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Pharmaceutical Sciences and Drug Design

Volume 2 (2022)

Development and Validation of an RP-HPLC Method for Simultaneous Quantification of Azelnidipine and Metoprolol Succinate in Synthetic Mixtures
Downloads: 60
Views: 613
Written by Leela Prasad Kowtharapu   Published on Vol 2 , 2022
This study outlines an RP-HPLC technique for quantifying azelnidipine and metoprolol succinate in a synthetic mixture. Azelnidipine, a calcium channel blocker, and metoprolol succinate, a beta-blocker, are both used for the management of hypertension. The method was optimized using a Shimadzu HPLC LC2010 system, equipped with a UV-VIS detector and a binary gradient system. A Hibar ODS C18 5 µm column (250 x 4.6 mm) was used for separation in isocratic mode, with a mobile phase consisting of meth
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Development and Validation of a Stability-Indicating UV Spectroscopic Method for Baricitinib in Bulk and Formulation
Downloads: 44
Views: 382
Written by Khagga Bhavya Sri   Published on Vol 2 , 2022
Baricitinib is a novel therapeutic agent recently approved for the treatment of moderate to severe rheumatoid arthritis, severe alopecia areata, and since 2022, COVID-19 in hospitalized adults requiring supplemental oxygen. This drug acts as a selective inhibitor of Janus kinase 1 and 2. This study aimed to establish and validate a stability-indicating UV spectroscopic method for the measurement of baricitinib in both bulk and formulated forms. A straightforward, precise, and cost-effective UV m
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Development and Enhancement of Liquisolid Compact Containing Rifampicin and Quercetin: An In-Vitro and In-Vivo Investigation
Downloads: 42
Views: 272
Written by Oluwatoyin A. Adeleke   Published on Vol 2 , 2022
The main objective of this study was to develop liquisolid compacts containing rifampicin and quercetin with enhanced gastrointestinal absorption and dissolution characteristics. To achieve the desired formulations, non-volatile liquid carriers such as propylene glycol, PEG 200, and Tween 20 were selected due to their superior drug solubility properties. The liquisolid formulations were subsequently blended with carrier and coating materials to produce a free-flowing and compressible powder. Avi
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RP-HPLC-Based Quantification of Ciprofloxacin in Active and Pharmaceutical Preparations
Downloads: 42
Views: 241
Written by Ahsan Zamir Siddiqi   Published on Vol 2 , 2022
A straightforward and highly sensitive isocratic reversed-phase HPLC technique has been developed for the detection and quantification of ciprofloxacin in pharmaceutical formulations, which has been validated following ICH guidelines. This study introduces a straightforward, cost-effective HPLC technique that delivers accurate results, a low limit of quantification (LOQ), and reduced analysis time. The separation process was performed on a C18 reversed-phase column, using a mobile phase of aceto
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An Overview of the Transdermal Drug Delivery System
Downloads: 36
Views: 299
Written by Yi You Huang   Published on Vol 2 , 2022
The transdermal drug delivery system (TDDS) has emerged as a significant advancement in drug administration, offering numerous benefits in pharmaceutical treatments. Transdermal patches, which deliver drugs through the skin, provide a systemic effect by allowing the drug to penetrate the dermis. This approach offers advantages such as continuous drug absorption, more stable plasma concentrations, reduced first-pass metabolism, fewer side effects, ease of use, and the ability to terminate treatme
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Development and Validation of a Stability-Indicating RP-HPLC Method for Related Substances in Dolutegravir Dispersible Tablets
Downloads: 26
Views: 272
Written by Kinga Vindis   Published on Vol 2 , 2022
A rapid, simple, and robust reverse-phase HPLC method was developed and validated for the quantification of related substances in dolutegravir 10 mg dispersible tablets. This study primarily aimed to establish a new RP-HPLC method to quantify impurity B (a degradation impurity) as a related substance, following USP guidelines. Chromatographic separation was performed using a phenyl-hexyl column (250 × 4.6 mm, 5µ) with a mobile phase consisting of 45% buffer (sodium dihydrogen phosphate dihydrate
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Chemometric-Based UV Spectrophotometric Approach for the Estimation of a Newly Developed Anti-Tubercular Liquisolid Formulation
Downloads: 38
Views: 354
Written by Sobhy M. El-adl   Published on Vol 2 , 2022
This study proposes a numerical approach based on spectroscopic data combined with partial least squares (PLS) multivariate analysis to simultaneously quantify quercetin and rifampicin in raw materials and liquisolid formulations. Spectral measurements were obtained for rifampicin and quercetin over a linear concentration range of 2–10 µg/ml for each compound. A total of 25 simulated mixtures were generated, including 16 calibration and 9 validation sets, using a wavelength interval of λ = 15 nm
