Papers by Keyword: Micelle

Abstract: An amphiphilic graft copolymer with poly(acrylamide-methacrylate) as a main chain and octylphenyl polyoxyethylene as side chains (P(AM-MA)-g-C8PhEO10) was successfully synthesized via free radical copolymerization. The structure and the composition of the graft copolymer were characterized by FTIR, 1H-NMR and elemental analysis (EA) in detail. The absolute molecular weight of the copolymer is 1.304×106, as determined by static light scattering (SLS). The molar ratio of acrylamide monomer to the macromonomer is 33:1 in the copolymer and 53 C8PhEO10 branch chains attach to a P(AM-MA) backbone. The micellar behavior of P(AM-MA)-g-C8PhEO10 was preliminarily studied by means of surface tension measurements, transmission electron microscope (TEM) in aqueous solution. It was found that the stable spherical micelles with core-shell structure are formed and polymolecular micelles are larger and more compact than monomolecular micelles. In addition, the graft copolymer has favorable thermal stability.

Abstract: 6-arm star-shaped Poly (ε-caprolactone)-dextran (sPCL-dextran) was synthesized and characterized. The core of the star polymer is dipentaerythritol, the inner block in the arm is hydrophobic poly (ε-caprolactone) (PCL), and the outer block in the arm is hydrophilic dextran. The synthesis involves three steps: (1) The ring-opening polymerization of ε-caprolactone (CL) initiated by dipentaerythritol produces 6-arm star-shaped PCL (sPCL-OH). (2) The sPCL-OH reacts with acryloyl chloride to get star-shaped PCL with acrylate end group (sPCL-CH=CH₂). (3) The amino ended dextran (dextran-NH₂) is then attached to sPCL-CH=CH₂ terminus by Micheal addition to form star-shaped sPCL-dextran. The architecture of products was characterized with ¹H NMR, GPC and element analysis. Micellization of sPCL-dextran in aqueous solutions was investigated by DLS. The results showed that the micelle size (R_h) and size distribution are related to the concentration of the sPCL-dextran. Salt, pH value and temperature have no obvious influence on the R_h.

Abstract: Polyethylene Glycol Oleate was synthesized by esterification of polyethylene glycol and Oil acid using DMAP as a catalyst. The double bonds of the product in the core of micelles were cross-linked by the initiation of (NH₄)₂S₂O₈ during the micelles formed. Applications of the noncross-linked and cross-linked polyethylene glycol oleate in drug delivery were studied, which indicates that drug efficiency decreased after micelles were core cross-linked, but release rate of MTX from core cross-linked micelles seems slower than that from noncross-linked micelles.

Abstract: Monodispersed gold nanocubes of highly uniform size were fabricated by a simple electrochemical method. The lengths of the edges of the gold nanocubes were about 30 nm. The growth solution was prepared from two cationic surfactant solutions as micelle templates with added acetone solvent. The primary surfactant was hexadecyltrimethylammonium bromide (CTAB) and the co-surfactant was tetradodecylammonium bromide (TTAB).

Abstract: Gelatin, a hydrophilic protein derived from collagen, has been widely used in drug delivery system because of its biocompatibility and biodegradability. However, its high water solubility limited its interaction with hydrophilic drugs. The current works propose a method to improve surface activity of gelatin by modifying it into an amphiphilic molecule via conjugating with cholesterol. High contents of cholesterol were conjugated to amino groups (-NH2) of gelatin using N,N’-Disuccinimidyl carbonate. Cholesterol contents were varied from 100% by mole of free -NH2 group in gelatin. The reduction of free -NH2 groups on gelatin determined by 2,4,6-trinitrobenzenesulfonic acid (TNBS) decreased with the increases of cholesterol used in the conjugation. The percentage of reduction of -NH2 content was 74.63 by mole respectively. Hydrophilicity/hydrophobicity changes were evaluated from water and ethylene glycol contact angles. The conjugated-gelatin were aggregated to form micelles at a critical micelle concentration (CMC) of 8 mg/ml in DI water (pH 5), determined by surface tension testing. Average size of the micelles were in range of 459.05±54.59 nm. The micelles were tested for curcumin entrapment for a cancer research.

Abstract: The polyaniline (PANI) coated titania (TiO2) has been prepared with ammonium persulfate (APS) as an oxidant in sodium dodecylsulfate(SDS) micellar aqueous solution. These nanosized powders could transfer into the organic phase. With increase in the amount of SDS, the dispersibility into the organic solvent was increased. Consequently, the electrical conductivity of the product was also decreased. The obtained composites showed 14.16 S/cm of conductivity at maximum while the value was almost independent on the polyaniline coating ratio in range of 100~20wt%. The conductivity value of composite with 20wt% polyaniline was 70000 times higher than that of raw titania. Modified titania had properties of polyaniline and titania together. In addition these composite showed the photoconductive response against the UV irradiation, which might show the existence of P-N junction between titania and polyaniline. The detailed structure and property analyses with X-ray, UV-spectroscopy, electron microscopy and so on will be discussed in relation to the synthetic conditions

Abstract: To improve the specific accumulation in tumor sites and aqueous solubility of atRA, the core-shell type of folate-PEG-g-PEI/atRA nanoparticles were prepared by complexation between cationic PEI segments in the copolymers and anionic charged atRA, and then characterized by 1HNMR, ELS, XRD, and TEM. In vitro atRA release from the nanoparticles was investigated as a function of drug content in sink condition. Cytotocicity of atRA against HepG2, KB cell lines were also evaluated by MTT assay. The lower the drug content, the faster atRA release. atRA incorporated in folate-PEG-g-PEI/atRA nanoparticles showed much higher cytotoxic effect compared with atRA itself.

Abstract: A naphthalocyanine dendrimer (DNPcZn) was synthesized as a potential candidate of photosensitizer for photodynamic therapy. DNPcZn exhibited strong Q band absorption around 780 nm, a useful wavelength for high tissue penetration. A polyion complex (PIC) micelle (DNPcZn/m) system was formed via an electrostatic interaction of anionic DNPcZn and poly(ethylene glycol)-poly(L-lysine) block copolymers (PEG-b-PLL).

Abstract: Well-defined block copolymers consisting of a hydrophilic poly (ethylene oxide) (PEO) and lipophobic poly (1H,1H-perfluorooctyl methacrylate) (PFOMA) were synthesized with controlled molecular weight via atom transfer radical polymerization (ATRP). The block copolymers formed stable micelles where PEO is the shell and PFOMA is the core in chloroform. The micellar morphology of PEO5K-b-PFOMA5K was found to be spherical with average diameter of ca. 12 nm, while meandering cylindrical with average diameter of ca. 13 nm was observed for PEO5K-b-PFOMA13K by TEM analysis. The self-assembled structures were reorganized to thermodynamically stable morphologies upon annealing above glass transition temperature (Tg). For example, spherical shape of PEO5K-b-PFOMA5K and cylindrical domain of PFOMA block in PEO5K-b-PFOMA5K became ordered cylindrical and continuous phase, respectively.