Effects of teat dipping disinfectant containing biodegradable iodophor microspheres on preventing dry period intramammary infection in dairy cows
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(3) (: 2003 12 30) 1. Effects of teat dipping disinfectant containing biodegradable iodophor microspheres on preventing dry period intramammary infection in dairy cows Cheol-Yong Hwang, Jong-Min Kim, Hwa-Young Youn, Bo Han, and Hong-Ryul Han* College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea College of Veterinary Medicine, China Agricultural University, Beiijing 10094, China (Accepted December 30, 2003). 1. Abstract : 1% iodophor loaded microspheres of PLGA (Poly[DL-Lactide-co-Glycolide]) were prepared by solvent evaporation method and were applied to the cows on dry period for evaluating it’s preventive effects on intramammary infections. The morphology of the microspheres were evaluated using scanning electron microscopy and their releasing patterns were investigated. On investigating idophor releasing patterns of the microsphere, burst releasing pattern was detected until 2 days after in vitro incubation and sustained releasing was observed until 4 weeks. In field trial of teat dipping solution containing idophor loaded microspheres in dry cows showed significant preventive effects of intramammary infection caused by S. aureus, S. agalactiae, coagulase negative Staphylococci and coliform bacteria (p<0.05). Key words : microsphere, teat dipping solutin, iodophor, dairy cow. . W s tu vw E 5 ; xK l )y
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(23) iodophor microsphere ! "# $%&' (" )*. 115. Table 1. Vermont teat skin and teat end evaluation system TEAT END CONDITION SCORING 0. Teat end has been subjected to physical or chemical injury(e.g. stepped on or frostbitten) not related to treatment or the quarter is nonlactating.. 1. Teat end sphincter is smooth with no evidence of irritation.. 2. Teat end has a raised ring.. 3. Teat end sphincter is roughened with slight cracks but no redness is present.. 4. Teat end sphincter is inverted with many cracks, giving a “flowered” appearance. Teat end may have old but healing scabs.. 5. Teat end is severely damaged and ulcerative with scabs or open lesions. Large or numerous warts are present that interfere with teat end function. TEAT SKIN CONDITION SCORING. 0. Teat skin has been subjected to physical injury(e.g. stepped on or frostbitten) not related to the treatment or the quarter is nonlactating.. 1. Teat skin is smooth and free from scales, cracks, or chapping.. 2. Teat skin shows some evidence of scaling.. 3. Teat skin is chapped. Some small warts may be present.. 4. Teat skin is chapped and cracked. Redness, indicating inflammation, is present. Numerous warts may be present.. 5. Teat skin is severely damaged and ulcerative with scabs or open lesions. Large or numerous warts are present that interfere with teat end function.. Ù,- )y$ J}×,4 D/ V 10% + U 1% idophor Ù,- )y$ à}×P. V )y 0 cloxacillin + b gh (êùa 500 , Virbac, France)$ ¹×P. #X V; D/ VW V V_ v 1A, V 0Ê èH %& â ×,4 áâU 5% calf blood\ 0.1% esculin ªKU Ù
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(29) ¾}Ä Ê àVQ ¹ áâE "òÙW 265 nm D ôL õvE Table 2. Iodophor encapsulation efficiency of PLGA microspheres prepared with solvent evaporation method (wave length=265 nm) Number Absorbance of sample 1 2 3. 0.47 0.46 0.51. Standard absorbance. Encapsulation efficiency. 0.69 (1 g/100 ml). 69.6%. ów 0.48- 1% iodophor ÙW ó w 0.69$ [,- ~ G/U iodophor-loaded microsphere 10 mgW iodophor (LÈ 69.6%P(Table 2). Table 3. Releasing pattern of iodophor in microshperes expressed by mean absorbance Time 0 1 2 3 4 7 14 21 28. day day days days days days days days days. Mean absorbance 0.142 0.474 0.395 0.216 0.206 0.197 0.177 0.292 0.332. Fig. 2. Scanning electron micrograph showing the change in surface morphology in vitro incubation. A : 1day (×150), B : 1week (×350). C : 3weeks (×350), D : 4week (×350)..
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(35) %E ¸W = 7 G}h lP. W )$E µ Ô" microsphereW qr qr K!Ó û VØh l ¸ = W& 8« µkÜ ¡ ³,. Table 4. Effects of teat dipping disinfectant for preventing of dry period new intramammary infection in dairy cows Groups Treatment Control Total. No. of Quarters 331 334 665. Organism S. aureus a. 9 32 41. *CNS : coagulase negative staphylococci species. a Statistical difference from controls (p<0.05).. S. agalactiae 5 18 23. a. CNS* 19 40 59. a. other streptococci. Coliforms. 3 9 12. 1a 7 8.
