Malay Dolai
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Malay Dolai has a total of 168 co-authors. Here are the top co-authors by number of shared publications:
- Avijit Kumar Das
Department of Chemistry, Christ University, Hosur Road, Bangalore, Karnataka, 560029, India
14 shared publications - Bhriguram Das
Department of Chemistry, Vidyasagar University, Midnapore-721102, West Bengal, India
10 shared publications - Urmila Saha
Department of Chemistry, Indian Association for the Cultivation of Science, Raja SC Mullick Road, Kolkata 700032, WB, India
10 shared publications Sujata Maiti Choudhury
Cancer Nanotherapeutics Laboratory, Biochemistry, Molecular Endocrinology, and Reproductive Physiology Division, Department of Human Physiology, Vidyasagar University, Midnapore- 721 102, West Bengal, India
9 shared publications- Mahammad Ali
Department of Chemistry
8 shared publications - Gopinatha Suresh Kumar
Organic and Medicinal Chemistry Division, CSIR-Indian Institute of Chemical Biology, Kolkata 700 032, India
7 shared publications
Latest Publications
- 5 October 2026
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 50 (38) , 16422-16430
Selective fluorogenic turn-on detection of Zn 2+ : crystallographic analysis of the ligand with theoretical insights, anticancer activity, and bioimaging applications
A fluorescent sensor, ( E )- N ′-(3-ethoxy-2-hydroxybenzylidene) picolinohydrazide (EVH), was designed and synthesized for the selective fluorescence recognition of Zn 2+ in semi-aqueous media.
- 5 October 2026
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 50 (38) , 16422-16430
Selective fluorogenic turn-on detection of Zn 2+ : crystallographic analysis of the ligand with theoretical insights, anticancer activity, and bioimaging applications
A fluorescent sensor, ( E )- N ′-(3-ethoxy-2-hydroxybenzylidene) picolinohydrazide (EVH), was designed and synthesized for the selective fluorescence recognition of Zn 2+ in semi-aqueous media.
- 7 August 2026
- Published by Elsevier in Journal of Molecular Structure
- Vol. 1379
Mannich Base Supported Mn(III) Complex: A Mononuclear Catalyst for Catecholase Mimicry
- 7 August 2026
- Published by Elsevier in Journal of Molecular Structure
- Vol. 1379
Mannich Base Supported Mn(III) Complex: A Mononuclear Catalyst for Catecholase Mimicry
- 2 June 2026
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 55 (24) , 9465-9473
Crystallographic and theoretical insights into a fluorogenic turn-on probe for selective Fe 3+ detection with biomolecular binding and in vitro anticancer studies
A fluorescent probe (HMC) has been developed for the selective turn-on detection of Fe 3+ exhibiting significant fluorescence enhancement and a visible emission color change from colorless to green.
- 2 June 2026
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 55 (24) , 9465-9473
Crystallographic and theoretical insights into a fluorogenic turn-on probe for selective Fe 3+ detection with biomolecular binding and in vitro anticancer studies
A fluorescent probe (HMC) has been developed for the selective turn-on detection of Fe 3+ exhibiting significant fluorescence enhancement and a visible emission color change from colorless to green.
- Open Access
- 1 June 2026
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 16 (32) , 29751-29757
A furano– ortho –vanillin conjugate for fluorogenic ratiometric and selective Zn 2+ sensing: theoretical insights and biological studies
A fluorescent sensor BFC was designed and synthesized in order to identify the selective fluorescence recognition of Zn 2+ in semi-aqueous environments.
- 1 June 2026
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 16 (32) , 29751-29757
Open AccessA furano– ortho –vanillin conjugate for fluorogenic ratiometric and selective Zn 2+ sensing: theoretical insights and biological studies
A fluorescent sensor BFC was designed and synthesized in order to identify the selective fluorescence recognition of Zn 2+ in semi-aqueous environments.
- 25 May 2026
- Published by Royal Society of Chemistry (RSC) in Analytical Methods
Ratiometric fluorescent detection of phosgene in liquid and gas phases using a tautomeric dye: a combined experimental and theoretical study
A new fluorescent probe, designated as (( E )-2-((2-hydroxy-3-methoxybenzylidene)amino)-2-(hydroxymethyl)propane-1,3-diol (HHP), was synthesized for selective detection of phosgene via a fluorescence-based cyclization mechanism.
- 25 May 2026
- Published by Royal Society of Chemistry (RSC) in Analytical Methods
Ratiometric fluorescent detection of phosgene in liquid and gas phases using a tautomeric dye: a combined experimental and theoretical study
A new fluorescent probe, designated as (( E )-2-((2-hydroxy-3-methoxybenzylidene)amino)-2-(hydroxymethyl)propane-1,3-diol (HHP), was synthesized for selective detection of phosgene via a fluorescence-based cyclization mechanism.
