LALCHAND DAYANAND DEVHARE

D. Devhare graduated from Sharad Powar college of Pharmacy Nagpur in 2013 with a B. Pharm in Pharmaceutical Sciences and Post graduated from same college in 2015 with a M. Pharm in Quality Assurance and Doctorate from Oriental University Indore in 2023 with Ph. D.
The author also has a qualification such as DNYS, PGDBM, PGDFSQM and BEMS. At present the author is working as Principal at Manwatkar College of Pharmacy, Ghodpeth, Chandrapur, Maharashtra, India. He has more than 30 publication in various reputed national and international journals, attained more than 25 conferences worldwide, Grant 11 patent in different country, Life member in different association and Award received “Bharat Gaurav Puraskar”, “ Ambedkar Manavi Hakk Puraskar” “India Proud Book of Records” & “Best Paper Award”. As well as he is an author of another 11 books.

EDUCATION

Graduated from Sharad Powar College of Pharmacy Nagpur in 2013 with a B. Pharm in Pharmaceutical Sciences and Post graduated from the same college in 2015 with an M. Pharm in Quality Assurance and Doctorate from Oriental University Indore in 2023 with Ph. D.
The author also qualifies such as DNYS, PGDBM, PGDFSQM, and BEMS.

RESEARCH, TEACHING, or OTHER INTERESTS

Medicine, Multidisciplinary, Health Informatics, General Medicine

Scopus Publications

Quality by Design Approach to Nasal Mucoadhesive Microspheres: Enhanced Sumatriptan Succinate Delivery through Formulation and Characterization
Shivanee . Vyas, Anitha K N, Niranjan Babu Mudduluru, and Lalchand D Devhare
Dr. Yashwant Research Labs Pvt. Ltd.
The primary therapeutic indications for sumatriptan succinate (STS) include the treatment of migraine and cluster headaches. To enhance mucoadhesion, sodium carboxymethyl cellulose (SCMC) and hydroxyl propyl methyl cellulose (HPMC K15M) were used in this study to develop nasal mucoadhesive microspheres of STS. A central composite design, facilitated by Design Expert software, was employed to assess the impact of polymer concentrations on mucoadhesion, involving nine different formulations. The study’s findings indicated that the microspheres were uniformly sized and spherical and that the polymers were compatible with STS. The optimal formulation, consisting of 220.711 mg of SCMC and 150 mg of HPMC K15M, demonstrated the highest level of mucoadhesion. This combination effectively regulated the discharge of STS from the mucoadhesive microspheres and significantly improved their mucoadhesive properties. These results suggest that the strategic use of SCMC and HPMC K15M can enhance the performance of nasal mucoadhesive microspheres, ensuring a controlled release of STS and improved adhesion to mucosal surfaces. This has the potential to optimize the therapeutic efficacy of STS in treating migraine and cluster headaches.


Therapeutic and Phytochemical Properties of Thymoquinone Derived from Nigella sativa
Gaurav Tiwari, Monisha Gupta, Lalchand D. Devhare, and Ruchi Tiwari
Bentham Science Publishers Ltd.
Background: Nigella sativa (N. sativa), commonly known as black seed or black cumin, belongs to the family Ranunculaceae. It contains several phytoconstituents, Thymoquinone (TQ), thymol, thymohydroquinone, carvacrol, and dithymoquinone. TQ is the main phytoconstituent present in N. sativa that is used as an herbal compound, and it is widely used as an antihypertensive, liver tonic, diuretic, digestive, anti-diarrheal, appetite stimulant, analgesic, and antibacterial agent, and in skin disorders. Objective: The study focused on collecting data on the therapeutic or pharmacological activities of TQ present in N. sativa seed. Methods: Antidiabetic, anticancer, immunomodulator, analgesic, antimicrobial, anti-inflammatory, hepato-protective, renal protective, and antioxidant properties of TQ have been studied by various scientists. Conclusion: TQ seems to have a variety of consequences on how infected cells behave at the cellular level.


