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Nifedipin-Yüklü Partiküler İlaç Tașıyıcı Sistemlere Genel Bir Bakıș

Yıl 2014, Sayı: 2, 73 - 95, 01.06.2014

Öz

Dihidropridin grubuna ait bir kalsiyum kanal blokeri olan nifedipin NF başlıca antianjinal ve antihipertansif etkilere sahiptir. NF’nin sudaki çözünürlüğü oldukça düşüktür ve yüksek oranda fotooksidasyona uğrar. NF’nin hemen salım yapan dozaj şekillerinin çeşitli sakıncaları ilk-geçiş etkisinden dolayı düşük oral biyoyararlanım, çoklu dozlama, plazma NF konsantrasyonunda dalgalanmalar ve hipotansiyon, taşikardi gibi yan etkiler mevcuttur. Bu derlemede, NFnin fizikokimyasal ve farmakolojik özelliklerinden kısaca bahsedildikten sonra NF’nin stabilitesi ve farmakolojik etkileri açısından sakıncalarını gidermek/iyileştirmek üzere geliştirilen partiküler ilaç taşıyıcı sistemlerle ilgili çalışmalar ele alınarak sunulmuştur.

Kaynakça

  • Sweetman S. Martindale: The complete drug reference, Electronic version. London, Pharmaceutical Press, 2007
  • h t t p s : / / w w w . r s c . o r g / M e r c k - I n d e x / m o n o g r a p h / m o n o 1 5 0 0 0 0 6 6 1 3 / nifedipine?q=unauthorize (28.08.2014)
  • Hayashi, K., Homma, K., Wakino, S., Tokuyama, H., Sugano, N., Saruta, T., Itoh, H.: T-type Ca Channel Blockade as a Determinant of Kidney Protection, Keio J Med, 59 (3), 84–95 (2010)
  • Friedrich, H., Nada, A., Bodmeier, R.: Solid State and Dissolution Rate Characterization of Co-ground Mixtures of Nifedipine and Hydrophilic Carriers, Drug Dev Ind Pharm, 31, 719–728 (2005)
  • http://www.who.int/medicines/publications/essentialmedicines/en/index.html (28.08.2014)
  • Conde-Agudelo, A., Romero, R., Kusanovic, J.P.: Nifedipine in the Management of Preterm Labor: A Systematic Review and Metaanalysis, Am J Obstet Gynecol. 204(2),134.e1-20 (2011)
  • Shen, J.B., Jiang, B., Pappano, A.J.: Comparison of L-type Calcium Channel Blockade By Nifedipine and/or Cadmium in Guinea Pig Ventricular Myocytes, J Pharmacol Exp Ther, 294(2),562-570 (2000)
  • Verhoeven, F.A., Moerings, E.P., Lamers, J.M., Hennemann, G., Visser, T.J., Everts, M.E.: Inhibitory Effects of Calcium Channel Blockers on Thyroid Hormone Uptake in Neonatal Rat Cardiomyocytes, Am J Physiol Heart Circ Physiol, 281(5),H1985-1991 (2001)
  • Lipscombe, D., Helton, T.D., Xu, W.: L-type Calcium Channels: The Low Down, J Neurophysiol. 92(5), 2633-2641 (2004)
  • Sousa, C.P., Navarro, C.M., Sposto, M.R.: Clinical Assessment of Nifedipine-Induced Gingival Overgrowth in A Group of Brazilian Patients, ISRN Dent, doi: 10.5402/2011/102047 (2011)
  • Lucas, R.M., Howell, L.P., Wall, B.A.: Nifedipine-induced Gingival Hyperplasia. A Histochemical and Ultrastructural Study, J Periodontol, 56(4),211-215 (1985)
  • Fami, M.J., Ho, N.T., Mason, C.M.: Another Report of Adverse Reactions to İmmediate- Release Nifedipine, Pharmacotherapy,18(5),1133-1135 (1998)
  • Mansoor, A.F., Keefer, L.A.H.: The Dangers of Immediate-Release Nifedipine for Hypertensive Crises, CME Credit (Jefferson Medical College), 27(7), 362-365 (2002)
  • Li, H., Yan, G., Wu, S., Wang, Z., Lam, K.Y.: Numerical Simulation of Controlled Nifedipine Release From Chitosan Microgels, J Appl Polym Sci, 93, 1928-1937 (2004)
