Relevant bibliographies by topics / Solid dosage form

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Solid dosage form'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Solid dosage form"

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Yamuna, Choudhary, Goyal Anju, and Vaishnav Rajat. "Process Validation of Solid Dosage Form." Pharmaceutical and Chemical Journal 7, no. 1 (2020): 46–54. https://doi.org/10.5281/zenodo.13952198.

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Process validation is an essential part for the safety of drug products and also to maintain the quality of the products. It is a fundamental component for assuring the quality system used by pharmaceutical industries. Process validation is the key element to ensure the identity, purity, safety, and efficacy of drug products. The process validation precisely focused on the aim and method of analysis. The Process validation reduces product recalls and troubleshooting assignments which results in more economical manufacturing process and quality products. In this article an overview is given on
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Prathamesh, Regade* Nikita Patil Komal Bhusare Sardar Shelke Nilesh Chougule. "Evalution Tests Of Different Dosage Forms An Overview." International Journal of Pharmaceutical Sciences 2, no. 7 (2024): 673–87. https://doi.org/10.5281/zenodo.12721342.

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The pharmaceutical industry continually strives to develop and enhance drug delivery systems to meet the diverse needs of patients. This study undertakes a comprehensive evaluation of solid, liquid, and semisolid dosage forms commonly used in pharmaceutical formulations. The research encompasses a range of parameters, including physicochemical properties, stability, bioavailability, and patient acceptability, to provide a holistic view of these formulations. For Solid pharmaceutical formulations, like tablets and capsules, we explore factors impacting dissolution rates, disintegration, The imp
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Andrews, Gavin P. "Advances in solid dosage form manufacturing technology." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 365, no. 1861 (2007): 2935–49. http://dx.doi.org/10.1098/rsta.2007.0014.

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Currently, the pharmaceutical and healthcare industries are moving through a period of unparalleled change. Major multinational pharmaceutical companies are restructuring, consolidating, merging and more importantly critically assessing their competitiveness to ensure constant growth in an ever-more demanding market where the cost of developing novel products is continuously increasing. The pharmaceutical manufacturing processes currently in existence for the production of solid oral dosage forms are associated with significant disadvantages and in many instances provide many processing proble
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Verma, Navneet Kumar, Uma Srivastava, Satya Prakash Singh, Shweta Yadav, and Pragya Mishra. "A Review on Solid Dosage form: Tablet." Scholars Academic Journal of Pharmacy 13, no. 06 (2024): 219–26. http://dx.doi.org/10.36347/sajp.2024.v13i06.003.

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Tablet is defined as solid pharmaceutical dosage form containing drug substance generally with suitable diluents and prepared by either compression or molding methods. Tablets remain popular as a dosage form because of the advantages afforded, both to the manufacturer (e.g. simplicity and economy of the preparation, stability, and convenience in packing, shipping and dispensing) and the patient. Because of their composition, method of manufacture or intended use, tablets present a variety of characteristics and consequently there are several categories of tablets. Tablet formulation and design
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Lee, Jaemin, Chanwoo Song, Inhwan Noh, Sangbyeong Song, and Yun-Seok Rhee. "Hot-Melt 3D Extrusion for the Fabrication of Customizable Modified-Release Solid Dosage Forms." Pharmaceutics 12, no. 8 (2020): 738. http://dx.doi.org/10.3390/pharmaceutics12080738.

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In this work, modified-release solid dosage forms were fabricated by adjusting geometrical properties of solid dosage forms through hot-melt 3D extrusion (3D HME). Using a 3D printer with air pressure driving HME system, solid dosage forms containing ibuprofen (IBF), polyvinyl pyrrolidone (PVP), and polyethylene glycol (PEG) were printed by simultaneous HME and 3D deposition. Printed solid dosage forms were evaluated for their physicochemical properties, dissolution rates, and floatable behavior. Results revealed that IBF content in the solid dosage form could be individualized by adjusting th
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Pandey, Shubham, Sujeet Pratap Singh, and Dr Tarkeshwar P. Shukla. "Review–Formulation Development of Semi-Solid Dosage Form." INTERANTIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT 07, no. 09 (2023): 1–11. http://dx.doi.org/10.55041/ijsrem25878.

