1.Measurement of Transendothelial Potential Difference to Evaluate the Chondroitin Sulfate Effect in TC-l99 Cornea Preservation Media.
Journal of the Korean Ophthalmological Society 1992;33(2):109-113
Chondroitin sulfate (CS) in corneal preservation medium can porolong corneal preservation time. The solutions used in the experimental chambers were made of TC-199 (GIB Co.) either by itself of by adding 1% CS (Sigma) to the TC-199. The evaliation of the viability of corneas can be made by monitoring their physiological parameter. Thus, we monitored the transendothelial electrical potential difference (p.d.) across deepithelialized rabbit corneas. We found that TC-199 containing 1% CS maintained higher p.d.'s than the same solution without CS.
Chondroitin Sulfates*
;
Chondroitin*
;
Cornea*
2.Two colorimetric assays verify that calcium sulfate promotes proliferating activity of human gingival fibroblasts.
Min CHAE ; Su Yeon KIM ; Soo Yeon KIM ; Suk Won LEE
The Journal of Korean Academy of Prosthodontics 2007;45(3):382-388
STATEMENT OF PROBLEM: The role of calcium sulfate in stimulating the growth of gingival soft tissue has been reported in few studies. Such a unique property of calcium sulfate could serve as a trouble-solving broker in compensating for the lack of soft tissues in various oral surgeries. PURPOSE: The purpose of this study was to compare the proliferating activities of human gingival fibroblasts seeded on various bone graft barrier materials of calcium sulfate, collagen, and polytetrafluorethylene (PTFE). MATERIAL AND METHODS: Two calcium sulfates (CAPSET(R) and CalForma(R), Lifecore Biomedical Inc., St. Paul, Minnesota, USA), a resorbable natural collagen (Bio-Gide(R), Geistlich Pharma Ag., Wolhusen, Switzerland), and a non-resorbable PTFE (TefGen-FD(R), Lifecore Biomedical Inc., St. Paul, Minnesota, USA) served as the human gingival fibroblasts'substrates and comprised the four experimental groups, whereas the untreated floors of culture plastics were used in the control group, in this study. Cells were trypsinized, seeded, and incubated for 48 h. The proliferating activities of fibroblasts were determined by XTT and SRB assay and absorbance (optical density, OD) was measured. One-way ANOVA was used to analyze the differences in the mean OD values between the groups of CAPSET, CalForma, Bio-Gide, TefGen, and the control (p<0.05). RESULTS: From the XTT assay, the mean OD value of the control group, the highest, was significantly greater than that of any of the four experimental groups followed by CalForma, CAPSET, TefGen, and Bio-Gide. Further, the mean OD value of CalForma, was significantly greater compared to that of Bio-Gide. From the SRB assay, Calforma showed the highest mean OD value, which was significantly greater than that of any other groups, followed by the control, CAPSET, Bio-Gide, and TefGen. The mean OD values of both the control and CAPSET were significantly greater compared to that of TefGen (p<0.05). CONCLUSION: Assessment of the viability and proliferation of cultured fibroblasts seeded and incubated for 48 h on various barrier-material substrates using XTT and SRB assay showed that calcium sulfate CalForma(R) promotes the proliferating activity of human gingival fibroblasts.
Calcium Sulfate*
;
Calcium*
;
Collagen
;
Fibroblasts*
;
Humans*
;
Minnesota
;
Plastics
;
Polytetrafluoroethylene
;
Sulfates
;
Transplants
;
Trypsin
3.Production and application of 3-phosphoadenosine-5- phosphosulfate.
Zhengxiong ZHOU ; Guocheng DU ; Zhen KANG
Chinese Journal of Biotechnology 2019;35(7):1222-1233
Sulfated compounds are widely present in cytoplasm, on cell surface, and in extracellular matrix. These compounds play important roles in cell development, differentiation, immune response, detoxication, and cell signal transduction. 3-Phosphoadenosine-5-phosphosulfate (PAPS) is the universal sulfate group donor for the biosynthesis of sulfated compounds. Up to now, the synthesis of PAPS is still too expensive for industrial applications. This review focuses on the recent progress of PAPS production and summaries the application of PAPS, particularly in the production of glucosinolate, heparin, condroitin sulfate, and oxamniquine production.
