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  • Walter de Gruyter GmbH  (2)
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  • Walter de Gruyter GmbH  (2)
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  • 1
    In: Green Processing and Synthesis, Walter de Gruyter GmbH, Vol. 5, No. 5 ( 2016-10-1), p. 459-466
    Abstract: In this report, magnetic Fe 3 O 4 nanoparticles were functionalized with chitosan-grafted-poly(ethylene glycol) methyl ether (CTS-mPEG) for paclitaxel (PTX) delivery. The Fe 3 O 4 nanoparticles were prepared via the chemical coprecipitation method and then coated with CTS-mPEG (Fe 3 O 4 @CTS-mPEG) by a simple method. The formation of Fe 3 O 4 @CTS-mPEG was characterized by several methods including proton nuclear magnetic resonance spectroscopy, Fourier transform infrared, and X-ray diffraction. Furthermore, the superparamagnetic properties of Fe 3 O 4 @CTS-mPEG were demonstrated by a vibrating sample magnetometer; the saturation magnetization reached 23 emu g –1 . The sizes and morphologies of Fe 3 O 4 and Fe 3 O 4 @CTS-mPEG nanoparticles were determined by transmission electron microscopy. The result indicated that Fe 3 O 4 @CTS-mPEGs were nearly spherical in shape with an average diameter of 20 nm, compared with the 12-nm Fe 3 O 4 particles. Especially, PTX was effectively loaded into the coated nanoparticles, 86.9±3.4% for drug loading efficiency, and slowly released up to 120 h. These results suggest the potential applications of Fe 3 O 4 @CTS-mPEG in the development of stable drug delivery systems for cancer treatment.
    Type of Medium: Online Resource
    ISSN: 2191-9550 , 2191-9542
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2016
    detail.hit.zdb_id: 2645923-1
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  • 2
    In: Green Processing and Synthesis, Walter de Gruyter GmbH, Vol. 5, No. 6 ( 2016-01-1)
    Abstract: Porous nanosilica (PNS) has been attracting much attention in fabrication of nanocarriers for a drug delivery system (DDS). However, the unmodified PNS-based carriers exhibited a significant initial burst release of drug, which may limit their potential clinical application. In this study, PNS was surface conjugated with cyclodextrin (CD) which was functionalized with adamantylamine-polyethylene glycol (APEG) for 5-fluorouracil (5-FU) delivery, in which case CD was used due to its ability to form a stable inclusion complex with 5-FU and APEG. The conjugated PNS (PNSC@APEG) was successfully prepared with spherical shape and diameter around 50 nm, determined by transmission electron microscopy (TEM). In addition, 5-FU was efficiently trapped in PNSC@APEG particles, which were around 63.4%±3.8% and was slowly released up to 3 days in phosphate buffer saline (PBS). Furthermore, the cell proliferation kit I (MTT) assay data showed that PNSC@APEG was a biocompatible nanocarrier. These results indicated that PNSC@APEG nanoparticles have a great potential as novel carriers for anticancer drug delivery.
    Type of Medium: Online Resource
    ISSN: 2191-9550 , 2191-9542
    Language: Unknown
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2016
    detail.hit.zdb_id: 2645923-1
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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