Erdi Metecan, Saruwatari Michele S, Rozyyev Selim, Acha Christopher, Ayyub Omar B, Sandler Anthony D, Kofinas Peter
Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, Maryland 20742, United States.
Sheikh Zayed Institute for Pediatric Surgical Innovation, Joseph E. Robert Jr. Center for Surgical Care, Children's National Medical Center, Washington, District of Columbia 20010, United States.
ACS Appl Mater Interfaces. 2023 Mar 8. doi: 10.1021/acsami.3c00283.
Formation of asymmetric, rigid scar tissue known as surgical adhesions is caused by traumatic disruption of mesothelial-lined surfaces in surgery. A widely adopted prophylactic barrier material (Seprafilm) for the treatment of intra-abdominal adhesions is applied operatively as a pre-dried hydrogel sheet but has reduced translational efficacy due its brittle mechanical properties. Topically administered peritoneal dialysate (Icodextrin) and anti-inflammatory drugs have failed to prevent adhesions due to an uncontrolled release profile. Hence, inclusion of a targeted therapeutic into a solid barrier host matrix with improved mechanical properties could provide dual utility in adhesion prevention and as a surgical sealant. Spray deposition of poly(lactide--caprolactone) (PLCL) polymer fibers through solution blow spinning has yielded a tissue-adherent barrier material with previously reported adhesion prevention efficacy due to a surface erosion mechanism that inhibits deposition of inflamed tissue. However, such an approach uniquely presents an avenue for controlled therapeutic release through mechanisms of diffusion and degradation. Such a rate is kinetically tuned via facile blending of "high" molecular weight (HMW) and "low" molecular weight (LMW) PLCL with slow and fast biodegradation rates, respectively. Here, we explore viscoelastic blends of HMW PLCL (70% w/v) and LMW PLCL (30% w/v) as a host matrix for anti-inflammatory drug delivery. In this work, COG133, an apolipoprotein E (ApoE) mimetic peptide with potent anti-inflammatory properties was selected and tested. studies with PLCL blends presented low (∼30%) and high (∼80%) percent release profiles over a 14-day period based on the nominal molecular weight of the HMW PLCL component. Two independent mouse models of cecal ligation and cecal anastomosis significantly reduced adhesion severity versus Seprafilm, COG133 liquid suspension, and no treatment control. The synergy of physical and chemical methods in a barrier material with proven preclinical studies highlights the value of COG133-loaded PLCL fiber mats in effectively dampening the formation of severe abdominal adhesions.
手术中,间皮衬里表面受到创伤性破坏会导致形成不对称、坚硬的瘢痕组织,即手术粘连。一种广泛应用于治疗腹腔内粘连的预防性屏障材料(Seprafilm),在手术中作为预干燥水凝胶片使用,但由于其脆性机械性能,其转化效果有所降低。局部施用的腹膜透析液(艾考糊精)和抗炎药物由于释放特性无法控制,未能预防粘连。因此,将靶向治疗剂纳入具有改善机械性能的固体屏障宿主基质中,可在预防粘连和作为手术密封剂方面提供双重效用。通过溶液吹纺法喷涂聚(丙交酯-己内酯)(PLCL)聚合物纤维,得到了一种组织粘附性屏障材料,由于其表面侵蚀机制抑制了炎症组织的沉积,此前已报道其具有预防粘连的功效。然而,这种方法独特地提供了一种通过扩散和降解机制进行可控治疗释放的途径。通过分别将具有缓慢和快速生物降解速率的“高”分子量(HMW)和“低”分子量(LMW)PLCL进行简单混合,可以对这种速率进行动力学调节。在此,我们探索将HMW PLCL(70% w/v)和LMW PLCL(30% w/v)的粘弹性共混物作为抗炎药物递送的宿主基质。在这项工作中,选择并测试了具有强大抗炎特性的载脂蛋白E(ApoE)模拟肽COG133。基于HMW PLCL组分的标称分子量,对PLCL共混物进行的研究显示,在14天内的释放率分别为低(约30%)和高(约80%)。与Seprafilm、COG133液体悬浮液和未治疗对照相比,两种独立的盲肠结扎和盲肠吻合小鼠模型显著降低了粘连严重程度。屏障材料中物理和化学方法的协同作用以及已证实的临床前研究突出了负载COG133的PLCL纤维垫在有效抑制严重腹部粘连形成方面的价值。