• 폴리머
• /
• 제28권1호
• /
• pp.24-34
• /
• 2004

여러 종류의 불소고분자내로 다양한 유기용매들의 동적 흡수 평형 (혹은 팽윤) 실험을 진행하였다. 불소로 포화된 고분자는 이상적 흡수 거동을 나타내었으나 부분적으로 치환된 불소고분자는 최종 흡수단계에서 가속화되는 비이상적 흡수 거동을 나타내었다. 회귀분석에 의해 픽-확산 거동으로부터 벗어나는 정도를 최소자승법 (즉, ∑ ［측정값-예측값］$^2$)으로 구한 결과 -퍼플루오로알콕시 공중합체, 폴리(에틸렌 테트라플루오로에틸렌) 공중합체, 폴리(비닐리덴 플루오라이드), 폴리(에틸렌 클로로트리플루오로에틸렌) 공중합체에 대해 각각 3.0${\times}$$10^{-4}$, 1.75${\times}$$10^{-3}$, 8.68${\times}$$10^{-3}$, 1.75${\times}$$10^{-2}$의 수치를 나타내었다. 응력-변형 실험 결과 비-픽 확산 거동은 팽윤된 불소고분자의 기계적 성질 (탄성률과 인장 강도) 변화와 상관관계가 있음을 알 수 있었다. 비이상적 흡수 거동의 주요 원인은 치환된 수소 혹은 염소와 불소원자 간의 전기음성도 차이에 기인한 사슬 간극성 결합 구조가 침투성분의 가소화 효과에 의해 비선형적 이완이 진행되면서 비-픽 확산이 진행되기 때문이다. 따라서 부분적으로 치환된 불소고분자를 차단성 혹은 선택적 투과기능이 요구되는 분야에 적용할 때 가소화 성분에 대한 용해 및 확산 거동에 대한 신중한 고찰이 필요하다.

• 폴리머
• /
• 제38권2호
• /
• pp.180-187
• /
• 2014

그래핀옥사이드(GO)와 전도성 고분자(PPy, PANI, PEDOT)로 이루어진 나노복합체를 제자리 화학중합을 통하여 제조하였으며, 전도성 고분자의 함량 증가에 따른 특성변화를 분석하였다. GO에 존재하는 반응성 그룹 그리고 GO-poly(4-styrene sulfonic acid)(PSSA) 복합체 및 세 종류 나노복합체에서 고분자의 존재를 확인하였으며, GO와 PSSA 또는 전도성 고분자 사이의 상호작용이 제안되었다. GO-PSS/PEDOT 나노복합체의 경우 PEDOT 함량이 증가함에 따라 라만 스펙트럼의 $I_D/I_G$ 값이 감소하였으며 특성 피크 위치도 크게 변화하였다. GO-PSS/PEDOT 나노복합체의 경우 PEDOT이 GO-PSSA 층을 박리시켜 그들 분자층 사이로 내부 삽입되어 있는 형태를 취하며 GO 또는 GO-PSSA 분자층이 열차단층으로 작용하게 되어 나노복합체는 GO 또는 GO-PSSA보다 열안정성이 향상되었다. 또한 GO-PSSA와 PEDOT 사이에 형성된 균일한 hybridization 모폴로지를 확인하였으며, GO-PSS/PEDOT 나노복합체의 경우 가장 우수한 전기전도성을 보여 주었다.

• Journal of Periodontal and Implant Science
• /
• 제48권5호
• /
• pp.305-316
• /
• 2018

Purpose: The aim of the present study was to evaluate the biocompatibility and barrier function of mussel adhesive protein (MAP)-loaded collagen membranes in guided bone regeneration (GBR). Methods: Eight male New Zealand white rabbits were used. Four circular defects (diameter: 8 mm) were created in the calvarium of each animal. The defects were randomly assigned to 1) a negative control group, 2) a cyanoacrylate (CA)-loaded collagen membrane group (the CA group), 3) a MAP-loaded collagen membrane group (the MAP group), and 4) a group that received a polycaprolactone block with MAP-loaded collagen membrane (the MAP-PCL group). Specimens were harvested at 2 weeks (n=4) and 8 weeks (n=4) postoperatively for observational histology and histometric analysis. Results: In the histologic analysis, MAP was completely absorbed without any byproducts. In contrast, some of the CA adhesive remained, showing an inflammatory reaction, at 8 weeks. In the MAP-PCL group, the MAP-loaded collagen membranes served as a barrier membrane despite their fast degradation in GBR. No significant difference was found in the amount of new bone between the MAP-PCL and MAP groups ($1.82{\pm}0.86mm^2$ and $2.60{\pm}0.65mm^2$, respectively). Conclusions: The MAP-loaded collagen membrane functioned efficiently in this rabbit calvarial GBR model, with excellent biocompatibility. Further research is needed to assess clinical applications in defect types that are more challenging for GBR than those used in the current model.

