4.7 Article

Development of 99mTc-Labeled Human Serum Albumin with Prolonged Circulation by Chelate-then-Click Approach: A Potential Blood Pool Imaging Agent

Journal

MOLECULAR PHARMACEUTICS
Volume 16, Issue 4, Pages 1586-1595

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.8b01258

Keywords

chelate-then-click; human serum albumin; SPECT; blood pool imaging; ADIBO-HSA

Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2017R1D1A1B03035556]
  2. Ministry of Health and Welfare Korea [HI18C0886]
  3. National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2017M2A2A7A01021401, 2017M3A9G5082640]
  4. National Research Foundation of Korea [2017M2A2A7A01021401, 2017M3A9G5082640] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Technetium-(99m)-labeled human serum albumin (Tc-99m-HSA) has been utilized as a blood pool imaging agent in the clinic for several decades. However, Tc-99m-HSA has a short circulation time, which is a critical shortcoming for a blood pool imaging agent. Herein, we developed a novel Tc-99m-labeled HSA with a long circulation time using click chemistry and a chelator, 2,2'-dipicolylamine (DPA), (Tc-99m-DPA-HSA). Specifically, we examined the feasibility of copper-free strain-promoted alkyne-azide cycloaddition (SPAAC) for the incorporation of HSA to the [Tc-99m (CO)(3)(H2O)(3)](+) system by adopting a chelate-then-click approach. In this strategy, a potent chelate system, azide-functionalized DPA, was first complexed with [Tc-99m (CO)(3)(H2O)(3)](+), followed by the SPAAC click reaction with azadibenzocyclooctyne-functionalized HSA (ADIBO HSA) under biocompatible conditions. Radiolabeling efficiency of azide-functionalized DPA (Tc-99m-DPA) was >98%. Click conjugation efficiency of Tc-99m-DPA with ADIBO HSA was between 76 and 99% depending on the number of ADIBO moieties attached to HSA. In whole-body in vivo single photon emission computed tomography images, the blood pool uptakes of Tc-99m-DPA-HSA were significantly enhanced compared to those of Tc-99m-HSA at 10 min, 2, and 6 h after the injection (P < 0.001, 0.025, and 0.003, respectively). Furthermore, the blood activities of Tc-99m-DPA-HSA were 8 times higher at 30 min and 10 times higher at 3 h after the injection compared to those of conventional Tc-99m-HSA in ex vivo biodistribution experiment. The results exhibit the potential of Tc-99m-DPA-HSA as a blood pool imaging agent and further illustrate the promise of the pre labeling SPAAC approach for conjugation of heat-sensitive biological targeting vectors with [Tc-99m (CO)(3)(H2O)(3)](+).

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