Dr Vaishali Ravindra Undale

@pharmacy.dypvp.edu.in

Professor Department of Pharmacology
Dr.D.Y.Patil Institue of Pharmaceutical Sciences and Research

Dr Vaishali Ravindra Undale


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https://researchid.co/vaishali.undale

EDUCATION

M Pharm, Ph D in pharmacology

RESEARCH, TEACHING, or OTHER INTERESTS

Pharmacology, Toxicology and Pharmaceutics, Neuroscience, Drug Discovery, Pharmaceutical Science
51

Scopus Publications

Scopus Publications

  • Advances in Parkinson's disease management using umbilical cord-derived mesenchymal stem cells
    Nishant Mante, Vaishali Undale, Avinash Sanap, Ramesh Bhonde, Supriya Kheur, Pratima Tambe, Avinash Kharat
    Journal of Neuroimmunology, 2026
  • Interplay of oxidative stress and neuroinflammation in alzheimer’s: insights into age-driven pathogenesis
    Sayed Mohammad Firdous, Shibam Chakrabortty, Vaishali R. Undale, Shouvik Mallik, Mostafa Gouda
    Inflammopharmacology, 2026
  • Calcium Bioavailability Comparison of Calcined Pearl Powder and Triturated Pearl Powder in Wistar Rats
    Payal Pradeep Wavhal, Amol H. Waghmare, Vaishali Undale, Nilima S. Dharkar
    Research Journal of Pharmacy and Technology, 2026
    Background: Pearl has been used in Ayurvedic medicine since many centuries. The two formulations i.e., Triturated Pearl powder) and Incinerated Pearl powder are used in a variety of disorders. Pearl, containing Calcium Carbonate in Aragonite form, is known to possess anti-osteoporotic, bone regenerating, sedative, anti-epileptic, and cognition-enhancing properties. Although micronized and nano-sized pearl powders have been studied for bioavailability, the pharmacokinetics of these Ayurvedic formulations of Pearl are unknown. This study elucidated the difference in bioavailability of calcium from two different forms of particle size reduction viz., trituration (heatless) and incineration (extreme heat). Methods: A single dose, randomized study was conducted on Wistar rats to observe the bioavailability of MP and MB along with Standard control Calcium lactate intervention and Normal Control Calcium levels in rats without intervention. After administration of corresponding drugs, blood sample was collected from each group at 30 min, 60 min, 3 hours, 6 hours, 12 hours and 24 hours. Calcium levels from blood samples were estimated using o-cresolphthalein complexone (oCPC) method. Results: Using collected data, Sr. Calcium levels at aforementioned time intervals, Maximum plasma concentration (Cmax), Time taken to reach maximum concentration (Tmax) and Area under the curve (AUC) were determined. Conclusion: It was noted that serum calcium levels were significantly higher in triturated pearl powder than in other calcium compounds (p<0.05), thus demonstrating that method of particle size reduction and form of the compound in final drug is crucial to enhance the bioavailability.
  • Comparative Analysis of Traditional and Modern Extraction Methods
    Vaishali Undale, Nayan Chaudhari, Samruddhi Bharud, S. M. Firdous
    Botanical Extracts Research Methods and Applications in Pharmaceutical Sciences, 2026
    Extraction methods play a pivotal role in the isolation of bioactive compounds from herbal or natural sources, forming the basis for developing effective phytopharmaceuticals and nutraceuticals, directly influencing the efficacy, safety, and quality of the final products. Traditionally, extraction methods such as maceration, percolation, decoction, and Soxhlet extraction have been widely employed due to their simplicity, cost-effectiveness, and historical precedence. These methods, however, often require longer processing times, higher solvent consumption, and may result in lower yields or degradation of thermolabile components. In contrast, modern extraction techniques—including ultrasound-assisted extraction (UAE), microwave-assisted extraction (MAE), supercritical fluid extraction (SFE), and pressurized liquid extraction (PLE)—have emerged as innovative alternatives. These advanced methods offer significant advantages such as reduced extraction time, lower solvent usage, higher selectivity, and improved preservation of sensitive phytochemicals. The need for efficient extraction arises from the growing demand for standardized, high-quality herbal nutraceuticals with consistent therapeutic profiles. Effective extraction not only maximizes the yield of desired constituents but also minimizes the presence of unwanted or toxic compounds, ensuring product safety and regulatory compliance. In conclusion, while traditional extraction techniques remain relevant for small-scale and preliminary extractions due to their simplicity and accessibility, modern extraction methods are increasingly important for industrial-scale production, high-throughput, and standardized herbal drug development, offering superior efficiency, reproducibility, and sustainability. The choice of extraction method should be guided by the nature of the target compounds, desired product quality, and scalability requirements. Ultimately, the integration of modern extraction technologies is essential for advancing the field of herbal nutraceuticals and meeting the evolving demands of the global market. This chapter provides a comprehensive comparative analysis of traditional and modern extraction methods, evaluating their principles, operational parameters, advantages, and limitations in the context of phytopharmaceuticals and nutraceuticals.
