Current Indian Science - Current Issue
Volume 3, Issue 1, 2025
- Special Issue: Herbal Medicine as Anti-infective Agents
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Phytochemicals as Therapeutic Agents for ESKAPE Pathogens
BackgroundThe worldwide increase of antimicrobial resistance in ESKAPE pathogens, which includes Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter sp., constitutes a substantial public health hazard, constraining treatment alternatives and elevating morbidity and mortality rates. As traditional antibiotics diminish in efficacy, phytochemicals are capturing interest due to their varied antibacterial characteristics and decreased susceptibility to developing antibiotic resistance. Phytochemicals, such as alkaloids, terpenes, phenolics, flavonoids, and organosulfur compounds, have multi-target processes that might provide innovative strategies for addressing infections caused by ESKAPE pathogens.
ObjectiveThe investigation sought to evaluate the effectiveness and mechanisms via which different phytochemicals could hinder and destroy the resistance pathways of ESKAPE bacteria, emphasizing their potential to serve as therapeutic agents in combating antimicrobial resistance.
ResultsInvestigation demonstrates that some phytochemicals may disrupt many bacterial functions, such as cell wall production, membrane integrity, quorum sensing, and biofilm development in ESKAPE pathogens. For example, carvacrol from essential oils has shown efficacy against S. aureus by reducing staphyloxanthin synthesis and altering regulatory proteins, including SarA. Furthermore, conessine has altered resistance in A. baumannii by inhibiting the AdeIJK efflux pump. Flavonoids like resveratrol and curcumin have shown synergistic benefits with conventional antibiotics by improving their effectiveness while minimizing toxicity. These chemicals address several resistance pathways, impairing the ability of infections to build resistance.
ConclusionPhytochemicals provide an opportunity to facilitate the development of novel therapies targeting antimicrobial resistance in ESKAPE bacteria. Extensive efficacy and distinctive multi-target mechanisms of phytochemicals provide them promising candidates for combination therapy, possibly reinstating antibiotic effectiveness and decelerating the development of resistance. Additional investigation into the increase of bioavailability and clinical usage is essential to fully exploring the medicinal potential of phytochemicals.
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Review Understanding of the Many Facets of Cancer and the Management of Skin Cancer
Authors: Arushi Saloki, Aditya Shrivastava, Sarita Gaikwad and Swarnlata SarafCancer is a complex disorder characterized by the unregulated proliferation of cells that have the potential to invade other regions of the body. It stems from genetic alterations in various cell types, resulting in tumor formation. These growths are classified as benign (noncancerous) or malignant (cancerous). Unlike benign tumors, which typically remain localized, malignant tumors can spread, infiltrate nearby tissues, and establish secondary growth in organs far from the original site. The treatment approach depends on the specific type and progression of cancer, encompassing options such as surgical intervention, radiation-based therapies, drug-based treatments, immune system-boosting techniques, and therapies targeting particular cellular mechanisms. Skin cancer is a common occurrence among various cancer types, especially in populations with lighter skin tones. Skin cancer is a prevalent form of cancer, particularly in the Caucasian population. The most common skin cancers are basal cell carcinoma (BCC), squamous cell carcinoma (SCC), and melanoma. BCCs, which arise from the basal layer of the epidermis, are often treated with surgery, topical therapies, or cryotherapy depending on their risk and location. Mohs micrographic surgery is effective for high-risk or recurrent BCCs, whereas topical treatments such as 5-fluorouracil and imiquimod are used for superficial BCCs. Early diagnosis through biopsy and various imaging techniques is crucial for effective management. Advances in treatment, including targeted therapies and improved surgical techniques, continue to enhance patient outcomes and reduce recurrence rates. Understanding these diverse aspects of cancer and skin cancer will help devise effective treatment strategies and improve patient prognosis.
