Dr Prasenjit Mondal

@brainwareuniversity.ac.in

Professor
Department of Pharmaceutical Technology, Brainware University

Dr Prasenjit Mondal


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Dr. Prasenjit Mondal is presently working as an Professor at the Department of Pharmaceutical Technology, Brainware University, Ramakrishnapur road. Barasat, West Bengal. He worked several pharmaceutical Institution throughout India, with 16 years of teaching and research experience. He awarded doctoral degree from Jawaharlal Nehru Technological University, Hyderabad in the year of 2017. He has 3 Indian patents in his credit. He is the author of a three academic book in his credit. He is an active reviewer of several Clarivate Analytics (previously Thomson Reuters) indexed reputed national and international journals and editorial board members of several reputed Scopus, SCI indexed journals. He has published 74 research articles in various high impact international and national journals. He supervised more than 35 Postgraduate students for their research proposal, 20 Undergraduate students. He is also supervising one PhD students. He receives the various grants like travel grant(

EDUCATION

M. Pharm, PhD

RESEARCH, TEACHING, or OTHER INTERESTS

Pharmaceutical Science
33

Scopus Publications

574

Scholar Citations

13

Scholar h-index

15

Scholar i10-index

Scopus Publications

  • Toxicological Evaluation of Polysaccharide-Based Multi-Particulate Oral Drug Delivery System
    Subhabrota Majumdar, Sailee Chowdhury, Prasenjit Mondal, Sajal Kumar Jha, Rana Mazumder
    Journal of Pharmaceutical Innovation, 2026
  • EVALUATION OF HEPATOPROTECTIVE POTENTIAL OF APOCYNACEAE FAMILY PLANTS IN RAT MODELS OF ALCOHOL, PARACETAMOL, AND RANITIDINE-INDUCED HEPATOTOXICITY
    Subba Rao Chamakuri, ASHISH SUTTEE, PRASENJIT MONDAL, Dasari Priyanka
    Asian Journal of Pharmaceutical and Clinical Research, 2025
    Objectives: This study aimed to evaluate the hepatoprotective activity of the methanolic leaf extract of Plumeria pudica (PP) against hepatotoxicity induced by Paracetamol, ethanol, and ranitidine in rat models. Methods: The presence of key bioactive constituents, such as saponins and flavonoids in the methanolic extract of PP leaves was confirmed through gas chromatography-mass spectrometry analysis. Rats were divided into six groups (n=6/group). Hepatotoxicity was induced using Paracetamol, ethanol, and ranitidine. Silymarin served as the standard reference drug. The extract was administered at various doses, and hepatoprotective activity was assessed in comparison with the control group. Results: Treatment with PP extract significantly reduced the levels of aspartate transaminase, alanine transaminase, serum total bilirubin, total protein, triglycerides, and cholesterol when compared to the toxicant-treated group (Group II). Histopathological examination revealed reduced hepatic necrosis and inflammation, supporting the biochemical findings. Conclusion: The methanolic leaf extract of PP demonstrated significant (p<0.05*, p<0.01**, p<0.001***) hepatoprotective effects in rat models of drug- and alcohol-induced liver injury. These effects are attributed to the presence of saponins and flavonoids, which may contribute to membrane stabilization and antioxidant properties.
  • Design, Synthesis, and Pharmacological Evaluation of Novel Isatin Scaffolds as Potent Anti-Inflammatory and Antibacterial Agents
    Prasenjit Mondal, Sreejan Manna, Paramita Ganguly, Zainab Irfan, Sumanta Mondal
    Chemistryselect, 2025
    In this study, novel Mannich bases were synthesized from Schiff bases of isatin using various secondary amines. The compounds were structurally characterized using FTIR, ¹H NMR, ¹3C NMR, mass spectrometry, and elemental analysis. Their anti‐inflammatory potential was evaluated both in vitro and in vivo, with compounds IS‐SM1, IS‐SM5, and IS‐S1 showing significant activity (IC₅₀ values: 29.84, 34.64, and 31.89 µg/mL) comparable to the standard (IC₅₀: 29.17 µg/mL). Molecular docking studies using AutoDock Vina revealed strong binding affinities (scores ranging from −7.4 to −8.9) against cyclooxygenase‐1, further supported by interaction analysis using Discovery Studio 2021. Additionally, IS‐S1, IS‐SM1, IS‐SM4, and IS‐SM5 demonstrated notable antibacterial activity, with inhibition zones ranging from 24.43 to 26.93 mm against Gram‐positive and 17.11 to 22.53 mm against Gram‐negative bacteria. These findings confirm the dual anti‐inflammatory and antibacterial potential of the synthesized compounds. The current reaction scheme holds promise for further structural modifications—such as acetylation, cyclization, and chalcone formation—to explore additional pharmacological activities like anticancer, antitubercular, and antidiabetic effects, thus opening new avenues in medicinal chemistry research.