  • Evaluation of Anti-arthritic Activity of ArthoCan – V50 Tablets using CFA induced Rheumatoid Arthritis in Wistar rats
    Swagata Tavhare, Smita Jadhav, Vaishali Undale, Sarang Deshpande, Vini Mehta
    Natural Resources for Human Health, 2026
    Current pharmacological therapy for Rheumatoid arthritis (RA) has long-term safety issues. The polyherbal formulation ArthoCan-V50 is comprised of <i>Boswellia serrata</i>, <i>Vitex negundo</i>, <i>Zingiber officinale</i>, <i>Ricinus communis</i>, <i>Curcuma longa</i>, and <i>Cannabis sativa</i>. These plants are individually known for their anti-inflammatory and anti-arthritic properties, but their combination has not been previously tested for arthritis. Hence, the study is designed to assess the anti-arthritic efficacy of ArthoCan-V50 tablets in a CFA-induced (Complete Freund’s Adjuvant) Rheumatoid Arthritis (RA) rat model and to confirm safety through an acute toxicity study. Wistar rats were induced with RA using a CFA. These rats were treated with varying doses of ArthoCan-V50 (50 mg, 100 mg, and 200 mg) per 200 gm rats. Body weight, paw volume, arthritic score, haematological and biochemical markers (TNF-α, IL-1β, CRP, RF), and antioxidant enzymes superoxide dismutase (SOD), glutathione (GSH), and catalase (CAT) were evaluated. Histopathological changes were assessed using ImageJ analysis. Acute oral toxicity was studied using OECD Guideline 423. ArthoCan-V50 tablets significantly reduced the inflammation, as observed by a decrease in paw thickness, arthritic scores, and levels of pro-inflammatory cytokines (TNF-α, IL-1β) and acute-phase proteins C-reactive protein (CRP) and rheumatoid factor (RF). Also, the tablets restored the levels of antioxidant enzymes while simultaneously improving the histological architecture of joints. The 200 mg dose showed the strongest therapeutic effect. The 2000 mg/kg dose displayed no toxicity or mortality signs, indicating an ample safety margin. Evidence suggests that ArthoCan-V50 possesses strong anti-inflammatory, antioxidant, and anti-arthritic activities, with acceptable safety indexes. Although the CFA-induced RA rat model may not fully reflect human autoimmune or chronic RA, the study data suggest that ArthoCan-V50 has potential as a significant adjunctive therapy in the treatment of rheumatoid arthritis and can further be studied in human patients.
