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Journal articles on the topic 'Suranaree University of Technology'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Benjaoran, Vacharapoom, and Patranid Parinyakulset. "Green initiative in Suranaree University of Technology in Thailand." MATEC Web of Conferences 174 (2018): 01028. http://dx.doi.org/10.1051/matecconf/201817401028.

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Suranaree University of Technology (SUT) has participated in the Universitas Indonesia (UI) GreenMetric World University Rankings since 2013. It attempts to pursue campus sustainability programs and policies. The rankings is broadly based on the frameworks of environment, economy, and equity. The measurement criteria are divided into six categories with different point weighting i.e. setting and infrastructure, energy and climate change, waste, water, transportation, and education. These criteria heavily and directly involve the tasks and responsibilities of SUT's the Division of Buildings and Ground. A lot of environmental challenges in civil engineering and infrastructure works need to be achieved. The results of this year self-assessment show that although the university is in the developing stage, it can preserve both natural and planted forests more than 90%. It takes seriously role in green initiative by contributing 30% of total budget on sustainable efforts each year. It receives four national awards in the recognition of energy conservation initiative for green buildings. The university establishes the Integrated Solid Waste Management Plant (ISWM Plant) based on mechanical and biological treatment (MBT) which turns general wastes into valuable and sellable refuse-derived fuel (RDF). Moreover, these sustainable movements are in the continuous improvement process.

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2

Suksaweang, Sanong, Seekaow Churproong, and Naporn Uengarporn. "Effectively Controlled and Prevented the Spreading of Pandemic H1N1/2009 at Suranaree University of Technology." American Journal of Clinical Pathology 138, suppl 2 (November 1, 2012): A257. http://dx.doi.org/10.1093/ajcp/138.suppl2.195.

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3

Karuchit, Sudjit, Wichayanee Puttipiriyangkul, and Tanyarut Karuchit. "Carbon Footprint Reduction from Energy-Saving Measure and Green Area of Suranaree University of Technology, Thailand." International Journal of Environmental Science and Development 11, no. 4 (2020): 170–74. http://dx.doi.org/10.18178/ijesd.2020.11.4.1246.

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4

Prasetyadi, A., and A. Koonsrisuk. "Evaluation of the Centralized HVAC Chilled Water Pumps of Suranaree University of Technology Hospital Main Building." IOP Conference Series: Materials Science and Engineering 722 (January 21, 2020): 012006. http://dx.doi.org/10.1088/1757-899x/722/1/012006.

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5

Prasetyadi, A., and A. Koonsrisuk. "Minimization of Energy and Water Cost for the Main Building of Suranaree University of Technology Hospital (SUTH)." IOP Conference Series: Materials Science and Engineering 886 (July 28, 2020): 012039. http://dx.doi.org/10.1088/1757-899x/886/1/012039.

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6

Saowakon, Naruwan, Piyada Ngernsoungnern, Pornpun Watcharavitoon, Apichart Ngernsoungnern, and Rachain Kosanlavit. "Formaldehyde exposure in gross anatomy laboratory of Suranaree University of Technology: a comparison of area and personal sampling." Environmental Science and Pollution Research 22, no. 23 (August 2, 2015): 19002–12. http://dx.doi.org/10.1007/s11356-015-5078-2.

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7

Klysubun, Wantana, Pinit Kidkhunthod, Pongjakr Tarawarakarn, Panidtha Sombunchoo, Chanapa Kongmark, Sukit Limpijumnong, Saroj Rujirawat, Rattikorn Yimnirun, Gamolwan Tumcharern, and Kajornsak Faungnawakij. "SUT-NANOTEC-SLRI beamline for X-ray absorption spectroscopy." Journal of Synchrotron Radiation 24, no. 3 (April 4, 2017): 707–16. http://dx.doi.org/10.1107/s1600577517004830.

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The SUT-NANOTEC-SLRI beamline was constructed in 2012 as the flagship of the SUT-NANOTEC-SLRI Joint Research Facility for Synchrotron Utilization, co-established by Suranaree University of Technology (SUT), National Nanotechnology Center (NANOTEC) and Synchrotron Light Research Institute (SLRI). It is an intermediate-energy X-ray absorption spectroscopy (XAS) beamline at SLRI. The beamline delivers an unfocused monochromatic X-ray beam of tunable photon energy (1.25–10 keV). The maximum normal incident beam size is 13 mm (width) × 1 mm (height) with a photon flux of 3 × 108to 2 × 1010 photons s−1(100 mA)−1varying across photon energies. Details of the beamline and XAS instrumentation are described. To demonstrate the beamline performance,K-edge XANES spectra of MgO, Al2O3, S8, FeS, FeSO4, Cu, Cu2O and CuO, and EXAFS spectra of Cu and CuO are presented.

