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首页> 外文期刊>Materials science & engineering, C. Materials for Biogical applications >Ceria-containing uncoated and coated hydroxyapatite-based galantamine nanocomposites for formidable treatment of Alzheimer's disease in ovariectomized albino-rat model
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Ceria-containing uncoated and coated hydroxyapatite-based galantamine nanocomposites for formidable treatment of Alzheimer's disease in ovariectomized albino-rat model

机译:含二氧化铈的未涂覆和涂覆的羟基磷灰石基加兰他敏纳米复合材料,在去卵巢白化病大鼠模型中用于阿尔茨海默氏病的强大治疗

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This paper upraises delivery and therapeutic actions of galantamine drug (GAL) against Alzheimer's disease (AD) in rat brain through attaching GAL to ceria-containing hydroxyapatite (GAL@Ce-HAp) as well ceria-containing carboxymethyl chitosan-coated hydroxyapatite (GAL@Ce-HAp/CMC) nanocomposites. Physicochemical features of such nanocomposites were analyzed by XRD, FT-IR, Raman spectroscopy, UV-vis spectrophotometer, N-2-BET, DIS, zeta-potential measurements, SEM, and HR-TEM. Limited interactions were observed in GAL@Ce-HAp with prevailed existence of dispersed negatively charged rod-like particles conjugated with ceria nanodots. On contrary, GAL@Ce-HAp/CMC was well-structured developing aggregates of uncharged tetragonal-shaped particles laden with accession of ceria quantum dots. Such nanocomposites were i.p. injected into ovariectomized AD albino-rats at galantamine dose of 2.5 mg/kg/day for one month, then brain tissues were collected for biochemical and histological tests. GAL@Ce-HAp adopted as a promising candidate for AD curativeness, whereas oxidative stress markers were successfully upregulated, degenerated neurons in hippocampal and cerebral tissues were wholly recovered and A beta-plaques were vanished. Also, optimizable in-vitro release for GAL and nanoceria were displayed from GAL@Ce-HAp, while delayed in-vitro release for those species were developed from GAL@Ce-HAp/CMC. This proof of concept work allow futuristic omnipotency of rod-like hydroxyapatite particles for selective delivery of GAL and nanoceria to AD affected brain areas. (C) 2016 Elsevier B.V. All rights reserved.
机译:本文通过将GAL与含二氧化铈的羟基磷灰石(GAL @ Ce-HAp)以及含二氧化铈的羧甲基壳聚糖包衣的羟基磷灰石(GAL @)结合,提高了加兰他敏药物(GAL)在大鼠脑中对阿尔茨海默病(AD)的递送和治疗作用。 Ce-HAp / CMC)纳米复合材料。通过XRD,FT-IR,拉曼光谱,紫外可见分光光度计,N-2-BET,DIS,ζ电位测量,SEM和HR-TEM分析了此类纳米复合材料的理化特征。在GAL @ Ce-HAp中观察到有限的相互作用,普遍存在与二氧化铈纳米点缀合的分散的带负电的棒状颗粒。相反,GAL @ Ce-HAp / CMC具有良好的结构,可形成带有二氧化铈量子点的不带电四边形颗粒的聚集体。这样的纳米复合材料是ip。加兰他敏剂量为2.5 mg / kg /天,将其注射入卵巢切除的AD白化病大鼠中,持续1个月,然后收集脑组织进行生化和组织学测试。 GAL @ Ce-HAp被认为是AD治愈的有希望的候选者,而氧化应激标志物已成功上调,海马和脑组织中退化的神经元被完全恢复,Aβ斑块消失了。此外,从GAL @ Ce-HAp展示了GAL和nanoceria的最佳体外释放,而从GAL @ Ce-HAp / CMC展示了这些物种的延迟体外释放。这种概念上的证明可以使棒状羟基磷灰石颗粒具有未来的全能性,从而可以将GAL和纳米氧化铈选择性地递送至受AD影响的大脑区域。 (C)2016 Elsevier B.V.保留所有权利。

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