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Preparation, characterization, and in vitro release of folic acid-conjugated chitosan nanoparticles loaded with methotrexate for targeted delivery

机译:叶酸偶联壳聚糖纳米粒的制备,表征和体外释放以靶向递送

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摘要

To reduce the toxicity of methotrexate (MTX) and increase the targeting of nanoparticles, the MTX-Ioaded chitosan (CS) covalently bonded with folic acid (FA) nanoparticles were prepared, and sodium tripolyphosphate was used as the cross-linking agent. FA was successfully conjugated to CS confirmed by 'H-NMR and Fourier transform infrared spectrometer (FT-IR). The prepared FA-CS nanoparticles were characterized by FT-IR spectroscopy to confirm the cross-linking reaction between FA-CS and cross-linking agent. X-ray diffraction was performed to reveal the crystalline nature of the drug after encapsulation. The average diameters of the nanoparticles ranged from 293.9 ± 24.2 to 401.5 ± 20.4 nm with a narrow particle size distribution. In vitro release pattern in phosphate buffer saline (pH 6.8) indicated that the characteristics of the MTX-loaded nanoparticles appeared to have an initial burst effect and followed by a slow, sustained drug release. FA or low molecular weight FA conjugate fragments were also released from the nanoparticles, which might have potential to reduce toxic effects of MTX within the body.
机译:为了降低甲氨蝶呤(MTX)的毒性并提高纳米粒子的靶向性,制备了与叶酸(FA)纳米粒子共价结合的MTX碘化壳聚糖(CS),并将三聚磷酸钠用作交联剂。通过1 H-NMR和傅里叶变换红外光谱仪(FT-IR)证实,FA已成功偶联到CS。通过FT-IR光谱对所制备的FA-CS纳米颗粒进行表征,以确认FA-CS与交联剂之间的交联反应。进行X射线衍射以揭示包封后药物的结晶性质。纳米粒子的平均直径在293.9±24.2到401.5±20.4 nm范围内,具有窄的粒度分布。在磷酸盐缓冲盐水(pH 6.8)中的体外释放模式表明,MTX负载的纳米颗粒的特性似乎具有初始爆发效应,然后缓慢,持续地释放药物。 FA或低分子量FA缀合物片段也从纳米颗粒释放,这可能具有减少MTX在体内的毒性作用的潜力。

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