The area of Research Experience: (a) Chemical synthesis of peptide, peptoid, peptide-based small molecules, and drug modification using peptide for targeted delivery, (b) Targeted delivery of a theranostic agent to cancer cells in vitro as well as in vivo mice model, (c) Bioimaging, confocal fluorescence microscopy, AFM, TEM, SEM imaging, (d) Study the aggregation of amyloid-beta peptide inside the cell like environment and SH-SY5Y cell line and its inhibition, (e) Anti-fouling, anti-bacterial study with synthesized molecules.
EDUCATION
Doctor of Philosophy ( (2011-2016) in Chemistry from the Department of Organic and Medicinal Chemistry Division, CSIR-Indian Institute of Chemical Biology (CSIR-IICB), Kolkata, India. (Guide: Prof. Surajit Ghosh)
CSIR-UGC NET with JRF (2011) in Chemical Science with rank CSIR-46
Master of Science (M.Sc.) (2009-2011) in Chemistry from the University of Calcutta, Raja-bazar Science College. Marks obtained: 77.5%
Bachelor of Science (B.Sc.) (2006-2009) in Chemistry (Honours) from the University of Calcutta, Ramakrishna Mission Vivekananda Centenary College, Rahara. Marks Obtained: 68.4%
Higher Secondary (2006) from West Bengal Council of Higher Secondary Examination. Sodepur High School. Marks Obtained: 78.9%
Class 10 Madhyamik (2004) from West Bengal Board of Secondary Education. Marks Obtained: 83.4%
Exploration of the Anticancer Efficacy and In Silico Drug Screening Study of Fe(II) and Fe(III) Complexes of Schiff Base and Phenanthroline Ligand Jansi Rani J, Evangeline Lawrence, Arjita Ghosh, Abhijit Saha, Anbalagan Moorthy, Sovan Roy Chemmedchem, 2026 To check the hard–soft nature of metals on biological interaction, heteroleptic compounds [Fe II (L1)(L2)](1) and [Fe III (L1)(L2)]Cl (2) were prepared where ligands are (2‐hydroxy‐1‐naphthylidene‐ o ‐aminophenol) [ L1 ] and 1,10‐phenanthroline [ L2 ]. Complexes are characterized by Fourier transform infrared spectra (FTIR), high resolution mass spectrometry (HRMS), and UV–vis spectroscopic techniques. Square pyramidal geometry of the complex 1 was determined using computational study [density functional theory (DFT) function (B3LYP/ LANL2DZ)]. The characteristic Fe(II) to Fe (III) oxidation and Fe(III) to Fe(II) reduction peaks were observed in the desired potential range for complexes 1 and 2 , respectively. Iron complexes demonstrated anticancer effective hydrolytic DNA cleavage efficacy and efficient groove binding prosperity toward DNA with intrinsic and apparent binding constant values of the order of 10 5 M −1 . The complexes displayed good binding capabilities to carrier protein bovine serum albumin (BSA). The experimental DNA and BSA binding nature was validated through molecular docking study. Absorption, Distribution, Metabolism, Excretion, and Toxicity (ADMET)drug screening profiling indicates that complex 1 satisfies all of Lipinski rule with good cell permeability, solubility, lipophilicity, and nontoxicity. Complexes show efficient anticancer activity in MCF‐7 cell lines through apoptotic pathway. Complex 1 is found to have better biological activity compared to 2 due to softer nature of Fe(II) ion.
Hydrogen-Bond-Driven Molecular Recognition: A UV-Spectroscopic Strategy for Positional Isomer Discrimination Using (4,5-Diphenyl-1H-Imidazol-2-Yl) Aniline and Picric Acid Hemanathan Elango, Shyam Ganesh, Adithya Prabhakaran, Abhijit Saha Chempluschem, 2026 A simple method, UV–Visible spectroscopy, was used to detect the positional isomers of imidazole derivatives. We synthesized 4,5‐diphenyl‐1H‐imidazol‐2‐yl‐aniline molecules, where ‐NH2 is present at different positions (ortho, meta, and para) and detected the para isomer using picric acid (PA). PA forms a binary self‐assembled complex with the para derivatives due to an acid–base reaction and causes a detectable shifting (33 nm) in the absorption band. The binary self‐assembled complex, between PA and para isomer, was characterized by UV, FT‐IR, differential scanning calorimetry (DSC), scanning electron microscopy (SEM), 1H‐NMR, and mass spectrometry. We also discussed the probable mechanism of interaction involved in the self‐assembly process and why the other isomers do not interact with the PA. This manuscript reveals a way of detecting positional isomers using the stereochemical aspects of acid–base reaction.
