Kinoshita, Ryo Tokushima University|Kumamoto University
異島, 優 Tokushima University 徳島大学 教育研究者総覧
Chuang, Victor T. G. Curtin University
Watanabe, Hiroshi Kumamoto University
清水, 太郎 Tokushima University KAKEN研究者をさがす
安藤, 英紀 Tokushima University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
奥平, 桂一郎 Osaka Medical and Pharmaceutical University KAKEN研究者をさがす
Otagiri, Masaki Sojo University
石田, 竜弘 Tokushima University 徳島大学 教育研究者総覧 KAKEN研究者をさがす
Maruyama, Toru Kumamoto University
human serum albumin
enhanced permeability and retention effect
Human serum albumin (HSA) is a versatile drug carrier with active tumor targeting capacity for an antitumor drug delivery system. Nanoparticle albumin-bound (nab)-technology, such as nab-paclitaxel (Abraxane®), has attracted significant interest in drug delivery research. Recently, we demonstrated that HSA dimer (HSA-d) possesses a higher tumor distribution than HSA monomer (HSA-m). Therefore, HSA-d is more suitable as a drug carrier for antitumor therapy and can improve nab technology. This study investigated the efficacy of HSA-d-doxorubicin (HSA-d-DOX) as next-generation nab technology for tumor treatment. DOX conjugated to HSA-d via a tunable pH-sensitive linker for the controlled release of DOX. Lyophilization did not affect the particle size of HSA-d-DOX or the release of DOX. HSA-d-DOX showed significantly higher cytotoxicity than HSA-m-DOX in vitro. In the SUIzo Tumor-2 (SUIT2) human pancreatic tumor subcutaneous inoculation model, HSA-d-DOX could significantly inhibit tumor growth without causing serious side effects, as compared to the HSA binding DOX prodrug, which utilized endogenous HSA as a nano-drug delivery system (DDS) carrier. These results indicate that HSA-d could function as a natural solubilizer of insoluble drugs and an active targeting carrier in intractable tumors with low vascular permeability, such as pancreatic tumors. In conclusion, HSA-d can be an effective drug carrier for the antitumor drug delivery system against human pancreatic tumors.
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