• Journal of Periodontal and Implant Science
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• 제28권4호
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• pp.611-632
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• 1998

Chitosan has been known as a wound healing agent. The purpose of this study was to evaluate the biocompatibility and guided bone regenerative effect of chitosan and chitosan-cellulose membranes. The effects of chitosan and chitosan-cellulose membranes on the growth and survival of human periodontal ligament cells were examined by rapid colorimetric MTT(tetrazolium) assay, and the tissue response and resorption pattern were observed by implanting the membranes into the subcutaneous tissue of the back of rats for 6 weeks. To evaluate the guided bone regenerative potential of membranes, the amount of newly formed bone in the rat calvarial defects(8mm in diameter) was measured by histomorphometry and radiomorphometry 1,2 and 4 weeks after implantation of membranes. Chitosan and chitosan-cellulose membranes showed no adverse effect on the growth and survival of human periodontal ligament cells. When membranes were subcutaneously implanted, inflammatory reaction was observed at 1 week and which gradually subsided 2weeks after implantation. Membranes remained intact throughout the experimental period of 6 weeks. Radiomorphometric analysis of the craniotomy sites revealed that chitosan and chitosan-cellulose membrane implanted sites showed increased radiopacity over control. Statistically significant differences with control were found in chitosan-cellulose membrane implanted group at 2 and 4 weeks, and chitosan membrane implanted group at 4 weeks(P<0.05). Histomorphometric data indicated a pattern of osseous healing similar to radiomorphometric analysis. There was a statistically significant difference between control and chitosan-cellulose membrane implanted group at 4 weeks(P<0.05). These results implicate that chitosan and chitosan-cellulose membrane might be useful for guided bone regeneration.

• 멤브레인
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• 제28권3호
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• pp.205-213
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• 2018

본 연구에서는 가교막을 poly(2,6-dimethyl-1,4-phenylene oxide)(PPO)에 브롬화반응을 통해 제조한 Br-PPO를 주사슬로 성공적으로 제조하였고, 키토산과 4차암모늄이 포함된 키토산을 가교제로 사용하였다. 제조된 가교막은 트리메틸아민 용액에 함침하여 후처리를 진행하였다. 그리고 가교도는 가교제 비율을 이용하여 조절하였다. 이렇게 제조된 A-PPO + chitosan 가교막과 A-PPO + QA-chitosan 가교막의 이온교환막으로써의 가능성을 여러 특성평가로 확인하였다. Chitosan을 사용한 가교막보다 QA-chitosan을 사용한 가교막이 가교가 더 잘 이루어졌으며, QA-chitosan의 함량이 증가할수록 이온교환용량이 1.18 meq/g에서 1.53 meq/g까지 증가하는 경향, 함수율이 21.6%에서 42.2%까지 증가하는 경향을 나타내었다.

• Journal of Life Science
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• 제9권1호
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• pp.17-21
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• 1999

Chitosan derivitives, a sulfated N-acetylchitosan was synthesized, and artificial skin of sulfated N-acetylchitosan and N-carboxyl butyl chitosan were investigated. Sulfated derivatives of chitosan were analyzed by {TEX}${13}^C${/TEX}-NMR and the structure on N-acetyl chitosan 3,6-O-disulfate were confirmed. Rabbits underwent a midline laparotomy followed either by a bilateral peritoneal sidewall abraison(3.0×1.5cm). The injured surface was then covered with 0.2mm thick sulfated N-acetyl chitosan membrane. Sulfated N-acetyl chitosan membrane was found to reduce postsurgical bleeding after abraison of peritoneal surface treated with sulfated N-acetyl chitosan membrane. Sulfated N-acetyl chitosan implanted rabbit showed quick wound healing than N-carboxybutyl chitosan. With a sterilization procedure of chemical sterilization, sulfated N-acetyl chitosan seem to be better substitutes than N-carboxybutyl chitosan.

