본 연구의 목적은 640 nm LED 조사와 아로마테라피가 목 피부 상태에 미치는 영향을 체계적 으로 평가하고 비교하는 것이다. 20명의 여성 참여자를 대상으로 A그룹(640 nm LED 조사 + 아로마테라 피)와 B그룹(640 nm LED 조사만)으로 나뉘어, 주 2회씩, 총 8회의 실험을 진행하였다. 실험 결과, 수분 함량은 A그룹(p<0.01)과 B그룹(p<0.001) 모두 유의하게 나타났으며, 주름 지수는 A그룹(p<0.01)과 B그룹 (p<0.05) 모두 유의하게 나타났다. 또한, 치밀도 변화는 A그룹(p<0.001)과 B그룹(p<0.05) 모두 유의하게 나타났으며, 탄력 변화는 A그룹(p<0.001)과 B그룹(p<0.001) 모두 유의하게 나타났다. 피부색 변화는 A그 룹에서는 (p>0.05) 유의하지 않았고, B그룹에서는 (p<0.05) 유의하게 나타났다. 기미 및 색소 침착 변화는 A그룹에서 (p<0.05) 유의하게 나타났으며, B그룹에서는 (p>0.05) 유의하지 않았다. 이러한 결과는 아로마 테라피와 640 nm LED 조사를 병행하는 것이 목 피부 상태를 향상시키는 데 높은 효과를 나타낼 수 있음 을 시사한다.

This study was conducted to determine the changes in ginsenosides content according to additional UV-A, and UV-B LED irradiation before harvesting the ginseng sprouts. One-year-old ginseng seedlings (n=100) were transplanted in a tray containing a ginseng medium. The ginseng sprouts were grown for 37 days at a temperature of 20°C (24h), a humidity of 70%, and an average light intensity of 80 μmol·m-2·s-1 (photoperiod; 24h) in a container-type plant factory. Ginseng sprouts were then transferred to a custom chamber equipped with UV-A (370 nm; 12.90 W·m-2) and UV-B (300 nm; 0.31 W·m-2) LEDs and treated for 3 days. Growth parameters and ginsenoside contents in shoot and root were conducted by harvesting on days 0 (control), 1, 2, and 3 of UV treatments, respectively. The growth parameters showed non-significant differences between the control and the UV treatments (wavelengths or the number of days). Ginsenoside contents of the shoot was highly improved by 186% in UV-A treatment compared to the control in 3 days of the treatment time. The ginsenoside contents of the roots was more improved in UV-A 1-day treatment and UV-B 3-day treatment, compared to the control by 171% and 160%, respectively. As a result of this experiment, it is thought that UV LED irradiation before harvesting can produce sprout ginseng with high ginsenoside contents in a plant factory.

본 연구는 수출 과정에서 UVA + LED처리가 절화백합의 품 질과 수명에 미치는 영향을 알아보고자 저장·수송 과정별 시 뮬레이션 실험을 수행하였다. 실험재료는 오리엔탈 백합 ‘Siberia’를 사용하였으며, 이 때 절화는 습식조건으로 증류수와 상업용 절화보존제(Chrysal SVB, 1/3 tablet/L)를 처리하였다. 동시에 UVA가 혼합된 청색(448nm), 적색(634nm과 661nm) LED를 3일간 처리하였고, 봄철과 여름철 일본 수출 환경과 동 일한 조건으로 생장상의 환경을 설정하였다. 그 결과, 수송 과정 중 수확 후부터 경매단계까지는 봄철에 비해 여름철이 꽃의 크 기가 크고, 상대 생체중과 수분 흡수율은 높았다. 경매 후 상대 생체중, 수분 흡수율, 잎의 엽록소 함량 등은 봄철이 높았으며, 인공광원 처리 유무에 따른 절화 품질은 처리간 유의적 차이가 없었다. 봄철과 여름철의 절화수명은 증류수와 절화보존제 처 리구에 비해 UVA + LED를 조사한 처리구에서 연장되었다. 봄 철 절화수명은 증류수 처리 18일, 절화보존제 처리 22일, UVA + Red LED 처리 22.5일로 나타났으며 UVA + Blue LED처리가 25.3일로 다른 처리에 비해 2~7일 연장되었다. 여름철 절화수명 은 증류수와 절화보존제 처리 16일, 적색 LED 처리 18일, 청색 LED 처리가 20일로 나타났다. 결론적으로 절화수명은 청색 LED 처리에서 절화 수명 연장 효과가 확인되었다.