Optimizing Verapamil Hydrochloride In-situ Delivery: A Strategic Formulation Approach using Box-Behnken Design for Enhanced Performance and Comprehensive Evaluation of Formulation Parameters
Ram K Choudhary, Sulochana Beeraka, Biresh K Sarkar, G Dharmamoorthy, and Lalchand Devhare
Dr. Yashwant Research Labs Pvt. Ltd.
This study focuses on formulating and assessing an in-situ gastro-retentive gel for precise delivery of verapamil hydrochloride to the stomach, aiming to extend its residence time and improve targeted delivery. Gels were synthesized in-situ using a cation-controlled gelation method, incorporating varied blends of pectin and HPMCK4M. Design Expert’s box behnken design was employed to assess responses such as buoyancy lag time, water uptake, and cumulative drug discharge. Results revealed that the developed gels exhibited a total float time exceeding 10 hours, with formulation T-2 showing the least floating lag time and a cumulative drug release of 99.40 ± 3.24% over 10 hours. This suggests effective prolongation of the gastric residence time, enabling controlled verapamil hydrochloride release. Additional evaluations, including appearance, pH, viscosity, in-vitro gel formation, drug content, density, and gel force, supported the robustness of the developed gels. Subsequent in-vitro dissolution and stability studies affirmed consistent active ingredient content, highlighting formulation stability over time. In conclusion, this study demonstrates that the in-situ gels effectively extend gastric residence time, facilitating controlled verapamil hydrochloride release, marking significant advancements in drug delivery systems and targeted drug delivery within the gastrointestinal tract.


Synthesis, DNA Binding, Molecular Docking and Anticancer Studies of Copper (II), Nickel (II), and Zinc (II) Complexes of Primaquine-based Ligand
M Gnana Ruba Priya, Lal Prasanth ML, Lalchand D Devhare, Shaik K Yazdan, and Sachinkumar Gunjal
Dr. Yashwant Research Labs Pvt. Ltd.
In a research study, a metal-based complex demonstrated anticancer properties. The process involved the synthesis of a compound called 7-chloro-N-[5-(diethylamino)pentan-2-yl]-N-[sulfanyl(carbonothioyl)]quinolyn-4-amine, which incorporated a primaquine-based dithiocarbamate ligand. This synthesis method utilized sodium hydroxide and carbon disulfide at temperatures of 0 to 5℃. Nickel(II), copper(II), and zinc(II) ions were employed as the metal-complexed ligands through various chromatographic and spectroscopic techniques that enhanced their purity. Metal compounds, such as cisplatin and its analogs, were widely used to treat different cancer types. Presently, researchers are exploring alternative metal-based complexes as potential agents against cancer, aiming to mitigate toxic effects linked to medications made of platinum. Investigations conducted in-silico revealed that the ligand preferred interacting with DNA’s minor groove, assembling a single hydrogen bond between an adenine hydrogen atom and the oxygen element of the carbonyl compound in the pyrrolidinone unit. Compared to cisplatin, copper complexes can overcome drug resistance by lowering their toxicity. The findings indicate that these primaquine analogs have the potential to lay the foundation for a novel and efficacious category of cancer chemotherapeutics.


Design Development and Characterization of Nicardipine Solid Lipid Nano-Particulars
Kotha Kranthi Kumar, Vema Kiran, Ram Kumar Choudhary, Lalchand D Devhare, and Sachinkumar Dnyaneshwar Gunjal
Dr. Yashwant Research Labs Pvt. Ltd.
The present work was designed and characterized nicardipine solid lipid nano-particulars and formulated into capsule. The formulation was evaluated and stability also as per the specified limits. The nanoparticles were prepared by solid hydrophilic adsorbents. The obtained ratio of 1:1:1:2 of drugs, soy PC, DMPC, and labrasol shows the highest dissolved in water. The liquid form was converted into a solid product using an adsorbent like anhydrous lactose and aerosil 200. The above results indicated aerosil 200 containing which helped in enhanced dissolve state in water. The results indicated the formulation trial-6 %drug content -100.2, entrapment efficiency 84.13 ± 1.64, zeta potential measurement 0.789 ± 0.32, Drug release rate at 3rd hour 81.6% and relative bioavailability of optimized nanoparticle formulation (CNF-6) was significantly increased. As a result, the produced lipid-based formulation shown potential as a method for improving the transfer of lipophilic chemicals that are weakly water-soluble to the aqueous phase, hence improving oral bioavailability