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8

Li, Kaijian, Ayut Limphirat, and Nuanwan Sanguansak. "Study of dose rate in the brain model based on the neutron beam of SUT-MNSR." EPJ Web of Conferences 239 (2020): 24002. http://dx.doi.org/10.1051/epjconf/202023924002.

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Boron neutron capture therapy (BNCT) is tumor-cell targeted radiotherapy that has significant superiority over conventional radiotherapies. The most neutron beams used for BNCT are from the reactors with high power, new design Miniature Neutron Source Reactor(MNSR) with 45kW with BNCT beam for Suranaree University of Technology(SUT) is being designed and built. According to SUT-MNSR physics design, SUT-MNSR will have the epithermal neutron beam for BNCT treatment. The dose rate distribution in the body should be estimated before SUT-MNSR is used for BNCT clinical trials (Brain tumor). This paper introduces the simulation for SUT-MNSR neutron beam by Monte Carlo N-Particle Transport Code (MCNP), and the establishment of human brain model and physics dose rate distribution in brain tumor by MCNP program.The brain model is established according to the different element in the skin, skull and tissue, the distribution of neutron dose and Gamma dose in the brain model were calculated.

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9

Lorthongpanich, C., C. Laowtammathron, S. Muenthaisong, T. Vetchayan, M. Ketudat-Cairns, B. Likitdecharote, and R. Parnpai. "55IN VITRO DEVELOPMENT OF ENUCLEATED DOMESTIC CAT OOCYTES RECONSTRUCTED WITH SKIN FIBROBLASTS OF DOMESTIC AND LEOPARD CATS." Reproduction, Fertility and Development 16, no. 2 (2004): 149. http://dx.doi.org/10.1071/rdv16n1ab55.

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The domestic cat is a valuable model for studies in assisted reproductive technology in felid species. Therefore, in this experiment we evaluated the in vitro developmental potential of enucleated domestic cat oocytes reconstructed with somatic cells from domestic and leopard cats. Skin fibroblasts were isolated from female domestic and leopard cats. The oocytes were collected by aspiration of follicles from ovaries that were superovulated with 200IU PMSG. In vitro-matured oocytes were enucleated and individual donor cells (diameter 14–16μm) were inserted into the perivitelline space of the enucleated oocyte. Fusion was performed at 26–27h post-maturation by placing a cell-oocyte couplet between both tips of the needle electrode and electrostimulating with a 2-DC pulse (30V, 30μs) in fusion medium containing 0.3M Mannitol+0.1mM MgCl2. Activation was performed 1 to 2h post-fusion by incubation in 7% ethanol at room temperature for 5min followed by cultured in 10μgmL−1 cycloheximide and 1.25μgmL−1 cytochalasin D at 38°C in 5% O2, 5% CO2, 90% N2 conditions. After activation, the reconstructed embryos were cultured in 100-μL droplets of Tyrode’s medium (Gomez et al., 2003 Theriogenology 60, 239–251.) supplemented with 0.3% BSA at 38°C in a 5% O2, 5% CO2, 90% N2 environment for 2d. Then, 8-cell embryos were cultured in 100-μL droplets of Tyrode’s medium supplemented with 10% FCS at 38°C in a 5% O2, 5% CO2, 90% N2environment for 5d. The cleavage rates of oocytes reconstructed with either donor cell types were not different. The percentages of blastocyst formation from parthenogenotes and nuclear transfer embryos derived from domestic cat fibroblasts (8/56, 14.3% and 7/51, 13.7%, respectively) were significantly higher than that for nuclear transfer embryos constructed with leopard cat fibroblasts (3/45, 6.7%). These results indicate that enucleated domestic cat oocytes reconstructed with skin fibroblasts of leopard cats can develop to the blastocyst stage. This experiment was supported by Suranaree University of Technology. Table 1 In vitro development of domestic cat oocytes reconstructed with domestic and leopard skin fibroblasts and parthenogenetic activation

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10

Laowtammathron, C., T. Terao, C. Lorthongpanich, S. Muenthaisong, T. Vetchayan, S. Hochi, and R. Parnpai. "104EFFECT OF HATCHING STATUS ON VITRIFICATION OF CLONED BOVINE BLASTOCYSTS." Reproduction, Fertility and Development 16, no. 2 (2004): 174. http://dx.doi.org/10.1071/rdv16n1ab104.