  • Fu, E., Nieh, S., Hsiao, C.T., Hsieh, Y.D., Wikesjö, U.M., Shen, E.C.: Nifedipine-Induced Gingival Overgrowth in Rats: Brief Review and Experimental Study, J Periodontol, 69, 765- 71 (1998)
  • Snider, M.E., Nuzum, D.S., Veverka A.: Long-acting Nifedipine in the Management of the Hypertensive Patient, Vasc Health Risk Manag, 4, 1249-1257 (2008)
  • http://www.accessdata.fda.gov/scripts/cder/ob/docs/tempai.cfm (29.08.2014)
  • Pawar, A.P., Shelake, M.R., Bothiraja C., Kamble R.N.: Development of Photostable Gastro Retentive Formulation for Nifedipine Using Low-Density Polypropylene Microporous Particles, J Microencapsul, 29, 409–416 (2012)
  • Emara, L.H., Badr, R.M., Elbary, A.A.: Improving the Dissolution and Bioavailability of Nifedipine Using Solid Dispersions and Solubilizers, Drug Dev Ind Pharm, 28, 795–807
  • Jagdale, S.C., Jadhav, V.N., Chabukswar, A.R., Kuchekar, B.S.: Solubility Enhancement, Physicochemical Characterization and Formulation of Fast-Dissolving Tablet of Nifedipine- Betacyclodextrin Complexes, BJPS, 48(1), 131-145 (2012)
  • Lalitha, Y., Lakshmi, P.K.: Enhancement Of Dissolution of Nifedipine by Surface Solid Dispersion Technique, Int J Pharm Pharm Sci, 3(3), 41-46 (2011)
  • Annapureddy, T., Preetha, J.P., Kumar, A.N., Reddy, M.S.: Enhancement of Solubility of Nifedipine by Liquisolid Compacts Technique, IAJPR, 3(4), 3433-3465 (2013)
  • Hecq, J., Deleers, M., Fanara, D., Vranckx, H., Amighi, K.: Preparation and Characterization of Nanocrystals for Solubility and Dissolution Rate Enhancement of Nifedipine, Int J Pharm, 299, 167-177 (2005)
  • Kim, Y.I., Fluckiger, L., Hoffman, M., Lartaud-Idjouadiene, I., Atkinson, J., Maincent, P.: The Antihypertensive Effect of Orally Administered Nifedipine-Loaded Nanoparticles in Spontaneously Hypertensive Rats, Br J Pharmacol, 120(3), 399-404 (1997)
  • Aydın, A.: Preterm Eylemin Durdurulmasında Ritodrin ve Nifedipinin Tedavi Etkinliklerinin Maternal ve Fetal Etkilerinin Karşılaştırılması, Uzmanlık Tezi, İstanbul (2005)
  • http://dailymed.nlm.nih.gov/dailymed/drugınfo.cfm?setid=4617417a-08df-4417- a944-dfc30de183db&cfıd=871840&cftoken=1cb8b1d12050b1e5-01802f95-b47e-e996- d69a38ae78d4dbe4 (29.08.2014)
  • http://dailymed.nlm.nih.gov/dailymed/archives/fdadrugınfo.cfm?archiveid=9958 (29.08.2014)
  • http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8ebcb33c-f43b-4b36-9f94- 9774b2a59e06 (29.08.2014)
  • http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2934261f-3606-439e-8418- 12438aae1b2a (29.08.2014)
  • Patel, N., Polak, S., Jamei, M., Rostami-Hodjegan, A., Turner, D.B.: Quantitative Prediction of Formulation-Specific Food Effects and Their Population Variability From In Vitro Data With The Physiologically-Based ADAM Model: A Case Study Using The BCS/BDDCS Class II Drug Nifedipine, Eur J Pharm Sci, 57,240-249 (2014)
  • Lin, X., Tang, D., Du, H.: Self-assembly and Controlled Release Behaviour of The Water- İnsoluble Drug Nifedipine From Electrospun PCL-Based Polyurethane Nanofibres, J Pharm Pharmacol, 65, 673-681 (2013)
