Pharmacy Research Journals

Pharmacy Research Journals-58
Background: Fitness to practise (Ft P) impairment (failure of a healthcare professional to demonstrate skills, knowledge, character and/or health required for their job) can compromise patient safety, the profession’s reputation, and an individual’s career.In the United Kingdom (UK), various healthcare professionals’ Ft P cases (documents about the panel hearing(s) and outcome(s) relating to the alleged Ft P impairment) are publicly available, yet reviewing these to learn lessons may be time-consuming given the number of cases across the professions and amount of text in each.

Background: Fitness to practise (Ft P) impairment (failure of a healthcare professional to demonstrate skills, knowledge, character and/or health required for their job) can compromise patient safety, the profession’s reputation, and an individual’s career.

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Hence, there is a requisite for a technology-based product (formulation) to overcome such issues without compromising on the therapeutic response.

The drugs belong to Biopharmaceutical Classification System Class II and Class IV characterized by a low solubility, and to overcome the solubility problem, nanotechnology is most useful technique.

The purpose of this review is to focus on various methods of preparation, characterization properties, and applications of nanosuspension.

Pharmacy practice-based research networks (PBRNs) are relatively new compared to their primary care forebears, representing a unique set of research challenges.

Affiliations:1Asian University , Department of Pharmaceutical Sciences, Indian College of Science, Pune – 411038, Maharastra, India. E-mail: Phone: methods have---------------------- compounds. To the best of our knowledge no reports were found for simultaneous estimation of gymnemagenin and 18β-glycyrrhetinic acid by HPTLC method. It is therefore necessary to develop methods for rapid, precise ----------------- and inherent quality MATERIALS AND METHODS Solvents and chemicals Instrumentation and Chromatographic Conditions RESULTS AND DISCUSSION: HPTLC Method optimization ( table 1,2,3, and fig.1.2.3.

) legends of table and fig has to be given above the table and fig.

The validated HPLC method is applied to measure IM released from IM-coated stents.

The chromatographic separation was achieved on C18 column (250 mm × 4.6 mm i.e., 5 μm) with a mobile phase consisting of methanol-water-glacial acetic acid (:0.03%, v/v) at a flow rate of 1.0 ml/min.

Although a large number of new drug molecules with varied therapeutic potentials have been discovered in the recent decade, most of them are still in developmental process.

This can be attributed to the limited aqueous solubility which governs the bioavailability of such drug molecules.

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