표고 톱밥배지 재배시 녹색LED 광량에 따른 생육특성 분석 결과 5 umol ·m -2 · s -1에서 3주기 기준 배지당 자실체 의 수량은 239 g으로 형광등 202 g 대비 18% 증수효과가 있었으며, 자실체 폴리페놀 함량은 형광등 107 ppm에 대 비 78.4 ppm으로 27% 정도 낮았지만 에르고스테롤 함량 은 형광등 145 ppm 대비 307 ppm으로 2.1배 높은 함량을 보였다. 전력소모량은 형광등 대비 15.9%의 에너지 절감 율을 보였으며, 전등의 에너지 효율이 77.5%로 가장 컸다.

In previous studies, we selected green LED(light emitting diodes) for suitable wavelength of light by higher commercial yields and lower ratio of abnormal fruit body in Lentinula edodes. In this study, we aim to select efficient irradiation intensity of green LED. Stronger irradiation intensity of green LED resulted in more polyphenol contents of fruit body. In four level of irradiation intensity, 5, 10, 15, 20umol/m2/sec there was no big difference in commercial yields and characteristics of fruit body. In addition, Lower irradiation intensity resulted in smaller amount of electircity used. In conclusion, we selected 5umol/m2/sec for suitable irradiation intensity in Lentinula edodes with sawdust substrate cultivation.

The purpose of the present study is to investigate the optimal wavelength, frequency and energy density for set up the photobiologic treatment of periodontal disease. To establish the present study, λ scan of 500㎚ to 900㎚ was used to search the optimal wavelength for maximal proliferation of human gingival fibroblasts. Cell proliferation assay was carried out as MTT assay. Light intensity of 0.8 to 3.25mW, frequency of 0 to 584㎐ and 0 to 2hours was applied for investigation of optimal energy density, frequency and applied duration. Finally, 628㎚ with 1mW/cm2 for 1hour of LED irradiation resulted in maximal proliferation of gingival fibroblasts. These results suggest that LED irradiation on gingival fibroblast show different proliferation according to the condition of irradiation, and demonstrate that LED irradiation can control the quantity of cell proliferation.

The process 0 1' wound healing needs the deposition of collagen and non-collagenous compounds, followed by the remodelling of extracellul ar matrix Recently, it has known that LEDs irradiation can help wound healing to accelerate the cell proliferation. But its mec hanism is not elucidated yot. The purpose of the present study is to observe the expression level of extracellular matrix by 635nm LEDs ir radiation. Human gingival fibroblasts were primary cultured, treated arac hidonic acid (때 and followed by LEDs irradiation. To observe the mRNA expression of extracellular matrix, cDNA mlcroarray was ca n‘ ied out 1n present study, 3 experimental groups were categorized into control, AA-treated group, and AA-treated with LEDs irradiation group. The differential expressions of MMP-1, -2, -3, - 10, - 11, -14, -16, - 17, -25 and TIMP-1, -2, -3. -4 were observed. Especially, mRNA expression of T1MP-3 was 10 fold decreased in arach idonic acid -treated with 635nm LEDs irradiation group. Finally, LEDs irradation can affect the expression level of MMPs and TIMPs, which lead to prolifer ation of gingival fibroblasts and result in would healing

