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[Development of gene delivery system using PLGA nanospheres]

[Development of gene delivery system using PLGA nanospheres] Research Abstract Details 

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  • [Development of gene delivery system using PLGA nanospheres] Abstract Text:

    kohei taharaKohei Tahara,hiromitsu yamamotoHiromitsu Yamamoto,hirofumi takeuchiHirofumi Takeuchi,yoshiaki kawashimaYoshiaki Kawashima,kohei taharaKohei Tahara,hiromitsu yamamotoHiromitsu Yamamoto,hirofumi takeuchiHirofumi Takeuchi,yoshiaki kawashimaYoshiaki Kawashima,kohei taharaKohei Tahara,hiromitsu yamamotoHiromitsu Yamamoto,hirofumi takeuchiHirofumi Takeuchi,yoshiaki kawashimaYoshiaki Kawashima,

    The development of nonviral vectors for the efficient and safe delivery to cells has long been awaited to facilitate gene therapy. Recently, many nonviral vectors modified with cationic lipids, cationic polymers, etc. have been reported. However, those nonviral vectors with cationic materials require improved stability, longer duration of gene expression, and reduced cytotoxicity. We successfully prepared mucoadhesive poly (lactide-co-glycolide) nanospheres (PLGA NS) by modifying the nanoparticulate surface with chitosan to improve mucosal peptide absorption after oral and pulmonary administration. Furthermore, we found that nucleic acid, which was not dispersed in the organic solvent, could be dispersed by forming a complex with cationic lipid. Using this phenomenon, polynucleic acids for gene therapy (plasmid DNA, antisense oligonucleotide, small interfering RNA, etc.) can be encapsulated into the matrix of the polymer particles with the emulsion solvent diffusion method. The advantages of this preparation method are its simple process and avoidance of an ultrasonication process for submicronization of particles. The resultant nanospheres show better cellular uptake and different gene therapeutic effects compared with conventional vectors due to their improved adherence to cells and sustained release of polynucleic acid in the cells. In conclusion, chitosan-coated PLGA NS can possibly be applied in nonviral vectors for gene therapy.

    [Development of gene delivery system using PLGA nanospheres] Publishing Authors By Initials

    k taharaK Tahara,h yamamotoH Yamamoto,h takeuchiH Takeuchi,y kawashimaY Kawashima,k taharaK Tahara,h yamamotoH Yamamoto,h takeuchiH Takeuchi,y kawashimaY Kawashima,k taharaK Tahara,h yamamotoH Yamamoto,h takeuchiH Takeuchi,y kawashimaY Kawashima,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

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    [Development of gene delivery system using PLGA nanospheres] Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Yakugaku zasshi : Journal of the Pharmaceutical So

    VOLUME: 127

    Page Numbers: 1541-8

    Journal Abbreviation: Yakugaku Zasshi

    ISSN: 0031-6903

    DAY: 5

    MONTH: Oct

    YEAR: 2007

    [Development of gene delivery system using PLGA nanospheres] Information

    Number of References:

    LANGUAGE: jpn

    NlmUniqueID: 413613

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    Grant and Affiliation Information for [Development of gene delivery system using PLGA nanospheres]

    AFFILIATION: Laboratory of Pharmaceutical Engineering, School of Pharmacy, Aichi Gakuin University, 1-100 Kusumoto-cho, Chikusa-ku, Nagoya 464-8650, Japan. tahara@dpc.agu.ac.jp

    Country: Japan

    Japan Research PublicationJapan Research Publication

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    MEDLINETA: Yakugaku Zasshi

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