Platelet membrane biomimetic nanoparticles for tumor photothermal therapy: a preliminary in vitro study
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Supported by Project of Science and Technology Plan of Sichuan Province (2023NSFSC1862), The Joint Project Between Luzhou Municipal People’s Government and Southwest Medical University (2023LZXNYDJ009), Foundation of Southwest Medical University (2019ZQN144, 2023QN004), and Innovation and Entrepreneurship Training Program for College Students in Sichuan Province (S202310632132).

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    Abstract:

    Objective To prepare indocyanine green (ICG)-loaded platelet membrane biomimetic liposome (ICG-PLP) for tumor photothermal therapy, and to preliminarily evaluate its in vitro characteristics. Methods ICG-PLP was prepared by an ultrasound method, and its particle size and zeta potential were determined using a laser particle size analyzer. The encapsulation efficiency of ICG-PLP was detected by ultraviolet spectrophotometry. The photothermal properties of ICG-PLP were investigated under 808 nm near-infrared ray irradiation (2 W/cm2), and the retention of platelet membrane proteins was observed by sodium dodecylsulfate-polyacrylamide gel electrophoresis. The uptake of ICG-PLP by mouse macrophage RAW264.7, human non-small cell lung cancer cell A549, mouse melanoma cell B16-F10, and mouse breast cancer cell 4T1 was observed by a laser confocal microscope. Furthermore, the phototoxicity of ICG-PLP was detected by methyl thiazolyl tetrazolium assay, and the safety of ICG-PLP was preliminarily evaluated according to hemolysis rate and cytocompatibility. Besides, the in vivo retention time of ICG, ICG-loaded liposome and ICG-PLP in healthy SD rats was observed after tail vein injection. Results ICG-PLP was successfully prepared and its encapsulation efficiency, particle size, zeta potential, and the polydispersity index were (97.68±0.01)%, (109.77±0.76) nm, (-21.23±0.84) mV, and 0.22±0.01, respectively. ICG-PLP well retained the proteins on platelet membrane and showed good photothermal properties. Platelet membrane enhanced the uptake of biomimetic nanoparticles by tumor cells A549, B16-F10, and 4T1, and reduced the phagocytosis of biomimetic nanoparticles by macrophages. ICG-PLP exhibited a favorable photothermal therapy effect and could kill tumor cells. Additionally, ICG-PLP displayed a good safety. After intravenous administration, ICG-PLP prolonged the in vivo retention time of ICG in healthy SD rats. Conclusion ICG-PLP has been successfully constructed. It has a great potential in targeted drug delivery and tumor photothermal therapy.

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History
  • Received:December 28,2023
  • Revised:May 07,2024
  • Adopted:
  • Online: August 23,2024
  • Published: August 20,2024
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