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Cancer Cell Radiobiological Studies Using In-House-Developed α-Particle Irradiator.

Nilsson, Jenny ; Bauden, Monika LU orcid ; Nilsson, Jonas LU ; Strand, Sven-Erik LU and Elgqvist, Jörgen LU (2015) In Cancer Biotherapy & Radiopharmaceuticals 30(9). p.386-394
Abstract
An α-particle irradiator, enabling high-precision irradiation of cells for in vitro studies, has been constructed. The irradiation source was a (241)Am source, on which well inserts containing cancer cells growing in monolayer were placed. The total radioactivity, uniformity, and α-particle spectrum were determined by use of HPGe detector, Gafchromic™ dosimetry film, and PIPS(®) detector measurements, respectively. Monte Carlo simulations were used for dosimetry. Three prostate cancer (LNCaP, DU145, PC3) and three pancreatic cancer (Capan-1, Panc-1, BxPC-3) cell lines were irradiated by α-particles to the absorbed doses 0, 0.5, 1, and 2 Gy. For reference, cells were irradiated using (137)Cs to the absorbed doses 0, 1, 2, 4, 6, 8, and 10... (More)
An α-particle irradiator, enabling high-precision irradiation of cells for in vitro studies, has been constructed. The irradiation source was a (241)Am source, on which well inserts containing cancer cells growing in monolayer were placed. The total radioactivity, uniformity, and α-particle spectrum were determined by use of HPGe detector, Gafchromic™ dosimetry film, and PIPS(®) detector measurements, respectively. Monte Carlo simulations were used for dosimetry. Three prostate cancer (LNCaP, DU145, PC3) and three pancreatic cancer (Capan-1, Panc-1, BxPC-3) cell lines were irradiated by α-particles to the absorbed doses 0, 0.5, 1, and 2 Gy. For reference, cells were irradiated using (137)Cs to the absorbed doses 0, 1, 2, 4, 6, 8, and 10 Gy. Radiation sensitivity was estimated using a tetrazolium salt-based colorimetric assay with absorbance measurements at 450 nm. The relative biological effectiveness for α-particles relative to γ-irradiation at 37% cell survival for the LNCaP, DU145, PC3, Capan-1, Panc-1, and BxPC-3 cells was 7.9 ± 1.7, 8.0 ± 0.8, 7.0 ± 1.1, 12.5 ± 1.6, 9.4 ± 0.9, and 6.2 ± 0.7, respectively. The results show the feasibility of constructing a desktop α-particle irradiator as well as indicate that both prostate and pancreatic cancers are good candidates for further studies of α-particle radioimmunotherapy. (Less)
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author
; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Cancer Biotherapy & Radiopharmaceuticals
volume
30
issue
9
pages
386 - 394
publisher
Mary Ann Liebert, Inc.
external identifiers
  • pmid:26560194
  • wos:000364485500003
  • scopus:84946908215
  • pmid:26560194
ISSN
1557-8852
DOI
10.1089/cbr.2015.1895
project
Pancreatic cancer
language
English
LU publication?
yes
id
dcaff552-c71b-472b-bbc6-675387f332a6 (old id 8235921)
alternative location
http://www.ncbi.nlm.nih.gov/pubmed/26560194?dopt=Abstract
date added to LUP
2016-04-01 10:06:38
date last changed
2022-02-02 06:28:34
@article{dcaff552-c71b-472b-bbc6-675387f332a6,
  abstract     = {{An α-particle irradiator, enabling high-precision irradiation of cells for in vitro studies, has been constructed. The irradiation source was a (241)Am source, on which well inserts containing cancer cells growing in monolayer were placed. The total radioactivity, uniformity, and α-particle spectrum were determined by use of HPGe detector, Gafchromic™ dosimetry film, and PIPS(®) detector measurements, respectively. Monte Carlo simulations were used for dosimetry. Three prostate cancer (LNCaP, DU145, PC3) and three pancreatic cancer (Capan-1, Panc-1, BxPC-3) cell lines were irradiated by α-particles to the absorbed doses 0, 0.5, 1, and 2 Gy. For reference, cells were irradiated using (137)Cs to the absorbed doses 0, 1, 2, 4, 6, 8, and 10 Gy. Radiation sensitivity was estimated using a tetrazolium salt-based colorimetric assay with absorbance measurements at 450 nm. The relative biological effectiveness for α-particles relative to γ-irradiation at 37% cell survival for the LNCaP, DU145, PC3, Capan-1, Panc-1, and BxPC-3 cells was 7.9 ± 1.7, 8.0 ± 0.8, 7.0 ± 1.1, 12.5 ± 1.6, 9.4 ± 0.9, and 6.2 ± 0.7, respectively. The results show the feasibility of constructing a desktop α-particle irradiator as well as indicate that both prostate and pancreatic cancers are good candidates for further studies of α-particle radioimmunotherapy.}},
  author       = {{Nilsson, Jenny and Bauden, Monika and Nilsson, Jonas and Strand, Sven-Erik and Elgqvist, Jörgen}},
  issn         = {{1557-8852}},
  language     = {{eng}},
  number       = {{9}},
  pages        = {{386--394}},
  publisher    = {{Mary Ann Liebert, Inc.}},
  series       = {{Cancer Biotherapy & Radiopharmaceuticals}},
  title        = {{Cancer Cell Radiobiological Studies Using In-House-Developed α-Particle Irradiator.}},
  url          = {{https://lup.lub.lu.se/search/files/1570615/8864967.pdf}},
  doi          = {{10.1089/cbr.2015.1895}},
  volume       = {{30}},
  year         = {{2015}},
}