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Mohamed Abbas Ibrahim

Microencapsulation, Parma (Italy), September 18-21, 2005. 4. T. Schaefer, P. Holm and H. G. Kristensen, Melt granulation in a laboratory scale high shear mixer, Drug Dev. Ind. Pharm. 19 (1990) 1249-1277; DOI: 10.3109/03639049009115960. 5. O. L. Sprockel, M. Sen, P. Shivanand and W. Prapaitrakul, A melt extrusion process for manufacturing matrix drug delivery systems, Int. J. Pharm. 155 (1997) 191-199; DOI: 10.1016/S0378- -5173(97)00165-8. 6. C. De Brabander, C. Vervaet and J. P. Remon, Development and evaluation of sustained

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Chinam Patra, Arethi Kumar, Hemant Pandit, Satya Singh and Meduri Devi

References Martindale, The Extra Pharmacopoeia , 31 st ed., The Pharmaceutical Press, London 1996, pp. 936-937. M. J. Serlin, M. L. Orme, M. Maciver, G. J. Green, R. G. Sibeon and A. M. Beckenridge, Pharmacodynamics and pharmacokinetics of conventional and long acting propranolol in patients with moderate hypertension, J. Clin. Pharmcol. 15 (1983) 519-526. B. Taylan, Y. Capan, O. Guven, S. Kes and A. A. Hincal, Design and evaluation of sustained release and buccal adhesive

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Amelia Avachat, Pralhad Bornare and Rakesh Dash

. Shivakumar, P. B. Patel and B. G. Desai, Design and statistical optimization of glipizide loaded lipospheres using response surface methodology, Acta Pharm.   57 (2007) 269-285; DOI: 10.2478/v10007-007-0022-8. M. K. Das and P. C. Senapati, Furosemide-loaded alginate microspheres prepared by ionic cross linking technique: Morphology and release characteristics, Indian J. Pharm. Sci.   70 (2008) 77-84; DOI: 10.4103/0250-474X.40336. Y. Samuelov, M. Donbrow and M. Friedman, Sustained release of drugs from ethylcellulose

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Barnabas Wilson, Patel Pritesh Babubhai, M. S. Sajeev, Josephine Leno Jenita and S. R. Brahmani Priyadarshini

-614; DOI: 10.1016/j.ejpb.2004.03.037. 6. K. R. Reddy, S. Mutalik and S. Reddy, Once-daily sustained release matrix tablets of nicorandil: Formulation and in vitro evaluation, AAPS Pharm. Sci. Tech. 4 (2003) 480-488; DOI: 10.1208/pt040461. 7. B.Wilson, P. H. Sitarambhai, M. S. Sajeev and G. Vinothapooshan, Design and evaluation of sustained release matrix tablets of levofloxacin for effective treatment of microbial infection, Int. J. Drug Deliv . 3 (2011) 305-314. 8. Pharmacopoeia of India, Ministry of Health and

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Alexandru Gavan, Alina Porfire, Cristina Marina and Ioan Tomuta

, Design of oral sustain release drug delivery of quetiapine fumarate, J. Drug Discov. Ther. 2 (2014) 7-11. 9. S. Tiwari and A. Rajabi-Siahboomi, Applications of complementary polymers in HPMC hydrophilic extended release matrices, Drug Deliv. Technol. 9 (2009) 20-27. 10. J. Djuriš, D. Medarević, M. Krstić, I. Vasiljević, I. Mašić and S. Ibrić, Design space approach in optimization of fluid bed granulation and tablets compression process, Sci. World J. (2012) 1-10; DOI: 10.1100/2012/185085. 11

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Ahmed Refaat, Magda Sokar, Fatma Ismail and Nabila Boraei

. Collett and C. Moreton, Modified-Release per Oral Dosage Forms, in Pharmaceuticals: the Science of Dosage Form Design (Ed. M. E. Aulton), Churchill Livingstone, New York 2001, pp. 289-305. 10. M. K. Raval, R. V. Ramani and N. R. Sheth, Formulation and evaluation of sustained release entericcoated pellets of budesonide for intestinal delivery, Int. J. Pharm. Investig. 3 (2013) 203-211. DOI: 10.4103/2230-973X.121294. 11. M. H. Kumar, K. Samatha, A. Balaji and M. S. Shankar, Recent novel advancements in pellet formulation. A Review, Int. J

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Bistra Kostova and Dimitar Rachev

References M. Gohel, T. Patel and Sh. Bariya, Studies in preparation and evaluation of pH-independent sustained-release matrix tablets of verapamil HCl using directly compressible Eudragits, Pharm. Dev. Technol. 8 (2003) 323-333; DOI: 10.1081/PDT-120024686. K. Gabr, Effect of organic acids on release patterns of weakly basic drugs from innert sustained release matrix tablets, Eur. J. Pharm. Biopharm. 38 (1992) 199-202. M. Dimitrov and N. Lambov, Study of verapamil hydrochloride

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Anurag Verma, Ashok Bansal, Amitava Ghosh and Jayanta Pandit

) 313-339. L. S. Wan, P. W. Heng and L. F. Wong, Relationship between swelling and drug release in a hydrophilic matrix, Drug Dev. Ind. Pharm . 19 (1993) 1201-1210; DOI: 10.3109/03639049309063012. P. J. Cox, K. A. Khan, D. L. Munday and J. Sujja-areevath, Development and evaluation of a multiple-unit oral sustained release dosage form for S (+)-ibuprofen: preparation and release kinetics, Int. J. Pharm.   193 (1999) 73-84; DOI: 10.1016/S0378-5173(99)00320-8.

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Gamal Mohamed El Maghraby, Ehab Mostafa Elzayat and Fars Kaed Alanazi

References 1. G. M. Jantzen and J. R. Robinson, Sustained and Controlled Release Drug Delivery Systems, Marcel Dekker, New York, 1996, pp. 575-610. 2. S. Miyazaki, H. Aoyama, N. Kawasaki, W. Kubo and D. Attwood, In situ-gelling gellan formulations as vehicles for oral drug delivery, J. Control. Release 60 (1999) 287-295; DOI: 10.1016/ S0168-3659(99)00084-X. 3. S. Miyazaki, W. Kubo and D. Attwood, Oral sustained delivery of theophylline using in situ gelation of sodium alginate, J. Control. Release 67 (2000) 275

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Muhammad Hanif, Hafeez Ullah Khan, Samina Afzal, Asif Mahmood, Safirah Maheen, Khurram Afzal, Nabila Iqbal, Mehwish Andleeb and Nazar Abbas

characterization of sustained release ketoprofen entrapped carnauba wax microparticles, Drug Dev. Ind. Pharm. 38 (2012) 1-11; 4. C. M. Adeyeye and J. C. Price, Development and evaluation of sustained release ibuprofen-wax microspheres. I. Effect of formulation variables on physical characteristics, Pharm. Res. 8 (1991) 1377-1383; 5. Y. A. Goma, I. A. Darwish, N. A. Boraei and L. K. El-Khordagui, Formulation of wax oxybenzone microparticles using a factorial