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1.
Maxillofacial Plastic and Reconstructive Surgery ; : 10-2018.
Article in English | WPRIM | ID: wpr-741570

ABSTRACT

BACKGROUND: The objective of this study was to evaluate the changes in gene expression after incubation of cells with proteins released from different silk mat layers. METHODS: A silk cocoon from Bombyx mori was separated into four layers of equal thickness. The layers were numbered from 1 to 4 (from the inner to the outer layer). The proteins were released by sonication of a silk mat layer in normal saline. The concentration of proteins was determined by spectrophotometry. They were incubated with RAW264.7 cells, and changes in the expression of genes were evaluated by cDNA microarray analysis and quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR). RESULTS: Layer 1 and 4 groups had higher protein concentrations compared to those in layer 2 and 3 groups. The genes associated with inflammation and angiogenesis showed significantly higher expression in layer 1 and 4 groups. The results of qRT-PCR were in agreement with those of the cDNA microarray analysis. CONCLUSIONS: The silk mat from the middle portion of the silkworm cocoon yielded a lower protein release and caused an insignificant change in the expression of genes that are associated with inflammation and angiogenesis.


Subject(s)
Angiogenesis Inducing Agents , Bombyx , Gene Expression , Inflammation , Macrophages , Oligonucleotide Array Sequence Analysis , Silk , Sonication , Spectrophotometry
2.
Maxillofacial Plastic and Reconstructive Surgery ; : 192-200, 2014.
Article in English | WPRIM | ID: wpr-203359

ABSTRACT

PURPOSE: The objective of this study was to evaluate the interaction between 4-hexylresorcinol (4HR) and antibody as that affects the performance of a silk-4HR combination graft for soft tissue augmentation in an animal model. METHODS: The silk graft materials consisted of four types: silk+10% tricalcium phosphate (TCP) (ST0), silk+10% TCP+1% 4HR (ST1), silk+10% TCP+3% 4HR (ST3), and silk+10% TCP+6% 4-HR (ST6). The antibody binding assay tested the 4HR effect and scanning electron microscopic (SEM) exam was done for silk grafts. The animal experiment used a subcutaneous pocket mouse model. The graft - SH0 or SH1 or SH3 or SH6 - was placed in a subcutaneous pocket. The animals were killed at one, two, and four weeks, postoperatively. The specimens were subjected to histological analysis and lysozyme assay. RESULTS: Groups with 4HR applied showed lower antibody binding affinity to antigen compared to groups without 4HR. In the SEM examination, there was no significant difference among groups. Histological examinations revealed many foreign body giant cells in ST0 and ST1 group at four weeks postoperatively. Both ST3 and ST6 groups developed significantly lower levels of giant cell values compared to ST0 and ST1 groups (P<0.001) at four weeks postoperatively. In the lysozyme assay, the ST1 and ST3 groups showed denser signals than the other groups. CONCLUSION: 4HR combined silk implants resulted in high levels of vascular and connective tissue regeneration.


Subject(s)
Animals , Mice , Animal Experimentation , Composite Tissue Allografts , Connective Tissue , Giant Cells , Giant Cells, Foreign-Body , Hexylresorcinol , Metabolism , Models, Animal , Muramidase , Regeneration , Silk , Transplants
3.
Maxillofacial Plastic and Reconstructive Surgery ; : 111-115, 2014.
Article in English | WPRIM | ID: wpr-17204

ABSTRACT

PURPOSE: This study evaluated powdered burn wound dressing materials from wild silkworm fibroin in an animal model. METHODS: Fifteen rats were used in this experiment. Full-thickness 2x2 cm burn wounds were created on the back of rats under anesthesia. In the two experimental groups, the wounds were treated with two different dressing materials made from silkworm fibroin. In the Control Group, natural healing without any dressing material was set as control. The wound surface area was measured at five days, seven days and 14 days. Wound healing was evaluated by histologic analysis. RESULTS: By gross observation, there were no infections or severe inflammations through 14 days post-injury. The differences among groups were statistically significant at seven days and 14 days, postoperatively (P<0.037 and 0.001, respectively). By post hoc test, the defect size was significantly smaller in experimental Group 1 compared with the Control Group and experimental Group 2 at seven days postoperatively (P=0.022 and 0.029, respectively). The difference between Group 1 and Group 2 was statistically significant at 14 days postoperatively (P<0.001). Group 1 and control also differed significantly (P=0.002). Group 1 showed a smaller residual scar than the Control Group and Group 2 at 14 days post-injury. Histologic analysis showed more re-epithelization in Groups 1 and 2 than in the Control Groups. CONCLUSION: Burn wound healing was accelerated with silk fibroin spun by wild silkworm Antheraea pernyi. There was no atypical inflammation with silk dressing materials. In conclusion, silk dressing materials can be used for treatment of burn wound.


