Scar management in burn injuries using drug delivery and molecular signaling: Current treatments and future directions

被引:98
|
作者
Amini-Nik, Saeid [2 ,4 ]
Yousuf, Yusef [1 ,2 ,3 ]
Jeschke, Marc G. [1 ,2 ,4 ,5 ,6 ]
机构
[1] Univ Toronto, Inst Med Sci, Toronto, ON, Canada
[2] Sunnybrook Res Inst, Toronto, ON, Canada
[3] Univ Toronto, Lab Med & Pathobiol, Toronto, ON, Canada
[4] Univ Toronto, Div Plast Surg, Dept Surg, Toronto, ON, Canada
[5] Univ Toronto, Dept Immunol, Toronto, ON, Canada
[6] Sunnybrook Hlth Sci Ctr, Ross Tilley Burn Ctr, Toronto, ON, Canada
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
GROWTH-FACTOR-BETA; PULSED-DYE-LASER; WNT/BETA-CATENIN PATHWAY; DEPENDENT TRANSCRIPTIONAL ACTIVATION; FIBROBLAST COLLAGEN-SYNTHESIS; GAMMA-SECRETASE INHIBITOR; IMIQUIMOD 5-PERCENT CREAM; BLACK SOUTH-AFRICANS; NF-KAPPA-B; HYPERTROPHIC SCARS;
D O I
10.1016/j.addr.2017.07.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent decades, there have been tremendous improvements in burn care that have allowed patients to survive severe burn injuries that were once fatal. However, a major limitation of burn care currently is the development of hypertrophic scars in approximately 70% of patients. This significantly decreases the quality of life for patients due to the physical and psychosocial symptoms associated with scarring. Current approaches to manage scarring include surgical techniques and non-surgical methods such as laser therapy, steroid injections, and compression therapy. These treatments are limited in their effectiveness and regularly fail to manage symptoms. As a result, the development of novel treatments that aim to improve outcomes and quality of life is imperative. Drug delivery that targets the molecular cascades of wound healing to attenuate or prevent hypertrophic scarring is a promising approach that has therapeutic potential. In this review, we discuss current treatments for scar management after burn injury, and how drug delivery targeting molecular signaling can lead to new therapeutic strategies. Crown Copyright (C) 2017 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 154
页数:20
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