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In Vitro Evaluations of Macrophage-T...
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Attarwala, Husain.
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In Vitro Evaluations of Macrophage-Targeted Anti-Inflammatory Gene Delivery and Transfection using Nanoparticles-in-Emulsion Formulations.
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
In Vitro Evaluations of Macrophage-Targeted Anti-Inflammatory Gene Delivery and Transfection using Nanoparticles-in-Emulsion Formulations./
作者:
Attarwala, Husain.
面頁冊數:
57 p.
附註:
Source: Masters Abstracts International, Volume: 49-03, page: .
Contained By:
Masters Abstracts International49-03.
標題:
Biology, Genetics. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1483819
ISBN:
9781124390178
In Vitro Evaluations of Macrophage-Targeted Anti-Inflammatory Gene Delivery and Transfection using Nanoparticles-in-Emulsion Formulations.
Attarwala, Husain.
In Vitro Evaluations of Macrophage-Targeted Anti-Inflammatory Gene Delivery and Transfection using Nanoparticles-in-Emulsion Formulations.
- 57 p.
Source: Masters Abstracts International, Volume: 49-03, page: .
Thesis (M.S.)--Northeastern University, 2010.
Purpose: Multi-compartmental delivery systems can effectively deliver therapeutic payloads by overcoming different extra- and intra-cellular barriers. The main objective of this study was to develop DNA-encapsulated solid nanoparticles-in-emulsion formulation to enhance gene delivery and transfection in macrophages.
ISBN: 9781124390178Subjects--Topical Terms:
1017730
Biology, Genetics.
In Vitro Evaluations of Macrophage-Targeted Anti-Inflammatory Gene Delivery and Transfection using Nanoparticles-in-Emulsion Formulations.
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Source: Masters Abstracts International, Volume: 49-03, page: .
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Adviser: Mansoor M. Amiji.
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Purpose: Multi-compartmental delivery systems can effectively deliver therapeutic payloads by overcoming different extra- and intra-cellular barriers. The main objective of this study was to develop DNA-encapsulated solid nanoparticles-in-emulsion formulation to enhance gene delivery and transfection in macrophages.
520
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Methods: Type B gelatin based nanoparticles were prepared by ethanol water solvent displacement method. Safflower oil-containing water in oil in water multiple emulsion was prepared by a two step emulsification technique with the help of Silverson homogenizer L4RTRTM. EGFP-N1 plasmid DNA that expresses enhanced green fluorescent protein (GFP) was encapsulated in solid type B gelatin nanoparticles (GNP) which were further encapsulated in the innermost aqueous phase of safflower oil containing water in oil in water (W/O/W) multiple emulsion (ME). Fluorescence microscopy and GFP-specific ELISA were performed for qualitative and quantitative determination of plasmid EGFP-N1 gene transfection in murine adherent alveolar macrophages J774A.1.
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Results: Particle size of the NiE formulations was found to be less than or equal to 5 um in diameter. Results obtained from gene transfection evaluations showed that plasmid EGFP-N1 or mIL-10 loaded NiE formulations offered higher and sustained GFP expression compared GFP expression observed with plasmid EGFP-N1 or mLI-10 loaded ME and GNP formulations or plasmid DNA complexed with LipofectinRTM, a cationic lipid based standard gene transfection reagent in J774A.1 murine adherent alveolar macrophage cell lines.
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Conclusion: The results of this study show that DNA-containing solid gelatin nanoparticles can be encapsulated in the innermost aqueous phase of the W/O/W multiple emulsions to form NiE formulations. EGFP-N1 or mIL-10 plasmid-loaded NiE formulations were capable producing sustained gene transfection in J774A.1 murine adherent alveolar macrophage cell lines. In addition mIL10 transfection using NiE formulation showed highest amount of TNF&agr; and IL-1beta suppression upon LPS stimulation.
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http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1483819
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