/10.1111/j.1349-7006.1996.tb03129.x Text en
spellingShingle Article
Shinkai, Masashige
Yanase, Mitsugu
Honda, Hiroyuki
Wakabayashi, Toshihiko
Yoshida, Jun
Kobayashi, Takeshi
Intracellular Hyperthermia for Cancer Using Magnetite Cationic Liposomes: In vitro Study
title Intracellular Hyperthermia for Cancer Using Magnetite Cationic Liposomes: In vitro Study
title_full Intracellular Hyperthermia for Cancer Using Magnetite Cationic Liposomes: In vitro Study
title_fullStr Intracellular Hyperthermia for Cancer Using Magnetite Cationic Liposomes: In vitro Study
title_full_unstemmed Intracellular Hyperthermia for Cancer Using Magnetite Cationic Liposomes: In vitro Study
title_short Intracellular Hyperthermia for Cancer Using Magnetite Cationic Liposomes: In vitro Study
title_sort intracellular hyperthermia for cancer using magnetite cationic liposomes: in vitro study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921008/
https://www.ncbi.nlm.nih.gov/pubmed/9045948
http://dx.doi.org/10.1111/j.1349-7006.1996.tb03129.x
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