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Semi-solid dosage forms are generally found in medicines for all types of patients. Though, they have specific advantages, along with fast efficacy due to the devoid of dissolution time and quick absorption in the skin surface. Semi-solid formulations have been broadly used in pharmacy due to their high dosing adjustability, easy use off, and rapid onset of action. Keywords: Semi-solid dosage forms, Gels, Ointment, Cream
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Virmani, Reshu, Tarun Virmani, Charan Singh, Geeta Singh, and Sameer Rastogi. "Validation of Solid Dosage form (Tablets): A Review." Research in Pharmacy and Health Sciences 1, no. 1 (2015): 6–12. http://dx.doi.org/10.32463/rphs.2015.v01i01.02.

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Abdoh, A., M. M. Al‐Omari, A. A. Badwan, and A. M. Y. Jaber. "Amlodipine Besylate–Excipients Interaction in Solid Dosage Form." Pharmaceutical Development and Technology 9, no. 1 (2004): 15–24. http://dx.doi.org/10.1081/pdt-120027414.

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Moribe, Kunikazu, Noboru Sekiya, Takayuki Fujito, et al. "Stabilization mechanism of limaprost in solid dosage form." International Journal of Pharmaceutics 338, no. 1-2 (2007): 1–6. http://dx.doi.org/10.1016/j.ijpharm.2006.12.047.

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Mattes, Robert, Denise Root, Yinqi Zhou, Chaoju Xiao, James Johnson, and Atul Shukla. "NIR Prediction of Solid Dosage Form Dissolution Profiles." NIR news 20, no. 5 (2009): 10–11. http://dx.doi.org/10.1255/nirn.1136.

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Dissertations / Theses on the topic "Solid dosage form"

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Massinga, Pedro Horacio. "Gel-based solid dosage form for pesticide delivery." Diss., University of Pretoria, 2008. http://hdl.handle.net/2263/23498.

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The aim of this research was to develop a solid dosage form containing 1.5 g of the pesticide cypermethrin. The dosage should be stable in a tropical climate. In addition, it is to disintegrate and disperse in 10 L of tap water within 3 minutes. Such dissolution should yield a 150 ppm dispersion of cypermethrin, stable for at least one week. This provides for a dip dispersion to treat ticks and fly infestation on livestock. A new solid dosage was formulated as the scope of this research. It is a gel-based solid dosage form. Polymer electrolyte ASP4 - a copolymer of methacrylic acid, ethyl acry
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Nqabeni, Luxolo. "Development of an antiretroviral solid dosage form using multivariate analysis." Thesis, Nelson Mandela Metropolitan University, 2007. http://hdl.handle.net/10948/705.

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The aim of pharmaceutical development is to design a quality product and the manufacturing process to deliver the product in a reproducible manner. The development of a new and generic formulation is based on a large number of experiments. Statistics provides many tools for studying the conditions of formulations and processes and enables us to optimize the same while being able to minimize our experimentation. The purpose of this study was to apply experimental design methodology (DOE) and multivariate analysis to the development and optimization of tablet formulations containing 150 mg lamiv
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Phillips, Justin. "Dextrin nanocomposites and deep eutectic solvents as matrices for solid dosage forms." Diss., University of Pretoria, 2020. http://hdl.handle.net/2263/81724.

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Controlled-release formulations for pesticide applications act as depot systems that continuously release the active ingredients into the environment over a speci ed period, usually from months to years. However, some applications require fast-dissolving drug delivery. The interest of this research is in fast-release of water-insoluble pesticides into aquatic environments. This study considered the use of dextrin starch and urea eutectics as fast release, solid dosage carrier forms that contain an active ingredient. The chosen active for this study is an acaricide called amitraz (N-methy
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Lopez, Lopez Felipe. "Better medicines for children : elucidating patient acceptability to guide flexible solid oral dosage form design." Thesis, University College London (University of London), 2017. http://discovery.ucl.ac.uk/10028121/.

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A medicine will not elicit its desired therapeutic effect if the patient is not able or willing to take it. The specific needs of the target population must be taken into account in the design of medicines. Evaluation of the effect of formulation factors on patient’s acceptability could guide the development of better medicines for children. Flexible solid oral dosage forms, including multiparticulates and (oro)dispersible formulations, offer advantages over conventional solid and liquid dosage forms to meet the needs of paediatric patients. These advantages include favourable stability profil
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Grout, B. F. "Novel applications of at-line near-infrared spectroscopy as process analytical technology for solid dosage form pharmaceutical analysis." Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1395997/.

