The Design Graphene-Based Nanosheets as a New Nanomaterial in Anti-Cancer
Therapy and Delivery of Chemotherapeutics and Biological Nano Drugs for
Liposomal Anti-Cancer Nano Drugs and Gene Delivery
Alireza Heidari*
Faculty of Chemistry, California South University (CSU), 14731 Comet St. Irvine, CA 92604, USA
- Corresponding Author:
- Alireza Heidari
Faculty of Chemistry, California South University (CSU)
14731 Comet St. Irvine, CA 92604, USA
Tel: +1-775-410-4974
E-mail: Scholar.Researcher.Scientist@gmail.com
Received Date: June 20, 2017; Accepted Date: June 26, 2017; Published Date: June 30, 2017
Citation: Heidari A (2017) The Design Graphene-Based Nanosheets as a New Nanomaterial in Anti-Cancer Therapy and Delivery of Chemotherapeutics and Biological Nano Drugs for Liposomal Anti-Cancer Nano Drugs and Gene Delivery. Br Biomed Bull 5:305.. doi:10.21767/2471-9897.1000305
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
The design Graphene-based nano sheets as a new nanomaterial in anti-cancer therapy and delivery of chemotherapeutics and biological nano drugs for liposomal anticancer nano drugs and gene delivery using nanofunctionalization of metal complexes for molecular imaging and anti-cancer therapy under synchrotron radiation has been studied more seriously in recent years and many researchers have investigated the theoretical aspects of pharmaceutical enzymatic reactions in much detail. Many kinetic models have been applied to these reactions [1-10].
Michaelis-Menten kinetics and Briggs-Haldane kinetics models are among the most successful models applied to enzymatic reactions and are widely taught in biochemical and chemical engineering in the design Graphene-based nano sheets as a new nanomaterial in anti-cancer therapy and delivery of chemotherapeutics and biological nano drugs for liposomal anticancer nano drugs and gene delivery using nanofunctionalization of metal complexes for molecular imaging and anti-cancer therapy under synchrotron radiation [10-15].
These models are used in a variety of biochemical situations other than enzyme-substrate interaction, including antigenantibody binding, nucleic acids-nucleic acids hybridization, amino acids-amino acids or Branched-Chain Amino Acids (BCAA) Branched Chain Amino Acids (BCAA) interactions and for designing Graphene-based nano sheets as a new nanomaterial in anti-cancer therapy and delivery of chemotherapeutics and biological nano drugs for liposomal anti-cancer nano drugs and gene delivery using nano-functionalization of metal complexes for molecular imaging and anti-cancer therapy under synchrotron radiation [15-20].
It can be used to characterize a generic biochemical reaction, in the same way that the Langmuir equation and Langmuir adsorption model can be used to model generic adsorption of bimolecular species. When an empirical equation of this form is applied to microbial growth, it is sometimes called a Monod equation or an activated sludge model.
Furthermore, these models are usually defined as a set of differential equations such as Verhulst equation, von Bertalanffy model, replicator dynamics, Hodgkin-Huxley model and Lotka-Volterra equations also known as the predator-prey equations, are a pair of first-order and non-linear differential equations frequently used to describe the population dynamics of two species that interact, one as a predator and the other as prey. It should be noted that the rate law or rate equation for a chemical reaction is a differential equation that links the reaction rate with concentrations or pressures of reactants and constant parameters (normally rate coefficients and partial reaction orders) [21-25].
To design Graphene-based nano sheets as a new nanomaterial in anti-cancer therapy and delivery of chemotherapeutics and biological nano drugs for liposomal anticancer nano drugs and gene delivery using nanofunctionalization of metal complexes for molecular imaging and anti-cancer therapy under synchrotron radiation. In addition, a set of differential equations are present in the investigation of thermodynamics, kinetics and quantum mechanics. The complete solution of this set is usually very difficult, complex and may be obtained using numerical methods and computer programming [26-30].
