Biodegradable Alginate-Chitosan Hollow Nanospheres for Codelivery of Doxorubicin and Paclitaxel for the Effect of Human Lung Cancer A549 Cells.

A biodegradable alginate coated chitosan hollow nanosphere (ACHN) was prepared by a hard template method and used for codelivery of doxorubicin (DOX) and paclitaxel (PTX) to investigate the effect on human lung cancer A549 cells. PTX was loaded into the nanometer hollow structure of ACHN through ads...

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Publicado en:BioMed Research International Vol. 2018; pp. 1 - 12
Autores principales: Tao, Liu, Jiang, Jie, Gao, Yu, Wu, Chao, Liu, Ying
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 1/28/2018
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 1/28/2018
      vid: 2018
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2018/4607945
        127598601
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        atl: Biodegradable Alginate-Chitosan Hollow Nanospheres for Codelivery of Doxorubicin and Paclitaxel for the Effect of Human Lung Cancer A549 Cells.
      aug:
        au:
          Tao, Liu
          Jiang, Jie
          Gao, Yu
          Wu, Chao
          Liu, Ying
        affil: Nursing College, Jinzhou Medical University, 40 Songpo Road, Linghe, Jinzhou, Liaoning 121000, China
      sug:
        subj:
          Doxorubicin Pharmacodynamics
          Paclitaxel Pharmacodynamics
          Lung Neoplasms Drug Therapy
          Alginates
          Polysaccharides
          Cell Line, Tumor Drug Effects
          Nanoparticles
          Human
          Doxorubicin Administration and Dosage
          Paclitaxel Administration and Dosage
          Drug Interactions
          X-Rays
          Calorimetry Methods
          Spectrophotometry, Infrared Methods
          Delayed-Action Preparations
          Cytotoxicity Tests, Immunologic
          Cell Proliferation
          Drug Therapy, Combination
      ab: A biodegradable alginate coated chitosan hollow nanosphere (ACHN) was prepared by a hard template method and used for codelivery of doxorubicin (DOX) and paclitaxel (PTX) to investigate the effect on human lung cancer A549 cells. PTX was loaded into the nanometer hollow structure of ACHN through adsorption method. DOX was coated on surface of ACHN through electrostatic interaction. Drug release studies exhibited a sustained-release effect. According to X-ray diffraction patterns (XRD), differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FT-IR) analysis, DOX structure in the loading samples (DOX-PTX-ACHN) was of amorphous state while PTX was microcrystalline. Cytotoxicity experiments showed ACHN was nontoxic as carrier material and the combination of DOX and PTX in DOX-PTX-ACHN exhibited a good inhibiting effect on cell proliferation. Cell uptake experiments demonstrated that DOX-PTX-ACHN accumulated in the cytoplasm. Degradation experiments illustrated that ACHN was a biodegradable material. In summary, these results clearly indicate that ACHN can be utilized as a potential biomaterial to transport multiple drugs to be used in combination therapy.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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