• 한국식품영양학회지
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• 제37권1호
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• pp.48-56
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• 2024

Effects of glutamic acid (Glu) and monosodium glutamate (MSG) on oxidative stability of oil-in-water (O/W) emulsions with different emulsifier charges during riboflavin (RF) photosensitization were evaluated by analyzing headspace oxygen content and conjugated dienes. Cetyltrimethylammonium bromide (CTAB), Tween 20, and sodium dodecyl sulfate (SDS) were used as cationic, neutral, and anionic emulsifiers, respectively. Glu acted as an antioxidant in CTAB- and Tween-20-stabilized O/W emulsions during RF sensitization, whereas Glu acted as prooxidants in SDS-stabilized O/W emulsions in the dark. However, adding MSG did not have a constant impact on the degree of oxidation in O/W emulsions irrespective of the emulsifier charge. In RF-photosensitized O/W emulsions, the emulsifier charge had a greater influence on antioxidant properties of Glu than on those of MSG.

• Journal of the Korean Wood Science and Technology
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• 제25권3호
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• pp.75-82
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• 1997

To improve the quality of coated paper, the continuous research to the coating components and development of alternative latices is required. Recently, amphoteric latex is getting a great concern due to their changable properties of surface charge through controlling pH and some methods have been tried to prepare amphoteric latices. This study was carried out to synthesize amphoteric latex using seeding polymerization method with low concentration emulsifier. Styrene was used as a main monomer in addition to acrylonitrile for a hydrophilic comonomer. acrylic acid for a anionic comonomer and N,N-dimethylaminoethyl methacrylate for a cationic comonomer. Particle size and viscosity of latex were greatly affected by addition of acrylic acid and ammonium persulfate as an initiator. Negative charge of latex in alkali condition was changed to zero to positive charge in around pH 4.

• Food Science and Biotechnology
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• 제16권6호
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• pp.999-1005
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• 2007

An oil-in-water (O/W) emulsion [20 wt% com oil, 0.5-6.0 wt% fish gelatin (FG), pH 3.0] was produced by high pressure homogenization, and the influence of pH, protein concentration, and homogenization condition on the formation of FG-stabilized emulsions was assessed by measuring particle size distribution, electrical charge, creaming stability, microstructure, and free FG concentration in the emulsions. Optical microscopy indicated that there were some large droplets ($d>10\;{\mu}m$) in all FG-emulsions, nevertheless, the amount of large droplets tended to decrease with increasing FG concentration. More than 90% of FG was present free in the continuous phase of the emulsions. To facilitate droplet disruption and prevent droplet coalescence within the homogenizer, homogenization time was adjusted in O/W emulsions stabilized by 2.0 or 4.0 wt% FG. However, the increase in the number of pass rather promoted droplet coalescence. This study has shown that the FG may have some limited use as a protein emulsifier in O/W emulsions.

• 폴리머
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• 제34권6호
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• pp.491-494
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• 2010

무유화 에멀젼 공중합법을 이용하여 180~200 nm의 지름을 가지는 단분산성 폴리(스티렌/디비닐벤젠/비닐 아세테이트) [poly(ST-co-DVB-co-VAc)] 고분자 나노입자를 합성하였으며, 제조된 단분산성 고분자 나노입자의 표면을 비누화반응을 통하여 개질하여 단분산성 폴리(스티렌/디비닐벤젠/비닐알코올) [poly(ST-co-DVB-co-VA)] 나노입자를 제조하였다. 합성된 입자를 반응염료와 반응시켜 적색과 청색 단분산성 폴리(스티렌/디비닐벤젠/비닐알코올) 나노입자를 제조하였으며, 입자의 형태, 분산성 및 표면전하를 전자현미경, 시차열분석기, UV/Vis 흡광기 및 제타 전하 측정장치를 이용하여 규명하였다.

• 폴리머
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• 제28권6호
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• pp.524-530
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• 2004

스티렌, 폴리(에틸렌 글리콜) 메타크릴레이트 (PEG-MMA) 혹은 폴리(에틸렌 글리콜) 디메타크릴레이트 (PEG-diMMA)를 중성 매질에서 무유화제 (emulsifier-free) 유화 중합하여 표면에 에틸렌 글리콜기를 갖는 폴리스티렌 입자를 합성하였고, 이로부터 동결 건조되어진 분말을 제조하였다. 고분자 분말은 FT-TR 분광기로 구조를 확인하였고, 광산란 입도 분석기와 주사 전자 현미경 (SEM)을 이용하여 입자 크기와 분산도를 조사하였다. 스티렌에 대하여 공단량체 PEG-MMA는 2∼5 mol%, PEG-diMMA는 1 mol% 농도 부근에서 균일한 입자 크기를 얻을 수 있었다. 합성된 입자의 표면 전하를 유전 매질 내에서 ELS-8000 광산란법을 이용하여 제타 포텐셜을 측정하였다. 스티렌에 대하여 PEG-MMA 5 mol%에서 183 mV의 아주 높은 제타 포텐셜이 측정되었다.

