Water-soluble nanoparticles from random copolymer and oppositely charged surfactant, 3a -: Nanoparticles of poly(ethylene glycol)-based cationic random copolymer and fatty acid salts

被引:14
作者
Kizhakkedathu, JN
Nisha, CK
Manorama, SV
Maiti, S
机构
[1] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V6T 2B5, Canada
[2] Univ British Columbia, Ctr Blood Res, Vancouver, BC V6T 2B5, Canada
[3] Indian Inst Chem Technol, CSIR, Mat Sci Grp, Inorgan & Phys Chem Div, Hyderabad 500007, Andhra Pradesh, India
[4] CSIR, Inst Genomics & Integrat Biol, Delhi 110007, India
关键词
colloids; drug delivery systems; nanoparticles; surfactants;
D O I
10.1002/mabi.200500023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this report, we investigate the nanoparticle formation between random copolymers (RCPs) of methoxy-poly(ethylene glycol) monomethacrylate (MePEGMA) and (3-(riiethaeryloylamino)propyl)trimethylammonium chloride (MAPTAC and oppositely charged natural surfactants, sodidium oleate and sodium laurate, using turbidimetric titration, steady-state fluorescence, dynamic light scattering, and electron microscopy. Though sodium oleate and sodium laurate are sparingly soluble in water, the nanoparticle complexes formed between the RCPs and these surfactants are soluble in the entire range of compositions studied here, including the stoichiometric electronetural complexes. The spherical nature of these nanoparticle complexes is revealed by electron microscopic (EM) analysis. Dynamic light scattering (DLS) showed that the average diameters of the nano-particles are in the range 50 to 150 nm, which is supported by EM analysis. Pyrene fluorescence experiments suggested that these soluble nanoparticles have hydrophobic cores, which may solubilize hydrophobic drug molecules. The polarity index (I-1/I-3) obtained from the pyrene fluorescence spectra and the conductometric measurements showed that the nanoparticles are in the order of 10(-4) m. Further, the complexation of such poorly water-soluble amphiphilic surfactants with polymers offers a useful method for the immobilization of hydrophobic compounds towards water-soluble drug carrier formulations.
引用
收藏
页码:549 / 558
页数:10
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