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透明质酸在泊洛沙姆 F-127/F-108 水凝胶中用于关节成形术后疼痛:对物理化学性质和持续药物释放的结构要求的影响。

Hyaluronic acid in Pluronic F-127/F-108 hydrogels for postoperative pain in arthroplasties: Influence on physico-chemical properties and structural requirements for sustained drug-release.

机构信息

Human and Natural Sciences Center, ABC Federal University, Santo André, SP, Brazil.

Nuclear and Energy Research Institute, São Paulo, SP, Brazil.

出版信息

Int J Biol Macromol. 2018 May;111:1245-1254. doi: 10.1016/j.ijbiomac.2018.01.064. Epub 2018 Jan 12.

DOI:10.1016/j.ijbiomac.2018.01.064
PMID:29339288
Abstract

In this study, we reported the hyaluronic acid (HA) on supramolecular structure of Pluronic F-127 (PLF-127) and/or Pluronic F-108 (PLF-127) hydrogels, as well as their effects on release mechanisms, looking forward their application as lidocaine (LDC) drug-delivery systems in arthroplastic surgeries. We have studied the HA-micelle interaction using Dynamic Light Scattering (DLS), the micellization and sol-gel transition processes by Differential Scanning Calorimetry (DSC) and Rheology., of PL-based hydrogels and. The presence of HA provided the formation of larger micellar dimensions from ~26.0 to 42.4nm. The incorporation of HA did not change the micellization temperatures and stabilized hydrogels rheological properties (G'>G″), showing no interference on PL-thermoreversible properties. Small-Angle-X-ray Scattering (SAXS) patterns revealed that HA incorporation effects were pronounced for PLF-127 and PLF-108 systems, showing transitions from lamellar to hexagonal phase organization (HA-PLF-127) and structural changes from cubic to gyroid and/or cubic to lamellar. The HA insertion effects were also observed on drug release profiles, since lower LDC release constants (K=0.24-0.41mM·h) were observed for HA-PLF-127, that presented a hexagonal phase organization. Furthermore, the HA-PL systems presented reduced in vitro cytotoxic effects, pointed out their tendency to self-assembly and possible application as drug delivery systems.

摘要

在这项研究中,我们报道了透明质酸(HA)对 Pluronic F-127(PLF-127)和/或 Pluronic F-108(PLF-127)水凝胶的超分子结构,以及它们对释放机制的影响,以期将其作为透明质酸(HA)作为关节成形术中的利多卡因(LDC)药物传递系统。我们使用动态光散射(DLS)研究了 HA-胶束相互作用,使用差示扫描量热法(DSC)和流变学研究了 PL 基水凝胶的胶束化和溶胶-凝胶转变过程。PL 基水凝胶的存在提供了更大的胶束尺寸,从~26.0nm 至 42.4nm。HA 的掺入并未改变胶束化温度并稳定了水凝胶的流变性能(G'>G″),表明对 PL-热可逆性质没有干扰。小角 X 射线散射(SAXS)图谱表明,HA 的掺入对 PLF-127 和 PLF-108 体系的影响明显,表现为从层状到六方相组织(HA-PLF-127)的转变,以及从立方到准晶和/或立方到层状的结构变化。HA 的插入效应也观察到在药物释放曲线中,因为对于呈现六方相组织的 HA-PLF-127,观察到较低的 LDC 释放常数(K=0.24-0.41mM·h)。此外,HA-PL 系统表现出降低的体外细胞毒性作用,指出它们的自组装倾向和作为药物传递系统的可能应用。

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