  • Formulation and Evaluation of Seed Oils Against UV-Induced Skin Damage
    Lata Kothapalli, Rakesh Ozarkar, Asha Thomas, Sonali Supe, Vaishali Undale
    Drug Delivery Letters, 2026
    Background: Reactive Oxygen Species (ROS) are generated due to UV exposure. These interact with proteins, fatty acids, and DNA, resulting in oxidative damage and photoaging. Seed oils of muskmelon (MSO), watermelon (WSO), and pumpkin (PSO), known for their rich content of essential fatty acids, carotenoids, tocopherols, phenolics, and flavonoids, are underutilised for their antioxidant activity. Objective: The present study evaluated the emulgel formulation containing MSO, WSO, and PSO against UV-induced photoaging in an animal model. Materials and Methods: Physicochemical parameters were determined, and oleic acid was quantified as an analytical marker for fatty acids present in the oils, along with phenolics and flavonoids, which provide an added advantage to the functional properties of cold-pressed seed oils. Oils were evaluated for antioxidant properties using the DPPH assay. Further, an emulgel was formulated using Carbopol 934 as the base and screened for effectiveness against UV-induced photoaging in rats. Results: Using HPTLC, the methyl ester of fatty acid equivalent to oleic acid content was estimated, with WSO showing 48.95%, higher than MSO and PSO. The total phenolic content of MSO was 0.746 mg/g GAE, and the total flavonoid content was 0.416 ± 0.10 mg/g QAE, the highest among the three oils. The prepared formulation contained a mixture of all three oils in a 1:1:1 ratio (F1 (3%) and F2 (6%)). The emulgels were evaluated and showed antioxidant potential. The emulgel caused no skin rashes or erythema when applied to the dorsal surface of rat skin before UV exposure. Histopathological data and biochemical analysis suggest that the formulation has significant potential against photoaging. Discussion: These seeds are known for their health benefits and are commonly consumed as food or dietary supplements. The combination of cold-pressed seed oils in an emulgel helped inactivating ROS and restoring skin homeostasis. However, the stability and release profile require further investigation. Conclusion: It can be concluded that the emulgel containing the combined oils (F2) shows potential for further development as a skincare product.
  • Exploring the Potential of Dolutegravir in Alzheimer's Disease Treatment: Insights from Network Pharmacology and In Silico Docking Studies
    Karishma M. Rathi, Nikhil S. Sakle, Vaishali R. Undale, Ravindra D. Wavhale, Ritesh P. Bhole, Pawan N. Karwa
    Central Nervous System Agents in Medicinal Chemistry, 2026
    Background: The search for effective treatments for neurodegenerative diseases, particularly Alzheimer's disease, has been fraught with challenges. Alzheimer's disease accounts for 60-80% of dementia cases globally, affecting approximately about 50 million people. Currently, drug repurposing has emerged as a promising strategy in new drug development, attracting significant attention from regulatory agencies, such as the US FDA. Aim: This study aimed to investigate the potential therapeutic role of dolutegravir in Alzheimer's disease (AD) treatment using a novel network pharmacology approach. Specifically, it explored the interaction of dolutegravir with key molecular targets involved in AD pathology, predicted its effects on relevant biological pathways, and evaluated its viability as a new therapeutic candidate. Objective: This study employed a network pharmacology framework to evaluate dolutegravir, an antiretroviral drug, as a potential treatment for Alzheimer's disease, shedding light on its possible therapeutic mechanisms. Method: A network pharmacology approach was used to predict the drug targets of dolutegravir. Gene Ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed to identify interacting pathways. Additionally, protein- protein interaction (PPI) network analysis was conducted to assess key interactions and molecular docking studies were performed to evaluate the binding affinity of dolutegravir to the predicted targets. Result: PPI network analysis revealed that dolutegravir interacted with several key targets, including BRAF, mTOR, MAPK1, MAPK3, NOS1, BACE1, CAPN1, CASP3, CASP7, CASP8, CHUK, IKBKB, PIK3CA, and PIK3CD. KEGG pathway analysis suggested that dolutegravir could influence amyloid-beta formation, amyloid precursor protein metabolism, and the cellular response to amyloid-beta. Molecular docking results showed the highest binding affinity of dolutegravir for PI3KCD (-8.5 kcal/mol) and MTOR (-8.7 kcal/mol). Conclusion: The findings indicated that dolutegravir holds significant potential in modulating key pathways involved in Alzheimer's disease pathogenesis. These results provide a strong foundation for further investigations into the therapeutic efficacy and safety of dolutegravir in the treatment of Alzheimer's disease. The use of drug repurposing strategies, leveraging Dolutegravir's established pharmacological profile, offers a promising route for accelerated therapeutic development in AD.
