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Targeted Delivery System Based on Gemcitabine-Loaded Silk Fibroin Nanoparticles for Lung Cancer Therapy Publisher Pubmed



Mottaghitalab F1 ; Kiani M1 ; Farokhi M3 ; Kundu SC4 ; Reis RL4 ; Gholami M2 ; Bardania H5 ; Dinarvand R1 ; Geramifar P5 ; Beiki D5 ; Atyabi F1
Authors
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Authors Affiliations
  1. 1. Nanotechnology Research Centre, Faculty of Pharmacy, Pharmaceutical Science Research Center, Tehran University of Medical Sciences, Tehran, 141556451, Iran
  2. 2. National Cell Bank of Iran, Pasteur Institute of Iran, Tehran, 1316943551, Iran
  3. 3. 3Bs Research Group, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, University of Minho, AvePark - Barco Taipas, Guimaraes, 4805-017, Portugal
  4. 4. Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, 7591994799, Iran
  5. 5. Research Center for Nuclear Medicine, Shariati Hospital, Tehran University of Medical Sciences, Tehran, 141551339, Iran

Source: ACS Applied Materials and Interfaces Published:2017


Abstract

Here, a targeted delivery system was developed based on silk fibroin nanoparticles (SFNPs) for the systemic delivery of gemcitabine (Gem) to treat induced lung tumor in a mice model. For targeting the tumorigenic lung tissue, SP5-52 peptide was conjugated to Gem-loaded SFNPs. Different methods were used to characterize the structural and physicochemical properties of the SFNPs. The prepared nanoparticles (NPs) showed suitable characteristics in terms of size, zeta potential, morphology, and structural properties. Moreover, the targeted Gem-loaded SFNPs showed higher cytotoxicity, cellular uptake, and accumulation in the lung tissue in comparison to the nontargeted SFNPs and control groups. Afterward, a mice model with induced lung tumor was developed by intratracheal injection of Lewis lung carcinoma (LL/2) cells into the lungs for assessing the therapeutic efficacy of the prepared drug delivery system. The histopathological assessments and single-photon-emission computed tomography-CT radiographs showed successful lung tumor induction. Moreover, the obtained results showed higher potential of targeted Gem-loaded SFNPs in treating induced lung tumor compared with that of the control groups. Higher survival rate, less mortality, and no sign of metastasis were also observed in those animals treated with targeted NPs based on the histological and radiological analyses. This study presented an effective anticancer drug delivery system for specific targeting of induced lung tumor that could be useful in treating malignant lung cancers in future. © 2017 American Chemical Society.
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