4.6 Article

A Novel Method of Magnetic Nanoparticles Functionalized with Anti-Folate Receptor Antibody and Methotrexate for Antibody Mediated Targeted Drug Delivery

期刊

MOLECULES
卷 27, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27010261

关键词

targeted drug delivery; anti-folate receptor antibody; methotrexate; anti-methotrexate; folate receptors; immunotherapy; cancer treatment

资金

  1. Key project of science and technology research of Chongqing Municipal Education Commission [kjzd-k201902802]
  2. Project of the Chongqing Education Science Research Program [2018-GX-462]
  3. Key project of education and teaching reform in Chongqing Medical and Pharmaceutical College [CQYGZJG1909]
  4. Talent introduction project of Chongqing Medical and Pharmaceutical College [ygz2016302]
  5. King Khalid University [RGP.2/156/42]

向作者/读者索取更多资源

Therapeutic effects of anticancer medicines can be improved by targeting the specific receptors on cancer cells. In this research project, a novel formulation of targeting drug delivery was designed and its anticancer effects were analyzed. The results showed that the engineered nanomedicines demonstrated good cytotoxicity against cancer cells, indicating their potential in targeted drug delivery.
Therapeutic effects of anticancer medicines can be improved by targeting the specific receptors on cancer cells. Folate receptor (FR) targeting with antibody (Ab) is an effective tool to deliver anticancer drugs to the cancer cell. In this research project, a novel formulation of targeting drug delivery was designed, and its anticancer effects were analyzed. Folic acid-conjugated magnetic nanoparticles (MNPs) were used for the purification of folate receptors through a novel magnetic affinity purification method. Antibodies against the folate receptors and methotrexate (MTX) were developed and characterized with enzyme-linked immunosorbent assay and Western blot. Targeting nanomedicines (MNP-MTX-FR Ab) were synthesized by engineering the MNP with methotrexate and anti-folate receptor antibody (anti-FR Ab). The cytotoxicity of nanomedicines on HeLa cells was analyzed by calculating the % age cell viability. A fluorescent study was performed with HeLa cells and tumor tissue sections to analyze the binding efficacy and intracellular tracking of synthesized nanomedicines. MNP-MTX-FR Ab demonstrated good cytotoxicity along all the nanocomposites, which confirms that the antibody-coated medicine possesses the potential affinity to destroy cancer cells in the targeted drug delivery process. Immunohistochemical approaches and fluorescent study further confirmed their uptake by FRs on the tumor cells' surface in antibody-mediated endocytosis. The current approach is a useful addition to targeted drug delivery for better management of cancer therapy along with immunotherapy in the future.

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