School of Nanoscience and Technology, Shivaji University, Kolhapur, Maharashtra 416004, India.
Department of Physics, Shivaji University, Kolhapur, Maharashtra 416004, India.
J Colloid Interface Sci. 2018 Nov 1;529:415-425. doi: 10.1016/j.jcis.2018.06.006. Epub 2018 Jun 15.
Magnetic nanoparticles (MNPs) with higher magnetization are highly desirable for targeted drug delivery (TDD) systems, as it helps accumulation of drug at the target site. However, functionalization of MNPs for drug binding reduces the magnetization which affects the efficacy of TDD. Herein we report direct functionalization of MNPs with (3-Aminopropyl)triethoxysilane (APTES) which preserves the magnetization. Grafting density estimated by TGA and BET analysis showed monolayer grafting of APTES on MNP surface. MNPs were comprehensively characterized by XRD, HR-TEM, SQUID-VSM and FTIR. Anti-cancerous drug telmisartan (TEL) was loaded on monolayer APTES grafted MNPs. In-vitro controlled drug release and cytotoxicity study on PC-3 human prostate cancer cell line of TEL conjugated MNPs are also discussed. This functionalization strategy can be extended to other biomedical applications where higher magnetization is desired.
磁性纳米粒子(MNPs)具有更高的磁化强度,非常适合靶向药物输送(TDD)系统,因为它有助于药物在靶部位的积累。然而,为了药物结合而对 MNPs 进行功能化会降低磁化强度,从而影响 TDD 的效果。在此,我们报告了 MNPs 与(3-氨丙基)三乙氧基硅烷(APTES)的直接功能化,该方法保留了磁化强度。通过 TGA 和 BET 分析估算的接枝密度表明 APTES 在 MNP 表面的单层接枝。通过 XRD、HR-TEM、SQUID-VSM 和 FTIR 对 MNPs 进行了全面表征。将抗癌药物替米沙坦(TEL)负载在单层 APTES 接枝的 MNPs 上。还讨论了 TEL 缀合的 MNPs 在 PC-3 人前列腺癌细胞系中的体外控释药物和细胞毒性研究。这种功能化策略可以扩展到其他需要更高磁化强度的生物医学应用中。