Exosome Applications in Skin Regeneration and Wound Healing Hemanathan Elango, Shyam Ganesh, Adithya Prabhakaran, Abhijit Saha Exosome Therapies from Bench to Bedside in Chronic Disease, 2026 Skin regeneration and wound healing are natural processes that are initiated when skin is injured or its integrity is disrupted. In some cases, the physiological healing process is insufficient for skin regeneration, and the patient experiences difficulties in the wound-healing process. A new biocompatible treatment strategy to expedite skin regeneration and enhance the wound-healing process is urgently needed. The biologically active nanoparticles named exosomes are released by cells as small extracellular vesicles (EV), which play an essential role in intercellular communication, interactions via growth factors, nucleotides, transporting proteins, and lipids. The exosomes can reduce the inflammatory response and promote angiogenesis, cell proliferation, and extracellular matrix (ECM) deposition. Thus, exosomes can regulate all phases of skin tissue regeneration and wound healing. In this chapter, the exosomes’ role in skin regeneration and tissue regeneration has been discussed. It describes strategies for making engineered exosomes with therapeutic cargos like microRNAs. The chapter also explains the wound-repairing mechanism and emphasizes the role of exosomes in skin regeneration. Additionally, this presents the use of engineered exosomes and exosome-loaded scaffolds, particularly hydrogels, to enhance skin regeneration and wound healing.
Tuning Anticancer Properties via Electron Distribution: Inducing Apoptosis Through Downregulation of Reactive Oxygen Species and Docking Studies on Bcl-2 Protein by a 2,4,5-Trisubstituted-1H-Imidazole Compound Hemanathan Elango, Subhabrata Guha, Suganya Ganesan, Shyam Ganesh, Ganesh Munuswamy‐Ramanujam, Gaurav Das, Rabindra Nath Das, Abhijit Saha Chemistryselect, 2025 Reactive oxygen species (ROS) are important in cancer treatment. Up‐ or downregulation of ROS leads to apoptotic death of cancer cells. The electron distribution can control the up‐ or down‐regulation of ROS. How the electron distribution controls the anticancer property of molecules is discussed in this study using the example of imidazole derivatives. We synthesized six different 2‐(substituted phenyl)‐4,5‐diphenyl‐1 H‐imidazole compounds and characterized them by mass, UV, FTIR, 1 H, and 13 C NMR spectroscopy. All the compounds can scavenge ROS and inhibit the proliferation of MCF‐7 breast cancer cells, but to different extents. Out of the six, Compound 5 ( meta isomer) has the highest negative electrostatic potential, and it showed the best ROS scavenging activity and highest anticancer activity. ROS scavenging and anticancer activity were measured by 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) inhibition and 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5 2,5‐diphenyltetrazolium bromide (MTT) assay, respectively, and we got inhibitory concentration (IC 50 , for Compound 5) values of 3.39 ± 0.04 mg/mL and 4.59 ± 0.22 µM, respectively, which is the lowest among the six compounds. A clear correlation was observed between the negative charge density and IC 50 values of the compounds. Compound 5 showed the highest anticancer activity but less cytotoxicity toward the non‐cancerous MCF‐10A cell line. Compound 5 reduces intercellular ROS of MCF‐7 breast cancer cells and thereby induces caspase 3/7 activation, nuclear fragmentation, and apoptotic death of MCF‐7 cancer cells. Compound 5 also blocks the antiapoptotic Bcl‐2 protein as revealed by a molecular docking study.
Sensing Redox Reaction by SPR Peak Shifting: Bioinspired Innovative Functionalization Enables Silver Nanoparticles as Ascorbic Acid Sensors Hemanathan Elango, Shyam Ganesh, Abhijit Saha Chemistryselect, 2025 Surface plasma resonance (SPR) of nanoparticles has garnered significant attention among emerging analytical techniques due to their unique optical sensing properties. SPR peak shifts due to a change in local refractive index, and electrical interactions because of the binding of other molecules to the nanoparticle's surface. In this manuscript, we explore the SPR peak shifting due to redox reaction on the nanoparticle's surface and apply this SPR peak shifting for ascorbic acid (AA) sensing by cysteine‐coated silver nanoparticles (Cys–AgNPs). The SPR peak shifting of Cys–AgNPs was measured by UV–vis spectroscopy. We observed a red shift, depending on the concentration of AA when added to Cys–AgNPs. We observed a 46 nm SPR shift with 2 mM of AA in the case of Cys–AgNPs. However, no shift occurred with bare AgNPs. A redox reaction between L‐cysteine and AA occurring on the nanoparticle's surface is the reason for the shift. The sensing method is sensitive and selective to AA. The SPR peak shifting is not affected by the presence of biomolecules like fructose, glucose, alanine, glycine, and bovine serum albumin (BSA). This manuscript showed the simple synthesis of cysteine‐coated silver nanoparticles (Cys–AgNPs) and their characterization by UV–vis spectroscopy, dynamic light scattering (DLS), zeta potential, FT‐IR, XRD, SEM, TEM analysis, and SPR‐based AA sensing.