  • Evaluation of Hepatoprotective Potential of Lamiaceae Family Plants in Rat Models of Alcohol, Paracetamol and Ranitidine-Induced Hepatotoxicity
    , Subba Rao Chamakuri, Ashish Suttee, , Prasenjit Mondal, , Dasari Priyanka, and
    International Journal of Drug Delivery Technology, 2025
    The whole plant of Leucas zeylanica (Lamiaceae) was tested for hepatoprotection in Wistar rats after paracetamol (PCM), ethyl alcohol (ALC), and ranitidine (RTD) produced hepato the albino mouse acute toxicity maximum dosage was 2000 mg/kg. Six animal groups were utilized in all models. Modelling followed Silymarin. MELZWP contains saponins, carbohydrates, flavonoids, tannins, and phenolic from Leucas zeylanica whole plant. LD50 experiments showed these extracts did not kill or alter mice at 2000 mg/Kg body weight. Silymarin and MELZWP dosages increased thiopental sleeping time, wet liver weight, and volume than PCM, ALC, and RTD-induced hepatotoxic mice. Albumin (ALB) and protein (PRO) increased whereas ALT, ALP, AST, CHO, BILT, and TG dropped. Steatosis, necrosis, and other histological abnormalities were disallowed. Saponins and flavonoids protect the liver, study finds
  • Synthesis, Molecular Docking and Pharmacological Evaluation of Some New Schiff and Mannich Bases of 5-Methylisatin Derivatives
    Prasenjit Mondal, Saptarshi Samajdar, Piyali Khamkat, Vivek Barik, Sudip Kumar Mandal
    Asian Journal of Chemistry, 2024
    Two novel series of Schiff and Mannich based 5-methylisatin were synthesized by Mannich reactions and evaluated for anthelmintic and antibacterial activities. The Mannich bases were synthesized from the Schiff base using various secondary amines and formaldehyde along with the derivatives of piperazinyl groups. N-Methyl piperazinyl (ICP-2B and ICM-2B) and piperidinyl derivatives (ICP-2C and ICM-2C) were found to have a highly significant anthelmintic potential. For compound ICP-2B, the paralysis time was observed at 4.936 ± 0.12 min at low concentration (0.1 % w/v) and 1.95 ± 0.10 min at high concentration (1% w/v). At low concentration (0.1%), compound ICM-2B, the paralysis time is 4.43 ± 0.17 min; at high concentration (1% w/v), it is 1.675 ± 0.08 min. These data indicated that compounds ICP-2B and ICM-2B has immense potential as anthelminthic and antimicrobial drug in future. Moreover, the in vitro study was confirmed by molecular docking studies, indicating both compounds ICP-2B and ICM-2B can find its use as novel drug against various pathogenic helminthes and bacteria.
  • A Novel RP-Chiral Separation Technique for the Quantification of Brivaracetam and its process Related Isomeric Impurities using High Performance Liquid Chromatography
    Sandip Kumar Dey, Sumanta Mondal, Prasenjit Mondal, Kausik Bhar
    Research Journal of Pharmacy and Technology, 2023
    Reverse‐phase high‐performance liquid chromatography method has been developed for the determination of brivaracetam (BRV) with its stereoisomeric impurities (BRV-SS), (BRV-RR) and (BRV- RS). Brivaracetam with its impurities has been eluted with good resolution using the chiral column, chiralpakIG (250 × 4.6mm, 5µ) column at the detection wavelength of 210nm with the flow rate of 0.50ml/minute. The separation was achieved with the mobile phase consisted of methanol: acetonitrile and trifluoroacetic acid in the volume ratio of 90:10:0.1. The column temperature was maintained at 30°C and detection wavelength was maintained at 210 nm. Brivaracetum (BRV), and stereoisomeric impurities, BRV-SS, BRV-RR and BRV-RS, were eluted at 13.829, 11.810, 10.448 and 9.449 min, respectively. The method showed adequate specificity, sensitivity, linearity, accuracy, precision, and robustness inline to ICH tripartite guidelines. The limit of detections were 0.2 μg/mL for BRV-SS and BRV-RR, for BRV-RS it was found 0.1μg/mL.The limit of quantification limits were 0.5μg/mL for BRV-SS, BRV-RR and for BRV-RS as well.The developed method was found to be linear over the concentration range of 0.5-20µg/mL for BRV-RS, for BRV-RR and BRV-RS it was 0.5-3µg/mLfor stereoisomeric impurities with a correlation coefficient of 0.999. The developed method was found precise (%RSD = 0.5%, 0.6% and 0.5% for BRV-SS, BRV-RR and BRV-RS,) accurate (with 96%–107% recovery) and found robust. The validation parameters of the developed method were within the limits as per the regulation of ICH Q2(R1) guidelines. Therefore, in this present method a good separation was achieved specifically for the identification of brivaracetam and its processed related stereoisomeric impurities using high performance liquid chromatography and found suitable for the quantification of stereoisomeric impurities of brivaracetam in bulk scale as well.
