Lili Tian, Taishan Liu, Yingxue Jiang, Bingyu He, Hong Hao
{"title":"更正:\"多功能水凝胶传感器具有坚韧、自愈能力和高灵敏度,可用于运动监测和伤口愈合\" [Chem. Eng. J. 497 (2024) 154890]","authors":"Lili Tian, Taishan Liu, Yingxue Jiang, Bingyu He, Hong Hao","doi":"10.1016/j.cej.2025.161900","DOIUrl":null,"url":null,"abstract":"The authors regret they found an error in <span><span>Fig. 5</span></span>e and <span><span>Fig. 6</span></span>g. The green channel in <span><span>Fig. 5</span></span>e, f should be labeled as CD68 instead of CD86, and we mistakenly used the MHPBA-GO group images in <span><span>Figs. 5</span></span>e and <span><span>6</span></span>e. This error was caused by confusion in folder naming during image classification. We have attached the correct MHPBA-GO group images in <span><span>Figs. 5</span></span>e and <span><span>6</span></span>g. The fluorescence images in <span><span>Figs. 5</span></span>e and <span><span>6</span></span>g are intended to semi-quantitatively highlight the differences in INOS and CD31 positivity between different groups. The INOS and CD31 positivity of the MHPBA-GO group in <span><span>Figs. 5</span></span>e and <span><span>6</span></span>g was originally calculated based on the images of the MHPBA-GO group, and the results remain unchanged. This correction does not affect the conclusions of this paper. We sincerely apologize for the inconvenience caused and hope to correct this error by providing the corrected <span><span>Figs. 5</span></span>e and <span><span>6</span></span>g.<figure><span><img alt=\"\" aria-describedby=\"cn0005\" height=\"596\" src=\"https://ars.els-cdn.com/content/image/1-s2.0-S1385894725027263-gr1.jpg\"/><ol><li><span><span>Download: <span>Download high-res image (1MB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span><span><span><p><span>Fig. 5</span>. Cytocompatibility, antimicrobial, and anti-inflammatory of MHPBA-GO hydrogels. (a) Cell viability in the control, HPBA, and MHPBA-GO groups (n = 3). (b) Live/Dead staining of L929 cells after being treated with MHPBA-GO hydrogels for 1, 2, and 3 days, respectively, scale bar: 100 µm. (c) Images of survival bacteria (<em>E. coli</em> and S. aureus) clones on culture plates after contact with the control, HPBA, MHPBA-GO, and MHPBA-GO Laser groups respectively (n = 3). (d) Bacterial viability in control, HPBA, MHPBA-GO, and MHPBA-GO Laser groups (n = 3) against <em>E. coli</em> and <em>S. aureus</em>. (e) Fluorescence images and (g) quantitative analysis of INOS after treatment with DHE (n = 3). (f) Fluorescence images and (h) quantitative analysis of CD206 after treatment with DHE (n = 3). (i) Quantitative analysis of the M2/M1 ratio. The scale bar in e and f is 50 μm. INOS (red): M1 macrophages, CD206 (red): M2 macrophages and nuclei were stained with DAPI (blue), data are shown as mean ± SD (n = 3). *p < 0.05, **p < 0.01, ***p < 0.001.</p></span></span></figure><figure><span><img alt=\"\" aria-describedby=\"cn0010\" height=\"577\" src=\"https://ars.els-cdn.com/content/image/1-s2.0-S1385894725027263-gr2.jpg\"/><ol><li><span><span>Download: <span>Download high-res image (1MB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span><span><span><p><span>Fig. 6</span>. In vivo diabetic wound healing assessment of multifunctional MHPBA-GO hydrogels. (a) Treatment schedule of diabetic wounds treated by different hydrogels. (b) Images of diabetic wounds at different times. (c) Simulate wound healing traces. (d) Quantitative analysis of the wound area (n = 4). (e) H&E staining of trauma tissue in different groups. (f) MT images of wound tissues. (g) Fluorescence images and (k) quantitative analysis of the relative coverage area of CD31 for different groups. (h) Fluorescence images and (l) quantitative analysis of ROS scavenging. (i) Epidermis thickness in different groups on day 10. (j) Collagen deposition in all groups based on MT staining. The scale bar in e, f, g, and h is 50 μm. Data are shown as mean ± SD (n = 3). *p < 0.05, **p < 0.01, ***p < 0.001.