Alireza Heidari*
Faculty of Chemistry, California South University, USA
- *Corresponding Author:
- Alireza Heidari
Faculty of Chemistry, California South University
14731 Comet St. Irvine, CA 92604, USA
Tel: 1-775-410-4974
E-mail: Scholar.Researcher.Scientist@gmail.com
Received Date: May 22, 2017; Accepted Date: May 23, 2017; Published Date: May 30, 2017
Citation: Heidari A. Delivery in DNA/RNA of Human Cancer Cells’ Membranes under Synchrotron Radiations: A Payload–Based Perspective. Arch
Chem Res. 2017, 1:2. doi: 10.21767/2572-4657.100011
Copyright: © 2017 Heidari A. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which
permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Editorial
Chemists have been fascinated for a long time with
phenomenon of bimolecular spectroscopy and dynamics of
Nano-sized molecules and clusters as cross-linking–induced anticancer
and immune oncology Nano drugs delivery in DNA/RNA
of human cancer cells’ membranes under synchrotron radiations
[1-21]. This concept generally associated with anti-cancer and
immune oncology Nano drugs delivery under synchrotron
radiations, now extends equally well to synchrotron chemistry.
Despite its continuing very frequent use in the scientific
literature, anti-cancer and immune oncology Nano drugs
delivery under synchrotron radiations like many other useful and
popular chemical concepts is non-reductive and lacks an
unambiguous basis. It has no precise quantitative definition and
is not directly measureable experimentally. In other words, anticancer
and immune oncology Nano drugs delivery under
synchrotron radiations is a virtual quantity, rather than a
physical observable. Since anti-cancer and immune oncology
Nano drugs delivery under synchrotron radiations is not a
directly measureable quantity, its magnitude is now generally
evaluated in terms of structural, energetic and magnetic criteria.
However, magnetic properties are the most closely related to
anti-cancer and immune oncology Nano drugs delivery under
synchrotron radiations, as they depend directly on the induced
ring currents associated with cyclic electron delocalization. The
main purpose of this editorial is to show how the different
criteria can be used to describe the Nano drugs delivery under
synchrotron radiations of various Nano-sized molecules and
clusters as cross-linking-induced anti-cancer and immune
oncology Nano drugs in DNA/RNA of human cancer cells’
membranes.
On the other hand, functionalized cross-linking-induced anti–
cancer and immune–oncology Nano drugs delivery in DNA/RNA
of human cancer cells’ membranes under synchrotron radiations
are found in a variety of Nano-sized molecules and clusters using
biomolecular spectroscopies such as 1HNMR, 13CNMR,
31PNMR, Attenuated Total Reflectance Fourier Transform
Infrared (ATR-FTIR) and FT-Raman. Consequently, many synthetic
methodologies have been developed for constructing these anticancer
and immune oncology Nano drugs delivery under synchrotron radiations, most of which were based on
cycloaddition/elimination or condensation reactions. Since
Michael reactions hydrophobic effects could strongly enhance
the rate of some anti–cancer and immune oncology Nano drugs
delivery under synchrotron radiations reactions and
rediscovered the use of water as solvent in synchrotron
chemistry in 2010s. Anti-cancer and immune oncology Nano
drugs delivery under synchrotron radiations reactions in water
without using harmful organic solvents are one of the current
focuses today specially in our environmentally vigilant societies.
In this editorial, we wish to report a one-pot, three-component
reaction of different Nano-sized molecules and clusters as crosslinking-
induced anti-cancer and immune oncology Nano drugs
delivery in DNA/RNA of human cancer cells’ membranes under
synchrotron radiations in refluxing water.
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