Overview of Small Molecules Used in Nanoparticle Functionalization to Prevent Protein Corona Formation and Improve the Therapeutic Potential Shyam Ganesh, Hemanathan Elango, Abhijit Saha Chemistryselect, 2025 Nanoparticles (NP's) have become increasingly important in drug design due to their potential to improve the delivery and efficacy of curative agents. The development of protein corona (PC) occurs on the outer layer of NP's when NPs are exposed to biological medium, affecting the NP's nature. PC significantly impacts the distribution of NPs in vivo by disturbing their interactions with biological systems. The PC prevents the ligands attached to the NP from coming into contact with the target cells' surface by hiding them on the NP's surface. Several strategies have been developed to inhibit PC formation. In the review paper, we discussed those strategies, mainly the utilization of grafting methods, zwitterionic coating with a variety of derivatives (sulfobetaine, carboxybetaine, phospholipids), and PEG coating controlling the size and shape of nanoparticles to prevent the formation of the protein corona. How these coatings significantly reduce the nonspecific absorption of lipids and proteins onto the NP surface and prevent the formation of the PC, has been discussed in this review paper. Moreover, we discuss the formation of PC, types of PC, and the effects of PC on the NP's therapeutic applications in this review.
pH and Medium Polarity-Induced Self-Assembly of Fmoc-Tryptophan into Multiple Superstructures: An Experimental and Theoretical Investigations Suman Nayak, Nanjundan Raghul, Abhijit Saha, Rabindranath Lo, Priyadip Das Chempluschem, 2025 Self‐assembly of functionalized molecular building blocks is an effective and resource‐saving bottom‐up technique to generate multiple superstructures with various functionality and morphologies. The nature of the molecule and the factors controlling the overall self‐assembly process are extremely vital in fundamental aspects of self‐assembly, which deliver insights into the fabrication of multiple assemblies with specific functionality. The self‐assembly of suitably functionalized amino acids leads to the formation of diverse structures with distinct properties, making them ideal bio‐organic scaffolds for various applications. The present study reports, the pH and solvent polarity‐induced self‐assembly of 9‐fluorenylmethoxycarbonyl (Fmoc)‐Tryptophan into various self‐assembled superstructures with morphological individualities, explore the plausible pathway of morphological transformation of Fmoc‐Trp into multiple superstructures having a wide range of well‐defined morphologies, including spheres, hollow spheres, nanoflowers, nanosheets, nanorods, and cube‐like structures, as characterized through conventional microscopic techniques. Detailed UV–vis, fluorescence, powder X‐ray diffraction analysis, and Fourier transform infrared analyses reveal significant insights into the intermolecular interactions, which trigger the overall self‐assembly process. The computational studies, including full geometry optimization and molecular dynamics simulations, are conducted to investigate the aggregation properties of modified amino acids (Fmoc‐Trp). These studies highlight the crucial role of π–π stacking and hydrogen bonding in tuning the overall self‐assembly with morphological variation.
