실험재료는 시중에서 판매되는 우육(등심) 부위를 이용하였으며, 생육 시료의 함기포장과 진공포장은 폴리에틸렌 필름을 이용하였고, 전자선 조사(0, 1, 2, kGy)를 실시한 후 $2{\sim}4^{\circ}C$의 냉장실에서 보관하면서 저장기간 별(0, 7, 14일) 실험에 사용하였다. 가열 시료는 oven에서 육 내부가 $70^{\circ}C$가 될 때까지 가열한 다음 함기 포장과 진공포장을 즉시 실시한 후 생육 시료와 같은 조건으로 전자선 조사를 실시한 다음 $2{\sim}4^{\circ}C$의 냉장실에서 보관하면서 생육 시료와 같은 저장기간별 콜레스테롤 산화물의 발생 종류와 발생량을 조사한 결과는 다음과 같다. 가열하지 않은 우육 등심의 함기 포장에서는 $7{\alpha}-hydroxycholesterol,\;{\beta}-epoxide,\;7{\beta}-hydroxycholesterol$, 7-ketocholesterol이 $0.5{\mu}g/g$ 이상 발생하였으며, 전 저장기간 동안 cholestanetriol과 ${\alpha}-epoxide$은 극소량($0.5\;{\mu}g/g$ 이하)발생하였다. 가열하지 않은 우육 등심의 진공포장에서는 전 저장기간 동안 $7{\alpha}-hydroxycholesterol$, 7-ketocholesterol, cholestanetriol과 ${\alpha}-epoxide$은 극소량$(0.5\;{\mu}g/g$ 이하) 발생하였다. 우육 등심을 가열한 후 함기포장에서는 전 저장기간 동안 cholestanetriol과 ${\alpha}-epoxide$은 극소량$(0.5\;{\mu}g/g$ 이하)였지만, $7{\alpha}-hydroxycholesterol\;(1.53{\sim}26.81),\;{\beta}-epoxide\;(1.07{\sim}5.23),\;7{\beta}-hydroxycholesterol\;(40.64{\sim}101.30)$, 7-ketocholesterol $(7.16{\sim}33.91)$. 모든 결과에서 처리구에 따른 콜레스테롤 산화물의 전체 발생량은 조사 수준이 증가할수록 유의적으로 증가하였으며(P<0.05), 저장기간이 경과함에 따라 전체 발생량이 유의적으로 증가하였다(P<0.05).
실험재료는 시중에서 판매되는 우육(등심) 부위를 이용하였으며, 생육 시료의 함기포장과 진공포장은 폴리에틸렌 필름을 이용하였고, 전자선 조사(0, 1, 2, kGy)를 실시한 후 $2{\sim}4^{\circ}C$의 냉장실에서 보관하면서 저장기간 별(0, 7, 14일) 실험에 사용하였다. 가열 시료는 oven에서 육 내부가 $70^{\circ}C$가 될 때까지 가열한 다음 함기 포장과 진공포장을 즉시 실시한 후 생육 시료와 같은 조건으로 전자선 조사를 실시한 다음 $2{\sim}4^{\circ}C$의 냉장실에서 보관하면서 생육 시료와 같은 저장기간별 콜레스테롤 산화물의 발생 종류와 발생량을 조사한 결과는 다음과 같다. 가열하지 않은 우육 등심의 함기 포장에서는 $7{\alpha}-hydroxycholesterol,\;{\beta}-epoxide,\;7{\beta}-hydroxycholesterol$, 7-ketocholesterol이 $0.5{\mu}g/g$ 이상 발생하였으며, 전 저장기간 동안 cholestanetriol과 ${\alpha}-epoxide$은 극소량($0.5\;{\mu}g/g$ 이하)발생하였다. 가열하지 않은 우육 등심의 진공포장에서는 전 저장기간 동안 $7{\alpha}-hydroxycholesterol$, 7-ketocholesterol, cholestanetriol과 ${\alpha}-epoxide$은 극소량$(0.5\;{\mu}g/g$ 이하) 발생하였다. 우육 등심을 가열한 후 함기포장에서는 전 저장기간 동안 cholestanetriol과 ${\alpha}-epoxide$은 극소량$(0.5\;{\mu}g/g$ 이하)였지만, $7{\alpha}-hydroxycholesterol\;(1.53{\sim}26.81),\;{\beta}-epoxide\;(1.07{\sim}5.23),\;7{\beta}-hydroxycholesterol\;(40.64{\sim}101.30)$, 7-ketocholesterol $(7.16{\sim}33.91)$. 모든 결과에서 처리구에 따른 콜레스테롤 산화물의 전체 발생량은 조사 수준이 증가할수록 유의적으로 증가하였으며(P<0.05), 저장기간이 경과함에 따라 전체 발생량이 유의적으로 증가하였다(P<0.05).
