跳转至内容
Merck
CN

Cartilage repair: 2013 Asian update.

Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association (2013-11-30)
James H P Hui, Deepak Goyal, Norimasa Nakamura, Mitsuo Ochi
摘要

Despite financial and regulatory hurdles, Asian scientists and clinicians have made important contributions in the area of cartilage repair. Because it is impossible to include observations on all the published articles in one review, our attempt is to highlight Asian progress in this area during recent years (2005 to the present), reviewing research development and clinical studies. In the former, our discussion of in vitro studies focuses on (1) potential sources of stem cells--such as mesenchymal stem cells (MSCs) from marrow, cord blood, synovium, and mobilized peripheral blood--which are capable of enhancing cartilage repair and (2) the use of growth factors and scaffolds with and without cells. Our discussion of animal studies attempts to summarize activities in evaluating surgical procedures and determining the route of cell administration, as well as studies on matrices and scaffolds. It ranges from the use of small animals such as rats and rabbits to larger animals like pigs and dogs. The local adherent technique, enhancement of microfracture with poly(l-lactic-co-glycolic acid) scaffold, adenovirus-mediated bone morphogenic protein (BMP) genes, and MSCs--whether they are magnetically labeled, suspended in hyaluronic acid, or immobilized with transforming growth factor-β (TGF-β)--have all been able to engineer a repair of the osteochondral defect. Although published Asian reports of clinical studies on cartilage repair are few, the findings of relevant trials are summarized in our discussion of these investigations. There has been a long history of use of laboratory-derived MSCs for cartilage repair. Recent progress has suggested the potential utility of cord blood and mobilized peripheral blood in this area, as well as more injectable bone marrow (BM)-derived stem cells. Finally, we make a few suggestions on the direction of research and development activities and the need for collaborative approaches by regulatory agencies.

材料
产品编号
品牌
产品描述

Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, bacterial glycosaminoglycan polysaccharide
Sigma-Aldrich
乳酸, meets USP testing specifications
Sigma-Aldrich
乳酸, 88%, FCC
Sigma-Aldrich
聚乳酸, Mw ~60,000
Sigma-Aldrich
乳酸, natural, ≥85%
Sigma-Aldrich
乳酸 溶液, ACS reagent, ≥85%
Sigma-Aldrich
透明质酸 钠盐 来源于公鸡鸡冠, avian glycosaminoglycan polysaccharide
Sigma-Aldrich
DL-乳酸, ~90% (T)
Supelco
乳酸, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
透明质酸 钠盐 来源于牛玻璃体液
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 8,000-15,000
透明质酸钠, BRP, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
DL-乳酸, 85 % (w/w), syrup
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 1,000,000-1,250,000
Sigma-Aldrich
透明质酸 钠盐 来源于兽疫链球菌, bacterial glycosaminoglycan polysaccharide
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 1,500,000-1,750,000
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 30,000-50,000
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 2,000,000-2,400,000
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 1,200
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 300,000-500,000
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 10,000-30,000
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 2,000,000-2,200,000
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 50,000-90,000
Sigma-Aldrich
透明质酸 钠盐 来源于马链球菌, mol wt 15,000-30,000