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Cadet college Rawalpindi management software CCRMS with website

Thesis Info

Author

Darr,Yasir Rashid

Supervisor

Imran Khan

Department

Department of Computer Science & Software Engineering

Program

MS

Institute

International Islamic University

Institute Type

Public

City

Islamabad

Province

Islamabad

Country

Pakistan

Thesis Completing Year

2014

Thesis Completion Status

Completed

Page

112

Subject

Computer Science

Language

English

Other

MA/MSC 005.3 DAC

Added

2021-02-17 19:49:13

Modified

2023-02-17 21:08:06

ARI ID

1676721499053

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اردو کے اہم مدونین (مولوی عبدالحق)

اردو کے اہم مدونین (بابائے اردومولوی عبدالحق)
حالات زندگی:
مولوی عبدا لحق برِ صغیر پاک ہند کے عظیم اردو مفکر، محقق، ماہر لسانیات، معلم، بانی انجمن ترقی اردو اور اردو کالج کے بانی تھے، ا?پ کو بابائے اردو کے لقب سے یاد کیا جاتا ہے۔آپ کی تاریخ پیدائش کے حوالے سے کافی اختلاف پایا جاتا ہے ،لیکن بقول ممتاز حسین مولوی عبدالحق 20 اپریل،1870ء کوبرطانوی ہندوستان کے ضلع میرٹھ کے ہاپوڑ کے قریب سراوہ نامی ایک گاؤں میں پیدا ہوئے۔مولوی صاحب کے والد شیخ علی حسین نے عہد مغلیہ میں اسلام قبول کیا۔ان کے سپرد محکمہ مال کی اہم خدمات رہیں۔مغلیہ دور میں انہیں جو مراعات حاصل تھیں وہ انگریز وں کے دور میں بھی برقرار رہیں۔
تعلیم و تربیت:
مولوی عبدالحق نے ابتدائی تعلیم گھر پرحاصل کی۔ثانوی تعلیم میرٹھ سے حاصل کی۔ 1894ء میں علی گڑھ سے بی اے کیا۔علی گڑھ میں سر سید احمد خان کی شخصیت سے بہت متاثر ہوئے۔1895ء میں حیدر آباد کے ایک سکول میں ملازمت اختیار کی۔اورنگ آباد میں صدر محتتم تعلیمات کے عہدے پر فائز رہے۔عثمانیہ کالج اورنگ آباد میں 1920ء تک بحیثیت پرنسپل فرائض سر انجام دیتے رہے۔
انجمن ترقی اردو:
جنوری 1902ء میں آل انڈیا محمڈن ایجوکیشن کانفرنس علی گڑھ کے تحت ایک علمی شعبہ قائم کیا گیا جس کانام انجمن ترقی اردو تھا۔ مولانا شبلی نعمانی اس کے سیکرٹری رہے تھے۔ عزیز مرزا کے بعد 1912ء میں مولوی عبدالحق سیکرٹری منتخب ہوئے جنھوں نے بہت جلد انجمن ترقی اردو کو ایک فعال ترین علمی ادارہ بنا دیا۔ مولوی عبدالحق اورنگ آباد (دکن ) میں ملازم تھے ،وہ انجمن کو اپنے ساتھ لے گئے اور اس طرح حیدر آباد دکن اس کا مرکز بن گیا۔
فروغ اردو کے لیے انجمن کی خدمات:
انجمن کے زیر اہتمام ایک لاکھ سے زائد جدیدعلمی ، فنی اور سائنسی اصطلاحات کا اردو...

Untamed Subjectivity upon Blasphemy: Comparative Subjectivity of the National and International English and National Urdu Print Media upon Reporting a Blasphemy Case in Pakistan

Objectivity of news have always been a debate, even the trusted source of information, the newspapers are not ‘clean’ so to say. Contrary to the codes of neat journalism, news reports are often found reflecting ideological, economic, regional, religious and pre-determined viewpoints. In the current study the researcher has purposely picked the blasphemy case of Aasiya Bibi from year 2010 involving Salman Taseer (late), then the Governor of Punjab and Mumtaz Qadri (late) the member of elite police force who shot Mr. Taseer and was later hanged in 2016. The researcher analyzed level of subjectivity in the news stories and editorial of two international and three national newspapers, The Guardian, The New York Time and The Dawn, Daily Jang and the Daily Express respectively. Through the scientific method of analyzing the content it is observed that in such cases, even the pioneers of print medium and the self-proclaimed champions of the codes of journalism are found overwhelmingly subjective.