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Bovine blastocysts produced by nuclear transplantation have mechanical slits in their zonae pellucidae, and therefore initiate hatching earlier than the non-manipulated embryos. The present study was undertaken to examine whether the hatching stage of cloned blastocysts is among the factors influencing their survival after vitrification and warming. Cloned bovine blastocysts were produced by using adult ear fibroblast cells as reported previously (Parnpai et al., 2002, Theriogenology 57, 443), except that fused couplets were co-cultured with bovine oviductal epithelial cells in mSOFaa medium supplemented with 0.1% linoleic acid-albumin (LAA)+0.2% BSA (Hochi et al., 1999, Theriogenology 52, 497–504). Hatching blastocysts harvested on Day 7 were classified into one of three groups according to the ratio of extruding embryonic diameter from zona (D2) to embryonic diameter inside the zona (D1); category-A: D2/D1=0.01–0.70; category-B: D2/D1=0.71–1.00; category-C: D2/D1=1.01–1.70. The blastocysts were first exposed to 10% DMSO+10% ethylene glycol in TCM199+20% FCS for 2min, and then equilibrated in 20% DMSO+20% ethylene glycol+0.5M sucrose with or without 10% Ficoll in TCM199+20% FCS for 30s. One to three blastocysts were placed on a Cryotop sheet (Kitazato Supply Co., Tokyo, Japan) and vitrified in liquid nitrogen. The samples were warmed in 0.5M sucrose solution for 2min and transferred into TCM199+20% FCS in five steps (5min per step). The post-warm survival of the blastocysts was assessed by in vitro culture for 24h. When Ficoll-free vitrification solution was used, post-warm survival rate of the category-A blastocysts (77%, 23/30) was not significantly different (ANOVA test) from those of category-B and category-C blastocysts (74%, 20/27; and 80%, 24/30; respectively). Inclusion of 10% Ficoll in the vitrification solution did not improve (ANOVA test) the post-warm survival rates of cloned blastocysts (category-A: 65%, 22/34; category-B: 54%, 15/28; category-C: 59%, 19/32). Groups of fresh nonsurgical embryos, vitrified with or without Ficoll, yielded 66.7% (4/6), 66.7% (2/3) and 40.0% (2/5), respectively, of recipients pregnant at 48 days of gestation. In conclusion, cloned bovine blastocysts, regardless of their hatching stages, were relatively resistant to cryopreservation by vitrification. (Supported by Thailand Research Fund and R&D Fund of Suranaree University of Technology.)

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11

Parnpai, R., C. Laowtammathron, T. Terao, C. Lorthongpanich, S. Muenthaisong, T. Vetchayan, and S. Hochi. "116DEVELOPMENT INTO BLASTOCYSTS OF SWAMP BUFFALO OOCYTES AFTER VITRIFICATION AND NUCLEAR TRANSFER." Reproduction, Fertility and Development 16, no. 2 (2004): 180. http://dx.doi.org/10.1071/rdv16n1ab116.

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Oocyte cryopreservation in the domestic species is still at the experimental stage, but recent studies indicated that vitrification characterized by ultra-rapid cooling rate is promising for cryopreservation of bovine oocytes. In the present study, denuded buffalo oocytes were vitrified by minimum volume cooling procedure (Kuwayama and Kato, 2000, J Assist Reprod Genet 17, 477) after IVM or after IVM and enucleation, and developmental potential into blastocysts of the post-warm oocytes after somatic cell nuclear transplantation was examined. Cumulus-oocyte complexes were matured, denuded, and enucleated as described previously (Parnpai et al., 1999, Buffalo J 3, 371–384). The presumptive metaphase-II (M-II) oocytes before and after enucleation were first equilibrated in 7.5% DMSO+7.5% ethylene glycol+20% FCS in TCM199 for 10 min, and then exposed to 15% DMSO+15% ethylene glycol+0.5M sucrose+20% FCS in TCM199 for 1min. Five oocytes were placed on a Cryotop sheet (Kitazato Supply Co., Tokyo, Japan) and vitrified in liquid nitrogen. The samples were warmed in 0.5M sucrose solution for 5min, directly transferred into TCM199+20% FCS, and kept at room temperature for 1h before being used for a cloning experiment. The post-warm oocytes were fused with ear skin fibroblasts by two DC pulses (26V, 17μs) and activated with 7% ethanol for 5min and then 10μg/mL cycloheximide and 1.25μg/mL cytochalasin-D for 5h. The reconstructed embryos were cultured in mSOFaa+0.2% BSA+0.1% linoleic acid albumin for 2 days, and then co-cultured with bovine oviductal epithelial cells for an additional 5 days. Post-warm morphological survival of M-II oocytes (80%, 187/235) was similar to that of enucleated oocytes (75%, 158/212). Vitrified M-II oocytes were successfully enucleated (96%, 136/142) as were fresh control oocytes (88%, 143/162). Fusion rates of M-II oocytes vitrified before and after enucleation (81%, 94/116 and 78%, 106/136, respectively) were also similar to those of fresh oocytes (81%, 100/123). Percentages of reconstructed embryos developing into hatching blastocysts on Day 7 were 5% (5/91), 6% (6/103), and 8% (8/99) in the groups of oocytes vitrified before and after enucleation, and of fresh control oocytes, respectively (ANOVA tests were not significant different). These results indicate that swamp buffalo oocytes cryopreserved by ultra-rapid vitrification procedure can be used successfully for subsequent somatic cell nuclear transplantation. (Supported by Thailand Research Fund and R&D Fund of Suranaree University of Technology)