  • Gürsoy, A.Z., “Giriş”, Gürsoy, A.Z. (Ed.), Kontrollü Salım Sistemleri, İstanbul, Kontrollü Salım Sistemleri Derneği, (2002), 3.
  • Chandana, N., Gopinath, H., Bhowmik, D., Williamkeri, Thirupathi, R.A.: Modified Release Dosage Forms, JCHPS, 6(1), 13-21 (2013)
  • Kaş, H.S., “İlaç taşıyıcı partiküler sistemler”, Gürsoy, A.Z. (Ed.), Kontrollü Salım Sistemleri, İstanbul, Kontrollü Salım Sistemleri Derneği, (2002), 65-102.
  • Li, D.X., Kim, J.O., Oh, D.H., Lee, W.S., Hong, M.J., Kang, J.Y., Choi, J.S., Woo, J.S., Yong, C.S., Choi, H.G.: Development of Nifedipine-Loaded Coated Gelatin Microcapsule as a Long Acting Oral Delivery, Arch Pharm Res, 32(1), 127-132 ( 2009)
  • http://eudragit.evonik.com/product/eudragit/en/products-services/eudragit-products/ enteric-formulations/Pages/default.aspx (16.02.2015)
  • Mallick, S., Gupta, B.K., Ghosal, S.K.: Assessment of Bioavailability of Experimental Controlled Release Microcapsules of Nifedipine, Acta Pol Pharm, 57(3), 175-180 (2000)
  • Varde, N.K., Pack, D.W.: Microspheres for Controlled Release Drug Delivery, Expert Opin Biol Ther, 4(1), 35-51 (2004)
  • Chuo,W.H., Tsai, T.R., Hsu, S.H., Cham, T.M.: Preparation and In-vitro Evaluation of Nifedipine Loaded Albumin Microspheres Cross-Linked by Different Glutaraldehyde Concentrations, Int J Pharm, 144, 241–245 (1996)
  • Dhawan, S., Singla, A.K.: Nifedipine Loaded Chitosan Microspheres Prepared by Emulsification Phase-Separation, Biotech Histochem, 78, 243-254 (2003)
  • Kumbar, S.G., Aminabhavi, T.M.: Synthesis and Characterization of Modified Chitosan Microspheres: Effect of the Grafting Ratio on the Controlled Release of Nifedipine through Microspheres, J Appl Polym Sci, 89, 2940–2949 (2003)
  • Dinarvand, R., Kouchakzadeh, Z., Moghadam, S.H., Atyabi, F.: Effect of Microencapsulation on Photo-Stability of Nifedipine, Iranian J Pharm Res, 5(4), 239-244 (2006)
  • Cilurzo, F., Selmin, F., Minghetti, P., Gennari, C.G., Demartin, F., Montanari, L.: Characterization and Physical Stability of Fast-Dissolving Microparticles Containing Nifedipine, Eur J Pharm Biopharm, 68, 579–588 (2008)
  • Guyot, M., Fawaz, F.: Nifedipine Loaded-Polymeric Microspheres: Preparation and Physical Characteristics, Int J Pharm, 175, 61–74 (1998)
  • Soppimath, K.S., Kulkarni, A.R., Aminabhavi, T.M.: Encapsulation of Antihypertensive Drugs in Cellulose-Based Matrix Microspheres: Characterization and Release Kinetics of Microspheres and Tableted Microspheres, J Microencapsul, 18(3), 397-409 ( 2001)
  • Sansdrap, P., Moës, A.J.: Influence of Additives on the Release Profile of Nifedipine from Poly(DL-lactide-co-glycolide) Microspheres, J Microencapsul, 5(5), 545-553 (1998)
  • Soppimath, K.S., Aminabhavi, T.M.: Ethyl Acetate as a Dispersing Solvent in the Production of Poly(DL-lactide-co-glycolide) Microspheres: Effect of Process Parameters and Polymer Type, J Microencapsul,19(3), 281-292 (2002)
  • Hombreiro Pérez, M., Zinutti, C., Lamprecht, A., Ubrich, N., Astier, A., Hoffman, M., Bodmeier, R., Maincent, P.: The Preparation and Evaluation of Poly(Epsilon-Caprolactone) Microparticles Containing Both aLipophilic and a Hydrophilic Drug, J Control Release, 65(3), 429-438 (2000)
