• Radiation Oncology Journal
• /
• 제7권1호
• /
• pp.15-22
• /
• 1989

Diethone의 피부에 대한 방사선 보호작용을 평가하기 위하여 Wistar계 랫드에 단일 X-선(20, 30, 40 Gy) 조사 후 시간경과와 선량변화에 따른 급성 피부반응을 연구하였다. 40Gy 선량에서 Diethone군의 피부반응기간은 24.7일로 대조군(29.8일)과 바셀린(29.2일) 투여군에 비하여 약$17\%$의 피부반응 기간이 뚜렷이 감소되었다. 피부반응이 최고도에 달한 10일 동안의 평균치는 Diethone군(2.43)이 대조군(2.91)과 바셀린(2.81)군에 비하여 현저히 감소되었다. 피부반응 Score 2.5에서 구한 등가효과 선량의 반응감소 계수(DRF)는 1.41로 피부보호효과가 있었다. 본 실험 결과로 보아 방사선 피부보호제를 국소적으로 도포함으로써 일반적인 치료선량보다 많은 방사선량을 거대하고 방사선내성이 있는 종양에 조사함으로로써 치료효과를 향상시킬 수 있을 것으로 기대한다.

• 한국환경보건학회지
• /
• 제19권3호
• /
• pp.64-73
• /
• 1993

The study was conducted to investigate the mechanism of tumor promotion as the time courses and the doses of promoter, and the effect of plant fiavonoids on the TPA-induced ODC responses. The results are summarized as follows: 1. A single, toppical application of 17 nmole of the potent tumor promoter, 12-O-tetradecanoyl phorbol-13-acetate, resulted in an induction of mouse epidermal Ornithine Decarboxylase with a peak at 5 hours after treatment and maximized 5.1 times as large as ODC activities of control. 2. Dose-response curve indicated that the tumor promotion increases proportionally between 1.7 and 170 nmole of TPA. This dose dependency relationship indicated that the ability of TPA to stimulate ODC is linked its ability to promote tumors. 3. Naturally occurring plant fiavonoids with anticarcinogenic and antipromotional activities were tested for their abilities to inhibit ODC response induced by skin tumor promoter TPA. Intra peritoneal administration of fiavonoids compounds (rutin, naphthofiavone, baicalein, quercitrin) and herbal drugs (sophorae rios, crataegi fructus, armeniacae semen) inhibited 17 nmole TPA-induced ODC activities in mouse epidermis in vivo.

• Biomolecules & Therapeutics
• /
• 제4권2호
• /
• pp.202-204
• /
• 1996

Clonidine, an antihypertensive drug, stimulates postsynaptic $\alpha_2$adrenergic receptors in the CNS and lowers arterial pressure by erects on both cardiac output and peripheral resistance. However, many patients experience that sedation and xerostomia occured upon oral administration of clonidine. These side effects are due to high plasma peak concentration and can be avoided when clonidine is given transdermally. In this study, we performed the skin irritation test for transdermal administration of clonidine patch on New Zealand white rabbits. Twelve New Zealand white rabbits were divided into two groups according to the dose levels, respectively. After transdermal administration of clonidine patch with two doses, clinical manifestations, body weight loss and postmortem findings were observed. We could not find any significant evidence of skin irritation by transdermal administration of clonidine patch.

• Journal of Radiation Protection and Research
• /
• 제44권3호
• /
• pp.110-117
• /
• 2019

Background: This study aimed to estimate occupational doses and patient peak skin doses (PSDs) during interventional radiology procedures. Materials and Methods: We examined data from brain embolization (n = 30), hepatic chemoembolization (n = 50), and uterine embolization (n = 12). The PSDs were measured using radiochromic film around the patient's head (group 1) or abdominal/pelvic region (group 2). Acquisition technical data and kerma-area products (KAP) were also recorded. Occupational doses were measured using $Instadose^{TM}$ dosimeters near the left eye region (LER), chest, and left ankle. Results and Discussion: The third quartile (median) KAP values were $408.1(235.3)Gy{\cdot}cm^2$ for group 1 and $584.4(449.4)Gy{\cdot}cm^2$ for group 2. The average PSDs were greatest during vascular procedures, reaching 1,004.4 (786.4) mGy, and the highest PSD was 2,352.6 mGy (during hepatic chemoembolization). The third quartile (median) occupational doses were 0.35 (0.21) mSv at the LER, 0.25 (0.15) mSv at the chest, and 1.47 (0.64) mSv at the left ankle. Occupational doses at the LER were higher than at the chest, which highlights the importance of protective glasses and suspended shields. The occupational doses at the ankle region were also high, which highlights the importance of using a lead-lined curtain attached to the table. Conclusion: The results indicate that physicians can reach, for eye region, the weekly occupational dose limit after around 15 procedures, even when using proper protection. The average PSD values were below the threshold for tissue reactions, although the complexity of these procedures emphasises the importance of considering related risks.

