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    DESIGN FORMULATION AND EVALUATION OF GASTRORETENTIVE FLOATING TABLETS OF STAVUDINE Mourya Adarsh*, Mrs.P. Haritha Sunil*, Praveen Kanna, Sampath.M Department of Pharmaceutics, St.Pauls College of Pharmacy, Hayathnagar, Telangana, India Abstract: The purpose of the present research work was to design, formulate and evaluate the floating tablets of Stavudine, a gastro retentive drug delivery system. Direct compression was used to prepare the tablets using HPMC K4M, HPMC K15M and Carbopol 974(p) as

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    very safe mode of administration when compared to other forms. The main reason for using natural disintegrates are 1) they are obtained naturally from plants, 2) they are less in cost, 3) they have no very less side effects when compared to synthetic and semi synthetic agents.Since the oral route of administration is most effective and can be easily administrated without any need of others, the drug becomes effective to the body immediately after 4 to 5 minutes of administration of the drug through

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    Introduction In the past years, drug delivery via the nasal route has established itself as a competitor and an alternative route over other routes of administration. It provides a higher degree of patient compliance and drugs can be painlessly self-administered by the patient (Illum, 2003). Drugs administered through nasal route are absorbed rapidly and can reach therapeutically effective plasma levels quickly due to highly permeable membranes and rich vasculature of the nasal cavity (Majithiya

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    FACULTY OF ENGINEERING TECHNOLOGY Bachelor of Engineering Technology (Pharmaceutical) with Honours BTP2153 Pharmaceutical Formulation Method ASSIGNMENT 1 NAME: KONG YEE TONG MATRIC NO: TD 14004 LECTURER: DR. KRISHNAMOORTHY MASILAMANI DUE DATE: 9 MAY 2016 1.0 INTRODUCTION Based on United State Pharmacopeia, pastes are defined as semisolid dosage forms that contain one or more drug substances intended for topical application. (Pharmaceutical Dosage Form, 2009) Pastes are also intended for

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    Case Study Of Haidilao

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    Moreover, they falsely believed that what happened in the kitchen would not be released to the public and did no harm to the customers’ health. It would cost them large amounts of money and human resource to change this situation. Considering the interests of the store, they thought they better not change the situation and decided to keep it as a

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    Loratadine Hcl (LOR)

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    Introduction Loratadine HCl (LOR) , which is chemically designated as ethyl 4 (8-chloro 5,6 dihydro,11H- benzo[5,6] cyclohepta[1,2 b]pyridin- 11- ylidene) -1- piperidinecarboxylate Hydrochloride is a tricyclic, piperidine derivative of antihistamines [1,2]. It is a second generation antihistamines, so it has non–sedating properties. Loratadine are newer drugs that are much more selective for peripheral H1 receptors as opposed to the central nervous system H1 receptors and cholinergic receptors

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    we are in life, the possibilities are endless. I however, have chosen something I feel will benefit myself as a person, and hopefully those around me. Healthcare administration is a booming field, and something that is although new, becoming more and more prevalent. This is a field connecting to leadership, management, and administration skills to the public’s health systems, hospitals, and more. I have always been told that I am a

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    Budget Justification The budget requested in this competitive renewal application is about 20% more than the current budget. The primary reason for this increase is due to an increased expenditure in breeding animals and animal service charges as we expanded the use of animals in the proposed grant. In the past 4 years, employee salaries at the UT Heath Center were increased by about 10%. This contributed a minor fraction of the increase. We used a 3% cost escalation in preparing the budget for

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    Synthesis of Aspirin Ling Tecson Gamido, Mitchiko Mariel M. Mizukami Abstract Acetylsalicylic acid, or also known as aspirin is known to be a drug that relives people of pain and is commonly used even today. It is synthesized from salicylic acid and ethanoic anhydride, both of small quantities. Phosphoric acid was used as a catalyst in the synthesis to speed up the process. Esterification is involved and the final product is aspirin with the presence of acetic acid as the byproduct. In order

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    This property is measured by the dissolution test. Accurate bioavailability can be obtained from the drug levels in the blood after its administration.  Tablets must be elegant in appearance, characteristic shape, color and other markings necessary to identify the product.  Tablets must retain all these functional attributes which include drug stability and efficacy.(Remington.,1998). Advantages

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