</p></span></span></figure>","PeriodicalId":270,"journal":{"name":"Chemical Engineering Journal","volume":"104 1","pages":""},"PeriodicalIF":13.3000,"publicationDate":"2025-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Corrigendum to “Multifunctional hydrogel sensor with Tough, self-healing capabilities and highly sensitive for motion monitoring and wound healing” [Chem. Eng. J. 497 (2024) 154890]\",\"authors\":\"Lili Tian, Taishan Liu, Yingxue Jiang, Bingyu He, Hong Hao\",\"doi\":\"10.1016/j.cej.2025.161900\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The authors regret they found an error in <span><span>Fig. 5</span></span>e and <span><span>Fig. 6</span></span>g. The green channel in <span><span>Fig. 5</span></span>e, f should be labeled as CD68 instead of CD86, and we mistakenly used the MHPBA-GO group images in <span><span>Figs. 5</span></span>e and <span><span>6</span></span>e. This error was caused by confusion in folder naming during image classification. We have attached the correct MHPBA-GO group images in <span><span>Figs. 5</span></span>e and <span><span>6</span></span>g. The fluorescence images in <span><span>Figs. 5</span></span>e and <span><span>6</span></span>g are intended to semi-quantitatively highlight the differences in INOS and CD31 positivity between different groups. The INOS and CD31 positivity of the MHPBA-GO group in <span><span>Figs. 5</span></span>e and <span><span>6</span></span>g was originally calculated based on the images of the MHPBA-GO group, and the results remain unchanged. This correction does not affect the conclusions of this paper. We sincerely apologize for the inconvenience caused and hope to correct this error by providing the corrected <span><span>Figs. 5</span></span>e and <span><span>6</span></span>g.<figure><span><img alt=\\\"\\\" aria-describedby=\\\"cn0005\\\" height=\\\"596\\\" src=\\\"https://ars.els-cdn.com/content/image/1-s2.0-S1385894725027263-gr1.jpg\\\"/><ol><li><span><span>Download: <span>Download high-res image (1MB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span><span><span><p><span>Fig. 5</span>. Cytocompatibility, antimicrobial, and anti-inflammatory of MHPBA-GO hydrogels. (a) Cell viability in the control, HPBA, and MHPBA-GO groups (n = 3). (b) Live/Dead staining of L929 cells after being treated with MHPBA-GO hydrogels for 1, 2, and 3 days, respectively, scale bar: 100 µm. (c) Images of survival bacteria (<em>E. coli</em> and S. aureus) clones on culture plates after contact with the control, HPBA, MHPBA-GO, and MHPBA-GO Laser groups respectively (n = 3). (d) Bacterial viability in control, HPBA, MHPBA-GO, and MHPBA-GO Laser groups (n = 3) against <em>E. coli</em> and <em>S. aureus</em>. (e) Fluorescence images and (g) quantitative analysis of INOS after treatment with DHE (n = 3). (f) Fluorescence images and (h) quantitative analysis of CD206 after treatment with DHE (n = 3). (i) Quantitative analysis of the M2/M1 ratio. The scale bar in e and f is 50 μm. INOS (red): M1 macrophages, CD206 (red): M2 macrophages and nuclei were stained with DAPI (blue), data are shown as mean ± SD (n = 3). *p < 0.05, **p < 0.01, ***p < 0.001.</p></span></span></figure><figure><span><img alt=\\\"\\\" aria-describedby=\\\"cn0010\\\" height=\\\"577\\\" src=\\\"https://ars.els-cdn.com/content/image/1-s2.0-S1385894725027263-gr2.jpg\\\"/><ol><li><span><span>Download: <span>Download high-res image (1MB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span><span><span><p><span>Fig. 6</span>. In vivo diabetic wound healing assessment of multifunctional MHPBA-GO hydrogels. (a) Treatment schedule of diabetic wounds treated by different hydrogels. (b) Images of diabetic wounds at different times. (c) Simulate wound healing traces. (d) Quantitative analysis of the wound area (n = 4). (e) H&E staining of trauma tissue in different groups. (f) MT images of wound tissues. (g) Fluorescence images and (k) quantitative analysis of the relative coverage area of CD31 for different groups. (h) Fluorescence images and (l) quantitative analysis of ROS scavenging. (i) Epidermis thickness in different groups on day 10. (j) Collagen deposition in all groups based on MT staining. The scale bar in e, f, g, and h is 50 μm. Data are shown as mean ± SD (n = 3). *p < 0.05, **p < 0.01, ***p < 0.001.