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The principal aim of this research was to assess at-line Near Infrared Spectroscopy (NIRS) to support Process Analytical Technology (PAT) applications within solid dosage form manufacturing. The history of PAT was traced from implementation of process analytical applications prior to the 2003 United States, Food and Drug Administration PAT initiative through to current time. The use of NIRS within the PAT context was reviewed, highlighting two areas in solid dosage manufacturing where further research of at-line NIRS is warranted; material testing and finished dosage form analysis. Novel appli
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Kindgen, Sarah M. [Verfasser]. "Hydrodynamics and solid dosage form disintegration/dissolution : immediate release tablets and novel in situ polyelectrolyte gastroretentive drug delivery systems / Sarah M. Kindgen." Mainz : Universitätsbibliothek der Johannes Gutenberg-Universität Mainz, 2015. http://d-nb.info/1225749581/34.

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Yin, Xianzhen. "Structure Pharmaceutics Based on Synchrotron Radiation X-Ray Micro- Computed Tomography: From Characterization to Evaluation and Innovation of Pharmaceutical Structures." Thesis, University of Bradford, 2016. http://hdl.handle.net/10454/17378.

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Drug delivery systems (DDS) are essentially pharmaceutical products for human therapy, typically involving a mixture of active ingredients and excipients. Based upon quantitative characterization of structure, the thesis introduces the concept of classifying the architecture of DDS into four levels by their spatial scale and the life time period. The primary level is recognised as the static structure of the whole dosage form with a size from μm to cm with the final structure generated by formulation design. The secondary level categorises the structures of particles or sub-units to for
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MODICA, DE MOHAC Laura. "Novel Drug Delivery System for Treatment-Resistant Schizophrenia." Doctoral thesis, Università degli Studi di Palermo, 2021. http://hdl.handle.net/10447/478483.

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Ibrahim, Mohamed Asim Y. "Co-processing of drugs and co-crystal formers and its effect on pharmaceutical dosage-form performance. Co-crystallization of urea/ 2-methoxybenzamide, caffeine/ malonic acid, caffeine/ oxalic acid and theophylline/ malonic acid systems: Solid-state characterization including imaging, thermal, X-ray and Raman spectroscopic techniques with subsequent evaluation of tableting behaviour." Thesis, University of Bradford, 2008. http://hdl.handle.net/10454/12760.

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This dissertation has focused on the solid-state characterization of different co-crystal system as well as the effect of co-crystallization of these systems on pharmaceutical dosage form performance. Urea/ 2-MB, caffeine/ malonic acid, caffeine/ oxalic acid and theophylline/ malonic acid co-crystals were prepared using co-grinding- and co-precipitation techniques. In addition, the synthesis of co-crystals through two novel methods has been demonstrated. This includes compaction and convection mixing. The solid-state characterization of the co-crystals has been carried out using XRPD, Raman sp
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Ibrahim, Mohamed Asim Yousif. "Co-processing of drugs and co-crystal formers and its effect on pharmaceutical dosage-form performance : co-crystallization of urea/2-methoxybenzamide, caffeine/malonic acid, caffeine/oxalic acid and theophylline/malonic acid systems : solid-state characterization including imaging, thermal, X-ray and Raman spectroscopic techniques with subsequent evaluation of tableting behaviour." Thesis, University of Bradford, 2008. http://hdl.handle.net/10454/12760.

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This dissertation has focused on the solid-state characterization of different co-crystal system as well as the effect of co-crystallization of these systems on pharmaceutical dosage form performance. Urea/ 2-MB, caffeine/ malonic acid, caffeine/ oxalic acid and theophylline/ malonic acid co-crystals were prepared using co-grinding- and co-precipitation techniques. In addition, the synthesis of co-crystals through two novel methods has been demonstrated. This includes compaction and convection mixing. The solid-state characterization of the co-crystals has been carried out using XRPD, Raman sp
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Books on the topic "Solid dosage form"

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Carstensen, Jens Thurø. Pharmaceutical principles of solid dosage forms. Technomic Pub., 1993.

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Burrows, Jane L. Solid dosage forms for ophthalmic drug delivery. University of Portsmouth, 2002.

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1941-, Shargel Leon, and Kanfer Isadore, eds. Generic drug product development: Solid oral dosage forms. Marcel Dekker, 2005.

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Qiu, Yihong, Yisheng Chen, and Geoff G. Z. Zhang. Developing solid oral dosage forms: Pharmaceutical theory and practice. Edited by ScienceDirect (Online service). Academic, 2009.

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United States. Food and Drug Administration., ed. Bioequivalence of solid oral dosage forms: A presentation to the U.S. Food and Drug Administration hearing on bioequivalence of solid oral dosage forms September 29 - October 1, 1986. The Association, 1986.

