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      Gold nanoparticles improve the embryonic developmental competency of artificially activated mouse oocytes

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          Abstract

          Currently, artificial oocyte activation has attracted wide attention in assisted reproduction due to extensive range of applications, particularly in somatic cell nuclear transfer and deriving pluripotent stem cell lines and it is the unique model to determine the role of paternal genome. Numbers of artificial activating agents have been used extensively to induce the oocytes activation; however, embryos developmental competency of artificially activated oocytes is still very low. In the present study, we determined the functional impact of strontium chloride supplementation with gold nanoparticles (AuNPs) in artificial oocytes activation and subsequent embryonic development. Oocytes were activated artificially in the culture medium containing 250 nM AuNPs with constant concentration of strontium chloride 10.00 mM. We found that adding 250 nM AuNPs with constant concentration of strontium chloride (10.00 mM for 3 hr) in culture medium improves the proportion of embryos reaching to the morula and blastocyst stages from 61.00% and 42.00% (controls) to 75.00% and 58.00% (250 nM AuNPs), respectively. In addition, foster mothers receiving AuNPs-treated embryos showed more implantation percentage and pregnancy rate relative to females received control embryos. Finally, embryos treated with 250 nM AuNPs concentration showed no toxic effect in term of blastocyst development. Collectively, our findings suggest the potential role of AuNPs in early embryonic development for mouse oocytes activated artificially and provide new insights in the field of animal biotechnology and assisted reproduction in humans.

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          Most cited references37

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          Gold nanoparticles in nanomedicine: preparations, imaging, diagnostics, therapies and toxicity.

          This critical review provides an overall survey of the basic concepts and up-to-date literature results concerning the very promising use of gold nanoparticles (AuNPs) for medicinal applications. It includes AuNP synthesis, assembly and conjugation with biological and biocompatible ligands, plasmon-based labeling and imaging, optical and electrochemical sensing, diagnostics, therapy (drug vectorization and DNA/gene delivery) for various diseases, in particular cancer (also Alzheimer, HIV, hepatitis, tuberculosis, arthritis, diabetes) and the essential in vitro and in vivo toxicity. It will interest the medicine, chemistry, spectroscopy, biochemistry, biophysics and nanoscience communities (211 references).
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            Particle size-dependent organ distribution of gold nanoparticles after intravenous administration.

            A kinetic study was performed to determine the influence of particle size on the in vivo tissue distribution of spherical-shaped gold nanoparticles in the rat. Gold nanoparticles were chosen as model substances as they are used in several medical applications. In addition, the detection of the presence of gold is feasible with no background levels in the body in the normal situation. Rats were intravenously injected in the tail vein with gold nanoparticles with a diameter of 10, 50, 100 and 250 nm, respectively. After 24 h, the rats were sacrificed and blood and various organs were collected for gold determination. The presence of gold was measured quantitatively with inductively coupled plasma mass spectrometry (ICP-MS). For all gold nanoparticle sizes the majority of the gold was demonstrated to be present in liver and spleen. A clear difference was observed between the distribution of the 10 nm particles and the larger particles. The 10 nm particles were present in various organ systems including blood, liver, spleen, kidney, testis, thymus, heart, lung and brain, whereas the larger particles were only detected in blood, liver and spleen. The results demonstrate that tissue distribution of gold nanoparticles is size-dependent with the smallest 10nm nanoparticles showing the most widespread organ distribution.
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              Classification of cell death: recommendations of the Nomenclature Committee on Cell Death.

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                Author and article information

                Journal
                Vet Res Forum
                Vet Res Forum
                VRF
                Veterinary Research Forum
                Urmia University Press (Urmia, Iran )
                2008-8140
                2322-3618
                December 2021
                15 December 2021
                : 12
                : 4
                : 415-420
                Affiliations
                [1 ]Department of Theriogenology, Faculty of Veterinary Sciences, University of Veterinary and Animal Sciences, Lahore, Pakistan;
                [2 ]Institute of Molecular Biology and Biotechnology, University of Lahore, Lahore, Pakistan;
                [3 ]Department of Physics, Faculty of Natural Sciences, University of Engineering and Technology, Lahore, Pakistan.
                Author notes
                [* ]Correspondence Amjad Riaz. DVM, PhD, Department of Theriogenology, Faculty of Veterinary Sciences, University of Veterinary and Animal Sciences, Lahore, Pakistan. E-mail: dramjadriaz@uvas.edu.pk
                Article
                10.30466/vrf.2020.119759.2829
                9010841
                c1ce1ed7-6645-48cc-8228-d795ee869415
                © 2021 Urmia University. All rights reserved

                This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, ( https://creativecommons.org/licenses/by-nc/4.0/) which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.

                History
                : 19 January 2020
                : 6 July 2020
                Categories
                Original Article

                embryonic development,gold nanoparticles,mice,oocytes,parthenogenesis

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