키토산이 백서 태자 두개관세포에 미치는 영향

김정경,정현주,김영준,김옥수,Kim, Jeong-Kyung,Chung, Hyun-Ju,Kim, Young-Joon,Kim, Ok-Su 대한치주과학회 2004 Journal of Periodontal & Implant Science Vol.34 No.4

The effect of chitosan, a carbohydrate biopolymer extracted from chitin, on periodontal regeneration is of particular interest. The purpose of this study was to evaluate the effect of chitosan on primary rat calvarial cells in vitro, with special focus on their proliferative properties by cell activity and the amount of total protein synthesis. The experimental groups were cultured with chitosan in concentration of 0.01, 0.1, 1.0, 2.0 and 5.0 mg/ml for MTT assay. In the experimental groups, cells were cultured with chitosan in concentration of 0.01, 0.1, 1.0 and 2.0 mg/ml. Each group was characterized by examining alkaline phosphatase activity at 3 and 7 days and the ability to produce mineralized nodules of rat calvarial cells at 14 and 21 days. The results were as follows: 1. The cell activity was not reduced in the concentration of $0.01{\sim}1.0$ mg/ml whereas the cell activity was reduced in the concentration of 5.0 mg/ml than the control at day 1 and 3 (p<0.05). 2. Primary rat calvarial cells treated with chitosan in the concentration 0.01 mg/ml and 0.1 mg/ml showed more protein synthesis than the control at day 3 (p<0.01), But primary rat calvarial cells treated with chitosan showed more protein synthesis than in control but they didn't have statistically difference among groups at day 7. 3. At 3 and 7 days, alkaline phosphatase activity was significantly increased in the concentration of 0.01 mg/ml. 0.1 mg/ml and 1.0 mg/ml (p<0.05). 4. The percentage of mineralized bone nodule was more in the concentration of chitosan 0.1 mg/ml and 1.0 mg/ml than the control. These results suggested that chitosan has a positive effect on the bone formation of primary rat calvarial cells in the concentration of 0.1 mg/ml and 1.0 mg/ml.

다문화가족 미취학자녀의 보육ㆍ교육서비스 선호요인 비교분석

김수봉(Kim, Soo-Bong),심옥수(Shim, Ok-Su) 한국유아교육·보육복지학회 2013 유아교육·보육복지연구 Vol.17 No.3

본 연구는 다문화가족 미취학자녀의 보육ㆍ교육서비스 시설 이용 여부 및 선호요인 분석을 통해 다문화 구성원의 사회적응을 위한 대안 모색을 시도한다. 이를 위해 2009년 「다문화가족실태조사」를 활용하였으며, 분석 대상은 다문화가족 미취학자녀 29,543명으로 로지스틱회귀모형을 구축하여 보육ㆍ교육서비스 이용 여부와 선호요인을 분석하였으며, 주요 결과는 다음과 같다. 첫째, 다문화가족 미취학자녀의 보육ㆍ교육서비스 시설 이용에 영향을 미치는 것은 결혼이주여성의 연령과 국적, 한국어 능력, 거주기간, 경제활동, 자녀의 출생 순위, 건강상태, 생활만족도, 동거 성인 수, 가구생활수준, 배우자 동거 등으로 나타났다. 둘째, 다문화가족이 이용하는 보육ㆍ교육서비스 중 상대적으로 유치원을 선호하는 경우는 다문화가족 미취학자녀가 둘째 또는 셋째이거나, 가구소득이 많을수록, 중국(한족 등), 학력이 높은 경우인 반면, 학원을 선호하는 경우는 동부지역 거주, 거주기간이 길수록, 국내가족의 생활수준이 높다고 인식할수록 학원을 선택하였으며, 어린이집(보육시설)은 결혼이주여성이 경제활동을 하는 경우에 상대적으로 높았다. 이러한 분석결과를 토대로 다문화가족의 삶의 질 향상을 위한 가족기능 및 역량강화를 위한 가족단위의 정책방안을 제시하였다. The main purpose of this study is to comparison the influencing factors on the selection of child-care and preschool of multi-cultural families with preschool children. For this study, analyzed from the first countris survey data of the multi-cultural families, conducted in 2009. The finding of the study are as follows; The main factors on the choice of child-care and preschool facilities are age, country of immigrant, ability of korean, residential period, economic activities, health state, birth order of kinder(second kinder), number of adult in family, spouse, satisfaction of life, and level of life. There were differences among the multi-cultural families in considerations for the child-care and preschool. First, the factors of selecting kindergartens were second or third kinder, family income, chinese(hangog), and education level. Second, the factors of selecting private institutes(hakwon) were residential district, residential period, perception level of life in Korea. Third, the immigrant take part in economic activities, they prefer chilid-care facilities to kindergartens or for-profit private institutes(hakwon). In conclusion, we need the implementation strategies for child-care facilities that reflected on the personalized service. Above all, social understanding of multi-cultural families shoud be improved.