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United States. Food and Drug Administration. Division of Field Investigations., ed. Guide to inspections of oral solid dosage forms pre/post approval issues for development and validation. Division of Field Investigations, Office of Regional Operations, Office of Regulatory Affairs, U.S. Food & Drug Administration, 1994.

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Storey, Richard A., and Ingvar Ymen. Solid state characterization of pharmaceuticals. John Wiley & Sons, 2011.

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J, Habib Muhammad, ed. Pharmaceutical solid dispersion technology. Technomic Pub. Co., 2001.

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United States. Food and Drug Administration. Division of Field Investigations, ed. Guide to inspections of oral solid dosage forms pre/post approval issues for development and validation. Division of Field Investigations, Office of Regional Operations, Office of Regulatory Affairs, U.S. Food & Drug Administration, 1994.

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G, Brittain H., ed. Polymorphism of pharmaceutical solids. 2nd ed. Informa Healthcare, 2009.

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Book chapters on the topic "Solid dosage form"

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Narang, Ajit S., Divyakant Desai, and Sherif Badawy. "Impact of Excipient Interactions on Solid Dosage Form Stability." In Excipient Applications in Formulation Design and Drug Delivery. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20206-8_5.

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Lyngberg, Olav, Lieve Bijnens, Jeroen Geens, Alex Marchut, Steve Mehrman, and Elisabeth Schafer. "Applications of Modeling in Oral Solid Dosage Form Development and Manufacturing." In Methods in Pharmacology and Toxicology. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-2996-2_1.

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Chandra, Phool, Zeeshan Ali, Neetu Sachan, Nishat Fatma, and Anurag Verma. "Grafted Polysaccharide as an Excipient for the Formulation of Solid Dosage Form." In Graft Copolymers for Biomedical and Tissue Engineering Applications. Apple Academic Press, 2025. https://doi.org/10.1201/9781003597742-12.

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Peeters, Michiel, Thomas De Beer, and Ashish Kumar. "Near-infrared Spectroscopy as Process Analytical Technology in Continuous Solid Dosage Form Manufacturing." In Continuous Pharmaceutical Processing and Process Analytical Technology. CRC Press, 2022. http://dx.doi.org/10.1201/9781003149835-13.

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Muliadi, Ariel R., Alamelu Banda, and Chen Mao. "Recent Progress in Roll Compaction Process Development for Pharmaceutical Solid Dosage Form Manufacture." In Continuous Pharmaceutical Processing. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-41524-2_7.

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Chang, Qing, Lisheng Kang, Keri Varner, Joyce Bridges, Norman Sesi, and Margo Palmieri. "An Excipient Library Approach to Analytical Development for Low-Dose, Solid Oral Dosage Form Drug Products." In Formulation and Analytical Development for Low-Dose Oral Drug Products. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470386361.ch14.

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Nickerson, Beverly, and Garry Scrivens. "Sample Preparation for Solid Oral Dosage Forms." In Sample Preparation of Pharmaceutical Dosage Forms. Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-9631-2_7.

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Murtaza, Ghulam, Munazza Ijaz, Hafsa Anam, and Saba Shamim. "Stability Studies of Solid Dosage Forms." In Drug Stability and Chemical Kinetics. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-6426-0_16.

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Brunaugh, Ashlee D., Hugh D. C. Smyth, and Robert O. Williams III. "Modified Release Solid Oral Dosage Forms." In AAPS Introductions in the Pharmaceutical Sciences. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-31745-4_4.

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Borde, Shambhavi, Dhirender Singh, Navneet Sharma, Dunesh Kumari, and Harsh Chauhan. "Solid Dosage Forms: Formulation and Characterization." In Handbook of Space Pharmaceuticals. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-50909-9_15-1.

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Conference papers on the topic "Solid dosage form"

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de Paula, Renato M., Victor V. Keasler, and Timothy J. Tidwell. "Evaluation of Preservative Chemistries to Control Microbial Activity During Well Completion." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-06069.

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Abstract Microbiologically-influenced corrosion (MIC) poses a serious concern to the production and the integrity of pipelines, vessels and tanks. High water content directly increases the risk for MIC as it results in an increase of the microbial load in the system. Compared to conventional production systems, unconventional fields are at a higher risk for premature MIC due to large volumes of water used to initially fracture the formation. Thus, microbial control during hydraulic fracturing is a critical step to prevent corrosion and maintain the integrity of the well. The use of traditional
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Keasler, Victor, Brian Bennett, Robert J. Franco, Don Lefevre, and Babatunde Moninuola. "Implementation of a Microbial Control Program for an Offshore Production System in Nigeria." In CORROSION 2011. NACE International, 2011. https://doi.org/10.5006/c2011-11235.