  • Quantification of Alectinib in spiked rabbit plasma using liquid chromatography-electro spray ionization-tandem mass spectrophotometry: An application to pharmacokinetic study
    H. K. Sundeep Kumar, Suman Acharyya, Prasenjit Mondal, Pratap Kumar Patra, Satyabrata Sahu
    Current Chemistry Letters, 2023
    The current technique was developed to estimate the amount of alectinib present in spiked rabbit plasma using liquid chromatographic mass spectrometry. The liquid-liquid extraction method was used, and chromatographic separation was carried out on a C18 (4.6mm id x 50mm) analytical column with a mobile phase consisting of acetonitrile and water with 0.1% formic acid at a volume ratio of 75:25. Alectinib's product m/z +483.2 (parent) 396.1 (product) and the internal standard m/z +447.5 (parent) 380.3 (product) were both obtained using positive ion mode. The calibration curve was linear from 0.5 to 600 ng/ml. The percentage extraction recovery (98.15% → 98.86%), demonstrated excellent matrix and analyte selectivity (% interference = 0), and satisfactory stability study results in all types (% nominal 94.94% → 99.63%). The intra and interday accuracy with % nominal 97 → 98.8%, precision % CV ≤ 2% in all quality control levels. The rabbit model's pharmacokinetic parameters were examined, and alectinib's area under the curve (AUC 0—∞) was 4269 ± 8.13 hr.ng/ml. The half-life of elimination (t1/2) is 8.52 ± 6.66 hours. The currently established approach was used in rabbit blood samples for pharmacokinetic investigations of commercial formulations since it was thought to be a novel, verified bioanalytical method based on experimental results.
  • Synthesis, characterization and SAR studies of Novel Series of Spiro β-Lactam of 5-methyl-indole-2,3-dione derivatives as a potential antibacterial and anthelmintic agent
    Prasenjit Mondal, Sumanta Mondal
    Current Chemistry Letters, 2022
    A novel series of spiro cyclo-indolyl β-lactam compounds of the 5-methyl-indole-2,3-dione derivatives has been synthesized from the new Schiff bases Isatin, using the Staudinger synthesis. FT-IR, 1H-NMR, 13C-NMR, mass spectroscopy, and elemental analyses were used to describe the produced chemicals. The anthelmintic potency of the produced compounds was evaluated using standard albendazole. The antibacterial activity also tested for the synthesized compounds by calculating the zone of inhibition using cup plate method and by comparison with the standard Ampicillin against the five different pathogens (Bacillus subtilis (ATCC-1086), Pseudomonas auroginosa (ATCC-1232), Escherichia coli, (ATCC-3273), Proteus mirabilis (ATCC-224), and Staphylococcus aureus (ATCC-449)). The result of anthelmintic potential, when compared to conventional albendazole (PT: 1.324±0.12, DT: 1.421±0.21), synthesized compounds ICP-3B (PT: 1.883±0.24, DT: 1.943±0.02) and ICM-3B (PT: 1.758±0.27, DT: 1.675±0.32) were shown significant activity in terms of paralysis and death time. In the antibacterial study, the compound ICP-3B has shown 20.53mm clear zone of inhibition at 100 µg/mL against the bacteria Bacillus subtilis in comparison to the standard ampicillin (23.04 mm zone). The compound ICM-3B, clearly shows the inhibition zone of 21.27 mm against Bacillus subtilis, 24.64 mm against pseudomonas aeruginosa, 20.62mm against E. coli, 20.41 mm against Proteus mirabilis and 23.65 mm against the bacteria staphylococcus aureus at the level of 100µg/mL. It was confirmed that the compounds were synthesized as expected in the reaction scheme based on the collected spectrum and elemental data. The obtained anthelmintic ant antibacterial results also affirm the potentiality of the synthesized compounds. The further compounds can be synthesised as well as other pharmacological activities can be tested for these compounds with the concept of molecular modelling.
