Size control of self-assembled nanoparticles by an emulsion/solvent evaporation method

被引:0
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作者
Minsu Lee
Yong Woo Cho
Jae Hyung Park
Hesson Chung
Seo Young Jeong
Kuiwon Choi
Dae Hyuk Moon
Sang Yoon Kim
In-San Kim
Ick Chan Kwon
机构
[1] Korea Institute of Science and Technology,Biomedical Research Center
[2] University of Ulsan College of Medicine,Asan Institute for Life Sciences
[3] University of Ulsan College of Medicine,Department of Nuclear Medicine, Asan Medical Center
[4] College of Environment and Applied Chemistry,Department of Advanced Polymer and Fiber Materials
[5] Kyung Hee University,Department of Otolaryngology, Asan Medical Center
[6] University of Ulsan College of Medicine,Department of Biochemistry, School of Medicine
[7] Kyungpook National University,undefined
来源
关键词
Nanoparicles; Size control; Colloidal stability; Glycol chitosan; Fluorescein isothiocyanate; Lactose;
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学科分类号
摘要
A novel and simple method for size control of self-assembled nanoparticles is suggested in this paper. Polymeric nanoparticles were prepared from amphiphilic chitosan derivatives fluorescein isothiocyanate (FITC)-conjugated glycol chitosans (FGCs). The attachment of hydrophobic FITC onto hydrophilic glycol chitosan induced the amphiphilic conjugate to form self-assembled nanoparticles in aqueous media, depending on degree of substitution. The size of self-assembled nanoparticles was controlled by a novel emulsion/solvent evaporation method. Adding a small amount of an immiscible solvent with water (chloroform) to FGC nanoparticle suspensions in aqueous media followed by ultrasonification and solvent evaporation led to partial dissociation and subsequent reformation of nanoparticles. The evaporation of chloroform facilitated the hydrophobic association, which resulted in more dense and hardened hydrophobic cores. The size of nanoparticles was closely related with the FGC concentration in the emulsion. The mean diameters of self-assembled nanoparticles were 150–500 nm at the FGC concentrations of 0.3–2.5 mg/ml. Higher FGC concentration resulted in larger particles. The polydispersity factors (μ2/Γ2) of the reformed nanoparticles were fairly low (0.001–0.094), indicating narrow size distribution. The FGC nanoparticles were stable in phosphate-buffered saline at 37°C up to 20 days. Lactose was a good excipient for maintaining the structural integrity of nanoparticles during freeze-drying. Without lactose, the freeze-dried nanoparticles were not homogeneously redispersed in aqueous media. However, the freeze-dried nanoparticles with lactose were spontaneously redispersed in aqueous milieu with their own sizes.
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页码:506 / 512
页数:6
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