Formulation and Evaluation of Mosquito Repellent Stick
Bobde K Shriram, Lalchand D Devhare, Archana Mehrotra, Savita S Deokar, and Surya P Singh
Dr. Yashwant Research Labs Pvt. Ltd.
Most of mosquito-repellent products and devices are made up of synthetic materials presenting market which causes various harmful effects on human beings. The resistance can be developed by the mosquito due to continuous exposure at high doses. Hence, the present research work represents the development and evaluation of mosquito repellent sticks with the help of various herbal products such as starch powder, wood powder, charcoal powder, eucalyptus oil, coconut oil, lavender oil, lemongrass and cinnamon oil, peppermint and citronella, neem oil making them ozone-friendly, financial effective, non-harmful.


Design and Development of Novel Mini Tablet Cap Technology for the Treatment of Cardiovascular Diseases
Anil K. Adimulapu, Lalchand D. Devhare, Anasuya Patil, Nilesh O. Chachda, and G. Dharmamoorthy
Dr. Yashwant Research Labs Pvt. Ltd.
Objectives: The purpose of the investigation was to extend and evaluate the novel mini tablet cap for treating cardiovascular disease at a desired combinational therapeutic activity and to improve patient compliance. A cheap four-in-one pill can guard against heart attacks and stroke. Methods and Materials: The drug product was manufactured by mini tablet cap technology. The technology was designed to initially use hydrochlorothiazide, simvastatin immediate release, metoprolol succinate, and asprin sustained release to reach the therapeutic levels at prolonged therapy. The two mini-bilayer tablets were prepared by wet granulation method and compression coated with a hydrophobic and hydrophilic polymer like ethyl cellulose and super disintegrating agents to release simvastatin and hydrochlorothiazide immediately. Results: Fourier transformer infrared spectroscopy (FTIR) studied the interaction studies of four chosen drugs. The mini tablet cap technology was designed as two mini bi-layer tablets in a capsule. The quantitative detection of four individual drugs was determined by using the RP-HPLC method. It was found that RP-HPLC is sensitive, reproducible, and valid for determining the mini tablet cap. The in-vitro drug release studies found that simvastatin and hydrochlorothiazide release 90% immediately within 20 minutes. Metoprolol and aspirin controlled the release for up to 24 hours, and drug release kinetics found that the drug release behavior of the optimized formulation followed first-order kinetics. Conclusion: The mini tablet cap is one of the best dosage forms to treat cardiovascular diseases. Because it was reported, the combination of these four drugs reduces mortality by 83% in high-risk patients with heart diseases, hypertension, diabetes, and obesity. The novel mini tablet cap approach data revealed a promising formula for improved relief of patient complaints during treatment or prevention of cardiovascular diseases


Synthesis, Characterisation, Molecular Docking Studies and Biological Evaluation of Novel Benzothiazole Derivatives as EGFR Inhibitors for Anti-breast Cancer Agents
Gnana R. Priya M, Lalchand D. Devhare, G. Dharmamoorthy, Mahendra V. Khairnar, and R. Prasidha
Dr. Yashwant Research Labs Pvt. Ltd.
Novel (2-anilino-N-(4,6-dimethyl-1,3-Benzosulfonazol-2-yl) ethanamide derivatives were synthesized and characterized by spectroscopy methods. All the compounds assessed for in-vitro antimicrobial activities on three strains are S. aureus, S. epidermis and E. coli by using disc plate method (25 μg/mL). Compounds 5a-5j showed good to excellent antimicrobial activity for three different strains compared to standard ciprofloxacin. Further screened by in-vitro cytotoxic activity against MCF-7 cell lines. Some compounds were 5i, 5c, 5b,5d and 5i showed high cytotoxic activities of IC50 values 73, 53,37,32 and 24 μg/mL, reference drug as Gefitinib against MCF-7 cell lines and MCF-12A. Further carried out docking studies using Schrodinger software to analyze the orientations, interactions and binding modes of these derivatives at the adenine -5-triphosphate binding site of EGFR (PDB ID: 2ITY), which indicated that the ligands show good interactions with active site residues in this structural benzothiazole class, and are considered lead compounds for further development as anti-breast cancer drugs


