• Journal of Chest Surgery
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• 제49권4호
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• pp.232-241
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• 2016

Background: Paraplegia is a devastating complication following operations on the thoracoabdominal aorta. We investigated whether histidine-tryptophan-ketoglutarate (HTK) solution could reduce the extent of ischemia/reperfusion (IR) spinal cord injuries in a rat model using a direct delivery method. Methods: Twenty-four Sprague-Dawley male rats were randomly divided into four groups. The sham group (n=6) underwent a sham operation, the IR group (n=6) underwent only an aortic occlusion, the saline infusion group (saline group, n=6) underwent an aortic occlusion and direct infusion of cold saline into the occluded aortic segment, and the HTK infusion group (HTK group, n=6) underwent an aortic occlusion and direct infusion of cold HTK solution into the occluded aortic segment. An IR spinal cord injury was induced by transabdominal clamping of the aorta distally to the left renal artery and proximally to the aortic bifurcation for 60 minutes. A neurological evaluation of locomotor function was performed using the modified Tarlov score after 48 hours of reperfusion. The spinal cord was harvested for histopathological and immunohistochemical examinations. Results: The spinal cord IR model using direct drug delivery in rats was highly reproducible. The Tarlov score was 4.0 in the sham group, $1.17{\pm}0.75$ in the IR group, $1.33{\pm}1.03$ in the saline group, and $2.67{\pm}0.81$ in the HTK group (p=0.04). The histopathological analysis of the HTK group showed reduced neuronal cell death. Conclusion: Direct infusion of cold HTK solution into the occluded aortic segment may reduce the extent of spinal cord injuries in an IR model in rats.

• Journal of Chest Surgery
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• 제25권2호
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• pp.125-130
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• 1992

To evaluate the effect of oxygenation[95% O2+5% CO2] of St. Thomas Hospital No.2 cardioplegic solution[Plegisol], 20 isolated perfused rat hearts were studied under hyp-othermic[20oC] ischemic arrest for 2 hours with infusion of cardioplegic solution every 30 minutes throughout the ischemic period. Ten isolated hearts were studied with the oxygenated cardioplegic solution and 10 another isolated hearts with the nonoxygenated one. Mean oxygen tensions of the nonoxygenated and oxygenated cardioplegic solutions were 150mmHg and 470mmHg, respectively. Two in 10 hearts infused with the nonaxygenated cardioplegic solution were not recovered from nonworking heart due to persistent ventricular fibrillation. In comparing hem-odynamic parameters between both groups, the mean postischemic recovery[expressed as a percentage of its preischemic control value] was significantly greater with the oxygenated solution[in 10 recovered hearts] than the nonoxygenated solution[in 8 recovered hearts] [95.9$\pm$1.8% compared with 88.5$\pm$2.9% in peak aortic pressure, p<0.05, 75.7$\pm$5.2% compared with 43.5$\pm$6.5% in aortic flow, p<0.01, 75.5$\pm$4.6% compared with 54.1$\pm$5.6% in cardiac output, p<0.01, 78.3$\pm$4.6% compared with 60.3$\pm$4.6% compared with 60.3$\pm$6.2% in stroke volume, p<0.05, and 80.4$\pm$5.3% compared with 58.6$\pm$7.0% in dP/dT, p<0.05]. It is concluded that oxygenation of St. Thomas Hospital No.2 cardioplegic solution improves cardiac electrical stability and postischemic hemodynamic recovery after ischemic arrest in the isolated perfused rat heart.

• 핵의학기술
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• 제16권2호
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• pp.139-148
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• 2012

이 실험은 검사를 매일 실행하고, 동결건조된 표준액을 매번 녹여서 사용하는 검사실은 그 안정성에 대하여 고민을 할 필요는 없지만, 검사를 일주일에 한번 또는 두 번 정도 실행하는 검사실에 대한 보고라고 할 수도 있다. 동결 건조한 표준물질은 용해한 후 다시 동결을 할 경우 보통 $-20^{\circ}C$이하에서 유효기간까지 보관하라는 식으로만 표현 되어져 있고, 이는 몇 번을 녹인 후 재사용해도 안정한가에 대해서는 표현된 바가 없기에 이번 실험은 동결건조한 표준용액을 녹임과 동결을 여러 번 번복하였을 때와 냉장보관을 하였을 시에 표준용액의 변화도와 이것이 결과에 미치는 영향을 비교 평가하였다. 시판되고 있는 방사면역측정법을 이용한 체외진단키트 중 동결건조표준용액으로 되어진 부갑상선호르몬(PTH), 부신피지자극호르몬(ACTH), 황체형성호르몬(LH) kit를 같은Lot.NO.로 구성하였다. 이를 D.W.로 각 용량에 맞게 용해한 후 3개의 대조군으로 분리하였다. 제1대조군은 녹임, 동결을 번복하는 방법으로 하였고 제2대조군은 용해한 후 Test tube에 1회 사용할 만큼 분주하여 동결을 하였고 제3대조군은 냉장보관으로 하였다. 표준액과 환자농도값 날짜 별로 비교하였고, pH Test를 하였으며 날짜 별 단순회귀분석 및 결정계수 산출을 하였으며 Excel Paired t-Test (p-value)를 하여서 유의수준관계를 분석하였다. 위에서 실험한 ACTH, PTH, LH의 동결건조 표준액은 반드시 냉동보관을 할 것을 권고한다. 이는 다른 동결건조표준액도 같은 방법으로 보관을 해야 할 것이다.