키토산이 치은섬유아세포에 미치는 영향

김옥수,정현주,Kim, Ok-Su,Chung, Hyun-Ju 대한치주과학회 2002 Journal of Periodontal & Implant Science Vol.32 No.1

The aim of this study was to evaluate the effects of chitosan coating on the attachment, proliferation, functional and morphological change of human gingival fibroblasts. Primary culture of human gingival fibroblasts were grown in Dulbecco's modified Eagle's medium with 10% fetal bovine serum and 1% antibiotics. In experimental group, cells were inoculated in the multiwell plates coated with chitosan in concentration of 0.02, 0.2, and 2 mg/ml. Cell counting and MTT assay were done after 0.5, 1.5, 3, 6 and 24 hours of incubation to evaluate the cell attachment, and then after 2 and 7 days of culture to evaluate the cell proliferation. The alkaline phosphatase activity was measured after 4 and 7 days of culture and the ability to produce mineralized nodules was evaluated after 21 days of culture. The results were as follows : The morphology of cells on the chitosan-coated well was round or spheric. Round cells were aggregated since 6 hours of culture and showed nodule-like appearance after 24 hours of culture and did not achieved confluency at 7 days. The attachment of gingival fibroblasts was inhibited by chitosan coating with a tendency of dose dependent pattern. But, cellular activity of unit cell was higher than control. The proliferation of gingival fibroblasts was inhibited by chitosan coating at 2 mg/ml(P<0.01), while the cell proliferation at 0.02, 0.2 $mg/m{\ell}$ was comparable to the control well. Total alkaline phosphatase activity was inhibited by chitosan coating and decreased in the course of time. While ALP activity of unit cell was the highest at 2mg/ml after 4 days of culture. Finally, gingival fibroblasts produced the mineralized nodule at 2 mg/ml. In summary, the attachment, proliferation, and alkaline phosphatase activity of gingival fibroblasts were influenced differently by the concentration of coated chitosan. From this study, it could be used as the matrix of tissue engineering for gingiva without inhibition on proliferation of gingival fibroblasts using chitosan at the optimal concentration (0.02mg/ml).

PTMSP-NaA Zeolite 복합막에 의한 수소-질소 기체 분리에 관한 연구

김옥수,윤석일,Kim, Ok-Su,Yun, Seok Il 한국막학회 2015 멤브레인 Vol.25 No.2

PTMSP에 0~50 wt% NaA Zeolite를 첨가하여 PTMSP-NaA Zeolite 복합막을 제조하고, PTMSP-NaA Zeolite 복합막의 특성을 FT-IR, $^1H$-NMR, GPC, DSC, TGA, SEM에 의해서 조사하였다. PTMSP-NaA Zeolite 복합막의 수소와 질소에 대한 투과도와 선택성을 NaA Zeolite 함량에 따라 조사하였다. TGA측정에 의하면 PTMSP에 NaA Zeolite가 첨가되었을 때 복합막의 감량이 완결되는 온도는 낮아졌고, 감량(wt%)도 작아졌다. SEM관찰에 의하면 NaA Zeolite는 PTMSP-NaA Zeolite 복합막 내에 $2{\sim}5{\mu}m$ 크기로 분산되어 있었다. PTMSP-NaA Zeolite 복합막에 대한 $N_2$와 $H_2$의 투과도는 NaA Zeolite 함량이 증가하면 증가하였다. 그리고 PTMSP-NaA Zeolite 복합막의 $N_2$에 대한 $H_2$의 선택성은 NaA Zeolite함량이 증가하면 감소하였다. PTMSP-NaA zeolite composite membranes were prepared by adding 0~50 wt% NaA zeolite to PTMSP. The membranes were characterized by FT-IR, $^1H$-NMR, GPC, DSC, TGA, SEM. The permeabilities of $H_2$ and $N_2$ gases through PTMSP-NaA zeolite composite membranes was studied as a function of NaA zeolite contents. According to TGA measurements, when zeolite was inserted into the polymer, weight loss temperature and weight loss wt% of PTMSP-NaA zeolite composite membranes were decreased. Based on SEM observation, NaA zeolite was dispersed in the PTMSP-NaA zeolite composite membrane with the size $2{\sim}5{\mu}m$. The permeability of PTMSP-NaA zeolite composite membranes increased added as NaA zeolite content increased. On the contrary, the selectivity ($H_2/N_2$) of the composite membranes decreased as NaA zeolite content increased. PTMSP-NaA zeolite composite membrane showed better permeability and selectivity ($H_2/N_2$) of $H_2$ and $N_2$ than PTMSP-NaY zeolite composite membrane.