Cell Differentiation
;
Chondroitin Sulfates
;
Phosphoadenosine Phosphosulfate
;
metabolism
;
Sulfates
4.Chondroitin sulfate in Corneal Preaervation Media Assessed by monitoring the Transendothelial Electrical Potential Difference.
Ha Bum LEE ; Kyung Hwa LEE ; Hyo Sub KIM
Journal of the Korean Ophthalmological Society 1989;30(6):893-897
Recently a great deal of attention has been focused on increasing corneal preservation time, and chondroitin sulfate in corneal preservation media can prolong corneal preservation time. So far evaluation of the effectiveness of this and some additives have been based on determining the state of the cornea at the end of the preservation period. We have accomplished this by monitoring in vitro the transendothelial electrical potential difference across deepithelialized rabbit cornea. We found that corneas stored in basal salt plus glucose containing chondroitin sulfate maintained higher transendothelial potential difference than corneas stored in the same solutions without chondroitin sulfate. The beneficial effects of chondroitin sulfate were opthimal at the 1% concentration.
Chondroitin Sulfates*
;
Chondroitin*
;
Cornea
;
Glucose
5.Long-lasting Allergic Patch Test Reaction.
Dong Yoon LEE ; Young Jin KIM ; Ji Yeoun LEE ; Tae Young YOON
Korean Journal of Dermatology 2012;50(3):259-261
A long-lasting allergic patch test reaction (LLAPTR) is generally defined as a positive patch test reaction that persists for weeks or months, at least 2 weeks after application of the allergen. Several allergens, including gold sodium thiosulfate, have been reported as causes of LLAPTR, however, it has never been described in the Korean dermatologic literature. We report a case of LLAPTR to Cl+Me-Isothiazolinone (Kathon CG) and p-tert-butylphenol formaldehyde resin (PTBP-FR) in a 45-year-old woman with suspected allergic contact dermatitis.
Allergens
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Dermatitis, Allergic Contact
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Female
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Formaldehyde
;
Gold Sodium Thiosulfate
;
Humans
;
Middle Aged
;
Patch Tests
;
Resins, Synthetic
;
Thiazoles
;
Thiosulfates
6.Analysis of chondroitin sulfate content of Cervi Cornu Pantotrichum with different processing methods and different parts.
Rui-Ze GONG ; Yan-Hua WANG ; Yin-Shi SUN
China Journal of Chinese Materia Medica 2018;43(3):556-562
The differences and the variations of chondroitin sulfate content in different parts of Cervi Cornu Pantotrichum(CCP) with different processing methods were investigated. The chondroitin sulfate from velvet was extracted by dilute alkali-concentrated salt method. Next, the chondroitin sulfate was digested by chondroitinase ABC.The contents of total chondroitin sulfate and chondroitin sulfate A, B and C in the samples were determined by high performance liquid chromatography(HPLC).The content of chondroitin sulfate in wax,powder,gauze,bone slices of CCP with freeze-drying processing is 14.13,11.99,1.74,0.32 g·kg⁻¹, respectively. The content of chondroitin sulfate in wax,powder,gauze,bone slices of CCP with boiling processing is 10.71,8.97,2.21,1.40 g·kg⁻¹, respectively. The content of chondroitin sulfate in wax,powder,gauze,bone slices of CCP without blood is 12.47,9.47,2.64,0.07 g·kg⁻¹, respectively. And the content of chondroitin sulfate in wax,powder,gauze,bone slices of CCP with blood is 8.22,4.39,0.87,0.28 g·kg⁻¹ respectively. The results indicated that the chondroitin sulfate content in different processing methods was significantly different.The content of chondroitin sulfate in CCP with freeze-drying is higher than that in CCP with boiling processing.The content of chondroitin sulfate in CCP without blood is higher than that in CCP with blood. The chondroitin sulfate content in differerent paris of the velvet with the same processing methods was arranged from high to low as: wax slices, powder, gauze slices, bone slices.
Animals
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Chondroitin Sulfates
;
analysis
;
Deer
;
Horns
;
chemistry
7.Optimized culture medium and fermentation conditions for lipid production by Rhodosporidium toruloides.
