Chatterjee Shreya, Das Amrita, Datta Pallab, Thomas Sabu, Ghosal Kajal
Department of Pharmaceutical Technology, Jadavpur University, Kolkata 700032, India.
Department of Pharmaceuticals, National Institute of Pharmaceutical Education and Research, Kolkata, India.
Int J Biol Macromol. 2025 Mar;293:139246. doi: 10.1016/j.ijbiomac.2024.139246. Epub 2024 Dec 30.
AIM & BACKGROUND: Increased efficacy with reduced side effects in cancer treatment is achieved through targeted distribution of anti-cancer medications. Because of their biocompatibility, biodegradability, low toxicity, and target ability under magnetic field, magnetic nanoparticles (MNP) based chitosan nanocomposite have attracted attention among other delivery technologies.
MNPs were synthesised using the co-precipitation method. After the successful synthesis of MNPs, it was successfully encapsulated with 5-fluorouracil (5-FU) within chitosan beads, making it ideal for targeted drug delivery to treat breast cancer cells. The properties of MNP-based drug-loaded chitosan nanocomposite were characterised by various characterization techniques like scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), Fourier-transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), vibrating sample magnetometry (VSM), atomic force microscopy (AFM). Entrapment efficiency and cytotoxicity studies of MNP-based drug-loaded chitosan nanocomposites by MTT were also conducted. The release study of the drug from MNP-based drug-loaded chitosan nanocomposite under different pH conditions was also investigated.
Instrumental analysis showed successful preparation of MNP-based drug-loaded chitosan nanocomposite. The entrapment efficiency of MNP-based drug-loaded chitosan nanocomposite was 85 % to 90 %. MTT study also proved its toxicity against breast cancer cells, and with increased concentration percentage, cell viability decreases. The release study showed that the release of the drug from MNP-based drug-loaded chitosan nanocomposite varied under different pH conditions.
Hence, MNP-based drug-loaded chitosan nanocomposite has the potential to be utilised as a targeted drug delivery vehicle for the treatment of breast cancer cells.
通过抗癌药物的靶向分布可提高癌症治疗的疗效并减少副作用。基于其生物相容性、生物可降解性、低毒性以及在磁场下的靶向能力,基于磁性纳米颗粒(MNP)的壳聚糖纳米复合材料在其他递送技术中受到关注。
采用共沉淀法合成磁性纳米颗粒。成功合成磁性纳米颗粒后,将其与5-氟尿嘧啶(5-FU)成功包封在壳聚糖微球内,使其成为靶向递送治疗乳腺癌细胞的理想药物。通过扫描电子显微镜(SEM)、高分辨率透射电子显微镜(HRTEM)、傅里叶变换红外光谱(FTIR)、粉末X射线衍射(PXRD)、振动样品磁强计(VSM)、原子力显微镜(AFM)等多种表征技术对基于MNP的载药壳聚糖纳米复合材料的性能进行了表征。还通过MTT法对基于MNP的载药壳聚糖纳米复合材料进行了包封率和细胞毒性研究。同时研究了基于MNP的载药壳聚糖纳米复合材料在不同pH条件下的药物释放情况。
仪器分析表明成功制备了基于MNP的载药壳聚糖纳米复合材料。基于MNP的载药壳聚糖纳米复合材料的包封率为85%至90%。MTT研究也证明了其对乳腺癌细胞的毒性,随着浓度百分比的增加,细胞活力下降。释放研究表明,基于MNP的载药壳聚糖纳米复合材料在不同pH条件下的药物释放情况有所不同。
因此,基于MNP的载药壳聚糖纳米复合材料有潜力用作治疗乳腺癌细胞的靶向药物递送载体。