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评价透明质酸及其片段的物理和生物学特性。

Evaluation of the physical and biological properties of hyaluronan and hyaluronan fragments.

机构信息

Wound Biology Group, Tissue Engineering and Reparative Dentistry, School of Dentistry, Cardiff University, Heath Park, Cardiff, CF14 4XY, UK.

出版信息

Int J Pharm. 2011 Nov 25;420(1):84-92. doi: 10.1016/j.ijpharm.2011.08.031. Epub 2011 Aug 22.

DOI:10.1016/j.ijpharm.2011.08.031
PMID:21884772
Abstract

Hyaluronan (HA) has been extensively used for various medical applications, including osteoarthritis, tissue augmentation and ocular surgery. More recently, it has been investigated for use in polymer therapeutics as a carrier for drugs and biologically active proteins, thanks to its biodegradability, biocompatibility and inherent biological properties. Such biological functions are strongly dependent on HA's chain length, yet the molecular weight of HAs used in polymer conjugates varies widely and is inconsistent with its intended application. Therefore, this study aimed to determine the ideal chain length of HA to be used in polymer conjugates for enhanced tissue repair. HA fragments (M(w) 45,000-900,000g/mol) were prepared by acid hydrolysis of rooster comb HA and their physicochemical and biological properties were characterized. Such HA fragments had a highly extended, almost rod-like solution conformation and demonstrated chain length- and concentration-dependent viscosity, while exposure to HAase caused a rapid reduction in HA viscosity, which was most significant for the native HA. Initial HA hydrolysis rate by HAase varied strongly with HA chain length and was dependent on the formation of a stable enzyme-substrate complex. When normal human dermal fibroblasts were exposed to the different HA fragments for 72h, only native (900,000g/mol) HA reduced proliferation at 1000μg/mL. Conversely, only the smallest HA fragment (70,000g/mol) reduced the proliferation of chronic wound fibroblasts, at 1000μg/mL. The 70,000g/mol HA fragment also promoted the greatest cell attachment. These observations demonstrate that low molecular weight (70,000-120,000g/mol) HA fragments would be best suited for the delivery of proteins and peptides with applications in chronic wound healing and paves the way for the rationalized development of novel HA conjugates.

摘要

透明质酸(HA)已广泛应用于各种医学领域,包括骨关节炎、组织填充和眼科手术。最近,由于其可生物降解性、生物相容性和固有生物学特性,它被研究用于聚合物治疗学作为药物和生物活性蛋白的载体。这种生物学功能强烈依赖于 HA 的链长,但是用于聚合物缀合物的 HA 的分子量变化很大,与其预期的应用不一致。因此,本研究旨在确定用于聚合物缀合物以增强组织修复的理想 HA 链长。通过酸水解鸡冠 HA 制备 HA 片段(M(w)45,000-900,000g/mol),并对其理化和生物学性质进行了表征。这些 HA 片段具有高度伸展的、几乎棒状的溶液构象,表现出链长和浓度依赖性的粘度,而暴露于 HAase 会导致 HA 粘度迅速降低,对于天然 HA 最为显著。HAase 对不同 HA 片段的初始水解速率与 HA 链长强烈相关,并且依赖于稳定的酶-底物复合物的形成。当正常的人真皮成纤维细胞暴露于不同的 HA 片段 72h 时,只有天然(900,000g/mol)HA 在 1000μg/mL 时降低增殖。相反,只有最小的 HA 片段(70,000g/mol)在 1000μg/mL 时降低慢性伤口成纤维细胞的增殖。70,000g/mol 的 HA 片段还促进了最大的细胞附着。这些观察结果表明,低分子量(70,000-120,000g/mol)HA 片段最适合用于蛋白质和肽的递送,在慢性伤口愈合中有应用前景,并为新型 HA 缀合物的合理化发展铺平了道路。

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