The purpose 01' pl'esent study was to examine the molecular events in apoptosis by CoCl2, mimicking hypoxic cond ition and recovering effects by LED ir l'adiation on Human SH-SY5Y neuroblastoma cells The SOUl'ce 0 1' light for ir l'adiation was a continuous-wave LED emitting at a wavelenl양h of 590 nm, and manufactured that ene rgy density was 5 mW!cm2 on sample surface, After ir l'adiation, cell viabi lity was measured with BrdU , cell morphol ogy was examined with Diff- Quik staining, cell signaling was monitored with various apoptosis-related molecules using RNase Pl'otection Assay(RPA) , W11en treated with CoC12, apoptotic induction was found in the SH-SY5Y cells in a concentration-dependent and time-dependent manner , Diff-Quik s taining was revealed that DNA fragmentation re presented apoptosis was examined in CoC12-tl'eated group, Moreover, RPA assay of SH-SY5Y cclls lIs ing val'iolls apoptosis-related molecllles showed that the apoptotic cell population was mcreased J-loweve. there was sorne signifïcant change in LED irradiatied cells aftel' treatement of CoC12 The main mechanism for Lhese a poptosis appearecl to be mito c hondriεt - m ecliated pathway, such as cytochrome- c‘ caspase-9, caspase-3, pro-apototic protein ßax, anti-apototic protein Bcl-2, and death receptor• mediated pathway, such as Fas, cas pase- 8, a ncl TNFRl These results demonstrate that CoCI2 induce apoptosis in SH-SY5Y via different dual apop tosis pathway through death receptor pathway as well as mitochondria- dependent pathway and LED irradiation can recl llces the CoCl2-induced apoptosis by blocking their internal signaling pathway

LEDs have been shown to be a safe, efficient, light-weight, and less-expensive alternative to heal wound. LED irradiation at the same biostimulatory wavelength of previous laser studies have similar biochemical effects The purpose of present study is to evaluate the effects of wound healing by LED irradiation. Thirty 34-day-old sprague dawley were used for present study. 1.5mm diameter defected holes were formed in both ear lobes of rat by rubber dam punch. 635nm and 890nm irradiation was performed by LED for 2 weeks, followed by histologíc examination staíned with H&E and Masson trichrome. Also, RT-PCR was carried out to find out the mRNA expression level in gingival fjbroblast irradiated by 635nm for 1 hour. In gross exarnination, wound healing was observed in irradiated group comparing to control For microscopic exarnination, repair by connective tissues was filled in defects of irradiated group, while dense cellular bands consisting of fjbroblasts and capi llaries were found at the end of defect in control By staining of masson trichrome, amount of collagens were found in irradiated group. In a result of RT-PCR, mRNA expressions of TGF- ß , MMP-1,3 and Timp-3 were down-regulated in irradiated group comparing with their expression in control group. Taken together, LED irradiation increase the prolifeation and the activity of fibroblasts and down-regualted the TGF-ß , MMP- 1,3 and Timp- 3 mRNA, followed by activation of would healing.

μ방lt emitting diodes (LED) devices are commercially introduced as an alternative for low-Ievellaser therapy (11ι，T) ， and it has several advantages over lasers such as a safe, efficient, and less-expensive altemative to treat wounds. And LED irradiation at the same biostimulatory wavelength has similar bíochemical effεαs. In the present study, to asses whether the I핑ht-emitting diode (LED) irradíation can stimulate bone regeneration, irradiated bony defects with or without grafting materials on rat calvaria were compared to corresponding nonirradiated control. Fifty male Sprague-Dawly rats weighing about 150g, were used. Factors for present study were designed as follows, 1) presence or absence of grafting materials, 2) with or without irradiation, and 3) number of irradiation. Two weeks after operation, rats were sacrifìced. Radiologic and 비stomorphologic fmdings were evaluated. Macrospically, there were no incidents of infection, dehiscence, hematoma and necrosis during study. Radiological findings showed greater radiopacity in the graft group and radiopacity increased as the number of irradiation increase. And microscopically, new bαle formation was great in the graft group and increased as the number of irradiation increase, Present study has shown that LED irradiation improved bone regeneration through radiologic and histomorphologic fmdings in rat.

