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Quaid -I - Azam School System of Islamabad

Thesis Info

Author

Bushra Bibi

Department

Abhinav Publications

Program

MSc

Institute

Quaid-i-Azam University

Institute Type

Public

City

Islamabad

Province

Islamabad

Country

Pakistan

Thesis Completing Year

2013

Thesis Completion Status

Completed

Subject

Information Technology

Language

English

Other

Call No: DISS / M.Sc / IT 107

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676715766187

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ضرب کلیم

یہ ،مجموعہ جولائی 1936 ء میں شائع ہوا۔ بال جبریل کی اشاعت کے ایک ہی سال بعد اردو کلام کا بہت سا حصہ جمع ہو گیا۔ بیماری کے باوجود شعر کے نزول کی کیفیت جاری رہتی ۔ اس کتاب میں بہت سے موضوعات ہیں۔ 183 عنوانات پر مشتمل اس مجموعہ کلام میں علیحدہ کوئی غزل نہیں ہے بلکہ درمیان میں ہی پانچ غزلیات کا عنوان دیا گیا ہے۔ کوئی طویل نظم نہیں ہے۔ بلکہ ”محراب گل افغان کے افکار“ کا عنوان دے کر 20 افکار پیش کیے گئے ہیں۔ افکار کے علاوہ پانچ موضوعات کو مرکزی حیثیت دی گئی ہے۔ (۱) اسلام اور مسلمان (۲) تعلیم و تربیت (۳) عورت (۴) ادبیات ، فنون لطیفہ اور (۵) سیاسیات مشرق و مغرب۔ سرورق پر لکھا ہے۔ ضرب کلیم یعنی ” اعلان جنگ دور حاضر کے خلاف۔ اقبال نے اپنی کتاب کے موضوع کی وضاحت کے لیے سرورق پر کبھی کچھ نہیں لکھا۔ رفیع الدین ہاشمی
لکھتے ہیں:
”یہ اقبال کا پہلا مجموعہ ہے جس کے سرورق پر انہوں نے کتاب کے نام اور
موضوع کی وضاحت کے لیے تو ضیحی الفاظ (اعلان جنگ دور حاضر کے خلاف)
درج کیے بلکہ ایک قطعے سے اس کی مزید تشریح بھی کی “(30)

علاج کے لیے بھو پال گئے تو شیش محل یا ریاض منزل میں لکھی جانے والی نظمیں بھی اس مجموعہ کلام میں شامل ہیں۔ ”ضرب کلیم“ کا مطالعہ اس بات کا منہ بولتا ثبوت ہے کہ شاعر مشرق پر شاعری کی دیوی مہربان ہے۔ حکیم الامت مرض الموت میں مبتلا ہو چکے ہیں مگر فکر وفن کا نزول جاری ہے۔

PENERAPAN PEMBELAJARAN KOOPERATIF MODEL GROUP INVESTIGATION (GI) UNTUK MENINGKATKAN MOTIVASI DAN HASIL BELAJAR BIOLOGI

Model pembelajaran mempengaruhi motivasi dan hasil belajar Biologi siswa sekolah menengah atas. Berdasarkan observasi awal, diketahui bahwa pembelajaran Biologi di kelas X-1 SMA Negeri 7 Malang memiliki beberapa ciri, yaitu (1) motivasi belajar siswa cenderung kurang, (2) dalam menyelesaikan suatu tugas, siswa dengan karakteristik yang sama cenderung mengelompok sehingga terbentuk kelompok homogen yang tidak seimbang di kelas, dan (3) metode ceramah yang diterapkan oleh guru tidak menarik minat siswa sehingga mempengaruhi hasil belajarnya. Berdasarkan kondisi tersebut maka dilakukan penelitian dengan menggunakan pembelajaran kooperatif model Group Investigation (GI) untuk meningkatkan motivasi dan hasil belajar Biologi siswa. Jenis penelitian ini adalah penelitian tindakan kelas dengan menggunakan pendekatan kualitatif dan dirancang dalam dua siklus. Hasil penelitian menunjukkan penerapan pembelajaran kooperatif model GI dapat meningkatkan motivasi dan hasil belajar Biologi siswa. Motivasi belajar siswa meningkat sebesar 31, 48% yaitu dari 46, 15% dengan kategori cukup pada siklus I menjadi 77, 63% dengan kategori baik pada siklus II. Hasil belajar siswa juga mengalami peningkatan, terlihat dari nilai rata-rata siswa sebesar 81, 94% pada siklus I menjadi 89, 18% pada siklus II dan siswa yang tuntas belajar juga mengalami peningkatan dari 79, 49% pada siklus I menjadi 97, 44 % pada siklus II. Hasil angket juga menunjukkan bahwa siswa menyukai dan lebih termotivasi untuk belajar Biologi setelah mengikuti pembelajaran dengan pembelajaran kooperatif model GI.

