RADIOISOTOPES

Online ISSN: 1884-4111 Print ISSN: 0033-8303
RADIOISOTOPESは日本アイソトープ協会が発行する学術論文誌です
Radioisotopes 75(1): 45-59 (2026)
doi:10.3769/radioisotopes.750108

原著Article

125I標識linear-polyglycerol lactosomeの複数回投与における腫瘍集積の初期評価Initial Evaluation of Tumor Accumulation during Multiple Dosing of 125I-labeled Linear-polyglycerol-modified Lactosome

1東北医科薬科大学薬学部Faculty of Pharmaceutical Sciences, Tohoku Medical and Pharmaceutical University

2福井大学高エネルギー医学研究センターBiomedical Imaging Research Center, University of Fukui

3浜松医科大学光医学総合研究所Institute of Photonics Medicine, Hamamatsu University School of Medicine

受付日:2025年7月30日Received: July 30, 2025
受理日:2025年11月6日Accepted: November 6, 2025
発行日:2026年3月15日Published: March 15, 2026
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Lactosomeは親水性部位にpoly(sarcosine)70,疎水性部位にpoly(L-lactic acid)30(PSar70-block-PLLA30)を有する両親媒性ポリデプシペプチドから成るミセル粒子であり,Enhanced Permeability and Retention (EPR)効果により腫瘍集積性を示す。しかし,初回投与により抗lactosome IgMの産生が誘発され,複数回投与後は肝臓に捕捉され腫瘍集積性が失われるAccelerated Blood Clearance(ABC)現象が発現する。複数回投与後の腫瘍集積を維持するために,重合度が10 merから成るlinear-poly(glycerol)10lin-PG10)で修飾したlactosomeから形成される新規ナノ粒子(lin-PG10 lactosome)を調製した。Lin-PG10とPLLA30を含む両親媒性ポリマーを合成し,Film法によりlactosomeに修飾した。Lin-PG10 lactosomeのIgM産生は,投与7日後に採取したマウス血漿を用いてELISA法により評価した。N-[125I]Iodobenzoyl poly(L-lactic acid)30125I-BzPLLA30)を組み込んで125I標識10%lin-PG10 lactosomeを調製し,Colon-26移植マウスを用いて1回目および2回目投与時の生体内分布を比較した。10%lin-PG10 lactosomeはlactosomeと比較して抗lactosome IgMの産生が抑制された。Colon-26移植マウスを用いた生体内分布評価では,1回目の投与では腫瘍への集積が認められたが,2回目の投与では腫瘍への集積量の減少が認められ,十分な改善には至らなかった。このことから,改良の余地はあるものの,lactosomeに官能基を導入することで抗体産生を抑制できる可能性が示唆された。

Lactosome is a polymeric micelle composed of an amphiphilic polydepsipeptide, a hydrophilic block poly(sarcosine)70, and a hydrophobic block poly(L-lactic acid)30(PSar70-block-PLLA30), which accumulates in solid tumors through the enhanced permeability and retention effect. However, following administration its pharmacokinetics shift from tumor accumulation to liver sequestration due to anti-lactosome IgM production triggered by the initial administration. This phenomenon is called Accelerated Blood Clearance. To enhance tumor accumulation after multiple doses, a novel nanoparticle composed of lactosome modified with linear-poly(glycerol)10 (lin-PG10) (lin-PG10 lactosome) was prepared. Amphiphilic polymer with lin-PG10 and PLLA30 were synthesized and modified into lactosome by the Film method. IgM production of lin-PG10 lactosome was evaluated by ELISA using mice plasma collected 7 days after dosing. 125I-labeled 10%lin-PG10 lactosome was prepared by incorporating N-[125I]iodobenzoyl poly(L-lactic acid)30(125I-BzPLLA30). Biodistribution was compared 1st and 2nd doses using Colon-26 bearing mice. 10%lin-PG10 lactosome was reduced anti-lactosome IgM production compared with lactosome. Evaluation of biodistribution in Colon-26 bearing mice showed that the 1st dose showed accumulation in tumors, but the 2nd dose showed a reduction in the amount of accumulation in tumors, which was not sufficient improvement. This suggests that antibody production may be inhibited by introducing functional groups into lactosomes, although there is room for improvement.

Key words: nanocarrier; accelerated blood clearance phenomenon; polyglycerol

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