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12

Liang, Y. Y., D. N. Ye, C. Laowtammathron, T. Phermthai, and R. Parnpai. "211 IN VITRO PRODUCTION OF SWAMP BUFFALO EMBRYOS BY INTRACYTOPLASMIC SPERM INJECTION: EFFECT OF CHEMICAL ACTIVATION TREATMENTS." Reproduction, Fertility and Development 21, no. 1 (2009): 203. http://dx.doi.org/10.1071/rdv21n1ab211.

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Intracytoplasmic spern injection (ICSI) in the buffalo has not yet been well examined. Several factors involved affect the success rates of this technique, particularly the postinjection activation procedure. The objective of this study was to evaluate the effects of chemical activation treatments on in vitro development of oocytes after ICSI. A single spermatozoa was injected into the cytoplasm of an in vitro-matured oocyte using a micromanipulator under an inverted microscope. The ICSI oocytes were assigned to the following chemical activation treatments: (1) exposed to 5 μm ionomycin (Io) in Emcare medium for 5 min and placed in Emcare medium for 3 h, or (2) exposed to 7% ethanol (EtOH) in Emcare medium for 5 min and placed in Emcare medium for 3 h. The treated oocytes that extruded a second polar body were then selected and cultured either in (A) 1.9 mm 6-dimethylaminopurine (6-DMAP) in mSOF medium for 3 h, or (B) 10 μg mL–1 of cychloheximide (CHX) for 5 h. The treated oocytes were further cultured in mSOF medium supplemented with 3 mg mL–1 of fatty acid-free BSA at 38.5°C under a humidified atmosphere of 5% O2, 5% CO2, and 90% N2 for 2 d. Thereafter, 8-cell-stage embryos were selected and co-cultured with buffalo cumulus cells in mSOF medium at 38.5°C under a humidified atmosphere of 5% CO2 in air for another 5 d. The medium was changed daily and the development of embryos was recorded at the same time the medium was changed. The sham-injected oocytes were treated and cultured along with ICSI oocytes. With 8 replications for each activation treatment, 336 oocytes were used for ICSI. With 6 replications for each activation treatment, 211 oocytes were used for sham injection. The cleavage of ICSI oocytes treated with Io + 6-DMAP, EtOH + 6-DMAP, and EtOH + CHX was 76.2, 69.4, and 78.3%, respectively, which was significant higher (P < 0.01) than ICSI oocytes treated with Io + CHX (52.4%) and also significant higher (P < 0.01) than sham-injected oocytes in all treatments. The highest blastocyst rate was observed in ICSI oocytes treated with Io + 6-DMAP (28.6%), which was not significantly different from ICSI oocytes treated with EtOH + CHX (24.4%). The blastocyst rates of ICSI oocytes treated with Io + 6-DMAP and EtOH + CHX were significantly higher than ICSI oocytes treated with Io + CHX (5.9%) and EtOH + 6-DMAP (16.5%) and also were significantly higher than sham-injected oocytes in all treatments. In conclusion, our study demonstrated that activated ICSI of swamp buffalo oocytes with Io + 6-DMAP or EtOH + CHX gave the highest cleavage and blastocyst rates. This work was supported by the Thailand Research Fund and Suranaree University of Technology.

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13

Srirattana, K., C. Laowtammathron, R. Devahudi, S. Imsoonthornruksa, A. Sangmalee, W. Tunwattana, C. Lorthongpanich, et al. "52 EFFECT OF TRICHOSTATIN A ON DEVELOPMENTAL POTENTIAL OF INTER-SPECIES CLONED GAUR (BOS GAURUS) EMBRYOS." Reproduction, Fertility and Development 21, no. 1 (2009): 126. http://dx.doi.org/10.1071/rdv21n1ab52.

