含细胞外基质肽聚合物颗粒治疗杜氏肌营养不良的科技展望。

Livia Alves Filgueiras, Francisco Thiago Bandeira Silva, Francisco das Chagas Alves Lima, Anderson Nogueira Mendes
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引用次数: 0

摘要

杜氏肌营养不良症是一种神经肌肉疾病,总体发病率在1 / 5000新生儿之间。携带者可能表现出进行性肌肉无力,导致骨骼肌进行性变性,产生心脏和呼吸系统疾病。考虑到缺乏有效的治疗方法,已经开发了不同的治疗方法,例如蛋白质合成和细胞外基质衍生物,可用于改善肌肉再生,维持或修复。同时,使用其他抗炎药物或生物制剂替代与这些细胞外基质衍生物结合的皮质类固醇可能更有效地控制杜氏肌营养不良的进展。讨论了细胞外基质衍生多肽(如laminin-111衍生物)和在聚合物颗粒中使用具有抗炎活性的精油用于治疗杜氏肌营养不良的应用。为此,对2012- 2024年LM-111多肽与杜氏肌营养不良的相关专利文献和科学论文进行了综述。许多专利集中在姑息技术,寻求延长疾病的进行性影响,考虑到控制炎症过程。技术和科学前景表明,需要继续研究可以作为治疗营养不良的系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Scientific and Technological Prospecting on Polymeric Particles Containing Extracellular Matrix Peptides for the Treatment of Duchenne Muscular Dystrophy.

Duchenne muscular dystrophy is a neuromuscular disease with an overall incidence of between 1 in 5,000 newborn males. Carriers may manifest progressive muscle weakness, resulting from the progressive degeneration of skeletal muscles, generating cardiac and respiratory disorders. Considering the lack of effective treatments, different therapeutic approaches have been developed, such as protein synthesis and extracellular matrix derivatives that can be used to improve muscle regeneration, maintenance, or repair. At the same time, the use of other anti-inflammatory drugs or biological agents to replace corticosteroids conjugated to these extracellular matrix derivatives may act more effectively in controlling the progression of Duchenne muscular dystrophy. Extracellular matrix-derived peptides (e.g. laminin-111 derivatives) and the use of essential oils with antiinflammatory activity in polymeric particles for application in the treatment of Duchenne muscular dystrophy are discussed. For this purpose, the literature of patents and scientific articles from 2012- 2024 on LM-111 peptides and Duchenne muscular dystrophy was reviewed. Many patents focus on palliative technologies that seek to prolong the progressive effects of the disease, considering the control of the inflammatory process. The technological and scientific prospecting suggests the need for continuous research on systems that can serve as a treatment for Dystrophy.

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