</p></span></span></figure>\",\"PeriodicalId\":270,\"journal\":{\"name\":\"Chemical Engineering Journal\",\"volume\":\"104 1\",\"pages\":\"\"},\"PeriodicalIF\":13.3000,\"publicationDate\":\"2025-04-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Engineering Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1016/j.cej.2025.161900\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.cej.2025.161900","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
Corrigendum to “Multifunctional hydrogel sensor with Tough, self-healing capabilities and highly sensitive for motion monitoring and wound healing” [Chem. Eng. J. 497 (2024) 154890]
The authors regret they found an error in Fig. 5e and Fig. 6g. The green channel in Fig. 5e, f should be labeled as CD68 instead of CD86, and we mistakenly used the MHPBA-GO group images in Figs. 5e and 6e. This error was caused by confusion in folder naming during image classification. We have attached the correct MHPBA-GO group images in Figs. 5e and 6g. The fluorescence images in Figs. 5e and 6g are intended to semi-quantitatively highlight the differences in INOS and CD31 positivity between different groups. The INOS and CD31 positivity of the MHPBA-GO group in Figs. 5e and 6g was originally calculated based on the images of the MHPBA-GO group, and the results remain unchanged. This correction does not affect the conclusions of this paper. We sincerely apologize for the inconvenience caused and hope to correct this error by providing the corrected Figs. 5e and 6g.
Download: Download high-res image (1MB)
Download: Download full-size image
Fig. 5. Cytocompatibility, antimicrobial, and anti-inflammatory of MHPBA-GO hydrogels. (a) Cell viability in the control, HPBA, and MHPBA-GO groups (n = 3). (b) Live/Dead staining of L929 cells after being treated with MHPBA-GO hydrogels for 1, 2, and 3 days, respectively, scale bar: 100 µm. (c) Images of survival bacteria (E. coli and S. aureus) clones on culture plates after contact with the control, HPBA, MHPBA-GO, and MHPBA-GO Laser groups respectively (n = 3). (d) Bacterial viability in control, HPBA, MHPBA-GO, and MHPBA-GO Laser groups (n = 3) against E. coli and S. aureus. (e) Fluorescence images and (g) quantitative analysis of INOS after treatment with DHE (n = 3). (f) Fluorescence images and (h) quantitative analysis of CD206 after treatment with DHE (n = 3). (i) Quantitative analysis of the M2/M1 ratio. The scale bar in e and f is 50 μm. INOS (red): M1 macrophages, CD206 (red): M2 macrophages and nuclei were stained with DAPI (blue), data are shown as mean ± SD (n = 3). *p < 0.05, **p < 0.01, ***p < 0.001.
Download: Download high-res image (1MB)
Download: Download full-size image
Fig. 6. In vivo diabetic wound healing assessment of multifunctional MHPBA-GO hydrogels. (a) Treatment schedule of diabetic wounds treated by different hydrogels. (b) Images of diabetic wounds at different times. (c) Simulate wound healing traces. (d) Quantitative analysis of the wound area (n = 4). (e) H&E staining of trauma tissue in different groups. (f) MT images of wound tissues. (g) Fluorescence images and (k) quantitative analysis of the relative coverage area of CD31 for different groups. (h) Fluorescence images and (l) quantitative analysis of ROS scavenging. (i) Epidermis thickness in different groups on day 10. (j) Collagen deposition in all groups based on MT staining. The scale bar in e, f, g, and h is 50 μm. Data are shown as mean ± SD (n = 3). *p < 0.05, **p < 0.01, ***p < 0.001.
期刊介绍:
The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.