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This study was carried out to investigate the effect of trichostatin A (TSA) treatment on interspecies cloned gaur (Bos gaurus) embryos development and implantation rate after transfer to bovine (Bos taurus) recipients. The bovine (Bos taurus) enucleated oocytes were used as recipient cytoplasm for male and female gaur fibroblasts. After electrical fusion, oocytes were separated into two groups, TSA treatment and control. For the TSA group, the oocytes were placed in EmCare (ICPbio, Ltd., Auckland, New Zealand) holding medium + 50 nm TSA for 1 h. The fused oocytes were activated by 7% ethanol + 50 nm TSA for 5 min at room temperature and 10 μg mL–1 cycloheximide + 1.25 μg mL–1 cytochalasin D + 50 nm TSA at 38.5°C under 5% CO2 in air for 5 h. Then the embryos were cultured in mSOFaa medium + 3 mg mL–1 bovine serum albumin (BSA) + 50 nm TSA up to 10 h. After 10 h, the reconstructed embryos were transferred to embryo culture medium without TSA and culture for 2 days at 38.5°C under 5% CO2, 5% O2, 90% N2. The control embryos were cultured with the same culture system without TSA supplementation. Eight-cell stage embryos were selected and co-cultured with bovine oviductal epithelial cells in culture medium at 38.5°C under 5% CO2 in air for 5 days. Half volume of the culture medium was replaced daily. Two blastocysts at days 7 or 8 derived from male fibroblasts of treated and non-treated TSA were non-surgically transferred to each synchronized estrous bovine recipients. The statistical analysis was done by ANOVA and the comparison of means by Duncan’s Multiple Range Test (DMRT). The development to blastocyst stage was not different among male and female, treated and non-treated TSA embryos which range between 34.8 to 39.3%. The pregnancy rate at 40 days after recipients received cloned embryos derived from male fibroblasts treated v. non-treated TSA was 11% (2/18) v. 10% (1/10) (Table 1). One recipient which received a non-treated embryo gave birth by C-section on March 4, 2008. The male gaur calf died from respiratory problem at 12 h after birth. Eight bovine microsatellite markers analysis confirmed that the newborn gaur was derived from the donor gaur fibroblast. In this study, TSA has no effect on pre-implantation cloned gaur embryos development either derived from male or female gaur fibroblasts. Cloned gaur calves could be produced by interspecies cloning using bovine oocytes as recipient cytoplasm. Table 1.Pregnancy and birth rates after transferred cloned gaur embryos derived from male fibroblasts to recipients This study was supported by National Center for Genetic Engineering and Biotechnology (BIOTEC) and Suranaree University of Technology.

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14

Liang, Y. Y., T. Phermthai, T. Nagai, T. Somfai, and R. Parnpai. "83 EFFECTS OF CYTOCHALASIN B AND VITRIFICATION PROCEDURE ON SURVIVAL AND IN VITRO MATURATION OF SWAMP BUFFALO OOCYTES CRYOPRESERVED AT THE IMMATURE STAGE." Reproduction, Fertility and Development 23, no. 1 (2011): 147. http://dx.doi.org/10.1071/rdv23n1ab83.