• 공업화학
• /
• 제7권5호
• /
• pp.813-822
• /
• 1996

온실효과에 주요한 기여를 하는 이산화탄소를 줄이기 위하여 새로운 형태의 고분자인 폴리(알킬렌 카보네이트)가 합성되어졌다. 이산화탄소와 여러 가지 에폭시드로부터 칼복시산의 아연염을 촉매로 하여 교대 공중합체가 만들어졌다. 중합체의 수 평균 분자량은 50,000 정도이면 중합 분산도는 5~10 정도로 비교적 넓은 분포를 갖는다. 이 중합체는 비 결정성이고, 투명한 물질로써 열분해가 쉽게 일어난다. 높은 온도와 불활성 분위기 하에서도 완벽한 분해가 일어나 탄소 잔류물을 남기지 않는 것으로 알려졌다. 간단한 에폭시드와의 공중합체의 물리적인 성질을 개선하기 위하여 입체 장애가 큰 에폭시드와의 삼원 공중합체도 만들 수 있다. 이러한 분해성을 이용하여 세라믹, 금속, 전자 산업용 바인더나 lost-foam casting에 활용이 검토되었다. 또한 포장용 필름이나 가소제로의 활용도 연구될 수 있을 것으로 기대된다.

• 한국막학회:학술대회논문집
• /
• 한국막학회 1997년도 추계 총회 및 학술발표회
• /
• pp.69-70
• /
• 1997

Polyimides and related polymers, when synthesized from aromatic monomers, have generally rigid chain structures resulting in a low gas permeability. The rigidity of polymer chains reduces the segmental motion of chains and works as a good barrier against gas transport. To overcome the limit of use as materials of gas separation membranes due to low gas permeability, block copolymers with the incorporation of flexible segments like siloxane linkage and ether linkage have been studied. These block copolymers have microphase-separated structures composed of microdomains of flexible poly(dimethylsiloxane) or polyether segments and of rigid polyimides segments. In case of rigid-flexible block copolymers, the characteristics of both phases for gas permeation are of great difference. The permeation of gas molecules occurs favorably through microdomains of flexible segments, whereas those of rigid segments hinder the permeation of gas molecules. Accordingly the increase of content of flexible segments in a rigid polymer matrix will increase the gas permeability of the membrane linearly. However, this prediction does not satisfy enough many experimental results and in particular the drastic increase of the permeability is observed in a certain volume fraction. It was proposed that the gas transport mechanism is dominated by diffusion rather than gas solubility in a certain content of flexible phase if solution-diffusion mechanism is adopted. However, the transition from solubility-dependent to diffusion-dependent cannot be explained by the understanding of mechanism itself. Therefore, we consider an effective chemical path which permeable phase can form in a microheterogenous medium, and percolation concept is introduced to describe the permeability transition at near threshold where for the first time a percolation path occurs. The volume fraction of both phases is defined as V$_{\alpha}$ and V$_{\beta}$ in block copolymers, and the volume of $\beta$ phase in the threshold forming geometrically a traversing channel is defined as V$_{\betac}$. The formation mechanism of shortest chemical channel is schematically depicted in Fig. 1.

• Advances in Traditional Medicine
• /
• 제7권1호
• /
• pp.51-64
• /
• 2007

Mucus is an aqueous gel complex with a constitution of about 95% water, high molecular weight glycoprotein (mucin), lipid, salts etc. Mucus appears to represent a significant barrier to the absorption of some compounds. Natural mucoadhesive agent was isolated and purified from the aqueous extract of the seeds of prosopis pallida (PP). Formulated tablet with the isolated material by wet granulation method. Some natural edible substances are in consideration for candidates as mucoadhesive agents to claim more effective controlled drug delivery as an alternative to the currently used synthetic mucoadhesive polymers. Subjected the materials obtained from natural source i.e. PP and standard synthetic substance, sodium carboxymethyl cellulose for evaluation of mucoadhesive property by various in vitro and in vivo methods. Through standard dissolution test and a model developed with rabbit, evaluated in vitro controlled release and bioadhesive property of theophylline formulation. Mucoadhesive agent obtained from PP showed good mucoadhesive potential in the demonstrated in vitro and in viνo models. The results suggest that the mucoadhesive agent showed controlled release properties by their application, substantially. In order to assess the gastrointestinal transit time in vivo, a radio opaque X-ray study performed in healthy rabbit testing the same controlled release formulation with and without bioadhesive polymer. Plasma levels of theophylline determined by the HPLC method and those allowed correlations to the in vitro mucoadhesive study results. Better correlation found between the results in different models. PP may acts as a better natural mucoadhesive agent in the extended drug delivery system.