Subject(s)
Animals , Rats , Anesthesia , Bandages , Bombyx , Burns , Cicatrix , Fibroins , Inflammation , Models, Animal , Moths , Silk , Wound Healing , Wounds and Injuries
4.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 30-36, 2014.
Article in English | WPRIM | ID: wpr-785256

ABSTRACT


Subject(s)
Head , Neck , Pterygoid Muscles
5.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 293-298, 2012.
Article in Korean | WPRIM | ID: wpr-785172

ABSTRACT

0.05). Regenerated bone volume (mm3) of 1% TC-loaded SFM, SFM, and control were 36.56+/-8.50, 25.86+/-8.17, and 19.09+/-5.07 at 8 weeks postoperatively, respectively (P<0.05).CONCLUSION: The 1% TC-loaded SFM showed more bone regeneration than the SFM and the uncovered control, in guided bone regeneration.


Subject(s)
Animals , Humans , Rabbits , Bone Regeneration , Eosine Yellowish-(YS) , Fibroins , Hematoxylin , Membranes , Parietal Bone , Silk , Tetracycline
6.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 459-466, 2011.
Article in Korean | WPRIM | ID: wpr-785117

ABSTRACT

0.05).CONCLUSION: The rabbit calvarial defect was not successfully repaired by silk fibroin/nano-hydroxyapatite/corn starch composite scaffold and may have been due to an inflammatory reaction caused by silk powder. In the future, the development of composite bone graft material based on various components should be performed with caution.


Subject(s)
Animals , Rabbits , Bone Regeneration , Fibroins , Osteogenesis , Parietal Bone , Silk , Starch , Transplants , X-Ray Microtomography , Zea mays
7.
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons ; : 293-300, 2011.
Article in Korean | WPRIM | ID: wpr-785089
8.
Journal of the Korean Association of Oral and Maxillofacial Surgeons ; : 366-374, 2010.
Article in Korean | WPRIM | ID: wpr-109510

ABSTRACT

INTRODUCTION: This study evaluated the capability of silk fibroin (SF) and recombinant human bone morphogenetic protein-2 loaded SF (SF-BMP) as a bone defect replacement matrix when grafted in a calvarial bone defect of rats in vivo. MATERIALS AND METHODS: A total 70 calvarial critical size defects (5.0 mm in diameter) made on 35 adult female Sprague-Dawley rats were used in this study. The defects were transplanted with (1) rhBMP-2 loaded silk fibroin graft (SF-BMP: 0.8+10 microg), (2) Silk fibroin (SF: 10 microg), and (3) no graft material (Raw). The samples were evaluated with soft x-rays, alkaline phosphatase activity, calcium/phosphate quantification, histological and histomorphometric analysis at postoperative 4 and 8 weeks. RESULTS: The SF-BMP group (48.86+/-14.92%) had a significantly higher mean percentage bone area than the SF group (24.96+/-11.01%) at postoperative 4 weeks.(P<0.05) In addition, the SF-BMP group (40.01+/-12.43%) had a higher % bone area at postoperative 8 weeks than the SF group (33.26+/-5.15%). The mean ratio of gray scale levels to the host bone showed that the SF-BMP group (0.67+/-0.08) had a higher mean ratio level than the SF group (0.61+/-0.09) at postoperative 8 weeks. These differences were not statistically significant.(P=0.168 and P=0.243, respectively) CONCLUSION: The rhBMP-2 loaded silk fibroin graft revealed fewer immunoreactions and inflammation as well as more new bone formation than the pure silk fibroin graft. Therefore, silk fibroin may be a candidate scaffold for tissue engineered bone regeneration.


Subject(s)
Adult , Animals , Female , Humans , Rats , Alkaline Phosphatase , Bone Morphogenetic Protein 2 , Bone Regeneration , Fibroins , Inflammation , Osteogenesis , Rats, Sprague-Dawley , Recombinant Proteins , Silk , Tissue Scaffolds , Transforming Growth Factor beta , Transplants
9.
Journal of Veterinary Science ; : 105-109, 2006.
Article in English | WPRIM | ID: wpr-32320

ABSTRACT

Recombinant human epidermal growth factor (rhEGF) stimulates the proliferation and migration of epithelial cells in human cell culture systems and animal models of partial-thickness skin wounds. This study investigated the effect of a topical rhEGF ointment on the rate of wound healing and skin re-epithelialization in a rat full thickness wound model, and verified whether or not the rhEGF treatment affected both myofibroblast proliferation and collagen synthesis in the dermis. When rhEGF (10 microgram/g ointment) was applied topically twice a day for 14 days, there was significantly enhanced wound closure from the 5th to the 12th day compared with the control (ointment base treatment) group. A histological examination at the postoperative 7th day revealed that the rhEGF treatment increased the number of proliferating nuclear antigen immunoreactive cells in the epidermis layer. In addition, the immunoreactive area of alpha-smooth muscle actin and the expression of prolyl 4-hydroxylase were significantly higher than those of the control group. Overall, a topical treatment of rhEGF ointment promotes wound healing by increasing the rate of epidermal proliferation and accelerating the level of wound contraction related to myofibroblast proliferation and collagen deposition.


Subject(s)
Animals , Male , Rats , Actins/genetics , Administration, Topical , Cell Proliferation/drug effects , Collagen/biosynthesis , Epidermal Growth Factor , Gene Expression Regulation , Myoblasts, Skeletal/drug effects , Proliferating Cell Nuclear Antigen/genetics , Rats, Sprague-Dawley , Wound Healing/drug effects
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