Antiepileptic drug-loaded and multifunctional iron oxide@silica@gelatin nanoparticles for acid-triggered drug delivery

• Published in: Scientific reports 2024-05, Vol.14 (1), p.11400-11400, Article 11400
• Main Authors: Ghane, Nazanin, Khalili, Shahla, Khorasani, Saied Nouri, Das, Oisik, Ramakrishna, Seeram, Neisiany, Rasoul Esmaeely
• Format: Article
• Language: English
• Subjects: 639/166; 639/301; Anticonvulsants - administration & dosage; Anticonvulsants - chemistry; Antiepileptic agents; Antiepileptic drug; Blood-brain barrier; Byggkonstruktion; Controlled release; Cytotoxicity; Drug Carriers - chemistry; Drug delivery; Drug delivery systems; Drug Delivery Systems - methods; Drug development; Drug Liberation; Epilepsy; Ferric Compounds - chemistry; Gelatin; Gelatin - chemistry; Humanities and Social Sciences; Humans; Hydrogen-Ion Concentration; Iron oxides; Magnetic Iron Oxide Nanoparticles - chemistry; Magnetite Nanoparticles - chemistry; multidisciplinary; Nanoparticles; Nanoparticles - chemistry; Particle Size; pH effects; pH-sensitivity; Phenytoin; Phenytoin - administration & dosage; Phenytoin - chemistry; Science; Science (multidisciplinary); Silica; Silicon Dioxide - chemistry; Structural Engineering; Superparamagnetic nanoparticles
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-62248-z

The current study developed an innovative design for the production of smart multifunctional core-double shell superparamagnetic nanoparticles (NPs) with a focus on the development of a pH-responsive drug delivery system tailored for the controlled release of Phenytoin, accompanied by real-time monitoring capabilities. In this regard, the ultra-small superparamagnetic iron oxide@silica NPs (IO@Si MNPs) were synthesized and then coated with a layer of gelatin containing Phenytoin as an antiepileptic drug. The precise saturation magnetization value for the resultant NPs was established at 26 emu g -1 . The polymeric shell showed a pH-sensitive behavior with the capacity to regulate the release of encapsulated drug under neutral pH conditions, simultaneously, releasing more amount of the drug in a simulated tumorous-epileptic acidic condition. The NPs showed an average size of 41.04 nm, which is in the desired size range facilitating entry through the blood–brain barrier. The values of drug loading and encapsulation efficiency were determined to be 2.01 and 10.05%, respectively. Moreover, kinetic studies revealed a Fickian diffusion process of Phenytoin release, and diffusional exponent values based on the Korsmeyer-Peppas equation were achieved at pH 7.4 and pH 6.3. The synthesized NPs did not show any cytotoxicity. Consequently, this new design offers a faster release of PHT at the site of a tumor in response to a change in pH, which is essential to prevent epileptic attacks.