Masaki Takahisa, Rathi Ramesh, Zentner Gaylen, Leypoldt John K, Mohammad Syed F, Burns Gregory L, Li Li, Zhuplatov Sergey, Chirananthavat Thanit, Kim Seung-Jung, Kern Steven, Holman John, Kim Sung Wan, Cheung Alfred K
Departments of Medicine, Bioengineering, Pathology, Pharmaceutics, and Surgery, and Animal Resource Center, University of Utah, Salt Lake City, Utah, USA.
Kidney Int. 2004 Nov;66(5):2061-9. doi: 10.1111/j.1523-1755.2004.00985.x.
Neointimal hyperplasia occurs commonly at the anastomoses of arteriovenous grafts for chronic hemodialysis, causing stenosis and occlusion. Antiproliferative drugs may be effective in inhibiting hyperplasia, but local drug delivery would be required to minimize systemic side effects. We examined the feasibility of local drug delivery to inhibit neointimal hyperplasia at dialysis grafts in a canine model.
Bilateral polytetrafluoroethylene loop grafts (10-cm length and 6-mm internal diameter) were placed between the femoral artery and ipsilateral femoral vein of five mongrel dogs. At the time of surgery or 1 to 5 weeks later, 2 mL of a thermosensitive biodegradable copolymer (ReGel) mixed with 0.26 mg or 0.65 mg paclitaxel were applied to the external surface of one graft around the anastomoses to provide a depot for sustained release of the drug. ReGel alone without paclitaxel was applied to the contralateral graft as a control. The grafts and the connecting vessels were explanted at eight or nine weeks, and the cross-sections were examined histologically. The degree of hyperplasia at the anastomoses was graded by five blinded independent reviewers, with scores ranging from 0 to 5.
The median (25th-75th percentile) hyperplasia score of both arterial and venous anastomoses was 1.80 (0.90-3.05) in the grafts treated with ReGel alone, and 0.95 (0.70-1.50) in the grafts treated with ReGel/paclitaxel (N= 8; P < 0.05 by Wilcoxon signed rank test). There were no noticeable localized or systemic complications attributed to the treatments in these animals. Paclitaxel levels in the plasma obtained from forelimb veins were undetectable (<10 ng/mL).
These results suggest that the local delivery of antiproliferative agents using a thermosensitive, injectable biodegradable copolymer (ReGel) for sustained delivery is a promising strategy to inhibit neointimal hyperplasia of arteriovenous hemodialysis grafts.
内膜增生常见于慢性血液透析的动静脉移植物吻合处,可导致狭窄和闭塞。抗增殖药物可能有效抑制增生,但需要局部给药以尽量减少全身副作用。我们在犬模型中研究了局部给药抑制透析移植物内膜增生的可行性。
在5只杂种犬的股动脉和同侧股静脉之间植入双侧聚四氟乙烯环行移植物(长度10 cm,内径6 mm)。在手术时或1至5周后,将2 mL与0.26 mg或0.65 mg紫杉醇混合的热敏性可生物降解共聚物(ReGel)应用于一个移植物吻合口周围的外表面,以提供药物缓释库。将不含紫杉醇的单纯ReGel应用于对侧移植物作为对照。在8或9周时取出移植物和连接血管,进行组织学检查。由5名不知情的独立评审员对吻合处的增生程度进行分级,分数范围为0至5。
单纯用ReGel处理的移植物中,动脉和静脉吻合处增生评分的中位数(第25-75百分位数)为1.80(0.90-3.05),而用ReGel/紫杉醇处理的移植物中为0.95(0.70-1.50)(N = 8;Wilcoxon符号秩检验,P < 0.05)。这些动物中没有因治疗引起的明显局部或全身并发症。从前肢静脉采集的血浆中未检测到紫杉醇水平(<10 ng/mL)。
这些结果表明,使用热敏性、可注射的可生物降解共聚物(ReGel)进行抗增殖药物的局部给药以实现持续释放,是抑制动静脉血液透析移植物内膜增生的一种有前景的策略。