• 멤브레인
• /
• 제16권2호
• /
• pp.85-105
• /
• 2006

Poly(lactic acid) (PLA)는 옥수수나 설탕수와 같은 재생자원에서 추출된 환경친화적 재료로서 이에 대한 관심이 증대되고 있다. PLA는 선형 지방족 열가소성 polyester로써, lactide와 lactic acid 모노머의 고리 개환 중합법에 의해 제조된다. PLA는 높은 기계적 능력과 열가소성, 직물능력과 생체적합성을 가지고 있어서, 다양한 end-use application에 유망한 고분자이다. 그러나 열점도, 충격인자, 열변형온도(HDT), gas barrier 특성 등과 같은 다른 몇몇 특성들은 충분히 만족시키지 못한다. 최근에, clay의 실리케이트 층에 용액이나 용융법을 이용한 고분자의 삽입은 순수 고분자나 전형적인 복합체에 비해 기계적, 열적, 광학적, 그리고 물리화학적 특성에서 훌륭한 증진을 꾀할 수 있는 나노복합재료를 제조하기 위한 가장 좋은 기술이다. 층상실리케이트는 자연적으로 풍부하고, 경제적이며, 환경친화적 물질이다. 본 논문에서는 생분해성 고분자를 기초로 한 재생자원 poly(lactic acid)의 여러 합성과 특징, 그리고 그것의 층상실리케이트 나노복합체 분리막으로의 응용과 특징을 알아보고자 하였다.

• 한국정밀공학회지
• /
• 제24권4호
• /
• pp.138-146
• /
• 2007

Some biodegradable polymers and other materials such as hydrogels have shown the promising potential for surgical applications. Post surgical adhesion caused by the natural consequence of surgical wound healing results in repeated surgery and harmful effects. Recently, scientists have developed absorbable anti-adhesion barriers that can protect a tissue from adhesion in case they are in use; however, they are dissolved when no longer needed. Although these approaches have been attempted to fulfill the criteria for adhesion prevention, none can perfectly prevent adhesions in all situations. Overall, we developed a new method to fabricate an anti-adhesion membrane using biodegradable polymer and hydrogel. It employed a highly accurate three-dimensional positioning system with pressure-controlled syringe to deposit biopolymer solution. The pressure-activated microsyringe was equipped with fine-bore nozzles of various inner-diameters. This process allowed that inner and outer shapes could be controlled arbitrarily when it was applied to a surgical region with arbitrary shapes. In order to fulfill the properties of the ideal barriers f3r preventing postoperative adhesion, we adopted the pre-mentioned method combined with surface modification with the hydrogel coating by which anti-adhesion property was improved.

• Journal of Pharmaceutical Investigation
• /
• 제30권3호
• /
• pp.179-189
• /
• 2000

Clebopride malate(Cm) is a new benzamide drug which has a potent central antidopaminergic activity possessing antiemetic and anxiolytic properties. A purpose of this study was to assess the feasibility of formulating sustained release preparation by dispersing a drug in hydrophilic polymeric matrices and double layered tablets(DLT), using HPMC, carbopol, PEO, PVP/VA and other polymers as a rate controlling barrier. The matrix and DLT showed optimum dissolution pattern up to 8 hours and the contents of polymer were optimized at 30% level in this preparation. After an oral administration in beagle dog, Cm concentration was determined by use of GC-ECD and pharmacokinetic parameters were calculated by Vallner's method. The AUC of DLT showed similar results and the duration of action was increased 55% compared to that of regular release dosage form. The calculated absorption rate effectiveness(ARE) and controlled release effectiveness(CRE) for DLT increased 50% compared to that of matrix, the overall effectiveness(E) of this product appears to be about 70%. in vivo effectiveness test, DLT showed significant differences from control on antiemetic action of Cm. In consequence, it was possible to conclude that double layered tablet might be a good candidate for the sustained release dosage forms.

• 한국응용과학기술학회지
• /
• 제28권2호
• /
• pp.170-177
• /
• 2011

Transdermal drug delivery(TDS) offers many important advantages. For instance, it is easy and painless, it protects the active compound from gastric enzymes, and it avoids the hepatic first-pass effect. Also, it is simple to terminate the therapy if any adverse or undesired effect occurs. But skin is a natural barrier, and only a few drugs can penetrate the skin easily and in sufficient quantities to be effective. Therefore, in recent years, numerous studies have been conducted in the area of penetration enhancement. The most commonly used transdermal system is the skin patch using various types of technologies. Compared with other method of dosage, it is possible to use for a long term. It is also possible to stop the drug dosage are stopped if the drug dosage lead to side effect. Polysaccharide, such as xanthan gum and algin were selected as base materials of TDS. Also, these polymers were characterized in terms of enhancers and drug contents. Among these polysaccharide, the permeation rate of Paroxetine such as lipophilic drug was the fastest in xanthan gum matrix in vitro. We used glycerin, PEG400 and PEG800 as enhancers. Since dermis has more water content(hydration) than the stratum corneum, skin permeation rate at steady state was highly influenced when PEG400 was more effective for lipophilic drug. Proper selection of the polymeric materials which resemble and enhance properties of the delivering drug was found to be important in controlling the skin permeation rate.