Background : This experiment was conducted to study the characteristics of Korean ginseng (Panax ginseng C. A. Meyer) growth by LED artificial light source in the plastic house using multi-stage cultivation facility and artificial soil. Methods and Results : Seedlings of Korean ginseng cultivar cultivated from 6:00 am to 6:00 pm by adjusting the ratio of 1 : 1, 2 : 1 and 3 : 1 for red light and blue light for the LED light quality test. Controls were tested by treating the white light (fluorescent lamps) for the same time. The average temperature inside the plastic house remained above 25℃, then below 25℃ after mid-August and below 20℃ after mid-September. The temperature near the roots of the artificial soils was higher than 26℃ in late July and early August and lowered to 20℃ or lower in all treatments in September. The pH of the soil was in the standard range, but the EC value was 2.89 in the soil before the test and 5.83 in the white light treatment, higher than the standard range of 1.0. The light intensities were 95.3 μmol and 94.9 μmol in the 3 : 1 and 2 : 1 ratios of red and blue light, respectively. The photosynthetic rate was 1.72 μmole CO2/㎡/s in 3 : 1 treatment and 1.9 times higher than white light treatment. As the red light ratio increased, the light amount and photosynthetic rate increased. Growth characteristics of aerial parts (plant height, leaf length etc.) by LED irradiation were longer than that of white light treatment in the 2 : 1 or 3 : 1 treatment of red light and blue light. The root length was the longest at 13.7 ㎝ in the 3 : 1 treatment of red and blue light, taproot length were 6.9 ㎝ and 6.6 ㎝ in the 2 : 1 treatment and 3 : 1 treatment, respectively, longer than 4.3 ㎝ in white light. Root fresh weight was the heaviest (3.6 g/plant) in 3 : 1 treatment for red and green lights. Conclusion : It was confirmed that the rate of photosynthesis of Korean ginseng was higher than that of white light treatment and the growth characteristics of aerial and root parts were excellent at the ratio of 3 : 1 of LED red light and blue light in plastic house using multi-stage cultivation facility and artificial soil.

UV light irradiation is known to give beneficial effects on fresh produce preservation. A container system equipped with UV-LED was fabricated for storing cherry tomatoes under computer-controlled conditions of intermittent on-off cycles (1 hour on/1 hour off). Wavelength (365 and 405 nm) and physical location of the LED (2 and 5 cm above fruit) were studied as variables affecting the respiration, ethylene production and quality preservation of the fruits at 10 and 20℃. 365 nm wavelength gave much higher radiation intensity than 405 nm, and intensity on surface decreased in inverse proportion to square of distance from LED. When compared to non-irradiated control, UV-LED irradiation decreased the respiration by 5-10% at 10℃ while there was no obvious effect at 20℃. Ethylene production was reduced when the fruits were placed at 5 cm distance, while there was no significant difference from control at 2 cm location. The reduction of ethylene production at 5 cm was more pronounced at 20℃. UV-LED irradiation was shown to have delayed increase or lower concentration in carotenoids compared to control treatment. Any negative effect of UV-LED irradiation on ascorbic acid content and firmness was not observed.

This study was conducted to assess the response of LED (Light-emitting diode) irradiation on the growth characteristics and saponin contents of Panax ginseng C. A. Meyer. LED irradiation showed a positive effect for most of the parameters studied. The content of chlorophyll a in leaves was increased by 4.9~36.5%, under LED and fluorescent light conditions compared to the control. The content of chlorophyll b was also increased by 44.4~55.6% under blue and red LED compared to the control except under the red plus blue LED condition. The shoot and root weight were increased by 20~60% and 14.8~59.3%, respectively under LED and fluorescent light conditions compared to the control. The total saponin content was increased by 1.8% under blue LED compared to the control, while total saponin content was decreased by 8.8~11.5% under red LED, red plus blue LED and fluorescent light conditions.