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A Random Forest Approach to Analyzing Molecular Descriptors of COX-2-Selective Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)
Downloads: 32
Views: 202
Written by Liza Tybaco Billones   Published on Vol 2 , 2022
The pursuit of next-generation non-steroidal anti-inflammatory drugs (NSAIDs) remains a critical focus in pharmaceutical research, given that over a billion individuals experience pain and inflammation. A key strategy in this effort involves developing a quantitative correlation between the anti-inflammatory potential and the molecular descriptors of cyclooxygenase-2 (COX-2) inhibitors, which will facilitate the identification and advancement of novel NSAIDs that minimize adverse effects associa
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Microsponge Technology: A Promising Approach for Targeted Topical Drug Delivery
Downloads: 33
Views: 385
Written by Maja Simonoska Crcarevska   Published on Vol 2 , 2022
In recent years, pharmaceutical companies have focused on controlled-release dosage forms, including solid, semi-solid, and topical preparations, due to their improved efficacy and better patient acceptance. However, transdermal drug delivery systems face challenges for compounds intended for skin application. Traditional topical treatments often have drawbacks such as unpleasant odors, greasiness, and skin irritation. In some cases, topical treatments do not achieve sufficient systemic circulat
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Anlotinib Combined with Chemoradiotherapy Improves Survival in Postoperative Lymph Node Recurrent Esophageal Squamous Cell Carcinoma: A Propensity Score-Matched Real-World Study
Downloads: 21
Views: 89
Written by James Carter   Published on Vol 2 , 2022
Anlotinib, a multitarget tyrosine kinase inhibitor, has demonstrated notable activity against esophageal squamous cell carcinoma (ESCC). This study summarizes real-world outcomes comparing chemoradiotherapy (CRT) combined with anlotinib versus CRT alone in individuals who developed lymph node relapse following curative surgery. Records of patients with nodal recurrence treated with CRT with or without anlotinib between January 2017 and December 2019 were retrospectively reviewed. Tumor response,
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Inhibition of cGAS/STING-Mediated Cellular Senescence Underlies the Protective Effect of Ginsenoside Rg1 in Experimental Pulmonary Hypertension
Downloads: 29
Views: 66
Written by Klara Novak   Published on Vol 2 , 2022
Pulmonary hypertension (PH) is a life-threatening disease of the pulmonary vasculature for which effective therapeutic options remain scarce. Although ginsenoside Rg1 has shown beneficial activity in alleviating PH, the molecular basis of its action has not been fully clarified. This work aimed to elucidate the signaling mechanisms through which ginsenoside Rg1 improves PH. A rat model of PH was used to evaluate the therapeutic impact of ginsenoside Rg1 via cardiopulmonary hemodynamic analysis a
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Perillaldehyde Inhibits Colorectal Cancer by Targeting SRD5A1 to Induce Autophagy via Suppression of the PI3K/AKT Pathway
Downloads: 28
Views: 64
Written by Daniel Rivera   Published on Vol 2 , 2022
Colorectal cancer (CRC) ranks as the third most prevalent malignancy worldwide, and effective treatment options remain limited. Perillaldehyde (PAH), a key bioactive component derived from Perilla, has shown promise in managing CRC, yet its underlying mechanisms are not fully understood. This work investigates the anti-CRC potential of PAH and elucidates its mode of action, aiming to support its development as a candidate therapeutic agent. For the in vitro portion, we employed CCK-8 assays, col
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Dehydrolithocholic Acid (DHLCA) Ameliorates Diabetic Kidney Disease by Activating TGR5/FXR Signaling and Remodeling the Gut Microbiota
Downloads: 27
Views: 95
Written by Liam Wilson   Published on Vol 2 , 2022
Diabetic kidney disease (DKD) is one of the primary causes of long-term loss of renal function internationally. In recent years, bile acids (BAs) have emerged as important metabolic signals influencing glucose control and kidney physiology. This project explored how disturbances in BA pathways contribute to DKD advancement. Plasma BA concentrations were quantified in healthy individuals (HC), subjects with type 2 diabetes mellitus (T2DM), and patients diagnosed with DKD using ultra-high-performa
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Ciprofol and Remimazolam Preserve Arrhythmia Inducibility Comparable to Propofol During Pediatric Supraventricular Tachycardia Ablation: A Retrospective Comparative Study
Downloads: 30
Views: 84
Written by Maria Rossi   Published on Vol 2 , 2022