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(54) 1. Arshady, R. Microspheres and microcapsules, a survey of manufacturing techniques : Part III Solvent evaporation. Poly. Eng. Sci. 1990, 30, 915-924. 2. Boddie, R. L. and Nickerson, S. C. Efficacy of two iodophor postmilking teat germicides against Streptococcus agalactiae. J. Dairy Sci. 1990, 73, 27902793. 3. Coti, B., Pavanetto, F. and Genta I. Use of polylactic acid for the preparation of microparticulate drug delivery system. J. Microencapsulation. 1992, 9, 153166. 4. Craven, N. Efficacy and Financial Value of Antibiotic Treatment of Bovine Clinical Mastitis during Lactationa Review. Br. Vet. J. 1987, 143, 410-422. 5. Dodd, F. H., Westgarth, D. R., Neave, F. K. and Kingwill, R. G. Mastitis - the strategy of control. J. Dairy Sci. 1969, 52, 689-691. 6. Gottardi, W. Disinfection, sterilization and preservation pp.183, 3rd ed. Lippincott, Philadelphia, 1983. 7. Heller, J. Biodegradable polymers in controlled drug delivery. CSC Crit. Rev. Ther. Drug Carrier Systems, 1984, 1, 39-90. 8. Jeffery, H., Davis, S. S. and O'Hagan, D. T. The preparation and characterization of poly(lactide-coglycolide) microparticle I : Oil-in-water emulsion solvent evaporation. Int. J. Pharm. 1991, 77, 169-175. 9. Johnson, P. and Lloyed-Jones, J. G. Drug delivery systems, pp. 12-55, 1st ed. Ellis Horwood, England Chicheste, 1987. 10. Kingwill, R. G., Neave, F. K., Dodd, F. H., Griffin, T. K. and Westgarth, D. R. The effect of a mastitis control system of levels of subclinical and clinical mastitis in two years. Vet. Rec. 1993, 87, 94-98. 11. Linhardt, R. J. Polymers and Aggregate systems, pp. 53-96, VCH Publishers, New York, 1988. 12. Mehta, R. C., Jeyanthi, R. S., Calis, B. C., Thanoo,.
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(56) Burton, K. W. and DeLuca, P. P. Biodegradable microspheres as depot system for parental delivery of peptide drugs. J. Control Release. 1994, 29, 375-384. Myllys, V., Honkanen-Buzalski, T. and Huovinen, P. Association of changes of in bacterial ecology of bovine mastitis with changes in the use of milking machines and antibacterial drugs. Acta Vet. Scand. 1994, 35, 363-369. Natzke, R. P. Therapy : one component in a mastitis control system. J. Dairy Sci. 1971, 54, 1895-1898. Neave, F. K., Dodd, F. H., Kingwill, R. G. and Westgarth, D. R. Control of mastitis in the dairy herd by hygiene and management. J. Dairy Sci. 1969, 52, 696-702. Nickerson, S. C. and Stephen, C. Choosing the best teat dip for mastitis control and milk quality. In Proc of National Mastitis Council Milk Quality Conference. p. 43-54, 2001. Nickerson, S. C., Watts, J. L., Boddie, R. L. and Pankey, J. W. Evaluation of 5% and 1% iodophor teat dips on commercial dairies. J. Dairy Sci. 1986, 69, 1693-1698. Pankey, J. W., Eberhart, R. J., Cuming, A. L., Daggett, R. D., Farnsworth, R. J. and McDuff, C. K. Update on postmilking teat antisepsis. J. Dairy Sci. 1984, 67, 1336-1341. Pankey, J. W. and Philpot, W. N. Hygiene in the prevention of udder infections. I. Comparative efficacy of four teat dips. J. Dairy Sci. 1975, 58, 202-207. Philpot, W. N. and Nickerson, S. C. Winning the fight against mastitis. pp. 44-53, 1st ed. Westfalia . Surge Inc, 2000. Roberson, J. R., Fox, L. K., Hancock, D. D. and Gay,. 22.. 23. 24.. 25.. 26. 27.. 28.. 29.. J. M. Ecology of Staphaphylococcus aureus isolated form various sites on dairy farms. J. Dairy Sci. 1994, 77, 3354-3364. Sah, H., Toddywala, R. and Chien, Y. W. Continuous release of protein from biodegradable microcapsules and in vivo evaluation of their potential as a vaccine adjuvant. J. Control Release. 1995, 35, 137-144. Schultze, W. D. and Smith, J. W. Effectiveness of postmilking teat dips. J. Dairy Sci. 1972, 55, 426-431. Smith, A., Neave, F. K., Dodd, F. H., Jones, A. and Gore, D. N. Methods of reducing the incidence of udder infection in dry cow. Vet. Rec. 1966, 79, 233. Sturesson, C., Carlfors, J., Edsman, K. and Andersson, M. Preparation of biodegradable poly (lactic-co-glycolic)acid microspheres and their in vitro release of timolol maleate. Int. J. Pharm. 1993, 89, 235244. Urarov, O., Evans, J. M., Marshall, M. and Sizer, D. Dry cow therapy. Vet. Rec. 1967, 81, 241-243. Wang, H. T., Schmitt, E., Flanagan, D. R. and Linhardt, R. J. Influence of formulation methods on the in vitro controlled release of protein from poly(ester) microspheres. J. Control Release. 1991, 17, 23-32. Watts, P. J., Davies, M. C. and Melia, C. D. Microencapsulation using emulsification/solvent evaporation; an overview of techniques and applications. CRC. Crit. Rev. Ther. Drug Carrier Syst. 1990, 7, 235259. Yong, C. S., Kwon, M. R., Park, S. H. and Oh, D. M. Preparation and characterization of poly(d,l-lactic acid) microspheres containing alprazolam. J. Korea Pharm. Sci. 1996, 26, 13-22..
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The influence of age and gender on remifentanil EC 50 for preventing microemulsion propofol injection pain.. - Remifentanil EC 50 on propofol injection
Pusposes: This study is to identify relations between knowledge, awareness and practice on nosocomial infection of operating room nurses and affecting factors
Effects of salt on hydrate-containing phase equilibria were experimentally determined for H-Lw equilibria and predicted for three-phase ( H-I-V C2H6 , H-L W -V C2H6 , H-L W
Ji Min Nam, Ji Hyun Kim, Sunghwan Kim, Kyu Hong Lee, Jong Man Park, Yong Jin Jeong, and Ki Nam Kim(KAERI) P04E09 Cold Spray Coating Technique with FeCrAI Alloy Powder