Liposomal Encapsulation of Chlorambucil with a Terpyridine-Based, Glutathione-Targeted Optical Probe Facilitates Cell Entry and Cancer Cell Death Mallayasamy Siva, Kiran Das, Priya Rana, Abhijit Saha, Debasish Mandal, Atanu Barik, Adele Stewart, Biswanath Maity, Priyadip Das ACS Applied Bio Materials, 2025 The nitrogen mustard alkylating agent chlorambucil (CBL) is a critical component of chemotherapeutic regimens used in the treatment of chronic lymphocytic leukemia. The cancer cell-killing actions of CBL are limited by glutathione (GSH) conjugation, a process catalyzed by the GSH transferase hGSTA1-1 that triggers CBL efflux from cells. In the cancer cell microenvironment, intracellular GSH levels are elevated to counterbalance oxidative stress generated due to the high glycolytic demand. As many chemotherapeutic drugs trigger cell death through mechanisms that depend on reactive oxygen species (ROS), antioxidant capacity in cancer cells also represents a barrier to anticancer therapies. Here, we demonstrate that a heightened GSH content in cancer cells can also be exploited for cell-selective drug delivery. We successfully synthesized a malononitrile conjugate terpyridine-based derivative L1, which specifically reacts with GSH in the presence of other biologically relevant amino acids including cysteine (Cys) and homocysteine (Hcy). The significant change in the electronic spectra of L1 in the presence of GSH confirmed GSH detection, which was further corroborated by density functional theory calculations. We next encapsulated CBL into L1-containing, anthracene-functionalized, and 10,12-pentacosadiynoic acid (PCDA)- and 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC)-based liposomes (Lip-CBL-L1). We established successful CBL encapsulation and release from L1-containing liposomes in GSH-enriched cancer cells in vitro. Both Lip-CBL-L1 and the L1-lacking Lip-CBL control displayed cell-killing activity. However, human triple-negative breast cancer cells MDAMB231, human lung cancer cells A549, and murine leukemic WEHI cells were more sensitive to the cytotoxic effects of Lip-CBL-L1 compared to the nonmalignant cells (AC16 and HEK293). Indeed, in these cancer cell lines, Lip-CBL-L1 induced greater ROS generation compared to that of Lip-CBL. Together, our results provide initial evidence of the feasibility of exploiting the unique oxidant environment of cancer cells for optimized drug delivery.
Fabrication of biotin functionalised SiO2 EM grid for studying biotin tagged biomolecules Indian Journal of Chemistry Section A Inorganic Physical Theoretical and Analytical Chemistry, 2013
Tuning Anticancer Properties via Electron Distribution: Inducing Apoptosis Through Downregulation of Reactive Oxygen Species and Docking Studies on Bcl‐2 Protein by a 2, 4, 5 … H Elango, S Guha, S Ganesan, S Ganesh, G Munuswamy‐Ramanujam, ... ChemistrySelect 10 (44), e03541 , 2025 2025
Sensing Redox Reaction by SPR Peak Shifting: Bioinspired Innovative Functionalization Enables Silver Nanoparticles as Ascorbic Acid Sensors H Elango, S Ganesh, A Saha ChemistrySelect 10 (34), e02048 , 2025 2025
Overview of Small Molecules Used in Nanoparticle Functionalization to Prevent Protein Corona Formation and Improve the Therapeutic Potential S Ganesh, H Elango, A Saha ChemistrySelect 10 (25), e02177 , 2025 2025 Citations: 1
pH and Medium Polarity‐Induced Self‐Assembly of Fmoc‐Tryptophan Into Multiple Superstructures: An Experimental and Theoretical Investigations S Nayak, N Raghul, A Saha, R Lo, P Das ChemPlusChem 90 (6), e202500036 , 2025 2025 Citations: 3
Sticky tubes co-assembled by functionalised diphenylalanine and polydopamine nanoparticles form biocompatible antifouling coating S Sivagnanam, S Nayak, A Halder, O Mukherjee, A Saha, P Das RSC advances 15 (5), 3672-3685 , 2025 2025 Citations: 3
Liposomal Encapsulation of Chlorambucil with a Terpyridine-Based, Glutathione-Targeted Optical Probe Facilitates Cell Entry and Cancer Cell Death M Siva, K Das, P Rana, A Saha, D Mandal, A Barik, A Stewart, B Maity, ... ACS applied bio materials 8 (1), 570-581 , 2024 2024 Citations: 2
