Abstract
The current study intends to investigate a novel drug delivery system (DDS) based on niosomes structure (NISM) and bovine serum albumin (BSA) which was formulated to BSA coated NISM (NISM-B). Also, selenium nanoparticles (SeNPs) have been prepared by BSA mediated biosynthesis. Finally, the NISM-B was hybridized with SeNPs and was formulated as NISM-B@SeNPs for drug delivery applications. Physicochemical properties of all samples were characterized by UV–Vis spectroscopy, FT-IR, DLS, FESEM, and EDX techniques. The cytotoxicity of all samples against A549 cell line was assessed by cell viability analysis and flow cytometry for apoptotic cells as well as RT-PCR for the expression of MDR-1, Bax, and Bcl-2 genes. Besides, in vivo biocompatibility was performed by LD50 assay to evaluate the acute toxicity. The proposed formulation has a regular spherical shape and approximately narrow size distribution with proper zeta-potential values; the proposed DDS revealed a good biocompatibility. The compound showed a significant cytotoxic effect against A549 cell line. Although the Bax/Bcl-2 expression ratio was significantly in NISM-B@SeNPs- treated cancer cells, the expression of MDR-1 was non-significantly lower in NISM-B@SeNPs-treated cancer cells. The obtained results suggest that the proposed DDS presents a promising approach for drug delivery, co-delivery and multifunctional biomedicine applications.
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Abbreviations
- BSA :
-
Bovine serum albumin
- NISM-B :
-
BSA coated NISM
- cDNA :
-
Complementary DNA
- DDS :
-
Drug delivery system
- DLS :
-
Dynamic light scattering
- FESEM :
-
Field emission scanning electron microscope
- FT-IR :
-
Fourier-Transform Infrared
- HAS :
-
Human serum albumin
- LD 50 :
-
Median lethal dose
- MDR :
-
Multidrug resistance
- MLV :
-
Multilamellar vesicles
- NISM :
-
Niosomes
- KBr :
-
Potassium bromide
- PDI :
-
Polydispersity index
- PI :
-
Propidium iodide
- RBC :
-
Red blood cells
- RT :
-
Reverse-transcribed
- RESs :
-
Reticulo-endothelial systems
- SeNPs :
-
Selenium nanoparticles
- UV–Vis :
-
Ultraviolet–Visible
- ULV :
-
Unilamellar vesicles
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Acknowledgments
This study was supported financially by Zanjan University of Medical Sciences, Zanjan, Iran (Grant Number: A-12-1244-11 & Ethical Code: IR.ZUMS.REC.1398.438).
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MG: Methodology, Conceptualization, Software, and Writing—original draft. BJ: Supervision, Project administration, Writing—review and editing, and Final approved. NM: Methodology. BR: Methodology. MPL: Methodology. SSE: Methodology. AS: Project administration and Writing—review and editing.
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Behrooz Johari received the grant from Zanjan University of Medical Sciences. All the authors declare no financial or commercial conflict of interests that could negatively influence the study.
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11033_2020_5704_MOESM1_ESM.tif
Fig. S1. (A, B) Rheological behavior of all samples. Non-Newtonian rheological behavior was observed for all samples. (C) Stability of all samples according to Z-Average (nm) as time dependent. Values with P< .05(*) and P< .01(**) were regarded statistically meaningful. Supplementary file1 (TIF 627 kb)
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Gharbavi, M., Johari, B., Mousazadeh, N. et al. Hybrid of niosomes and bio-synthesized selenium nanoparticles as a novel approach in drug delivery for cancer treatment. Mol Biol Rep 47, 6517–6529 (2020). https://doi.org/10.1007/s11033-020-05704-z
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DOI: https://doi.org/10.1007/s11033-020-05704-z