키토산이 배양중인 치주인대세포에 미치는 영향

김옥수,정현주,Kim, Ok-Su,Chung, Hyun-Ju 대한치주과학회 2001 Journal of Periodontal & Implant Science Vol.31 No.1

The aim of this study was to evaluate the effects of chitosan coating on the attachment, proliferation, functional and morphological change of periodontal ligament cells. Primary human periodontal ligament cells were cultured in dulbecco's modified Eagle's medium with 10% fetal bovine serum and 1% antibiotics. In experimental group, cells of 4th to 7th passage were inoculated in the multiwell plates coated with chitosan in concentration of 0.22, 0.2, and $2mg/m{\ell}$. Cell counting and MTT assay were done after 0.5, 1.5, 3, 6 and 24 hours of incubation to evaluate the cell attachment, and then after 2 and 7 days of culture to evaluate the cell proliferation. The alkaline phosphatase activity was measured after 4 and 7 days of culture and the ability to produce mineralized modules was evaluated after 21 days of culture. The results were as follows : 1. The morphology of periodontal ligament cells on the chitosan coating was round or spheric. Round cells were aggregated after 6 hours of culture. Aggregated cells on the chitosan coated surface showed nodule-like appearance after 24 hours of culture and not achieved confluency at 7 days. 2. During early period of culture, the attachment of periodontal ligament cells were inhibited by chitosan coating. Inhibition of cell attachment tended to increase with the concentration of chitosan. 3. At the chitosan concentration of 0.02 and $0.2mg/m{\ell}$, periodontal ligament cells were more rapidly proliferated at 7 days, compared to the control group. At the concentration of $2mg/m{\ell}$, the proliferation of periodontal ligament cells was inhibitied(p<0.01). 4. Alkaline phosphatase activity of periodontal ligament cells was increased in chitosan coated group, especially at the concentration of $0.02mg/m{\ell}$after 4 days of culture.5. Periodontal ligament cells produced mineralized nodules on chitosan coated wells without the addition of mineralized nodule forming materials (ascorbic acid, ${\beta}-glycerophosphat$, dexamethasone). With the addition of mineralized nodule forming materials, periodontal ligament cells produced more mineralized nodules at the concentration of $0.02mg/m{\ell}$, compared to the control. In summary, the attachment, proliferation, cell activity, and alkaline phosphatase activity of periodontal ligament cells depended on the concentration of coated chitosan. Chitosan stimulated mineralized nodule formation by periodontal ligament cells. At the appropriate concentration($0.02mg/m{\ell}$), chitosan could increase alkaline phosphatase activity and stimulate the formation of mineralized nodule by periodontal ligament cells. These results suggest that chitosan can be used as an adjunct for bone graft material, and the matrix of tissue engineering for periodontal regeneration, especially bone regeneration.

백서에서 Pulsed Nd : YAG Laser에 의한 치은절제술후의 치유양상

김옥수,정현주,Kim, Ok-Su,Chung, Hyun-Ju 대한치주과학회 1996 Journal of Periodontal & Implant Science Vol.26 No.1

