Noncommutative quantum mechanics of a harmonic oscillator under linearized gravitational waves

We consider the quantum dynamics of a harmonic oscillator in noncommutative space under the influence of linearized gravitational waves (GW) in the long wave-length and low-velocity limit. Following the prescription in \cite{ncgw1} we quantize the system. The Hamiltonian of the system is solved by using standard algebraic iterative methods. The solution shows signatures of the coordinate noncommutativity via alterations in the oscillation frequency of the harmonic oscillator system from its commutative counterpart. Moreover, it is found that the response of the harmonic oscillator to periodic GW, when their frequencies match, will oscillate with a time scale imposed by the NC parameter. We expect this noncommutative signature to show up as some noise source in the GW detection experiments since the recent phenomenological upper-bounds set on spatial noncommutative parameter implies a length-scale comparable to the length-variations due to the passage of gravitational waves, detectable in the present day GW detectors.Comment: 6 pages Late

DESIGN AND CHARACTERISATION OF TRANSDERMAL PATCHES OF PHENFORMIN HYDROCHLORIDE

Objective: In present work was designed to develop suitable transdermal matrix patches of Phenformin hydrochloride using various hydrophilic (HPMC) and hydrophobic (EUDRAGID) polymers as matrix formers.Methods: Transdermal patches containing Phenformin hydrochloride were prepared by the solvent casting evaporation technique.Results: Revealed that prepared patches showed good physical characteristics, no drug-polymer interaction and no skin irritation was observed. The in vitro release study revealed that F3 formulation showed maximum release in 24 h. Formulation F3 was subjected for accelerated stability studies. The F3 formulation was found to be stable as there was no drastic change in the Physico-chemical properties of the patches, which was also confirmed by FTIR.Conclusion: Thus conclusion can be made that stable transdermal patches of Phenformin hydrochloride has been developed. F1, F2, F3, F4 formulations showed highest cumulative percentage drug release of 98.13%, 95.50%, 98.65%, 97.21% were obtained during in vitro drug release studies after 24 h. The release of Phenformin hydrochloride appears to be dependent on lipophilicity of the matrix. Moderately lipophillic matrices showed best release. The predominant release mechanism of drug through the fabricated matrices was believed to be by diffusion mechanism. Based upon the in vitro dissolution data the F3 formulation was concluded as optimized formulation

SUBLINGUAL DRUG DELIVERY: AN INDICATION OF POTENTIAL ALTERNATIVE ROUTE

Sublingual literally meaning is under the tongueâ€, refers to a method of administrating substance via mouth in such a way that the substance is rapidly absorbed via blood vessels under tongue. Sublingual route is a useful when rapid onset of action is desired with better patient compliance than orally ingested tablets. Drugs that are given sublingually reach directly in to the systemic circulation through the ventral surface of the tongue and floor of the mouth. The portion of drug absorbed through the sublingual blood vessels bypasses the hepatic firstâ€pass metabolic processes giving acceptable bioavailability. As nowadays most of the people need effective relief within a short period of time so sublingual is the most suitable form of administration. New sublingual technologies address many pharmaceutical and patient needs, ranging from enhanced lifeâ€cycle management to convenient dosing for paediatric, geriatric, and psychiatric patients with dysphagia

