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    Pharmacokinetics Analysis

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    Following intravenous administration, there is no absorption process since the drug is directly introduced into the blood stream. However, for oral routes, there will be an absorption process that occurs. Following ingestion of a drug it begins to dissolve in the GI fluids and is absorbed into the blood. While the transportation of the drug in the gut wall, if any process becomes saturated, then increases…

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    Advantages Of Ointments

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    Topical ointments Introduction: An ointment is semi solid topical preparation applied to external application with rubbing effect. It may be a vehicle or media for a drug or it may serve like a protective or emollient. Ointments show plastic flow characteristics. When the ointment is applied it is definite yield value and the resistant to flow drops as the applications to the skin is continued. Body: • Uses : There are two types of ointments: A- Medicated: used to treat different…

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    Figure 2.1.3 TPGS concentration and Paclitaxel solubility are directly related. Figure created by M. Varma, 200522. TPGS has been incorporated into various drug formulations partly because of its ability to overcome multidrug resistance (MDR). By inhibiting P-glycoprotein (P-gp) activity, the relative cytotoxicity of drugs such as doxorubicin, vinblastine, and paclitaxel was increased19. P-gp is a drug efflux pump, a.k.a. multidrug resistance protein 1 (MDR1), located in the cell membranes of…

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    Solubility

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    ABSTRACT Solubility is the phenomenon of dissolution of solid in liquid phase to give a homogenous system.Solubility is one of the important parameter to achieve desired concentration of drug in systemic circulation for pharmacological response to be shown. Poor watersolubledrugs often require high doses in order to reach therapeutic plasma concentrations after oral administration. Low aqueoussolubility is the major problem encountered with formulation development of new chemical entities. Any…

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    Microneedles Insulin is most effectively taken through direct injection, which is most typically done through a needle. Traditional needles are bulky and are oftentimes associated with pain. Microneedles are much smaller in dimensions, making them able to effectively release insulin into the body while not reaching nerve cells which would cause pain and discomfort. Microneedles are designed to puncture only the top 20–50 μm of the skin, because the stratum corneum, which is the outer layer…

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    Lornoxicam Research Paper

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    OBJECTIVE: To deliver lornoxicam into systemic circulation by engineering ethosomal gel formulation. RATIONAL OF WORK: Because of their improved pervasion of medication through skin.  lornoxicam is BCS class II medication causes gastric bothering when managed orally  ethosomes are stages for the conveyance of vast and differing gathering of medications.  due to their generally safe profile.  better understanding agreeability can be utilized as a part of the manifestation of gel,…

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    The aim of the present investigation is to intend, develop and evaluate a pulsatile drug delivery containing a core-in-cup based system of dry coated tablet of ketoprofen based on chronomodulated approach for management of Rheumatoid Arthritis. This pulsatile system contained a core tablet surrounded by an impermeable outer shell and top cover layer. Core tablet contained the active ingredient acting as reservoir, ethylcellulose was used to form an impermeable outer shell, the top cover layer…

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    Medication Observation Paper

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    Focus Objectives 1. Develop at least two (2) complete nursing diagnoses related to medication administration. Impaired Oral Mucous Membrane related to Medication side effects as evidenced by dry mouth and difficulty swallowing. (546) Risk for Aspiration related to impaired swallowing. (67) Impaired Tissue Integrity related to Excess fluid volume as evidenced by damaged tissue surrounding the subcutaneous area. Risk for Infection related to tissue destruction. 2. Identify the six rights of…

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    Unit 5-Gids Case Study

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    2- The fluctuations in plasma drug concentration are minimized and side effect associates with concentration are also minimized. 3- Complete absorption of drug from the floating formulation is expected even at alkaline pH of intestine. The dissolution occurs in gastric fluid and after emptying of the stomach contents the dissolved drug is available for absorption in small intestine. 4- Because of site‐specific absorption from the upper part of the GIT, Drugs that have poor bioavailability are…

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    t 's been a few years since I 've been to Clementon, so having the day off last Wednesday I took a ride up to see the town. In the 1970s I lived in an apartment on Blackwood-Clementon Road in Lindenwold and had a friend who lived on top of the Park Grill. The town had a distinct look, with its older buildings, pool hall, and feed store – something you don 't usually see at the mall. Most of my time there was spent drinking beer in the Park Grill or drinking beer and eating seafood at the Palm…

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