Propofol remains a widely applied intravenous anesthetic in children. Newer agents, including ciprofol and remimazolam, produce little to no injection discomfort and maintain more consistent hemodynamics. This investigation assessed how these three drugs influence the ability to provoke arrhythmias in pediatric supraventricular tachycardia (SVT). Clinical records of children with SVT who received radiofrequency ablation under general anesthesia between May 2020 and June 2024 were reviewed. After
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Tacrolimus versus Cyclophosphamide and Mycophenolate Mofetil in Pediatric IgA Vasculitis Nephritis: Superior Early Remission and Long-Term Renal Outcomes in a Large Single-Center Cohort
Downloads: 23
Views: 67
Written by Peter Mwangi   Published on Vol 2 , 2022
IgA vasculitis nephritis (IgAVN) is a frequent form of secondary glomerular disease in childhood. Although consensus documents generally acknowledge the therapeutic value of cyclophosphamide (CYC), guidance regarding tacrolimus (TAC) and mycophenolate mofetil (MMF) remains variable. Existing data indicate that TAC can work safely and effectively in IgAVN, but the long-term influence of different immunosuppressants is still not clearly defined. This study was designed to compare TAC, CYC, and MMF
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Ciprofol Dose Requirements for Successful Anesthesia Induction in Unpremedicated Children: An Up-and-Down Sequential Analysis
Downloads: 20
Views: 87
Written by Mason Clark   Published on Vol 2 , 2022
This investigation sought to identify the median effective dose (ED50) and the 90% effective dose (ED90) of ciprofol that can reliably provide sedation for the induction of general anesthesia in children, refine dosing recommendations, and support clinical decision-making. Children 3–12 years old scheduled for elective procedures requiring general anesthesia and endotracheal intubation were recruited. The initial participant received 0.4 mg/kg of intravenous ciprofol. Dose adjustments for all fo
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GnRH Agonist Pretreatment Prior to Hormone Replacement Therapy Improves Live Birth Rates in Frozen-Thawed Embryo Transfer Among Overweight and Obese Women: A Large Retrospective Cohort Study
Downloads: 22
Views: 68
Written by Eli Mitchell   Published on Vol 2 , 2022
Excess body weight is frequently associated with suboptimal endometrial readiness and poorer reproductive success in frozen-thawed embryo transfer (FET) cycles. Administering a depot gonadotropin-releasing hormone agonist (GnRH-a) prior to starting hormone replacement therapy (HRT) has been suggested to enhance endometrial performance through several biological pathways; however, whether this strategy benefits overweight or obese individuals has not been clearly determined. This retrospective an
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Glucocorticoid-Associated Infection Risk in Severe Drug-Induced Liver Injury: A Machine Learning Prediction Model Identifying Globulin as the Key Predictor
Downloads: 38
Views: 93
Written by Ahmed Idris   Published on Vol 2 , 2022
Glucocorticoids are widely used in managing severe drug-induced liver injury (DILI) to enhance clinical improvement and reduce the length of hospital stay, yet they may elevate susceptibility to infections. This work aimed to build a model capable of forecasting infection following glucocorticoid administration in individuals with DILI. A retrospective review was carried out on patients diagnosed with severe DILI who received glucocorticoid treatment at the Fifth Medical Center of the Chinese Pe
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Piperine-Rich Baolier Capsule Promotes Cholesterol Excretion and Attenuates Atherosclerosis via LXRα Activation and Upregulation of ABCA1, ABCG5/8, and CYP7A1
Downloads: 27
Views: 75
Written by Avery Cole   Published on Vol 2 , 2022
Baolier capsule (BLEC), a traditional Mongolian formulation, is prescribed for managing hypercholesterolemia and atherosclerosis (AS). Yet, its therapeutic efficacy, key constituents, and molecular actions in these disorders remain insufficiently defined. This work sought to clarify the pharmacodynamic profile of BLEC, identify its principal bioactive molecules, and delineate its mechanisms against hypercholesterolemia and AS. Liver-specific LXRα knockout ApoE−/− mice were generated via adeno-as
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Gui-Qi-Yi-Shen Granules Ameliorate IgA Nephropathy in Transgenic Mice by Suppressing TLR4/MyD88/NF-κB and IL-6/JAK2/STAT3 Signaling: An Integrated Network Pharmacology and Transcriptomic Study
Downloads: 32
Views: 61
Written by Diana Brkovic   Published on Vol 2 , 2022
IgA nephropathy (IgAN) remains a major cause of renal failure and mortality, and available treatments are still limited. Gui-qi-yi-shen (GQYS) granules—an established traditional Chinese medicinal formula—have long been used for IgAN, yet the molecular basis of their therapeutic effects is not fully defined. This study aimed to clarify how GQYS mediates its beneficial actions in IgAN. Eight-week-old Itgam-IRES-hCD89 mice were assigned to four experimental groups: IgAN, low-dose GQYS (GQYS-L, 5.2
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