FAST DISSOLVING TABLET USING SOLID DISPERSION TECHNIQUE: A REVIEW

Fast dissolving tablets are also called as mouth-dissolving tablets, melt-in mouth tablets, orodispersible tablets, quick dissolving etc. Fast dissolving tablets are those when put on tongue disintegrate instantaneously releasing the drug, which dissolve or disperses in the saliva. The faster the drug dissolved into solution, quicker the absorption and onset of clinical effect. Oral routes of drug administration have wide acceptance up to 50-60% of total dosage forms. Fast dissolving tablet containing solid dispersion was developed to improve the dissolution of drug and stability of solid dispersion. They are disintegrating and/or dissolve rapidly in the saliva without the need for water. Thus it is regarded as the safest, most convenient and most economical method of drug delivery having the highest patient compliance. The later part of the article focus on the progress in methods of manufacturing, evaluation and various latest technologies involved in the development of Fast dissolving tablets. Solid dispersion is basically a drug–polymer two-component system; the drug–polymer interaction is the determining factor in its design and performance. It also discusses about modern characterization technique to characterize solid dispersion. In this review, it is intended to discuss the recent advances related on the area of solid dispersion technology. Different methods are also been used for preparation of solid dispersions such as Melting method, Solvent method, Melting solvent method, Melt extrusion method, lyophilisation Technique, Melt Agglomeration Process, The Use Of Surfactant, Electro spinning and Super Critical Fluid Technology. The introduction of fast dissolving dosage forms has solved some of the problems encountered in administration of drugs to the pediatric and elderly patient, which constitutes a large proportion of the world's population. Solid dispersions have attracted considerable interest as an efficient means of improving the dissolution rate and hence the bio availability of a range of poorly water-soluble drugs. The focus of one part of the review article is based on solid dispersion mainly advantages, disadvantages, types, the method of preparation, and characterization of the solid dispersion at laboratory and industrial level

Comparison of hemodynamic alterations and post-operative profile of sevoflurane and propofol during laparoscopic cholecystectomies

Background: Modern laparoscopic surgeries with insufflation of gas into peritoneal cavity are gold standard treatment for cholelithiasis. Propofol, a GABA receptor positive allosteric modulator and Sevoflurane, an inhalational anesthetic are used for maintenance of general anesthesia. In laparoscopy, significant hemodynamic changes occur. Searching in field of anesthesia is going on for anesthetic agent for better recovery. Aims and Objectives: Objective of the study is to compare sevoflurane with propofol for intraoperative hemodynamic changes and post-operative recovery profile of patient’s undergone laparoscopic cholecystectomies under general anesthesia. Secondary objective is to compare post-operative complications. Materials and Methods: A prospective, randomized, single-blinded, and comparative study done after permission from the institutional ethical committee and informed consent from patients. Total 84 patients of 20–50 years age of either sex were scheduled for laparoscopic cholecystectomy, divided in two equal groups – Group P, induced with propofol and anesthesia was maintained with propofol (100–120 μg/kg/min), nitrous oxide and oxygen and Group S induced with propofol and anesthesia was maintained using sevoflurane (1–2%), nitrous oxide, and oxygen. Results: We found that time for eye opening was 9±1.21 min in Group P and 8±1.34 min in Group S. Time for following verbal command was 10±1.20 min in Group P and 9±1.32 min in Group S. Time for speaking name by patient was 11±1.20 min in Group P and 10±1.34 min in Group S. Difference between two groups regarding eye opening, following verbal command, and time to speak own name are highly significant with P8 was 14±1.30 min in Group P and 13±1.37 min in Group S. Difference between two groups is also highly significant with P8 were significantly shorter in sevoflurane group. Conclusion: From our study, maintenance of general anesthesia with sevoflurane is associated with faster recovery from anesthesia

Study on the Perspective of Mechanical Properties and Corrosion Behaviour of Stainless Steel, Plain and TMT Rebars

In the present research, the effects of various alloying elements and microstructural constituents on the mechanical properties and corrosion behaviour have been studied for four different rebars. The microstructures of stainless steel and plain rebar primarily reveal equiaxed ferrite grains and ferrite-pearlite microstructures, respectively, with no evidence of transition zone, whereas tempered martensite at the outer rim, followed by a narrow bainitic transition zone with an internal core of ferrite-pearlite, has been observed for the thermomechanically treated (TMT) rebars. The hardness profiles obtained from this study display maximum hardness at the periphery, which decreases gradually towards the centre, thereby providing the classical U-shaped hardness profile for TMT rebars. The tensile test results confirm that stainless steel rebar exhibits the highest combination of strength (≈755 MPa) and ductility (≈27%). It has been witnessed that in Tafel plots, the corrosion rate increases for all the experimental rebars in 1% HCl solution, which is well expected because the acid solutions generally possess a higher corrosive environment than seawater (3.5% NaCl) due to their acidic nature and lower pH values. However, all the experimental results obtained from Tafel and Nyquist plots correlate well for both 1% HCl and 3.5% NaCl solutions