Characterization and Stabilization of a New 64Cu-Labeled Anti-EGFR Antibody NCAB001 for the Early Detection of Pancreatic Cancer with Positron Emission Tomography

  • Pharmaceutics. 2021 Dec 28;14(1):67. doi: 10.3390/pharmaceutics14010067.
Hiroki Matsumoto  1  2 Chika Igarashi  1 Tomoko Tachibana  1 Fukiko Hihara  1 Atsuo Waki  1 Ming-Rong Zhang  1 Sei Yoshida  3 Kenichiro Naito  3 Hiroaki Kurihara  2 Makoto Ueno  4 Kimiteru Ito  5 Tatsuya Higashi  1 Yukie Yoshii  1  2
Affiliations
  • 1. Institute for Quantum Medical Science, National Institutes for Quantum Science and Technology, Chiba 263-8555, Japan.
  • 2. Department of Diagnostic Radiology, Kanagawa Cancer Center, Yokohama 241-8515, Japan.
  • 3. Department of Research, NanoCarrier Co., Ltd., Tokyo 104-0031, Japan.
  • 4. Department of Gastroenterology, Kanagawa Cancer Center, Yokohama 241-8515, Japan.
  • 5. Department of Diagnostic Radiology, National Cancer Center Hospital, Tokyo 104-0045, Japan.
Abstract

Early diagnosis of pancreatic Cancer using current imaging modalities remains challenging. We have developed a new approach to identify tumor lesions ≥ 3 mm in the pancreas by positron emission tomography (PET) with a new intraperitoneally administered 64Cu-labeled anti-epidermal growth factor receptor (EGFR) antibody (encoded as NCAB001), called 64Cu-NCAB001 ipPET. Generally, in clinical research, a radiometal-antibody complex must be prepared immediately before use at the imaging site. To make 64Cu-NCAB001 ipPET available to daily clinical practices in a sustainable way, the NCAB001-chelator conjugate and 64Cu-NCAB001 must be characterized and stabilized. NCAB001 was manufactured under cGMP conditions. NCAB001 was conjugated with a bifunctional chelator (p-SCN-Bn-PCTA), and the antibody-chelator conjugate (PCTA-NCAB001) was characterized by LC/MS and ELISA. Thereafter, to effectively manufacture 64Cu-NCAB001, we developed a new formulation to stabilize PCTA-NCAB001 and 64Cu-NCAB001. An average of three PCTA chelators were conjugated per molecule of NCAB001. The relative binding potency of PCTA-NCAB001 was comparable to cetuximab. The formulation consisting of acetate buffer, glycine, and polysorbate-80 stabilized PCTA-NCAB001 for a year-long storage. Additionally, this formulation enabled the stabilization of 64Cu-NCAB001 for up to 24 h after radiolabeling with a sufficient radioactivity concentration for clinical use. These results may accelerate the future use of 64Cu-NCAB001 ipPET in clinical settings for the early diagnosis and treatment of pancreatic Cancer.

Keywords
64Cu-NCAB001; ipPET; process development; radiometal-antibody complex; stability.
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