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Showing 1 to 20 of 87 for “"Active pharmaceutical ingredients"”.

  1. NOVEL SYNTHETIC PROCESSES FOR THE INDUSTRIAL PREPARATION OF ACTIVE PHARMACEUTICAL INGREDIENTS

    … for the industrial preparation of two emerging active pharmaceutical ingredients (API). Specifically, the process for the preparation of a new paclitaxel prodrug, namely octadecanedioc acid-paclitaxel, was defined. This paclitaxel derivate has shown better results in vivo trials, against a wide …

    milano Repository record for NOVEL SYNTHETIC PROCESSES FOR THE INDUSTRIAL PREPARATION OF ACTIVE PHARMACEUTICAL INGREDIENTS (opens in a new tab)

  2. Microfluidic platforms for screening of crystallization conditions of active pharmaceutical ingredients

    Item reinstated by Sarah Shreeves (sshreeve@illinois.edu) on 2012-05-19T10:00:13Z Item was in collections: University of Illinois Dissertations and Theses (ID: 204) Dissertations and Theses - Chemical and Biomolecular Engineering (ID: 591) No. of bitstreams: 4 Thorson_Michael.pdf: 901648 bytes, …

    uiuc Repository record for Microfluidic platforms for screening of crystallization conditions of active pharmaceutical ingredients (opens in a new tab)

  3. Crystallization of active pharmaceutical ingredients using microfluidic platforms and meniscus-guided coating

    … times and large development cost has led the pharmaceutical industry to evaluate and improve pharmaceutical development and manufacturing procedures. Emphasis has been placed on the connection between drug development and discovery, especially on characterization of candidate drugs earlier in …

    uiuc Repository record for Crystallization of active pharmaceutical ingredients using microfluidic platforms and meniscus-guided coating (opens in a new tab)

  4. Optimal handling of Highly Active Pharmaceutical Ingredients during milling and blending operations

    … thesis investigates best practices for Highly Active Pharmaceutical Ingredient (HAPI) milling and blending. We utilize a qualitative analysis centering on a benchmarking study and quantitative analyses using a probabilistic capacity simulation and tradeoff methodology. The analyses indicate …

    mit Repository record for Optimal handling of Highly Active Pharmaceutical Ingredients during milling and blending operations (opens in a new tab)

  5. CONTINUOUS-FLOW STRATEGIES FOR THE PREPARATION OF ACTIVE PHARMACEUTICAL INGREDIENTS AND RELEVANT INTERMEDIATES

    … continuous-flow strategies for the synthesis of active pharmaceutical ingredients (APIs) and key intermediates, with the aim of improving reaction efficiency, safety, and scalability. The work focuses on the integration of modern synthetic methodologies with enabling technologies such as flow …

    milano Repository record for CONTINUOUS-FLOW STRATEGIES FOR THE PREPARATION OF ACTIVE PHARMACEUTICAL INGREDIENTS AND RELEVANT INTERMEDIATES (opens in a new tab)

  6. Heterogeneous nucleation of active pharmaceutical ingredients on polymers : applications in continuous pharmaceutical manufacturing

    … nucleation and crystal growth in the absence of active mass transfer would have too small a throughput and too large a footprint to be useful. The main reasons were long average nucleation induction times and slow crystal growth in the absence of convection. A set of batch desupersaturation …

    mit Repository record for Heterogeneous nucleation of active pharmaceutical ingredients on polymers : applications in continuous pharmaceutical manufacturing (opens in a new tab)

  7. Study of controlled release of active pharmaceutical ingredients from functionalized nanoclays and polymer matrices

    … structure-property-processing relationships of pharmaceutical polymer-based products. They are: a) modification of a pharmaceutical anionic nanoclay with two different Active Pharmaceutical Ingredients (APIs) to produce nanohybrid API carriers intended to be used alone or in acrylic polymer …

    njit Repository record for Study of controlled release of active pharmaceutical ingredients from functionalized nanoclays and polymer matrices (opens in a new tab)

  8. Physicochemical and computational approaches for the prediction of the manufacturability of active pharmaceutical ingredients

    Tablets have aided the delivery of active pharmaceutical ingredients (APIs) to patients since the 1800s, however tablet failure, such as punch sticking and tablet hardness issues, during manufacturing is still common. The techniques currently available for the prediction of manufacturability of …

    greenwich Repository record for Physicochemical and computational approaches for the prediction of the manufacturability of active pharmaceutical ingredients (opens in a new tab)

  9. Preformulation solid-state supramolecular beneficiation of selected active pharmaceutical ingredients and a novel drug candidate

    … selected compounds for use in the formulation of pharmaceutical products. The compounds selected were: Clevudine, an established drug that is currently in use for the treatment of chronic hepatitis B infections, 6-(3- (Methylsulfonyl)phenyl)-3-(4-(methylsulfonyl)phenyl)-imidazo[1,2-b]pyridazine …

    cape-town Repository record for Preformulation solid-state supramolecular beneficiation of selected active pharmaceutical ingredients and a novel drug candidate (opens in a new tab)

