• 제목/요약/키워드: C-26 Colon Carcinoma

검색결과 23건 처리시간 0.018초

황기 및 천년초 첨가가 홍삼음료의 품질에 미치는 영향 (Effect of Astragali Radix and Opuntia humifusa on Quality of Red Ginseng Drink)

  • 유상권;김성원;정경환;문성권;유광원;최원석
    • 산업식품공학
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    • 제14권4호
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    • pp.299-306
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    • 2010
  • 본 연구에서는 홍삼음료의 다양화 및 기능성 강화와 여러 기능성을 가진 황기의 식품으로의 활용에 역점을 두고, 기존의 증점제를 대신하여 동결건조 천년초열매를 첨가한 새로운 기능성 홍삼음료을 개발하고자 하였다. 먼저 높은 항산화활성을 지닌 황기추출물을 얻고자 추출용매의 지용성정도를 달리하면서(100(증류수) : 0(95% 에탄올), 75 : 25, 50 : 50, 25 : 75) $80^{\circ}C$에서 추출한 추출물의 항산화활성을 측정한 결과, ABTS 및 DPPH radical 소거능 실험에서 증류수의 비율이 증가할수록 추출물의 항산화력이 증가하는 것으로 나타났다. 추출용매의 온도에 의한 황기추출물의 항산화활성 차이를 알아보고자 추출용액의 온도를 달리하면서(60, $80^{\circ}C$) 추출한 추출물의 항산화활성을 비교해 본 결과, $80^{\circ}C$에서의 추출물이 증류수와 에탄올혼합비율과는 상관없이 대부분 $60^{\circ}C$ 추출물보다 높은 값을 나타내었다. 기존의 점증제를 대신하여 다양한 기능성을 함유한 천연물 소재인 천년초분말을 선택하였으며, 구아검용액과 농도별 점도를 비교해 본 결과, 구아검 0.1%(w/v) 용액과 비슷한 점도를 나타내기 위해서는 천년초분말의 경우 1-2%(w/v)의 농도가 필요한 것으로 분석되었다. 황기와 천년초 첨가가 홍삼용액의 저장성($35^{\circ}C$)에 미치는 영향을 조사하기 위하여 이들 용액의 pH와 총미생물수를 7일 동안 측정하였다. 홍삼용액에 황기와 천년초를 첨가한 경우, 저장 1일째 부터 pH가 급격히 감소하기 시작하였으며, 저장 3일째에는 pH가 약 3.6까지 떨어진 다음, 저장 6일 이후에는 다소 pH가 증가하였으며, 천년초분말을 첨가한 용액에서는 황기의 농도증가에 의한 유의적 pH 감소는 나타나지 않았다. 천년초를 첨가한 홍삼용액의 경우 황기의 농도와는 상관없이 저장 7일째 미생물의 성장을 관찰할 수 없었으며, 천년초를 첨가하지 않은 시료에 비해 6 log cycle 이상의 큰 살균효과를 나타내었다. 황기(3, 5%, w/v), 천년초(1.2%, w/v)를 함유한 홍삼용액(5%, w/v)이 대장암 및 뇌종양세포 증식에 미치는 영향을 각각 0.5 mg/mL과 1 mg/mL의 농도에서 살펴본 결과, 종양세포에 대한 의미 있는 증식억제효과는 나타나지 않았다.

생약으로부터 조제된 수증기 증류물의 면역활성 (Effect of Steam Distillates Prepared from Herbal Medicines on Immunostimulating Activity)

  • 이창호;김인호;김영언;김용조;황종현;유광원
    • 한국식품영양과학회지
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    • 제33권4호
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    • pp.626-632
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    • 2004
  • 30종의 생약으로부터 조제된 열수추출물 중, 가시오가피 (대조군의 75.6% 억제), 백출(71.3%), 인삼(70.0%), 감초 (66.3%) 및 당귀 (63.1%)는 2.5 mg/kg body weight의 농도에서 colon 26-M3.1 lung carcinoma에 대한 매우 높은 종양전이 억제활성을 나타내었으나, 갈근(58.6%)과 진피(54.9%)를 제외한 다른 생약의 열수추출물은 그다지 높은 활성을 보여주지 않았다. 또한 진피(대조군의 1.80배),백출(1.73배), 가시오가피와 감초(1.64배) 등은 100$\mu\textrm{g}$/mL의 농도에서 Peyer's patch 세포를 매개로 한 조혈작용도 증강시킴을 알 수 있었다. 한편, 음료로서의 식품학적인 물성을 개선하고 비활성 성분을 제거하기 위하여, 열수추출물에서 활성을 나타낸 생약을 수증기 증류물로 조제하여 면역활성을 비교한 결과, 백출, 감초와 가시오가피가 2.5 mg/kg body weight에서 유의적인 종양전이 억제활성을 나타내었으며(각각 58.7%, 50.3%와 41.9%), 백출은 0.25 mg/kg body weight의 저농도에서도 높은 종양전이 억제활성을 보여주었다(49.7%). 또한 수증기 증류물을 Peyer's patch 세포와 처리한 결과, 백출과 가시오가피는 10 $\mu\textrm{g}$/mL의 낮은 농도에서도 골수세포의 증식작용을 유의적으로 증가시키고 있음을 나타내었다(각각 1.49배와 1.28배). 수증기 증류물이 열수추출물보다 다소 낮은 면역 활성을 가지고 있다 할지라도, 백출 및 가시오가피 등과 같은 전통 생약은 열수추출물 뿐만 아니라 수증기 증류물에서도 높은 면역 활성을 가지고 있음을 보여주었다. 그러므로 이러한 결과는 생약으로부터 조제된 수증기 증류물이 기능성 음료로서 식품산업에 이용될 수 있는 가능성을 시사하고 있다.