  • Dental Pulp Mesenchymal Stem Cell-Secretome Gel Reverse Areca Nut Induced Oral Submucous Fibrosis in Mice: A Pilot Study
    Nishant Mante, Supriya Kheur, Avinash Sanap, Avinash Kharat, Pranjali Potdar, Poonam Suryawanshi, Ravindra Badhe, Vaishali Undale, Nitika Monga, Ramesh Bhonde
    Journal of Oral Pathology and Medicine, 2026
    ObjectivesOral submucous fibrosis is a pre‐malignant disorder caused by habitual areca nut consumption. This pilot study investigated the therapeutic potential of dental pulp mesenchymal stem cell‐secretome chitosan gel in a mice model of areca nut extract‐induced oral submucous fibrosis.Materials and MethodsAngiogenic potential of dental pulp mesenchymal stem cell‐secretome was validated using a chick yolk sac membrane assay. Oral submucous fibrosis was induced in male Swiss albino mice (n = 40) via intraoral areca nut extract administration for 3 months. Post‐induction, animals were divided into disease control, DPMSCs‐S, and DPMSCs‐S gel groups. Treatments were administered intraorally twice weekly for 1 month. Therapeutic efficacy was assessed through measurements of mouth opening, histopathology, oxidative stress markers (LDH, MDA, SOD), and fibrotic gene expression (COL1, COL3, α‐SMA).ResultsDental pulp mesenchymal stem cells’ secretome contains pro‐angiogenic growth factors. Dental pulp mesenchymal stem cells’ secretome gel significantly improved mouth opening, restored epithelial architecture, and reduced collagen deposition. Histological staining and gene expression analyses confirmed the reversal of fibrosis and downregulation of COL1, COL3, and α‐SMA. Additionally, the gel reduced LDH and MDA levels and enhanced SOD activity, indicating antioxidant effects. The gel showed superior efficacy over the secretome alone.ConclusionDPMSCs‐S gel demonstrates significant anti‐fibrotic, antioxidant, and regenerative potential in reversing ANE‐induced OSMF in mice. These findings warrant further investigation into larger, long‐term preclinical studies.
  • Evaluation of joint pain–relieving activity of Scitican-50 tablet using Mono-Iodoacetate and complete Freund’s adjuvant–induced joint pain in wistar rats
    Sarang Deshpande, Smita Jadhav, Swagata Tavhare, Vaishali Undale, Vini Mehta
    Natural Resources for Human Health, 2025
    Current treatment of Rheumatoid arthritis and osteoarthritis is limited by side effects and cost. Scitican-50, a polyherbal formulation containing <i>Cannabis sativa</i>, <i>Ferula asafoetida</i>, <i>Piper nigrum</i>, <i>Strychnos nux-vomica</i>, and <i>Zingiber officinale</i>, offers a multi-targeted, plant-based approach. This study aimed to evaluate the joint pain-relieving, anti-inflammatory, and chondroprotective effects of Scitican-50 in monosodium iodoacetate (MIA) and complete Freund’s adjuvant (CFA) induced arthritic models in rats. Scitican-50’s joint pain-relieving activity was assessed in CFA and MIA induced arthritis models in healthy female Wistar rats (180–200 g, 6–8 weeks). Acute toxicity was evaluated per OECD 423 at 2000 mg/kg. Rats received Scitican-50 (50, 100, 200 mg/kg) or diclofenac (10 mg/kg) for 28 days. Efficacy was measured via pain threshold, inflammation, cytokine levels (TNF-α, IL-1β), and joint histology. Scitican-50 demonstrated dose-dependent efficacy in arthritic rats. Pain latency improved from 4–5 s to 7–9 s by Day 28 (p < 0.01–0.001), and paw edema reduced from 11 mm to 8 mm (p < 0.01). Knee and ankle thickness significantly declined with 100–200 mg/kg doses (p < 0.01), and radiographs showed reduced joint damage. In the MIA model, Scitican restored body weight (p < 0.05), normalized food/water intake, and improved hematological parameters, including red blood cells (RBC), white blood cells (WBC), and Hemoglobin (Hb) (p < 0.001). TNF-α and IL-1β levels decreased significantly (p < 0.01), and histology confirmed chondroprotection with cell counts comparable to diclofenac (p < 0.001). Scitican-50 exhibited dose-dependent analgesic, anti-inflammatory, and chondroprotective effects in CFA and MIA arthritis models and significantly improved pain thresholds, reduced joint swelling, normalized hematological and cytokine levels (p < 0.01–0.0001), and preserved joint structure.