  10. Developing strategies and equipment for continuous isolation of active pharmaceutical ingredients (APIs) by filtration, washing and drying

    In pharmaceutical sector, compounds forming the drug and especially the activep harmaceutical ingredients (API's) are required to be pure, in accordance with the regulatory authorities' rules. The isolation stage is used to remove the impure liquid phase and to remove surface impurities from the …

    strathclyde Repository record for Developing strategies and equipment for continuous isolation of active pharmaceutical ingredients (APIs) by filtration, washing and drying (opens in a new tab)

  11. Modeling, optimization, and sensitivity analysis of a continuous multi-segment crystallizer for production of active pharmaceutical ingredients

    … a new type of crystallizer for the production of pharmaceuticals. The multi-segment, multi-addition plug-flow crystallizer (MSMA-PFC) offers better control over supersaturation in one dimension compared to a batch or stirred-tank crystallizer. Through use of a population balance framework, we have …

    purdue-thes Repository record for Modeling, optimization, and sensitivity analysis of a continuous multi-segment crystallizer for production of active pharmaceutical ingredients (opens in a new tab)

  12. Effect of Compression Force on Agglomeration of Micronized Active Pharmaceutical Ingredients: Techniques to Prevent API Agglomeration During Compression

    … to increase surface area of poorly soluble Active Pharmaceutical Ingredient’s (API). This size reduction improves the dissolution rate and permeability thereby increasing the bioavailability for hydrophobic API’s.</p> <p>Tablets and capsules are the most marketed and easy to manufacture …

    tenn-hsc Repository record for Effect of Compression Force on Agglomeration of Micronized Active Pharmaceutical Ingredients: Techniques to Prevent API Agglomeration During Compression (opens in a new tab)

  13. The sorption fate of active pharmaceutical ingredients in soils receiving high wastewater inputs and implications for risk assessments

    … access to medicines have led to an increase in active pharmaceutical ingredients (APIs) entering sewerage networks. Wastewater in lower and lower middle-income countries use that use wastewater for irrigation may use untreated or poorly treated wastewater resulting in the potential for greater …

    plymouth Repository record for The sorption fate of active pharmaceutical ingredients in soils receiving high wastewater inputs and implications for risk assessments (opens in a new tab)

  14. Design of a rapid, continuous, small-scale device for creating dry powders from concentrated suspensions containing active pharmaceutical ingredients

    Current methods of producing pharmaceutical compounds are large batch processes. The minimum time-to-patient for drug manufacturing is approximately 100 days. Using a continuous manufacturing process, the time-to-patient could be reduced to less than ten days. The scope of this paper encompasses …

    mit Repository record for Design of a rapid, continuous, small-scale device for creating dry powders from concentrated suspensions containing active pharmaceutical ingredients (opens in a new tab)

  15. NOVEL SUSTAINABLE STRATEGIES FOR THE SYNTHESIS OF ACTIVE PHARMACEUTICAL INGREDIENTS (APIS) AND BIOACTIVE MOLECULES THROUGH THE EXPLOITATION OF ISOLATED ENZYMES AS BIOCATALYSTS

    … on the development of sustainable entries to bioactive compounds, small molecules, and chiral synthons of pharmaceutical and industrial interest, by combining the ability of various biocatalysts alongside traditional organic synthetic protocols. Both commercially available and in-house expressed, …

    milano Repository record for NOVEL SUSTAINABLE STRATEGIES FOR THE SYNTHESIS OF ACTIVE PHARMACEUTICAL INGREDIENTS (APIS) AND BIOACTIVE MOLECULES THROUGH THE EXPLOITATION OF ISOLATED ENZYMES AS BIOCATALYSTS (opens in a new tab)

  16. Co-crystal screening of poorly water-soluble active pharmaceutical ingredients. Application of hot stage microscopy on curcumin-nicotinamide system and construction of ternary phase diagram of fenbufen-nicotinamide-water co-crystal system.

    … motivated by the fact that a number of active pharmaceutical ingredient (API) co-crystals with improved dissolution have recently been synthesized. Hence, co-crystallization technique highlights an alternative means to improve the performance of curcumin. Within our work evidences for a …

    bradford Repository record for Co-crystal screening of poorly water-soluble active pharmaceutical ingredients. Application of hot stage microscopy on curcumin-nicotinamide system and construction of ternary phase diagram of fenbufen-nicotinamide-water co-crystal system. (opens in a new tab)

  17. Assessment of a marine polysaccharide for use as excipient in pharmaceutical hot-melt extrusion

    Pharmaceutical Hot Melt Extrusion (HME) is currently investigated by both industry and academia as a method for manufacturing solid oral dosages with improved bioavailability of poorly-water soluble active pharmaceutical ingredients (APIs) and control drug release of water-soluble APIs. Although …

    njit Repository record for Assessment of a marine polysaccharide for use as excipient in pharmaceutical hot-melt extrusion (opens in a new tab)

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