釉基質 的英文怎麼說
中文拼音 [yòujīzhí]
釉基質
英文
ganoin-
Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel
結果如下：皮下包埋卜周者，無細胞真皮基質漸與周圍組織粘附，顏色由蒼白轉紅；皮下包埋3周者，無細胞真皮基質與周圍組織緊密枯附，盾晰葉辯；術后卜周，包埋的基質面積變化較包埋前無統計學差異o川0引，術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ） 。光鏡下術后卜周，宿主的淋巳組織細胞、成纖維細胞浸入生長，釉附在膠原纖維上，少量血管內皮細胞浸入基質；術后34周，無細胞真皮基質內較多的血管形成，故可認為無細胞真皮基質免疫原性低，能誘導宿主的成纖維細胞、巨噬細胞浸入生長，為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合移棺的研究， sd大鼠10隻，在其背部卜方造成全厚皮膚缺損的創面Results placement of a zinc oxide phosphorat protective base at cej level decreased hydrogen peroxide. penetration dramatically
結果漂白前平齊釉牙骨質界水平制備磷酸鋅水門汀基，過氧化氫漏量顯著減少。This paper probed into the composition of sanitary ware refire glazes and the repairing process of the flaw on the surface of sanitary ware glaze. investigated the effect of sanitary ware refiring process to the quantity of product and proposed the firing curves of sanitary ware refiring based on it
探討了衛生陶瓷重燒釉的組成，衛生陶瓷釉面缺陷的修補工藝，研究了衛生陶瓷重燒燒成工藝對產品質量的影響，在此基礎上提出了衛生陶瓷重燒的燒成曲線。The effects of enamel matrix proteins on cell proliferation of cultured human periodontal ligament cells
釉基質蛋白對牙周膜成纖維細胞增殖活性的影響The effects of enamel matrix proteins and bone morphogenetic protein 2 on cell proliferation by cultured human periodontal ligament cells
釉基質蛋白和骨形成蛋白對牙周膜成纖維細胞增殖活性的影響The effects of enamel matrix proteins and bone morphogenetic protein 2 on cell mineralogical property by cultured human periodontal ligament cells
釉基質蛋白和骨形成蛋白對牙周膜成纖維細胞礦化能力的影響Shanghai ceramics of institute of china academy of sciences has its own pigment industrial park. it ' s main products vary from advanced print colors, stains for glazes to nano - inorganic pigment
中科院上海硅酸鹽研究所高性能色料研發及生產基地，主要產品為高品質釉用色料、印刷色料、納米無機顏料。分享友人