2,348 research outputs found

    Author interview: Q and A with Dr Ian Sanjay Patel on we’re here because you were there: immigration and the end of empire

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    In this author interview, we speak to Dr Ian Sanjay Patel about his new book, We’re Here Because You Were There: Immigration and the End of Empire, which explores post-war immigration laws, the afterlives of British imperial citizenship and related attempts to reimagine and rejuvenate British imperialism after 1945. Contributing to transnational histories of decolonisation, the book also explores the interconnections between human rights, post-war migration and international diplomacy. Author Interview with Dr Ian Sanjay Patel, author of We’re Here Because You Were There: Immigration and the End of Empire. Verso. 2021

    Embedded in the Body: the Poetry, History and Politics of Migritude with Shailja Patel (2021-02-25)

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    Online discussion, reading and Q&A; Thursday, February 25 at 4:00PM CST; Shailja Patel is the bestselling author of Migritude, taught in over 100 colleges and universities worldwide. Patel's poems have been translated into 17 languages, and been featured in the Smithsonian. The Nobel Women's Initiative honored her with a Global Feminist Spotlight. She is currently a Research Associate at Five College Women's Studies Research Center.Women, Gender & Sexuality Studies program; Alworth Institute for International Studies; Department of Anthropology, Sociology & Criminology; English program; Writing Studies programPatel, Shailja. (2021). Embedded in the Body: the Poetry, History and Politics of Migritude with Shailja Patel (2021-02-25). Retrieved from the University Digital Conservancy, https://hdl.handle.net/11299/220654

    The Patel trials: further evidence of the need to reform the Griffith Codes

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    This article argues that the two trials of Dr Jayant Patel for criminal medical negligence under s 288 of the Criminal Code 1899 Act (Qld) highlight the inadequacies of the duty provisions in the Griffith Codes of Queensland and Western Australia. The difficulties with these duty provisions extend beyond causation and go to the heart of the construction of the Griffith Codes. The fundamental problem lies in the wording of s 23 of both the Queensland and the Western Australia Codes, the principal section dealing with criminal responsibility, which allows a prosecution for criminal negligence under two alternative routes with different standards of proof, and the importation of common law criminal negligence into the duty provisions in the absence of a specified fault element in the relevant Code sections. It is further contended that other criminal law jurisdictions in Australia, such as the Criminal Code 1995 (Cth), offer a better model for the prosecution of criminal negligence cases that flow from breach of a specified duty. The article has greatly benefited from comments provided to the author by Justice HG Fryberg, who conducted the second Patel trial

    dc121p-patel

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    Abstract Researchers have used machine learning algorithms to solve hard problems in a variety of domains, enabling exciting, new applications of computing. However, research results have not transferred to software solutions. In part, this is because developing software with machine learning algorithms is itself difficult. My dissertation work aims to understand why using machine learning is difficult and to create tools that lower the bar so that more developers can effectively use machine learning

    Preparation, optimization and characterization of multiple unit microspheres containing kollidone SR

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    The present investigation described the influence of viscosity and drug: Polymer ratio on Hydrochlorothiazide release. Floating microspheres loaded with hydrochlorothiazide were prepared by Emulsion solvent evaporation method. The prepared microspheres were evaluated by micromeritics properties, in vitro drug release, floating ability and drug entrapment efficiency

    Optimization of fast disintegration tablets using pullulan as diluent by central composite experimental design

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    The objective of this work was to apply central composite experimental design to investigate main and interaction effect of formulation parameters in optimizing novel fast disintegration tablets formulation using pullulan as diluents. Face centered central composite experimental design was employed to optimize fast disintegration tablet formulation. The variables studied were concentration of diluents (pullulan, X1), superdisintigrant (sodium starch glycolate, X2), and direct compression aid (spray dried lactose, X3). Tablets were characterized for weight variation, thickness, disintegration time (Y1) and hardness (Y2). Good correlation between the predicted values and experimental data of the optimized formulation methodology in optimizing fast disintegrating tablets using pullulan as a diluent

    Validated Stability-Indicating RP-HPLC Method for the Simultaneous Determination of Azelnidipine and Olmesartan in Their Combined Dosage Form

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    A simple, rapid, and highly selective RP-HPLC method was developed for the simultaneous determination of Azelnidipine (AZL) and Olmesartan (OLM) drug substances in the fixed dosage strength of 16 mg and 20 mg, respectively. Effective chromatographic separation was achieved using a Hypersil GOLD C18 column (150 mm × 4.6 mm internal diameter, 5 μm particle size) with a mobile phase composed of methanol, acetonitrile, and water in the ratio of 40:40:20 (by volume). The mobile phase was pumped using a gradient HPLC system at a flow rate of 0.5 mL/min, and quantification of the analytes was based on measuring their peak areas at 260 nm. The retention times for Azelnidipine and Olmesartan were about 8.56 and 3.04 min, respectively. The reliability and analytical performance of the proposed HPLC procedure were statistically validated with respect to system suitability, linearity, ranges, precision, accuracy, specificity, robustness, detection, and quantification limits. Calibration curves were linear in the ranges of 2–48 μg/mL for Azelnidipine and 2.5–60 μg/mL for Olmesartan with correlation coefficients >0.990. The proposed method proved to be selective and stability-indicating by the resolution of the two analytes from the forced degradation (hydrolysis, oxidation, and photolysis) products. The validated HPLC method was successfully applied to the analysis of AZL and OLM in their combined dosage form
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