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Intratumoral Injection of (188)Re labeled Cationic Polyethylenimine Conjugates: A Preliminary Report

(188)Re(Rhenium) is easily obtained from an in-house (188)W/(188)Re generator that is similar to the current (99)Mo/(99m)Tc generator, making it very convenient for clinical use. This characteristic makes this radionuclide a promising candidate as a therapeutic agent. Polyethylenimine (PEI) is a cat...

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Autores principales: Kim, Eun-Mi, Jeong, Hwan-Jeong, Heo, Young-Jun, Moon, Hyung-Bae, Bom, Hee-Seung, Kim, Chang-Guhn
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816324/
https://www.ncbi.nlm.nih.gov/pubmed/15483337
http://dx.doi.org/10.3346/jkms.2004.19.5.647
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author Kim, Eun-Mi
Jeong, Hwan-Jeong
Heo, Young-Jun
Moon, Hyung-Bae
Bom, Hee-Seung
Kim, Chang-Guhn
author_facet Kim, Eun-Mi
Jeong, Hwan-Jeong
Heo, Young-Jun
Moon, Hyung-Bae
Bom, Hee-Seung
Kim, Chang-Guhn
author_sort Kim, Eun-Mi
collection PubMed
description (188)Re(Rhenium) is easily obtained from an in-house (188)W/(188)Re generator that is similar to the current (99)Mo/(99m)Tc generator, making it very convenient for clinical use. This characteristic makes this radionuclide a promising candidate as a therapeutic agent. Polyethylenimine (PEI) is a cationic polymer and has been used as a gene delivery vector. Positively charged materials interact with cellular blood components, vascular endothelium, and plasma proteins. In this study, the authors investigated whether intratumoral injection of (188)Re labeled transferrin (Tf)-PEI conjugates exert the effect of radionuclide therapy against the tumor cells. When the diameters of the Ramos lymphoma (human Burkitt's lymphoma) xenografted tumors reached approximately 1 cm, 3 kinds of (188)Re bound compounds (HYNIC-PEI-Tf, HYNIC-PEI, (188)Re perrhenate) were injected directly into the tumors. There were increases in the retention of (188)Re inside the tumor when PEI was incorporated with (188)Re compared to the use of free (188)Re. The (188)Re HYNIC-Tf-PEI showed the most retention inside the tumor (retention rate=approximately 97%). H&E stain of isolated tumor tissues showed that (188)Re labeled HYNIC-PEI-Tf caused extensive tumor necrosis. These results support (188)Re HYNIC-PEI-Tf as being a useful radiopharmaceutical agent to treat tumors when delievered by intratumoral injection.
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spelling pubmed-28163242010-02-04 Intratumoral Injection of (188)Re labeled Cationic Polyethylenimine Conjugates: A Preliminary Report Kim, Eun-Mi Jeong, Hwan-Jeong Heo, Young-Jun Moon, Hyung-Bae Bom, Hee-Seung Kim, Chang-Guhn J Korean Med Sci Original Article (188)Re(Rhenium) is easily obtained from an in-house (188)W/(188)Re generator that is similar to the current (99)Mo/(99m)Tc generator, making it very convenient for clinical use. This characteristic makes this radionuclide a promising candidate as a therapeutic agent. Polyethylenimine (PEI) is a cationic polymer and has been used as a gene delivery vector. Positively charged materials interact with cellular blood components, vascular endothelium, and plasma proteins. In this study, the authors investigated whether intratumoral injection of (188)Re labeled transferrin (Tf)-PEI conjugates exert the effect of radionuclide therapy against the tumor cells. When the diameters of the Ramos lymphoma (human Burkitt's lymphoma) xenografted tumors reached approximately 1 cm, 3 kinds of (188)Re bound compounds (HYNIC-PEI-Tf, HYNIC-PEI, (188)Re perrhenate) were injected directly into the tumors. There were increases in the retention of (188)Re inside the tumor when PEI was incorporated with (188)Re compared to the use of free (188)Re. The (188)Re HYNIC-Tf-PEI showed the most retention inside the tumor (retention rate=approximately 97%). H&E stain of isolated tumor tissues showed that (188)Re labeled HYNIC-PEI-Tf caused extensive tumor necrosis. These results support (188)Re HYNIC-PEI-Tf as being a useful radiopharmaceutical agent to treat tumors when delievered by intratumoral injection. The Korean Academy of Medical Sciences 2004-10 2004-10-30 /pmc/articles/PMC2816324/ /pubmed/15483337 http://dx.doi.org/10.3346/jkms.2004.19.5.647 Text en Copyright © 2004 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Eun-Mi
Jeong, Hwan-Jeong
Heo, Young-Jun
Moon, Hyung-Bae
Bom, Hee-Seung
Kim, Chang-Guhn
Intratumoral Injection of (188)Re labeled Cationic Polyethylenimine Conjugates: A Preliminary Report
title Intratumoral Injection of (188)Re labeled Cationic Polyethylenimine Conjugates: A Preliminary Report
title_full Intratumoral Injection of (188)Re labeled Cationic Polyethylenimine Conjugates: A Preliminary Report
title_fullStr Intratumoral Injection of (188)Re labeled Cationic Polyethylenimine Conjugates: A Preliminary Report
title_full_unstemmed Intratumoral Injection of (188)Re labeled Cationic Polyethylenimine Conjugates: A Preliminary Report
title_short Intratumoral Injection of (188)Re labeled Cationic Polyethylenimine Conjugates: A Preliminary Report
title_sort intratumoral injection of (188)re labeled cationic polyethylenimine conjugates: a preliminary report
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816324/
https://www.ncbi.nlm.nih.gov/pubmed/15483337
http://dx.doi.org/10.3346/jkms.2004.19.5.647
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