  • Liquid chromatography-electro spray ionization-tandem mass spectroscopy method for the quantification of alogliptin in spiked human plasma
    S. Biswal, S. Mondal, P. Mondal
    Egyptian Pharmaceutical Journal, 2021
    Background Alogliptin is the inhibitor of dipeptidyl peptidase-4. It acts to regulate blood sugar by increasing the amount of insulin in the body. Aim A liquid chromatography–mass spectroscopy/mass spectroscopy method was developed for the estimation of alogliptin in spiked human plasma. Liquid–liquid extraction technique was adopted for the extraction of alogliptin from human plasma. Materials and methods The chromatographic separation was performed on a Waters Symmetry shield RP C-18 column with 4.6-mm internal diameter, 5-μm particle size, 100A° pore size analytical column at a flow rate of 1.0 ml/min using a mixture of 0.3% formic acid and acetonitrile in the ratio of 20 : 80% v/v as mobile phase. Positive ion mode was selected to obtain the product ion m/z +339.19 (parent) →245.11 (product) for alogliptin and m/z +303.39 (parent) →232.16 (product) for internal standard. Results The developed method was satisfactorily validated as per United State Food and Drug Administration guidelines for the bioanalytical study because it exhibits excellent intraday and interday accuracy with % nominal 91.06→98.48% and precision percentage coefficient variation less than or equal to 2% in all quality control levels. Alogliptin revealed its linearity with correlation coefficient (r2=0.99) in the concentration range of 40.17–16 096 ng/ml, showed acceptable % extraction recovery (96.18→98.36%), and showed excellent matrix and analyte selectivity (% interference=0), as well as matrix effect (matrix factor 0.931 at lower quantitation limit and 1.14 at high quality control level). The stability study results of bench top, freeze thaw, autosampler, and short-term and long-term showed the accuracy in the range of 92.52–99.16% and percentage coefficient variation in the range of 0.22–1.93. Conclusion The method was successfully optimized and validated as per the United State Food and Drug Administration bioanalytical method development guidelines. The applicability of the developed method undoubtedly can further extend during preclinical and clinical trials.
  • A novel ultra performance liquid chromatography-PDA method development and validation for darunavir in bulk and its application to marketed dosage form
    Sumanta Mondal, Sabyasachi Biswal, Prasenjit Mondal
    Journal of Pharmacy and Bioallied Sciences, 2021
    Aims and Objective: The aim of this study was to develop and validate a novel ultra-performance liquid chromatographic method for estimation of darunavir in a bulk and tablet dosage form. Materials and Methods: The chromatographic separation was achieved using DIKMA Endoversil (2.1 mm x 50 mm, 1.7 µm) column. A mixture of 40% buffer (0.1% octa sulfonic acid) and 60% acetonitrile was used as a mobile phase with the isocratic elution mode and eluent was monitored at 281nm using UV detector. The method was continued and validated in accordance with International Conference on Harmonization Guidelines. Validation study revealed the specificity and reliability of the method. Results: In this method, darunavir was eluted with retention time of 0.516 min. Calibration curve plots were found linear over the concentration ranges 10–50 μg/mL for darunavir. Limit of detection was 0.02 μg/mL and limit of quantification was found 0.07 μg/mL. The present method was also found stable in force degradation study. Conclusion: The empirical evidences of all the study results revealed the suitability of the estimation of darunavir in bulk and tablet dosage form without any interference from the excipients.
  • A tangy twist review on hog-plum: Spondias pinnata (l.f.) kurz
    Sumanta Mondal, Kausik Bhar, Naresh Panigrahi, Prasenjit Mondal, Sridhar Nayak, Rudra Pratap Barik, Koyyana Aravind
    Journal of Natural Remedies, 2021
  • Carbon Tetrachloride, Alcohol and Ranitidine Induced Hepatotoxicity and Its Protection by Bark Extracts of Bassia Latifolia in Wister Rats
    Manish Kumar Thimmaraju, Prasenjit Mondal, Kola Venu, Bookya Padmaja, Gummadi Sridhar Babu, Rudra Dinesh Kumar, Konda Ravi Kumar
    Journal of Herbs Spices and Medicinal Plants, 2020
  • Herb-drug interaction study between Aloe vera and glimepiride in normal and diabetic rats
    Prasenjit Mondal, Kola Venu, ManishKumar Thimmaraju, Shaik Chanbasha
