全國中小學科展

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2025年

短期睡眠剝奪對小鼠免疫系統的影響

現代社會中,睡眠剝奪已成為普遍問題,人們對其對免疫系統及整體健康的負面影響愈加關注。本研究使用特製的旋轉鼠籠讓小鼠連續72小時保持清醒,探討急性睡眠剝奪對小鼠免疫反應的影響。研究發現NK細胞與脾臟中的記憶CD8 T細胞比例明顯減少,顯示細胞毒性功能受損或記憶免疫反應下降。與此同時,抗炎細胞因子的表達增加,而促炎細胞因子和相關基因的表達則有顯著下調。此外,雖然觀察到B細胞比例有所增加,這可能是免疫系統在細胞免疫功能受損時,維持免疫穩態的反應。這些發現揭示了睡眠剝奪可能抑制免疫系統造成損害。本研究強調適量睡眠對維持免疫平衡的重要性,並指出睡眠不足可能促進慢性免疫問題的發展。在此基礎上,後續研究可探討短期睡眠剝奪與腫瘤及免疫系統的關聯,並延伸至長期剝奪的影響。

開發回收PET合成UiO-66並應用於催化合成羥甲香豆素

本研究利用乙二醇處理後的聚對苯二甲酸(PET)及氯氧化鋯,以創新的無溶劑方式”solvent-free PET-to-MOF conversion”合成一類金屬有機框架材料(MOF) ── UiO-66(Zr),並發現此材料可用於催化Pechmann condensation、以間苯二酚和乙醯乙酸乙脂合成羥甲香豆素。於190℃之環境下,乙二醇處理6小時的EG-PET可合成出晶型最接近模擬模型的UiO-66晶體;而我們開發的合成方法中,最佳的反應條件為反應物質量比(氯氧化鋯:PET)= 2:1、130℃合成24小時。 對於合成出的UiO-66(Zr),我將其進行了XRD、FTIR、BET、SEM檢測,結果符合UiO-66(Zr)的特徵;唯比表面積僅有約900 平方公尺/克,推測此方法合成出的材料之有機linker數量和一般UiO-66(Zr)有所差異。 對於催化合成羥甲香豆素之反應,我們首先發現UiO-66(Zr)可作為非勻相催化劑參與此反應;且實驗結果顯示,相較於溶劑熱合成的UiO-66(Zr),以本研究的方法所得之UiO-66(Zr)作為催化劑可得到更高產率的羥甲香豆素。

降脂轉肌–將脂肪轉變成肌肉的可能性探討

先前研究發現一種多元不飽和脂肪酸 15-keto-PGE2 能減少肌肉慢性發炎以及增加肌肉生長因子胰島素的敏感性,具有增加肌肉的潛力。我們探討此脂肪酸在小鼠中將脂肪組織轉成肌肉組織的可能性。 我們先以 15-keto-PGE2 治療肥胖型肌少症小鼠後,再以全基因組mRNA定序,發現在小鼠皮下脂肪中,肌肉特異基因表現量高度上升。透過基因表現路徑分析軟體 GSEA證實此脂肪酸會高度引發皮下脂肪中,與肌肉分化、肌肉收縮與肌肉結構相關的生物路徑。另外, 15-keto-PGE2 也可以誘導脂肪前驅細胞3T3-L1中與肌肉生成相關的基因表現。 最後,我們發現以 15-keto-PGE2 治療的老年肥胖型肌少症小鼠,體重、血糖、脂肪比例下降,肌肉質量及力量上升,證實了它在體內同時減少脂肪並增加肌肉量的效果。

Synthesis of Nanocomposite Nanocellulose From Durio zibethinus L. and TiO2 NPs as Potential Food Packaging Antibacterial (E. coli Wild Type and Resistance)