A computational program have been made progress to pass the computational barrier for designing Graphene-based nano sheets as a new nanomaterial in anti-cancer therapy and delivery of chemotherapeutics and biological nano drugs for liposomal anti-cancer nano drugs and gene delivery using nanofunctionalization of metal complexes for molecular imaging and anti-cancer therapy under synchrotron radiation. The program is very user friendly and even an elementary user can learn the program, easily. There is a main menu and one can choose the proper enzyme kinetics from the right box of the main menu entitled by “Type of Enzyme Kinetics”.
Different kinetic models have different parameters and so whenever a certain kinetic model is selected, certain kinetic parameters are also highlighted in the main menu. The user may also select the time interval and the name of the file to which the computational results must be saved. After entering the kinetic parameters, initial values, time intervals and file name, then the user must double click on the “calculate” to design Graphene-based nano sheets as a new nanomaterial in anticancer therapy and delivery of chemotherapeutics and biological nano drugs for liposomal anti-cancer nano drugs and gene delivery using nano-functionalization of metal complexes for molecular imaging and anti-cancer therapy under synchrotron radiation and also must double click on the “plot” to draw Eadie- Hofstee diagram and Lineweaver-Burk plot as with the Michaelis-Menten and Briggs-Haldane equations graphical methods may be used to fit the coefficients of the Monod equation or an activated sludge model [31-33].
The design Graphene-based nano sheets as a new nanomaterial in anti-cancer therapy and delivery of chemotherapeutics and biological nano drugs for liposomal anticancer nano drugs and gene delivery using nanofunctionalization of metal complexes for molecular imaging and anti-cancer therapy under synchrotron radiation has been considered for many years. In this editorial, first, immobilization process has been evaluated in different periods from various point views and it is tried to be totally considered its relation with pharmaceutical products in the world high-tech factories. For evaluation of biocatalyst performance in a specific process, it is necessary to be aware of the nature of kinetics and transport phenomenon in that biocatalyst.
A logical assumption system is evaluated in both steady state and unsteady state and conditions include three geometric shapes: Slap cylinder and sphere with the use of Michaelis-Menten kinetics and Briggs-Haldane kinetics mechanisms and then obtained computational results from both models to compare with experimental data. This comparison illustrates that although time duration for transforming system from unsteady state to steady state is too short (model is capable to calculate this time), the computational results of the unsteady state are closer to the experimental data.
Therefore, prediction the condition of biocatalyst performance will be more accurate to design Graphene-based nano sheets as a new nanomaterial in anti-cancer therapy and delivery of chemotherapeutics and biological nano drugs for liposomal anti-cancer nano drugs and gene delivery using nanofunctionalization of metal complexes for molecular imaging and anti-cancer therapy under synchrotron radiation.
References
- Heidari A, Brown C (2015) Study of composition and morphology of cadmium oxide (cdo) nanoparticles for eliminating cancer cells. JNanomedicine Res 2: 20.
- Heidari A (2016) Extraction and preconcentration of N-Tolyl-Sulfonyl-Phosphoramid-Saeure-Dichlorid as an anti- cancer drug from plants: A pharmacognosy study. J Pharmacogn Nat Prod 2: e103.
- Heidari A (2016) Future Prospects of Point Fluorescence Spectroscopy, Fluorescence Imaging and Fluorescence Endoscopy in Photodynamic Therapy (PDT) for Cancer Cells, J Bioanal Biomed 8: e135.
- Heidari A (2016) A Bio-spectroscopic study of DNA density and color role as determining factor for absorbed irradiation in cancer cells.Adv Cancer Prev 1: e102.
- Heidari A (2016) Anti-Cancer effect of UV irradiation at presence of cadmium oxide (CdO) nanoparticles on DNA of cancer cells: A photodynamic therapy study. Arch Cancer Res 4: 1.
