Academic literature on the topic 'Dosage formulation'

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Dissertations / Theses on the topic "Dosage formulation"

1

Buys, Johannes Jacobus. "Formulation and evaluation of mebendazole dosage forms / Kobus Buys." Thesis, North-West University, 2003. http://hdl.handle.net/10394/190.

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Parasites in the restricted sense are those members of the animal kingdom which derive their means of well-being from other members of the animal kingdom, at the same time depriving their host of some (sometimes all) of its well-being. Parasitic diseases are much more widespread than many people realise. These diseases affect not only impoverished people in remote countries but they can be important health problems for rich and poor throughout the world. Different parasites infect our domestic animals and cause great losses; they have a great influence on the growing, production and overall re
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2

Palazzolo, Robert D. (Robert David) 1973. "Formulation of oral dosage forms by three dimensional printing." Thesis, Massachusetts Institute of Technology, 1998. http://hdl.handle.net/1721.1/50617.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 1998.<br>Includes bibliographical references (p. 93).<br>Pharmaceutical grade materials were used in the fabrication of fast-release and extended-release oral dosage forms. Tablets were processed by employing a method of solid freeform fabrication known as three dimensional printingTM (3DPTM). A microcrystalline cellulose powder was used in combination with pH-dependent and permeable polymeric binder solutions. Release studies in acidic media were performed using both dye and drug (antihistamine)
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Injety, Sahana. "Formulation of a nevirapine co-crystal as a liquid dosage form." University of the Western Cape, 2016. http://hdl.handle.net/11394/5060.

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Magister Pharmaceuticae - MPharm<br>Co-crystals are a solid phase phenomena that could enhance the physicochemical properties of an active pharmaceutical ingredient. A co-crystal has never been incorporated into a liquid dosage form with the assurance of maintaining its co-crystal state until absorption under defined conditions. This study aims to develop a liquid formulation with a nevirapine co-crystal. A protocol was developed to investigate all the five co-formers that were used to make the nevirapine co-crystals to-date. The most appropriate co-former was selected for a liquid dosage form
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4

Raiwa, Araya [Verfasser]. "Formulation development strategies for oral extended release dosage form / Araya Raiwa." Berlin : Freie Universität Berlin, 2011. http://d-nb.info/1025490363/34.

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5

Wheate, Nial. "Pharmaceutical Drug Design, Formulation, Testing, and Use." Thesis, The University of Sydney, 2020. https://hdl.handle.net/2123/22097.

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This compilation of my research has been organised into nine different sections based on the sub-themes on my research into medicines. Section one deals principally with my research and impact into the examination of the interactions of multinuclear platinum-based chemotherapy drugs with their cellular target, DNA. Section two covers the design and synthesis of new drugs including multinuclear platinum drugs and a new drug class of platinum drugs based on phenanthroline. Section three details my investigation of macrocycles as potential delivery vehicles for drugs; in particular, the deli
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6

Owaisat, Suzan. "A novel oral dosage form with drug independent formulation and variable controlled release." Diss., Temple University Libraries, 2015. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/342831.

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Pharmaceutical Sciences<br>Ph.D.<br>A unique dosage form which uses a hydrophilic polymer was developed to provide for a predicable release of several drugs. This drug release could be optimized for controlled release using erosion. It can also be designed to release drug utilizing electrochemical processes. The accuracy of drug delivery in terms of dose and timing is of utmost importance for the patient’s health status and compliance. A well-designed drug delivery technology offers many advantages to the patient. These advantages include: reduction in dose frequency, reduction of drug side ef
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Bohloko, Ntseliseng Selloane. "Development and formulation of an intranasal dosage form for cyclizine hydrochloride / Ntseliseng Selloane Bohloko." Thesis, North-West University, 2004. http://hdl.handle.net/10394/403.

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A comprehensive review of the nasal route of administration, in particular the nasal drug delivery system has been presented. The physicochemical properties, mode of action and pharmacology of H1-receptor antagonists, in particular cyclizine HCl, have been highlighted. The techniques for the assessment of toxicity (in-vitro ciliary beat frequency (CBF) studies for human nasal explants and morphology studies of the rat nasal mucosa), synthesis of cyclizine lactate, solubility studies of both cyclizine HCI and cyclizine lactate, viscosity determination of the gel formulated and assessment of the
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8

Gu, Alice. "Development of a Cucurbituril Suspension-Based Dosage Formulation and its Ability to Taste Mask Paracetamol." Thesis, The University of Sydney, 2021. https://hdl.handle.net/2123/25943.

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Medication non-adherence as a result of aversion to the bitter taste of active pharmaceutical ingredients and/or an inability to swallow solid dosage forms presents a challenge to the optimal use of medicines. The aims of this study were to examine the interactions of cucurbit[n]urils (CB[n]; n = 6, 7, 8) with paracetamol, and CB[7] with common pharmaceutical excipients, to design an effective oral suspension dosage formulation with CB[n]s as a potential taste masking excipient, and to assess the ability of CB[7] to reduce the bitter taste of paracetamol in rats. 1H NMR spectrometry was used t
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9

Hamid, Rezaei. "EFFECT OF MOLECULAR WEIGHT OF POLYETHYLENE GLYCOLS ON THEIR FUNCTION AS LUBRICANT SPARING BINDERS IN TABLET TECHNOLOGY." University of Cincinnati / OhioLINK, 2001. http://rave.ohiolink.edu/etdc/view?acc_num=ucin984508148.

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10

Marais, Johannes Francois. "The formulation of different dosage forms with the anthelmintics : Levamisole, Niclosamide and Oxyclozanide / J.F. Marais." Thesis, North-West University, 2003. http://hdl.handle.net/10394/390.

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Different formulations of dosage forms of niclosamide, levamisole HCI or levamisole HCI and oxyclozanide have been used on the local market for a very long time. Unfortunately, the spectrum of each of the drugs alone has a very narrow therapeutic index. Together, however, they have a broad spectrum of action and it is a solution to most of the helminths infestations today. Because of the increasing cost to produce livestock, it is important to formulate a product that is not only pharmacologically effective but also cost effective. A combination dosage form plays a big role in decreasing the c
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