According to the 印尼n Association of Olefin Aromatic and Plastic Industries/INAPLAS, 2019 national plastic consumption still relies on plastic packaging at 65% and surprisingly, around 60% of plastic waste is absorbed by the food and beverage industry. The waste has been widely sought to be environmentally friendly, one of which is by developing biodegradable packaging. The purpose of this research is to make durian peel cellulose nanocomposites impregnated with TiO2 NPs, to form antibacterial properties against E. coli wild type and resistance. In this research, there are research methods consisting of nanocomposite synthesis, PSA test, FTIR, physical characteristics test and resistance test. The results analyzed that the nanocomposite nanocellulose-TiO2 NPs was successfully made using a 1:1 ratio and had a particle size of 458.7 nm based on the PSA test, which is classified as a nano size. The success of nanocomposite synthesis was proven by the results of FTIR analysis, which showed the formation of 698.65cm-1 and 1633.99cm-1 spectra, indicating the peak of TiO2 NPs and O-H functional groups on TiO2 NPs, as well as 1028.98cm-1 and 1158.42cm-1 showing C-O and C-O-C bonds in cellulose. The antibacterial test performed showed no significant activity in disc diffusion and well diffusion tests against E. coli wild type and resistance. This is potentially caused by inhomogeneous particle size variation. Physical characteristics test showed that the tensile strength test (0.075 > 0.0125 MPa) Durio Nano-Pack is superior to styrofoam, but the compressive strength test (0.125 > 0.875 MPa) shows the opposite. In this study, nanocomposite has a potential innovation that provides good mechanical properties and has a dual function mechanically as bio-based food packaging and chemically as antibacterial. Further research is needed to improve the particle size homogeneity of nanocomposites, modify the impregnation method, so that it has the potential to develop multifunctional materials that excel in various applications.

Mattress Ventilation System

One of the worldwide hidden problems with lack of attention is Bedsores. Simply, These are ulcers, that happen on the areas of the skin that are under pressure while lying on the bed for a prolonged time. This can be infected to anyone in the world. The common group who face these bed sores are..... •Elderly patients, •Spinal cord injury patients, •Stroke patients, •Coma patients, •People who have faced accidents Bed sores develop when the blood supply is cut off for more than 2-3 hours to the skin, (Position changing time depends on the patient's condition) The continuous pressure is the cause for that and also the temperature generated between the skin and the bed surface increases the metabolism of the tissues. When the skin temperature increases by 1°C, the risk of bed sores increases approximately 14 times. So, The skin temperature in the range of 29.4°C to 37.1°C is correlated with the tissue damage score. Not only that shearing and moisture are the other considerable factors for this problem. This infection has 4 stages. Sometimes in the 4th stage of the bed sores can cause death.

以果蠅建立單純型表皮水皰症(EBS)模型、建立藥物篩選流程並以雙醋瑞因(Diacerein)進行測試

遺傳性表皮分解性水泡症(EB)是種罕見疾病,因突變使角蛋白異常,造成表皮組織脆弱易形成水泡,單純型水泡症(EBS)是最常見的類型。此計畫旨在:(一)建立果蠅EBS疾病模型;(二)探討溫度對病徵的影響;(三)以此果蠅EBS疾病模型發展藥物篩選平台。初步使用Diacerein測試,評估對EBS症狀的改善效果。 目前顯示突變角蛋白K5/K14R125C會形成積聚體,與正常K5/K14形成的角蛋白網絡不同;全程25℃培養,約32%果蠅翅膀有水泡,亦符合EBS病徵。篩藥平台建置已完成色素和溶劑DMSO劑量測試,初步顯示Diacerein有助病徵緩解。目前將擴大統計不同溫度對 EBS果蠅死亡率、水泡發生率和角蛋白積聚形成比例。希望以本研究建立的果蠅EBS疾病模型與篩藥平台,能為罕見遺傳疾病療程開發奠定基礎。

關於Repunit數列 之餘數性質探討

在這篇作品中,主要研究Repunit數列=在模n之下的餘數數列循環性質。我們探討了Repunit餘數數列在什麼條件下 為純循環週期數列、混循環週期數列和完全純循環週期數列,同時給出了循環週期的公式及上界。接著我們發現一階非齊次線性遞迴數列在模n之下的循環週期與c進制Repunit數列在模 n/gcd(n,c)之下的循環週期相同,並且進一步探討餘數數列在什麼條件下為純循環數列、混循環循環數列和完全純循環數列。

Evaluating the Impact of the AI-Powered Interactive Journal “I Am Great Because of Me” on Reducing Impostor Syndrome Among High Performing Students