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Formulation and Evaluation of Solid Dispersion Lipid Particles of Curcumin for Improving Bioavailability
Authors: More V. Apoorva, Dhokchawle V. Bharat, Tauro J. Savita and Kulkarni R. SavitaBackgroundTo overcome the drugs’ low bioavailability and/ or solubility, the development of novel oral delivery approaches using lipid-based formulations has been of growing interest. Curcumin being a Class IV drug, has poor solubility and poor permeability. One of the biggest obstacles to its use in therapeutic treatment is this.
ObjectiveIn order to increase drug bioavailability, this research aimed to create Solid Dispersion Lipid Particles (SDSLs), in which Solid Dispersion (SD) was enclosed in solid lipid particles as the drug's core packaging.
MethodsFor this, Curcumin (CUR) was selected as a model drug, PEG 6000 was used as a polymer, Stearic acid was used as the lipid phase, and Poloxomer 188 was used as a surfactant. Different batches of SD were formulated by solvent evaporation method. SDSLs were prepared by the melt-emulsification ultrasonication method and characterized for their % yield, % drug loading, % drug encapsulation efficiency, zeta potential, FTIR spectroscopy, XRD studies, in vitro drug release, and ex vivo permeation.
ResultsThe optimized formulation showed the highest % EE and sustained in vitro drug release. The release mechanism was Super Case II, and the Higuchi equation was the best fit for the data.
ConclusionSDSLs have sustained release effects and demonstrated enhanced ex vivo permeability which could lead to improved bioavailability. These studies demonstrate that SDSL could be a promising oral formulation for enhanced bioavailability.
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Optimizing Congo Red Dye Removal Using Sodium Borohydride-reduced Bent/Fe NPs and Bentonite in Aqueous Solutions
Authors: Mandira Debnath, Manash Pratim Barman, Dipanwita Basak, Debasis Borah and Hemaprobha SaikiaBackgroundThe presence of synthetic dyes like Congo Red in wastewater poses serious and persistent environmental health hazards as a result of their toxicity and stability. Therefore, developing an efficient and reusable adsorbents for the elimination of dye is quite important in order to address water pollution challenges.
ObjectiveThe study aims to classify the efficacy of sodium borohydride-reduced Bent/Fe NPs and crude bentonite in removing Congo Red dye from aqueous solutions.
MethodsSodium Borohydride was utilized in order to synthesize Bent/Fe NPs, dragging its reducing capacities in order to enhance its adsorption properties. Batch adsorption experiments were performed in order to estimate the removal efficacy under multiple conditions consisting of initial dye concentration, pH and contact time. Adsorption isotherms and kinetics were analyzed using Freundlich and pseudo-second-order models.
ResultsBent/Fe NPs exhibited significant removal efficiency, reaching up to 91.97% removal of Congo Red dye with an initial concentration of 40 mg/L in alkaline conditions. Adsorption data was found to align well with the Freundlich isotherm model, signifying heterogeneous adsorption sites. It also fitted well with pseudo-second-order kinetic model indicating that chemisorption is the dominant mechanism taking place. Also, the adsorbent displayed excellent reusability, preserving substantial efficiency up to three cycles.
ConclusionSodium borohydride reduced Bent/Fe NPs offer an assuring, efficient and reusable solution for Congo Red dye removal from aqueous solution. The high adsorption capacity and, its affinity with alkaline conditions and its excellent reusability make them a feasible choice for wastewater treatment applications.
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Biopolymers in Floating Drug Delivery Systems
Authors: Moumita Das Kirtania, Laboni Das, Gopa Roy Biswas and Kajal GhosalFloating drug delivery systems are significant for gastric retention characteristics and improving the absorption and bioavailability of drugs. Several polymers have been used in such systems as drug carriers. Biopolymers, including alginate, chitosan, guar gum, and gelatin obtained from plant or animal sources have also been applied in such systems. Such biopolymers are biocompatible and biodegradable and provide suitable characteristics for swelling and hydrogel formation. The present review summarizes several biopolymers used in floating drug delivery including their sources, structure, and recent research studies for gastric retention.