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Cryopreservation of oocytes from swamp buffaloes of high genetic and individual values is important for conservation of animal genetic resources. This study investigated the effect of cytochalasin B (CB) pretreatment and the efficiencies of solid surface vitrification (SSV) and cryotop (CT) vitrification methods to cryopreserve immature buffalo oocytes. Cumulus oocyte complexes harvested from abattoir-derived ovaries were randomly separated into 5 groups: 1) CT method with pretreatment by 7.5 μg mL–1 CB in base medium (BM, TCM-199 HEPES+20% FBS) for 15 min [CT(+)CB]; 2) CT method without CB pretreatment [CT(–)CB]; 3) SSV method with pretreatment by 7.5 μg mL–1 CB in BM for 15 min [SSV(+)CB]; 4) SSV method without CB pretreatment [SSV(–)CB]; and 5) fresh control. Immature oocytes were partially denuded, and those with 2 layers of cumulus cells were placed in 10% dimethylsulfoxide (DMSO) + 10% ethylene glycol (EG) for 1 min followed by exposure to 20% DMSO + 20% EG + 0.5 M sucrose in BM for 30 s. The oocytes were then vitrified either by SSV or CT method and stored in liquid nitrogen. Vitrified oocytes were thawed by placing them directly in warming solution (0.5 M sucrose in BM) for 5 min at 38.5°C and then washed in BM for 5 min. Oocyte viability was assessed by fluorescein diacetate staining. Surviving oocytes were in vitro matured (IVM) for 23 h (Parnpai et al. 1999 Buffalo J. 15, 371–384) and their meiotic progression was investigated by nuclear staining. Data were analysed by 1-way ANOVA. The survival rate of oocytes in CT groups [CT(+)CB, 82%; CT(–)CB, 82%] was significantly lower (P < 0.05) than that of the control group (100%), but significantly higher (P < 0.05) than those in the SSV groups [SSV(+)CB, 71%; SSV(–)CB, 72%]. After IVM, the proportions of viable oocytes were similar among vitrified groups [CT(+)CB, 84%; CT(–)CB, 86%; SSV(+)CB, 80%; SSV(–)CB, 79%], but significantly lower than those of the control group (96%). Pretreatment with CB did not increase oocyte survival. Among vitrified groups the highest maturation rate was obtained in CT(–)CB (32%), which was significantly higher than that of SSV(+)CB (13%). Vitrified oocytes in all groups reached metaphase-II at significantly lower rates compared with the control group (55%). In conclusion, CB did not improve the survival and maturation of vitrified oocytes. Higher survival and maturation rates in CT groups indicate the superiority of this method. This work was supported by Thailand Research Fund, Suranaree University of Technology and Japan Society for the Promotion of Science – National Research Council of Thailand (JSPS-NRCT) scientific cooperation program.

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15

Jomnonkwao, Sajjakaj, Onanong Sangphong, Buratin Khampirat, Siradol Siridhara, and Vatanavongs Ratanavaraha. "Public transport promotion policy on campus: evidence from Suranaree University in Thailand." Public Transport 8, no. 2 (March 8, 2016): 185–203. http://dx.doi.org/10.1007/s12469-016-0122-2.

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16

Cox, Mike. "University Technology Transfer." SCRIPT-ed 1, no. 3 (September 15, 2004): 388–407. http://dx.doi.org/10.2966/scrip.010304.388.

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Gering, Thomas. "University Technology Licensing." Industry and Higher Education 9, no. 2 (April 1995): 72–77. http://dx.doi.org/10.1177/095042229500900202.

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In the mid-1980s, European universities began to set up intellectual property (IP) programmes following the models created by US universities. Contrary to widespread opinion, it can be shown that the recently developed patent policies of European universities do not conflict in principle with basic scientific objectives nor with the special legal framework in European countries. However, there is still confusion concerning the motivations for universities to become involved in this aspect of technology transfer and also the economic and strategic potential of such programmes and their effect on higher education in general. European universities still suffer from antitrust policies which severely restrict their opportunities in licensing markets. The argument set out in this article is that they can and should profit from experience in the USA, where universities now have the title to all IP created in government-sponsored research and the right freely to license this IP to industry. Recent evidence regarding the royalties earned, the number of patents granted to universities and the industrial sectors in which these technologies have been exploited provides valuable information for European institutions. Despite its risks, university technology licensing is of strategic importance to university development and can generate substantial income. To achieve these benefits, it is necessary to establish a medium- to long-term policy for the development of the university technology licensing function.

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18

Okamoto, Takashi, and Shigeki Ono. "Kochi University of Technology." JOURNAL OF THE ILLUMINATING ENGINEERING INSTITUTE OF JAPAN 84, no. 4 (2000): 252–53. http://dx.doi.org/10.2150/jieij1980.84.4_252.

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19

Schouten, M. J. W. "Eindhoven University of Technology." Tribology International 18, no. 1 (February 1985): 45–47. http://dx.doi.org/10.1016/0301-679x(85)90008-8.

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20

De Moortel, Kevin, and Thomas Crispeels. "International university-university technology transfer: Strategic management framework." Technological Forecasting and Social Change 135 (October 2018): 145–55. http://dx.doi.org/10.1016/j.techfore.2018.05.002.

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21

Randazzese, L. P. "Exploring university-industry technology transfer of CAD technology." IEEE Transactions on Engineering Management 43, no. 4 (1996): 393–401. http://dx.doi.org/10.1109/17.543981.

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22

Srivastava, Pradeep, and Sunita Chandra. "Technology Commercialization: Indian University Perspective." Journal of technology management & innovation 7, no. 4 (December 2012): 121–31. http://dx.doi.org/10.4067/s0718-27242012000400010.

