WEKO3
アイテム
Quantitative Radionuclide Imaging Analysis of Enhanced Drug Delivery Induced by Photoimmunotherapy
https://repo.qst.go.jp/records/85633
https://repo.qst.go.jp/records/85633dc545695-bd3e-4cd9-89ad-1ed4be6d1c3f
Item type | 学術雑誌論文 / Journal Article(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2021-08-12 | |||||
タイトル | ||||||
タイトル | Quantitative Radionuclide Imaging Analysis of Enhanced Drug Delivery Induced by Photoimmunotherapy | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Kuribayashi, Winnaung
× Kuribayashi, Winnaung× Tsuji, Atsushi× Sugyo, Aya× Fujinaga, Masayuki× Ming-Rong, Zhang× Higashi, Tatsuya× Winnaung, Kuribayashi× Atsushi, Tsuji× Aya, Sugyo× Masayuki, Fujinaga× Zhang, Ming-Rong× Tatsuya, Higashi |
|||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Photoimmunotherapy (PIT) is an upcoming potential cancer treatment modality, the effect of which is improved in combination with chemotherapy. PIT causes a super-enhanced permeability and retention (SUPR) effect. Here, we quantitatively evaluated the SUPR effect using radiolabeled drugs of varying molecular weights (F-5FU, In-DTPA, Tc-HSA-D, and In-IgG) to determine the appropriate drug size. PIT was conducted with an indocyanine green-labeled anti-HER2 antibody and an 808 nm laser irradiation. Mice were subcutaneously inoculated with HER2-positive cells in both hindlimbs. The tumor on one side was treated with PIT, and the contralateral side was not treated. The differences between tumor accumulations were evaluated using positron emission tomography or single-photon emission computed tomography. Imaging studies found increased tumor accumulation of agents after PIT. PIT-treated tumors showed significantly increased uptake of F-5FU ( < 0.001) and Tc-HSA-D ( < 0.001). A tendency toward increased accumulation of In-DTPA and In-IgG was observed. These findings suggest that some low- and medium-molecular-weight agents are promising candidates for combined PIT, as are macromolecules; hence, administration after PIT could enhance their efficacy. Our findings encourage further preclinical and clinical studies to develop a combination therapy of PIT with conventional anticancer drugs. | |||||
書誌情報 |
International Journal of Molecular Sciences 巻 22, 号 15, p. 8316, 発行日 2021-08 |
|||||
出版者 | ||||||
出版者 | MDPI | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1422-0067 | |||||
PubMed番号 | ||||||
識別子タイプ | PMID | |||||
関連識別子 | 34361080 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.3390/ijms22158316 | |||||
関連サイト | ||||||
識別子タイプ | DOI | |||||
関連識別子 | https://doi.org/10.3390/ijms22158316 |