  • Kumar, S.V., Shelke, N.B., Prasannakumar, S., Sherigara, B.S., Aminabhavi, T.M.: Microspheres of Copolymeric N-vinylpyrrolidone and 2-ethoxyethyl Methacrylate for the Controlled Release of Nifedipine, J Polym Res, 18(3), 359-366 (2011)
  • Saigal, A., Ng, W.K., Tan, R.B., Chan, S.Y.: Development of Controlled Release Inhalable Polymeric Microspheres for Treatment of Pulmonary Hypertension, Int J Pharm, 450(1-2), 114-122 (2013)
  • Shelke, N.B., Aminabhavi, T.M.: Synthesis and Characterization of Novel Poly(Sebacic Anhydride-Co-Pluronic F68/F127)Biopolymeric Microspheres for the Controlled Release of Nifedipine, Int J Pharm, 345, 51–58 (2007)
  • Giovannelli, L., Bellomi, S., Pattarino, F., Albertini, B.: Characterization of Nifedipine Microparticles Prepared by Hot Air Coating Technique, Int J Pharm, 293(1-2), 225-234
  • Pattarino, F., Giovannelli, L., Bellomi, S.: Effect of Poloxamers on Nifedipine Microparticles Prepared by Hot Air Coating Technique, Eur J Pharm Biopharm, 65, 198–203 (2007)
  • Huang, J., Wigent, R.J., Bentzley, C.M., Schwartz, J.B.: Nifedipine Solid Dispersion in Microparticles of Ammonio Methacrylate Copolymer and Ethylcellulose Binary Blend for Controlled Drug Delivery. Effect of Drug Loading on Release Kinetics, Int J Pharm, 319(1- 2),44-54 (2006)
  • Devrim, B., Canefe, K.: Midede Kalış Süresini Uzatan İlaç Şekilleri, Ankara Ecz. Fak. Derg, 35 (1), 69 - 94 (2006)
  • Zhao, L., Wei, Y.M., Yu, Y., Zheng, W.W.: Polymer Blends Used to Prepare Nifedipine Loaded Hollow Microspheres for a Floating-Type Oral Drug Delivery System: In vitro Evaluation, Arch Pharm Res, 33(3), 443-450 (2010)
  • Granada, A., Tagliari, M.P., Soldi, V., Silva, M.A., Zanetti-Ramos, B.G., Fernandes, D., Stulzer, H.K.: Nifedipine-loaded Polymeric Nanocapsules: Validation of a Stability-indicating HPLC Method to Evaluate the Drug Entrapment Efficiency and In vitro Release Profiles, J AOAC Int, 96(2), 276-281 (2013)
  • Li, P., Dai, Y.N., Zhang, J.P., Wang, A.Q., Wei, Q.: Chitosan-alginate Nanoparticles as a Novel Drug Delivery System for Nifedipine, Int J Biomed Sci, 4(3), 221-228 (2008)
  • Barman, R.K., Iwao Y, Funakoshi Y, Abdul-Hackam Ranneh, Noguchi S, Wahed, M.I.I. Itai, S. Development of Highly Stable Nifedipine Solid–Lipid Nanoparticles, Chem Pharm Bull, 62(5), 399–406 (2014).
  • Barman, R.K., Iwao Y, Islam R, Funakoshi Y, Noguchi S, Wahed, M.I.I. Itai, S.: In vivo Pharmacokinetic and Hemocompatible Evaluation of Lyophilization Induced Nifedipine Solid-Lipid Nanoparticle, Pharmacol & Pharm, 5, 455-461(2014).
  • Kamiya, S., Yamada, M., Kurita, T., Miyagishima, A., Arakawa, M., Sonobe, T.: Preparation and Stabilization of Nifedipine Lipid Nanoparticles. Int J Pharm, 354(1-2), 242-247 (2008)
  • Plumley, C., Gorman, E.M., El-Gendy, N., Bybee, C.R., Munson, E.J., Berkland, C.: Nifedipine Nanoparticle Agglomeration as a Dry Powder Aerosol Formulation Strategy, Int J Pharm, 369(1-2), 136-143 (2009)
  • Jeong, Y.I., Sun, H.S., Shim, Y.H., Kim, C., Park, S.H., Choi, K.C., Cho, C.S.: Nifedipine Encapsulated Core-Shell Type Nanoparticles Based on Poly(Gamma-Benzyl L-Glutamate)/ Poly(Ethylene Glycol) Diblock Copolymers, J Microencapsul, 21(4),445-453 (2004)

