Raj Kumar Koninti

ORCID: 0009-0003-8748-7834
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Research Areas
  • Photochemistry and Electron Transfer Studies
  • DNA and Nucleic Acid Chemistry
  • Spectroscopy and Quantum Chemical Studies
  • Advanced biosensing and bioanalysis techniques
  • Porphyrin and Phthalocyanine Chemistry
  • Supramolecular Chemistry and Complexes
  • Cancer therapeutics and mechanisms
  • Luminescence and Fluorescent Materials
  • Molecular Sensors and Ion Detection
  • RNA Interference and Gene Delivery
  • Nanoparticle-Based Drug Delivery
  • Liquid Crystal Research Advancements
  • Ionic liquids properties and applications
  • Graphene and Nanomaterials Applications
  • Boron Compounds in Chemistry
  • Biosensors and Analytical Detection
  • Gold and Silver Nanoparticles Synthesis and Applications
  • Organic Light-Emitting Diodes Research
  • Surfactants and Colloidal Systems
  • Polymer Surface Interaction Studies
  • Organic Electronics and Photovoltaics
  • Photochromic and Fluorescence Chemistry
  • Mass Spectrometry Techniques and Applications
  • Bioactive Compounds and Antitumor Agents
  • biodegradable polymer synthesis and properties

Pusan National University
2024

Indian Institute of Science Education and Research Pune
2013-2023

Kyushu University
2021

Indian Institute of Science Bangalore
2013-2015

Indian Institute of Science Education and Research Berhampur
2013-2014

Indian Institute of Science Education and Research Mohali
2013-2014

Indian Institute of Science Education and Research Kolkata
2013-2014

Indian Institute of Science Education and Research, Bhopal
2013-2014

Indian Institute of Science Education and Research, Tirupati
2013-2014

Abstract Mechanistic details of DNA compaction is essential blue print for gene regulation in living organisms. Many vitro studies have been implemented using several agents. However, these compacting agents may some kinds cytotoxic effects to the cells. To minimize this aspect, research works had performed, but people never focused green solvent, i.e. room temperature ionic liquid as agent. best our knowledge, first ever report where we shown that guanidinium...

10.1038/srep09137 article EN cc-by Scientific Reports 2015-03-16

Host–guest interactions between cucurbit[7]uril (CB7) and a cardiotonic drug, milrinone, have been explored using steady state pico-second time-resolved techniques. A novel fluorescence switch from ultraviolet (UV) to visible (cyan) is observed as consequence of upward pKa shift the drug inside nano-cavity cucurbit[7]uril.

10.1039/c3cp54895c article EN Physical Chemistry Chemical Physics 2014-01-01

Graphene oxide based molecular switching of ellipticine (E) has been utilized to probe its efficient loading onto graphene (GO) and subsequent release intra-cellular biomolecules like DNA/RNA. The green fluorescence E switches blue in GO back with polynucleotides. intensified emission the ellipticine-GO (E-GO) complex human serum albumin (HSA), a bluish upon addition dsDNA. Electron microscopy reveals formation distinctive 3D assemblies involving biomolecule(s) probably through non-covalent...

10.1039/c3nr06081k article EN Nanoscale 2013-12-12

Herein, we have reported a new strategy for the synthesis of highly stable fluorescent copper nanoclusters (CuNCs) with l-cysteine (Cys) as protecting ligand within water nanopool reverse micelles (RMs). In present work, efforts are also given to address origin excitation-dependent fluorescence spectral shift CuNCs. From our experiments, elucidated that broad from CuNCs in RMs consists two spectrally overlapped bands corresponding metal-core and surface states The intrinsic emission...

10.1021/acs.jpcc.7b11457 article EN The Journal of Physical Chemistry C 2018-02-21

The G-quadruplex (GQ-DNA), an alternative structure motif of DNA, has emerged as a novel and exciting target for anticancer drug discovery. GQ-DNA formed in the presence monovalent cations (Na(+)/K(+)) by human telomeric DNA is point interest due to their direct relevance cellular aging abnormal cell growths. Small molecules that selectively stabilize structures are considered be potential therapeutic agents. Herein, we probe proflavine (a well-known intercalator, hence acting...

10.1021/jp506267b article EN The Journal of Physical Chemistry B 2014-09-02

Abstract The effect of cucurbit[7]uril (CB[7]) nano‐caging on the photophysical properties, particularly excited‐state proton transfer (ESPT) reaction, an eminent anti‐cancer drug, topotecan (TPT), is demonstrated through steady‐state and time‐resolved fluorescence measurements. TPT in water (pH 6) exists exclusively as cationic form (C) ground state. However, drug emission mainly comes from zwitterionic (Z*) TPT, attributed to water‐assisted ESPT between 10‐hydroxyl group water, which leads...

10.1002/cphc.201300461 article EN ChemPhysChem 2013-07-22

Mesoporous silica nano-channel (MCM-41) based molecular switching of a biologically important anticancer drug, namely, ellipticine (EPT) has been utilized to probe its efficient loading onto MCM-41, and subsequent release intra-cellular biomolecules, like DNA. By exploiting various spectroscopic techniques (like, steady state fluorescence, time-resolved fluorescence circular dichroism), it shown that EPT can be easily translocated from MCM-41 DNA without using any external stimulant. Blue...