  • From computational screening to zebrafish testing: repurposing of doxazosin, donepezil, and dolutegravir for neuroprotective potential in Alzheimer’s disease
    Karishma M. Rathi, Vaishali R. Undale, Ravindra D. Wavhale, Firdous Sayed Mohammed, Pawan N. Karwa, Harsh Patil
    Naunyn Schmiedeberg S Archives of Pharmacology, 2025
  • Disease microenvironment preconditioning: An evolving approach to improve therapeutic efficacy of human mesenchymal stromal cells
    Nishant Mante, Vaishali Undale, Avinash Sanap, Ramesh Bhonde, Pratima Tambe, Manoj Bansode, Rajesh Kumar Gupta
    International Immunopharmacology, 2025
  • Development of Voriconazole Proliposome Based Dry Powder for Inhalation: A Design of Experiment Approach
    Sanjeevani Deshkar, Alisha Vas, Roshani Pagar, Prabhanjan Giram, Asha Thomas, Vaishali Undale
    Pharmaceutics, 2025
  • Novel Combination of Traditional Ayurvedic Herb Piper longum L. and Modern Stem Cell Therapy for the Reversal of Glucocorticoid-Induced Osteoporosis
    Avinash Sanap, Ramesh Bhonde, Madhura Shekatkar, Avinash Kharat, Supriya Kheur, Vaishali Undale, Nilima Dharkar, Girish Tillu, Kalpana Joshi
    Molecular Nutrition and Food Research, 2025
  • A Snapshot on Clinical Trials on Zotarolimus DES: A Repurposing Drug against Myocardial Infarction
    Vaishali R. Undale, Shweta K. Lembhe, Shital D. Satone, Pratiksha Hase
    International Journal of Angiology, 2025
  • Comparative Study of Aqueous and Alcoholic Extracts of Roots of Bauhinia variegata Linn. on Cafeteria Diet Induced Obesity
    Aryaa Ankalikar, Agadi Hiremath Viswanthaswamy, Vaishali Undale
    Indian Journal of Pharmaceutical Education and Research, 2025
  • Development and Optimization of Transferosomal Gel for Efficient Topical Delivery of Berberine Hydrochloride
    Sanjeevani S. Deshkar, Arati S. Halyali, Asha B. Thomas, Vaishali R. Undale, Roshani R. Pagar, Dheeraj H. Nagore
    Drug Delivery Letters, 2025
  • Silver Nanoparticle-Infused Aloe Polysaccharides/Polyvinyl Alcohol/Sodium Alginate Nanofiber Sheet for Enhanced Burn Wound Healing
    Vinita Patole, Prathamesh Gadge, Abhay Shirode, Ganesh Ingavle, Vaishali Undale, Sanjeevani Deshkar, Avinash Sanap, Abhishek Jha, Ashlesha Pandit, Prabhanjan Giram
    Current Drug Delivery, 2025
  • Gallic acid–guar gum and chitosan-based polyelectrolyte complex film exhibited enhanced wound healing in full-thickness excision wound model
    V. Patole, Dhaneshwari Swami, Ganesh Ingavle, Isha Behere, Divya Ottoor, Nikita Vyawahare, Abhishek Jha, S. Deshkar, Vaishali R. Undale, Avinash Sanap, Supriya Kheur, Avinash Kumar
    Journal of Biomaterials Science Polymer Edition, 2025
  • The prospective role of mesenchymal stem cells in Parkinson's disease
    Pratima Tambe, Vaishali Undale, Avinash Sanap, Ramesh Bhonde, Nishant Mante
    Parkinsonism and Related Disorders, 2024
  • Effect of Combination of Alcoholic Extract of Zingiber Officinale (AEZO) and Hydroalcoholic Extract of Brassica Oleracea (HAEBO) on Papain Induced Osteoarthritis in Wistar Rats
    Pawan Karwa, Pooja Kamble, Surabhi Jarare, Addepalli V, Vaishali Undale, Shubhangi Shelar
    International Journal of Pharmaceutical Sciences and Nanotechnology, 2024
  • An Insight into the Molecular Mechanisms of Neuroinflammation
    Firdous Sayeed Mohammed, Snehasis Kundu, Vaishali R. Undale, Mayur Mali, Nahla S. Zidan, et al.
