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성견에서 교정적 고정원으로서의 티타늄 미니스크류에 대한 연구 : An experimental investigation in dogs
윤병수,최병호,이원유,김경남,심형보,박진형 대한치과교정학회 2001 대한치과교정학회지 Vol.31 No.5
교정치료에서 원하는 치아이동을 위해서는 안정된 고정원이 필요한데 티타늄 미니스크류가 매식과 제거가 쉽고, 구강 내 여러 부위에서 적용이 가능하고, 환자가 느끼는 불편감이나 비용적인 부담이 적고, 제거 후에 치유가 빠르게 진행될 수 있는 등의 장점이 있어 최근에 교정적 고정원으로 사용되기 시작하였다. 티타늄 미니스크류를 교정적 고정원으로 사용한 임상 예들이 여러 편 발표되었는데 미니스크류의 이완이 가장 큰 실패의 원인으로 보고되고 있다. 그러나 지금까지 보고된 논문들에서 교정적 고정원으로 안정성을 줄 수 있는 스크류의 식립 길이에 관한 연구가 없는 상태이다. 교정적 고정원으로 미니스크류를 효과적으로 사용하기 위해서는 식립 부위에 따른 골구조와 골밀도 차이를 고려한 식립 길이에 관한 기준이 필요하다. 이에 본 연구에서는 성견의 상악골과 하악골에서 직경 2mm 티타늄 미니스크류를 다양한 길이로 식립하고 교정력을 적용한 후 그 안정성을 평가하여 교정적 고정원으로 사용될 수 있는 미니스크류의 식립 길이를 결정하고자 하였다. 미니스크류가 상악에서는 6mm이상, 하악에서는 4mm 이상이 골 내에 식립될 때 8주 동안 200g의 교정력에 동요도나 위치변화를 보이지 않았다. 식립 부위로는 부착치은 부위 치근 사이에 식립될 때 구강청결이 유지되고 미니스크류 주변 치은조직에 자극을 주지 않아 정상적인 조직으로 유지 될 수 있었다. 또한 교정력 적용 8주 후 치근단 방사선 사진검사에서 스크류 주변 치근 흡수나 치조골 흡수, 치주 인대 손상이 관찰되지 않았다. 따라서 상 ㆍ 하악 골밀도와 골구조의 차이를 고려하여 미니스크류의 골내 식립 길이를 적절히 조절함으로써 교정적 고정원으로 티타늄 미니스크류가 효과적으로 사용될 수 있다고 생각된다. Titanium miniscrews are being used increasingly as an anchorage for tooth movement, because they are easy to place and to remove, increase the number of sites available, give minimum strain to patients regarding surgical procedures, and offer uneventful healing after removal. The use of titanium miniscrews as an orthodontic anchorage has been reported in clinical case reports, but clinicians hove experienced screw loosening when using such screws. To our knowledge, there are no published reports evaluating the stability of miniscrews. Information about the length of miniscrews used in relation to the location is of some importance, as stability will vary depending on bone quality. The purpose of this study was to evaluate a variety of lengths of miniscrews (diameter: 2mm) which were inserted in maxilla or mandible and to demonstrate in a dog moedl which miniscrew provides fundamental stability in the jaws. 10 mm long miniscrews in the maxilla and 8mm long miniscrews in the mandible showed no clinical mobility and retained their position throughout an 8 weeks force (200g) application. The mucosal condition around the screws was healthy in cases in which miniscrews were inserted in the alveolar bone between the roots and the head of the screws emerged into the attached gingiva. When the force application was terminated, radiographic analysis revealed neither root resorption nor periodontal pathology around the miniscrews that remained stable during the entire treatment period. This study suggests that if titanium miniscrews with adequate length are properly used depending on the location, they provide sufficient stability for orthodontic anchorage.
Won-Bo Shim,Jung-Sook Kim,Ji-Young Kim,Jin-Gil Choi,Jung-Hyun Je,Nina Sergeevna Kuzmina,Sergei Alexandrovich Eremin,Duck-Hwa Chung 한국식품과학회 2008 Food Science and Biotechnology Vol.17 No.3
A non-instrumental immunochromatographic (ICG) strip-test and direct competitive enzyme-linked immunosorbent assay (DC-ELISA) for aflatoxin B1 (AFB1) determination were developed and optimized. The detection limits of ICG striptest and DC-ELISA were 0.5 and 0.004 ng/mL, respectively, and these methods possessed a cross-reaction to aflatoxins. The results of spiked samples by both methods were coincided with the amount spiked AFB1 and the comparative analyses of 172 real samples by 2 immunoassays and high performance liquid chromatography (HPLC) showed a good agreement. Especially, the ICG strip-test is easier to perform and quicker, but less sensitivity than DC-ELISA. Both methods could analyze a high sample throughput with short time, but the sample throughput of ICG strip-test was better. Therefore, the ICG strip-test can be used as a simple, easy, non-instrumental, and fast screening technique for AFB1 determination.
