h. eftekhari
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Performance evaluation is one of the most significant issues in management taken into consideration by a number of academics and researchers who have developed various parametric and non-parametric methods used for performance measurement and evaluation. Among these models, Data Envelopment Analysis (DEA) is regarded as one of the most widely used models for performance evaluation. DEA is a powerful mathematical tool and a non-parametric technique to measure the relative efficiency of a group of homogeneous Decision-Making Units (DMUs). This approach carried out an evaluation by assigning weights to the inputs and outputs of each decision-making unit. The difference in the input and output weights in this technique is one of the objections to this method that threatens the assessment of the underlying basis. In this study, a model was presented to find a solution to this problem. The proposed model is a one-phase linear model and has less computational complexity than other models. To validate this model, the numerical exam of Kao & Hung (2005) was implemented and the results of the presented model were compared with those of other models; in addition, the Spearman correlation coefficient was calculated. The results showed that the proposed model had a more significant correlation coefficient than other models, had a more resolution than other models, and eliminated the shortcomings of Classic base models. After the validation of the model, the pharmaceutical companies in Tehran Stock Exchange were evaluated by means of the proposed model and CCR model. The indices of the study were obtained from previous studies and the opinions of experts were taken into account to confirm these indices. The data used in the present study and the actual values of these indices were obtained from ``codal.ir website'' according to each company's financial status. Moreover, sensitivity analysis was performed on the outputs of these companies. The results showed that Alborz Pharmaceutical and Shafa Pharmaceutical Investment companies were the most effective units in both models, and Farabi Pharmaceutical Company was the most inefficient one. Besides, the results indicated that the units under study showed more sensitivity than the first output.
Keywords: Performance evaluation, data envelopment analysis, common weights, pharmaceutical companies, Tehran stock exchange -
مقدمه
ژل موضعی داپسون تاثیر مناسبی در درمان آکنه نشان می دهد. این مطالعه جهت ساخت نمونه داپسون موضعی در کشور انجام گرفته است.
هدفتعیین فرمولاسیون مناسب برای تهیه فرم ژنریک این دارو در درمان آکنه .
مواد و روش ها:
برای ساخت ژل داپسون نخست تعدادی پایه ژل با استفاده از ماده ژل ساز کربومر P934 با درصد 3/0درصد تا 5درصد ساخته شد و از نظر ویژگی های ظاهری بررسی شد. سپس، ماده ی موثره ی داپسون در حلال دی اتیلن گلایکول مونو اتیل اتر حل و در پایه ژل بارگذاری شد. برای بهینه سازی فرمولاسیون با استفاده از برنامه طراحی آزمایش،در گام نخست 13 و سپس 17 نمونه از ژل طراحی شد و هر دو دسته نمونه ها نیز از نظر خواص ظاهری،pH و خواص ریولوژیک بررسی شدند و بر پایه استاندارد های فارماکوپه دو نمونه نهایی انتخاب شد. این دو نمونه نیزاز دید ریولوژی ، pHو آزادسازی بررسی و مقایسه شدند.
نتایجنمونه های اولیه پایه ژل با میزان کربومردر محدوده 1درصد تا 5/3درصد مناسب تشخیص داده شد . 13 نمونه تهیه شده pH در محدوده 7-5 و ویسکوزیته در محدوده 2980000-16530(cp) داشتند و ویسکوزیته 17 نمونه دوم در محدوده 760000-1100(cp) بود.ویسکوزیته نمونه 1درصد نهایی 268000-14075 (cp) و آزادسازی آن 1/78درصد و ویسکوزیته نمونه 2درصد نهایی 557000-92660 (cp) و آزادسازی آن 76درصد اندازه گیری شد.
نتیجه گیری:
ویسکوزیته وآزادسازی هر دو نمونه در محدوده ویسکوزیته پذیرفتنی فارماکوپه قرار داشت .با توجه به این که نمونه 1درصد، میزان کربومر کمتری نسبت به نمونه 2درصددارد, از نظر اقتصادی مقرون به صرفه تر است. بنابراین، به نظر می رسد نمونه 1درصد با pH=5 مناسب تر باشد.
کلید واژگان: آکنه ولگاریس، داپسون، دارو درمانیIntroductionDapsone gel (5%) is found to be effective in treating acne. The study was to develop a topical formulation of dapsone in Iran.
ObjectiveDetermination of appropriate formulation for generic form of this drug in the treatment of acne.
Materials and MethodsSamples of the base of gel were made in the range of 0.3%-5% by dissolving Carbomer 934P in distilled water, and their physical properties and pH were evaluated. Then, Dapsone was dissolved in its appropriate solvent, diethylene glycol monoethyl ether (DEG) and were introduced into gel base. Afterwards, using Design Expert software 13 samples and in the next step 17 samples were designed, made and their rheological properties and pH were evaluated. Then, two formulations were selected and were characterized by drug content, physicochemical properties, rheology and stability and found to be in accordance with the US Pharmacopeia.
ResultsThe gel bases containing carbomer in the range of 1-3% were appropriate. The pH value of gel bases in first 13 samples were between 5-7 and the viscosity range between 16530-2980000(cp). The viscosity of range of 17 designed samples was between 1100-760000(cp). The final sample with 1% carbomer content had the viscosity range of 14075-268000(cp) and drug release of 78/1% after 3 hours. The sample with 2% carbomer content had the viscosity range of 92660-557000(cp) and drug release of 76% after 3 hours.
ConclusionViscosity and drug release of both samples were in accordance with pharmacopeia. However, the sample containing 1% carbomer is more commercially suitable and more appropriate lowering pH of the skin.
Keywords: Acne Vulgaris, Dapsone, Drug Therapy
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