A Robust and Sustainable HPLC Refractive Index Method Using Box–Behnken Design for Simultaneous Determination of Glycerin and Propylene Glycol Prasanth Katakam, Bharat Kumar Tripuramallu, Satish Kumar Konidala, Ravi Kumar Pedapati, Kishore Rapolu, Srinivas Torati Separation Science Plus, 2026 Glycerin (Gly) and propylene glycol (PG) are widely used excipients in pharmaceutical formulations, and their accurate and reliable quantification is essential for quality control (QC). The present study describes the development, optimization, and validation of a robust, sustainable, and environmentally conscious high‐performance liquid chromatography (HPLC) refractive index method for the simultaneous determination of glycerin and PG using a quality‐by‐design (QbD) approach. The optimized chromatographic conditions employed an Inertsil ODS‐3, 5 µm, 4.6 mm × 250 mm column with a mobile phase of water and methanol (90:10, v/v), flow rate of 0.5 mL/min, and column temperature of 40°C. The method was validated in accordance with International Council for Harmonization (ICH) guidelines. Accuracy results were found to be 99.1%–99.9% for Gly and 99.7%–99.9% for PG. Precision results were found Gly 0.3% and PG 0.4% relative standard deviation. Correlation coefficient ( r 2 ) was obtained >0.998 for two components. Analytical solutions are stable for 67 h at ambient conditions. The environmental sustainability of the method was assessed using AGREE, AGREEprep, Green Analytical Procedure Index (GAPI), ComplexGAPI, and Blue Applicability Grade Index (BAGI) tools, indicating a favorable greenness profile due to low organic solvent usage and simple sample preparation. The proposed method is reliable, cost‐effective, and suitable for routine QC applications while aligning with green analytical chemistry principles.
MULTITARGET NEUROPROTECTIVE POTENTIAL OF MYRISTICA MALABARICA AND SESBANIA GRANDIFLORA: AN INTEGRATED HR-LCMS, IN VITRO AND MOLECULAR DOCKING APPROACH IN DIABETES-ASSOCIATED COGNITIVE DYSFUNCTION Jagadeeshwar Kolguri, Risy Namratha Jamullamudi, Nallapaty Srilakshmi, Sathish Kumar Konidala Genetics and Molecular Research, 2026 Diabetes-associated cognitive decline (DACD) is a progressive neurodegenerative condition characterized by impairments in learning, memory, and executive function, primarily driven by chronic hyperglycemia-induced oxidative stress and neuroinflammatory pathways. Despite the availability of therapies, effective multitarget interventions remain limited. The present study was employed for an integrated experimental and computational approach to evaluate the hypothesis that methanolic bark extracts of Myristica malabarica and Sesbania grandiflora possess multifunctional neuroprotective properties capable of modulating multiple molecular targets involved in DACD. Phytochemical characterization was performed by quantification of total phenolic and flavonoid contents, followed by HR-LCMS for metabolite profiling. Identified phytoconstituents were subjected to in silico pharmacokinetic evaluation (SwissADME) to determine drug-likeness, gastrointestinal absorption, and blood–brain barrier permeability. Of all, twelve compounds satisfying ADME criteria were selected for molecular docking studies using AutoDock Vina against key DACD-related targets, including acetylcholinesterase (AChE), monoamine oxidase-B (MAO-B), cyclooxygenase-2 (COX-2), glycogen synthase kinase-3β (GSK-3β), and the Keap1–Nrf2 complex. Additionally, in vitro antioxidant and enzyme inhibition assays were conducted. Statistical analysis was performed using two-way ANOVA followed by Tukey’s post hoc test, with significance set at p < 0.05. HR-LCMS analysis identified multiple bioactive phytoconstituents, of which twelve demonstrated favorable pharmacokinetic properties, including high gastrointestinal absorption and blood–brain barrier permeability. Docking studies revealed that compounds M4(Androsta-4,9(11)-diene-3,17-dione), M8(Pirenperone), and M9(Drotaverine) exhibited strong binding affinities across multiple targets, with docking scores comparable to or exceeding standard drugs, donepezil and selegiline. In vitro assays demonstrated significant antioxidant and enzyme inhibitory activities (p < 0.01), including oxidative stress marker reduction and modulation of key enzymes associated with neurodegeneration and inflammation. The findings confirm that M. malabarica and S. grandiflora exhibit multifunctional and multitarget neuroprotective effects, supporting their potential as promising phytotherapeutic candidates for the management of DACD. Further in vivo validation, mechanistic studies, and formulation development are warranted to facilitate clinical translation.
