1. Academic Validation
  2. Preclinical Pharmacokinetics and Biodistribution of LR004, a Novel Antiepidermal Growth Factor Receptor Monoclonal Antibody

Preclinical Pharmacokinetics and Biodistribution of LR004, a Novel Antiepidermal Growth Factor Receptor Monoclonal Antibody

  • Molecules. 2024 Jan 22;29(2):545. doi: 10.3390/molecules29020545.
Ying Zheng 1 2 Guifang Dou 1 Shuchen Liu 1 Zhiyun Meng 1 Eric I Tsao 3 Gang Yu 4 Xiaoxia Zhu 1 Ruolan Gu 1 Zhuona Wu 1 Yunbo Sun 1 Peng Han 1 Hui Gan 1
Affiliations

Affiliations

  • 1 Department of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, Beijing 100850, China.
  • 2 Artemisinin Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.
  • 3 Synermore Biologics Co., Ltd., Suzhou 215000, China.
  • 4 State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing 100850, China.
Abstract

LR004 is a novel chimeric (human/mouse) monoclonal antibody developed for the treatment of advanced colorectal carcinoma with detectable epidermal growth factor receptor (EGFR) expression. We aimed to investigate the preclinical pharmacokinetics (PK) and in vivo biodistribution of LR004. The PK profiles of LR004 were initially established in rhesus monkeys. Subsequently, 125I radionuclide-labeled LR004 was developed and the biodistribution, autoradiography, and NanoSPECT/CT of 125I-LR004 in xenograft mice bearing A431 tumors were examined. The PK data revealed a prolonged half-life and nonlinear PK characteristics of LR004 within the dose range of 6-54 mg/kg. The radiochemical purity of 125I-LR004 was approximately 98.54%, and iodination of LR004 did not affect its specific binding activity to the EGFR antigen. In a classical biodistribution study, 125I-LR004 exhibited higher uptake in highly perfused organs than in poorly perfused organs. Prolonged retention properties of 125I-LR004 in tumors were observed at 4 and 10 days. Autoradiography and NanoSPECT/CT confirmed the sustained retention of 125I-LR004 at the tumor site in xenograft mice. These findings demonstrated the adequate tumor targeting capabilities of 125I-LR004 in EGFR-positive tumors, which may improve dosing strategies and future drug development.

Keywords

EGFR; monoclonal antibody; nanoSPECT/CT; pharmacokinetics; radionuclide-based biodistribution; tumor-targeting.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-P991969
    EGFR抗体抑制剂