portable apparatus for the determination of the protein content of samples by neutron activation analysis.

• 1. 一种测定样品中蛋白质含量的装置 [P] . 中国专利： CN213398184U . 2021-06-08
• 2. 一种测定富含还原糖的蛋白样品中蛋白质含量的方法 [P] . 中国专利： CN106841079B . 2019.06.18
• 3. portable apparatus for the determination of the protein content of samples by neutron activation analysis. [P] . NL163627B . 1980-04-15

  机译： 用于通过中子活化分析测定样品蛋白质含量的便携式仪器。

• 4. METHOD AND TOOL FOR DETERMINATION OF FRACTURE GEOMETRY IN SUBTERRANEAN FORMATIONS BASED ON IN-SITU NEUTRON ACTIVATION ANALYSIS. [P] . MX2011004722A . 2011-09-01

  机译： 基于原位中子活化分析的地层裂缝几何确定方法和工具。

• 5. METHOD AND TOOL FOR DETERMINATION OF FRACTURE GEOMETRY IN SUBTERRANEAN FORMATIONS BASED ON IN-SITU NEUTRON ACTIVATION ANALYSIS. [P] . MX2011004722A . 2011-09-01

  机译： 基于原位中子活化分析的地层裂缝几何确定方法和工具。

• 1. Measurement of trace element content in bone samples using long-lived neutron activation products and high-resolution gamma-ray spectrometry [J] . Vladimir Zaichick, Sofia Zaichick 核技术（英文版） . 2016,第001期
• 2. Quantitative determination of Tamm-Horsfall Glycoprotein (Uromodulin) in urine samples using LC-MS/MS analysis. [C] . Nikolay V Voskoboev, Olga Bondar, Timothy S Larson, American Society for Mass Spectrometry Conference on Mass Spectrometry and Allied Topics . 2013
• 3. Part A: Speciation of aluminum metabolites in biological matrices employing chemical neutron activation analysis. Part B: Evaluation of methods for the determination of trimethylselenonium ion in urine [D] . Shoop, David Mark 1996
• 4. Determination of element composition and extraterrestrial material occurrence in moss and lichen samples from King George Island (Antarctica) using reactor neutron activation analysis and SEM microscopy [O] . Tomasz Mróz, Katarzyna Szufa, Marina V. Frontasyeva, -1
• 5. Research on the mass-determination method of As content in soil samples by its capability concerning for the microwave digestion method and epithermal neutron activation analysis. [O] . Yoshitsugu SHINOZUKA, Kazuhiro TOYODA 2001
• 6. Determination of Arsenic, Selenium and Antimony by Neutron Activation Analysis. Application to Hair Samples [R] . Das, H. A., Hoede, D., Nieuwendijk, B. J. T., 1983

• 1. BACKGROUND： Vibrio vulnifi cus inside the body could activate the NF-!B signaling pathwayand initiate the inflammatory cascade. The lung is one of the earliest organs affected by sepsisassociated with acute lung injury. High mobility group protein B1 （HMGB1） is an important late-actingpro-infl ammatory cytokine involving in the pathophysiology of sepsis. It is also involved in the injuryprocess in the lung, liver and intestine. There has been no report on the involvement of HMGB1 inVibrio vulnifi cus sepsis-induced lung injury.METHODS： Sixty rats were randomly divided into a normal control group （group A, n=10） anda Vibrio vulnificus sepsis group （group B, n=50）. Sepsis was induced in the rats by subcutaneousinjection of Vibrio vulnificus （concentration 6×108 cfu/mL, volume 0.1 mL/100g）） into the left lowerlimbs. The rats in group B were sacrifi ced separately 1, 6, 12, 24, and 48 hours after the infection.Their lungs were stored as specimens, lung water content was measured, and lung pathology wasobserved under a light microscope. The expressions of the HMGB1 gene and protein in the lungswere detected by RT-PCR and Western blot. Data were analyzed with one-way analysis of variance（ANOVA） and the LSD method for pair-wise comparison between the two groups. P〈0.05 wasconsidered statistically signifi cant.RESULTS： Compared to group A （0.652±0.177）, HMGB1 mRNA expression in the lungs ofgroup B was signifi cantly higher at 0 hour （1.161±0.358, P=0.013）, 24 hours （1.679±0.235, P=0.000）,and 48 hours （1.258±0.274, P=0.004） （P〈0.05）, and peaked at 24 hours. Compared to group A（0.594±0.190）, HMGB1 protein expression at 6 hours （1.408±0.567, P=0.026） after infection wassignificantly increased （P〈0. 05）, and peaked at 24 hours （2.415±1.064, P=0.000） after infection.Compared to group A （0.699±0.054）, lung water content was significantly increased at 6 hours（0.759±0.030, P=0.001）,12 hours （0.767±0.023, P=0.000）, 24 hours （0.771±0.043, P=0.000） and 48hours （0.789±0.137, P=0.000） after infection （P〈0.05）. Compared to group A, pathological changesat 12 hours in group B indicate marked pulmonary vascular congestion, interstitial edema andinfl ammatory infi ltration. Alveolar cavity collapse and boundaries of the alveolar septum could not beclearly identifi ed.CONCLUSION： Vibrio vulnifi cus sepsis can lead to injury in rat lungs, and increased HMGB1expression in lung tissue may be one of the mechanisms for injury from Vibrio vulnifi cus sepsis. [J] . Qiao-meng Qiu ,Zhong-wang Li ,Lu-ming Tang . 世界急诊医学杂志(英文) . 2011,第4期
• 2. Determination of Neutron Fluxes and Spectrum Shaping Factors in Irradiation Sites of Ghana’S Miniature Neutron Source Reactor (mnsr) by Activation Method After Compensation of Loss of Excess Reactivty [J] . R.B.M. Sogbadji ,B.J.B. Nyarko ,E.H.K. Akaho . 核科学与技术国际期刊（英文） . 2011,第2期
• 3. Determination of Mercuric Ion in Water Samples with a LED Exciting and CCD Based Portable Spectrofluorimeter [J] . Arsenio Munoz de la Pena ,Maria Isabel Rodriguez-Caceres ,Diego Bohoyo Gil . 美国分析化学（英文） . 2011,第5期
• 4. Application of Neutron Activation Analysis Technique for the Analysis of Soil Samples from Farmlands of Yebrage Hawariat, East Gojjam, Ethiopia [J] . Yihunie Hibstie Asres ,Ashok Kumar Chaubey ,Awoke Taddesse Hailu . 农业科学与技术：A . 2014,第004期
• 5. 放化中子活化分析法测定生物样品中的砷、镉、汞、铜和锌 [C] . 庄圭荪 . 第四次全国活化分析学术讨论会 . 1988
• 6. 用于测定谷物中蛋白质含量及深度分布的核分析方法研究 [A] . 罗小兵 . 2006