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ORIGINAL RESEARCH article

Front. Bioeng. Biotechnol.

Sec. Biomaterials

Volume 13 - 2025 | doi: 10.3389/fbioe.2025.1557772

This article is part of the Research Topic Advanced Functional Materials for Disease Diagnosis, Drug Delivery and Tissue Repair View all 15 articles

A Preclinical Study of a Novel Dual-Modality Contrast Agent in Rodent Models

Provisionally accepted
Xuelai Zhou Xuelai Zhou 1Kangli Jiang Kangli Jiang 1Yuxin Han Yuxin Han 1*Shuxu Yang Shuxu Yang 2*
  • 1 Zhejiang Poly Pharm. Co., Ltd, Hangzhou, China
  • 2 Department of Nephrology, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou, Jiangsu Province, China

The final, formatted version of the article will be published soon.

    Glioblastoma (GBM) is the most aggressive and prevalent primary malignant brain tumor in adults, with surgery being the main treatment. To improve surgical outcomes and extend patient survival, PL002 was developed as a dual-modality MRI/fluorescence imaging (FI) contrast agent. Preclinical studies in rodent models were conducted to assess its potential for clinical use. PL002, containing gadolinium (Gd³⁺) and indocyanine green (ICG), demonstrated high biocompatibility in L-O2, HEK293, and U-87 MG cells. In U-87 MG intracranial glioma mouse and healthy rat models, PL002 showed good in vivo imaging efficacy within a dosage range of 10-50 mg/kg, with a half-life of 2.51-4.87 hours. It primarily accumulated in organs with rich blood supply but maintained stable imaging effects in the brain for up to 72 hours. No abnormalities were observed in rats at a dosage of 100 mg/kg. Compared to Gadavist® and ICG, PL002 provided sustained support for MRI and FI of GBM for 72 hours, with a broad therapeutic window. This makes PL002 highly promising for preoperative assessment, intraoperative guidance, and postoperative verification of resection margins.

    Keywords: Gadolinium contrast agent, ICG, Magnetic Resonance Imaging, Fluorescence Imaging, Glioblastoma, Intraoperative navigation

    Received: 09 Jan 2025; Accepted: 03 Mar 2025.

    Copyright: © 2025 Zhou, Jiang, Han and Yang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Yuxin Han, Zhejiang Poly Pharm. Co., Ltd, Hangzhou, China
    Shuxu Yang, Department of Nephrology, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou, Jiangsu Province, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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