    Egyptian Pharmaceutical Journal, 2020
  • An eye-catching and comprehensive review on plumeria pudica jacq.(bridal bouquet)
    Plant Archives, 2020
  • Prevalence of vitamin D deficiency and its relationship with epileptic severity in a pediatric department of tertiary care hospital
    Venu Kola, Chandana Kamili, Shivaram Prasad, BattulaHarsha Vardhan, Kompelli Koushik, Nadigittu Akshita, Sanjana Yadav, Sharadha Radhakrishnan, Konde Abbulu, Prasenjit Mondal
    Egyptian Pharmaceutical Journal, 2020
  • Quantification of fosamprenavir in spiked human plasma using liquid chromatography-electrospray ionization-tandem mass spectrophotometry-application to pharmacokinetic study
    M. Thimmaraju, P. Mondal, K. Venu, G. Babu, Gaju Rajkumar, B. Padmaja
    Egyptian Pharmaceutical Journal, 2019
  • Toxicological evaluation of meloxicam and ketorolac loaded chitosan and PLGA nanoparticle formulations
    Latin American Journal of Pharmacy, 2019
  • Study on drug-drug interaction between carvedilol and gliclazide in normal and diabetic rats
    Latin American Journal of Pharmacy, 2019
  • Quantification of duloxetine in spiked human plasma using LC-MS/MS and its application to pharmacokinetic study
    Latin American Journal of Pharmacy, 2019
  • Evaluation of toxicological, diuretic, and laxative properties of ethanol extract from Macrothelypteris Torresiana (Gaudich) aerial parts with in silico docking studies of polyphenolic compounds on carbonic anhydrase II: An enzyme target for diuretic activity
    Sumanta Mondal, Naresh Panigrahi, Purab Sancheti, Ruchi Tirkey, Prasenjit Mondal, Sara Almas, Venu Kola
    Pharmacognosy Research, 2018
  • Antiarthritic potential of aqueous and ethanolic fruit extracts of 'Momordica charantia' using different screening models
    Pharmacognosy Research, 2018
  • A Novel UPLC-PDA Method for the Simultaneous Determination of Lamivudine, Zidovudine and Nevirapine in Bulk and Tablet Dosage Form
    Prasenjit Mondal, Kunta Mahender, Bookya Padmaja
    Analytical Chemistry Letters, 2018
  • Investigation of cytotoxic activity of prepared PLGA nanoparticle formulations of meloxicam in HT29 colon cancer cell lines
    Latin American Journal of Pharmacy, 2017
  • Quantification of blonanserin in human plasma using liquid chromatography- electrospray ionization-tandem mass spectrophotometry-application to pharmacokinetic study
    Mondal Prasenjit, Shobharani Satla, Ramakrishna Raparla
    Journal of Young Pharmacists, 2016
  • A novel simultaneous quantification method for escitalopram and etizolam in human plasma using liquid chromatography-ESI-tandem mass spectrophotometry-application to pharmacokinetic study
    Prasenjit Mondal, Satla Sobharani, Raparla Ramakrishna
    Current Pharmaceutical Analysis, 2016
  • A novel quantification method for the simultaneous estimation of losartan potassium and hydrochlorothiazide in bulk and tablet dosage form using simultaneous equation method
    Der Pharmacia Lettre, 2016
  • Novel extractive colorimetric and UV spectrophotometric estimation of etizolam in bulk and tablet by forming ion association complex with methyl orange and bromocresol green
    Prasenjit Mondal, A. Rama Narsimha Reddy, Gadapa Swarnamanju, Ramakrishna Raparla
    Toxicological and Environmental Chemistry, 2015
  • Novel stability indicating validated RP-HPLC method for simultaneous quantification of Artemether and lumefantrine in bulk and tablet
    Prasenjit Mondal, Satla Rani, Raparla Ramakrishna
    Current Pharmaceutical Analysis, 2014
  • A pivotal role of insulin like growth factor in malignant neoplasm
    International Journal of Pharmacy and Pharmaceutical Sciences, 2013
  • A new stability indicating validated method for the determination of aripiprazole in bulk and tablet dosage form using RP- HPLC
    International Journal of Pharmacy and Pharmaceutical Sciences, 2013
  • Development of new simple and economic validated RP-HPLC method for the determination of famciclovir in bulk and tablet dosage
    Der Pharmacia Lettre, 2013
  • A new validated simultaneous RP-HPLC method for estimation of escitalopram oxalate and etizolam in bulk and table dosage form
    Der Pharma Chemica, 2013
  • Synthesis of some new isoxazoline derivatives of chalconised indoline 2-one as a potential analgesic, antibacterial and anthelmimtic agents
    P. Mondal, S. Jana, A. Balaji, R. Ramakrishna, L.K. Kanthal
    Journal of Young Pharmacists, 2012