Recently, dental laser have been applied for removal of soft tissues, hemostasis and blood coagulation, removal of benign and malignant tumor, treatment of leukoplakia, aphthous ulcer and herpetic lesion, implant second surgery, removal of granulation tissue, frenectomy, clinical crown lengthening, gingivectomy, gingivoplasty, and treatment of dentin hypersensitivity. Even though the frequency of laser treatment is increasing, the research on the healing process after gingivectomy using pulsed Nd : YAG laser is very rare. The purpose of this study was to observe and compare the wound healing after gingivectomy using scalpel and pulsed Nd : YAG laser in the rat. Gingivectomy was performed using pulsed Nd : YAG laser(SUNRISE Technologies, U.S.A., 1.5 Watts, 10 pps) on the buccal gingiva of right maxillary first molar and using scalpel(No.12) on the contralateral side. Those sites treated by surgical scalpel were designated as the control, and by pulsed Nd : YAG laser as the experimental group. Animals were sacrificed at 1, 2, 3, 5, 7, 11 and 14 days postoperatively, and specimens were histologically observed under light microscope. The results were as follows : 1. Clinical observation Normal color and shape were observed at the 5th day ill the control group and the 7th day in the experimental group. 2. Histologic findings 1) In the control group, denser inflammatory infiltration was observed. 2) Epithelialization started at the 2nd day in the control group, similar to the experimental group, and completed at the 11th to the 14th day postoperatively. 3) In the experimental group, connective tissue showed the vacuole formation and degenerative change during early healing period. Healing of connective tissue was slower in the experimental group than in the control group by 2 days. 4) In the both groups, wound healing was completed at the 2nd week. From this study, gingivectomy using pulsed Nd : YAG laser seems to result in a little delayed wound healing process, compared to the gingivectomy using scalpel. Considering the clinical advantages of laser surgery, pulsed Nd : YAG laser might be useful device for gingivectomy.

상악 구개부 치은에 발생한 편평상피세포암의 증례보고

김옥수,정현주,Kim, Ok-Su,Chung, Hyun-Ju 대한치주과학회 1996 Journal of Periodontal & Implant Science Vol.26 No.1

Squamous cell carcinoma is the most common malignant tumor of the gingiva. Oral cancer accounts for 5 percent of all malignant tumors in the body, and 6 percent of these occur in the gingiva. We present one case of squamous cell carcinoma of the gingiva in 23-year-old female. She complained of gingival swelling and pain during mastication between left maxillary first molar and second molar. Since she had received scaling 2 years ago, food impaction occurred frequently in this site and an ulcerative lesion recurred several times. When she was referred from local clinic, she had a large, irregularly ulcerated lesion of palatal gingiva between left maxillary first molar and second molar, accompanying induration in center and slight elevation around ulcerative margin. The etiology could not be defined but we could diagnose by careful history taking and excisional biopsy of the recurrent ulcerative lesion. In addition, computed tomography and nuclear medicine imaging were undertaken. As a result, we finally diagnosed as moderately differentiated squamous cell carcinoma without metastases. It is concluded that if ulcerations do not respond to therapy in the usual manner, it should be biopsed and histologically evaluated for the definitive diagnosis and treatment.

Full-mouth disinfection의 단기간의 임상적 효과

이신화,김옥수,김영준,정현주,Lee, Shin-Hwa,Kim, Ok-Su,Kim, Young-Joon,Chung, Hyun-Ju 대한치주과학회 2007 Journal of Periodontal & Implant Science Vol.37 No.3

Full-mouth disinfection (Fdis) completes the entire scaling and root planing (SRP) in one stage within 24 hours for the prevention of microbial recolonization from untreated sites and ecological niches. The aim of this study is to compare the clinical short-term effects of modified Fdis with those of the conventional SRP in the therapy of moderate and severe chronic periodontitis. Modified Fdis group (5 patients) received the entire SRP within 24 hours using chlorhexidine solution (0.1%) and conventional SRP group (5 patients) received SRP per quadrant at one-week intervals. Clinical parameters were measured at baseline, one month and three months after both therapies. The results of this case report were as follows: 1. There were considerable decreases in sulcus bleeding index and plaque index one month after Fdis. 2. The mean probing depth of single-rooted teeth decreased more in Fdis group than conventional SRP group after therapy and, that of multi-rooted teeth decreased similarly in both groups. 3. The mean probing depth decreased 1.77mm in case of initial probing depth of 4-6mm and it decreased 4.13mm in case of initial probing depth of ${\geq}$ 7mm three months after Felis. 4. There were the smaller increases in gingival recession together with the larger gains in attachment in Fdis group than conventional SRP group after three months. Within the limitations of this study, one could conclude that Fdis has beneficial clinical effects in the treatment of moderate and severe chronic periodontitis and further research would be helpful including more subjects during a longer period to confirm the beneficial long-term effects of Fdis.