• 공업화학
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• 제4권2호
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• pp.416-422
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• 1993

성능이 우수한 킬레이트막을 개발하고자 chitosan에 글루타르알데히드를 가교시켜 막을 제조하였으며, 이 막을 통한 금속 이온의 투과 특성을 조사하였다. 막을 통한 이온의 투과는 downstream 용액의 pH의 영향을 크게 받았으며, 이 현산에 대하여 proton pump 메카니즘을 제안하였다. 막 표면에서의 착물형상에 의한 선택흡착성이 선택투과성에 영향을 미친다고 생각되며, $Mg^{2+}$과 $Cu^{2+}$의 혼합 용액에서 $Cu^{2+}$의 선택도는 9.5이었다.

• 한국재료학회지
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• 제31권7호
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• pp.375-381
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• 2021

Chitosan powder is synthesized by a deasetylation process of chitin, obtained from processing of dried shrimp shell powder. Subsequently, chitosan (CS) membranes filled by montmorillonite (MMT) particles and phosphotungstic acid are prepared, and characterized by FT-IR and SEM. The morphology, obtained by SEM for the composite membrane, showed that MMT filler is successfully incorporated and relatively well dispersed in the chitosan polymer matrix. Water and methanol uptake for the CS/MMT composite membranes decrease with increasing MMT loadings, but IEC value increases. In all prepared CS/MMT composite membranes, the CS membrane filled by 5 wt% MMT particles exhibits the best proton conductivity, while that with 10 wt% MMT loading exhibits the lowest methanol permeability; these values are 2.67 mS·cm^-1 and 3.40 × 10^-7 cm²·s^-1, respectively. The best membrane selectivity is shown in the CS/MMT10 composite membrane; this shows that 10 wt% filled MMT is the optimum loading to improve the performance of the chitosan composite membrane. These characteristics make the developed chitosan composite membranes a promising electrolyte for direct methanol fuel cell (DMFC) application.

• Korean Membrane Journal
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• 제5권1호
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• pp.25-30
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• 2003

Chitosan membranes crosslinked with glutaraldehayde that contained chiral environment were prepared. The chitosan membranes were characterized using FTIR and swelling index measurements. Their swelling index in water ranged from 100 to 70%, depending on the crosslinking time. The separation of D- and L-isomers of tryptophan was achieved through a pressure driven membrane separation process, using the self-supporting crosslinked chitosan membranes. The chiral separation performance of the membranes depended strongly on the swelling index of the membranes and the separation conditions such as concentration of feed solutions and different operating pressures. Especially when a chitosan membrane with a swelling index of 70% was used, almost complete optical resolution of D- and L-tryptophan was obtained ; enantiomeric excess (ee %) of 97.92% and flux of 2.26 g/㎡$.$h.

• 한국재료학회지
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• 제21권2호
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• pp.125-132
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• 2011

Fibrous chitosan membranes were fabricated as a substrate for skin applications using an electro-spinning process with different solvents and varying concentrations. Scanning electron microscopy (SEM) images confirmed that the formation of the chitosan fibrous membrane in trifluoroacetic acid was better than that in acetic acid. Fourier transform infrared spectroscopy showed that the chitosan fibers were cross-linked with glutaraldehyde, and that the cytotoxicity of the aldehyde groups was reduced by glycine and washing by NaOH and DI water. Chitosan cross-linked fibrous membranes were insoluble in water and could be washed thoroughly to wash away glycine and excess NaOH and prevent the infiltration of other water soluble bio-toxic agents using DI water. MTT assay method was employed to test the cytotoxicity of chitosan membranes during fabricating, treating and washing processes. After the dehydration of cell cultured chitosan membranes, cell attachment behavior on the material was evaluated using SEM method. Effect of the treatment processes on the biocompatibility of the chitosan membranes was shown by comparing of filopodium and lamellipodium of fibroblast cells on grown washed and unwashed chitosan fibrous membrane. The MTT assay and SEM morphology confirmed that the washed chitosan fibrous membrane increased cell attachment and cell growth, and decreased toxicity compared to results for the unwashed chitosan fibrous membrane.

