利鲁唑脑递送蛋白纳米杂化系统的合成与表征。

IF 2.2 Q2 PHARMACOLOGY & PHARMACY
Therapeutic delivery Pub Date : 2025-06-01 Epub Date: 2025-03-24 DOI:10.1080/20415990.2025.2478805
Ujjwal Gupta, Amit Kumar, Md Imtiyaz Alam, Paul Gajanan Balaji, Ankita Sharma, Awesh K Yadav
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引用次数: 0

摘要

目的:合成和表征利鲁唑脑递送蛋白纳米杂化体系。方法/材料:将富勒烯转化为羧化富勒烯(CF),制备与CF偶联的RZU-PNH负载的BSA纳米颗粒。结果:RZU-PNH的粒径为210±1.15 nm, zeta电位为-18.5±0.615 mV,包封效率为98.8±0.53%,负载效率为11.6±0.43%。RZU-PNH的XRD和CD分析表明,该蛋白的二级结构主要由α-螺旋和β-片组成。MTT实验显示,在浓度为20 μg/ml时,sh - sy5y和N2a细胞株的细胞存活率分别为88.60%和90.84%,RZU-PNH对小鼠鼻纤毛无明显毒性作用。结论:RZU-PNH制剂具有治疗肌萎缩性侧索硬化症的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and characterization of protein nanohybrid systems for the brain delivery of Riluzole.

Aims: Synthesis and Characterization of Protein NanoHybrid Systems for the Brain Delivery of Riluzole.

Methods/materials: Fullerene is converted into carboxylated fullerene (CF) and then, prepared RZU-loaded BSA nanoparticles conjugated with CF.

Results: The particle size and zeta potential of RZU-PNH were found to be 210 ± 1.15 nm and -18.5 ± 0.615 mV respectively, and entrapment efficiency and loading efficiency of RZU-PNH were found to be 98.8 ± 0.53% and 11.6 ± 0.43%, respectively. The XRD of the RZU-PNH shows the amorphism behavior and CD revealed that secondary structure of the protein mainly consists of α-helix andβ-sheet. The MTT assay showed 88.60% and 90.84% cell viability in both SH-SY5Yand N2a cell lines at a concentration of 20 μg/ml and also, no significant nasal ciliotoxicity was observed after incubation with RZU-PNH.

Conclusions: Obtained results indicated RZU-PNH formulation to treat amyotrophic lateral sclerosis.

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来源期刊
Therapeutic delivery
Therapeutic delivery PHARMACOLOGY & PHARMACY-
CiteScore
5.50
自引率
0.00%
发文量
25
期刊介绍: Delivering therapeutics in a way that is right for the patient - safe, painless, reliable, targeted, efficient and cost effective - is the fundamental aim of scientists working in this area. Correspondingly, this evolving field has already yielded a diversity of delivery methods, including injectors, controlled release formulations, drug eluting implants and transdermal patches. Rapid technological advances and the desire to improve the efficacy and safety profile of existing medications by specific targeting to the site of action, combined with the drive to improve patient compliance, continue to fuel rapid research progress. Furthermore, the emergence of cell-based therapeutics and biopharmaceuticals such as proteins, peptides and nucleotides presents scientists with new and exciting challenges for the application of therapeutic delivery science and technology. Successful delivery strategies increasingly rely upon collaboration across a diversity of fields, including biology, chemistry, pharmacology, nanotechnology, physiology, materials science and engineering. Therapeutic Delivery recognizes the importance of this diverse research platform and encourages the publication of articles that reflect the highly interdisciplinary nature of the field. In a highly competitive industry, Therapeutic Delivery provides the busy researcher with a forum for the rapid publication of original research and critical reviews of all the latest relevant and significant developments, and focuses on how the technological, pharmacological, clinical and physiological aspects come together to successfully deliver modern therapeutics to patients. The journal delivers this essential information in concise, at-a-glance article formats that are readily accessible to the full spectrum of therapeutic delivery researchers.
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