Overview on nifedipine loaded particulate drug delivery systems

Yıl 2014, Sayı: 2, 73 - 95, 01.06.2014

Öz

Nifedipine NF , a dihydropyridine calcium-channel blocker, has primarily antianginal and antihypertensive effects. It is a poorly water-soluble drug and highly sensitive to photo-oxidation. The immediate release NF dosage forms have several disadvantages such as low oral bioavailability due to first-pass effect, multiple dosing fluctuations in the plasma NF concentration and adverse effects such as hypotension, tachycardia . In this review, after briefly mentioned the physicochemical and pharmacological properties of NF, the studies with regard to the particulate drug delivery systems developed to eliminate/improve the drawbacks in terms of the stability and pharmacological effect of NF were presented.

Kaynakça

  • Sweetman S. Martindale: The complete drug reference, Electronic version. London, Pharmaceutical Press, 2007
  • h t t p s : / / w w w . r s c . o r g / M e r c k - I n d e x / m o n o g r a p h / m o n o 1 5 0 0 0 0 6 6 1 3 / nifedipine?q=unauthorize (28.08.2014)
  • Hayashi, K., Homma, K., Wakino, S., Tokuyama, H., Sugano, N., Saruta, T., Itoh, H.: T-type Ca Channel Blockade as a Determinant of Kidney Protection, Keio J Med, 59 (3), 84–95 (2010)
  • Friedrich, H., Nada, A., Bodmeier, R.: Solid State and Dissolution Rate Characterization of Co-ground Mixtures of Nifedipine and Hydrophilic Carriers, Drug Dev Ind Pharm, 31, 719–728 (2005)
  • http://www.who.int/medicines/publications/essentialmedicines/en/index.html (28.08.2014)
  • Conde-Agudelo, A., Romero, R., Kusanovic, J.P.: Nifedipine in the Management of Preterm Labor: A Systematic Review and Metaanalysis, Am J Obstet Gynecol. 204(2),134.e1-20 (2011)
  • Shen, J.B., Jiang, B., Pappano, A.J.: Comparison of L-type Calcium Channel Blockade By Nifedipine and/or Cadmium in Guinea Pig Ventricular Myocytes, J Pharmacol Exp Ther, 294(2),562-570 (2000)
  • Verhoeven, F.A., Moerings, E.P., Lamers, J.M., Hennemann, G., Visser, T.J., Everts, M.E.: Inhibitory Effects of Calcium Channel Blockers on Thyroid Hormone Uptake in Neonatal Rat Cardiomyocytes, Am J Physiol Heart Circ Physiol, 281(5),H1985-1991 (2001)
  • Lipscombe, D., Helton, T.D., Xu, W.: L-type Calcium Channels: The Low Down, J Neurophysiol. 92(5), 2633-2641 (2004)
  • Sousa, C.P., Navarro, C.M., Sposto, M.R.: Clinical Assessment of Nifedipine-Induced Gingival Overgrowth in A Group of Brazilian Patients, ISRN Dent, doi: 10.5402/2011/102047 (2011)
  • Lucas, R.M., Howell, L.P., Wall, B.A.: Nifedipine-induced Gingival Hyperplasia. A Histochemical and Ultrastructural Study, J Periodontol, 56(4),211-215 (1985)
  • Fami, M.J., Ho, N.T., Mason, C.M.: Another Report of Adverse Reactions to İmmediate- Release Nifedipine, Pharmacotherapy,18(5),1133-1135 (1998)
  • Mansoor, A.F., Keefer, L.A.H.: The Dangers of Immediate-Release Nifedipine for Hypertensive Crises, CME Credit (Jefferson Medical College), 27(7), 362-365 (2002)
  • Li, H., Yan, G., Wu, S., Wang, Z., Lam, K.Y.: Numerical Simulation of Controlled Nifedipine Release From Chitosan Microgels, J Appl Polym Sci, 93, 1928-1937 (2004)
