A High-Throughput Screening Strategy for Synthesizing Molecularly Imprinted Polymer Nanoparticles Selectively Targeting Tumors

被引:6
作者
Song, Qingmei [1 ]
Li, Yan [1 ]
Ma, Liang [2 ]
Li, Yuan [1 ]
Lv, Yongqin [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Life Sci & Technol, Natl Energy Res & Dev Ctr Biorefinery, State Key Lab Organ Inorgan Composites,IntJoint Bi, Beijing 100029, Peoples R China
[2] China Japan Friendship Hosp, Clin Lab, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
artificial antibodies; fluorescence imaging; high-throughput screening; imprinted nanoparticles; tumor targeting; HYDROGEL NANOPARTICLES; RECOGNITION; PROTEINS; AFFINITY;
D O I
10.1002/adhm.202400290
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Molecularly imprinted polymers (MIPs) show significant promise as effective alternatives to antibodies in disease diagnosis and therapy. However, the challenging process of screening extensive libraries of monomer combinations and synthesis conditions to identify formulations with enhanced selectivity and affinity presents a notable time constraint. The need for expedient methods becomes clear in accelerating the strategic development of MIPs tailored for precise molecular recognition purposes. In this study, an innovative high-throughput screening methodology designed to identify the optimal MIP formulation for targeting tumors is presented. Employing a microtiter plate format, over 100 polymer syntheses are conducted, incorporating diverse combinations of functional monomers. Evaluation of binding performance utilizes fluorescence-based assays, focusing on an epitope of the epidermal growth factor receptor (EGFR). Through this meticulously structured screening process, synthesis conditions that produced MIP nanoparticles exhibiting substantial specificity for EGFR targeting (KD = 10-12 m) are identified. These "bionic antibodies" demonstrate selective recognition of cancer cells in whole blood samples, even at concentrations as low as 5 cells mL-1. Further validation through fluorescent imaging confirms the tumor-specific localization of the MIPs in vivo. This highly efficient screening approach facilitates the strategic synthesis of imprinted polymers functioning as precision bioprobes. Through a high-throughput screening approach incorporating over 100 polymer formulations, MIP nanoparticles exhibiting substantial specificity and picomolar affinity for an epitope of the epidermal growth factor receptor are identified. These "bionic antibodies" demonstrate selective recognition of cancer cells in whole blood samples and tumor-specific localization in vivo, confirming their potential as precision diagnostic and analytical tools. image
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页数:15
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ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2023, 62 (19)