Synthesis and In-vivo Anticancer Evaluation of N-(4-oxo-2-(4-((5-aryl-1,3,4 thiadiazole-2yl) amino) Phenyl thiazolidine-3-yl) Benzamide derivative
Amit Chawla, Lalchand Devhare, G. Dharmamoorthy, Ritika ., and Sachin Tyagi
Dr. Yashwant Research Labs Pvt. Ltd.
The development of novel antitumor agents is paramount in the fight against drug resistance and its associated cardiotoxicity. The present study carried out a thorough anticancer evaluation of N- (4-oxo-2-(4-((5-aryl-1,3,4 thiadiazole-2yl) amino) phenyl thiazolidine-3-yl) benzamide (TH08) in Ehrlich ascites carcinoma (EAC) in Swiss albino mice. Our assessment included the measurement of tumor weight, the duration of survival for mice with tumors, and tumor cell growth inhibition. Additionally, we analyzed hematological parameters, like white and red blood cells and hemoglobin levels. The results we obtained clearly demonstrate that TH08 is a potent anticancer agent that exerts a positive effect on EAC cells. To determine TH08's effectiveness, We compared our findings to those achieved by using the standard medication, bleomycin. Our findings provide compelling evidence that TH08 has significant potential as a novel antitumor agent.


An updated review on recent developments and applications of fish collagen




Microemulgel-based Hydrogel of Diclofenac Sodium using Lipidium sativum as a Gelling Agent
Minal Sonule, Lalchand D Devhare, M Niranjan Babu, Sachinkumar D Gunjal, and S Varalaxmi
Dr. Yashwant Research Labs Pvt. Ltd.
Aim was to prepare hydrogel containing diclofenac sodium using Lipidium sativum as a gelling agent within a micro emulsion-based system. The oil phase consisted of soybean oil, while surfactants, namely Span 80 and Tween 20, were employed in the formulation. Absolute ethanol was used as a co-surfactant and were characterized by a phase diagram. The in-vitro permeation information is derived from the Franz diffusion. Different microemulsion was designed by screening of various components by performing pseudo-ternary phase diagram and then a solubility study. From this psudo-ternary phase diagram was constructed. In-vitro permeation data was screened from these results the topical delivery of diclofenac sodium microemulsion was clearly confirmed as being by means of w/o microemulsion systems. The optimized formulation of the microemulsion consist of soya bean oil 1.25 mL, span:Tween 20 : 2.5 mL, ethanol 1-mL, water 0.2 mL, L. sativum mucilage and it is compared with the marketed preparation. So, the micro emulsion-based hydrogel of diclofenac using L. sativum mucilage can be used as a gelling agent for a topical drug delivery system.


