载白藜芦醇壳聚糖修饰的中空二氧化锰纳米颗粒用于脊髓损伤的治疗。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Delivery Pub Date : 2022-12-01 DOI:10.1080/10717544.2022.2104957
Yingqiao Li, Zhiru Zou, Jinyu An, Qian Wu, Le Tong, Xifan Mei, He Tian, Chao Wu
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引用次数: 12

摘要

脊髓损伤(Spinal cord injury, SCI)是一种严重的中枢神经系统疾病,氧化应激、炎症反应及伴随的神经元凋亡等继发性损伤会加重病情。由于血脊髓屏障(BSCB)的存在,现有治疗脊髓损伤的药物难以到达损伤部位,其疗效受到限制。在这项研究中,我们设计了壳聚糖修饰的中空二氧化锰纳米颗粒(CM),用于递送白藜芦醇,以帮助其通过BSCB。白藜芦醇(Resveratrol, Res)是一种难溶性药物,通过吸附法将其吸附到CM中,其粒径约为130 nm,载药量达到21.39±2.53%。体外溶出实验表明,负载样品(CMR)的释出率为缓慢释放,在36 h时释出率约为87%。体外细胞水平和体内动物水平实验表明,CMR可通过降低活性氧(ROS)、丙二醛(MDA)、超氧化物歧化酶(SOD)水平,提高谷胱甘肽过氧化物酶(GSH)水平,显著缓解氧化应激。免疫荧光法(iNOS、IL-1β、Cl - caspase-3)和免疫印迹法(iNOS、cox-2、IL-1β、IL-10、Cl - caspase-3、bax、bcl-2)检测相关因子的表达,证实CMR还能减轻炎症和神经元凋亡。这些结果表明,CM作为一种潜在的中枢神经系统给药材料,适合于脊髓损伤的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Chitosan-modified hollow manganese dioxide nanoparticles loaded with resveratrol for the treatment of spinal cord injury.

Spinal cord injury (SCI) is a serious central nervous system disease, and secondary injury, including oxidative stress, the inflammatory response and accompanying neuronal apoptosis, will aggravate the condition. Due to the existence of the blood-spinal cord barrier (BSCB), the existing drugs for SCI treatment are difficulty to reach the injury site and thus their efficacy is limited. In this study, we designed chitosan-modified hollow manganese dioxide nanoparticles (CM) for the delivery of resveratrol to help it pass through the BSCB. Resveratrol (Res), a poorly soluble drug, was adsorbed into CM with a particle size of approximately 130 nm via the adsorption method, and the drug loading reached 21.39 ± 2.53%. In vitro dissolution experiment, the Res release of the loaded sample (CMR) showed slowly release behavior and reached about 87% at 36 h. In vitro at the cellular level and in vivo at the animal level experiments demonstrated that CMR could alleviate significantly oxidative stress by reducing level of reactive oxygen species (ROS), malondialdehyde (MDA), superoxide dismutase (SOD), and increasing glutathione peroxidase (GSH) level. Additionally, immunofluorescence (iNOS, IL-1β, and Cl caspase-3) and western blot (iNOS, cox-2, IL-1β, IL-10, Cl caspase-3, bax, and bcl-2) were used to detect the expression of related factors, which verified that CMR could also reduce inflammation and neuronal apoptosis. These results indicated that CM, as a potential central nervous system drug delivery material, was suitable for SCI treatment.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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