Yong-Hong LI ; Bo LIU ; Zong-Bao ZHAO ; Feng-Wu BAI
Chinese Journal of Biotechnology 2006;22(4):650-656
Culture medium and fermentation conditions for lipid production by Rhodosporidium toruloides were optimized with single factor and uniform design experiment. The best medium recipe was found with 70 g/L glucose, 0.1 g/L (NH4)2SO4, 0.75 g/L yeast extract, 1.5 g/L MgSO4. 7H2O, 0.4g/L KH2PO4, sterilized at 121 degrees C for 15 min, and then supplemented with ZnSO4 1.91 x 10(-6) mmol/L, CaCl2 1.50 mmol/L, MnCl2 1.22 x 10(-4) mmol/L and CuSO4 1.00 x 10(-4) mmol/L. The optimal fermentation conditions were as follows: 50 mL of medium (pH 6.0) in 250 mL Erlenmeyer flask with 10% inoculum (28h) under orbital shaking at 200 r/min for 120h at 30 degrees C. Under these conditions, yeast biomass accumulated lipids up to 76.1%.
Basidiomycota
;
growth & development
;
metabolism
;
Copper
;
pharmacology
;
Culture Media
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Fermentation
;
Hydrogen-Ion Concentration
;
Lipids
;
biosynthesis
;
Magnesium Sulfate
;
pharmacology
;
Zinc
;
pharmacology
8.A Comparative Evaluation of 4 degrees C Corneal Preservation Media, Optisol(R) and Likorol(R).
Journal of the Korean Ophthalmological Society 1996;37(5):776-781
We examined two different corneal preservatives, Optisol(R) and Likorol(R) which contain different concentrations of chondroitin sulfate and evaluated their ability to maintain cellular viability and corneal deturgescence. The corneal thickness(12 days storage, at 4 degrees C) and endothelial cell cytotoxicity (24, 48, 72, and 120 hours incubation at 35.5 degrees C) were measured in 8 paired human corneas. Corneas stored in Optisol were thinner than Likorol-stored corneas throughout the examination period. Alkaline Phosphatase activity and (3H)-Thymidine incorporation showed increased mitotic activity in endothelial cells cultured in Optisol when compared with Likorol-cultured cells. These results suggest that Optisol provides better maintenance of corneal deturgescence and increased corneal endothelial viability with prolonged storage time.
Alkaline Phosphatase
;
Chondroitin Sulfates
;
Cornea
;
Endothelial Cells
;
Humans
9.A Comparative Evaluation of 4degrees C Corneal Preservation Media, Optisol and Likorol.
Journal of the Korean Ophthalmological Society 1997;38(4):776-781
We examined two different corneal preservatives, Optisol and Likorol which contain different concentrations of chondroitin sulfate and evaluated their ability to maintain cellular viability and corneal deturgescence. The corneal thickness(12 days storage, at 4degrees C) and endothelial cell cytotoxicity(24, 48, 72, and 120 hours incubation at 35.5degrees C) were measured in 8 paired human corneas. Corneas stored in Optisol were thinner than Likorol-stored corneas throughout the examination period. Alkaline Phosphatase activity and [3H]-Thymidine incorporation showed increased mitotic activity in endothelial cells cultured in Optisol when compared with Likorol-cultured cells. These results suggest that Optisol provides better maintenance of corneal deturgescence and increased corneal endothelial viability with prolonged storage time.
Alkaline Phosphatase
;
Chondroitin Sulfates
;
Cornea
;
Endothelial Cells
;
Humans
10.Pharmacological Therapy in Osteoarthritis.
Journal of the Korean Medical Association 2003;46(11):958-964
Osteoarthdtis (OA) is a common, chronic, and painful disorder characterized by cartilage loss. It is the most common among all rheumatic disorders and is a major cause of disability. OA can be managed with a variety of pharmacological therapies, including acetaminophen, traditional nonsteroidal antiinflammatory drugs, cyclooxygenase2 inhibitors, intraarticular steroids, viscosupplements, glucosamine, chondroitin sulfate, and capsaicin. In this review, I describe the clinical efficacy and side effects of these pharmaceuticals and review diseasemodifying osteoarthritis drugs (DMOAD), such as glucosamine, diacerein, and avocado/soybean unsaponifiables, of which the clinical efficacy still remains to be determined.
Acetaminophen
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Capsaicin
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Cartilage
;
Chondroitin Sulfates
;
Glucosamine
;
Osteoarthritis*
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Steroids
;
Viscosupplements