• Maxillofacial Plastic and Reconstructive Surgery
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• 제32권4호
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• pp.299-305
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• 2010

Purpose: Adipose tissue is located beneath the skin, around internal organs, and in the bone marrow in humans. Its main role is to store energy in the form of fat, although it also cushions and insulates the body. Adipose tissue also has the ability to dynamically expand and shrink throughout the life of an adult. Recently, it has been shown that adipose tissue contains a population of adult multipotent mesenchymal stem cells and endothelial progenitor cells that, in cell culture conditions, have extensive proliferative capacity and are able to differentiate into several lineages, including, osteogenic, chondrogenic, endothelial cells, and myogenic lineages. Materials and Methods: This study focused on endothelial cell culture from the adipose tissue. Adipose tissues were harvested from buccal fat pad during bilateral sagittal split ramus osteotomy for surgical correction of mandibular prognathism. The tissues were treated with 0.075% type I collagenase. The samples were neutralized with DMEM/and centrifuged for 10 min at 2,400 rpm. The pellet was treated with 3 volume of RBC lysis buffer and filtered through a 100 ${\mu}m$ nylon cell strainer. The filtered cells were centrifuged for 10 min at 2,400 rpm. The cells were further cultured in the endothelial cell culture medium (EGM-2, Cambrex, Walkersville, Md., USA) supplemented with 10% fetal bovine serum, human EGF, human VEGF, human insulin-like growth factor-1, human FGF-$\beta$, heparin, ascorbic acid and hydrocortisone at a density of $1{\times}10^5$ cells/well in a 24-well plate. Low positivity of endothelial cell markers, such as CD31 and CD146, was observed during early passage of cells. Results: Increase of CD146 positivity was observed in passage 5 to 7 adipose tissue-derived cells. However, CD44, representative mesenchymal stem cell marker, was also strongly expressed. CD146 sorted adipose tissue-derived cells was cultured using immuno-magnetic beads. Magnetic labeling with 100 ${\mu}l$ microbeads per 108 cells was performed for 30 minutes at $4^{\circ}C$ a using CD146 direct cell isolation kit. Magnetic separation was carried out and a separator under a biological hood. Aliquous of CD146+ sorted cells were evaluated for purity by flow cytometry. Sorted cells were 96.04% positivity for CD146. And then tube formation was examined. These CD146 sorted adipose tissue-derived cells formed tube-like structures on Matrigel. Conclusion: These results suggest that adipose tissue-derived cells are endothelial cells. With the fabrication of the vascularized scaffold construct, novel approaches could be developed to enhance the engineered scaffold by the addition of adipose tissue-derived endothelial cells and periosteal-derived osteoblastic cells to promote bone growth.

• 자원리싸이클링
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• 제28권6호
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• pp.96-105
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• 2019

폐자동차파쇄잔재물(Automobile Shredder Residue, ASR)은 폐차 재활용시 발생되는 최종 폐기물로써 파분쇄, 공기분급, 자력선별 및 정전선별법과 같은 자원처리 공정을 이용하여 선별할 수 있다. 본 연구에서는 유도형 정전선별기를 이용하여 A SR의 선별효율 향상 및 예측을 위한 전도체(구리) 및 비전도체(유리)의 궤적분석이 수행되었다. 전도체의 궤적분석 결과, 0.5와 0.25 mm 조립자 구리선의 모사궤적은 실제궤적과 거의 일치하였다. 반면 0.06 mm 구리선의 관찰궤적은 (-) 전극으로 편향되었다. 이는 입자특성 및 상대습도에 의한 전하량의 영향 때문으로 판단된다. 비전도체의 경우 절연체 유리의 관찰궤적이 전도성 입자들의 궤적과 유사한 특징을 보이면서 (-) 전극으로 편향되었다. 현미경, SEM & EDS 분석결과 유리표면에서 미립의 철과 전도성 유기물과 같은 이물질 발견되었다. 이와 같이 이물질이 부착된 유리는 ASR 재활용을 위한 정전선별시 비철금속의 선별효율을 저하시키는 것으로판단된다. 향후 연구에서 유리에 부착된 이물질 제거를 위한 전처리 기술개발 및 개선된 궤적모사 연구가 요구된다.