Impostor Syndrome, a psychological phenomenon where individuals doubt their abilities despite evident achievements, can hinder personal and academic development. This study aims to evaluate the effectiveness of the interactive journal “I am Great Because of Me”, integrated with artificial intelligence (AI), in addressing Impostor Syndrome among high-performing students. The journal features innovative tools such as the Clance Impostor Phenomenon Scale (CIPS) test accessible via QR code, self-acknowledgement pages, and virtual consultations powered by AI chatbots. These elements aim to support self-reflection, provide real-time diagnostics, and deliver actionable recommendations for users. The ADDIE model was employed for the journal's development, incorporating feedback from experts and users. Likert scales and Cohen’s D analysis were used to evaluate satisfaction, usability, and impact. Results showed that 90.1% of students expressed high satisfaction with the journal’s accessibility, interactivity, and capacity to enhance self-awareness and motivation. A pre-test and post-test conducted on the intervention group revealed a significant reduction in Impostor Syndrome by 42.5%, with an effect size of 2.84, categorized as "very large." Features such as the self-acknowledgement worksheets helped students recognize their strengths, while AI consultations offered additional psychological support. Expert validation emphasized the journal’s clarity, relevance, and objectivity, noting the absence of bias in AI-driven suggestions. The journal was praised for its accurate content, ease of use, interactivity, and the protection of user data, ensuring a safe and private environment for self-development. Students found the journal beneficial not only for addressing Impostor Syndrome but also for fostering personal growth and self-confidence. This research demonstrates the potential of combining psychological theories with AI-driven tools in education. The journal “I am Great Because of Me” effectively aids students in overcoming Impostor Syndrome and improving self-perception. It serves as a scalable solution for schools and individuals aiming to tackle similar psychological challenges. Future studies are encouraged to explore its application in broader contexts to maximize its impact.

非牛頓流體於地下結構中的減震效果與減震裝置探討 The damping action and the effective damping structure of the non Newtonian fluid in the gap between basement wall and diaphragm wall

本研究探討臺灣常見的鋼筋華廈、鋼筋及鋼骨大樓,透過於地下室外牆與連續壁間填入非牛頓流體、牛頓流體及輕黏土,比較建物受震時加速度,發現地下結構中設置非牛頓流體減震裝置較牛頓流體、輕黏土更減震。而模擬器搖晃20-50秒時,非牛頓流體能顯著的減震,超過50秒後,非牛頓流體可能因沉澱而減震效果下降;在100秒後,無減震裝置的建築加速度上升,非牛頓流體再次出現明顯的減震效果;不同重心的建築質量分布導致不同的擴溶現象,使減震效果發生變化;較高的建物因力臂較長,重心高時產生較大的加速度。接著觀察光穿透吉利丁凍的偏折情形,發現受力面與地震方向垂直時,牆面受力明顯;若受力面和搖晃方向不垂直,柱的部分受力大,且觀察到力量有轉移的現象。最後,為建築設計超聲波測距模組,即時監測建築下陷或傾斜情形,以利即時修繕及重建。

Eradicating Cystic Fibrosis Biofilms by a Novel Non-Toxic, Multi-Pathway Salicylate Therapy

1.1. Cystic Fibrosis Biofilms Biofilms are bacterial aggregates in a matrix of polysaccharides, proteins and nucleic acids (Donlan, 2002). They account for 80% of all chronic infections and cause over 500,000 deaths annually. Cystic fibrosis (CF) is a genetic disorder characterized by mucus accumulation in the respiratory tracts (Morrison et al., 2020). This impairs mucociliary clearance, allowing chronic colonization by bacterial biofilms, leading to fatal respiratory failure, lung scarring, and necrosis of pulmonary epithelial tissues (Martin et al., 2021). 1.2. Obstacles in Current Treatments Three major therapies are used against CF biofilms: (1) aminoglycoside antibiotics like tobramycin, (2)non-aminoglycoside antibiotics such as ciprofloxacin and vancomycin, and (3) non-antibiotic therapies including flushing, chlorination, and ultraviolet disinfection. These have two major flaws. First, they are cytotoxic; 30% of patients experience acute kidney injury after three days of intravenous aminoglycoside therapy (Joyce et al., 2017). Furthermore, non-aminoglycoside therapies can cause phospholipid buildup in lysosomes of proximal tubule epithelial cells, accounting for 10-20% of acute renal failure cases. Second, antibiotic resistance due to horizontal gene transfer and mutations has significantly reduced treatment effectiveness. Therefore, cystic fibrosis biofilms remain a critical threat with few effective treatments. 1.3. Salicylate Derivatives This project tackled this issue using an innovative non-antibiotic approach with salicylate derivatives. Salicylates, a class of benzoic acids—benzene-based carboxylic acids (Figure 1)—used in painkillers and blood thinners, were investigated for their antibiofilm potential through a 3-step process: 1. Literature review: Identified three key biofilm therapeutic targets: quorum sensing, bacterial adhesion, and cell motility. Disrupting these pathways would result in biofilm eradication. 2. Molecule Identification: Recognized key molecules in each pathway: LasR, adhesins, and flagellin. Inhibiting these molecules would disrupt the pathways. 3. Screening: Found that salicylates could inhibit the identified molecules, though they had never been tested against cystic fibrosis biofilms.