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Abstract A 30-year-old offshore pipeline system in Nigeria was found to have severe internal corrosion, which was attributed to microbiologically influenced corrosion (MIC). A laboratory investigation was undertaken to develop a microbial and solids control program to overcome the most significant challenges including: the inability to pig the majority of the system, treating isolated sump tanks that likely harbor large quantities of bacteria, and minimizing internal corrosion of a critical pipeline delivering crude oil to the processing facility. The laboratory findings were presented at NACE
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Lu, Haiping, Tim Underwood, Zhenning Gu, and Bingbing Guo. "The Development of Novel Laboratory Test Method on Evaluation of Scale Inhibition and Dispersancy for Downstream Water Treatment Applications." In CORROSION 2020. NACE International, 2020. https://doi.org/10.5006/c2020-14491.

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Abstract Scale control is vital for cooling water operations, and evaluation of best-fit scale inhibitors for the application is essential, for the scale treatment. One of the traditional test methods for industrial water scale inhibitor screening is static bottle testing. Recently, in other industries, Kinetic Turbidity Test (KTT) has gained more acceptance for scale inhibitor evaluation. KTT uses an Ultraviolet-Visible (UV-Vis) spectrophotometer to monitor scale formation at various dosages of tested products, as function of reaction time. The technology can provide minimum dosage recommenda
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Fu, Bob. "Development of Non-Interfering Corrosion Inhibitors for Sour Gas Pipelines with Co-Injection of Kinetic Hydrate Inhibitors." In CORROSION 2007. NACE International, 2007. https://doi.org/10.5006/c2007-07666.

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Abstract Sour gas pipelines are often operated under the conditions that are conducive to corrosion and gas hydrate formation. In order to protect the integrity of the pipelines and to prevent potential solid hydrate blockages, the continuous application of corrosion inhibitors (CI) and kinetic hydrate inhibitors (KHI) is an attractive chemical solution to minimize the risk. However, CI and KHI are not always compatible with each other when co-injected. This study confirms that the presence of CI can significantly decrease the performance of KHI. The adverse effect is attributed to the interfe
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Sibychan, Jerrin Job, Nicola Sorace, Jason Melnick, et al. "Use of Discrete Element Method to Troubleshoot Aesthetic Defects in Pharmaceutical Tablets." In Foundations of Computer-Aided Process Design. PSE Press, 2024. http://dx.doi.org/10.69997/sct.148066.

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Pharmaceutically elegant tablets are an expectation from pharmacists, health care providers and consumers for solid oral dosage forms. The presence of non-aesthetically pleasing defects in solid oral dosage forms can result in complaints back to the manufacturer and potentially non-compliance with medicines. The purpose of this study was to simulate and analyze the design of a tablet core and the aqueous film-coating process, to gain a better understanding of tablet defect generation, and to help eliminate the defects from the finished product. This evaluation employs Discrete Element Method (
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Smith, James P., Ian H. Gilbert, Roger W. Kidder, and Syamsudin. "Inhibition of CO2 Corrosion in Multiphase Flow and Solids Production A Case History." In CORROSION 2001. NACE International, 2001. https://doi.org/10.5006/c2001-01029.

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Abstract Variability in corrosion rates, 0.1 to 10 mm/year, observed in an electrical submersible pump driven subsea pipeline system culminated in a search for a corrosion inhibitor and treatment program that successfully controls the cumulative impact of multiple types of flow and produced solids. The problems arising from these causative factors are further exacerbated by depleting sands that produce increasing CO2 mole fraction, often denoted by an increasing gas oil ratio, coupled with increasing water cuts. These factors act synergistically with multiphase flow corrosion to accelerate dam
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de Paula, Renato M., Victor V. Keasler, Brian Bennett, Jeffrey Caleb Clark, and Richard Cloud. "On-site Evaluation of Microbiologically Induced Corrosion and the Effects of Continuous Low Dosage Corrosion Inhibitor Application." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-4066.