내장신경차단에 관한 임상적 연구 (A Clinical Evaluation of Splanchnic Nerve Block)

  • 김수연;오흥근;윤덕미;신양식;이윤우;김종래
    • The Korean Journal of Pain
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    • 제1권1호
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    • pp.34-46
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    • 1988
  • Intractable pain from advanced carcinoma of the upper abdomen is difficult to manage. One method used to control pain associated with these malignancies is to block off the splanchnic nerve. In 1919 Kappis described a technique by which the splanchnic nerve of the upper abdomen could be anesthetized, using a percutaneous injection. This method has been used for the relief of upper abdominal pain due to hematoma and cancer of the pancreas, stomach, gall bladder, bile duct, and colon. During the Period from November 1968 to January 1986, this method was used in 208 cases of malignancy at Severance Hospital and clinically evaluated. Patients were retroactively grouped according to the stage of development of technique used. Twelve patients who received the treatment in the period from November 1968 to March 1977 were designate4i as group 1, 26 patients from April 1977 to April 1979 as group 2, and 170 from May 1979 to January 1986 as group 3. The results are as follows: 1) The number of patients receiving splanchnic nerve block has been increasing since 1977. 2) A total of 208 patients, including 133 males and 75 females, ranging in age from 18 to 84 and averaging 51. 3) The causes of pain were stomach cancer 90, pancreatic cancer 69, and miscellaneous cancer 49 cases respectively. 4) There were 57.7% who had surgery. and 3.7% of whom had chemotherapy before the splanchnic nerve block was done. 5) These blocks were carried out with the patient in the prone position as described by Dr. Moore. For group 2 and 3, C-arm image intensifier was used. In group 1, a 22 gauze loom long needle was inserted at the lower border of the 12th rib on each aide about 7\;cm from the midline. The average distance from the midline was $6.60{\pm}0.61\;cm$ on the left side and $6.60{\pm}0.83\;cm$ on the right side in group 2, and $5.46{\pm}0.76\;cm$ on the left side and $5.49{\pm}0.69\;cm$ on the right side in group 3. The average depth to which the needle was inserted was $8.60{\pm}0.52\;cm$ on the left side and $8.74{\pm}0.60\;cm$ on the right side in group 2, and $8.96{\pm}0.63\;cm$ on the left side and $9.18{\pm}0.57\;cm$ on the right side in group 3. 6) The points of the inserted needles were positioned in the upper quarter anteriorly, 51.8% on the left side and 54.4% n the right side of the L1 vertebra by lateral roentgenogram in group 3. The inserted needle points were located in the upper and anterolateral part, of the L1 vertebra 68.5% on the left side and 60.6won the right side, on the anteroposterior rentgenogram in group 3. The needle tip was not advanced beyond the anterior margin of the vertebral body. 7) In some case of group 3, contrast media was injected before the block was done. It shows, the spread upward along the anterior mal gin of the vertebral body. 8) The concentration and the average amount of drug used in each group was as follows: In group 1, $39.17{\pm}6.69\;ml$ of 0.5% -l% lidocaine or 0.25% bupivacaine were injected for the test block and one to three days after the test block $40.00{\pm}4.26\;ml$ of 50% alcohol was injected for the semipermanent block. In group 2, $13.75{\pm}4.88\;ml$ of 1% lidocaine were used as the test block and followed by $46.17{\pm}4.37\;ml$ of 50% alcohol was injected as the semipermanent block. In group 3, $15.63{\pm}1.19\;ml$ of 1% lidocaine for test block followed by $15.62{\pm}1.20\;ml$ of pure alcohol and $16.05{\pm}2.58\;ml$ of 50% alcohol for semipermanent block were injected. 9) The result of the test block was satisfactory in all cases. However the semipermanent block was 83.3 percent of the patients in group 1 who received relief from pain for at least 2 weeks after the block, 73.1% in group 2, and 91.8% in group 3. In these unsuccessful cases, 2 cases in group 1 were controlled by narcotics but 7 cases in group 2 and 14 cases in group 3 received the same splanchnic nerve block 1 or 2 times again within 2 weeks. But, in some cases it was 3 to i months before the 2nd block and in 1 cases even 7 years. 10) The most common complications of splanchnic nerve block were hypotensino(25.5%) occasional flushing of the face, nausea, vomiting, and chest discomfort. 11) For the patients in group 3, the supplemental block most commonly used was a continuous epidural block; it was used as a diagnostic block and to afford relief from pain before the splanchnic nerve block was done. 12) The interval between the receiving of the alcohol block and discharge was from 5 to 8 days in 61 cases(31.1%) and from 1 to 2 days in 48 cases(24.5%). From the above results, it can be concluded that the splanchnic nerve block done in the prone position with pure and 50% alcohol immediately after an effective test block with 1% lidocaine under C-arm fluoroscopic control is satisfactory and reliable. How to minimize the repeat block is still a problem to be solved.

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