RECENT SCHOLAR PUBLICATIONS

  • Novel Isatin Derivatives as Antidiabetic Agent
    SS Manami Sardar, Prasenjit Mondal , Teasha Chakrabarty
    Indian Journal of Natural Sciences 17 (95) , 2026
    2026
  • EVALUATION OF HEPATOPROTECTIVE POTENTIAL OF APOCYNACEAE FAMILY PLANTS IN RAT MODELS OF ALCOHOL, PARACETAMOL, AND RANITIDINE-INDUCED HEPATOTOXICITY
    SRAO CHAMAKURI, A SUTTEE, P MONDAL, D PRIYANKA
    EVALUATION 18 (8) , 2025
    2025
  • Design, Synthesis, and Pharmacological Evaluation of Novel Isatin Scaffolds as Potent Anti-Inflammatory and Antibacterial Agents
    SM Prasenjit Mondal, Sreejan Manna, Paramita Ganguly, Zainab Irfan
    chemistry select 10 (22) , 2025
    2025
    Citations: 2
  • Advanced UPLC-Photo Diode Array Method for Precise Quantification of Sotagliflozin in Bulk and Commercial Formulations
    AS Chatterjee B, Mondal P
    Oriental Journal of Chemistry 41 (2) , 2025
    2025
  • Advanced UPLC-Photo Diode Array Method for Precise Quantification of Sotagliflozin in Bulk and Commercial Formulations
    DP Subba Rao Chamakuri , Ashish Suttee, Prasenjit Mondal
    International Journal of Drug Delivery Technology 15 (1) , 2025
    2025
  • Beyond the Surface: An In-Depth Look at Tomato Flu
    JPKMA Mondal Prasenjit*, Biswas Supriti, Abbasuddin S.K.
    International Journal of Zoological Investigations 11 , 2025
    2025
  • Evaluation of Hepatoprotective Potential of Lamiaceae Family Plants in Rat Models of Alcohol, Paracetamol and Ranitidine-Induced Hepatotoxicity
    SR Chamakuri, A Suttee, P Mondal, D Priyanka
    Journal of King Saud University-Science 36 (11) , 2024
    2024
  • Medicinal plants effective against dengue fever in India: A brief review
    SDJ Ganguly P, Mandal SK, Mondal P
    Journal of Biochemicals and Phytomedicine 3 (1) , 2024
    2024
    Citations: 3
  • Synthesis, Molecular Docking and Pharmacological Evaluation of Some New Schiff and Mannich Bases of 5-Methylisatin Derivatives
    SK Mondal, P., Samajdar, S., Khamkat, P., Barik, V., & Mandal
    Asian Journal of Chemistry 36 (10) , 2024
    2024
  • Formulation and Evaluation of Propranolol Hydrochloride Sustained Release Matrix Tablets Using Different Grades of HPMC and MCC.
    P Khamkat, V Barik, BB Barik, A Chakraborty, D Patra, P Mondal, ...
    International Journal of Pharmaceutical Investigation 13 (4) , 2023
    2023
    Citations: 3
  • A Novel RP-Chiral Separation Technique for the Quantification of Brivaracetam and its process Related Isomeric Impurities using High Performance Liquid Chromatography
    sandip kumar dey sumanta mondal prasenjit Mondal
    Research Journal of Pharmacy and Technology 16 (7) , 2023
    2023
    Citations: 1
  • In silico studies on the phytochemical components of Lagenaria siceraria targeting aromatase receptors against breast cancer.
    M saptarshi samajdar
    insilico pharmacology 11 , 2023
    2023
  • In Quest of the Mysterious Holistic Vedic Herb Bacopa monnieri (L.) Pennell. Pharmacog Res
    M mondal
    Pharmacognosy research , 2023
    2023
    Citations: 27
  • A Promising Analytical Method has been Crafted, Validated, and Quantified for Estimating Theophylline Utilizing UV Spectroscopic and RP-HPLC Techniques in Conjunction with …
    MP Mondal
    Journal of pharmaceutical research international 35 (4) , 2023
    2023
    Citations: 2
  • Quantification of Alectinib in spiked rabbit plasma using liquid chromatography- electro spray ionization-tandem mass spectrophotometry: An application to pharmacokinetic study
    sandip kumar Prasenjit Mondal
    Current chemistry letters 12 (2) , 2023
    2023
  • An Insight into the Elusive Healer Plant “Luffa echinata Roxb.”.
    S Mondal, K Bhar, R Kumari, P Mondal, S Chakraborty, NY Teja
    Pharmacognosy Research 15 (1) , 2023
    2023
    Citations: 4
  • In Quest of the Mysterious Holistic Vedic Herb Bacopa monnieri (L.) Pennell
    Pharmacognosy research , 2023
    2023
  • GC-MS Analysis and Assessment of the Anthelmintic Potential of the Arial Parts of the Common Indian Vegetative Plant Lagenaria siceraria (Molina) Standley (LS).
    P Mondal
    International journal of pharmaceutical investigation , 2023
    2023
    Citations: 3
  • Investigating the antimicrobial effect of Loranthus europeaus leaf hydroalcoholic extract against methicillin-resistant Staphylococcus aureus
    MP Mohammadrezaei Khorramabadi R, Mandal SK, Bose A
    Journal of Biochemicals and Phytomedicine 1 (1) , 2022
    2022
    Citations: 5
  • Ideologues Established Yash Churna's Authenticity using Pharmacognostic, Physicochemical, and Chromatographic Approaches
    K Bhar, S Mondal, P Mondal
    NeuroQuantology 20 (10), 10498 , 2022
    2022