한국인 전반적 급진성 치주염 환자에서 IL-10 promoter 유전자 다변성에 관한 연구

류지선,김옥수,Ryn, Ji-Sun,Kim, Ok-Su 대한치주과학회 2007 Journal of Periodontal & Implant Science Vol.37 No.3

Genetic polymorphisms associated with aggressive periodontitis have previously been reported. Interleukin-10 is an immunoregulatory cytokine that plays a role in the pathogenesis of periodontitis. Individual capacity for IL-10 production appears to be under genetic influence, The aim of present investigation was to explore possible genetic association of IL-10 gene promoter polymorphisms with generalized aggressive periodontitis. The study population consisted of 37 generalized aggressive periodontitis patients from the Department of Periodontology, Chonnam National University Hospital and 27 control subjects, all the subjects were non-smokers, Genomic DNA was obtained from buccal swab. The IL-10promoter -597, -824, -1082 positions were genotyped by amplifying the polymorphic regions using polymerase chain reaction (PCR) , followed by restriction enzyme digestion and gel electrophoresis. IL-10-597 C (allele 1) to A (allele 2) and IL-10-824 C (allele 1) to T (allele 2) and IL-10-1082 G (allele 1) to A (allele 2) polymorphisms were examined. The results were as follows. 1. In patients, the distribution of genotypes C/C, C/A and NA at Il-10-597 was determined to be 13.5%, 37.8% and 48.7%, respectively and the distribution of genotypes at IL-10-824 was the same as that of IL-10-597. The distribution of genotypes G/G, G/A and NA at IL-10-1082 was found to be 2.7%, 16.2% and 81. 4%, respectively. No statistical difference in genotype distribution was found between the patient and control groups. 2. Allele 2 carriage rate at the three position of the IL-10 promoter region was higher in the control group than the patient group. 3. Allele 2 frequencies at IL-10-597 and -824 positions were higher in female group than male group and its difference was statistically significant(p<0.05). No significant difference in genotype distribution between the control and patient groups. Allele frequency between control and patient groups was not significantly different although allele 2 frequency at the three positions in the IL-10 promoter region appeared to be higher in control group. In conclusion, no clear association between IL-10 gene promoter polymorphisms and generalized aggressive periodontitis in Korean was observed.

한국인 전반적 급진성 치주염 환자에서 IL-6 유전자 다변성에 관한 연구

방선정,김일신,김옥수,김영준,정현주,Bang, Sun-Jung,Kim, Il-Shin,Kim, Ok-Su,Kim, Young-Jun,Chung, Hyun-Ju 대한치주과학회 2008 Journal of Periodontal & Implant Science Vol.38 No.4

Purpose: The purpose of this study was to investigate the association of generalized aggressive periodontitis with IL-6 promoter gene single nucleotide polymorphisms(SNP). Material and Methods: The study population consisted of 52 generalized aggressive periodontitis patients(GAP) and 30 periodontally healthy control subjects, who were systemically healthy non-smokers. Genomic DNA was obtained from buccal swab. The IL-6 promotor SNP at the positions of -597, -572, and -174 were genotyped by amplifying the polymorphic region using polymerase chain reaction(PCR), restriction enzyme digestion and gel electrophoresis. Result: The genotype distributions for G/G, G/A and A/A genotypes of IL-6 -597 were 30.8%, 40.4%, and 28.8% in the GAP group and 53.3%, 40%, and 6.7% in the control group and were statistically different between 2 groups(p<0.05). Allele 2 frequency of IL-6 -597 were significantly higher in the GAP group than the control group(p<0.01). At the position of IL-6 -572, the distribution for C/C, C/G and G/G genotypes were 23.1%, 55.8% and 21.2% in the GAP group and 20%, 33.3%, and 46.7% in the control group. In female subjects, the genotype distribution were significantly different between 2 groups(p<0.01). In male subjects, allele 2 frequency of IL-6-572 was significantly lower in the GAP group than the control group(p<0.05). The genotype distribution of IL-6 -174 in the GAP group were 96.2%, 3.8% for G/G, G/C genotypes whereas only the G/G genotype was detected in the control group. Conclusion: In conclusion, significant associations were found in IL-6 gene promoter(-597, -572) polymorphisms and generalized aggressive periodontitis. Further cohort study will be necessary in larger population.