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Applications of Selenium Nanoparticles in Phytoremediation
Authors: Nandha Kumar Subramani and Subhashree VenugopalHeavy metal contamination in soil and water poses a severe global environmental challenge, particularly in rapidly industrialized regions. While conventional remediation methods exist, their widespread implementation is hindered by high costs, time-intensive processes, and complex technical requirements. This review aimed to explore an innovative approach combining phytoremediation with green-synthesized selenium nanoparticles (Se-NPs) for enhancing heavy metal removal. Our analysis revealed that plants treated with green-synthesized Se-NPs exhibited more efficient uptake of heavy metals compared to traditional phytoremediation alone. Some key advantages include enhanced metal accumulation capacity, increased plant biomass production, and improved stress tolerance. The green synthesis of Se-NPs, primarily using plant extracts and biological materials, offers a sustainable and cost-effective alternative to chemical and physical synthesis methods. These biogenic Se-NPs exhibit dual benefits: promoting plant growth and remediation efficiency while demonstrating valuable biological properties, including antioxidant, antimicrobial, and anticancer activities. Our findings demonstrated that the integrated approach achieved 40–60% greater heavy metal removal compared to conventional methods while also reducing treatment costs by approximately 30%. The review also identified promising applications in large-scale soil restoration projects and agricultural land rehabilitation, suggesting a practical pathway for sustainable environmental remediation.
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Updated Assessment of Drug Delivery Techniques for the Treatment of Onychomycosis
Authors: Sarita Gaikwad, Arushi Saloki, Taranjeet Kukreja and Swarnlata SarafDermatophytes typically cause onychomycosis, which accounts for 50% of all nail diseases. Although formerly thought to be a cosmetic issue, it has recently gained attention because of its chronic nature and challenging treatment with relapses. Due to the lengthy treatment period and high expense associated with treating onychomycosis, numerous attempts have been made to overcome the hard nail barrier. Oral and topical medications are traditional treatments for onychomycosis. Despite their effectiveness, oral antifungal medications have hepatotoxic effects and can be mixed with other medications. Topical therapy improves patient compliance because it has no negative side effects. However, improper nail penetration poses a problem. Therefore, the goal of enhancing topical administration to effectively treat onychomycosis has been pursued for decades. Despite all efforts, issues with nail delivery have not been much closer to being resolved. Recently, the focus has shifted to novel drug delivery technologies, such as polymeric films, metallic nanoparticles, microemulsions, and nail lacquers, to enhance drug penetration and localized therapy. A global study is investigating their potential as efficacious treatment modalities. Thus, the goal of this review is to learn about innovative delivery methods for the treatment of onychomycosis, a persistent fungal disease.
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Optimization of L-Asparaginase Production from Endophytic Fungus Rhizomucor Variabilis Strain CBS 103.93 Isolated from Mushroom
Authors: M.S Vineetha, Sunil S. More, H.M. Dhanyashree, H. Poojashree, K. Rahul, A. Hemalatha, B. Bhavana, N. Gagana, S. Bhumika and Atheeth P.V.IntroductionAsparaginase, an enzyme that changes L-asparagine into L-aspartic acid, has attracted a lot of interest recently due to its potential to prevent the development of cancer.
MethodsIn the present study, the endophytic fungi isolated from wild mushrooms were tested for their ability to produce extracellular L-asparaginase.
ResultsThe isolated organism was identified as Rhizomucor variabilis strain CBS 103.93 by morphological and molecular identification. The enzyme and substrate incubation time of 10 minutes showed the highest production of L-asparaginase at 3.850 U/mL. Rhizomucor variabilis strain CBS 103.93 exhibited the highest enzyme activity on the fourth day of the incubation period at pH 7.0. The most beneficial carbon source was found to be mannitol, and substrate concentration at 1.5% resulted in maximum enzyme production. Inorganic nitrogen (NH4)H2PO4 and organic nitrogen source peptone exhibited maximum enzyme activity. Rhizomucor variabilis strain CBS 103.93 species produced the enzyme under optimal conditions, and a 5-fold increase (from 3.850 U/mL to 19.25 U/mL) was achieved after optimization in submerged fermentation.
