• Restorative Dentistry and Endodontics
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• v.29 no.4
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• pp.370-377
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• 2004

The purpose of this study was to regenerate human dental pulp tissues similar to native pulp tissues. Using the mixture of type I collagen solution, primary cells collected from the different tissues (pulp, gingiva, and skin) and NIH 3T3 ($1{\;}{\times}{\;}10^5{\;}cells/ml/well$) were cultured at 12-well plate at $37^{\circ}C$ for 14 days. Standardized photographs were taken with digital camera during 14 days and the diameter of the contracted collagen gel matrix was measured and statistically analyzed with student t-test. As one of the pulp tissue engineering, normal human dental pulp tissue and collagen gel matrix cultured with dental pulp cells for 14 days were fixed and stained with Hematoxyline & Eosin. According to this study, the results were as follows: 1. The contraction of collagen gel matrix cultured with pulp cells for 14 days was significantly higher than other fibroblasts (gingiva, skin) (p < 0.05), 2. The diameter of collagen gel matrix cultured with pulp cells was reduced to 70.4% after 7 days, and 57.1% after 14 days. 3. The collagen gel without any cells did not contract, whereas the collagen gel cultured with gingiva and skin showed mild contraction after 14 days (88.1% and 87.6% respectively). 4. The contraction of the collagen gel cultured with NIH 3T3 cells after 14 days was higher than those cultured with gingival and skin fibroblasts, but it was not statistically significant (72.1%, p > 0.05). 5. The collagen gel matrix cultured with pulp cells for 14 days showed similar shape with native pulp tissue without blood vessels. This approach may provide a means of engineering a variety of other oral tissue as well and these cell behaviors may provide information needed to establish pulp tissue engineering protocols.

• Journal of Korea Technical Association of The Pulp and Paper Industry
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• v.45 no.6
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• pp.72-77
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• 2013

Tissue and paper manufacturing companies have common problems with increasing cost of imported virgin pulp and the restriction of using woods in the forest. Possibility of using bagasse pulp for solving those problems was studied. In order to reduce the production cost and study the dependency on pulps, bagasse pulp has been studied for mixing with Sw-BKP and Hw-BKP. Optimum blending ratio of wood pulps and bagasse pulp to enhance tissue properties were analyzed. Various properties of the hand sheet after blending of wood pulp and bagasse pulp were measured. As results, the bagasse pulp could substitute the hard wood pulp with similar properties of tissue. Therefore, we judged that the bagasse pulp was suitable for replacement of the hardwood pulp.

• Restorative Dentistry and Endodontics
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• v.35 no.4
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• pp.238-245
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• 2010

Numerous cases about additional growth of roots or pulp tissue regeneration by using various intracanal medicaments in immature permanent teeth with periapical or pulpal disease have been reported. The underlying mechanism has not been clearly delineated, but it has been widely accepted that undifferentiated mesenchymal cells and stem cells are involved. Moreover, the growth and deposition of osteoid or cementoid tissues have been observed in regenerated pulp and roots. This new and non-invasive treatment has brightened the future of endodontics, and enlarged the vision of regenerative root canal treatment with multi-potent stem cells and various tissue engineering techniques.

• Journal of Korea Technical Association of The Pulp and Paper Industry
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• v.47 no.1
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• pp.93-101
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• 2015

The purpose of this study is to examine the reusability of the fluff pulp recycled from paper diaper. To do this, the physical and optical properties of each handsheet made from these fluff pulp sample as well as the properties of the fiber recycled from paper diaper were analyzed and compared with those of non-recycled diaper fluff pulp samples and conventional pulp samples. These comparisons show that the characteristics of fiber such as length, width, curl, kink of the pulp recycled from paper diaper were similar to those of non-recycled diaper fluff pulp as well as to those of commercial pulp. The fine content of recycled diaper fluff pulp was lower than that of other pulp samples, while the ash content of the former was higher than that of the latter. Furthermore, it was also found that the bulk of handsheets made from the recycled fluff pulp was higher than that of other pulp samples, while the formation of the former was worse than that of the latter. The mechanical properties of the handsheet sample made from the recycled diaper fluff pulp was higher than those of the unused diaper fluff pulp and was lower that those of commercial fluff pulp and softwood tissue pulp handsheet. But, it was higher than that of hardwood tissue pulp handsheet. The optical properties of recycled diaper fluff pulp handsheet was lower than those of each handsheet samples made from other pulps due to its low fine content.

