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Home > Feasibility Study of Girls Islamic Primary School at Jauharabad [Mba Progr]

Feasibility Study of Girls Islamic Primary School at Jauharabad [Mba Progr]

Thesis Info

Author

Rasheed, Abdur

Supervisor

Haq Nawaz Shah

Department

University of Management and Technology

Program

MBA

Institute

University of Management and Technology

Institute Type

Private

City

Lahore

Province

Punjab

Country

Pakistan

Thesis Completing Year

2002

Thesis Completion Status

Completed

Page

94 .

Subject

Education

Language

English

Other

Report presented in part requirement for MBA final Advisor: Haq Nawaz Shah; EN; Call No: TP 372.0954914 RAS-F

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676712749446

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قاضی محمد عدیل عباسی

قاضی محمد عدیل عباسی
جناب قاضی محمد عدیل عباسی مرحوم کی رحلت کی خبر دارالمصنفین میں بہت ہی رنج و الم کے ساتھ سنی گئی، مرحوم قوم و ملت دونوں کے لیے بہت ہی مخلصانہ جذبات رکھتے تھے، وہ ایک اچھے خدمت گزارِ ملت کے ساتھ ہی بڑے سچے محبِ وطن بھی تھے، انھوں نے اپنی علمی سرگرمیوں سے یہ عملی نمونہ پیش کیا کہ ایک سچا مسلمان ہی سچا محبِ وطن ہوسکتا ہے۔ قاضی صاحب نے اردو، علی گڑھ اور مسلمانوں کی دینی تعلیم کے لیے جو خدمات انجام دی ہیں وہ مدتِ مدید تک یاد رہیں گی۔ (صباح الدین عبدالرحمن، جون ۱۹۸۰ء)

قاضی محمد عدیل عباسی
جناب قاضی محمد عدیل عباسی کے انتقال کو کئی مہینے ہوگئے، دارالمصنفین سے ان کو جو اخلاص و تعلق تھا، اس کا تقاضا تھا کہ ان کے ذکر سے معارف خالی نہ رہے، اس لئے تاخیر کے باوجود اس تحریر کی اشاعت نامناسب نہ ہوگی۔
قاضی محمد عدیل صاحب کا تعلق ضلع بستی کے ایک کھاتے پیتے زمیندار گھرانے سے تھا مگر ابتداء ہی سے ان کا رجحان قوم پروری اور حب الوطنی کی تحریک کی جانب ہوگیا تھا، اس لئے کالج کی تعلیم چھوڑ کر وہ علمی سیاست میں داخل ہوگئے، ان کو اس میدان میں پنڈت جواہر لال نہرو، رفیع احمد قدوائی، مولانا حسین احمد مدنی اور مولانا حفظ الرحمان وغیرہ کے ساتھ کام کرنے کا موقع ملا، خلافت، ترک موالات اور ہندوستان چھوڑ دو، تحریکوں میں سرگرم حصہ لینے کی بنا پر وہ کئی بار جیل گئے۔
قاضی صاحب کی عملی زندگی کا آغاز صحافت سے ہوا ان کو اس کا ذوق کان پور میں مولانا حسرت موہانی مرحوم کی صحبت میں پیدا ہوا، پھر وہ مشہور قوم پرور اخبار مدینہ بجنور اور زمیندار لاہور سے وابستہ ہوئے، زمیندار اس زمانہ کا...

English in the Workplace: Business English as a Lingua Franca in Boardwalk Direct Selling Company

With the current international competition among global companies, Business English as a Lingua Franca (BEFL) has become a necessity. As for one, Boardwalk Direct Selling Company recognizes the adoption of the BEFL concept within the organization to equip its workforce with adequate English language skills at par with global standards. This study aims to assess the organization’s current English proficiency and the readiness of its employees to embrace BEFL. This also presents the major English language skills areas that need improvement through training intervention. A stratified sampling method is utilized to extract data via an online survey. Respondents are strategically chosen to represent different strata such as organizational departments or groups, job levels, tenure, and age. A convenient size of 34 respondents participated in this study. Generally, respondents acknowledge the importance of the English language skill set in their job functions and as criteria for their career growth. Half of the sampling population affirms their English language proficiency. However, the study reveals that Boardwalk employees are willing to subject themselves to improving their English skills, most particularly in speaking and writing aspects. Given their willingness, the employees recommend that the company strengthen its BEFL trainings across the organization. Moreover, with the current setup of mostly working from home due to COVID restrictions, majority of the employees prefer online learning.