ConclusionThe optimization processes are beneficial for the industrial production of L-asparaginase for use in the pharmaceutical and food industries. Hence, it is possible to say that it may find its future application in the pharmaceuticals industry and food industry.
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Citrus Pseudolimon: An Overview of Unexplored and Underutilised Plant from Genus Citrus
Authors: Hardeep Kaur, Ujjwal Kaushik, Neeraj Choudhary and Neha KukretiGenus Citrus, with a handful of the most extensively grown fruit crops in the world, is home to an unknown number of plant species. Since they are very perishable, many neglected citrus varietals are yet unexplored. Citrus pseudolimon Tan., sometimes known as Hill Lemon, is a lesser-known citrus species with relatively little research available on it when compared to other prominent citrus cultivars. To the best of our knowledge and search, there is no review article available detailing the in-depth phyto-pharmacological aspects of this plant with respect to its volatile and non-volatile contents. This review provides a thorough overview of this plant species with respect to the published material that is currently accessible. The current effort focuses on a thorough meta-analysis of the scientific literature and the most recent research updates that are currently accessible. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines, which are intended for systematic review writing, 481 publications were screened for material relevant to the chosen plant species. An effort has been made to compile the pertinent data about its pharmacological and phytochemical features.
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Integrative Healing: Exploring the Pharmacological Approach and Impact of Yoga on Depression Following Traumatic Brain Injury
Authors: Khushi Bajaj, Navneet Kaur, Pakhee Grewal and Hardik KumarTraumatic Brain Injury (TBI) is a complex type of brain damage caused by external factors. Depression is one of the major comorbidities that follow, making things more difficult for patients and caregivers. Post-traumatic depression is a serious condition that can increase rates of death and morbidity, especially as it gets worse. Though constant discussion exists about the best ways to treat the condition, a conclusive answer is still out of reach. Interestingly, traditional non-pharmacological treatments that have been used for a long time to treat a wide range of illnesses have just returned to prominence because they may be able to help prevent, treat, and even cure several mental conditions. Among these, yoga stands out as a particularly effective means of enhancing focus, which in turn supports mental health, productivity, and general well-being while reducing thoughts of suicide. Moreover, the technique exhibits a noticeable impact on the control of neurohumoral transmissions, which presents a possible treatment option for post-traumatic depression. This study explores in great detail the complex pathological relationship between traumatic brain injury and depression indicators, highlighting the critical role that yoga plays in the treatment of post-traumatic depression.
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Atopic Dermatitis: A Review on Nanocarrier-based Dermo-pharmaceutical Formulation for Inflammatory Effect
Authors: Taranjeet Kukreja and Swarnlata SarafAtopic dermatitis (AD), a disorder that is on the rise, affects about 20% of people globally, including children. It is believed that immunological inadequacies, pathogenic microorganisms, the environment, and anomalies in the function of the epidermal barrier interact intricately with the pathophysiology of AD. Studies on the impact of oxidative stress on many skin conditions have been carried out, but there aren’t many on AD. Topical corticosteroids and calcineurin inhibitors are among the available drugs; nonetheless, they cause burning sensations, skin atrophy, and systemic side effects that hinder patient adherence. These limitations emphasize how important it is to have a fresh approach to AD management. Inflammation, the biological reaction of the immune system, can be caused by a number of factors, such as pathogens, damaged cells, and poisonous substances. Herbal anti-inflammatory medications and their ingredients offer strong defence against a range of pro-inflammatory mediators in illnesses and conditions.
Due to their ability to protect, encapsulate, and discharge the cargo at the location of skin damage. Nanomaterials have attracted a lot of interest as a way to provide medications for skin conditions like AD. However, many unanswered questions remain, particularly when creating safe formulations and translating proven nanomedicines into usable products for clinical use. Lipidic, polymeric, metal, silica, liposomes, hydrocarbon gels, and many other formulations have been developed as carriers for poorly soluble and permeable pharmaceuticals. This field is still developing. This review aims to shed light on incidents linked to the pathophysiology of AD and the difficulties facing current AD treatments. The review emphasizes the advantages of different nanomedicines in resolving problems with existing products and their possible prospects for the future.
