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原位形成壳聚糖植入物负载盐酸雷洛昔芬和生物活性玻璃纳米粒子治疗骨损伤:配方和动物模型中的生物学评价。

In-situ forming chitosan implant-loaded with raloxifene hydrochloride and bioactive glass nanoparticles for treatment of bone injuries: Formulation and biological evaluation in animal model.

机构信息

Egyptian Patent Office, Academy of Scientific Research and Technology, Cairo, Egypt.

Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt.

出版信息

Int J Pharm. 2020 Apr 30;580:119213. doi: 10.1016/j.ijpharm.2020.119213. Epub 2020 Mar 9.

Abstract

In-situ forming implants receive great attention for repairing serious bone injuries. The aim of the present study was to prepare novel chitosan in-situ forming implants (CIFI) loaded with bioactive glass nanoparticles and/or raloxifene hydrochloride (RLX). Incorporating raloxifene hydrochloride (RLX) as a selective estrogen receptor modulator was essential to make use of its anti-resorptive properties. The prepared formulae were tested for their in-vitro gelation time, drug release, injectability, rheological properties, erosion rate and morphological properties. Results revealed that the formulation composed of 1% (w/v) chitosan with 2% (w/v) NaHCO and 1% (w/v) bioactive glass nanoparticles (CIFI-BG) possessed the most sustained drug release profile which extended over four months with low burst release effect compared to the same formulation lacking bioactive glass nanoparticles (CIFI). Selected formulations were tested for their ability to enhance bone regeneration in induced puncture in rate tibia. Results declared that these formulations were able to enhance bone regeneration after 12 weeks in comparison to the untreated tibial punctures and that containing bioactive glass could be considered as novel approach for treatment of serious bone injuries which require long term treatment and internal mechanical bone support during healing.

摘要

原位形成植入物因其可修复严重骨损伤而受到广泛关注。本研究的目的是制备新型壳聚糖原位形成植入物(CIFI),负载生物活性玻璃纳米粒子和/或盐酸雷洛昔芬(RLX)。将盐酸雷洛昔芬(RLX)作为一种选择性雌激素受体调节剂,对于利用其抗吸收特性非常重要。对所制备的配方进行了体外凝胶时间、药物释放、可注射性、流变学特性、侵蚀率和形态特性的测试。结果表明,由 1%(w/v)壳聚糖、2%(w/v)NaHCO 和 1%(w/v)生物活性玻璃纳米粒子组成的配方(CIFI-BG)具有最持久的药物释放曲线,与不含生物活性玻璃纳米粒子的相同配方(CIFI)相比,药物释放时间可延长四个月以上,且突释效应较低。对选定的配方进行了增强诱导性胫骨穿刺部位骨再生能力的测试。结果表明,与未经处理的胫骨穿刺相比,这些配方在 12 周后能够增强骨再生,并且含有生物活性玻璃的配方可以被认为是治疗严重骨损伤的新方法,严重骨损伤需要长期治疗和愈合过程中的内部机械性骨支撑。

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