  • Fu, E., Nieh, S., Hsiao, C.T., Hsieh, Y.D., Wikesjö, U.M., Shen, E.C.: Nifedipine-Induced Gingival Overgrowth in Rats: Brief Review and Experimental Study, J Periodontol, 69, 765- 71 (1998)
  • Snider, M.E., Nuzum, D.S., Veverka A.: Long-acting Nifedipine in the Management of the Hypertensive Patient, Vasc Health Risk Manag, 4, 1249-1257 (2008)
  • http://www.accessdata.fda.gov/scripts/cder/ob/docs/tempai.cfm (29.08.2014)
  • Pawar, A.P., Shelake, M.R., Bothiraja C., Kamble R.N.: Development of Photostable Gastro Retentive Formulation for Nifedipine Using Low-Density Polypropylene Microporous Particles, J Microencapsul, 29, 409–416 (2012)
  • Emara, L.H., Badr, R.M., Elbary, A.A.: Improving the Dissolution and Bioavailability of Nifedipine Using Solid Dispersions and Solubilizers, Drug Dev Ind Pharm, 28, 795–807
  • Jagdale, S.C., Jadhav, V.N., Chabukswar, A.R., Kuchekar, B.S.: Solubility Enhancement, Physicochemical Characterization and Formulation of Fast-Dissolving Tablet of Nifedipine- Betacyclodextrin Complexes, BJPS, 48(1), 131-145 (2012)
  • Lalitha, Y., Lakshmi, P.K.: Enhancement Of Dissolution of Nifedipine by Surface Solid Dispersion Technique, Int J Pharm Pharm Sci, 3(3), 41-46 (2011)
  • Annapureddy, T., Preetha, J.P., Kumar, A.N., Reddy, M.S.: Enhancement of Solubility of Nifedipine by Liquisolid Compacts Technique, IAJPR, 3(4), 3433-3465 (2013)
  • Hecq, J., Deleers, M., Fanara, D., Vranckx, H., Amighi, K.: Preparation and Characterization of Nanocrystals for Solubility and Dissolution Rate Enhancement of Nifedipine, Int J Pharm, 299, 167-177 (2005)
  • Kim, Y.I., Fluckiger, L., Hoffman, M., Lartaud-Idjouadiene, I., Atkinson, J., Maincent, P.: The Antihypertensive Effect of Orally Administered Nifedipine-Loaded Nanoparticles in Spontaneously Hypertensive Rats, Br J Pharmacol, 120(3), 399-404 (1997)
  • Aydın, A.: Preterm Eylemin Durdurulmasında Ritodrin ve Nifedipinin Tedavi Etkinliklerinin Maternal ve Fetal Etkilerinin Karşılaştırılması, Uzmanlık Tezi, İstanbul (2005)
  • http://dailymed.nlm.nih.gov/dailymed/drugınfo.cfm?setid=4617417a-08df-4417- a944-dfc30de183db&cfıd=871840&cftoken=1cb8b1d12050b1e5-01802f95-b47e-e996- d69a38ae78d4dbe4 (29.08.2014)
  • http://dailymed.nlm.nih.gov/dailymed/archives/fdadrugınfo.cfm?archiveid=9958 (29.08.2014)
  • http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8ebcb33c-f43b-4b36-9f94- 9774b2a59e06 (29.08.2014)
  • http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2934261f-3606-439e-8418- 12438aae1b2a (29.08.2014)
  • Patel, N., Polak, S., Jamei, M., Rostami-Hodjegan, A., Turner, D.B.: Quantitative Prediction of Formulation-Specific Food Effects and Their Population Variability From In Vitro Data With The Physiologically-Based ADAM Model: A Case Study Using The BCS/BDDCS Class II Drug Nifedipine, Eur J Pharm Sci, 57,240-249 (2014)
  • Lin, X., Tang, D., Du, H.: Self-assembly and Controlled Release Behaviour of The Water- İnsoluble Drug Nifedipine From Electrospun PCL-Based Polyurethane Nanofibres, J Pharm Pharmacol, 65, 673-681 (2013)
  • Gürsoy, A.Z., “Giriş”, Gürsoy, A.Z. (Ed.), Kontrollü Salım Sistemleri, İstanbul, Kontrollü Salım Sistemleri Derneği, (2002), 3.
  • Chandana, N., Gopinath, H., Bhowmik, D., Williamkeri, Thirupathi, R.A.: Modified Release Dosage Forms, JCHPS, 6(1), 13-21 (2013)