    Journal of Biological Regulators and Homeostatic Agents, 2024
  • Evaluation of Herbal Composite for Activity Against Anticancer Drug-induced Nephrotoxicity in Wistar Rats
    Akshay Narawade, Omkar Janjire, Vaishali Undale, Addepalli V, Suvarna Ingale, Pawan N Karwa, Vrushali Neve
    International Journal of Pharmaceutical Sciences and Nanotechnology, 2024
  • Inclusion of Pregnant Women in Clinical Trials: Need, Ethical and Scientific Considerations and Current Status
    Mahesh Asalkar, Hanif Shaikh, Priyanka V Mahadik, Parveen Shaikh, Anil Pardeshi, Shravani P Wakte, Krishna S Dakh, Vaishali R Undale, Anand S Kawade, Chandrashekhar Upasani
    Journal of South Asian Federation of Obstetrics and Gynaecology, 2024
  • TiO2 Nanoparticles Derived from Capparis Zeylanica: An Effective Treatment for Diabetic and Food Borne Infections
    M. Nilavukkarasi, S. Vijayakumar, Pradnya Jagtap, Vaishali Undale, Nilambari Gurav, Shailendra Gurav, R. Mythili, Sandhanasamy Devanesan, Mohamad S. Alsalhi, Woong Kim
    Waste and Biomass Valorization, 2024
  • Development and Evaluation of Self Micro-Emulsifying Formulation of Venlafaxine HCl with Improved Antidepressant Activity
    Sanjeevani Shekhar Deshkar, Shubhangi Vitthal Shekade, Nilesh Raghu, Vaishali Ravindra Undale
    Indian Journal of Pharmaceutical Education and Research, 2024
  • Rational drug repurposing for alzheimer’s treatment using in-silico ligand and structure-based approaches
    Karishma Rathi, Ravindra Wavhale, Ritesh Bhole, Vaishali Undale, Somdatta Chaudhari
    Brazilian Journal of Pharmaceutical Sciences, 2024
  • Knowledge, attitudes, awareness and factors associated with the uptake of influenza vaccine among pregnant women in urban Pune
    Hanif Shaikh, Vaishali Undale, Anil Pardeshi, Shweta Jadhav, Pratiksha Jagtap, Parth Aphale, Anand Kawade, Mahesh Asalkar, Suneth Agampodi, Aman Upaganlawar, Chandrashekhar Upasani
    Indian Journal of Obstetrics and Gynecology Research, 2024
  • Sub-Acute Toxicity Study of Hydro-Alcoholic Extracts of Sansevieria cylindrica and Plumeria obtusa in Wistar Albino Rats
    Sunil Shewale, Vaishali Undale, V. Addepalli, Vrushali Bhalchim, Shivani Desai, Vikas Wawale, Maruti Shelar, Shubham Padole, Shital Satone, Shweta Lembhe, Sameer Parekh, Pramod Pujari
    Toxicology International, 2023
  • Safety and Protective Effects of Influenza Vaccination in Pregnant Women on Pregnancy and Birth Outcomes in Pune, India: A Cross-Sectional Study
    Hanif Shaikh, Pranesha Koli, Vaishali Undale, Anil Pardeshi, Mahesh Asalkar, Sushant Sahastrabuddhe, Anand Kawade, Chandrashekhar Upasani
    Vaccines, 2023
  • Preliminary Pharmacognostic, Physicochemical and Phytochemical Evaluation of Plumeria-Obtuse Seed Pods
    Sunil Shewale, Vaishali Ravindra Undale, Maruti Shelar, Bhagyashri Warude, Mohini Kuchekar, Vrushali Bhalchim, Shital Satone, Shweta Lembhe, Sachin Gundecha
    Defence Life Science Journal, 2023
  • A Current Perspective on the Potential of Nanomedicine for Anti-Tuberculosis Therapy
    Khushboo Borah Slater, Daniel Kim, Pooja Chand, Ye Xu, Hanif Shaikh, Vaishali Undale
    Tropical Medicine and Infectious Disease, 2023
  • EXPLORING AVENUES FOR ALZHEIMER’S DRUGS: CURRENT STATUS AND FUTURE OUTLOOK
    K. Rathi, R. Wavhale, V. Undale V., R. Bhole, S. Dherange
    Russian Neurological Journal, 2023
  • A novel approach to develop an animal model for oral submucous fibrosis
    Madhura Shekatkar, Supriya Kheur, Avinash Sanap, Vaishali Undale, Avinash Kharat, Vrushali Bhalchim, Arati Dubewar, Ramesh Bhonde