Shim, Jin-Hyung,Jeong, Jae-hyang,Won, Joo-Yun,Bae, Ji-Hyeon,Ahn, Geunseon,Jeon, Hojun,Yun, Won-Soo,Bae, Eun-Bin,Choi, Jae-Won,Lee, So-Hyoun,Jeong, Chang-Mo,Chung, Ho Yun,Huh, Jung-Bo Institute of Physics Publishing Ltd 2018 Biomedical Materials Vol.13 No.1
<P>The appropriate porosity and pore size of barrier membranes were associated with the transportation of biomolecules required for new bone formation and angiogenesis. In this study, we fabricated three-dimensional (3D)-printed resorbable polycaprolactone (PCL) membranes with different porosities (30%, 50%, and 70%) to evaluate the effective pore size for guided bone regeneration (GBR) membranes. To analyze mechanical properties and cytocompatibility, PCL membranes prepared using extrusion-based 3D printing technology were compared in dry and wet conditions and tested in vitro. The proliferation rates and pattern of fibroblasts and preosteoblasts on PCL membranes with different porosities were determined using a cell counting kit-8 assay and scanning electron microscopy. PCL membrane porosity did not affect cell proliferation, but osteogenic differentiation and mechanical properties were increased with lower porosity (30%) on day 14 (p < 0.001). Similar results were found in an in vivo calvarial defect model; new bone formation was significantly higher in PCL membranes with lower porosity (p < 0.001). These results indicate that 3D-printed PCL with 30% porosity (130 mu m pore size) is an excellent pore size for GBR membranes.</P>
Won-Bo Shim,Gyeongyeol Kim,Hee-Jung Ryu,Minji Nam,Duck-Hwa Chung 한국식품과학회 2009 Food Science and Biotechnology Vol.18 No.3
A one-step simultaneous immunchromatographic (OS-ICG) assay using colloidal gold-monoclonal antibody (gold-MAb) conjugates was developed for the rapid multianalysis of aflatoxin B1 (AFB1) and ochratoxin A (OTA) in feed samples. Visual detection limits for AFB1 and OTA were 0.5 and 2.5 ng/㎖, respectively, and the results were obtained within 15 min. Matrix interference from the feed extracts was efficiently reduced by appropriate dilution with buffer. Cut-off values of the OS-ICG assay for the feed spiked with AFB1/OTA mixtures (5/5, 10/10, 25/25, 50/55, 100/100 ㎍/㎏) were 10 and 50 ㎍/㎏ for AFB1 and OTA. The comparative analyses of 65 feed samples by OS-ICG, enzyme-linked immunosorbent assay (ELISA), and high performance liquid chromatography (HPLC) showed good agreement. In this study, we confirmed that simultaneous analysis based on immunoassay is possible and it can be used as an on-site multianalysis of AFB1 and OTA in feed, food, and agricultural products.
( Won Bo Shim ),( Boris B. Dzantiev ),( Sergei A. Eremin ),( Duck Hwa Chung ) 한국미생물 · 생명공학회 2009 Journal of microbiology and biotechnology Vol.19 No.1
Individual immunochromatographic assays (ICG) for ochratoxin A (OTA) and zearalenone (ZEA) were optimized and used in the development of a one-step simultaneous immunochromatographic assay (OS-ICG) for the rapid multianalysis of two mycotoxins in corn samples. The nitrocellulose membrane of the OS-ICG was treated with OTA-bovine serum albumin (BSA), ZEA-ovalbumin (OVA), and anti-mouse IgG in the OTA test, ZEA test, and control zones, respectively. Monoclonal antibody-gold conjugates (OTA3 MAb-gold and ZEA2C5 MAb-gold) were sprayed onto the conjugate pad. The visual detection limits were 2.5 and 5 ng/ml for OTA and ZEA, resepectively, and the results were obtained within 15 min after starting the analysis. An efficient, simple, and rapid extraction method using 30% MeOH/PBS was established and validated by analyzing the corn samples spiked with OTA/ZEA mixtures (0/0, 5/10, 10/20, and 20/30 μg/kg). The cut-off values of the OS-ICG for the spiked corn were 5 and 10 μg/kg for OTA and ZEA, respectively. Natural corn samples were analyzed by OS-ICG, direct competitive enzyme-linked immunosorbent assay (DC-ELISA), and HPLC. Results of the OS-ICG were in good agreement with those obtained by DC-ELISA and HPLC. The developed OS-ICG offers a rapid, easy-to-use, and portable analytical system and can be used as a convenient qualitative tool for the on-site simultaneous determination of OTA and ZEA in cereals, food, and agricultural products in one analytical cycle.
FSR1 is essential for virulence and female fertility in Fusarium verticillioides and F. graminearum.
Shim, Won-Bo,Sagaram, Uma Shankar,Choi, Yoon-E,So, Jinny,Wilkinson, Heather H,Lee, Yin-Won APS Press 2006 Molecular plant-microbe interactions Vol.19 No.7
<P>Fusarium verticillioides (teleomorph Gibberella moniliformis) and F. graminearum (teleomorph G. zeae) are well known to cause devastating diseases on cereal crops. Despite their importance, our understanding of the molecular mechanisms involved in these host-pathogen interactions is limited. The FSR1 locus in F. verticillioides was identified by screening REMI mutants for loss of virulence in maize stalk rot inoculation studies. FSR1 encodes an 823-codon open reading frame interrupted by two introns. The Fsr1 protein shares 60% sequence identity with the Sordaria macrospora Pro11, a multimodular protein with four putative protein-protein binding domains (caveolin-binding domain, coiled-coil structure, calmodulin-binding motif, and seven-WD40 repeats), which plays a regulatory role in cell differentiation and ascocarp development. Our data demonstrate that FSR1 is essential for female fertility and virulence in F. verticillioides. Significantly, targeted disruption of the FSR1 ortholog in F. graminearum (FgFSR1) reduced virulence on barley and deterred perithecia formation. Cross-complementation experiments demonstrated that the gene function is conserved in the two Fusarium species. FSR1 is expressed constitutively, and we hypothesize that Fsr1 regulates virulence by acting as a scaffold for a signal transduction pathway. A survey of available genome databases indicates Fsr1 homologs are present in a number of filamentous fungi and animal systems but not in budding yeast or plants. A maximum likelihood analysis of this gene family reveals well-supported monophyletic clades associated with fungi and animals.</P>