Antioxidant and Antiulcer property of different solvent extracts of Cassia tora Linn.
Lalchand D. Devhare and Niharika Gokhale
A and V Publications
Aim: The fundamental objective and goal of the current research is to determine the effectiveness of Cassia tora in the treatment of gastric ulcers in order to produce an anti-ulcer medication of natural origin. Method: The plant material was successively extracted by the Soxhlet extraction technique with chloroform, methanol, butanol and water. The antioxidant activity of the plant extracts and the standard drugs were based on consideration of the radical scavenging influence of the stable "1,1-diphenyl-2-picrylhydrazyl" (DPPH) free radical action and hydrogen peroxide process. Two models, and non-steroidal anti-inflammatory induced ulcer and pyloric ligation, were analysed for methanolic extract of Cassia tora for its antiulcer activity. Results: Among all the extract, the percent of DPPH inhibition at 200 μg mL-1 for MECT extracts (Cassia tora methanolic extract) was 58.67±1.95. The overall scavenging potential for the H2O2 process was 68.23±0.19 at 200 μg mL-1 by MECT extract. Hence MECT extract was undertaken for the antiulcer property. Compared with control, there was a significant (p<0.05) decrease in free acidity, gastric volume, and total acidity in the extract-treated classes and ranitidine (standard). The Cassia tora methanolic extract demonstrated significant (p<0.05) inhibition activity, i.e. 59.42 and 69.59 percent at 500 mg mL-1 with the PL (Pylorus ligation) and NSAID (Non-steroidal anti-inflammatory drugs) process respectively. Conclusion: The findings of present study provide the scientific evidence to Cassia tora as a strong antiulcer and antioxidant agent.


Pharmacological assessment of antiulcer activity of gloriosa superba linn tubers in experimentally induced gastric ulcers
Vaibhav P Uplanchiwar
Medic Scientific
In a study, the potential of hydroalcoholic and petroleum ether extract of Gloriosa superba Linn (GS) tubers in the mitigation of antisecretory and antiulcer was studied. Both extracts were tested at 100, 200, and 400 mg/kg/p.o. using ethanol, and cold stress as toxicants. Both the extracts showed significant ulcer protection at the highest dose of 400mg/kg as compared to standard drug lansoprazole. To support its antiulcer potential, the plant was examined for radical - scavenging capability by lipid peroxidation. The extracts showed a comparative significant result. The flavonoids & polyphenols in the extracts verify the antioxidant potential. From the results, it was concluded that both hydroalcoholic and petroleum ether extracts of tubers of Gloriosa superba are having gastric ulcer protective activity.

RECENT SCHOLAR PUBLICATIONS

Autophagy: A Critical Review of Cellular Homeostasis and Pathophysiology
S Deogade, S Shende, C Prasad, M Dorlikar, P Urade, L Devhare
Asian Journal of Advanced Research and Reports 19 (2), 280-287 2025



Diverse Properties of Tinospora cordifolia (Giloy, Heart Leaved Moonseed) World Wild Use for Immunotherapies; Boosting the Body’s Defense and Immune Support
P Semwal, BK Sarkar, K Sonu, G Chand, LD Devhare, T Hooda
Emerging Paradigms for Antibiotic-Resistant Infections: Beyond the Pill, 471-487 2024



Combatting Antibiotic Resistance: Leveraging Fecal Microbial Transplantation for Gut Health
P Upreti, LD Devhare, LH Abdulmageed, YG Kumar, R Kumar, ...
Emerging Paradigms for Antibiotic-Resistant Infections: Beyond the Pill, 211-232 2024



Therapeutic and phytochemical properties of thymoquinone derived from Nigella sativa
G Tiwari, M Gupta, LD Devhare, R Tiwari
Current Drug Research Reviews Formerly: Current Drug Abuse Reviews 16 (2 2024



Next-Generation Drug Delivery Strategies for Personalized Healthcare
S Shende, L Devhare, C Prasad, A Khobragade, A Khapne
Pharmaceutical Research - Recent Advances and Trends 2, 28-62 2024



Case Study On Rubella Virus
D Devnani, KK Prasad, K Bongade, A Verma, T Choudhary, MK Posa, ...
Journal of Advanced Zoology 45 (2), 1133 2024



Diverse Properties of Tinospora cordifolia (Giloy, Heart Leaved
G Chand, LD Devhare, T Hooda
EMERGING PARADIGMS FOR ANTIBIOTIC-RESISTANT INFECTIONS: Beyond the Pill, 471 2024



