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میری آواز کو باغی کہہ سکتے ہو تو کہو

میری آواز اقبال کا شاہین
نحمدہ ونصلی علی رسولہ الکریم امّا بعد فاعوذ بااللہ من الشیطن الرجیم
بسم اللہ الرحمن الرحیم
معزز اسا تذہ کرام اور میرے ہم مکتب ساتھیو!
آج مجھے جس موضوع پرلب کشائی کرنی ہے وہ ہے:’’اقبال کا شاہین ‘‘
جنابِ صدر!
علامہ اقبال رحمۃ اللہ علیہ نے اپنے اشعار میں جو لفظ شاہین استعمال کیا ہے، اس سے مراد ان کی صرف ظاہری طور پر نظر آنے والا شاہین نہیں ہے، صرف ایک معروف پرندے کے طور پر ذکر کیا جانے والا شاہین نہیں آسمان کی بلندیوں پر محو پرواز طائرنہیں ہے۔
جناب صدر!
شاہین سے مراد وہ نوجوان نسل لیتے ہیں ، شاہین کی خصوصیات وہ نوجوان نسل میں پیدا کرنا چاہتے ہیں، نوجوان نسل کی اصلاح ہی ان کے لیے تعمیر وطن میں اہم کردار ادا کرسکتی ہے، وہ شاہیں کا ذکر کر کے انسانیت کو ان کا اصل مقام دلانے کی مساعی جمیلہ کرتے ہیں، وہ شاہین کی خصوصیات کے قائل ہیں ، وہ نو جوان نسل کو ارفع مقام پرمتمکن کرنے کے خواہشمند ہیں۔
نہیں تیرا نشیمن قصر سلطانی کے گنبد پر
تو شاہیں ہے بسیرا کر پہاڑوں کی چٹانوں میں
صدرِذی وقار!
اقبال کا حکیمانہ فلسفہ ’’شاہین کے روپ میں ہمیں یہ باور کراتا ہے کہ مسلمان کا مقصد حیات اس سرزمین پر خلافت الہی قائم کرنا ہے، دینِ اسلام کا بول بالا کرنا ہے، اپنے فکروعمل سے سنسار کوگلزار بنانا ہے، بلندی کردار اور پختگی اعمال سے اس جہاں کو امن و آشتی کا گہوارہ بنانا ہے۔ علم و حکمت کی روشن کرنوں سے دنیا پر چھائی گھٹاٹوپ تاریکیوں کو ختم کرنا ہے، اس لیے علامہ اقبالؒ نوجوان نسل سے یہ تمنا اور امید لگائے بیٹھے ہیں کہ وہ شاہین کی طرح اپنی بلند ہمتی، عمل پیہم، جہدِمسلسل، انتھک کوشش سے اپنے اوپر چھائی...

Dehumanization of Refugees: A Postcolonial Eco-Critical Study of Mohsin Hamid’s Exit West

This paper explores Mohsin Hamid’s literary representation of dehumanization of refugees in the age of globalization, the exploitation of humans and their land, as well as the impact of migration on the lives of the migrants in his novel Exit West. The research uses the theoretical framework of postcolonial ecocriticism by Huggan and Tiffin to critically analyze the primary text. This research employs qualitative method to draw parallels between the exploitation of humans and their environment in Hamid’s novel while exploring the dehumanized treatment of refugees, reasons of migration, and the role of war, science and technology in the destruction of environment in this particular narrative. Textual analysis, more specifically, content analysis is used as a method to link the global humanitarian and environmental crisis in the primary text under the Postcolonial Eco-critical ideology.

