METHOD FOR PRODUCING PACKING AND/OR STORING IMPLEMENT ADVANTAGEOUSLY PLANT-CULTIVATING VESSEL

• 1. 具有薄膜内容器的纸盒包装、用于生产纸盒包装的预制纸盒单元以及生产该种纸盒包装的方法 [P] . 中国专利： CN101687585B . 2012.02.08
• 2. 具有薄膜内容器的纸盒包装、用于生产纸盒包装的预制纸盒单元以及生产该种纸盒包装的方法 [P] . 中国专利： CN101687585A . 2010-03-31
• 3. Method of raising and of protecting a plant and plant-cultivating vessel for implementing the method [P] . 瑞士专利： CH646836A5 . 1984-12-28

  机译： 饲养和保护植物的方法以及实施该方法的植物栽培容器

• 4. METHOD OF MANUFACTURING PACKING VESSEL AND PACKING VESSEL PRODUCED BY THE METHODS [P] . 韩国专利： KR20070120386A . 2007-12-24

  机译： 制造包装容器的方法和用该方法生产的包装容器

• 5. PACKING MATERIAL, METHOD FOR PRODUCING PACKING MATERIAL, READING DEVICE, STORED-ARTICLE MANAGEMENT SYSTEM, DISCONNECTION DETECTION DEVICE, UNSEALING DETECTION LABEL, AND UNSEALING DETECTION SYSTEM [P] . 欧洲知识产权局专利： EP3693290A1 . 2020-08-12

  机译： 包装材料，包装材料的生产方法，读取设备，存储的物品管理系统，断开检测设备，拆封检测标签和拆封检测系统

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• 2. Method for pests detecting in stored grain based on spectral residual saliency edge detection [J] . Yao Qin, Yanli Wu, Qifu Wang, 粮油科技：英文版 . 2019,第002期
• 3. Adaptive Page Packing and Storing Method for PCM-Flash Hybrid Memory Structure [C] . Su-Kyung Yoon, Young-Sun Youn, Shin-Dug Kim 2015 IEEE 17th International Conference on High Performance Computing and Communications, 2015 IEEE 7th International Symposium on Cyberspace Safety and Security, 2015 IEEE 12th International Conference on Embedded Software and Systems . 2015
• 4. Development and application of multiple polymerase chain reaction assays to detect ochratoxin-producing Aspergillus and Penicillium, and trichothecene-producing Fusarium in stored and processed grain. [D] . Boddeda, Anuradha. 2008
• 5. Evaluation of Random Donor Platelets Produced from Buffy Coat Stored for 24 h at Ambient Temperature: Should This be Implemented in India? [O] . J. Philip, Kumarage Samantha, T. Chatterjee, 2015
• 6. The effect of packing methods on the field survival and growth of winter-stored plants of Scots pine. [O] . Långström, Bo 1970
• 7. SOME GEOMETRICAL PROPERTIES OF PACKINGS OF EQUAL SPHERES IN CYLINDRICAL VESSELS PART 1 - EXPLORATORY STUDY OF RANDOM PACKINGS IN SMALL VESSELS [R] . G. A. TINGATE 1970

• 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. Biorational control methods for protection of stored grain legumes against bruchid beetles [J] . Takashi Yamane . 农业科学（英文） . 2013,第12期
• 3. Development and Application of a Validated UHPLC Method for the Determination of Atropine and Its Major Impurities in Antidote Treatment Nerve Agent Auto-Injectors (ATNAA) Stored in the Strategic National Stockpiles [J] . Cheng H. Yen ,Adil Mohammad ,Miah Schneider . 药理与制药（英文） . 2017,第1期
• 4. 自主创新,全面提高PET包装容器的质量技术水平在塑料中空容器行业联合中心PET包装容器技术发展研讨会上的发言 [C] . . 中国包装联合会塑料制品包装委员会塑料中空容器行业联合中心第一届第三次年会暨PET包装容器技术交流研讨会 . 2007
• 5. 仿生设计在包装容器造型设计中的应用研究一水形态在女性化妆品包装容器造型设计的表现魅力 [A] . 姜萍 . 2012