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Jiemin Qiu,Weihao Ye,Congcong Chen,Zhiqiang Xu,Chaofan Hu,Jianle Zhuang,Hanwu Dong,Bingfu Lei,Guangqi Hu,Yingliang Liu 한국공업화학회 2023 Journal of Industrial and Engineering Chemistry Vol.117 No.-
UV absorbers are sustainable substances that inhibit the ultraviolet (UV) radiative degradation of polymers. In previous reports, the as-prepared carbon dots (CDs) possess only an absorption band at UVA(320–400 nm). To achieve broad-spectrum UV absorption (200–400 nm), increasing the concentrationof the CDs solution becomes common. However, a high concentration solution seriously affects the lighttransmittance due to its heavy yellow color. Furthermore, the promising organic UV absorbers cannotachieve broad-spectrum UV absorption. In this work, we initially synthesized three-component watersolublecarbon dots (OP–CDs), which delivers an excellent UV absorption (98 % UVA and 100 % UVB atthe concentration of 1.7 102 mg/mL; 99 % transmittance in visible light). Moreover, OP–CDs exhibitoutstanding stability at high temperatures and different pH. With the corporation of OP–CDs and polyvinylalcohol (PVA), a high-performance UV-shielding film was formed, leading to enhanced broadspectrumUV shielding performance and improved mechanical properties, resistance of photocatalyticactivity and anti-UV aging ability compared with pure PVA film. Notably, the PVA film remains hightransparency with the addition of OP–CDs. The study suggests that the corporation of OP–CDs and polymersis effective in anti-UV degradation.
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Xinyi Zhu,Tian Tian,Miao Ruan,Jia Rao,Wentao Yang,Xu Cai,Menghong Sun,Guangqi Qin,Zhonghua Zhao,Jiong Wu,Zhimin Shao,Ruohong Shui,Zhen Hu 한국유방암학회 2018 Journal of breast cancer Vol.21 No.3
Purpose: The characteristic expression of DNA damage response proteins in familial breast cancers with BRCA1, BRCA2, or non-BRCA1/2 mutations has not been analyzed in Chinese patients. Our study aimed to assess the differential expression of microcephalin 1 (BRIT1), ATM serine/threonine kinase (ATM), checkpoint kinase 2 (CHEK2), BRCA1, RAD51 recombinase (RAD51), and poly (ADP-ribose) polymerase 1 (PARP-1) and establish the profile of Chinese familial breast cancers with different mutation status. Methods: We constructed five tissue microarrays from 183 familial breast cancer patients (31 with BRCA1 mutations; 14 with BRCA2 mutations, and 138 with non-BRCA1/2 mutations). The DNA response and repair markers used for immunohistochemistry analysis included BRIT1, ATM, CHEK2, BRCA1, RAD51, and PARP-1. The expressions of these proteins were analyzed in BRCA1/2 mutated tumors. The association between pathologic characteristics with BRCA1/2 mutation status was also analyzed. Results: In familial breast cancer patients, BRCA1 mutated tumors were more frequent with high nuclear grade, estrogen receptor/progesterone receptor/human epidermal growth factor receptor 2 negative, low Ki-67, and positive CK5/6. BRCA1 mutated tumors had lower CHEK2 and higher cytoplasmic BRIT1 expression than BRCA2 and non-BRCA1/2 mutation tumors. BRCA2-associated tumors showed higher CHEK2 and cytoplasmic RAD51 expression than those in other groups. Nuclear PARP-1 expression in BRCA1/2-associated tumors was significantly higher than in non-BRCA1/2 mutation tumors. Moreover, we found quite a few of negative PARP-1 expression cases in BRCA1/2 mutated groups. Conclusion: The clinicopathologic findings of BRCA1-associated Chinese familial breast cancers were similar to the results of other studies. Chinese familial breast cancer patients with BRCA1/2 mutations might have distinctive expression of different DNA damage response proteins. The reduced expression of PARP-1 in Chinese BRCA1/2 mutated breast cancer patients could influence the therapeutic outcome of PARP-1 inhibitors.
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