• Restorative Dentistry and Endodontics
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• v.44 no.2
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• pp.20.1-20.8
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• 2019

Objectives: To achieve pulp-dentin complex regeneration with tissue engineering, treatment efficacies and safeties should be evaluated using in vivo orthotopic transplantation in a sufficient number of animals. Mice have been a species of choice in which to study stem cell biology in mammals. However, most pulp-dentin complex regeneration studies have used large animals because the mouse tooth is too small. The purpose of this study was to demonstrate the utility of the mouse tooth as a transplantation model for pulp-dentin complex regeneration research. Materials and Methods: Experiments were performed using 7-week-old male Institute of Cancer Research (ICR) mice; a total of 35 mice had their pulp exposed, and 5 mice each were sacrificed at 1, 2, 4, 7, 9, 12 and 14 days after pulp exposure. After decalcification in 5% ethylenediaminetetraacetic acid, the samples were embedded and cut with a microtome and then stained with hematoxylin and eosin. Slides were observed under a high-magnification light microscope. Results: Until 1 week postoperatively, the tissue below the pulp chamber orifice appeared normal. The remaining coronal portion of the pulp tissue was inflammatory and necrotic. After 1 week postoperatively, inflammation and necrosis were apparent in the root canals inferior to the orifices. The specimens obtained after experimental day 14 showed necrosis of all tissue in the root canals. Conclusions: This study could provide opportunities for researchers performing in vivo orthotopic transplantation experiments with mice.

• Journal of Korea Technical Association of The Pulp and Paper Industry
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• v.47 no.6
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• pp.147-153
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• 2015

Wet-tissue has been used for baby wipe, cleansing pads, industrial wipes, pain relief, personal hygiene, pet care, and healthcare at home, care facilities, restaurant, and hospital. Raw materials of wet-tissue are mainly natural fibers and synthetic fibers such as cotton, rayon, PET (polyethylene terephthalate) and so on. In this study, electrolytic water of NaCl solution was used as fluid in wet-tissue, and the effect of raw materials on antibacterial rate of wet-tissue was investigated. Rayon (100%) showed an excellent antibacterial rate compared with cotton (100%) and rayon:PET (50:50). Antibacterial rate increased as Cl concentration of electrolytic water increased. Absorption of rayon:PET (50:50) was uneven and antibacterial rate of wet-tissue slightly increased by increase of Cl concentration. Antibacterial rate of wet-tissue was 100% under the conditions of more than 1.5 mL of electrolytic water dosage, and dropped under 50% after storage period of 48 hours.

• Journal of Korea Technical Association of The Pulp and Paper Industry
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• v.36 no.4 s.107
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• pp.77-82
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• 2004

Expression-deliquoring tests using three types of paper sludges (tissue, newsprint, and paperboard) as deliquoring agent were carried out in order to investigate the effects of sludge dosage and pressure on the expression-deliquoring of slurry. The addition of deli­quoring agent causes expression-deliquoring of slurry to be faster than would be the case without the deliquoring agent. In case of the tissue sludge, the highest compression rate was achieved when $5\%$ of deliquoring agent was added, while in cases of the news­print and the paperboard sludge, $7\%$. Compression rate was increased as pressure increases. Porosity was decreased as pressure increases. The lowest porosity was observed when $5\%$ of tissue sludge was added. When compared the weight of cake where deliquoring agent was not added and the weight of cake that was fastest expression-deliquoring, there was about $17.5\%$ of the weight reduction

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• v.36 no.1
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• pp.7-15
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• 2010