• Clinical and Experimental Pediatrics
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• 제48권5호
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• pp.518-522
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• 2005

목 적 : 급성 세기관지염에 대한 치료로 보조 요법에 더해 기관지 확장제 흡입치료의 효과가 많이 보고되고 있다. 세기관지의 폐색에는 평활근의 수축이 관여하지만 어린 영아에서는 기관지 점막의 부종과 점액이나 상피세포 탈락물의 축적이 더 중요한 원인이기에, 본 질환으로 입원한 영아에서 ${\beta}_2$ 자극제와 정상 식염액을 혼합하여 흡입하는 대신, 점막 부종을 감소시키고 기도 축적물의 제거를 향상시킬 수 있는 고장성 식염액을 혼합하여 흡입했을 때의 치료효과를 알아보고자 하였다. 방 법 : 2003년 10월부터 2004년 5월까지 본원에 급성 세기관지염으로 입원한 1세 미만 환아 83명을 대상으로 하였다. 환아는 무작위로 두 그룹으로 나뉘어 입원과 동시에 초기 상태 평가가 이루어진 후 흡입 치료를 받았다. 치료는 이중 맹검법을 사용하여 fenoterol 2 mL(0.5 mg)에 0.9% saline solution 2 mL를 혼합하거나 fenoterol 2 mL에 3% saline solution 2 mL를 혼합하여 네뷰라이져로 6시간 간격으로 하루 4회 흡입하도록 하였다. 24, 48, 72시간째 흡입 전과 흡입 후 20분에 각각의 임상평가 점수를 측정하여 시간의 경과에 따른 변화를 검토하였고, 두 군의 총 입원일수도 비교하였다. 결 과 : 입원 72시간 동안, 두 그룹의 흡입 치료 직전의 임상평가 점수는 각각 시간이 지남에 따라 통계학적으로 유의하게 향상되었으며(P<0.05), 이는 3% 식염액 흡입군에서 유의하게 더 현저하였다(P<0.05). 평균 입원 일수는 0.9% 식염액 흡입군과 3% 식염액 흡입군 각각에서 $7.4{\pm}2.0$일과 $5.9{\pm}1.9$일로 두군간에 유의한 차이를 보였다(P<0.05). 흡입 치료와 관련된 부작용은 관찰되지 않았다. 결 론 : 급성 세기관지염으로 입원한 영아의 치료에서 3% saline solution에 혼합한 fenoterol 흡입 치료는 0.9% saline solution에 혼합한 fenoterol에 비해 더 효과적으로 임상 증상을 호전시켰다.

• 대한간호학회지
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• 제42권6호
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• pp.791-798
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• 2012

Purpose: The purpose of this study was to analyze the effectiveness of saline solution vs. heparinized-saline for maintenance of arterial lines and to detect changes in platelet and aPTT as physiological indexes. Methods: In this nonequivalent control group, non-synchronized, double-blind study the effects of heparinized and saline solution on the maintenance of arterial lines were compared. Fifty five patients received the heparinized solution and fifty nine patients received the saline solution. All patients who had surgery in K-university hospital between September and December 2011 were eligible for participation in the study. Results: There was no statistically significant difference between the saline and the heparin group in the maintenance time of the arterial lines or the number of irrigations. There was no statistically significant difference between the groups in changes in the number of platelets and aPTT for interaction between the groups and time intervals. Conclusion: The results indicate that saline solution can be used as an irrigation solution for the maintenance of arterial lines of adult surgical patients, rather than heparinized-saline, in view of potential risk factors in the use of heparin.

• 대한소아치과학회지
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• 제50권3호
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• pp.347-359
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• 2023

본 연구는 탈구된 치아의 저장 매체로서 polydeoxyribonucleotide (PDRN)의 적합성을 평가하고자 하였다. HBSS와 10, 25, 50, 100 ㎍/mL 농도의 PDRN 용액과 수돗물에 저장된 인간 치주인대 세포의 생존율을 측정하기 위해 Cell Counting Kit-8 assay와 Live/Dead assay를 시행하였다. 또한, PDRN의 항염증 효과를 평가하기 위한 NO 검출 및 qRT-PCR 실험을 진행하였다. 100 ㎍/mL 농도의 PDRN 용액에 저장된 치주인대 세포의 생존율이 다른 용액보다 유의하게 높았다(p < 0.01). 또한, 100 ㎍/mL 농도의 PDRN 용액은 유의하게 NO의 생산을 줄였다(p < 0.0001). 그리고, HBSS 용액에 비하여 50 및 100 ㎍/mL 농도의 PDRN 용액에서 유의하게 tumor necrosis factor α, interleukin (IL)-4, IL-6, 그리고 IL-10의 발현이 낮았다(p < 0.01). 이 연구를 통해 PDRN은 치주인대 세포에 세포 보존 및 항염증 효과를 가진 것으로 밝혀졌다. 이 연구는 효과적인 탈구치 저장매체의 개발을 위한 향후 추가적인 실험의 기반이 될 수 있을 것이라 생각한다.