A Robust LC-MS/MS Bioanalytical Strategy for Simultaneous Quantification of Tramadol HCl and Dexketoprofen Trometamol and Its Use in Pharmacokinetic Studies Adusumalli Srinivasa Rao, P. Bangaraiah, Sathish Kumar Konidala Biomedical Chromatography, 2026 This study reports the first bioanalytical method for simultaneous estimation of Tramadol HCl and dexketoprofen trometamol in rat plasma using Tapentadol as an internal standard. A validated LC‐MS/MS method was developed following USFDA guidelines. Analytes were extracted from plasma by protein precipitation technique using acetonitrile. Chromatographic separation was achieved on a Waters Symmetry Shield RP‐18 column (250 × 4.6 mm, 5 μm) with an isocratic mobile phase of acetonitrile and 0.1% formic acid in HPLC grade water (30:70 v/v) at a flow rate of 1.0 mL/min, yielding a 7‐min runtime. Detection was performed using electrospray ionization with ion transitions of m/z 222.3398 → 70.0307 for Tapentadol, m/z 264.4351 → 96.4527 for Tramadol HCl, and m/z 376.4239 → 100.4520 for dexketoprofen trometamol. The method showed good accuracy, with mean recoveries of 92.79%–98.15% for Tramadol HCl and 91.78%–98.37% for dexketoprofen trometamol. Excellent linearity was obtained, with r 2 values of 0.99983 (22.5–900 ng/mL) and 0.99963 (7.5–300 ng/mL), respectively. All validation parameters met acceptable criteria. The method is suitable for evaluating pharmacokinetic parameters that indicate drug efficacy and safety.
Network Pharmacology and Molecular Docking-Based in Silico Investigation of Anti-Atherosclerotic Phytoactives From Annona Reticulata and Ocimum Basilicum Premi Gelam, Ramayyappa Muddala, Siva Satya Narayana Kaipu, Sravani Boyapati, Rama Rao Vadapalli, Sathish Kumar Konidala, Kamma Harsha Sri Chemistryselect, 2026 Atherosclerosis (AS) remains a leading cause of cardiovascular morbidity and mortality, demanding the identification of novel and safer therapeutic strategies. While Ocimum basilicum (basil) and Annona reticulata (custard apple) have been traditionally reported to possess cardio protective effects, the underlying molecular mechanisms are not fully understood. In this study, we employed an integrative computational framework combining network pharmacology (NP), ADMET screening, molecular docking (MD), and pathway enrichment analysis to explore the multi‐target anti‐atherosclerotic potential of their phytoconstituents. Seven bioactive compounds with favorable drug‐likeness and pharmacokinetic properties were identified, of which four displayed strong binding affinities toward key targets such as HSP90AA1, STAT3, NF‐κB, and IL‐6. Gene Ontology (GO) and KEGG enrichment revealed their involvement in inflammatory signaling, oxidative stress regulation, and immune modulation pathways, central to AS progression. Toxicity predictions further supported their drug‐likeness and safety profile. Collectively, this systems‐level analysis provides mechanistic insights into the therapeutic potential of O. basilicum and A. reticulate bioactives and highlights their promise as leads for anti‐atherosclerotic drug development.
Validated LC-MS/MS Method for Quantification and Pharmacokinetic Analysis of Talazoparib and Enzalutamide in Rats Rajesh Guntupalli, Panchumarthy Ravisankar, Sathish Kumar Konidala Biomedical Chromatography, 2026 The FDA has approved Talazoparib and Enzalutamide for metastatic castration‐resistant prostate cancer (mCRPC) with homologous recombination repair (HRR) gene mutations, based on the TALAPRO‐2 Phase 3 trial. This study developed and validated an LC‐MS/MS method for simultaneous quantification of Talazoparib and Enzalutamide in rat plasma using Apalutamide as the internal standard. Chromatographic separation was achieved with a 70:30 (v/v) acetonitrile–0.1% formic acid system, 10 min runtime, and 1.0 mL/min flow rate. Retention times were 4.13 min (Talazoparib), 5.31 min (Enzalutamide), and 7.89 min (Apalutamide). Detection was performed in positive ionization mode using MRM transitions: m / z 381.35 → 240.56, 465.44 → 305.24, and 478.44 → 285.10, respectively. The method was linear over 0.05–2 ng/mL for Talazoparib and 4–160 ng/mL for Enzalutamide ( r 2 > 0.999). Accuracy and precision were within ±15%–20%, and recovery exceeded 98%. In pharmacokinetic studies on male Wistar rats, Talazoparib showed a C max of 0.88 ng/mL at 3 h and an AUC 0− t of 20 ng·h/mL, while Enzalutamide exhibited a C max of 76.18 ng/mL at 1 h and an AUC 0− t of 1702 ng·h/mL; both had 24 h half‐lives. The validated method enables sensitive, rapid, and reliable bioanalysis for preclinical pharmacokinetic evaluation.
