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通过核磁共振(NMR)和微型计算机断层扫描(micro-CT)对后肢悬吊大鼠模型中用于骨质流失的合成纳米包裹药物进行表征。

Characterization of synthesized NANO-encapsulated drug for bone loss on hind limb suspension rat model by NMR and micro-CT.

作者信息

Ni Qingwen, Dixon Hong, Gutierrez Gloria, Bi Long, Qin Yi-Xian

机构信息

Southwest Research Institute, San Antonio, TX, USA; Texas A&M International University, Laredo, TX, USA.

Southwest Research Institute, San Antonio, TX, USA.

出版信息

Adv Biosci Bioeng (N Y). 2013 Jun;1(1):1-7. doi: 10.11648/j.abb.20130101.11. Epub 2014 Jun 14.

DOI:10.11648/j.abb.20130101.11
PMID:28042594
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5199030/
Abstract

A formulation of nano-encapsulated enantiomer of (+) promethazine with desired release rate has been synthesized for establish a localized drug delivery system. It was tested on a hind limb suspension (HLS) disuse rat model, and by using a non-destructive Nuclear Magnetic Resonance (NMR) relaxation technique, and micro computed tomography (Micro-CT) analysis technique to qualitatively evaluate the effectiveness of the new bone formations as well as to compare the current commercial anti-bone loss drug Alendeonate. Our studies suggest that nano-encapsulated (+) promethazine in controlled release formulations conjugating bone-targeting functional groups are effective in promoting bone growth in a disuse rat model.

摘要

已合成具有所需释放速率的纳米封装(+)异丙嗪对映体配方,以建立局部给药系统。在大鼠后肢悬吊(HLS)废用模型上进行了测试,并使用无损核磁共振(NMR)弛豫技术和微型计算机断层扫描(Micro-CT)分析技术,定性评估新骨形成的有效性,并比较当前市售的抗骨质流失药物阿仑膦酸盐。我们的研究表明,在控释制剂中结合骨靶向官能团的纳米封装(+)异丙嗪可有效促进废用大鼠模型中的骨生长。

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