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2. The muscle strips incubated at 0°C developed a peak isometric tension of 53.3 g/cm2. This occurred after only 17 min incubation when the pH was 7.02, demonstrating the potential of chicken PM muscle to cold shorten. Peak isometric tension at 5°C was considerably lower than that generated at 0°C. However, as this occurred when the muscle pH was still high (6.70), this also indicated some potential to cold shorten at 5°C.
3. At 10° to 30°C, the muscle strips developed mean peak isometric tensions of 18 g/cm2 after 6 h incubation by which time the muscle pH had fallen to 6.00, demonstrating a limited potential to rigor shorten. In contrast, those incubated at 40°C developed a peak tension of 54.5 g cm2 after 75 min when the muscle pH was also around 6.00, thus indicating the potential for intensive rigor shortening at this temperature. Incubation temperature and the resultant muscle pH therefore determine the potential of chicken PM muscle to either cold shorten or rigor shorten.
4. Despite the differences found in isometric tension profiles, cooked meat texture after isometric tension measurement was not significantly different at any of the temperatures studied primarily because the muscle strips were essentially prevented from shortening. 相似文献
Design Blood and urine of dogs and horses were analysed after topical administration of three common nonsteroidal anti-inflammatory preparations.
Experimental method Dimethylsulphoxide was analysed using a gas chromatograph with a flame photometric detector. Phenylbutazone, its metabolites and lignocaine were analysed using a gas chromatograph with a mass selective detector.
Results Dimethylsulphoxide, phenylbutazone and ligno-caine were detected in dog urine after muliple applications of the preparations. The maximum concentration of dimethyl-sulphoxide in dog urine correlated with the concentration of dimethylsulphoxide in the preparation. Phenylbutazone penetrated the skin more effectively from the cream than from the solution or gel preparations. This penetration was independent of the concentration of dimethylsulphoxide.
Conclusion The superior penetration of phenylbutazone from the cream can be explained by it being present as a neutral molecule in an hydrophobic medium. It is proposed that phenylbutazone penetrates the skin of greyhounds most effectively by a hydrophobic lipid route which is likely to be different from the path by which dimethylsulphoxide penetrates the skin. 相似文献