Some commercial beef loins in raw state were packaged with PVDC as aerobic and vacuum condition. The other beef samples were cooked until core temperature arrived at $70^{\circ}C$ and then packaged immediately in the same way as the raw state. These samples were irradiated by electron bea...
Some commercial beef loins in raw state were packaged with PVDC as aerobic and vacuum condition. The other beef samples were cooked until core temperature arrived at $70^{\circ}C$ and then packaged immediately in the same way as the raw state. These samples were irradiated by electron beam (0, 1, 2 kGy), and then stored in refrigerator $(2{\sim}4^{\circ}C)$. Identity and quantity of cholesterol oxides were analysed at the 0, 7th, 14th day of storage. In the samples that were raw and packaged aerobically, $7{\alpha}-hydroxycholesterol,\;{\beta}-epoxide,\;7{\beta}-hydroxycholesterol$ and 7-ketocholesterol were detected over $0.5\;{\mu}g/g$. Cholestanetriol and${\alpha}-epoxide$ were detected at levels below $0.5\;{\mu}g/g$ during storage. In the samples that were raw and vacuum-packaged, $7{\alpha}-hydroxycholesterol$, 7-ketocholesterol and cholestanetriol were detected. In the samples that were cooked and packaged aerobically, cholestanetriol and ${\alpha}-epoxide$ were detected below $0.5\;{\mu}g/g$ during storage. $7{\alpha}-hydroxycholesterol,\;{\beta}-epoxide,\;7{\beta}-hydroxycholesterol$and 7-ketocholesterol were detected as $1.53{\sim}26.81,\;1.07{\sim}5.23,\;40.64{\sim}101.30\;and\;7.16{\sim}33.91\;{\mu}g/g$, respectively. In all results, total amounts of cholesterol oxide increased significantly as irradiation dose and storage time increased (P<0.05).
Some commercial beef loins in raw state were packaged with PVDC as aerobic and vacuum condition. The other beef samples were cooked until core temperature arrived at $70^{\circ}C$ and then packaged immediately in the same way as the raw state. These samples were irradiated by electron beam (0, 1, 2 kGy), and then stored in refrigerator $(2{\sim}4^{\circ}C)$. Identity and quantity of cholesterol oxides were analysed at the 0, 7th, 14th day of storage. In the samples that were raw and packaged aerobically, $7{\alpha}-hydroxycholesterol,\;{\beta}-epoxide,\;7{\beta}-hydroxycholesterol$ and 7-ketocholesterol were detected over $0.5\;{\mu}g/g$. Cholestanetriol and${\alpha}-epoxide$ were detected at levels below $0.5\;{\mu}g/g$ during storage. In the samples that were raw and vacuum-packaged, $7{\alpha}-hydroxycholesterol$, 7-ketocholesterol and cholestanetriol were detected. In the samples that were cooked and packaged aerobically, cholestanetriol and ${\alpha}-epoxide$ were detected below $0.5\;{\mu}g/g$ during storage. $7{\alpha}-hydroxycholesterol,\;{\beta}-epoxide,\;7{\beta}-hydroxycholesterol$and 7-ketocholesterol were detected as $1.53{\sim}26.81,\;1.07{\sim}5.23,\;40.64{\sim}101.30\;and\;7.16{\sim}33.91\;{\mu}g/g$, respectively. In all results, total amounts of cholesterol oxide increased significantly as irradiation dose and storage time increased (P<0.05).
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