• 한국염색가공학회지
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• 제20권6호
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• pp.8-17
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• 2008

Poly (vinyl acetate) (PVAc) was used as a precursor of PVA/PVAc (skin/core) bicomponent. In order to investigate the possibility of PVA particles for electrical applications, PVA/PVAc particles were produced with an emulsifier, SDS (Sodium Dodecyl Sulfate) and an initiator, V-50 (2,2'-azobis(2-amidinopropane)digydrochloride). In this study, we investigated the electrical property of PVA/PVAc (skin/core) particles. The hydroxyl group of the PVA/PVAc (skin./core) was confirmed by the analysis of PVAc and PVA/PVAc (skin/core) using Fourier Transform Infrared Spectroscopy (FT-IR). The zeta-potential of the PVA/PVAc (skin/core) and PVAc has similarity; however, charge control agent (CCA) treated PVA/PVAc (skin/core) particles has lower zeta-potential than untreated PVA/PVAc particles. The zeta-potential (negative values) of the PVA/PVAc (skin/core) were enhanced in proportion to the increased concentration of CCA.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 2003년도 The Korea-Japan Joint Symposium
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• pp.94-94
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• 2003

Cross-linked polystyrene (PS) particles with carboxyl and/or poly(ethylene glycol) units on surface were formed by an emulsifier-free emulsion polymerization using styrene, methacrylic acid (MA), and poly(ethylene glycol) dimethacrylate (PEG-diMMA) at pH 7, and followed by freeze-drying to give the corresponding powders. Monodisperse polymer particles could be obtained at a concentration of PEG-diMMA 1 mol% relative to styrene. Zeta potential of polymer surface was measured to be 91 mV at a polymer of PEG-diMMA 1 mol% and was dropped as the content of MA increased.

• 한국축산식품학회지
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• 제31권4호
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• pp.543-550
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• 2011

Various concentrations of whey protein isolate (WPI), such as 0.1, 0.5, 1.0, 2.5, and 5.0%(w/v), containing 1.0%(w/v) eugenol were prepared by high speed homogenization to formulate nanoemulsions (NEs) and to investigate their antimicrobial activity. The results showed that particle size decreased according to increases in WPI concentration. Similarly, the ${\zeta}$-potential value was reduced to a negative charge when using WPI concentrations >0.1%(w/v). In contrast, no significant differences in particle size were observed during 1 mon of storage, except for the 0.1%(w/v) WPI NE. The ${\zeta}$-potential value depended on the increase in WPI concentration and storage duration, except for NE1 and NE5, suggesting that a low or high concentration of emulsifier was not effective for maintaining the droplet form of the eugenol NE. The results of an antibacterial effect investigation indicated that the growth of Escherichia coli was inhibited based on an increase in eugenol concentration in all NE formulations. Moreover, a membrane permeability study showed that total leakage content increased according to incubation time.

• 폴리머
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• 제31권1호
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• pp.74-79
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• 2007

[ $PPy^+DBS^-$ ] 복합체는 유화중합에 의해 제조되었고 이때 iron(III) chloride($FeCl_3$)는 개시제로, dodecyl benzene sulfonic acid(DBSA)는 계면활성제 및 도판트로 사용되었다. Poly(2,6-dimethyl-1,4-phenylene oxide) (PPO)는 chlorosulfonic acid(CSA)를 사용하여 설폰화되었고 양극은 $PPy^+DBS^-$ 복합체, 도전제 그리고 바인더로 구성되며 이때 바인더로 PPO와 설폰화된 poly (2,6-dimethyl-1,4-phenylene oxide) (SPPO)를 사용하였다. $PPy^+DBS^-/SPPO$ 양극은 $PPy^+DBS^-/PPO$에 비해 약 50% 높은 충 방전 성능을 나타내었는데 이는 SPPO가 바인더뿐만 아니라 도판트로 작용했기 때문이다. 더욱이 바인더로 사용된 고분자의 설폰화는 전도성 고분자와의 coulombic attraction을 유발시켜 두 상간의 혼화성을 증가시켰을 뿐만 아니라 양극과 전해질 사이의 접촉면적을 증가시켜 전기화학적으로 우수한 성능을 나타나게 했다.

• Biomolecules & Therapeutics
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• 제18권1호
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• pp.99-105
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• 2010

The purpose of this study was to evaluate relative bioavailability of the coenzyme Q10 (CoQ10) in emulsion and three liposome formulations after a single oral administration (60 mg/kg) into rats. Emulsion formulation of CoQ10 was prepared by conventional method using Phospholipon 85G as an emulsifier, and three liposome formulations (neutral, anionic, and cationic) of CoQ10 were prepared by traditional lipid film hydration technique using Phospholipon 85G, cholesterol, and charge carrier lipids (1,2-dioleoyl-3-trimethylammonium-propane chloride salt for cationic liposome and 1,2-dimyristoyl-sn-glycero-3-phosphate monosodium salt for anionic liposome). Mean particle size of all CoQ10-loaded liposome was less than a micron, and size distribution of the liposome population was homogeneous. Bioavailability of CoQ10 in emulsion was 1.5 to 2.6-fold greater than liposome formulations in terms of $AUC_{0-24\;h}$. $T_{max}$ was 3 h when administered as emulsion while it was greater than 6 h in liposome formulations. Notably, it was approximately 8 h in cationic liposome. $C_{max}$ was highest in emulsion and was significantly decreased when administered as liposome. Charged liposome showed even lower $C_{max}$ than neutral liposome, especially in cationic liposome. In conclusion, therefore, it is suggested that clinicians and patients consider bioavailability issue a primary concern when choosing a CoQ10 product, especially when very high plasma level is required such as in the treatment of heart failure and Parkinson's disease.