Please use this identifier to cite or link to this item: https://doi.org/10.1007/s00396-004-1090-7
Title: Study on surfactant coating of polymeric nanoparticles for controlled delivery of anticancer drug
Authors: Mu, L.
Seow, P.-H.
Ang, S.-N.
Feng, S.-S. 
Keywords: Biodegradable polymer
Emulsifier
Microencapsulation
New delivery route
Oral drug delivery
Paclitaxel
Surfactant stabiliser
Taxol
Issue Date: Nov-2004
Source: Mu, L., Seow, P.-H., Ang, S.-N., Feng, S.-S. (2004-11). Study on surfactant coating of polymeric nanoparticles for controlled delivery of anticancer drug. Colloid and Polymer Science 283 (1) : 58-65. ScholarBank@NUS Repository. https://doi.org/10.1007/s00396-004-1090-7
Abstract: Biodegradable nanoparticles loaded with anticancer drug paclitaxel and appropriately coated with polyvinyl alcohol (PVA), polyethylene glycol (PEG) as well as D-α-tocopheryl polyethylene glycol 1000 succinate (TPGS) were produced and characterised by various analysis techniques such as laser light scattering (LLS) for particle size and size distribution, scanning electron microscopy (SEM) and atomic force microscopy (AFM) for particle morphology, X-ray photoelectron spectroscopy (XPS) and Fourier Transform Infrared-Photoacoustic Spectroscopy (FTIR-PAS) for surface chemistry, and high performance liquid chromatography (HPLC) for drug encapsulation efficiency (EE) and in vitro release kinetics. The emphasis was given to the possible effects of surface coating on the physicochemical and pharmaceutical properties of paclitaxel loaded nanoparticles. It was found that the type and amount of the surfactant could significantly affect the drug EE in the nanoparticles, the particles characteristics and their in vitro release behaviour. The surfactants dominated on the nanoparticles' surface and the coated nanoparticles displayed in spherical shape with relative smooth surface within the resolution scope of the equipment. The particle size and size distribution showed close relation to the surface coating, which may also be responsible for the drug encapsulation efficiency and the in vitro release kinetics. A favourable formulation of drug loaded nanoparticles of desired properties could be obtained by optimising the fabrication parameters. © Springer-Verlag 2004.
Source Title: Colloid and Polymer Science
URI: http://scholarbank.nus.edu.sg/handle/10635/64626
ISSN: 0303402X
DOI: 10.1007/s00396-004-1090-7
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