Niosomal Encapsulation of Anticancer Drugs and Assessment of Their Activity Through Cancer Cell Line

Niosomes are self-organizing non-ionic surfactant vesicles, which encapsulate aqueous volume of drug(s) with or without the addition of cholesterol and other lipid contents. Niosomes have the capability to encapsulate both lipophilic and hydrophilic drugs. They are alternative to liposomes, and their main benefits as compared to liposomes are their lower price, higher stability and better biodegradability. By making niosomes, the side effects of drugs have been reduced and the therapeutic efficacy has been increased. The first part of the study was to develop an optimized niosome formulation for the encapsulation of a poorly water-soluble drug by the ecological probe sonication method. Pluronic L121 and Span 60 were used as surface active agents and the optimization of the composition was made with the aid of Design of Experiment (DoE) concept. Rifampicin was used as a model drug. Concentration levels of charge inducing agent, dicetylphosphate (DCP), and Pluronic L121 were studied as variables. Prepared niosomes with varying concentrations of DCP and Pluronic L121 resulted in small sized niosomes with sizes ranging from 190 nm to 893 nm. During the four weeks stability testing, the particle sizes were reduced slightly. The formulation containing 2 mg of DCP resulted in most stable niosomes with 75.37% entrapment efficiency. All the niosomal formulations showed higher In vitro drug release rates as compared to bulk drug formulation. The rifampicin loaded niosomes prepared with Pluronic L121 and Span 60 resulted in stable, small sized niosomes with improved drug release profile. The second part of the study was carried out to produce niosome formulations for the encapsulation of a hydrophilic and poorly water-soluble drugs by the ecological probe sonication method. Pluronic L121 and Span 60 were used as surface active agents and the optimization of the composition was made with the aid of Design of Experiment (DoE) concept. Ceftriaxone sodium and Rifampicin were used as model drugs (hydrophilic and hydrophobic respectively). Concentration levels of charge inducing agent, dicetylphosphate (DCP), and Pluronic L121 were studied as variables. Prepared niosomes with varying concentrations of DCP and Pluronic L121 resulted in small sized niosomes with sizes ranging from 164 nm to 893 nm. During the four weeks stability testing, the particle sizes were reduced slightly. The formulations CR1 and CR2 resulted in most stable niosomes with (98.71% of rifampicin and 95.73% ceftriaxone) and (98.86% rifampicin and 95.88% ceftriaxone) entrapment efficiency of respective formulations. All the niosomal formulations showed higher In vitro drug release rates as compared to bulk drug formulations. The ceftriaxone and rifampicin loaded niosomes prepared with Pluronic L121 and Span 60 resulted in stable, small sized niosomes with improved drug release profile. In the third part of study, the niosome formulations were prepared for the encapsulation of anticancer drugs by the ecological probe sonication method. Pluronic L121 and Span 60 were used as surface active agents in niosomes and doxorubicin HCl and paclitaxel were used as anticancer drugs. Thorough physicochemical studies were performed for the niosomes and their cytotoxicity and activity were evaluated on MCF-7 and PC3- MM2 cancerous cell lines. Prepared niosomes were small with sizes ranging from 137 nm to 893 nm and entrapment efficiencies were high, ranging from 91.24% to 99.99%. During the four weeks stability testing, the particle sizes remained stable. The niosomal formulations showed In vitro sustained drug release profiles for doxorubicin HCL and increased clearly dissolution rate of poorly water-soluble paclitaxel. The incorporation of both the drugs into niosomes, improved cell penetration and antiproliferative activity of the drugs towards PC3 as compared to MCF-7 cell lines. As a conclusion, doxorubicin HCl and paclitaxel loaded niosome formulations resulted in relatively stable, small sized niosomes with improved drug release profiles, better cell penetration and antiproliferative activity. The niosomes showed more antiproliferative effect due to the presence of both drugs, which can overcome multidrug resistance. The present study suggested that the codelivery of anticancer drugs can be delivered by encapsulating in niosomes prepared from Pluronic L121 and Span 60. Through which improved in-vitro sustained release of both anticancer drugs, better cell penetration and antiproliferative activity. The further in-vivo evaluation can lead to treat different types of cancers in a better way without toxic effects with reduction in doses.