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Chemical Composition and Biological Activities of Natural Essential Oil Extracted from Flowers of Cassia sophera Linn.
BackgroundNatural essential oil comprises a galaxy of low-molecular-weight (usually less than 500 daltons) and volatile phytoconstituents that exhibit a handful of biological and pharmaceutical properties; they exhibit several applications chiefly in agriculture, cosmetic, perfumeries, and food industries.
MethodsThe extraction of essential oil from fresh flowers of C. sophera was performed by hydrodistillation, and the determination of its chemical composition was carried out by Gas Chromatography/Mass Spectrometry (GC-MS). The antibacterial activity of the essential oil was executed by the disc diffusion method against the four pathogenic bacteria. 1,1-Diphenyl-2-picrylhydrazyl (DPPH) was also performed for free radical scavenging assay, and a scanning electron microscopic study was also executed to get an idea of the effect of C. sophera essential oil on bacterial morphology.
ResultsThe GC/MS analysis indicated that the essential oil is constituted primarily of aromatic compounds (68.75%), and the principal compounds are the dialkyl phthalates esters (58.32%). The zones of inhibition range from 8-16 mm in the case of Gram-negative E. coli, whereas, in Gram-positive S. aureus, these range from 7-13.5 mm. The Minimum Inhibitory Concentration (MIC) was found to be 0.3 mg/mL against all the Gram-negative bacteria tested and 0.4 mg/mL against the Gram-positive bacteria S. aureus. The oil also showed moderate antioxidant properties by scavenging 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical with an IC50 value of 126 μg/mL.
ConclusionAs per the present study, the essential oil of C. sophera flowers may be suggested as a new potential source of natural antimicrobial and antioxidant agents.
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Phytochemicals for the Improvement of Cognitive Function through Cholinergic Anti-inflammatory Pathway
Authors: Dhananjay Kumar Singh, Bindu Kumari, Sonal Sinha and Kaneez FatimaCognition is the interdisciplinary scientific study of the brain and its processes, which include the intelligence and behaviour of living beings. Humans are generally equipped with a capacity for cognitive function at birth, but some conditions, such as infection and oxidative stress, lead to impaired cognition. Herbal drugs/phytochemicals are utilized in order to get better cognitive functions and alleviate symptoms associated with impaired cognition function. Yet, there still remains no complete cure for cognitive dysfunction, with most current treatments offering symptomatic relief. This has prompted us to review the importance of phytochemicals and the mechanism by which they may augment cognitive functions. For the present review, a comprehensive literature search was conducted by referring to the research and review articles published by authentic journals and available on web databases. Indeed, numerous plant-based drugs have traditionally been used to combat learning and memory-associated deficits, but many available drugs are potentially toxic alkaloidal cholinesterase inhibitors. Findings by various researchers exhibited that many plant-based drugs act through a different mechanisms, such as inhibition of acetylcholinesterase (AChE), activation of antioxidant defence, and augmenting the blood flow to the brain. The aim of the present review is to highlight the importance of phytochemicals in the modulation of cholinergic anti-inflammatory pathways (CAP) in neurodegenerative disease. For this, available literature was critically analysed. Through a comprehensive review of the recent research findings, this article concludes that medicinal plants serve as reservoirs of various successful drugs for cognition improvement, which belong to different classes of secondary metabolites. We also observe that phytochemicals can modulate cholinergic anti-inflammatory pathways (CAP) in neurodegenerative disease, although the mechanism of action of most natural/herbal extracts and their compounds is not yet fully explored.