In-situ eco-friendly synthesis of a biomimetic robust antibacterial nanohybrid via catecholamine-induced metallization AK Rajeev, N Sathish, H Elango, S Sivagnanam, S Nayak, P Das, A Saha Inorganic Chemistry Communications 170, 113172 , 2024 2024 Citations: 6
Benzimidazole-based small molecules as anticancer agents targeting telomeric G-quadruplex and inhibiting telomerase enzyme H Elango, RN Das, A Saha Future Medicinal Chemistry 16 (19), 2043-2067 , 2024 2024 Citations: 7
Importance of soft lithography AK Rajeev, N Sathish, A Saha Human organs-on-a-chip technology, 43-61 , 2024 2024 Citations: 6
Liposomes containing zinc-based chemotherapeutic drug block proliferation and trigger apoptosis in breast cancer cells M Siva, K Das, S Guha, S Sivagnanam, G Das, A Saha, A Stewart, B Maity, ... ACS applied bio materials 6 (12), 5310-5323 , 2023 2023 Citations: 9
Vanillin benzothiazole derivative reduces cellular reactive oxygen species and detects amyloid fibrillar aggregates in alzheimer’s disease brain PK Gharai, J Khan, R Mallesh, S Garg, A Saha, S Ghosh, S Ghosh ACS Chemical Neuroscience 14 (4), 773-786 , 2023 2023 Citations: 28
Platform for Active Vaccine Formulation Using a Two-Mode Enhancement Mechanism of Epitope Presentation by Pickering Emulsion G Mechrez, KA Mani, A Saha, O Lachman, N Luria, O Molad, ... ACS Applied Bio Materials 5 (8), 3859-3869 , 2022 2022 Citations: 1
Evidence for new enantiospecific interaction force in chiral biomolecules Y Kapon, A Saha, T Duanis-Assaf, T Stuyver, A Ziv, T Metzger, S Yochelis, ... Chem 7 (10), 2787-2799 , 2021 2021 Citations: 39
Nucleobase morpholino β amino acids as molecular chimeras for the preparation of photoluminescent materials from ribonucleosides R Bucci, A Bossi, E Erba, F Vaghi, A Saha, S Yuran, D Maggioni, ... Scientific Reports 10 (1), 19331 , 2020 2020 Citations: 20
Amphiphilic peptide with dual functionality resists biofouling A Saha, S Nir, M Reches Langmuir 36 (15), 4201-4206 , 2020 2020 Citations: 37
A bis-indole/carbazole based C5-curcuminoid fluorescent probe with large Stokes shift for selective detection of biothiols and application to live cell imaging P Bhattacharjee, S Chatterjee, A Achari, A Saha, D Nandi, C Acharya, ... Analyst 145 (4), 1184-1189 , 2020 2020 Citations: 17
AFM‐based spin‐exchange microscopy using chiral molecules A Ziv, A Saha, H Alpern, N Sukenik, LT Baczewski, S Yochelis, M Reches, ... Advanced Materials 31 (40), 1904206 , 2019 2019 Citations: 84
Multiplex optical detection and quantification of DNA fragments by metallo-peptide assemblies A Saha, M Reches Scientific Reports 9 (1), 8789 , 2019 2019 Citations: 3
Potential neuroprotective peptide emerged from dual neurotherapeutic targets: A fusion approach for the development of anti-Alzheimer’s lead P Mondal, G Das, J Khan, K Pradhan, R Mallesh, A Saha, B Jana, ... ACS Chemical Neuroscience 10 (5), 2609-2620 , 2019 2019 Citations: 20
MOST CITED SCHOLAR PUBLICATIONS
Indolicidin targets duplex DNA: structural and mechanistic insight through a combination of spectroscopy and microscopy A Ghosh, RK Kar, J Jana, A Saha, B Jana, J Krishnamoorthy, D Kumar, ... ChemMedChem 9 (9), 2052-2058 , 2014 2014 Citations: 138
AFM‐based spin‐exchange microscopy using chiral molecules A Ziv, A Saha, H Alpern, N Sukenik, LT Baczewski, S Yochelis, M Reches, ... Advanced Materials 31 (40), 1904206 , 2019 2019 Citations: 84
Excited state proton transfer in the lysosome of live lung cells: normal and cancer cells R Chowdhury, A Saha, AK Mandal, B Jana, S Ghosh, K Bhattacharyya The Journal of Physical Chemistry B 119 (6), 2149-2156 , 2015 2015 Citations: 62
Spatial position regulates power of tryptophan: discovery of a major-groove-specific nuclear-localizing, cell-penetrating tetrapeptide D Bhunia, P Mondal, G Das, A Saha, P Sengupta, J Jana, S Mohapatra, ... Journal of the American Chemical Society 140 (5), 1697-1714 , 2018 2018 Citations: 53
