586 research outputs found

    Innovative Biochemical Approaches for Early Cancer Detection and Prognostication

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    This examination explores "Imaginative Biochemical Methodologies for Early Malignant Growth Identification and Anticipation" by coordinating fluid biopsy, metabolomics, and proteomics. In the fluid biopsy tests, circulating tumor DNA (ctDNA), circulating tumor cells (CTCs), and exosomes have been examined, uncovering a tremendous distinction in ctDNA fixation between disease patients and controls (p = 0.023). Designated sequencing of ctDNA distinguished noteworthy hereditary changes, underlining the indicative capability of fluid biopsy. Metabolomic profiling divulged unmistakable metabolic movements, including raised lactate levels, predictable with the Warburg impact seen in malignant growth digestion. Proteomics examination distinguished differentially communicated proteins related to vital disease-related pathways, giving bits of knowledge into the atomic complexities of danger. This interdisciplinary exploration lines up with late examinations investigating AI in diabetes conclusion, the scene of imaginative techniques for gastric malignant growth discovery, and the use of nano biosensors for disease antigen 125 (CA-125) identification. Utilizing man-made consciousness and organization draws near, our work coordinates consistently into the developing scene of accuracy medication. The relative investigation highlights the novel commitments of our review, situating it as an extraordinary investigation of early disease discovery. As it explores customized restorative systems, our examination holds a guarantee for upsetting clinical practices and working on quiet results in the complicated domain of disease the executives

    Effect of Cross Linking on Evaluation of Chitosan Coated Pellets of Glipizide

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    The objective of the current work is to develop and evaluate the effect of cross linking on drug release of chitosan pellets of Glipizide. Hence the present work was aimed to formulate glipizide pellets with a view to achieve and to maintain the plasma concentration for considerable period by controlling the release so to decrease the occurrence of doses and also to recover the patient fulfillment. Here the pellets of glipizide are designed by Pan Coating technique with solution layering with and without cross linking by Gluteraldehyde effectively. Then the optimized formulations are aimed to study the effects of polymer and cross linking on different evaluation parameters including the drug release study. Finally the conclusion was to arrive at better formulation based on comparison amongst the studied ones

    A pharmacological evaluation of ethanol extract of alpinia calcarata rhizome for anti-oxidant, anti-inflammatory and anti-asthmatic properties

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    Alpinia calcarata rhizome ethanolic extract was tested for anti-asthmatic, antioxidant, and anti-inflammatory properties. Adaptogens normalize leukocytosis after milk consumption. Eosinophils are necessary for allergic illness development. The plant extract significantly reduced allergic asthma-related eosinophil cell count compared to the control group. Eosinophil count decreases cell recruitment and IL-4, IL-5, and IL-13, which affect cell count. Studies on milk-induced leukocytosis and eosinophils verified the plant extract's anti-asthmatic capabilities. In guinea pigs, goats, horses, dogs, and humans, histamine contracts trachea and bronchial muscles. Tracheas in guinea pigs test asthma drugs. The isolated guinea pig trachea contracts dose-dependently after H1 receptor stimulation. Alpinia calcarata reduced histamine-induced trachea constriction in solitary guinea pigs, proving its anti-asthmatic and H1 receptor antagonist capabilities. Hydrogen peroxide scavenging and reduction were used to test antioxidants. A hydrogen peroxide-scavenging Alpinia calcarata rhizome ethanol extract. Hydrogen peroxide scavenged less than ascorbic acid. Increasing Alpinia calcarata rhizome ethanolic extract dramatically lowered power. In vitro, ethanolic Alpinia calcarata rhizome extract stabilized rabbit red blood cell membranes and prevented protein denaturation. The ethanolic Alpinia calcarata rhizome extract was anti-asthmatic. Antioxidant and anti-inflammatory characteristics aid the plant's anti-astatic effects. Most asthma medications are steroidal. The phytochemical study identified steroids and flavonoids. Chemical moieties may make the plant anti-asthmatic. The findings support the conventional and advise more anti-asthmatic active component study

    Anti-Urolithiatic Activity of Cassia Auriculata Ethanolic Seed Extract in Wistar Rats

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    Background: Urolithiasis is a medical condition that, despite substantial research in the field of urology, has yet to find a cure within the allopathic medical approach. The process of stone development, known as nephrolithiasis, can occur within the kidney or any segment of the urinary tract, encompassing the ureters and bladder. Material and Methods: The seeds of Cassia auriculata (Linn.) were obtained in June 2021 from Mettukadai hamlet, located in the Erode District of Tamilnadu, India. The herbarium of the plant was meticulously assembled, verified, and afterwards deposited as a voucher specimen. The voucher specimen was retained within the college premises for future reference. Results: The current investigation involved conducting a preliminary phytochemical analysis on the ethanolic seed extract of Cassia auriculata Linn. The research revealed the existence of many phytochemical constituents, including Alkaloids, Flavanoids, Carbohydrate, Sterols, Phytosterols, Phenols, Terpenoids, Amino acids, and Anthraquinones. The acute toxicity experiments revealed that rats exhibited tolerance to a maximum dose of 2000 mg/kg body weight, and no discernible alterations in behavior were detected across all experimental groups. Hence, fractions equivalent to one-fourth and one-eighth of the maximum tolerated dose of 200 mg/kg body weight were selected for subsequent investigations. Conclusion: In summary, the findings suggest that the application of an ethanolic seed extract derived from Cassia auriculata Linn effectively decreased the progression of urinary stone formation. Additionally, it appears that the efficacy of the treatment impact surpasses that of its preventative counterpart