Simultaneous quantification of linezolid and pretomanid in BALB/c mice plasma using a validated LC-MS/MS method: Application to pharmacokinetic and lung distribution studies S. Siva Shanmugam, Sathish Kumar Konidala, S. Narayanan, R.K. Shandil Acta Chromatographica, 2026 A sensitive and selective LC–MS/MS method was developed and validated for the simultaneous quantification of pretomanid and linezolid in BALB/c mouse plasma and lung tissue in accordance with ICH M10 bioanalytical guidelines. Chromatographic separation was achieved on a C18 column with gradient elution using methanol and 0.1% formic acid in water. The method demonstrated linearity ( r 2 > 0.995), accuracy, precision, and recovery within the validated range of 10–20,000 ng mL −1 , without significant matrix effect. Stability under various storage and handling conditions was also confirmed. The validated assay was successfully applied to a pharmacokinetic study using a sparse sampling design, demonstrating reliable quantification of both analytes in plasma and lung tissue and confirming the applicability of the method to preclinical bioanalysis. The developed method provides a robust and validated analytical platform for the simultaneous determination of co-administered anti-tuberculosis agents and is suitable for future pharmacokinetic and tissue distribution studies in preclinical models.
Quantification of Belzutifan in Biological Samples: LC–MS/MS Method Validation and Pharmacokinetic Study in Rats Kamma Harsha Sri, Panchumarthy Ravisankar, Sathish Kumar Konidala, Srinivasa Babu Puttagunta Biomedical Chromatography, 2025 Belzutifan, an inhibitor of hypoxia inducible factor‐2α, is used to treat cancer associated with von Hippel Lindau disease. The quality control and pharmacokinetic study of this drug is crucial for effective chemotherapy. Since no bio‐analytical method has been reported, this work aimed to develop an LC–MS/MS technique for the determination of belzutifan and its application for pharmacokinetic profiling in rat plasma. Belzutifan and apalutamide (IS) were quantified on a symmetry shield (150 × 4.6 mm, 3.5 μm) column using acetonitrile and buffer (30:70% v/v) as the mobile phase, with a run time of 7 min. The spiked samples and quality controls were extracted with an optimized protein precipitation technique. Belzutifan and IS were quantified in MRM mode. The validation of the method in compliance with the US FDA's guidelines was performed. The analyte and IS were quantified at m/z 384.3422 → 311.4205 and 478.4154 → 341.1629, respectively. The results indicate linearity between 5 and 100 ng/mL concentration with r2 = 0.9997, which proved to be accurate with % recovery between 95.0% and 97.98%, along with other essential metrics within the accepted limits. The pharmacokinetic study demonstrates that the established LC–MS/MS method accurately quantifies the drugs in rat plasma and might be useful for routine quantification of belzutifan in biological matrices.
