دورية أكاديمية

Immunogenic antitumor potential of Prakasine nanoparticles in zebrafish by gene expression stimulation

التفاصيل البيبلوغرافية
العنوان: Immunogenic antitumor potential of Prakasine nanoparticles in zebrafish by gene expression stimulation
المؤلفون: Prakash S. K.
المصدر: Artificial Cells, Nanomedicine, and Biotechnology, Vol 51, Iss 1, Pp 41-56 (2023)
بيانات النشر: Taylor & Francis Group, 2023.
سنة النشر: 2023
المجموعة: LCC:Biotechnology
LCC:Medical technology
مصطلحات موضوعية: Nanoparticle, Prakasine nanoparticle, cytokine gene stimulation, cancer treatment, immunotherapy, Biotechnology, TP248.13-248.65, Medical technology, R855-855.5
الوصف: AbstractIn this study, non-toxic mercury nanoparticle was synthesized as per “Prakash theory of metal drugs” and nanoparticle’s characters has been demonstrated by employing several nanotechnological tools including XPS, XRD, EDAX. The size of the Prakasine nanoparticles (PRK-NP) ranged from 90–100 nm, confirmed using TEM, SEM, DLS and along with zeta potential of −29.5 mV before storage and −8.5 mV after storage. The FTIR provided information regarding the nanoparticle capping and functional groups. The study was further elaborated for determining PRK-NPs toxicity, genotoxicity, in-vivo toxicity, immunological anti-tumour activity, immunogenicity potential, gene expression profiling and confirmed by MTT and apoptosis assays, cancer zebrafish model studies and WBC proliferation assay. PRK-NPs revealed no cytotoxicity where cell viability was observed 99% in L6 mouse fibroblasts and 99% in MCF-7 cell lines. Also, the cell viability was to be 89.47% at a very high concentration of 320 µg/ml in HEK 293 cells. The PRK-NPs significantly reduced the tumour in zebrafish at dose of 90 μg/g by up regulating IL-1α, IL-1β, IL-2-ITK, IL-6, IL-8, IL-12, TNF-α and IFN-γ, and down regulating IL-4, IL-5, IL-10 and TGF-β compared to untreated controls without any adverse effects and toxicity. Thus, the current study beholds anticipation PRK-NPs may play a vital role in therapeutic.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 21691401
2169-141X
2169-1401
Relation: https://doaj.org/toc/2169-1401; https://doaj.org/toc/2169-141X
DOI: 10.1080/21691401.2023.2173217
URL الوصول: https://doaj.org/article/81882c7f2b9442b0b3825772f1f4b710
رقم الأكسشن: edsdoj.81882c7f2b9442b0b3825772f1f4b710
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21691401
2169141X
DOI:10.1080/21691401.2023.2173217