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Mitapivat: A Novel Drug Discovery for the Treatment of Hereditary Hemolytic Anaemias
Authors: Shikha Sharma and Utkarsh SharmaMitapivat (AG-348) is a novel, first-in-class oral small-molecule allosteric activator of the pyruvate kinase enzyme. Mitapivat has been shown to significantly upregulate both wild-type and numerous mutant forms of erythrocyte pyruvate kinase (PKR), increasing adenosine triphosphate (ATP) production and reducing levels of 2,3-diphosphoglycerate. Given this mechanism, mitapivat has been evaluated in clinical trials in a wide range of hereditary hemolytic anaemias, including pyruvate kinase deficiency (PKD), sickle cell disease, and thalassemia.
The technique entails searching numerous search engines, such as PubMed, Science Direct, and Sci Finder, for relevant citations to the current subject matter. This is done in order to obtain the data that is required. In relation to medicine, mitapivat has been examined for its ability to cure a wide variety of inherited haemolytic anaemias in clinical investigations. Some examples of these conditions include pyruvate kinase deficiency (PKD), sickle cell disease, and thalassemias.
It has been demonstrated that mitapivat is both safe and effective in treating adults with PKD in two phases III clinical trials, and the development of the medicine is very close to being finished. Based on these findings, mitapivat may end up becoming the very first medication in the history of the world to receive regulatory approval.
Allosteric activator of pyruvate kinase mitapivat has shown promise in treating various hereditary hemolytic anemias, including sickle cell disease, PKD, and alpha- and beta-thalassemia.
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Surface Solid Dispersion Technique for Solubility Enhancement of Nifedipine
IntroductionPoor solubility is a common challenge in pharmaceuticals, hindering oral bioavailability. High throughput screening has led to an increase in poorly soluble drug candidates. Enhancing solubility and dissolution rates is crucial for drug development. Various methods, including solid dispersion, aim to improve solubility. A solid dispersion formulation process involves dispersing one or more active chemicals in a solid state within an inert carrier or matrix. It can be made using solvent, melting, or melting-solvent procedures, among other techniques. By increasing the surface area and dispersibility of poorly soluble pharmaceuticals, this method improves their solubility and rate of dissolution, ultimately leading to an improvement in bioavailability.
BackgroundNifedipine solid dispersion emerged in the late 1970s to address its poor solubility and erratic bioavailability for cardiovascular treatment. Researchers explored methods like fusion, solvent evaporation, and melt extrusion to enhance its solubility and dissolution rate. Over the years, these efforts resulted in commercial products, highlighting the importance of solid dispersion in improving drug delivery and patient outcomes for nifedipine therapy.
AimThe aim of this work is to use the surface solid dispersion approach to increase the solubility of nifedipine.
ObjectiveThe objective of the study is to develop surface solid dispersion formulations of nifedipine, evaluate their physicochemical properties, assess solubility enhancement, analyze dissolution behavior and stability, and determine the potential of this technique to enhance the pharmaceutical performance of nifedipine.
Materials and MethodsNifedipine was dissolved in the solvent-ethanol, and a carrier was then added at various drug-to-carrier ratios. The mixture was allowed to sit for an hour before the solvent was evaporated on a water bath at 40-42ºC with occasional stirring. The resulting dried mass was pulverized, sieved, and then dried further at 40ºC for 3 hours. For further study the powder was stored in desiccators.
ResultsFormulation S3 shows better increase in the solubility by solid dispersion technique, increases solubility from 0.002576 ± 0.00013 to 0.04379 ± 0.00013. Dissolution profile data found to be improved from 98.45 ± 0.41 to 99.57 ± 0.088%.
ConclusionThis study explores the challenge of poor solubility in pharmaceutical formulation, focusing on Nifedipine. Surface solid dispersions (SSDs) are investigated as a solution, with various polymers showing promise in enhancing solubility. SSDs, particularly with sodium starch glycolate (SSG) as a carrier, significantly improve solubility, as confirmed by saturation solubility studies. Evaluation indicates SSD efficacy, with S3 emerging as a promising formulation. This study underscores the potential of SSD technology in addressing solubility challenges and improving drug bioavailability.
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