Davaran Soodabeh, Alimirzalu Samira, Nejati-Koshki Kazem, Nasrabadi Hamid Tayef, Akbarzadeh Abolfazl, Khandaghi Amir Ahmad, Abbasian Mojtaba, Alimohammadi Somayeh
Department of Medical Nanotechnology, Faculty of Advanced Medical Science, Tabriz University of Medical Sciences, Tabriz, Iran E-mail :
Asian Pac J Cancer Prev. 2014;15(1):49-54. doi: 10.7314/apjcp.2014.15.1.49.
Hydrogels are a class of polymers that can absorb water or biological fluids and swell to several times their dry volume, dependent on changes in the external environment. In recent years, hydrogels and hydrogel nanocomposites have found a variety of biomedical applications, including drug delivery and cancer treatment. The incorporation of nanoparticulates into a hydrogel matrix can result in unique material characteristics such as enhanced mechanical properties, swelling response, and capability of remote controlled actuation.
In this work, synthesis of hydrogel nanocomposites containing magnetic nanoparticles are studied. At first, magnetic nanoparticles (Fe3O4) with an average size 10 nm were prepared. At second approach, thermo and pH-sensitive poly (N-isopropylacrylamide -co-methacrylic acid-co-vinyl pyrrolidone) (NIPAAm-MAA- VP) were prepared. Swelling behavior of co-polymer was studied in buffer solutions with different pH values (pH=5.8, pH=7.4) at 37 °C. Magnetic iron oxide nanoparticles (Fe3O4) and doxorubicin were incorporated into copolymer and drug loading was studied. The release of drug, carried out at different pH and temperatures. Finally, chemical composition, magnetic properties and morphology of doxorubicin-loaded magnetic hydrogel nanocomposites were analyzed by FT- IR, vibrating sample magnetometry (VSM), scanning electron microscopy (SEM).
The results indicated that drug loading efficiency was increased by increasing the drug ratio to polymer. Doxorubicin was released more at 40 °C and in acidic pH compared to that 37 °C and basic pH.
This study suggested that the poly (NIPAAm-MAA-VP) magnetic hydrogel nanocomposite could be an effective carrier for targeting drug delivery systems of anti-cancer drugs due to its temperature sensitive properties.
水凝胶是一类能够吸收水或生物流体并膨胀至其干体积几倍的聚合物,这取决于外部环境的变化。近年来,水凝胶和水凝胶纳米复合材料已在多种生物医学应用中得到应用,包括药物递送和癌症治疗。将纳米颗粒掺入水凝胶基质中可产生独特的材料特性,如增强的机械性能、溶胀响应和远程控制驱动能力。
在本研究中,对含磁性纳米颗粒的水凝胶纳米复合材料的合成进行了研究。首先,制备了平均粒径为10 nm的磁性纳米颗粒(Fe3O4)。其次,制备了对温度和pH敏感的聚(N-异丙基丙烯酰胺-共-甲基丙烯酸-共-乙烯基吡咯烷酮)(NIPAAm-MAA-VP)。在37℃下,研究了该共聚物在不同pH值(pH = 5.8,pH = 7.4)缓冲溶液中的溶胀行为。将磁性氧化铁纳米颗粒(Fe3O4)和阿霉素掺入共聚物中,并研究了药物负载情况。在不同的pH值和温度下进行药物释放。最后,通过傅里叶变换红外光谱(FT-IR)、振动样品磁强计(VSM)、扫描电子显微镜(SEM)对负载阿霉素的磁性水凝胶纳米复合材料的化学成分、磁性和形态进行了分析。
结果表明,通过增加药物与聚合物的比例,载药效率提高。与37℃和碱性pH相比,阿霉素在40℃和酸性pH下释放更多。
本研究表明,聚(NIPAAm-MAA-VP)磁性水凝胶纳米复合材料因其温度敏感特性,可能是抗癌药物靶向给药系统的有效载体。