Metallic Biomaterials for Pharmaceutical and Biomedical Applications Metals in Medicine Volume 1 Metals for Tissue Engineering and Pharmaceutical Applications, 2025
Utilization of Palladium in Photothermal Therapy of Cancer Metals in Medicine Volume 2 Metallic Nanoparticles for Biomedical Applications, 2025
Pharmacognostic and Phytochemical Evaluation with Isolation and Anthelmintic Activity of Dypsis lutescens Leaf extracts Latin American Journal of Pharmacy, 2023
ZnCl2 catalyzed new coumarinyl-chalcones as cytotoxic agents Konidala Sathish Kumar, Vijay Kotra, Phani Kumar Kola, CH.B. Praveena Devi, Nutakki Anusha, Bollikolla Hari Babu, Syed Farooq Adil, Mohammed Rafi Shaik, Mujeeb Khan, Abdulrahman Al-Warthan, Osamah Alduhaish, M. Mujahid Alam Saudi Journal of Biological Sciences, 2021
Laser induced breakdown spectroscopy Sathish Kumar Konidala, Govindarao Kamala, Sravani Koralla Research Journal of Pharmacy and Technology, 2016
Stability-indicating RP-HPLC method development & validation for simultaneous determination of doxylamine succinate and dextromethorphan hydrobromide in pharmaceutical dosage forms Der Pharmacia Lettre, 2015
New validated visible spectrophotometric method for the determination of salbutamol sulphate in bulk and dosage form International Journal of Pharmacy and Technology, 2015
New validated RP-HPLC method for the determination of rizatriptan benzoate in bulk and pharmaceutical dosage form Indian Drugs, 2014
New validated RP-HPLC method for the determination of Ritonavir in bulk and pharmaceutical dosage form International Journal of Pharmacy and Pharmaceutical Sciences, 2013
Development and validation of UV spectroscopic method for determination of atazanavir sulphate in bulk and formulation International Journal of Pharmacy and Pharmaceutical Sciences, 2012
New Validated RP-HPLC method for the Determination of Atazanavir Sulphate in Bulk and Dosage form Der Pharma Chemica, 2012
Electrochemical sensors and biosensors for the pharmaceutical and environmental analysis International Journal of Pharmacy and Technology, 2011
Two dimensional gas chromatography International Journal of Pharmacy and Technology, 2011
RECENT SCHOLAR PUBLICATIONS
Development and validation of an LC–MS/MS method for Lazertinib in rat plasma using SFOD microextraction with pharmacokinetic application R Guntupalli, P Ravisankar, SK Konidala Microchemical Journal, 118412 , 2026 2026
A Robust LC‐MS/MS Bioanalytical Strategy for Simultaneous Quantification of Tramadol HCl and Dexketoprofen Trometamol and Its Use in Pharmacokinetic Studies AS Rao, P Bangaraiah, SK Konidala Biomedical Chromatography 40 (4), e70398 , 2026 2026
Network Pharmacology and Molecular Docking‐Based in Silico Investigation of Anti‐Atherosclerotic Phytoactives From Annona Reticulata and Ocimum Basilicum P Gelam, R Muddala, SSN Kaipu, S Boyapati, RR Vadapalli, SK Konidala, ... ChemistrySelect 11 (11), e06652 , 2026 2026
Validated LC‐MS/MS Method for Quantification and Pharmacokinetic Analysis of Talazoparib and Enzalutamide in Rats R Guntupalli, P Ravisankar, SK Konidala Biomedical Chromatography 40 (3), e70381 , 2026 2026
Simultaneous quantification of linezolid and pretomanid in BALB/c mice plasma using a validated LC-MS/MS method: Application to pharmacokinetic and lung distribution studies S Siva Shanmugam, SK Konidala, S Narayanan, RK Shandil Acta Chromatographica, 1326.2026. 01448 , 2026 2026
Development of a New Validated RP-HPLC Method for Simultaneous Estimation and Stability Study of Tegafur, Gimeracil and Oteracil in Combined Dosage Form. R Panchumarthy, SK Konidala, KH Sri, CS Kolakaluri, ... Indian Journal of Pharmaceutical Education & Research 60 , 2026 2026
Quantification of Belzutifan in Biological Samples: LC–MS/MS Method Validation and Pharmacokinetic Study in Rats KH Sri, P Ravisankar, SK Konidala, SB Puttagunta Biomedical Chromatography 39 (9), e70168 , 2025 2025 Citations: 1