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Abstract The ability to properly monitor microbial growth and corrosion rates on-site is a critical step towards the development of a successful mitigation strategy to control microbiologically influenced corrosion (MIC). Commonly, bacterial activity on pipelines and vessels is determined by extrapolation of microbial loads detection in the planktonic phase. This often leads to misleading decisions around chemical treatments. To establish a correlation between microbial activity on metal surfaces and the corrosion process, an on-site evaluation was implemented in a produced water system in Nor
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Brooks, Johnathon, Miriam Barber, and Haiping Lu. "Kinetic Turbidity Test Method for Scale Inhibitor Evaluation on Multifunctional Scales." In CORROSION 2021. AMPP, 2021. https://doi.org/10.5006/c2021-16959.

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Abstract One of the critical approaches for scale control is the proper selection and use of scale inhibitors. Laboratory tests help to select the appropriate scale inhibitor with the most common testing methods, including static bottle test and dynamic scaling loop test. Recently, Kinetic Turbidity Test (KTT) has gained increased recognition as a new testing method for scale inhibitor evaluation due to short testing time, simple sample preparation, and good reproducibility. There has been a good deal of research and studies on KTT as a technique for multifunctional scales, including calcium c
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Zhang, Naling, Ling Sang, Xiping Niu, et al. "Improving the Electrical Performances of 1200 V 4H-SiC MOSFETs by Optimizing the Doping Dose of p-Well." In 2024 21st China International Forum on Solid State Lighting & 2024 10th International Forum on Wide Bandgap Semiconductors (SSLCHINA: IFWS). IEEE, 2024. https://doi.org/10.1109/sslchinaifws64644.2024.10835394.

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Richter, Sonja, Jay Locklear, Mohsen Achour, Thomas Baugh, Probjot Singh, and Ross Goff. "Control of Corrosion Inhibitor Fouling in a Highly Sour System." In CORROSION 2018. NACE International, 2018. https://doi.org/10.5006/c2018-10918.

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Abstract Black tar-like fouling material was driving frequent shut-downs and increasing corrosion in the inlet area of a gas plant that processes lean gas with high acid gas content (68%CH4, 20%CO2 and 12%H2S). Analytical work indicated that the nitrogen containing corrosion inhibitor (CI) polymerized with sulfur compounds (polysulfides, elemental sulfur and/or H2S) in a type of a vulcanization process resulting in a hard-to-clean insoluble fouling product. Corrosion testing confirmed the role of the CI in creating this fouling. A customized autoclave testing was designed to include powdered e
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Reports on the topic "Solid dosage form"

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Rittman, P. D. Dose estimates for the solid waste performance assessment. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10185060.

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Smith III, F. G., B. T. Butcher, M. A. Phifer, and L. L. Hamm. Dose Calculation Methodology and Data for Solid Waste Performance Assessment and Composite Analysis at the Savannah River Site. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1178652.

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Smith, F., T. Butcher, L. Hamm, and W. Kubilius. DOSE CALCULATION METHODOLOGY AND DATA FOR SOLID WASTE PERFORMANCE ASSESSMENT AND COMPOSITE ANALYSIS AT THE SAVANNAH RIVER SITE. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1561208.

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Small Lung Nodule Volume Assessment and Monitoring in Low Dose CT Screening, Clinically Feasible Profile. Chair Artit Jirapatnakul, James Mulshine, and Kyle Myers. Radiological Society of North America (RSNA) / Quantitative Imaging Biomarkers Alliance (QIBA), 2023. http://dx.doi.org/10.1148/qiba/20231219.

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The goal of a QIBA Profile is to help achieve a useful level of performance for a given biomarker. The Claim (Section 2) describes the biomarker performance. The Profile Activities (Section 3) contribute to generating the biomarker. Requirements are placed on the Actors that participate in those activities as necessary to achieve the Claim. Assessment Procedures (Section 4) defines the technical methods to be used for evaluating conformance with profile requirements. This includes the steps needed for clinical sites and equipment vendors to be compliant with the Profile. This QIBA Profile (Sma
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Schwartz, Bertha, Vaclav Vetvicka, Ofer Danai, and Yitzhak Hadar. Increasing the value of mushrooms as functional foods: induction of alpha and beta glucan content via novel cultivation methods. United States Department of Agriculture, 2015. http://dx.doi.org/10.32747/2015.7600033.bard.

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During the granting period, we performed the following projects: Firstly, we differentially measured glucan content in several pleurotus mushroom strains. Mushroom polysaccharides are edible polymers that have numerous reported biological functions; the most common effects are attributed to β-glucans. In recent years, it became apparent that the less abundant α-glucans also possess potent effects in various health conditions. In our first study, we explored several Pleurotus species for their total, β and α-glucan content. Pleurotuseryngii was found to have the highest total glucan concentrati
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