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基于细菌纤维素的材料作为伤口愈合敷料

Bacterial Cellulose-Based Materials as Dressings for Wound Healing.

作者信息

Horue Manuel, Silva Jhonatan Miguel, Berti Ignacio Rivero, Brandão Larissa Reis, Barud Hernane da Silva, Castro Guillermo R

机构信息

Laboratorio de Nanobiomateriales, CINDEFI, Departamento de Química, Facultad de Ciencias Exactas, Universidad Nacional de La Plata (UNLP)-CONICET (CCT La Plata), Calle 47 y 115, La Plata B1900, Argentina.

Biopolymers and Biomaterials Laboratory-BioPolMat, University of Araraquara-UNIARA, Araraquara 14801-320, SP, Brazil.

出版信息

Pharmaceutics. 2023 Jan 27;15(2):424. doi: 10.3390/pharmaceutics15020424.

Abstract

Bacterial cellulose (BC) is produced by several microorganisms as extracellular structures and can be modified by various physicochemical and biological strategies to produce different cellulosic formats. The main advantages of BC for biomedical applications can be summarized thus: easy moldability, purification, and scalability; high biocompatibility; and straightforward tailoring. The presence of a high amount of free hydroxyl residues, linked with water and nanoporous morphology, makes BC polymer an ideal candidate for wound healing. In this frame, acute and chronic wounds, associated with prevalent pathologies, were addressed to find adequate therapeutic strategies. Hence, the main characteristics of different BC structures-such as membranes and films, fibrous and spheroidal, nanocrystals and nanofibers, and different BC blends, as well as recent advances in BC composites with alginate, collagen, chitosan, silk sericin, and some miscellaneous blends-are reported in detail. Moreover, the development of novel antimicrobial BC and drug delivery systems are discussed.

摘要

细菌纤维素(BC)由多种微生物作为细胞外结构产生,并且可以通过各种物理化学和生物学策略进行修饰,以产生不同的纤维素形式。BC在生物医学应用中的主要优点可总结如下:易于成型、纯化和扩大规模;高生物相容性;以及易于定制。大量与水相连的游离羟基残基的存在以及纳米多孔形态,使BC聚合物成为伤口愈合的理想候选材料。在此框架下,针对与常见病症相关的急性和慢性伤口,寻求适当的治疗策略。因此,详细报道了不同BC结构的主要特性,如膜和薄膜、纤维状和球状、纳米晶体和纳米纤维,以及不同的BC共混物,以及BC与藻酸盐、胶原蛋白、壳聚糖、丝胶蛋白的复合材料和一些其他共混物的最新进展。此外,还讨论了新型抗菌BC和药物递送系统的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16bb/9963514/d92114959559/pharmaceutics-15-00424-g001.jpg

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