Rhizophora apiculata extracts improved memory function through inhibition of acetylcholinesterase and oxidative stress in scopolamine-induced memory deficits in rats A Mande, M Narender, C Guntupalli, K Ramakrishna, SK Konidala Avicenna Journal of Phytomedicine , 2025 2025
Novel quinoline-4-thiazolidinone derivatives as anticancer agents targeting the biological macromolecular protein-EGFR tyrosine kinase with dual anticancer and antioxidant … SK Konidala, GR Kamala, RR Bhandare, AB Shaik Journal of Molecular Structure, 143607 , 2025 2025 Citations: 3
Metals in Medicine: Volume 1: Metals for Tissue Engineering and Pharmaceutical Applications S Sundram, R Malviya, GSNK Rao CRC Press , 2025 2025
Utilization of Palladium in Photothermal Therapy of Cancer SK Konidala, BS Padya, GSNK Rao, RR Budha Metals in Medicine, 371-392 , 2025 2025
Metallic Biomaterials for Pharmaceutical and Biomedical Applications S Chaudhary, RR Budha, GSNK Rao, SK Konidala Metals in Medicine, 41-57 , 2025 2025 Citations: 1
IN VIVO AND IN SILICO ANTI-ATHEROSCLEROTIC ACTIVITY OF ETHANOLIC LEAVES EXTRACT OF OCIMUM BASILICUM AND ANNONA RETICULATE. P Gelam, RR Vadapalli, SK Konidala, R Muddala, B Bonthagarala, ... Indian Drugs 62 (2) , 2025 2025 Citations: 1
Rational Design of Antibacterial Agents for Multidrug‐Resistant Infections SK Konidala, P Naresh, RN Jamullamudi, KH Sri, RR Bhandare, AB Shaik Computational Methods for Rational Drug Design, 403-421 , 2025 2025 Citations: 1
Simultaneous Quantification of Multi-Class Antimicrobials in Chicken Kidney and Liver by New Validated UPLC-MS/MS Method SK Konidala, S Narayanan, S Rk Hacettepe University Journal of the Faculty of Pharmacy 45 (1), 30-42 , 2025 2025
Quantification of Vactosertib an Inhibitor of TGFBR1 by LC–MS/MS in Rat Plasma and Its Pharmacokinetic Profiling RK Boggavarapu, J Chimakurthy, SK Konidala Biomedical Chromatography 39 (1), e6057 , 2025 2025 Citations: 1
Computational methods for rational drug design M Rudrapal John Wiley & Sons , 2024 2024 Citations: 13
HR-LCMS Metabolite Profiling and in silico Evaluation of the Antidiabetic Activity of Methanolic Leaf Extract of Chrozophora rottleri (Geiseler) A. Juss. Ex Spreng S Nallapaty, N Malothu, SK Konidala, AR Areti, C Guntupalli Indian Journal of Pharmaceutical Education and Research 58 (4), 1277-1286 , 2024 2024 Citations: 6
Acid Hydrolytic Degradation Profiling of Ezetimibe: Identification, Isolation, and Structural Elucidation of Its Degradants AK Modini, M Ranga, SK Konidala, P Ravisankar, KH Sri Separation Science Plus 7 (10), e202400135 , 2024 2024 Citations: 1
Synergistic amelioration of letrozole-induced polycystic ovary syndrome in rats: a therapeutic approach with apple cider vinegar and metformin combination RCSR Danduga, AS Kurapati, RA Shaik, PK Kola, SK Konidala, ... Reproductive Sciences 31 (9), 2861-2876 , 2024 2024 Citations: 1
MOST CITED SCHOLAR PUBLICATIONS
Emerging role of biopharmaceutical classification and biopharmaceutical drug disposition system in dosage form development: A systematic review R Samineni, J Chimakurthy, S Konidala Turkish journal of pharmaceutical sciences 19 (6), 706 , 2022 2022 Citations: 146
Multistep synthesis and screening of heterocyclic tetrads containing furan, pyrazoline, thiazole and triazole (or oxadiazole) as antimicrobial and anticancer agents RR Bhandare, CS Munikrishnappa, GVS Kumar, SK Konidala, ... Journal of Saudi Chemical Society 26 (3), 101447 , 2022 2022 Citations: 60
Design, multistep synthesis and in-vitro antimicrobial and antioxidant screening of coumarin clubbed chalcone hybrids through molecular hybridization approach SK Konidala, V Kotra, RCSR Danduga, PK Kola, RR Bhandare, AB Shaik Arabian Journal of Chemistry 14 (6), 103154 , 2021 2021 Citations: 53
Coumarin-chalcone hybrids targeting insulin receptor: Design, synthesis, anti-diabetic activity, and molecular docking SK Konidala, V Kotra, RCSR Danduga, PK Kola Bioorganic chemistry 104, 104207 , 2020 2020 Citations: 51
