4.8 Article

Methotrexate-loaded PLGA nanobubbles for ultrasound imaging and Synergistic Targeted therapy of residual tumor during HIFU ablation

Journal

BIOMATERIALS
Volume 35, Issue 19, Pages 5148-5161

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2014.02.036

Keywords

HIFU; Nanobubbles; Methotrexate; Ultrasound imaging; Cancer therapy

Funding

  1. National Natural Science Foundation of China [81070502, 81170585, 81100444, 81270021]
  2. Funding of National Key Clinical Department in China [201101ckZD]
  3. Chongqing Science Fund for Distinguished Young Scholars [cstc2013jcyjjq10004]
  4. Program for New Century Excellent Talents in University of Ministry of Education of China [NCET-13-1067]

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High intensity focused ultrasound (HIFU) has attracted the great attention in tumor ablation due to its non-invasive, efficient and economic features. However, HIFU ablation has its intrinsic limitations for removing the residual tumor cells, thus the tumor recurrence and metastasis cannot be avoided in this case. Herein, we developed a multifunctional targeted poly(lactic-co-glycolic acid) (PLGA) nanobubbles (NBs), which not only function as an efficient ultrasound contrast agent for tumor imaging, but also a targeted anticancer drug carrier and excellent synergistic agent for enhancing the therapeutic efficiency of HIFU ablation. Methotrexate (MTX)-loaded NBs were synthesized and filled with perfluorocarbon gas subsequently using a facile but general double emulsion evaporation method. The active tumor-targeting monoclonal anti-HLA-G antibodies (mAb(HLA-G)) were further conjugated onto the surface of nanobubbles. The mAb(HLA-G)/MTX/PLGA NBs could enhance the ultrasound imaging both in vitro and in vivo, and the targeting efficiency to HLA-G overexpressing JEG-3 cells has been demonstrated. The elaborately designed mAb(HLA-G)/MTX/PLGA NBs can specifically target to the tumor cells both in vitro and in vivo, and their blood circulation time in vivo was much longer than non-targeted MTX/PLGA NBs. Further therapeutic evaluations showed that the targeted NBs as a synergistic agent can significantly improve the efficiency of HIFU ablation by changing the acoustic environment, and the focused ultrasound can promote the on-demand MTX release both in vitro and in vivo. The in vivo histopathology test and immunohistochemical analysis showed that the mAb(HLA-G)/MTX/PLGA NBs plus HIFU group presented most serious coagulative necrosis, the lowest proliferation index and the highest apoptotic index. Therefore, the successful introduction of targeted mAb(HLA-G)/MTX/PLGA NBs provides an excellent platform for the highly efficient, imaging-guided and non-invasive HIFU synergistic therapy of cancer with the supplementary functions of killing residual tumor cells and preventing tumor recurrence/metastasis. (C) 2014 Elsevier Ltd. All rights reserved.

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