Rheological and Release Characteristics of Drugs of Different Solubilities from Semisolid Matrix Filled in Hard Gelatin Capsule

The re-introduced liquid/semisolid matrix technology, in recent past encompasses filling of hard gelatin capsules for thixotropic system at ambient and thermosoftened system at elevated temperature. Formulations in both of the above systems may contain dissolved or dispersed drugs. In the present work thixotropic gels were prepared using a series of hydrophilic poloxamers (Pluronic/Synperonic L31, L43, L62, L64, L92) of different viscosities and composition of polyoxyethhylene and polyoxypropylenein co-polymers thickened with hydrophilic silicon dioxide (Aerosil®A200) to form gel structure. Model drugs of varying solubilities, isoniazid, metronidazole, paracetamol and mefenamic acid were dispersed in gels of above poloxamers. The gel formulations were filled into hard gelatin capsules via syringe. The rheological characteristics, dispersion stability, and FTIR of the gels with and without drugs were investigated. The gels with drugs were additionally characterized for their release pattern. In preliminary studies, twenty separate gels of poloxamers L31, L64 were thickened with concentrations 1 to 10% w/w of Aerosil® A200 to incorporate isoniazid (unsifted, 10% w/w). Different concentration of Aerosil® A200 affected dispersion stability as well as release of the drug incorporated into gels. All gels were thixotropic and shear thinning. A little change in apparent viscosity on storage upto 30 days was noted. Disperse phase sedimentation was not observed with more viscous poloxamer and with higher concentration of silicon dioxide. Higher concentration of Aerosil® A200 resulted into stronger gel structure between silicon dioxide and poloxamers and thereby, hindered release of drug from a gel. Rheograms of poloxamers, L31 and L64 confirmed their Newtonian behaviour, in contrast to the thixotropic behaviour of all gels made with Aerosil® A200 concentrations (1-10% w/w) and 10% w/w isoniazid. Therefore, ii in-vitro release of highly water soluble drug, isoniazid could be controlled by poloxamer/A200 thixotropic gel system which depended upon concentration of Aerosil® A200, viscosity of poloxamer and the aqueous solubility of drug. In the further work, the effect of selected concentration of Aerosil® A200 (8% w/w) and five liquid poloxamers of different viscosities on release of drugs with characterized particle size (180-250 μm) and of different from semi solid matrix/ thixotropic gel filled into hard gelatin capsules was tested by in-vitro dissolution test. The drugs with different solublities used in this study were isoniazid, metronidazole, paracetamol and mefenamic acid. The interaction of drug in gel formulations was also determined by Fourier transform infrared (FTIR) spectroscopy. The release of drugs from different formulations was related to their aqueous solubility, viscosity of poloxamers, and poloxamer’s polyoxyethylene and polyoxypropylene proportions. In most of the formulations drug remains dispersed over a period of one month depending upon the viscosity of gels. Most of the gels showed little change in apparent viscosity on storage. The apparent viscosity for each gel was found to be dependent on the viscosity of poloxamers from which the gel was prepared. Like in preliminary work, rheograms of five pure poloxamers showed Newtonian behaviour whereas each gel exhibited thixotropic and shear thinning. In-vitro dissolution data of drugs from their respective stable gels followed first order kinetics. No chemical interaction or incompatibilities between drugs and polymers were noted by FTIR. Long term stability studies at International conference on harmonization (ICH) recommended conditions of temperature/relative humidity (30°C/65% RH) over one year revealed that almost all the gels retained their rheological, dispersion stability, release profile and chemical integrity. Thus, the hydrophilic semisolid matrix (gels) made by mixing poloxamer and Aerosil® (A200) was suitable for filling into hard gelatin capsules because of their rheological characteristics. The release of drugs with different solubilities could be modified by using poloxamers of different viscosity. Overall present research study demonstrates the effect of silicon dioxide on the microstructure of the gel prepared with various poloxamers which is evident from the rheological studies, FTIR and release pattern of the drugs