MOST CITED SCHOLAR PUBLICATIONS

  • Synthesis of some new isoxazoline derivatives of chalconised indoline 2-one as a potential analgesic, antibacterial and anthelmimtic agents
    P Mondal, S Jana, A Balaji, R Ramakrishna, LK Kanthal
    Journal of Young Pharmacists 4 (1), 38-41 , 2012
    2012
    Citations: 60
  • Synthesis Of Novel Mercapto-Pyrimidine And Amino-Pyrimidine Derivatives Of Indoline-2-One As Potential Antioxidant & Antibacterial Agents.
    KLK Mondal Prasenjit
    The Pharma Research 3 (1) , 2010
    2010
    Citations: 38
  • Evaluation of anthelmintic activity of carica papaya latex using pheritima posthuma
    LK Kanthal, P Mondal, S De, S Jana, S Aneela, K Satyavathi
    International Journal of Life Science and Pharma Research 2 (1), 10-2 , 2012
    2012
    Citations: 34
  • Synthesis and evaluation of 1, 3 Di-substituted schiff, mannich bases and spiro isatin derivatives
    P Mondal, S Jana, A Bose, M Banerjee
    Journal of Young Pharmacists 2 (2), 169-172 , 2010
    2010
    Citations: 34
  • Novel stability indicating validated rp-hplc method for simultaneous quantification of artemether and lumefantrine in bulk and tablet
    P Mondal, S Shobha Rani, R Ramakrishna
    Current Pharmaceutical Analysis 10 (4), 271-278 , 2014
    2014
    Citations: 33
  • In Quest of the Mysterious Holistic Vedic Herb Bacopa monnieri (L.) Pennell. Pharmacog Res
    M mondal
    Pharmacognosy research , 2023
    2023
    Citations: 27
  • An eye-catching and comprehensive review on Plumeria pudica Jacq.(Bridal Bouquet)
    SR Chamakuri, A Suttee, P Mondal
    Plant Arch 20 (2), 2076-2079 , 2020
    2020
    Citations: 20
  • A novel UPLC-PDA method for the simultaneous determination of lamivudine, zidovudine and nevirapine in bulk and tablet dosage form
    P Mondal, K Mahender, B Padmaja
    Analytical Chemistry Letters 8 (1), 131-138 , 2018
    2018
    Citations: 20
  • “Haripriya” god's favorite: Anthocephalus cadamba (Roxb.) Miq.-At a glance
    S Mondal, K Bhar, A Mahapatra, J Mukherjee, P Mondal, S Rahaman, ...
    Pharmacognosy Research 12 (1), 1-16 , 2020
    2020
    Citations: 18
  • Evaluation of toxicological, diuretic, and laxative properties of ethanol extract from Macrothelypteris torresiana (Gaudich) aerial parts with in silico docking studies of …
    S Mondal, N Panigrahi, P Sancheti, R Tirkey, P Mondal, S Almas, V Kola
    Pharmacognosy Research 10 (4), 408-416 , 2018
    2018
    Citations: 17
  • Development and validation of few UV spectrophotometric methods for the determination of valganciclovir in bulk and pharmaceutical dosage form