• 약학회지
• /
• 제38권5호
• /
• pp.483-487
• /
• 1994

The pharmacokinetic characteristics of an 1% flurbiprofen gel were evaluated using rats in reference to IV bolus and oral administration of the drug using rats. Following the transdermal application of the gel at the dose of 2 mg/kg as flurbiprofen, the $C_{max}$ and $T_{max}$ of the drug were $2.14\;{\mu}g/ml$ and 2 hr, respectively, whereas those after the oral administration of the drug as a suspension were $9.90\;{\mu}g/ml$ and 0.25 hr, respectively. These results indicate that, by the transdermal administration fo flubiprofen as the gel, the absorption of the drug was much slowed down and the lower $C_{max}$ compared to the oral administration may reduce the systemic side effects of the drug. The relative bioavailability of the flurbiprofen gel in reference to the oral dose was 48.5%. Tissue levels of flurbiprofen following the application of 50 mg of the 1% flurbiprofen gel onto ventral skin of rats showed that the maximum drug concentrations in the skin $(8.52\;{\mu}g/g)$ and the muscle $(2.06\;{\mu}g/g)$ occurred at 2 hrs postdose. The drug concentration in the both tissues remained relatively constant over the next 6 hrs following the peak concentration.

• 약학회지
• /
• 제42권4호
• /
• pp.437-446
• /
• 1998

The distribution, metabolism and excretion of CKD-602{20(S)-7-[2-(N-Isopropylamino)ethyl]camptothecin HCI), a new camptothecin derivative, were investigated in rats after a sing le administration of CKD-602. 1. The tissue levels of CKD-602 given to mice by the intravenous route at a dose of 20mg/kg were the highest in intestine, followed in descending order by kidney, liver, stomach,lung, heart, spleen and plasma. The concentrations of CKD-602 after 24hrs decreased to less than 2% of the peak level in most tissues except the skin. The urinary and fecal excretion of CKD-602 were 47.6% and 44.4% of the administered dose, respectively, with 0.7% remaining in the rinse. 2. After administration of CKD-602 at 10mg/kg in rats, metabolism of this compound was examined in plasma, urine, and feces. The plasma samples were collected for 24hr, urinary and fecal samples for 72hr. While any peak of CKD-602 in HPLC chromatograms was not detected from plasma and urine it was detected in feces (peaks, 9.8 min). However, additional peak area was about 0.5% of the peak area of parent CKD-602. Therefore, CKD-602 may be eliminated with the parent form and rarely metabolized in the body. 4. After I.v. administration of CKD-602 at 10mg/kg in rats, urinary and fecal excretions were examined for 72hrs post dose period. 87% of total urinary excretion of CKD-602 was excreted within 8hr after administration, 53%, and 32% of total fecal excreted amounts were determined in 0-24 hr and 24-48hr periods, respectively. The total excretion amounts of CKD-602 into urine and feces were 94% of the administered dose.

• Journal of Applied Biological Chemistry
• /
• 제58권4호
• /
• pp.363-368
• /
• 2015

The pharmacokinetics of florfenicol were studied in healthy and vibriosis-infected large yellow croaker (Pseudosciaena crocea) following administration of a single oral dose of $20mg{\cdot}kg^{-1}$ at $25{\pm}2^{\circ}C$. After oral administration, florfenicol levels in tissues (liver, kidney, muscle, serum, and skin) were analyzed using high-performance liquid chromatography. A two-compartment open model was used to describe the pharmacokinetics of florfenicol following oral administration. Compared to the healthy group, the absorption rate of vibriosis-infected fish significantly decreased, peak-time ($T_{max}$) delayed, maximum concentration ($C_{max}$) declined, total body clearance decreased, the elimination half-life ($T_{1/2{\beta}}$) was extended, and the area under the curve increased. These results indicate that a $20mg{\cdot}kg^{-1}$ oral dose of florfenicol administered once daily continuously for 4 or 5 days can be used for the treatment of Vibrio alginolyticus infection in large yellow croaker (Pseudosciaena crocea).