- 17 March 2026
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 55 (15) , 5920-5933
In situ transformed binuclear Co( ii ) and Ni( ii ) complexes as electrocatalysts for the water oxidation reaction
The Co- and Ni-based complexes were synthesized via in situ reaction of 2-cyanopyrimidine and hydroxylamine that forms homologous dinuclear cationic structures having excellent OER performance.
- 17 March 2026
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 55 (15) , 5920-5933
In situ transformed binuclear Co( ii ) and Ni( ii ) complexes as electrocatalysts for the water oxidation reaction
The Co- and Ni-based complexes were synthesized via in situ reaction of 2-cyanopyrimidine and hydroxylamine that forms homologous dinuclear cationic structures having excellent OER performance.
- Open Access
- 1 January 2026
- Published by CSIR-National Institute of Science Communication and Policy Research (NIScPR) in Indian Journal of Biochemistry and Biophysics
- Vol. 63 (1) , 19-28
Interaction of 7,8-dihydroxycoumarin with a biopolymer bromelain: Synthesis, spectroscopic and molecular docking insights
Dihydroxycoumarins which are present in nature as natural products in medicinal plants used for herbal treatment, have numerous pharmacological and therapeutic potentials. They can be developed as promising components of treatment in various medicinal fields. Regardless of several advantages, they have a few disadvantages like low molecular weight and low solubility which lowers the appropriate bioavailability. The strategy is to identify effective intake with a carrier for oral drug delivery. In this paper, we synthesized daphnetin (7,8-dihydroxycoumarin) which has various medicinal properties in a pot-economical multicomponent domino fashion, and explored its biophysical interaction with cysteine protease enzyme bromelain for the very first time using steady-state fluorescence and temperature variation experimentally at pH 7.4 since it has a proven record of enhancing the efficacy of drugs. The binding constant (or stability constant) of the bromelain-daphnetin interaction is determined from the double-logarithmic plot at three different temperatures, 288K, 298K, and 308K. The change of enthalpy and entropy revealed the major forces of interaction. Thus, bromelain can be used as a drug carrier for daphnetin.
- 1 January 2026
- Published by CSIR-National Institute of Science Communication and Policy Research (NIScPR) in Indian Journal of Biochemistry and Biophysics
- Vol. 63 (1) , 19-28
Open AccessInteraction of 7,8-dihydroxycoumarin with a biopolymer bromelain: Synthesis, spectroscopic and molecular docking insights
Dihydroxycoumarins which are present in nature as natural products in medicinal plants used for herbal treatment, have numerous pharmacological and therapeutic potentials. They can be developed as promising components of treatment in various medicinal fields. Regardless of several advantages, they have a few disadvantages like low molecular weight and low solubility which lowers the appropriate bioavailability. The strategy is to identify effective intake with a carrier for oral drug delivery. In this paper, we synthesized daphnetin (7,8-dihydroxycoumarin) which has various medicinal properties in a pot-economical multicomponent domino fashion, and explored its biophysical interaction with cysteine protease enzyme bromelain for the very first time using steady-state fluorescence and temperature variation experimentally at pH 7.4 since it has a proven record of enhancing the efficacy of drugs. The binding constant (or stability constant) of the bromelain-daphnetin interaction is determined from the double-logarithmic plot at three different temperatures, 288K, 298K, and 308K. The change of enthalpy and entropy revealed the major forces of interaction. Thus, bromelain can be used as a drug carrier for daphnetin.