    CURRENT TRENDS, MODERN SYNTHETIC APPROACH, SAR AND BIOLOGICAL ACTIVITIES OF BENZIMIDAZOLE DERIVATIVES

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    Abstract Background: Benzimidazole is a heterocyclic compound with a benzene ring fused to an imidazole ring. It is commercially available as a white, odorless, and tasteless powder. O-phenylenediamine and formic acid are condensed to form benzimidazole. The most common benzimidazole substance found in nature is N- riosyldimethylbenzimidazole, which functions as an axial ligand for cobalt in vitamin B12. Aim: The main objective of the review is to explore Current trends, modern synthetic approach, SAR and Biological activities of benzimidazole derivatives. Method and material: All the data were collected from online published article which in indexed in SCOPUS, WOS, and UGC. Result: Benzimidazole derivatives are generally well-tolerated, but they can cause side effects such as nausea, vomiting, and diarrhea. They can also interact with other medications, so it is important to talk to your doctor before taking them. Conclusion: In order to inform the reader on the chemical and pharmacological properties of these compounds, the goal of this article is to provide them a thorough overview of the substituted benzimidazoles

    An insight of development and validation of bio-analytical method in the reference of anti-diabetic drugs by using LC-MS/MS

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    Diabetes mellitus, which has high rates of disability and mortality, is one of the main causes of public health concerns worldwide. It currently poses serious medical and societal issues. Different bio-analytical techniques have been developed to identify the pharmaceutical formulation of the anti-diabetic drug. Due to the continual requirement to achieve improved sensitivity, accuracy, and speed of analysis in complex biological samples, the development of bio-analytical sample preparation techniques has grown more difficult over time (e.g., blood, serum, plasma, saliva, feces, and urine). This is a mini review, and its goal is to analyze how LC-MS/MS has been used to for the pharmaceutical formulation of the anti-diabetic drugs. The method was validated for linearity, accuracy, precision, specificity, selectivity, and stability

    Measurement of the double-differential inclusive jet cross section in proton-proton collisions at s\sqrt{s} = 5.02 TeV

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    International audienceThe inclusive jet cross section is measured as a function of jet transverse momentum pTp_\mathrm{T} and rapidity yy. The measurement is performed using proton-proton collision data at s\sqrt{s} = 5.02 TeV, recorded by the CMS experiment at the LHC, corresponding to an integrated luminosity of 27.4 pb1^{-1}. The jets are reconstructed with the anti-kTk_\mathrm{T} algorithm using a distance parameter of RR = 0.4, within the rapidity interval y\lvert y\rvert<\lt 2, and across the kinematic range 0.06 <\ltpTp_\mathrm{T}<\lt 1 TeV. The jet cross section is unfolded from detector to particle level using the determined jet response and resolution. The results are compared to predictions of perturbative quantum chromodynamics, calculated at both next-to-leading order and next-to-next-to-leading order. The predictions are corrected for nonperturbative effects, and presented for a variety of parton distribution functions and choices of the renormalization/factorization scales and the strong coupling αS\alpha_\mathrm{S}

    Measurement of the double-differential inclusive jet cross section in proton-proton collisions at s= \sqrt{s} = 5.02 TeV

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    The inclusive jet cross section is measured as a function of jet transverse momentum pT p_{\mathrm{T}} and rapidity y y . The measurement is performed using proton-proton collision data at s= \sqrt{s} = 5.02 TeV, recorded by the CMS experiment at the LHC, corresponding to an integrated luminosity of 27.4pb1\,\text{pb}^{-1}. The jets are reconstructed with the anti-kT k_{\mathrm{T}} algorithm using a distance parameter of R= R= 0.4, within the rapidity interval y< |y| < 2, and across the kinematic range 0.06 <pT< < p_{\mathrm{T}} < 1 TeV. The jet cross section is unfolded from detector to particle level using the determined jet response and resolution. The results are compared to predictions of perturbative quantum chromodynamics, calculated at both next-to-leading order and next-to-next-to-leading order. The predictions are corrected for nonperturbative effects, and presented for a variety of parton distribution functions and choices of the renormalization/factorization scales and the strong coupling αS \alpha_\mathrm{S} .The inclusive jet cross section is measured as a function of jet transverse momentum pTp_\mathrm{T} and rapidity yy. The measurement is performed using proton-proton collision data at s\sqrt{s} = 5.02 TeV, recorded by the CMS experiment at the LHC, corresponding to an integrated luminosity of 27.4 pb1^{-1}. The jets are reconstructed with the anti-kTk_\mathrm{T} algorithm using a distance parameter of RR = 0.4, within the rapidity interval y\lvert y\rvert<\lt 2, and across the kinematic range 0.06 <\ltpTp_\mathrm{T}<\lt 1 TeV. The jet cross section is unfolded from detector to particle level using the determined jet response and resolution. The results are compared to predictions of perturbative quantum chromodynamics, calculated at both next-to-leading order and next-to-next-to-leading order. The predictions are corrected for nonperturbative effects, and presented for a variety of parton distribution functions and choices of the renormalization/factorization scales and the strong coupling αS\alpha_\mathrm{S}
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