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23

Le, Khoa Van. "University of Technology, VNU-HCM." Science and Technology Development Journal 14, no. 2 (June 30, 2011): 97–105. http://dx.doi.org/10.32508/stdj.v14i2.1921.

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Plastic bags are associated with convenience and low cost. The over-use and disposal of plastic waste with non specifications are made the regrettable corollary to landscape and environment. Therefore, research on plastic bag use reduction measures in Ho Chi Minh City is necessary, and will contribute to improving public awareness about environmental protection, aiming at a sustainable consumption society in Ho Chi Minh City. This research gathered and analyzed documents regarding plastic bag’s effects on the environment; documents and figures related to plastic bag use management in the world; and combined with surveying, collecting related data about reducing plastic bag use in Ho Chi Minh City. Many measures from economic tools to enforcement, even through media campaigns are proposed to guaranty the success of the program; such as a ban of free plastic bags, a tax on using plastic bags, improving public awareness, setting up a system for plastic bag collection. In addition to, the potential conditions and solutions were studied for replacing plastic bags with environmentally friendly bags.

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24

Bray, Michael J., and James N. Lee. "University revenues from technology transfer." Journal of Business Venturing 15, no. 5-6 (September 2000): 385–92. http://dx.doi.org/10.1016/s0883-9026(98)00034-2.

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25

Herbst, Theo. "Music Technology at Stellenbosch University." Leonardo Music Journal 16 (December 2006): 65. http://dx.doi.org/10.1162/lmj.2006.16.65a.

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26

De Ritis, Anthony. "Music Technology at Northeastern University." Journal of the Acoustical Society of America 110, no. 5 (November 2001): 2625. http://dx.doi.org/10.1121/1.4776858.

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27

Vanderburg, Willem H. "Engineering Technology, and the University." IEEE Technology and Society Magazine 6, no. 4 (December 1987): 5–11. http://dx.doi.org/10.1109/mtas.1987.5010137.

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Schmitt, Roland W. "Technology Transfer and the University." Journal of Higher Education 63, no. 4 (July 1992): 476–78. http://dx.doi.org/10.1080/00221546.1992.11778384.

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Kumar, Umesh, and Neeta Sharma. "Cross River University of Technology." International Journal of Computer Trends and Technology 64, no. 1 (October 25, 2018): 7–11. http://dx.doi.org/10.14445/22312803/ijctt-v64p103.

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30

Brust, Melvin F. "Technology Transfer And The University." Journal of Applied Business Research (JABR) 7, no. 1 (October 20, 2011): 1. http://dx.doi.org/10.19030/jabr.v7i1.6253.

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This article contains a review of current thoughts on technology transfer and the role of the university in this process. Factors which affect the rate at which technology transfer takes place are briefly reviewed. Opportunities for universities to facilitate the process of technology transfer are discussed. The increasingly aggressive role being played by universities and the risks associated therewith are noted. The conclusion is reached that, with appropriate safeguards, benefits far outweigh the attendant risks.

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31

Schmitt, Roland W., and Gary W. Matkin. "Technology Transfer and the University." Journal of Higher Education 63, no. 4 (July 1992): 476. http://dx.doi.org/10.2307/1982127.

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32

Wright, Mike, Sue Birley, and Simon Mosey. "Entrepreneurship and University Technology Transfer." Journal of Technology Transfer 29, no. 3/4 (August 2004): 235–46. http://dx.doi.org/10.1023/b:jott.0000034121.02507.f3.

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Bao, Hung Hoang. "Information Technology in University Education." International Journal of Education and Learning 5, no. 2 (September 30, 2016): 9–14. http://dx.doi.org/10.14257/ijel.2016.5.2.02.

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34

Sandelin, Jon. "University Technology Transfer Through Licensing." Optics and Photonics News 9, no. 10 (October 1, 1998): 24. http://dx.doi.org/10.1364/opn.9.10.000024.

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35

Chatziioanou, Alypios, and Edward Sullivan. "University Technology and Research Parks." Industry and Higher Education 18, no. 2 (April 2004): 125–29. http://dx.doi.org/10.5367/000000004323051903.

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This paper discusses the history, prospects and impacts of university technology and research parks. The main question addressed is: what are the short-term and long-term impacts of such parks on engineering education and its mission? The first technology park, at Stanford, and other early parks are used as examples to assess some of these impacts. Most of the short-term impacts are positive: the parks provide more options for academic staff and students, enable rapid technology transfer and offer improved funding for academia. The longer-term impacts however, including the potential loss of academic independence and diversity as well as a reduction in the classroom involvement and availability of academic staff tend not to be closely Monitored. Programmes, curricula and academics' interests have been observed to shift in concert with commercial priorities. A better balance between short-term success and long-term benefits should be sought in future technology park developments.

