Department of Plastic Surgery, R. G. Kar Medical College and Hospital (RGKMCH), Kolkata 700004, India.
Mater Sci Eng C Mater Biol Appl. 2013 Oct;33(7):3986-93. doi: 10.1016/j.msec.2013.05.036. Epub 2013 May 25.
Chronic osteomyelitis is a challenging setback to the orthopedic surgeons in deciding an optimal therapeutic strategy. Conversely, patients feel frustrated of the therapeutic outcomes and development of adverse drug effects, if any. Present investigation deals with extensive approach incorporating in vivo animal experimentation and human application to treat chronic osteomyelitis, using antibiotic loaded porous hydroxyapatite scaffolds. Micro- to macro-porous hydroxyapatite scaffolds impregnated with antibiotic ceftriaxone-sulbactam sodium (CFS) were fabricated and subsequently evaluated by in vivo animal model after developing osteomyelitis in rabbit tibia. Finally 10 nos. of human osteomyelitis patients involving long bone and mandible were studied for histopathology, radiology, pus culture, 3D CT etc. up to 8-18 months post-operatively. It was established up to animal trial stage that 50N50H samples [with 50-55% porosity, average pore size 110 μm, higher interconnectivity (10-100 μm), and moderately high drug adsorption efficiency (50%)] showed efficient drug release up to 42 days than parenteral group based on infection eradication and new bone formation. In vivo human bone showed gradual evidence of new bone formation and fracture union with organized callus without recurrence of infection even after 8 months. This may be a new, alternative, cost effective and ideal therapeutic strategy for chronic osteomyelitis treatment in human patients.
慢性骨髓炎是骨科医生在决定最佳治疗策略时面临的一个具有挑战性的难题。相反,如果出现治疗效果不佳和药物不良反应,患者会感到沮丧。本研究采用广泛的方法,结合体内动物实验和人类应用,使用载抗生素的多孔羟磷灰石支架治疗慢性骨髓炎。制备了载抗生素头孢曲松-舒巴坦钠(CFS)的微孔到宏孔羟磷灰石支架,并在兔胫骨骨髓炎模型中进行了体内评估。最后,对 10 例涉及长骨和下颌骨的慢性骨髓炎患者进行了组织病理学、放射学、脓液培养、3D CT 等检查,术后随访 8-18 个月。在动物试验阶段证实,50N50H 样本(孔隙率为 50-55%,平均孔径为 110μm,较高的连通性(10-100μm)和中等的药物吸附效率(50%))在 42 天内比静脉注射组更有效地释放药物,从而实现了感染的消除和新骨的形成。体内人骨显示出新骨形成和骨折愈合的逐渐证据,形成有组织的骨痂,没有感染复发,即使在 8 个月后也是如此。这可能是一种新的、替代的、具有成本效益的、理想的慢性骨髓炎治疗策略,适用于人类患者。