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用于治疗骨关节炎的粘弹性补充疗法:从最初发现到现状与结果

Viscosupplementation for treatment of osteoarthritis: from initial discovery to current status and results.

作者信息

Balazs Endre A

机构信息

Matrix Biology Institute, Edgewater, New Jersey, USA.

出版信息

Surg Technol Int. 2004;12:278-89.


DOI:
PMID:15455338
Abstract

Viscosupplementation is a therapeutic modality based on the replacement of synovial fluid or exudates with an elastoviscous hyaluronan solution. The first clinical trials were carried out on race horses with painful osteoarthritis of traumatic origin. In the early 1970s, the clinical trials were extended to painful osteoarthritis in humans. Analgesic effects lasting longer than the residence time of the injected hyaluronan in joints were reported both in horses and humans. The hyaluronan used was a noninflammatory fraction of the molecule with an average molecular weight of 2-3 million at a 1% concentration. The analgesic effect of this elastoviscous hyaluronan solution was demonstrated in behavioral animal pain models. Later it was shown that the elastoviscous properties of hyaluronan solutions are the determining factors in reducing pain-elicited nerve activity in both normal and inflamed cat and rat joints. It also was demonstrated in animal arthritis models that elastoviscous hyaluronan solutions promote the healing of traumatic intra-articular wounds. From the mid-1980s, several hyaluronan preparations of greatly varying average molecular weight but with the same concentration were introduced as viscosupplementation-based therapeutic agents. The elastoviscous properties of these solutions varied also, because of the greatly varying average molecular weights (0.5-6.0 million), imitating the rheological properties of either healthy or pathological synovial fluid. Currently, viscosupplementation products available worldwide vary greatly in their elastoviscous properties, and their dosage is not standardized in terms of frequency of injections required or in regard to the removal of exudates before injection. The question of which patient at what stage of the disease responds best with long-lasting pain relief to the many therapeutic products marketed with greatly varying elastoviscous properties has not yet been answered. At the same time, viscosupplementation was introduced, the same highly elastoviscous hyaluronan solutions also were applied in ophthalmic surgery as viscosurgical tools to protect sensitive tissues in the eye during surgery and to be used as soft instruments for tissue manipulation. Modified hyaluronan products (gels) also were introduced for augmentation of the intercellular matrix in tissues (viscoaugmentation) and for separating tissues to prevent adhesions and excessive scar formation (viscoseparation). Hyaluronan and its derivatives (gels) also have been used for drug delivery. The therapeutic use of highly elastoviscous solutions and gels of hyaluronan and its derivatives to build intercellular matrices for supplementation, regeneration, and developing new tissues introduced the concept of matrix engineering into medical practice.

摘要

粘弹性补充疗法是一种基于用弹性粘性透明质酸溶液替代滑液或渗出液的治疗方式。最初的临床试验是在患有创伤性疼痛性骨关节炎的赛马身上进行的。20世纪70年代初,临床试验扩展到人类的疼痛性骨关节炎。在马和人类中都报告了止痛效果持续时间长于注射的透明质酸在关节中的停留时间。所使用的透明质酸是该分子的非炎性部分,浓度为1%时平均分子量为200万至300万。这种弹性粘性透明质酸溶液的止痛作用在动物行为疼痛模型中得到了证实。后来发现,透明质酸溶液的弹性粘性特性是降低正常和发炎的猫和大鼠关节中疼痛引发的神经活动的决定性因素。在动物关节炎模型中也证明,弹性粘性透明质酸溶液可促进创伤性关节内伤口的愈合。从20世纪80年代中期开始,引入了几种平均分子量差异很大但浓度相同的透明质酸制剂作为基于粘弹性补充疗法的治疗药物。由于平均分子量差异很大(0.5万至600万),这些溶液的弹性粘性特性也有所不同,模仿了健康或病理滑液的流变特性。目前,全球可用的粘弹性补充疗法产品在其弹性粘性特性方面差异很大,并且其剂量在所需注射频率或注射前渗出液清除方面尚未标准化。对于许多具有极大不同弹性粘性特性的市售治疗产品,哪种疾病阶段的患者对其反应最佳并能获得持久的疼痛缓解,这个问题尚未得到解答。与此同时,在引入粘弹性补充疗法的同时,同样的高弹性粘性透明质酸溶液也被用作眼科手术中的粘弹剂,以在手术期间保护眼睛中的敏感组织,并用作组织操作的软性器械。改性透明质酸产品(凝胶)也被引入用于增加组织中的细胞间基质(粘弹性增强)以及分离组织以防止粘连和过度瘢痕形成(粘弹性分离)。透明质酸及其衍生物(凝胶)也已用于药物递送。使用高弹性粘性的透明质酸及其衍生物溶液和凝胶来构建细胞间基质以进行补充、再生和开发新组织,将基质工程的概念引入了医学实践。

相似文献

[1]
Viscosupplementation for treatment of osteoarthritis: from initial discovery to current status and results.

Surg Technol Int. 2004

[2]
Viscosupplementation for osteoarthritis.

Am J Orthop (Belle Mead NJ). 2000-2

[3]
Effects of different molecular weight elastoviscous hyaluronan solutions on articular nociceptive afferents.

Arthritis Rheum. 2004-1

[4]
The pathophysiology of osteoarthritis and the implication of the use of hyaluronan and hylan as therapeutic agents in viscosupplementation.

J Rheumatol Suppl. 1993-8

[5]
An analysis of clinical studies of the use of crosslinked hyaluronan, hylan, in the treatment of osteoarthritis.

J Rheumatol Suppl. 1993-8

[6]
Analgesic effect of elastoviscous hyaluronan solutions and the treatment of arthritic pain.

Cells Tissues Organs. 2003

[7]
Intraarticular hyaluronan injections in the treatment of osteoarthritis: state-of-the-art review.

J Rheumatol Suppl. 1993-8

[8]
Viscosupplementation: a new concept in the treatment of osteoarthritis.

J Rheumatol Suppl. 1993-8

[9]
The molecular weight of therapeutic hyaluronan (sodium hyaluronate): how significant is it?

J Rheumatol. 1994-2

[10]
The role of elastoviscosity in the efficacy of viscosupplementation for osteoarthritis of the knee: a comparison of hylan G-F 20 and a lower-molecular-weight hyaluronan.

Clin Ther. 1999-9

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[2]
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Cartilage. 2025-6

[3]
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Pharmaceuticals (Basel). 2023-10-9

[4]
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Adv Exp Med Biol. 2023

[5]
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Cartilage. 2022-12

[6]
Viscosupplementation for knee osteoarthritis: systematic review and meta-analysis.

BMJ. 2022-7-6

[7]
Nanoforming Hyaluronan-Based Thermoresponsive Hydrogels: Optimized and Tunable Functionality in Osteoarthritis Management.

Pharmaceutics. 2022-3-17

[8]
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Nat Rev Rheumatol. 2022-5

[9]
Modulation of hyaluronan signaling as a therapeutic target in human disease.

Pharmacol Ther. 2022-4

[10]
Mechanotransducive Biomimetic Systems for Chondrogenic Differentiation In Vitro.

Int J Mol Sci. 2021-9-7

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