Quality by Design Approach to Nasal Mucoadhesive Microspheres: Enhanced Sumatriptan Succinate Delivery through Formulation and Characterization
S Vyas, KN Anitha, NB Mudduluru, LD Devhare
Drug Delivery 14 (3), 1644-1651 2024



Prophylactic and curative activity of Withania somnifera on experimentally induced calcium oxalate nephrolithiasis
L Devhare, C Prasad
Journal of medical pharmaceutical and allied sciences 13 (4), 6687-6695 2024



Synthesis, DNA binding, molecular docking and anticancer studies of copper (II), nickel (II), and zinc (II) complexes of primaquine-based ligand
MGR Priya, LML Prasanth, LD Devhare, SK Yazdan, S Gunjal
International Journal of Pharmaceutical Quality Assurance 15 (1), 69-75 2024



Optimizing verapamil hydrochloride in-situ delivery: A strategic formulation approach using Box-Behnken design for enhanced performance and comprehensive evaluation of
RK Choudhary, S Beeraka, BK Sarkar, G Dharmamoorthy, L Devhare
International Journal of Drug Delivery Technology 14 (1), 61-70 2024



Design Development and Characterization of Nicardipine Solid Lipid Nano-Particulars
KK Kumar, V Kiran, RK Choudhary, LD Devhare, SD Gunjal
International Journal of Drug Delivery Technology 14 (1), 71-78 2024



Research Methodology and Biostatistics.IIP Publication
DLDD Dr. Ram Kumar Choudhary, Mr. Kiran Kumar Kurella, Miss. Falgunee ...
2024



Toxicity Profile Study of Antihypertensive Drug Prazosin in Pregnant Wistar Rats.
YG Kumar, G Dharmamoorthy, LD Devhare, SD Gunjal, M Deshpande
Journal of Advanced Zoology 44 2023



A Study on Antidiabetic Potential of Dried Fruits Extract of Eucalyptus Globulus in Experimental Animals
K Krishna, PK Jain, LD Devhare, RK Sharma, OM Bagade, ...
Journal of Biomedical Engineering 40 (3), 99-110 2023



An updated review on recent developments and applications of fish collagen
R Tiwari, J Mishra, LD Devhare, G Tiwari
Pharma Times 55 (6), 28-36 2023



A BRIEF REVIEW ON: PHYTOCHEMICAL AND ANTIULCER PROPERTIES OF PLANTS (FABACEAE FAMILY) USED BY TRIBAL PEOPLE OF GADCHIROLI INDIA.
LD Devhare, N Gokhale
IJPSR 14 (4), 1572-1593 2023



Extraction phytochemical screening and comparative pharmacological evaluation of some indigenous plants for antiulcer activity
LD Devhare
Indore 2023



A Textbook of Social and Preventive Pharmacy. Pritam Publication.
LDD Konda V V S Krishna, Virendra Kumar Maurya, S. R. Fulmali, Praful N Giradkar
2023



Textbook of Pharmacotherapeutics. Pritam Publication
LDD Konda V V S Krishna, Amruta R. Patil, Anupama A. Kapadnis, Vinod M. Thakare
2023

MOST CITED SCHOLAR PUBLICATIONS

Antioxidant and Antiulcer property of different solvent extracts of Cassia tora Linn.
LD Devhare, N Gokhale
Research journal of pharmacy and technology 15 (3), 1109-1113 2022
Citations: 43



Acid neutralizing capacity and antimicrobial potential of selected solvent extract from various indigenous plants
LD Devhare, N Gokhale
Journal of Advanced Scientific Research 12 (04), 175-179 2021
Citations: 35



A recent review on bioavailability and solubility enhancement of poorly soluble drugs by physical and chemical modifications
L Devhare, PK Kore
Research chronicle in health sciences 2 (5), 299-308 2016
Citations: 35



A brief review on: phytochemical and antiulcer properties of plants (fabaceae family) used by tribal people of gadchiroli maharashtra
LD Devhare, N Gokhale
International journal of pharmaceutical sciences and research 14 (4), 1572-1593 2023
Citations: 30



