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中性电解水与常用局部抗菌剂对全层烧伤愈合的疗效:小鼠模型的临床前试验

Efficacy of neutral electrolyzed water vs. common topical antiseptics in the healing of full‑thickness burn: Preclinical trial in a mouse model.

作者信息

Delgado-Enciso Ivan, Aurelien-Cabezas Nomely S, Meza-Robles Carmen, Walle-Guillen Mireya, Hernandez-Fuentes Gustavo A, Cabrera-Licona Ariana, Hernandez-Rangel Alejandra E, Delgado-Machuca Marina, Rodriguez-Hernandez Alejandrina, Beas-Guzman Oscar F, Cardenas-Aguilar Citlaly B, Rodriguez-Sanchez Iram P, Martinez-Fierro Margarita L, Chaviano-Conesa Daniel, Paz-Michel Brenda A

机构信息

Department of Molecular Medicine, School of Medicine, University of Colima, Colima 28040, Mexico.

Department of Research, State Cancerology Institute of Colima, Health Services of The Mexican Social Security Institute for Welfare (IMSS-BIENESTAR Colima), Colima 28085, Mexico.

出版信息

Biomed Rep. 2024 Oct 10;21(6):189. doi: 10.3892/br.2024.1877. eCollection 2024 Dec.

DOI:10.3892/br.2024.1877
PMID:39479362
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11522847/
Abstract

Burn injuries impose challenges such as infection risk, pain management, fluid loss, electrolyte imbalance and psychological and emotional impact, on healthcare professionals, requiring effective treatments to enhance wound healing. The present study evaluated the efficacy superoxidized electrolyzed solution (SES), with low (SES-low) or high (SES-high) concentrations of active species, alone or in combination with a formulation in gel (G), in comparison with commonly prescribed treatments for burn injury, including nitrofurazone (NF) and silver sulfadiazine (S); normal saline was used as placebo (PI). A scald burn model was established in BALB/c mice. Measurements of the burned area and histological parameters such as inflammatory infiltration state, epithelial regeneration and collagen fibers were evaluated on days 3, 6, 9, 18 and 32 to assess healing score and status. All treatments achieved wound closure at day 32; histopathological parameters indicated that SES-low and SES-low + G performed better than the Pl and S groups (P<0.05). All treatments showed a lower count of inflammatory cells compared with S (P<0.05); for collagen deposition and orientation, SES-low + G showed a more uniform horizontal orientation compared with Pl, SES-high + G, NF and S groups (P<0.05). SES-Low was the most effective substance to induce favorable and organized healing, while S was the worst, inducing disorganized closure of the wound due to a pro-inflammatory effect.

摘要

烧伤会给医护人员带来诸多挑战,如感染风险、疼痛管理、体液流失、电解质失衡以及心理和情绪影响等,这就需要有效的治疗方法来促进伤口愈合。本研究评估了低浓度(低浓度超氧化电解溶液,SES-low)或高浓度(高浓度超氧化电解溶液,SES-high)活性成分的超氧化电解溶液单独使用或与凝胶制剂(G)联合使用的疗效,并与烧伤常用治疗药物,包括呋喃西林(NF)和磺胺嘧啶银(S)进行比较;生理盐水用作安慰剂(PI)。在BALB/c小鼠中建立烫伤模型。在第3、6、9、18和32天评估烧伤面积以及炎症浸润状态、上皮再生和胶原纤维等组织学参数,以评估愈合评分和状态。所有治疗在第32天均实现伤口闭合;组织病理学参数表明,SES-low和SES-low + G的表现优于PI组和S组(P<0.05)。与S组相比,所有治疗组的炎症细胞计数均较低(P<0.05);对于胶原沉积和排列,与PI组、SES-high + G组、NF组和S组相比,SES-low + G组呈现出更均匀的水平排列(P<0.05)。SES-Low是诱导良好且有序愈合的最有效物质,而S是最差的,因其促炎作用导致伤口愈合紊乱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/fb79f7f81db3/br-21-06-01877-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/a5fa5aedc844/br-21-06-01877-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/19b06671b4b9/br-21-06-01877-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/b6590026fd72/br-21-06-01877-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/7422353c70b0/br-21-06-01877-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/a8ccaf865973/br-21-06-01877-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/ed58c80e09eb/br-21-06-01877-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/7ad3631f9f84/br-21-06-01877-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/fb79f7f81db3/br-21-06-01877-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/a5fa5aedc844/br-21-06-01877-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/19b06671b4b9/br-21-06-01877-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/b6590026fd72/br-21-06-01877-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/7422353c70b0/br-21-06-01877-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/a8ccaf865973/br-21-06-01877-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/ed58c80e09eb/br-21-06-01877-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/7ad3631f9f84/br-21-06-01877-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b4/11522847/fb79f7f81db3/br-21-06-01877-g07.jpg

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