Диссертация (1141302), страница 30
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140–145.142. Parikh D. M. Handbook of Pharmaceutical Granulation Technology, ThirdEdition. – New York: Marcel Dekker Inc, 1997. – 676 p.143. Perrie Y., Rades T. Pharmaceutics – drug delivery and targeting. – London:Pharmaceutical Press, 2012. – 256 p.144. Pharmacopeia of the United State. USP 38/NF 33.
2015.145. Pharmaceutical Applications of Hot-Melt Extrusion: Part I / M. M. Crowley,F. Chang, M.A. Repka [et al] // Drug Development and Industrial Pharmacy. 2007. – N. 33. -P. 909 – 926.146. Physical characterizations and sustained release profiling of gastroretentivedrug delivery systems with improved floating and swelling capabilities / Ying206Chen Chen, H.O. Ho,T.Y.
Lee [et al] // International Journal of Pharmaceutics. 2013. – N. 1-2. - P. 162-169.147. Physical and technological parameters influencing floating properties ofmatrix tablets based on cellulose ethers / S. Baumgartner, J. Smid-Korber, F.Vreces [et al] // S T P Pharma. – 1998. – Vol. 5.
– N. 8. – P. 285-290.148. Plasticizing effect of ibuprofen induced an alteration of drug released fromKollidon SR matrices produced by direct compression / C. Wiranidchapong, N.Ruangpayungsak, P. Suwattanasuk [et al] // Drug development and industrialpharmacy. – 2015. – Vol. 43 – N. 6. – 1037-1046.149. Pluronic-g-poly(acrylic acid) copolymers as novel excipients for site specific,sustained release tablets / R. Barreiro-Iglesias, L. Bromberg, M. Temchenko [et al]// European Journal of Pharmaceutical Sciences.
– 2005. – N. 26. – P. 374–385.150. Poloxamer 407 microspheres for orotransmucosal drug delivery. Part I:Formulation, manufacturing and characterization // B. Albertini, N. Passerini, DiSabatino M. [et al] // International Journal of Pharmaceutics. – 2010. – N. 39. –P. 71–79.151. Preparation and characterization of Compritol 888 ATO matrix tablets for thesustained release of diclofenac sodium / M.
Roberts, L. Pulcini, S. Mostafa [et al] //Pharmaceutical Development and Technology. - 2013. – Vol. 20. – N. 4. - P. 507512.152. Preparation, characterisation and photosensitivity studies of solid dispersionsof diflunisal and Eudragit RS100® and RL100® / R. Pignatello, M. Ferro, DeGuidi G. [et al] // International Journal of Pharmaceutics.
– 1998. – Vol. 218. N. 1-2. – P. 27-42.153. Preparation of multiple-unit floating-bioadhesive cooperative minitablets forimproving the oral bioavailability of famotidine in rats / X. Zhu, X. Qi, Z. Wu [etal] // Drug Delivery. – 2014. – N. 21. P. 459–466.154. Properties of tablets containing granulations of ibuprofen and an acryliccopolymer prepared by thermal processes / M. Kidokoro, N.H.
Shah, A.W. Malick207[et al] // Pharmaceutical Development and Technology. -2001. – Vol. 6. – N. 2. –P. 263-275.155. Rathbone M. J., Hadgraft J., Roberts M. S. Modified-Release Drug DeliveryTechnology. – New York: Marcel Dekker Inc., 2002. – 1032 p.156. Rational Design of Oral Modified-Release Drug Delivery Systems.Developing Solid Oral Dosage Forms / Y.Qiu, Y. Chen, G.G.Z. Zhang [et al]. –San Diego: Academic Press, 2009. – P. 469-499.157. Relationship between slugging pressure and Brittle fracture tendency – a casestudy for Aspirin tablets / F.E. Eichie, R.S. Okor, M.U.
Uhumwangho [et al] //Tropical Journal of Pharmaceutical Research. – 2005. – Vol. 2. – N. 4. – P. 483487.158. Reza S., Quadir M. A., Haider S. Sh. Comparative evaluation of plastic,hydrophobic and hydrophilic polymers as matrices for controlled-release drugdelivery // Journal of Pharmacy and Pharmaceutical Sciences. – 2003. – Vol. 6. –N. 2. – P. 274-291.159. Saini Nisha, Mathew G., Lincy J. Matrix Tablets: An Effective Way for OralControlled Release Drug Delivery // Iranian Journal of Pharmaceutical Sciences. 2012.
– N. 8. - Р. 165-170.160. Sakr W., Alanazi F., Sakr A. Effect of Kollidon SR on the release ofAlbuterol Sulphate from matrix tablets // Saudi Pharmaceutical Journal. – 2011. –N. 19. - P. 19–27.161. Sarika Pundir, Ashutosh Badola, Deepak Sharma. Sustained release matrixtechnology and recent advance in matrix drug delivery system: a review //International Journal of Drug Research and Technology. -2013.
– N. 3. -Р. 12-20.162. Serajuddin A.T. Salt formation to improve drug solubility // Advanced DrugDelivery Reviews. – 2007. - Vol. 7 – N. 59. – P. 603-616.163. Sieg U., Flähmig. Die fibrinolytische Aktivität des peripheren und desuterinen Blutes und ihre Beeinflussung durch p-Aminomethylbezoesäure208(PAMBA) bei Gestosen // Zentralblatt für Gynäkologie.