10.1039/c6nr06285g article EN Nanoscale 2016-01-01

Host–guest interactions between an anticancer drug, ellipticine (EPT), and molecular containers (cucurbitruils (CBn) cyclodextrins (CD)) are investigated with the help of steady state time-resolved fluorescence measurements. Our experimental results confirm formation 1:1 inclusion complexes CB7 CB8. The protonated form EPT predominantly prevails in due to stabilization achieved through ion–dipole interaction host positively charged drug. Drug does not complex CB6, which is smaller cavity...

10.1021/jp408280p article EN The Journal of Physical Chemistry B 2013-10-18

Prototropical and photophysical properties of an anticancer drug, ellipticine, are explored inside the octyl-β-<sc>d</sc>-glucoside micelles using steady state time-resolved fluorescence spectroscopic techniques.

10.1039/c4cp01783h article EN Physical Chemistry Chemical Physics 2014-01-01

Here, we investigate the effect of urea in unfolding dynamics flavin adenine dinucleotide (FAD), an important enzymatic cofactor, through steady state, time-resolved fluorescence spectroscopic and molecular (MD) simulation studies. Steady state results indicate possibility induced FAD, inferred from increasing emission intensity FAD with urea. The TCSPC up-conversion suggest that stack–unstack severely gets affected presence leads to increase unstack conformation population 15% pure water...

10.1021/jp412339a article EN The Journal of Physical Chemistry B 2014-01-23

Femtosecond fluorescence upconversion measurements are employed to elucidate the mechanism of ultrafast double proton transfer dynamics BP(OH)2 inside molecular containers (cucurbit[7]uril (CB7) and β-cyclodextrin (β-CD)). up-converted signals in water consist growth followed by a long decay component (~650 ps). The appearance (~35 ps) signal indicates presence two-step sequential process water. Surprisingly, CB7 nano-cavity does not exhibit any characteristic process. Interestingly, exists...

10.1039/c3cp54038c article EN Physical Chemistry Chemical Physics 2013-10-26

A visible fluorescence switch of an eminent anti-carcinogen, ellipticine has been used to probe non-specific protein-DNA interaction. The unique pattern complexation is depicted for the first time through field emission scanning electron microscopy (FE-SEM) images and spectroscopic techniques.

10.1039/c3cp54422b article EN Physical Chemistry Chemical Physics 2013-12-02

Herein, we explored the photophysical properties of antimalarial, anticancer drug cryptolepine (CRYP) in presence macrocyclic host cucurbit[7]uril (CB7) and DNA with help steady-state time-resolved fluorescence techniques. Ground-state excited-state calculations based on density functional theory were also performed to obtain insight into shape, electron distribution, energetics molecular orbitals CRYP. CRYP exists two forms depending pH medium, namely, a cationic (charge transfer) form...

10.1002/cphc.201501011 article EN ChemPhysChem 2015-12-10

Reverse hexagonal (HII) liquid crystalline material based on glycerol monooleate (GMO) is considered as a potential carrier for drugs and other important biomolecules due to its thermotropic phase change excellent morphology. In this work, the dynamics of encapsulated water, which plays role in stabilization formation reverse mesophase, has been investigated by time dependent Stokes shift method using Coumarin-343 solvation probe. The mesophase transformation L2 have monitored small-angle...

10.1021/acs.jpcb.5b04370 article EN The Journal of Physical Chemistry B 2015-08-10

Controlling luminescence behaviors of organic chromophores is essential for their applications. As emissions from are strongly modulated by structural fluctuations and external environments, comprehensive understandings remain elusive. Here, we demonstrate the modulation photophysics benzophenone (Bzp), a prototypical triplet sensor molecule, encapsulating it into mesoporous silica nanomaterials (MSNs). We systematically probed photoluminescence property using time-resolved (TR-PL)...

10.1021/acs.jpcc.1c04283 article EN The Journal of Physical Chemistry C 2021-08-03

10.1016/j.jphotobiol.2014.08.007 article EN Journal of Photochemistry and Photobiology B Biology 2014-08-19

The excited state proton transfer (ESPT) dynamics of a potentially important anticancer drug, Topotecan (TPT), has been explored in aqueous reverse micelle (RM) using steady-state and time-resolved fluorescence measurements. Both the emission spectrum area normalized infer generation zwitterionic form TPT from cationic TPT, as result ESPT process −OH group to nearby water molecule. were found be severely retarded inside nanocavities RMs, yielding time constants 250 ps 1.0 ns, which is...

10.1021/jp5066902 article EN The Journal of Physical Chemistry B 2014-08-08

The modulation of kinetics and pathways in the ESIPT process proton transfer probes holds significant potential for advancing applications bio-imaging, drug delivery, OLEDs. One effective approach achieving this is altering H-bonding donating capability surrounding medium. To investigate this, we conducted a comprehensive study on excited state intramolecular double [2,2′-bipyridyl]-3,3′-diol (BP(OH)2) within confined spaces silica nanochannels, namely, MCM-41. MCM-41, known its versatile...

10.1016/j.chphi.2023.100285 article EN cc-by-nc-nd Chemical Physics Impact 2023-08-12

Excited-state intramolecular proton transfer (ESIPT) reactions are crucial in photoresponsive materials and fluorescent markers. The compound 4-aminophthalimide (4-AP) has been reported to exhibit solvent-assisted ESIPT protic solvents, such as methanol, wherein the solvent interacts with 4-AP form a six-membered hydrogen-bonded ring that is strengthened upon excitation. Although controversial observation of extensively studied, molecular mechanism yet be fully explored. In this study,...

10.3390/ijms252011038 article EN International Journal of Molecular Sciences 2024-10-14
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