Design, synthesis, biological and computational screening of novel pyridine-based thiadiazole derivatives as prospective anti-inflammatory agents N Podila, NK Penddinti, M Rudrapal, G Rakshit, SK Konidala, VS Pulusu, ... Heliyon 10 (8) , 2024 2024 Citations: 32
New Validated RP-HPLC method for the Determination of Atazanavir Sulphate in Bulk and Dosage form SK Konidala, K Sujana, AP Rani Der Pharma Chemica 4 (3), 1305-1310 , 2012 2012 Citations: 23
Identification, isolation, and structural characterization of novel forced degradation products of Darunavir using advanced analytical techniques like UPLC–MS, prep-HPLC, HRMS … AK Modini, M Ranga, U Puppala, M Kaliyapermal, MKR Geereddy, ... Chromatographia 86 (1), 63-78 , 2023 2023 Citations: 20
Novel RP-UPLC method development and validation for simultaneous quantification of emtricitabine, tenofovir and efavirenz in bulk and tablet dosage forms SK Konidala, R Samineni, YV Rao, J Chimakurthy, CS Kolakaluri, ... Research Journal of Pharmacy and Technology 15 (7), 3141-3146 , 2022 2022 Citations: 17
Development of orally active anti-inflammatory agents: In vivo and in silico analysis of naphthalene-chalcone derivatives based on 2-acetyl-6-methoxy naphthalene D Vasudha, A Jagadeesh, SK Konidala, H Yasin, SN Mali, RR Bhandare, ... Chemical Physics Impact 8, 100472 , 2024 2024 Citations: 16
ZnCl2 catalyzed new coumarinyl-chalcones as cytotoxic agents KS Kumar, V Kotra, PK Kola, CHBP Devi, N Anusha, BH Babu, SF Adil, ... Saudi Journal of Biological Sciences 28 (1), 386-394 , 2021 2021 Citations: 16
Development and validation of UV spectroscopic method for the determination of ranolazine in bulk and formulation DVSRS Doppa, SK Konidala, S Khanabhi Research Journal of pharmacy and Technology 12 (10), 5007-5010 , 2019 2019 Citations: 14
Computational methods for rational drug design M Rudrapal John Wiley & Sons , 2024 2024 Citations: 13
Laser Induced Breakdown Spectroscopy SK Sathish Kumar Konidala, Govindarao Kamala Research Journal of Pharmacy and Technology 9 (1), 91-100 , 2016 2016 Citations: 13
Development and validation of UV spectroscopic method for determination of atazanavir sulphate in bulk and formulation SK Konidala, K Sujana Int. J. Pharm. Pharm. Sci 4 (3) , 2012 2012 Citations: 13
Development and validation of RP-HPLC method for simultaneous estimation of Paracetamol and Flupirtine Maleate SK Konidala, A Penumala, VK Mugada, GR Kamala Asian Journal of Pharmaceutical Analysis 5 (2), 105-11 , 2015 2015 Citations: 12
Stability indicating RP-HPLC method for simultaneous estimation of ramipril and amlodipine besylate in pharmaceutical dosage form S Koralla, SK Konidala, KG Rao, SM Begum Asian Journal of Pharmaceutical Research 6 (4), 242-249 , 2016 2016 Citations: 10
DEVELOPMENT AND VALIDATION OF NEW SPECTROSCOPIC METHOD FOR THE ESTIMATION OF VALGANCYCLOVIR HCL IN BULK AND PHARMACEUTIC DOSAGE FORM OTDDDRS Sathish Kumar Konidala , N Yamini Sai Silpa, K Samrajyam World Journal of Pharmaceutical Research 3 (3), 4773-4782 , 2014 2014 Citations: 10
A simple and validated RP-HPLC method for the simultaneous determination of vildagliptin and metformin in bulk and pharmaceutical dosage forms SK Konidala, P Hemanth Int J Curr Pharm Res 6 (2), 31-35 , 2014 2014 Citations: 10
Evaluation of in vitro antidiabetic and antioxidant activity of leaf extracts of Ecbolium linneanum kurz.: GC-MS and HR-LCMS based metabolite profiling and an in silico approach S Nallapaty, N Malothu, SK Konidala, AR Areti Journal of Applied Pharmaceutical Science 14 (1), 247-260 , 2024 2024 Citations: 8
Development and validation of analytical method for estimation of balofloxacin in bulk and pharmaceutical dosage form by RP-HPLC R Samineni, J Chimakurthy, SK Konidala, V Yamarthy Research Journal of Pharmacy and Technology 15 (7), 2992-2996 , 2022 2022 Citations: 8