Complex human tissues harbor stem cells and precursor cells, which are responsible for tissue development or repair. Recently, dental tissues such as dental pulp, periodontal ligament (PDL), dental follicle have been identified as easily accessible sources of undifferentiated cells. These tissues contain mesenchymal stem cells that can be differentiate into bone, cartilage, fat or muscle by exposing them to specific growth conditions. In this study, the authors procured the stem cell from pulp, PDL, and dental follicle and differentiate them into osteoblast and examine the bone induction capacity. Dental pulp stem cell (DPSC), periodontal ligament stem cell (PDLSC), and dental follicle precursor cell (DFPC) were obtained from human 3rd molar and cultured. Each cell was analyzed for presence of stem cell by fluorescence activated cell sorter (FACs) against CD44, CD105 and CD34, CD45. Each stem cell was cultured, expanded and grown in an osteogenic culture medium to allow formation of a layer of extracellular bone matrix. Osteogenic pathway was checked by alizarin red staining, alkaline phosphatase (ALP) activity test and RT-PCR for ALP and osteocalcin (OCN) gene expression. According to results from FACs, mesenchymal stem cell existed in pulp, PDL, and dental follicle. As culturing with bone differentiation medium, stem cells were differentiated to osteoblast like cell. Compare with stem cell from pulp, PDL and dental follicle-originated stem cell has more osteogenic effect and it was assumed that the character of donor cell was able to affect on differential potency of stem cell. From this article, we are able to verify the pulp, PDL, and dental follicle from extracted tooth, and these can be a source of osteoblast and stem cell for tissue engineering.

• Restorative Dentistry and Endodontics
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• v.28 no.5
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• pp.419-424
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• 2003

이 연구의 목적은 원래의 치수조직과 유사한 조직을 재생하기 위한 pulp tissue engineering의 한 방법으로 건전한 조직으로부터 배양된 치수세포와 쥐의 조섬유세포(NIH 3T3 cell)를 Rat tail type I collagen solution에서 3차원적으로 관찰하기 위한 것으로, 콜라젠 젤의 수축량과 세포의 증식 량을 비교하였으며, 또한 마모된 사람치아의 표면과 배양용기에서 두 세포의 증식 량을 비교하여 다음과 같은 결과를 얻었다. 1. 콜라젠 젤에 NIH 3T3 세포를 배양한 경우 그 수축량은 최소였으나, 치수세포를 배양한 경우 그 수축량은 현저하였다. 2. 서로 다른 수의 치수세포를 콜라젠 젤에서 배양시킨 경우 세포 수가 많을수록 수축량이 증가하였으며, 세포가 없는 콜라젠 젤은 수축하지 않았다. 3. 치수세포를 콜라젠 젤에서 18일간 배양시킨 후 세포의 증식은 거의 없는 반면, NIH 3T3 세포는 계속 증식하였다. 4. 마모된 사람 치아 표면과 배양 용기에서 치수세포와 NIH 3T3세포를 배양한 경우 NIH 3T3세포가 치수세포에 비해 빠르게 증식 하였으며 , 특히 사람 치아의 표면에서 NIH 3T3세포가 현저히 빠른 증식을 보였다. 이상의 결과는 치수세포를 type I collagen gel에서 3차원 적으로 배양 후 치수조직의 재생을 유도하는 pulp tissue engineering에 관한 연구에 발판이 될 것으로 사료된다.

• Journal of Biosystems Engineering
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• v.38 no.2
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• pp.113-120
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• 2013

Purpose: Stem cells provide new opportunities in the regenerative medicine for human or animal tissue regeneration. In this study, we report an efficient method for the modulating behaviors of electro-active stem cells by micro-electric current stimulation (mES) without using chemical agents, such as serum or induction chemicals. Methods: Dental pulp stem cells (DPSCs) were cultured on the tissue culture dish in the mES system. To find a suitable mES condition to promote the DPSC functions, the response surface analysis was used. Results: We found that a working micro-current of 38 ${\mu}A$ showed higher DPSC proliferation compared with other working conditions. The mES altered the expressions of intracellular and extracellular proteins compared to those in unstimulated cells. The mES with 38 ${\mu}A$ significantly increased osteogenesis of DPSCs compared with ones without mES. Conclusions: Our findings indicate that mES may induce DPSC proliferation and differentiation, resulting in applying to DPSCs-based human or animal tissue regeneration.