-1969. – N. 51. - S. 1662 –1666.164. Siepmann J., Peppas N.A. Modeling of drug release from delivery systemsbased on hydroxypropyl methylcellulose (HPMC) // Advanced Drug DeliveryReviews. – 2012. – Vol. 64. – P. 163 -174.165. Singh B. N., Kim K. H. Floating drug delivery systems: an approach to oralcontrolled drug delivery via gastric retention // Journal of Controlled Release.
2000. – Vol. 3. – N. 63. - P. 235–259.166. Skoug J.W., Mikelsons M.V., Vigneron C.N., Stemm N.L. Qualitativeevaluation of the mechanism of release of matrix sustained-release dosage formsby measurement of polymer release // Journal of Controlled Release. -1993. –N. 27. P. 227–245.167. Solid lipid excipients – Matrix agents for sustained drug delivery / Y. Rosiaux[et al] // Journal of Controlled Release. - 2014. – N. 188. - P.
18-30.168. Solubility-pH profiles of some acidic, basic and amphoteric drugs / E. Shoghi,E.Fuquet, E. Bosch [et al] // The European Journal of Pharmaceutical Sciences. –2013. – Vol. 1-2. – N. 48. – P. 291-300.169. Staniforth J.N., Baichwal A.R. TIMERx: novel polysaccharide composites forcontrolled/programmed release of drugs in gastrointestinal tract // Expert OpinionDrugs.
– 2005. – Vol. 2. – N. 3. - P. 587-595.170. Study of morphine hydrochloride percolation threshold in Eudragit® RS–PMmatrices / L.M. Melgoza, I. Caraballo, J. Alvarez-Fuentes [et al] // InternationalJournal of Pharmaceutics. – 1998. – N. 170.
– P. 169-177.171. Strübing S., Metz H., Mäder K. Characterization of poly(vinyl acetate) basedfloating matrix tablets // Journal of Controlled Release. – 2008. – Vol 2. – N. 126.– P. 149–155.172. Tapaswi Rani Dash, Pankaj Verma. Matrix Tablets: An Approach towardsOral Extended Release Drug Delivery // International Journal of Pharma Research& Review. - 2012. – N. 2. - P. 12 - 24.209173. Technical Information-Quickstart. EUDRAGIT® L 100 and/or S 100. EvonikIndustries AG.- 2011. – Vol. 30.
– 2 p.174. The role of oral controlled release matrix tablets in drug delivery systems /AliNokhodchi, S. Raja, P. Patel [et al] // BioImpacts. - 2012. - N. 2. - P. 175-187.175. The role of compression force in floating tablet formula optimization / P.Colombo, D. Provasi, M. G. Borazza [et al] // Acta Pharmaceutica Technologica. –1989. – N. 35. –P. 168–170.176. Timmins P., Pygall S.R., Melia C.D.
Hydrophilic Matrix Tablets for OralControlled Release. – New York: Springer, 2014. – 326 p.177. Timmermans J., Moës A.J. How well do floating dosage forms float? //International Journal of Parmaceutics. – 1990. – N. 62. – P. 207 – 216.178. Ungnade H., Lamb R.W. The Absorption Spectra of Benzoic Acid and Esters// Journal of American Chemistry Society. – 1952. – Vol.
15. - N. 74. –P. 3789–3794.179. US 2006/0159749 A1, Int. Cl. A61K 9/20. Controlled release and tastemaking oral pharmaceutical composition / Roberto Villa, Massimo Pedrani, MauroAjani, Lorenzo Fossati (IT); YOUNG & THOMPSON. № US 2006/0159749 ;Appl. No.: 11/378,378; publ. date Jul. 20, 2006. 4 p.180. Using METHOCEL Cellulose Ethers for Controlled Release of Drugs inHydrophilicMatrixSystems[Электронный ресурс]. URL:http://www.colorcon.com/literature/marketing/mr/Extended%20Release/METHOCEL/English/hydroph_matrix_broch.pdf (дата обращения: 23.08.2016).181.
WO2007106960 A9. Controlled-release floating dosage forms VanderbistFr., Baudier Ph., Deboeck A., Amighi K., Goole J. (Laboratoires Smb S.A,Belgium) Publication date: 2007-09-27.182. WO/2007/106957. IPC: A61K 9/46, A61K 9/00, A61K 9/20. MULTIPLEUNITS CONTROLLED-RELEASE FLOATING DOSAGE FORMS. VanderbistFr., Baudier Ph., Deboeck A., Amighi K., Goole J. (Laboratoires Smb S.A,Belgium) Publication date: 2007-09-27.210183. Wilson C.
G., P. J. Crowley. Controlled Release in Oral Drug Delivery. NewYork: Springer, 2011. – 414 p.184. Yang L, Fassihi R. Examination of drug solubility, polymer types,hydrodynamics and loading dose on drug release behaviour from a triple-layerasymmetricconfigurationdeliverysystem//InternationalJournalofPharmaceutics. -1997. – N. 155. – P.
219–29.185. Yang W.-W., Pierstorff E. Reservoir-Based Polymer Drug Delivery Systems// Journal of Laboratory Automation. – 2012. – Vol. 17. – N. 1. – P. 50-58.186. Yoon Yeo, Kinam Park. A new microencapsulation method using anultrasonic atomizer based on interfacial solvent exchange // Journal of ControlledRelease. - 2004.
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