Solid Lipid Nanoparticles for Thermoresponsive Drug Delivery: Fabrication and Evaluation

Thermoresponsive drug delivery systems (DDS) are designed for the controlled and targeted release of therapeutic payload by exploiting the hyperthermic temperature (>39°C), which may be applied by some external means or an encountered symptom in inflammatory diseases such as cancer, arthritis etc. However, available thermoresponsive DDS, including liposomes, have complex method of preparation involving toxic solvents and reagents. Recently, we have shown for the first time that melting point of solid lipid nanoparticles (SLN) can be optimized for thermoresponsive drug release by tuning their melting point (MP). The objective of this study was to provide some strong evidence in support of hypothesis that thermoresponsive solid lipid nanoparticles (TSLN) undergo solid-liquid phase transition at their melting point (>39ºC) leading to faster drug release. Thermoresponsive lipid mixtures (TLM) were prepared by mixing solid (lauric, myristic, palmitic and stearic acid) and liquid (oleic and linoleic acid) natural fatty acids in different ratios (0.1:1 to 1:2) and melting point was measured by differential scanning calorimetry (DSC). A graph was plotted between liquid content in TLM and the MP, and TLM that would melt at 39°C were identified by using straight line equation of the graph. The solidliquid phase transition was assessed by determination of temperature dependent change in viscosity (low at 39°C) and light transmission (higher at 39°C) that are characteristic of liquids. TSLN containing a chemotherapeutic drug, either hydrophilic 5-fluorouracil (5-FU) or lipophilic paclitaxel, were synthesized by hot melt encapsulation method. It should be noted that the TLM and the TSLN were made by physical interaction of materials and no chemical reaction was needed. The TSLN showed desirable spherical shape (TEM), size (100-300 nm), physicochemical stability (FTIR analysis), high yield (>85%) and encapsulation efficinecy (5-FU >40% and paclitaxel >90%). In 5-FU loaded TSLN, drug release studies were first performed by USP type II dissolution apparatus in PBS (7.4) at 37°C and 39°C. A sustained release pattern was observed at 37°C and 22-34% 5-FU was released in 5 hrs. On the other hand, >90% drug was released at 39°C suggesting that the SLN show thermoresponsive drug release in agreement with our hypothesis. Drug release from SLN at 39°C was similar to model oleic acid and linoleic acid nanoemulsions which further supports our hypothesis. Next, a quick and real-time differential pulse voltammetry (DPV) based electrochemical chemical detection method was developed using a graphite electrode to detect change in current with 5-FU concentration while increasing voltage was applied on reference and counter electrodes. This method also showed that sustained release pattern of 5-FU at 37°C was converted to an immediate drug release when heated to 39°C, thus, confirming the thermoresponsive drug release. In case of paclitaxel loaded TSLN, drug release was minimum at 37°C and 70-100% drug release achieved after 60 hrs. On the other hand, whole drug was released in 4-7 hours at 39°C. This 15-20 time higher drug release at hyperthermic conditions confirmed the thermoresponsive drug release from the TSLN. Blank SLN were found to be biocompatible with human gingival fibroblast cells (PCS- 201-108) although and breast cancer cells (MDA-MB-231). However, 5-FU loaded SLN showed some cytotoxicity after 24 hours which was due to the release of drug. 5-FU loaded SLN showed thermoresponsive cytotoxicity to breast cancer cells (MDA-MB-231) as cytotoxicity was higher at 39°C (22-28%) compared to 37°C (<10%) within 1 hour. Similarly, paclitaxel loaded TSLN showed higher cytotoxicity to glioblastoma cells at 39°C (31% cell viability after one hour) compared to 37°C (18% cell viability). The higher cytotoxicity at 39°C was due to the higher drug release. Finally, the TSLN were evaluated for brain targeting across blood brain barrier (BBB) and an in vitro BBB model was used consisting astrocytes (CRL-2541) and endothelial cells (b.End3). The BBB model was optimized at 39°C for 1 hour duration due to retention of semipermeable nature and lack of paclitaxel and heat related toxicity. The TSLN showed higher permeability across BBB at 39°C which may be attributed to the deformable liquid state that squeezes through the tight junctions of BBB without any damaging effects. In conclusion, the novel TSLN reported in this thesis may serve as safe and effective platform of thermoresponsive targeting of cancer.
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