• 멤브레인
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• 제16권1호
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• pp.39-50
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• 2006

실리카 입자를 기공 형성제로 사용하여 다공성 키토산 및 키틴 막을 제조하였다. 다공성 막의 제조는 다음의 3단계 절차로서 수행되었다: (1) 키토산 용액에 실리카 입자를 첨가시켜 필름을 형성시킨 후, (2) 이 필름을 알카리 용액에 침지시켜 실리카 입자를 제거하여 다공성의 키토산 막을 제조하였으며, (3) 다공성 키토산 막을 acetic anhydride를 사용하여 아세틸화시킴으로서 다공성 키틴 막을 제조하였다. 물리적 강도가 우수하고, 적절한 순수 투과량을 갖는 다공성 키토산 막과 키틴 막의 최적 제막조건이 제시되었다. 단백질 친화성을 부여하기 위해 다공성 키토산 막에 반응성 염료인 Cibacron Blue 3GA를 고정화시켰으며, BSA 단백질 및 lysozyme 효소의 흡착실험을 수행하여 친화 키토산 막 및 키틴 막의 단백질 결합용량을 측정하였다. 친화 키토산 막의 BSA 단백질 결합용량은 약 22 mg/mL이었으며, 친화 키틴 막의 lysozyme 효소 결합용량은 약 26 mg/mL로서 이는 키토산 또는 키틴을 기반으로 하여 제조된 hydrogel bead의 단백질 결합용량보다 수${\sim}$수십 배 큰 값으로서, 향후 막여과 크로마토그래피용 친화 막으로의 효과적인 활용이 기대된다.

• 멤브레인
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• 제23권6호
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• pp.418-424
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• 2013

고분자 PDMS에 chitosan을 0.02~0.60 wt%까지 넣어 복합막을 제조하였고, SEM과 TGA에 의해서 막의 특성을 조사하였다. 기체투과 실험은 $30^{\circ}C$, $4kg/cm^2$ 조건에서 수행하였고, 복합막의 함량 변화에 따른 $H_2$와 $N_2$의 투과도와 선택도를 조사하였다. PDMS-chitosan 복합막의 $H_2$와 $N_2$ 투과도는 chitosan 함량이 증가하면 0~0.20 wt%까지는 증가하고 그 이상에서는 감소하였다. 그리고 선택도($H_2/N_2$)는 0~0.20 wt%까지는 감소하고 0.20~0.60 wt% 범위에서는 증가하였다. PDMS 고분자에 chitosan이 도입되어졌을 때 PDMS의 열적 안정성이 향상되었고, chitosan 함량이 증가했을 때 복합막의 표면은 거칠어지고 홀이 생성되었다.

• 멤브레인
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• 제24권5호
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• pp.358-366
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• 2014

Chitosan에 HNT (halloysite nanotube)의 함량을 0, 3, 5, 10 wt%로 가하여 chitosan-HNT 복합막을 제조하였다. 복합막의 구조는 FT-IR, XRD, TGA, SEM으로 알아보았다. 기체투과 실험은 $30^{\circ}C$, $4kg/cm^2$ 조건에서 수행하였고, chitosan-HNT 복합막의 HNT 함량 변화에 따른 $CO_2$와 $CH_4$의 기체투과도와 선택도를 조사하였다. Chitosan-HNT 복합막의 기체 투과도는 HNT 함량이 3 wt%에서 가장 큰 값을 보였고, 그 이상의 함량에서는 감소하였다. 선택도($CO_2/N_2$)는 0~10 wt% 범위에서 HNT 내의 OH기와 $CO_2$ 간의 친화력으로 인하여 증가하였고, 약 1.3~3.8의 값을 보였다.