  • Kaş, H.S., “İlaç taşıyıcı partiküler sistemler”, Gürsoy, A.Z. (Ed.), Kontrollü Salım Sistemleri, İstanbul, Kontrollü Salım Sistemleri Derneği, (2002), 65-102.
  • Li, D.X., Kim, J.O., Oh, D.H., Lee, W.S., Hong, M.J., Kang, J.Y., Choi, J.S., Woo, J.S., Yong, C.S., Choi, H.G.: Development of Nifedipine-Loaded Coated Gelatin Microcapsule as a Long Acting Oral Delivery, Arch Pharm Res, 32(1), 127-132 ( 2009)
  • http://eudragit.evonik.com/product/eudragit/en/products-services/eudragit-products/ enteric-formulations/Pages/default.aspx (16.02.2015)
  • Mallick, S., Gupta, B.K., Ghosal, S.K.: Assessment of Bioavailability of Experimental Controlled Release Microcapsules of Nifedipine, Acta Pol Pharm, 57(3), 175-180 (2000)
  • Varde, N.K., Pack, D.W.: Microspheres for Controlled Release Drug Delivery, Expert Opin Biol Ther, 4(1), 35-51 (2004)
  • Chuo,W.H., Tsai, T.R., Hsu, S.H., Cham, T.M.: Preparation and In-vitro Evaluation of Nifedipine Loaded Albumin Microspheres Cross-Linked by Different Glutaraldehyde Concentrations, Int J Pharm, 144, 241–245 (1996)
  • Dhawan, S., Singla, A.K.: Nifedipine Loaded Chitosan Microspheres Prepared by Emulsification Phase-Separation, Biotech Histochem, 78, 243-254 (2003)
  • Kumbar, S.G., Aminabhavi, T.M.: Synthesis and Characterization of Modified Chitosan Microspheres: Effect of the Grafting Ratio on the Controlled Release of Nifedipine through Microspheres, J Appl Polym Sci, 89, 2940–2949 (2003)
  • Dinarvand, R., Kouchakzadeh, Z., Moghadam, S.H., Atyabi, F.: Effect of Microencapsulation on Photo-Stability of Nifedipine, Iranian J Pharm Res, 5(4), 239-244 (2006)
  • Cilurzo, F., Selmin, F., Minghetti, P., Gennari, C.G., Demartin, F., Montanari, L.: Characterization and Physical Stability of Fast-Dissolving Microparticles Containing Nifedipine, Eur J Pharm Biopharm, 68, 579–588 (2008)
  • Guyot, M., Fawaz, F.: Nifedipine Loaded-Polymeric Microspheres: Preparation and Physical Characteristics, Int J Pharm, 175, 61–74 (1998)
  • Soppimath, K.S., Kulkarni, A.R., Aminabhavi, T.M.: Encapsulation of Antihypertensive Drugs in Cellulose-Based Matrix Microspheres: Characterization and Release Kinetics of Microspheres and Tableted Microspheres, J Microencapsul, 18(3), 397-409 ( 2001)
  • Sansdrap, P., Moës, A.J.: Influence of Additives on the Release Profile of Nifedipine from Poly(DL-lactide-co-glycolide) Microspheres, J Microencapsul, 5(5), 545-553 (1998)
  • Soppimath, K.S., Aminabhavi, T.M.: Ethyl Acetate as a Dispersing Solvent in the Production of Poly(DL-lactide-co-glycolide) Microspheres: Effect of Process Parameters and Polymer Type, J Microencapsul,19(3), 281-292 (2002)
  • Hombreiro Pérez, M., Zinutti, C., Lamprecht, A., Ubrich, N., Astier, A., Hoffman, M., Bodmeier, R., Maincent, P.: The Preparation and Evaluation of Poly(Epsilon-Caprolactone) Microparticles Containing Both aLipophilic and a Hydrophilic Drug, J Control Release, 65(3), 429-438 (2000)
  • Kumar, S.V., Shelke, N.B., Prasannakumar, S., Sherigara, B.S., Aminabhavi, T.M.: Microspheres of Copolymeric N-vinylpyrrolidone and 2-ethoxyethyl Methacrylate for the Controlled Release of Nifedipine, J Polym Res, 18(3), 359-366 (2011)
  • Saigal, A., Ng, W.K., Tan, R.B., Chan, S.Y.: Development of Controlled Release Inhalable Polymeric Microspheres for Treatment of Pulmonary Hypertension, Int J Pharm, 450(1-2), 114-122 (2013)
