Mitomycin loaded self-assembled colloidal prodrug nanoparticles for magnetic drug targeting

被引:3
作者
Amin, Keristina Wagdi K. [1 ,2 ]
Abdelghafour, Mohamed M. [1 ,3 ]
Hornok, Viktoria [4 ]
Kiss, Tamas [1 ]
Szabo, Diana [5 ]
Rovo, Laszlo [5 ]
Janovak, Laszlo [1 ]
机构
[1] Univ Szeged, Dept Phys Chem & Mat Sci, Rerrich Bela Ter 1, H-6720 Szeged, Hungary
[2] Suez Canal Univ, Dept Chem, Ismailia 41522, Egypt
[3] Zagazig Univ, Dept Chem, Zagazig 44519, Egypt
[4] Univ Szeged, Interdisciplinary Excellence Ctr, Dept Phys Chem & Mat Sci, Rerrich B Sqr 1, H-6720 Szeged, Hungary
[5] Univ Szeged, Dept Otorhinolaryngol Head & Neck Surg, Tisza Laj Krt 111, H-6720 Szeged, Hungary
关键词
Succinated PVA; Magnetic nanoparticles; Mitomycin; Self-assembly; Colloidal stability; Prolonged drug release; IRON-OXIDE NANOPARTICLES; POLYVINYL-ALCOHOL;
D O I
10.1016/j.jddst.2023.104948
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this work, we developed a stable and targeted polymeric drug delivery system (DDs) with good magnetic response that can form self-assembled nanoparticles and encapsulate therapeutic agents with hydroxyl and/or amino functional groups. A multifunctional drug (Mitomycin C, MMC) with anticancer and antibacterial properties was used as a model drug for encapsulation. Both the drug and the magnetic nanoparticles (MNPs, pre-pared by the coprecipitation method) were linked to the succinated polyvinyl-alcohol polymer (PVA-SA) in a single step reaction. The success of the conjugation reactions was confirmed by FTIR and XRD analyses. The MMC release experiments exhibited a rapid release profile for the free drug (k = 2.01 h-n) but a prolonged release profile (k = 47.97 h-n) for the conjugated drug. The magnetic response of the produced NPs was tested by exposing them to an external magnet. The results showed that the use of MNPs for precise targeting and PVA-SA for controlling the release rate can promote developing targeted DDs and can be useful to reduce unwanted side effects.
引用
收藏
页数:11
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