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مہر آپ جدوں مہربان کردا
مہر آپ جدوں مہربان کردا
رب مشکلاں سب آسان کردا
شاہ رگ دے کولوں وی ہے نیڑے
آپ وچ قرآن فرمان کردا
ہک وار دیدار نصیب ہوندا
جان لکھ کروڑ قربان کردا
میرا ہیں تے بن کے رہویں میرا
ایسے گل اُتّے بندہ مان کردا
دکھی دردی نوں لیندا لا سینے
اک وار چا یار احسان کردا
نِت پنڈ گناہاں دی کراں کٹّھی
نِت فضل ہے رب رحمان کردا
تیرے پیار اندر عمر گئی ساری
ہور سوچ کی ایہہ نادان کردا
عشق دسدا اپنا آپ جس دم
عقل سوچ دانائی حیران کردا
اسلامی تصوف کے مصادر اور مستشرقین كى آراء کا ایک تجزیاتی مطالعہ
The issue of the source and origin of Sufism in Islam is a complex one. A number of scholars, since the latter half of the nineteenth century have put forward conflicting claims. Earlier Orientalists thought that a Sufism developed from a single source while the latter scholars think a number of different sources should be considered as origin of Sufism. Both groups agree, however, in maintaining that Sufism is an addition to Islam and did not originally belong to Islam. Different opinions have been presented regarding the true source of Sufism, for example, Persian, Indian, Christian, Jewish and Neo-Platonic philosophies. The present paper intends to refute these charges of external influences on Islamic Sufism and attempts to show that the real origin of Islamic Sufism lies nowhere but in the teachings of the Holy Qur’an, Sunnah of the Prophet (peace be upon him) and lives of the blessed companions of the Prophet (peace be upon him).Analysis of Epidemiology Models by Non Standard Finite Difference Scheme and Laplace Adomian Decomposition Method
The present work has been planned through rational designing to develop targeted drug delivery system for alfuzosin HCl. Alfuzosin is basically selective antagonist of alpha 1 adrenoreceptors, indicated for treating benign prostatic hyperplasia. Its dose is 2.5 mg thrice daily and the treatment plan includes steady-state concentration of the drug throughout course of therapy. Due to readily absorbance and development of postural hypotension, it is not being indicated for treatment of hypertension. Through this research project, development of targeted systems like hydrogels and floating drug delivery system has been made in order to control the release of drug molecule. Regarding hydrogels; two different types of pH dependant three dimensional polymeric networks have been developed through free radical polymerization. In first phase; nine different formulations of pectin (Pec) have been evaluated in combination with acrylic acid and crosslinked through glutaraldehyde. In second phase; various grades of poly (ethylene glycol) (PEG) (Mw 400, 4000, 8000, 10000, 12000 & 20000) have been crosslinked with acrylic acid through N,N,,-Mehtylene-bis-acrylamide (MBAAm). After development of discs, these model systems were envisaged for various important elucidations like swelling studies, In-Vitro drug release analysis, Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (X RD) and Scanning Electron Microscopy (SEM). In order to predict releasing site and pattern; both dynamic and equilibrium swelling studies were conducted and implementation of various kinetic models has helped to elucidate kinetics of released molecule more efficiently. For both of the systems, frequency variations indicated by FTIR spectrum revealed interaction between the used polymers and monomers. Thermal stability has been reported by thermo gravimetric analysis while after copolymerization; increased enthalpy characters have been reported. In pectin based formulations, release of the drug followed zero order rates while in case of PEG based formulations; variations were reported in both rate and mechanism of drug release along with variations of molecular weights used. In both type of formulations, the drug release data is closely related to the swelling study’s findings and there is development of common character i.e. release of maximum amount of drug at pH 7.5. In floating drug delivery system, direct compression methodology has been adopted. The study has been aimed at developing floating system with non effervescent mechanism by using hydroxypropyl methylcellulose (HPMC) K100M, microcrystalline cellulose (MCC) PH 102, carbopol® and three grades of poly (ethylene glycol) (MW 10,000, 12,000 and 20,000). Various pre-compressional (angle of repose, compressibility index and Hausner’s ratio) and post compressional parameters (In-vitro buoyancy test, thickness, diameter, hardness, friability and In-vitro dissolution test) have been conducted to evaluate the suitability of developed dosage form for floating drug delivery system. The study is more focused towards evaluation of three grades of PEG (MW 10000, 12000, 20000) as all other parameters have been used as a constant quantity. Good matrix integrity has been found as all the formulations have presented total flotation time for more than 24 hours without disintegration. The formulation which doesn’t contain PEG has demonstrated first order along with fickian transport mechanism while all other formulations showed variation in their kinetic profile as the quantity and type of PEG varied. On the bases of revealed data of hydrogel and floating drug delivery system characterizations, it can be concluded that these systems are capable of delivering the drug molecule to the desired site in a predetermined mode of release.Journals by Discipline
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