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Osteoclasts and tumor cells dual targeting nanoparticle to treat bone metastases of lung cancer.
Bai, Shao-Bo; Liu, Dao-Zhou; Cheng, Ying; Cui, Han; Liu, Miao; Cui, Min-Xuan; Zhang, Bang-le; Mei, Qi-Bing; Zhou, Si-Yuan.
Affiliation
  • Bai SB; Department of Pharmaceutics, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
  • Liu DZ; Department of Pharmaceutics, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
  • Cheng Y; Department of Pharmaceutics, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
  • Cui H; Department of Pharmaceutics, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
  • Liu M; Department of Pharmaceutics, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
  • Cui MX; Department of Pharmaceutics, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
  • Zhang BL; Department of Pharmaceutics, School of Pharmacy, Fourth Military Medical University, Xi'an, China.
  • Mei QB; Key Laboratory of Gastrointestinal Pharmacology of Chinese Materia Medica of the State Administration of Traditional Chinese Medicine, Fourth Military Medical University, Xi'an, China.
  • Zhou SY; Department of Pharmaceutics, School of Pharmacy, Fourth Military Medical University, Xi'an, China; Key Laboratory of Gastrointestinal Pharmacology of Chinese Materia Medica of the State Administration of Traditional Chinese Medicine, Fourth Military Medical University, Xi'an, China. Electronic addre
Nanomedicine ; 21: 102054, 2019 10.
Article in En | MEDLINE | ID: mdl-31310809
Bone is one of the prone metastatic sites of lung cancer. Osteoclast plays an important role in bone resorption and the growth of bone metastases of lung cancer. In order to treat bone metastases of lung cancer, we reported a docetaxel (DTX)-loaded nanoparticle, DTX@AHP, which could target dually at osteoclasts and bone metastatic tumor cells. The in vitro drug release from DTX@AHP exhibited pH and redox responsive characteristics. DTX@AHP displayed high binding affinity with bone matrix. In addition, DTX@AHP significantly inhibited the differentiation of RAW264.7 into osteoclast and effectively inhibited the proliferation of osteoclasts and tumor cells in in-vitro 3D bone metastases model of lung cancer. DTX@AHP could accumulate in bone metastases sites in vivo. Consequently, DTX@AHP not only markedly inhibited the growth of bone metastases of lung cancer but also reduced osteolysis in tumor-bearing mice. DTX@AHP exhibited great potential in the treatment of bone metastases of lung cancer.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Nanoparticles / Docetaxel / Lung Neoplasms Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Nanomedicine Journal subject: BIOTECNOLOGIA Year: 2019 Document type: Article Affiliation country: China Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Nanoparticles / Docetaxel / Lung Neoplasms Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Nanomedicine Journal subject: BIOTECNOLOGIA Year: 2019 Document type: Article Affiliation country: China Country of publication: Estados Unidos