- Heidari A (2016)Biospectroscopicstudy on multi-component reactions (MCRs) in two a-type and b-type conformations of nucleic acids to determine ligand binding modes, binding constant and stability of nucleic acids in cadmium oxide (CdO) nanoparticles-nucleic acids complexes as anti-cancer drugs. Arch Cancer Res 4: 2.
- Heidari A (2016) Simulation of temperature distribution of DNA/RNA of human cancer cells using time-dependent bio-heat equation and Nd: YAG Lasers. Arch Cancer Res 4: 2.
- Heidari A (2016) Quantitative structure-activity relationship (QSAR) approximation for cadmium oxide (CdO) and rhodium (III) oxide (Rh2O3) nanoparticles as anti-cancer drugs for the catalytic formation of proviral DNA from Viral RNA using multiple linear and non-linear correlation approach. Ann Clin Lab Res 4: 1.
- Heidari A (2016) Biomedical study of cancer cells DNA therapy using laser irradiations at presence of intelligent nanoparticles. J Biomedical Sci 5: 2.
- Heidari A (2016) Novel and stable modifications of intelligent cadmium oxide (CdO) nanoparticles as anti-cancer drug in formation of nucleic acids complexes for human cancer cells’ treatment.BiochemPharmacol 5: 207.
- Heidari A (2016) Pharmaceutical and analytical chemistry study of cadmium oxide (CdO) nanoparticles synthesis methods and properties as anti-cancer drug and its effect on human cancer cells. Pharm Anal Chem Open Access 2: 113.
- Heidari A (2016) A chemotherapeutic and biospectroscopic investigation of the interaction of double-standard DNA/RNA-binding molecules with cadmium oxide (CdO) and rhodium (iii) oxide (Rh2O3) nanoparticles as anti-cancer drugs for cancer cells’ treatment. Chemo Open Access 5: e129.
- Heidari A (2016) Determination of ratio and stability constant of DNA/RNA in human cancer cells and cadmium oxide (CdO) nanoparticles complexes using analytical electrochemical and spectroscopic techniques. Insights Anal Electrochem 2: 1.
- Heidari A (2016) Combined theoretical and computational study of the belousov-zhabotinsky chaotic reaction and curtius rearrangement for synthesis of mechlorethamine, cisplatin, streptozotocin, cyclophosphamide, melphalan, busulphan and bcnu as anti-cancer drugs. Insights Med Phys1: 2.
- Heidari A (2016)Abinitio and density functional theory (DFT) studies of dynamic NMR shielding tensors and vibrational frequencies of DNA/RNA and Cadmium Oxide (CdO) nanoparticles complexes in human cancer cells. J NanomedineBiotherapeuticDiscov 6: e144.
- Heidari A (2016) Nitrogen, Oxygen, Phosphorus and Sulphurheterocyclic anti-cancer nano drugs separation in the supercritical fluid of ozone (O3) using Soave-Redlich-Kwong (SRK) and Pang-Robinson (PR) equations. Electronic J Biol 12: 4.
- Heidari A (2016) Study of the role of anti-cancer molecules with different sizes for decreasing corresponding bulk tumor multiple organs or tissues. Arch Can Res 4: 2.
- Heidari A (2016) Pharmacogenomics and pharmacoproteomics studies of Phosphodiesterase-5 (PDE5) inhibitors andpaclitaxel albumin-stabilized nanoparticles as sandwiched anti-cancer nano drugs between two DNA/RNA molecules of human cancer cells. J Pharmacogenomics Pharmacoproteomics 7: e153.
- Heidari A (2016) A comparative study on simultaneous determination and separation of adsorbed cadmium oxide (CdO) nanoparticles on DNA/RNA of human cancer cells using biospectroscopic techniques and dielectrophoresis(DEP) method. Arch Can Res 4: 2.