• 한국방사선학회논문지
• /
• 제15권4호
• /
• pp.401-408
• /
• 2021

양성자 치료는 방사선치료 중 하나로 브래그 피크로 알려진 물리적 특성을 활용한 방법이다. 양성자 치료계획 수립 시 주로 전산화단층촬영(CT)의 인체 횡단면 영상이 사용되고 있다. CT는 사용되는 관전압에 따라 HU가 변하게 되며 이는 구조물의 경계, 두께 변화로 이어진다. 본 연구는 Geant4를 이용하여 복합 물질로 구성된 두개골 팬텀에서 두께 변화에 따른 뇌 영역의 브래그 곡선의 변화를 살펴보았다. 먼저, 단일 물질로 구성된 팬텀에서 매질의 종류와 양성자의 입사에너지에 따른 브래그 곡선을 측정하여 Geant4 계산결과의 신뢰성을 확보하였다. 두개골 팬텀의 각 두께를 변동하였을 때 뇌 영역에서 발생하는 피크의 위치변화를 측정하였다. 연부조직의 두께를 변화하였을 때 피크의 위치 변화는 나타나지 않았으며, 피부의 두께를 변화하였을 때 피크의 변화는 적었으며, 주로 뼈의 두께를 변화할 때 피크의 위치 변화가 나타났다. 또한 뼈를 단독으로 변화하였을 때와 뼈를 다른 조직과 함께 변화하였을 때 피크의 위치 변화량은 동일하였다. 뼈의 정확한 두께 측정이 방사선치료계획의 선량-깊이 분포 예측에 주요 인자 중 하나임을 확인하였다.

• 대한수의학회지
• /
• 제40권3호
• /
• pp.497-504
• /
• 2000

To document that effects of hyperbaric oxygen(HBO) and ${\alpha}-tocopherol$ on full-thickness skin grafts in rat, we performed full-thickness skin grafts bilaterally on each rats. The HBO-treated rats were received HBO twice daily for 90 minutes at 2 ATA. Surgical control rats were not treated with HBO. ${\alpha}-tocopherol$ treated rats were received the agent via oral gastric tube daily for 3 days preoperative and a fourth dose 1 to 2 hours postoperative. HBO plus ${\alpha}-tocopherol$ treated rats were received HBO and ${\alpha}-tocopherol$ as mentioned above. Biopsy specimens were taken from each rat at the time of grafting and on days 2, 4, 7, 10, 14, 21, and 28, then were processed for tissue-concentration of total glutathione(GSHt), oxidized/reduced glutathione level, and thiobarbituric acid-reactive substance(TBARS) levels. The percentage of viable graft on day 10 ranged from 67 to 93%, and was not significantly different among the each other groups. The percentage of viable graft were, however, higher in HBO plus ${\alpha}-tocopherol$ treated rats(78.6%) than in HBO alone treated rats(59.1%), ${\alpha}-tocopherol$ alone treated rats(66.7%) and surgical control rats(58.2%). TBARS concentration had a significant increase from preoperative concentration at day 2, and peak concentration at day 4(p<0.01). Concentration then decreased to preoperative concentration at day 28. GSHt concentration of free skin graft had a similar patteren of change in four groups and decreased significantly from preoperative concentration at day 2, returning to preoperative concentration by day 7(surgical control, HBO-treated, and ${\alpha}-tocopherol-treated$, alone) and 28(HBO plus ${\alpha}-tocopherol-treated$). Percentage of the concentration of reduced glutathione decreased in surgical control, HBO-treated and, ${\alpha}-tocopherol-treated$(p<0.05), and HBO plus ${\alpha}-tocopherol-treared$(p<0.01) on day 7 after surgery, whereas the concentration of oxidized increased significantly in HBO-treated(p<0.05), ${\alpha}-tocopherol-treated$(p<0.05), and HBO plus ${\alpha}-tocopherol-treated$(p<0.01).