    S Mondal, GS Reddy, P Mondal, VS Prathyusha, AP Nair, ST Rahaman
    Pharmaceutical Methods 9 (2), 64-68 , 2018
    2018
    Citations: 17
  • A New Validated Simultaneous RP- HPLC Method for Estimation of Escitalopram oxalate and Etizolam in Bulk and Table Dosage Form
    R Prasenjit Mondal*, Santhosh. B , Sobha rani satla
    Der Pharma Chemica , 2013
    2013
    Citations: 17
  • Evaluation of antitumor potential of synthesized novel 2-substituted 4-anilinoquinazolines as quinazoline-pyrrole hybrids in MCF-7 human breast cancer cell line and A-549 human …
    R Bathula, P Mondal, R Raparla, SR Satla
    Future Journal of Pharmaceutical Sciences 6 (1), 44 , 2020
    2020
    Citations: 14
  • Antiarthritic potential of aqueous and ethanolic fruit extracts of" Momordica charantia" using different screening models
    V Kola, P Mondal, M Thimmaraju, S Mondal, N Rao
    Pharmacognosy Research 10 (3) , 2018
    2018
    Citations: 12
  • A New Stability Indicating High Performance Liquid Chromatography Method for the Estimation of Ruxolitinib in Bulk and Tablet Dosage Form.
    Sabyasachi Biswal, Sumanta Mondal, Prasenjit Mondal
    Pharmaceutical methods , 2019
    2019
    Citations: 11
  • Synthesis, characterization and SAR studies of Novel Series of Spiro β-Lactam of 5-methyl-indole-2,3-dione derivatives as a potential antibacterial and anthelmintic agent
    PMS Mondal
    Current chemistry letters 11 (4), 341-422 , 2022
    2022
    Citations: 9
  • Detection of secondary metabolites using HPTLC and GC-MS analysis and assessment of pharmacological activities of Phoenix loureiroi Kunth (Arecaceae) ethanolic leaves extract …
    S Mondal, P Mondal, SK Sahoo, N Panigrahi, S Almas, K Bhar, ...
    Discovery Phytomedicine 8 (2), 67-82 , 2021
    2021
    Citations: 9
  • Herb–drug interaction study between and glimepiride in normal and diabetic rats
    P Mondal, K Venu, MK Thimmaraju, S Chanbasha
    Egyptian Pharmaceutical Journal 19 (2), 124-135 , 2020
    2020
    Citations: 9
  • A New Stability Indicating Ultra Performance Liquid Chromatography-PDA Method for the Estimation of Valganciclovir in Bulk and Tablet Dosage Form.
    S Mondal, GS Reddy, P Mondal, VS Prathyusha, AP Nair, ST Rahaman
    Pharmaceutical Methods 9 (2) , 2018
    2018
    Citations: 9
  • Liquid chromatography–electro spray ionization–tandem mass spectroscopy method for the quantification of alogliptin in spiked human plasma
    S Biswal, S Mondal, P Mondal
    Egyptian Pharmaceutical Journal 20 (1), 82-91 , 2021
    2021
    Citations: 8