- Heidari A (2016)Cheminformaticsand system chemistry of cisplatin, carboplatin, nedaplatin, oxaliplatin, heptaplatin and lobaplatin as anti-cancer nano drugs: A combined computational and experimental study. J Inform Data Min 1: 3.
- Heidari A (2016) Linear and non-linear quantitative structure-anti-cancer-activity relationship (QSACAR) study of hydrous ruthenium (IV) oxide (RuO2) nanoparticles as non-nucleoside reverse transcriptase Inhibitors (NNRTIs) and anti-cancer nano drugs. J IntegrOncol 5: e110.
- Heidari A (2016) A Pharmacovigilancestudy on linear and non-linear quantitative structure (chromatographic) retention relationships (QSRR) models for the prediction of retention time of anti-cancer nano drugs under synchrotron radiations. J Pharmacovigil 4: e161.
- Heidari A (2016) DNA/RNA fragmentation and cytolysis in human cancer cells treated with diphthamidenano particles derivatives. Biomed Data Mining 5: e102.
- Heidari A (2016) A comparative study of conformational behavior of isotretinoin(13-Cis Retinoic Acid) and tretinoin (All-Trans Retinoic Acid (ATRA)) nano particles as anti-cancer nano drugs under synchrotron radiations using hartree-Fock (HF) and density functional theory (DFT) methods. Insights in Biomed 1: 2.
- Heidari A (2016) Chemotherapy a last resort for cancer treatment. Chemo Open Access 5: 4.
- Heidari A, Yoctosecond (2016) Quantitative structure-activity relationship (QSAR) and quantitative structure- property relationship (QSPR) under synchrotron radiations studies for prediction of solubility of anti-cancer nano drugs in aqueous solutions using genetic function approximation (GFA) algorithm. Insight Pharm Res 1: 1.
- Heidari A (2016) Cancer risk prediction and assessment in human cells under synchrotron radiations using quantitative structure activity relationship (QSAR) and quantitative structure properties relationship (QSPR) studies.Int J Clin Med Imaging 3: 516.
- Heidari A (2016) Integrating precision cancer medicine into healthcare, Medicare reimbursement changes and the practice of oncology: Trends in oncology medicine and practices. J Oncol Med andPract 1: 2.
- Heidari A (2017)Biomolecularspectroscopy and dynamics of nano-sized molecules and clusters as cross- linking-induced anti-cancer and immune-oncology nano drugs delivery in DNA/RNA of human cancer cells’ membranes under synchrotron radiations: A payload-based perspective. Arch Chem Res 1: 2.
- Heidari A (2017) Deficiencies in repair of double-standard DNA/RNA-binding molecules identified in many types of solid and liquid tumors oncology in human body for advancing cancer immunotherapy using computer simulations and data analysis. J ApplBioinformaComputBiol 6: 1.
- Heidari A (2017) Polymorphism in nano-sized graphene ligand-induced transformation of Au38-xAgx/xCux(SPh- tBu)24 to Au36-xAgx/xCux(SPh-tBu)24 (x = 1-12) nanomolecules for synthesis of Au144-xAgx/xCux[(SR)60, (SC4)60, (SC6)60, (SC12)60, (PET)60, (p-MBA)60, (F)60, (Cl)60, (Br)60, (I)60, (At)60, (Uus)60 and (SC6H13)60] nano clusters as anti-cancer nano drugs. J NanomaterMolNanotechnol 6: 3.
- Heidari A (2017) Biomedical resource oncology and data mining to enable resource discovery in medical, medicinal, clinical, pharmaceutical, chemical and translational research and their applications in cancer research.Int J Biomed Data Min 6: e103.
- Heidari A (2017) Study of synthesis, pharmacokinetics, pharmacodynamics, dosing, stability, safety and efficacy of olympiadanenanomolecules as agent for cancer enzymotherapy, immunotherapy, chemotherapy, radiotherapy, hormone therapy and targeted therapy under synchrotorn radiation. J Dev Drugs 6: e154.