γ-Fe 2 O 3 @carboxymethyl Cellulose as Potential Oral Nanomedicine for Iron Deficiency Anemia Treatment on Rats

氧化铁纳米粒子 羧甲基纤维素 氧化铁 药品 纳米氧化铁 口服 化学 缺铁 医学 纳米医学 血红蛋白 缺铁性贫血 纳米颗粒 内科学 药理学 核化学 生物利用度 贫血 材料科学 纳米技术 生物化学 有机化学 放射科 磁共振成像
作者
Bo Chen,Peng Zhao,Qiwei Wang,Zhanhang Guo,Xin Liu,Yan Li,Yue Zhang,Min Ji,Ning Gu
标识
DOI:10.11916/j.issn.1005-9113.20034
摘要

Oral iron supplements such as ferrous iron salts are major treatment agents for iron deficiency anemia (IDA) due to the convenience of large dose administration and good patient compliance. However, the gastrointestinal adverse impact caused by Fe2+ stimulus and low bioavailability severely impedes its therapeutic effects. In recent years, it has been found that nano iron-based nanoparticles with high surface-to-volume ratio and low iron ion leakage can alleviate the toxic effect and improve the gastrointestinal absorbance. For further clinical development, nano materials need to meet the pharmaceutical quality demand. Carboxymethyl cellulose (CMC) is a significant pharmaceutical ingredient applied in approved drug formulations, and polyglucosorbitol carboxymethylether (PSC) has been utilized in iron-based nanomedicine ferumoxytol synthesis, both of which can be firmly anchored on iron oxide by carboxyl chelation. In this work, iron oxide nanoparticles (NPs) modified with CMC were designed and synthesized, and the structure composition and physicochemical properties were distinctly characterized. Oral supplement effects on rat IDA were investigated and compared with other recently reported iron supplements including NPs modified with PSC. Results show that the oral nano iron supplement achieved the recovery of hemoglobin and serum iron level in only two weeks with high safety. The nano iron oxide modified with pharmaceutical excipients provides new potential approach for oral iron supplement available in clinics.
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