    Medical Oncology, 2022
  • Evaluation and Assessment of the Acute Toxic Potential of Sansevieria cylindrica and Plumeria obtusa Plant Extracts in Wistar Albino Rats
    Sunil Shewale, Vaishali Undale, Vrushali Bhalchim, Shivani Desai, Maruti Shelar, Shubham Padole, Sohan Chitlange, Vikas Wawale, Sameer Parekh, Pramod Pujari
    Journal of Natural Remedies, 2022
  • Antidiabetics Interactions with Herbs: A Compressive Review
    Kajal Jirapure, Vaishali Undale
    Current Diabetes Reviews, 2022
  • Zebrafish: Promising Model for Cancer Research
    Mayuri Gurav, Vaishali Undale
    Zebrafish Model for Biomedical Research, 2022
  • Evaluation of the Effect of Phytocomplex on Chondroprotective Biomarkers in an Experimental Model of Osteoarthritis in Rats
    , Shridhar PANDYA, Chetan SAVALIYA, , Dheeraj NAGORE, , Vaishali UNDALE, , Shubhada KHADE, , Nishant MANTE, and
    Medicina Moderna, 2022
  • Development & quantitative analysis of validated stability-indicating analytical method for estimation of valsartan and hydrochlorothiazide by high performance thin layer chromatography
    Sunil Shewale, Vaishali Undale, Maruti Shelar, Vrushali Bhalchim, Chandramohan Panchal, Sachin Gundecha
    Materials Today Proceedings, 2022
  • Ophidian bite: The balance between perception, idealism and realism
    Tropical Journal of Natural Product Research, 2021
  • Alpha-Synuclein: Biomarker for Parkinson’s Disease, It’s Estimation Methods, and Targeted Medicinal Therapies
    Shivani V. Dhokne, Vaishali R. Undale, Dinesh Chandra Agrawal, Sharad D. Pawar
    Medicinal Herbs and Fungi Neurotoxicity Vs Neuroprotection, 2021
  • Combination of zingiber officinale and brassica oleraceae extracts shows better anti-arthritic activity
    Vaishali. R. Undale, Asawari S. Thakare, Pooja V. Katkar
    Research Journal of Pharmacy and Technology, 2020
  • Novel targets for antimicrobials
    Vaishali Ravindra UNDALE, Suchita GUPTA, Kedar LAKHADIVE
    Turkish Journal of Pharmaceutical Sciences, 2020
  • Preclinical evaluation of antihypertensive activity of combination of herbs extract in wistar rats
    Bhavika D. Satone, Atul A. Deshmukh, Vaishali R. Undale
    Research Journal of Pharmacy and Technology, 2020
  • Curcumin potentiates therapeutic efficacy of metformin: A preclinical study in STZ-NA induced hyperglycemia in wistar rats
    Vaishali. R. Undale, Sujata S. Kurkute, Srutuja S. Jadhav
    Research Journal of Pharmacy and Technology, 2020
  • Oxidants, antioxidants in physical exercise
    Oxidative Stress and Antioxidant Defense Biomedical Value in Health and Diseases, 2019
  • Protective effect of Lepidium sativum against doxorubicin-induced nephrotoxicity in rats
    Research Journal of Pharmaceutical Biological and Chemical Sciences, 2010
  • Antiarthritic and antipyretic activity of Mitragyna parvifolia leaves
    Pharmacologyonline, 2009
  • Effect of Ageratum conyzoides Linn on clonidine and haloperidol induced catalepsy in mice
    Pharmacologyonline, 2009
  • Antiinflammatory effect of Premna latifolia leaves
    Pharmacologyonline, 2009
  • Evaluation of diuretic activity of aqueous and methanol extracts of Lepidium sativum Garden Cress (Cruciferae) in rats
    U Patel, M Kulkarni, V Undale, A Bhosale
    Tropical Journal of Pharmaceutical Research, 2009
  • Antinociceptive and anti-inflammatory effects of solvent extracts of Tagetes erectus Linn (Asteraceae)
    MNV Shinde, KG Kanase, VC Shilimkar, VR Undale, AV Bhosale
    Tropical Journal of Pharmaceutical Research, 2009