• 한국가금학회지
• /
• 제20권2호
• /
• pp.93-105
• /
• 1993

본 연구는 31 일령 broiler 병아리에 297 nm의 자외선을 조사하여 경과시간에 따라 다리의 피부를 채취하고 previtamin D$_3$(PreD$_3$), lumistero1$_3$(고), tachysterol$_3$(T$_3$), Vitamin D$_3$(VD$_3$) 및 provitaminD$_3$ (PreD$_3$) 함양을 측정코저 실시되었다. Broiler Hubbard계통 1일령 병아리 82수(2조사시간$\times$9 경과시간$\times$4회복＋10대조구)를 무창약등 육계사에 넣고 VD-결핍사료로 315간 사육한 후 조사선양 0.204mJ/$ extrm{cm}^2$ (30분 조사) 또는 0.409mJ/$\textrm{cm}^2$(60분 조사)로 UVB 등을 조사하였으며 0, 6, 12, 18, 30, 42, 66, 90또는 138시간 후에 다리의 피부를 채취하였다. 9% ethyl acetate/n-hexane으로 처리하여 지질을 추출하였으며 Sep-Pak silica cartridge로 정제한 후 순상 HPLC로 PreD$_3$, L$_3$, T$_3$, VD$_3$ 및 ProD$_3$의 함양을 분석하였다. UVB를 조사하지 않은 대조구 병아리의 다리 피부중에는 PreD$_3$, L$_3$, T$_3$, VD$_3$가 검출되지 않았으며 PreD$_3$ 함양은 966$\pm$89ng/$\textrm{cm}^2$이었다. 0.204 또는 0.409mJ/$\textrm{cm}^2$(30분 또는 60분) .조사시 다리 피부중 PreD$_3$의 mole %(절대함량 ng/$\textrm{cm}^2$)는 열사직후 각각 4.67%(44ng/$\textrm{cm}^2$) 또는 3.97%(37ng/$\textrm{cm}^2$)이었으며 시간이 경과됨에 따라 점차 감소되었다. 병아리의 다리 피부 면적은 25.81$\pm$0.50$\textrm{cm}^2$이었으며 다리 피부전체에서 합성된 PreD$_3$는 각각 0시간대에 961ng/$\textrm{cm}^2$, 738ng/$\textrm{cm}^2$이었다. 다리 피부중의 은 0시간 경과 시 각각 1.24%(12ng/$\textrm{cm}^2$) 또는 0.92%(9ng/$\textrm{cm}^2$)이었으며 시간이 지남에 따라 점차 감소되었다 함량은 각각 0.58%(5ng/$\textrm{cm}^2$) 또는 0.57%(6ng/$\textrm{cm}^2$)이었으며 역시 시간의 경과와 더불어 감소되었다. VD$_3$함량은 0시간대에 각각 2.13(21ng/$\textrm{cm}^2$) 또는 0.97%(16 ng/$\textrm{cm}^2$), 12시간대에 4.30%(33ng/$\textrm{cm}^2$) 또는 6.40%(76ng/$\textrm{cm}^2$)을 나타내었고 0.204mJ/$\textrm{cm}^2$ 조사시에는 18시간대에, 0.409mJ/$\textrm{cm}^2$ 처리시에는 30시간 후에 최고치를 보였다 PreD$_3$가 VD$_3$로 열전환되는데 각각 18 또는 30시간이 소요된다는 것을 시사한다. 다리 피부중의 PreD$_3$함량은 0시간대에 각각 948또는 815ng/$\textrm{cm}^2$이었으며 대조구의 ProD$_3$ 함량 966ng/$\textrm{cm}^2$에 비하면 18 또는 151ng/$\textrm{cm}^2$의 PreD$_3$가 PreD$_3$, L$_3$, T$_3$ 및 VD$_3$이성화된 것이다. mole %로 보았을 때는 각각 8.63%, 6.43%가 광합성물로 전변 된 것이다 결논적으로 자외선을 2배 .무사하였을 때 VD$_3$등 광생성물이 2배는 아니지만 더 많이 생성된다는 것이 증명되었다.