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Macho-Stadler, Inés, and David Pérez-Castrillo. "Incentives in university technology transfers." International Journal of Industrial Organization 28, no. 4 (July 2010): 362–67. http://dx.doi.org/10.1016/j.ijindorg.2010.02.009.

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Hsu, David W. L., Yung-Chi Shen, Benjamin J. C. Yuan, and Chiyan James Chou. "Toward successful commercialization of university technology: Performance drivers of university technology transfer in Taiwan." Technological Forecasting and Social Change 92 (March 2015): 25–39. http://dx.doi.org/10.1016/j.techfore.2014.11.002.

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TAKAMURA, Fujitoshi, Yoriko OHTA, Mitsunori OZAKI, and Izumi NISHIZAWA. "Technology circulation model of industry-university collaboration utilizing visualization technology of university and its practice." Transactions of the JSME (in Japanese) 82, no. 842 (2016): 16–00070. http://dx.doi.org/10.1299/transjsme.16-00070.

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39

Feng, Hui-I., Chia-Shen Chen, Chuan-Hung Wang, and Hsueh-Chiao Chiang. "The role of intellectual capital and university technology transfer offices in university-based technology transfer." Service Industries Journal 32, no. 6 (May 2012): 899–917. http://dx.doi.org/10.1080/02642069.2010.545883.

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Masuda, Masataka. "University Move and Corrosion Protection Technology." Zairyo-to-Kankyo 55, no. 10 (2006): 429. http://dx.doi.org/10.3323/jcorr.55.429.

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Olufikayo, Aderinlewo. "Federal University of Technology Akure, Nigeria." Revista Romana de Inginerie Civila/Romanian Journal of Civil Engineering 11, no. 3 (August 4, 2020): 298–311. http://dx.doi.org/10.37789/rjce.2020.11.3.2.

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Tolulope, Ojekale. "Federal University of Technology Akure, Nigeria." Revista Romana de Inginerie Civila/Romanian Journal of Civil Engineering 11, no. 3 (August 4, 2020): 337–53. http://dx.doi.org/10.37789/rjce.2020.11.3.6.

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43

KOYAMA, KIYOHITO. "Management of Technology Program, Yamagata University." FIBER 61, no. 12 (2005): P.315. http://dx.doi.org/10.2115/fiber.61.p_315.

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Phan, Phillip H., and Donald S. Siegel. "The Effectiveness of University Technology Transfer." Foundations and Trends® in Entrepreneurship 2, no. 2 (2006): 77–144. http://dx.doi.org/10.1561/0300000006.

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Chester, Victoria. "Using Tablet Technology for University Lectures." Bioscience Education 12, no. 1 (December 2008): 1–4. http://dx.doi.org/10.3108/beej.12.c5.

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Nakagawa, Keisuke, and Peter M. Yellowlees. "University of California Technology Wellness Index." Psychiatric Clinics of North America 42, no. 4 (December 2019): 669–81. http://dx.doi.org/10.1016/j.psc.2019.08.005.

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47

Harmon, Brian, Alexander Ardishvili, Richard Cardozo, Tait Elder, John Leuthold, John Parshall, Michael Raghian, and Donald Smith. "Mapping the university technology transfer process." Journal of Business Venturing 12, no. 6 (November 1997): 423–34. http://dx.doi.org/10.1016/s0883-9026(96)00064-x.

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Ulusoy, Gündüz, and Okyay Kaynak. "Technology Management: University—Industry—Government Collaboration." Industry and Higher Education 10, no. 6 (December 1996): 329–31. http://dx.doi.org/10.1177/095042229601000602.

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49

Thomson, H. G. "Technology Transfer from University to SMEs." Industry and Higher Education 12, no. 6 (December 1998): 377–78. http://dx.doi.org/10.1177/095042229801200609.

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The author summarizes current strategies at the University of Strathclyde in Scotland which respond to the need to collaborate effectively with local small and medium-sized enterprises (SMEs). These strategies are the results of four key policy strands: networking with local development agencies to improve industrial liaison; licensing IPR to SMEs; supporting initiatives from academic staff who wish to establish an institute or research centre which would address near-market needs of a local industry sector; and encouraging SMEs to collaborate with universities through national and international schemes.

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50

Slemon, Dean Gordon. "Industry-University Cooperation and Technology Transfer." IEEE Power Engineering Review PER-5, no. 12 (December 1985): 9–11. http://dx.doi.org/10.1109/mper.1985.5528592.

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