- Open Access
- 22 December 2025
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 16 (1) , 667-686
Rationally engineered PEGylated l -citrulline functionalized baicalein encapsulated HSA nanopolymer guided by molecular docking for tumor microenvironment responsive and redox modulated colon cancer therapy
Colon cancer remains a major global health burden characterized by uncontrolled proliferation, oxidative stress, and poor responsiveness to conventional therapies, underscoring the need for biocompatible and targeted nanotherapeutic interventions. In this study, a novel pH-responsive human serum albumin-based nanocarrier, HSA-BA@PEG-LC NPs, was designed for the efficient and selective delivery of baicalein (BA) to colon cancer cells. Molecular docking analysis demonstrated strong binding affinities of BA with Hsp90 inhibitors and with human serum albumin (HSA), as well as a notable interaction between L-citrulline (LC) and the cationic amino acid transporter 1 (CAT-1), highlighting their potential roles in anticancer modulation. The engineered nanoparticles exhibited a uniform spherical morphology (232 nm), low polydispersity index (PDI < 0.3), and high colloidal stability (−27.21 mV). Spectroscopic analyses (FTIR and 1H NMR) confirmed successful encapsulation of BA and PEG-LC surface conjugation, with an encapsulation efficiency of 86.62% and pH-dependent sustained release favoring acidic tumor conditions. In HCT-116 cells, HSA-BA@PEG-LC NPs demonstrated enhanced internalization, strong cytoplasmic accumulation, and pronounced cytotoxicity (IC50 = 5.42 µg mL−1), while maintaining safety toward normal lymphocytes. Mechanistically, treatment induced elevated ROS levels, GSH depletion, mitochondrial depolarization, nuclear condensation, cytoskeletal collapse, and G0/G1 cell-cycle arrest. Furthermore, the formulation displayed potent antioxidant activity across DPPH, NO, SOD, and lipid peroxidation assays, with IC50 values approaching ascorbic acid, validating synergistic PEG-LC functionalization and HSA-mediated stabilization as a promising redox-driven nanoplatform for targeted colon cancer therapy.
- 22 December 2025
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 16 (1) , 667-686
Open AccessRationally engineered PEGylated l -citrulline functionalized baicalein encapsulated HSA nanopolymer guided by molecular docking for tumor microenvironment responsive and redox modulated colon cancer therapy
Colon cancer remains a major global health burden characterized by uncontrolled proliferation, oxidative stress, and poor responsiveness to conventional therapies, underscoring the need for biocompatible and targeted nanotherapeutic interventions. In this study, a novel pH-responsive human serum albumin-based nanocarrier, HSA-BA@PEG-LC NPs, was designed for the efficient and selective delivery of baicalein (BA) to colon cancer cells. Molecular docking analysis demonstrated strong binding affinities of BA with Hsp90 inhibitors and with human serum albumin (HSA), as well as a notable interaction between L-citrulline (LC) and the cationic amino acid transporter 1 (CAT-1), highlighting their potential roles in anticancer modulation. The engineered nanoparticles exhibited a uniform spherical morphology (232 nm), low polydispersity index (PDI < 0.3), and high colloidal stability (−27.21 mV). Spectroscopic analyses (FTIR and 1H NMR) confirmed successful encapsulation of BA and PEG-LC surface conjugation, with an encapsulation efficiency of 86.62% and pH-dependent sustained release favoring acidic tumor conditions. In HCT-116 cells, HSA-BA@PEG-LC NPs demonstrated enhanced internalization, strong cytoplasmic accumulation, and pronounced cytotoxicity (IC50 = 5.42 µg mL−1), while maintaining safety toward normal lymphocytes. Mechanistically, treatment induced elevated ROS levels, GSH depletion, mitochondrial depolarization, nuclear condensation, cytoskeletal collapse, and G0/G1 cell-cycle arrest. Furthermore, the formulation displayed potent antioxidant activity across DPPH, NO, SOD, and lipid peroxidation assays, with IC50 values approaching ascorbic acid, validating synergistic PEG-LC functionalization and HSA-mediated stabilization as a promising redox-driven nanoplatform for targeted colon cancer therapy.
- Open Access
- 25 November 2025
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 50 (1) , 433-440
Mechanistic elucidation of irreversible chemodosimetric sensing of hydrazine through structural, computational, and bioimaging analyses
A fluorescent chemodosimeter, DBA, has been developed for the selective detection of hydrazine via an irreversible reaction pathway that leads to fluorescence enhancement.
- 25 November 2025
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 50 (1) , 433-440
Open AccessMechanistic elucidation of irreversible chemodosimetric sensing of hydrazine through structural, computational, and bioimaging analyses
A fluorescent chemodosimeter, DBA, has been developed for the selective detection of hydrazine via an irreversible reaction pathway that leads to fluorescence enhancement.
- Open Access
- 22 August 2025
- Published by Royal Society of Chemistry (RSC) in Inorganic Chemistry Frontiers
- Vol. 12 (21) , 6460-6472
From strong to weak interaction: reconciling SQUID and μSQUID-EPR data in anomalous Co( ii ) dimers
Sub-Kelvin μSQUID-EPR reveals unexpected spin interactions in Co( ii ) dimers, complementing conventional magnetic studies.
- 22 August 2025
- Published by Royal Society of Chemistry (RSC) in Inorganic Chemistry Frontiers
- Vol. 12 (21) , 6460-6472
Open AccessFrom strong to weak interaction: reconciling SQUID and μSQUID-EPR data in anomalous Co( ii ) dimers
Sub-Kelvin μSQUID-EPR reveals unexpected spin interactions in Co( ii ) dimers, complementing conventional magnetic studies.