  • Shelke, N.B., Aminabhavi, T.M.: Synthesis and Characterization of Novel Poly(Sebacic Anhydride-Co-Pluronic F68/F127)Biopolymeric Microspheres for the Controlled Release of Nifedipine, Int J Pharm, 345, 51–58 (2007)
  • Giovannelli, L., Bellomi, S., Pattarino, F., Albertini, B.: Characterization of Nifedipine Microparticles Prepared by Hot Air Coating Technique, Int J Pharm, 293(1-2), 225-234
  • Pattarino, F., Giovannelli, L., Bellomi, S.: Effect of Poloxamers on Nifedipine Microparticles Prepared by Hot Air Coating Technique, Eur J Pharm Biopharm, 65, 198–203 (2007)
  • Huang, J., Wigent, R.J., Bentzley, C.M., Schwartz, J.B.: Nifedipine Solid Dispersion in Microparticles of Ammonio Methacrylate Copolymer and Ethylcellulose Binary Blend for Controlled Drug Delivery. Effect of Drug Loading on Release Kinetics, Int J Pharm, 319(1- 2),44-54 (2006)
  • Devrim, B., Canefe, K.: Midede Kalış Süresini Uzatan İlaç Şekilleri, Ankara Ecz. Fak. Derg, 35 (1), 69 - 94 (2006)
  • Zhao, L., Wei, Y.M., Yu, Y., Zheng, W.W.: Polymer Blends Used to Prepare Nifedipine Loaded Hollow Microspheres for a Floating-Type Oral Drug Delivery System: In vitro Evaluation, Arch Pharm Res, 33(3), 443-450 (2010)
  • Granada, A., Tagliari, M.P., Soldi, V., Silva, M.A., Zanetti-Ramos, B.G., Fernandes, D., Stulzer, H.K.: Nifedipine-loaded Polymeric Nanocapsules: Validation of a Stability-indicating HPLC Method to Evaluate the Drug Entrapment Efficiency and In vitro Release Profiles, J AOAC Int, 96(2), 276-281 (2013)
  • Li, P., Dai, Y.N., Zhang, J.P., Wang, A.Q., Wei, Q.: Chitosan-alginate Nanoparticles as a Novel Drug Delivery System for Nifedipine, Int J Biomed Sci, 4(3), 221-228 (2008)
  • Barman, R.K., Iwao Y, Funakoshi Y, Abdul-Hackam Ranneh, Noguchi S, Wahed, M.I.I. Itai, S. Development of Highly Stable Nifedipine Solid–Lipid Nanoparticles, Chem Pharm Bull, 62(5), 399–406 (2014).
  • Barman, R.K., Iwao Y, Islam R, Funakoshi Y, Noguchi S, Wahed, M.I.I. Itai, S.: In vivo Pharmacokinetic and Hemocompatible Evaluation of Lyophilization Induced Nifedipine Solid-Lipid Nanoparticle, Pharmacol & Pharm, 5, 455-461(2014).
  • Kamiya, S., Yamada, M., Kurita, T., Miyagishima, A., Arakawa, M., Sonobe, T.: Preparation and Stabilization of Nifedipine Lipid Nanoparticles. Int J Pharm, 354(1-2), 242-247 (2008)
  • Plumley, C., Gorman, E.M., El-Gendy, N., Bybee, C.R., Munson, E.J., Berkland, C.: Nifedipine Nanoparticle Agglomeration as a Dry Powder Aerosol Formulation Strategy, Int J Pharm, 369(1-2), 136-143 (2009)
  • Jeong, Y.I., Sun, H.S., Shim, Y.H., Kim, C., Park, S.H., Choi, K.C., Cho, C.S.: Nifedipine Encapsulated Core-Shell Type Nanoparticles Based on Poly(Gamma-Benzyl L-Glutamate)/ Poly(Ethylene Glycol) Diblock Copolymers, J Microencapsul, 21(4),445-453 (2004)
Toplam 63 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Research Article
Yazarlar

Emrah Özakar Bu kişi benim

Evren Alğın Yapar Bu kişi benim

Meltem Çetin Bu kişi benim

Yayımlanma Tarihi 1 Haziran 2014
Yayımlandığı Sayı Yıl 2014 Sayı: 2

Kaynak Göster

Vancouver Özakar E, Yapar EA, Çetin M. Nifedipin-Yüklü Partiküler İlaç Tașıyıcı Sistemlere Genel Bir Bakıș. HUJPHARM. 2014(2):73-95.