Apoferritin nanocage delivers combination of microtubule and nucleus targeting anticancer drugs S Ghosh, S Mohapatra, A Thomas, D Bhunia, A Saha, G Das, B Jana, ... ACS Applied Materials & Interfaces 8 (45), 30824-30832 , 2016 2016 Citations: 45
Confocal microscopy of cytoplasmic lipid droplets in a live cancer cell: number, polarity, diffusion and solvation dynamics R Chowdhury, B Jana, A Saha, S Ghosh, K Bhattacharyya MedChemComm 5 (4), 536-539 , 2014 2014 Citations: 42
Evidence for new enantiospecific interaction force in chiral biomolecules Y Kapon, A Saha, T Duanis-Assaf, T Stuyver, A Ziv, T Metzger, S Yochelis, ... Chem 7 (10), 2787-2799 , 2021 2021 Citations: 39
Amphiphilic peptide with dual functionality resists biofouling A Saha, S Nir, M Reches Langmuir 36 (15), 4201-4206 , 2020 2020 Citations: 37
Novel hexapeptide interacts with tubulin and microtubules, inhibits Aβ fibrillation, and shows significant neuroprotection A Biswas, P Kurkute, S Saleem, B Jana, S Mohapatra, P Mondal, A Adak, ... ACS Chemical Neuroscience 6 (8), 1309-1316 , 2015 2015 Citations: 32
α-Cyclodextrin interacts close to vinblastine site of tubulin and delivers curcumin preferentially to the tubulin surface of cancer cell B Jana, S Mohapatra, P Mondal, S Barman, K Pradhan, A Saha, S Ghosh ACS Applied Materials & Interfaces 8 (22), 13793-13803 , 2016 2016 Citations: 30
Dual Functionalized Graphene Oxide Serves as a Carrier for Delivering Oligohistidine‐and Biotin‐Tagged Biomolecules into Cells B Jana, G Mondal, A Biswas, I Chakraborty, A Saha, P Kurkute, S Ghosh Macromolecular Bioscience 13 (11), 1478-1484 , 2013 2013 Citations: 29
Vanillin benzothiazole derivative reduces cellular reactive oxygen species and detects amyloid fibrillar aggregates in alzheimer’s disease brain PK Gharai, J Khan, R Mallesh, S Garg, A Saha, S Ghosh, S Ghosh ACS Chemical Neuroscience 14 (4), 773-786 , 2023 2023 Citations: 28
Cancer cell specific delivery of photosystem I through integrin targeted liposome shows significant anticancer activity A Saha, S Mohapatra, G Das, B Jana, S Ghosh, D Bhunia, S Ghosh ACS applied materials & interfaces 9 (1), 176-188 , 2017 2017 Citations: 28
In vitro reconstitution of a cell-like environment using liposomes for amyloid beta peptide aggregation and its propagation A Saha, G Mondal, A Biswas, I Chakraborty, B Jana, S Ghosh Chemical Communications 49 (55), 6119-6121 , 2013 2013 Citations: 25
Interaction of Aβ peptide with tubulin causes an inhibition of tubulin polymerization and the apoptotic death of cancer cells A Saha, S Mohapatra, P Kurkute, B Jana, P Mondal, D Bhunia, S Ghosh, ... Chemical Communications 51 (12), 2249-2252 , 2015 2015 Citations: 24
Targeting cytotoxicity and tubulin polymerization by metal–carbene complexes on a purine tautomer platform S Khanna, B Jana, A Saha, P Kurkute, S Ghosh, S Verma Dalton Transactions 43 (26), 9838-9842 , 2014 2014 Citations: 24
Rational design of amphiphilic peptides and its effect on antifouling performance SL Gaw, G Sakala, S Nir, A Saha, ZJ Xu, PS Lee, M Reches Biomacromolecules 19 (9), 3620-3627 , 2018 2018 Citations: 22
Synergistic anticancer effect of peptide‐docetaxel nanoassembly targeted to tubulin: Toward development of dual warhead containing nanomedicine S Mohapatra, A Saha, P Mondal, B Jana, S Ghosh, A Biswas, S Ghosh Advanced healthcare materials 6 (2), 1600718 , 2017 2017 Citations: 21
Nucleobase morpholino β amino acids as molecular chimeras for the preparation of photoluminescent materials from ribonucleosides R Bucci, A Bossi, E Erba, F Vaghi, A Saha, S Yuran, D Maggioni, ... Scientific Reports 10 (1), 19331 , 2020 2020 Citations: 20
Potential neuroprotective peptide emerged from dual neurotherapeutic targets: A fusion approach for the development of anti-Alzheimer’s lead P Mondal, G Das, J Khan, K Pradhan, R Mallesh, A Saha, B Jana, ... ACS Chemical Neuroscience 10 (5), 2609-2620 , 2019 2019 Citations: 20