Isolation and Characterization of Biologically Active Compounds from Selected Medicinal Plants

The main objective of this study was to discover new cancer chemopreventive and cytotoxic compounds from the natural sources to combat cancer. For the purpose, after an extensive survey based on the information gathered from local healers, six medicinally-important plants of Pakistan were selected for investigation. These plants included Euphorbia wallichii Hook F., Bergenia ciliata (Haw.) Sternb, Acer oblongifolium Hort. ex Dippel, Aster thomsonii C. B. Clarke, Opuntia dillenii (Ker Gawl) Haw. and Withania coagulans (Stocks) Dunal. For initial screening, total 59 extracts/fractions were prepared by using the different techniques including maceration, solvent-solvent extraction, flash column chromatography and solid phase extraction. All the extracts/fractions were tested for their anticancer and cancer chemopreventive activity by employing seven independent assays. Overall the results of the initial screening were very encouraging and led to the selection of the most potent plant material for further investigation. NFĸB activity plays a critical role in cancer development, progression and therapy and two of our samples from Withania coagulans demonstrated greater than 90% inhibition of TNF-α induced activity of NFĸB. Aromatase inhibitors are known to be effective for the treatment and prevention of breast cancer. One fraction from aerial parts of each plant, W. coagulans and Euphorbia wallichii, inhibited aromatase by 100% and 73%, respectively. Nitric oxide (NO) produced by inducible nitric oxide synthase (iNOS) plays critical role in inflammation, cell survival and tumor development and progression. Five of our samples, one from aerial parts of E. wallichii, one from Aster thomsonii, and three from fruit bearing aerial parts of W. coagulans, inhibited NO production significantly in lipopolysaccharide activated macrophage RAW 264.7 cells as a marker of iNOS inhibitor. No extracts or fractions was deemed active in RXRE assay. DPPH free radical scavenger has potential use to scavenge oxygen free radicals, which are the product of normal cellular metabolism and can attack and produce endogenous DNA lesions leading to genotoxicity, mutation and cancer. A total of 25 extracts/fractions exhibited ≥ 70% scavenging at 200 μg/ml concentration in DPPH assay, among them 13 were from roots and aerial parts of E. wallichii, 5 from B. ciliata, 6 from A. oblongifolium and one from A. thomsonii. QR1 is measured as overall representative of the phase II enzymes. Phase xiii Abstract II enzymes are primarily responsible for the metabolic detoxification of chemical carcinogens and other harmful oxidants, leading to the protection of cells against redox cycling, oxidative stress, and carcinogenesis. Therefore, induction of QR1 at the tumor initiation stage is suggestive for cancer prevention potential. A total of 10 extracts/fractions demonstrated potent induction of QR1 in a cell-based assay with CD (concentration required to double the enzyme activity) <10 μg/ml among them one is from A. oblongifolium and 9 from W. coagulans. A total of 8 extracts and fractions showed cytotoxicity in an SRB assay against MCF-7, LU-1 and MDA-MB 231 cancer cell lines, among them 3 are from E. waliichii and 5 from the W. coagulans. The overall results suggested that W. coagulans might be the most promising plant for further studies as the extracts/fractions from this plant showed highest and significant activity in most of the assays. After the initial screening, W. coagulans was selected to pursue further for isolation and purification of the pharmacologically relevant compounds. For this purpose, total 10 kg dry weight of the W. coagulans aerial part was extracted, fractionated and subjected to biological evaluation in the above described assays to confirm the biological activities and to find the most active fractions. Active fractions were further processed through sequential bioactivity guided fractionation utilizing various chromatographic techniques, which led to isolation of 9 biologically active pure compounds. Structure elucidation of these compounds was carried by utilizing mass spectrometry (MS), one dimensional nuclear magnetic resonance (1D-NMR), and two dimensional nuclear magnetic resonance (2D-NMR) techniques. Structural elucidation showed that these compounds belong to a very important, biologically active and chemically distinct class of natural products known as “withanolides”. On the basis of existing reports and spectroscopic results it is concluded that out of these 9 compounds 3 are new and 6 are already known withanolides. This study is a contribution towards the exploration of new withanolides as well as their potential use in cancer chemopreventive and anticancer drug discovery.