Development And Validation Of Vierordt's Spectrophotometric Method For Simultaneous Estimation Of Drotaverine And Nimesulide Combination
AAMLD Devhare
Research Chronicle in Health Sciences 3 (2), 22-28 2017
Citations: 29



Method development for determination of water content from various materials by spectrophotometry and it’s validation
LD Devhare, AP Ghugare, BP Hatwar, DC Goupale, LD Devhare
International journal of drug delivery 7 (4), 233-240 2015
Citations: 29



In silico anti-ulcerative activity evaluation of some bioactive compound from Cassia tora and Butea monosperma through moleculer docking approach
LD Devhare, N Gokhale
International journal of pharmaceutical sciences and research 14 (2), 1000-1008 2023
Citations: 28



Development and Validation of Analytical Methods for Drotaverine and Nimesulide Combination
AAMLD Devhare
Research Chronicle in Health Sciences 3 (3), 40-44 2017
Citations: 25



Quantitative Estimation of Bacoside A in Polyherbal Memory Enhancer Syrup for Memory Boosting Activity Using HPTLC Method.
LDD T. U. Tonde, R. H. Kasliwal
Research Chronicle in Health Sciences 2 (6), 315-320 2016
Citations: 25



An update on morphology, mechanism, lethality, and management of dhatura poisoning
S Singh, KH Minj, LD Devhare, SV Uppalwar, S Anand, A Suman, ...
European Chemical Bulletin 12 (5), 3418-3426 2023
Citations: 23



Pharmacological assessment of antiulcer activity of gloriosa superba linn tubers in experimentally induced gastric ulcers
VP Uplanchiwar, SY Raut, LD Devhare
Journal of medical pharmaceutical and allied science 10 (3), 2852-2856 2021
Citations: 23



Exploring the potential of Aerva Lanata extract in a herbal ointment for fungal infection treatment
PB Suruse, BA Jadhav, LG Barde, LD Devhare, S Singh, KH Minj, ...
Journal of Survey in Fisheries Sciences 10 (1), 1922-1932 2023
Citations: 22



Important role of food and nutritional security during Covid-19: A survey
LD Devhare, SS Bodhankar, P Warambhe, SV Uppalwar, DL Devhare, ...
cancer 4, 5 2023
Citations: 22



Formulation and in vitro evaluation of dental gel containing ethanglic extract of Mimosa pudica
SS Bodhankar, LD Devhare, AS Meshram, DW Moharkar, CB Badwaik
European Chemical Bulletin 12 (5), 1293-1299 2023
Citations: 22



Synthesis, characterisation, molecular docking studies and biological evaluation of novel benzothiazole derivatives as EGFR inhibitors for anti-breast cancer agents
RPM Gnana, LD Devhare, G Dharmamoorthy, MV Khairnar, R Prasidha
International Journal of Pharmaceutical Quality Assurance 14 (3), 475-480 2023
Citations: 21



In-vitro: micropropagation of mint and investigate the antibacterial activity of mint extract
SM Shende, P Bhandare, LD Devhare
Eur. Chem. Bull 12 (5), 780-784 2023
Citations: 21



Parenteral drug delivery approach: an overview
R Nikam Nikita, A Vaishnavi, D Lalchand
Journal of xidian university 17 (1), 386-400 2023
Citations: 19



Recent insight into some emerging natural resources with remarkable hepato protective potentials
G Katole, LD Devhare
International journal of pharmaceutical science and research 5 (1), 41-47 2020
Citations: 19



An updated review on recent developments and applications of fish collagen
R Tiwari, J Mishra, LD Devhare, G Tiwari
Pharma Times 55 (6), 28-36 2023
Citations: 18



Development And Characterization of Glycerogelatin Suppositories For Enhanced Efficacy
SM Shende, B Meshram, H Karemore, LD Devhare
European Journal of Pharmaceutical and Medical Research 10 (6), 522-528 2023
Citations: 18