• Macromolecular Research
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• 제17권8호
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• pp.597-602
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• 2009

Although the existing design principle of full-sequence ionic complement is convenient for the development of peptides, it greatly constrains the exploration of peptides with other possible assembly mechanisms and different yet essential functions. Herein, a novel designed half-sequence ionic complementary peptide (referred to as P9), AC-Pro-Ser-Phe-Asn-Phe-Lys-Phe-Glu-Pro-$NH_2$, is reported. When transferred from pure water to sodium chloride solution, P9 underwent a dramatic morphological transformation from globular aggregations to nanofibers. Moreover, the rheological experiment showed that the P9 could form a hydrogel with a storage modulus of about 30 Pa even at very low peptide concentration (0.5% (wt/vol)). The P9 hydrogel formed in salt solution could recover in a period of about 1,800 sec, which is faster than that in the pure water. The data suggestcd that the half-sequence, ionic complementary peptide might be worthy of further research for its special properties.

• Journal of Dental Anesthesia and Pain Medicine
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• 제23권5호
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• pp.273-280
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• 2023

Background: Intraoral local anesthesia is essential for delivering dental care; however, injection of this local anesthetic is perceived as the most painful and distressing agent for children, parents, and healthcare providers. Reducing pain as much as possible is essential to ensure smooth subsequent treatment procedures, especially in pediatric dentistry. In clinical practice, oral sucrose administration has been reported to decrease the pain during heel lance and cold pressor tests in neonates and children. This study aimed to determine whether the prior administration of a 30% sucrose solution reduced the pain related to inferior alveolar nerve block in children. Methods: A total of 42 healthy children aged 7-10 years requiring dental treatment of mandibular molars involving inferior alveolar nerve block were recruited. The participants' demographic details were recorded, height and weight were measured, and the anesthetic injection was delivered after receiving the respective intraoral sucrose solution and distilled water by the intervention (group 1) and control (group 2) group participants for 2 min. The subjective pain perceived during injection was measured using an animated emoji scale. The pain scores between the groups were compared using the Mann-Whitney U test. Results: The median pain score and range for the intervention and control groups were 4 (2 - 6) and 6 (4 - 8), respectively, and statistically significant differences (P < 0.001) were observed in the intervention group. Age, sex, height, and weight did not influence the analgesic effect of the sucrose solution. Conclusion: Oral administration of sucrose may relieve pain associated with inferior alveolar nerve block in children.

• 대한두경부종양학회:학술대회논문집
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• 대한두경부종양학회 2004년도 제21차 학술대회
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• pp.209-209
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• 2004

• Journal of Nutrition and Health
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• 제26권6호
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• pp.793-803
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• 1993

This study was designed to measure viscosity, osmolality and in vitro flow rates via nasogastric tubes for 6 types of commercially available and 9 hospital-blenderized enteral solutions and to examine the effect of viscosity and osmolaility of enteral formula on the flow rates in gravity drip administration. Each solution was infused through 18, 16, 14, 12 French sizes of silicone rubber tube. Flow rates were measured six times at $25^{\circ}C$ using formula bags and drip sets hung at a uniform height on a intravenous drip stand with tube uniformly positioned in collecting container. Viscosity ranged widely from 16.0 to 195.5 cps with mean, 64.61$\pm$64.42 for hospital-blenderized formula while mean viscosity of commercial formula was 7.60$\pm$4.84 cps. Mean osmolality of commercial formula and hospital-blenderized formula were 370$\pm$100.80, 540.33$\pm$89.37 mOsm/kg respectively. There was negative relationship between viscosity of formula and flow rates through tubes but no significant relationship between flow rates and osmolalty. Some of hospital-blenderized formula was too viscous to be infused througth tube with gravity drip administration and the recipe of formula requires to be modiifed. On the other hand, commercial formula with the low viscosity flows too rapidly with large bore size tubes. Smaller size of tube must be selected for hyperosmolar solution to decrease possible side effects associated with tube feeding. Two kinds of regression equations for flow rates obtained according to viscosity and tube sizes were also presented for the purpose of practical uses. In conclusion, this study emphasizes that viscosity of fomula, osmolality, patient's tolerance and comfort, caloric density should be considered in the selection of tubes for gravify drip administration.