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    المصدر: Revista Colombiana de Ciencias Químico-Farmacéuticas; Vol. 49 Núm. 2 (2020) ; Revista Colombiana de Ciencias Químico-Farmacéuticas; v. 49 n. 2 (2020) ; Revista Colombiana de Ciencias Químico-Farmacéuticas; Vol. 49 No. 2 (2020) ; 1909-6356 ; 0034-7418

    وصف الملف: application/pdf

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Jana, A comprehensive physicochemical, thermal, and spectroscopic characterization of zinc (II) chloride using X-ray diffraction, particle size distribution, differential scanning calorimetry, thermogravimetric analysis/differential thermogravimetric analysis, ultraviolet-visible, and Fourier transform-infrared Spectroscopy, Int. J. Pharm. Investig., 7, 33-40 (2017).; R.S. Leite, R.O. Macedo, S.M. Torres, C.C.N. Batista, L.O. Baltazar, S.A. Lima Neto, F.S. Souza, Evaluation of thermal stability and parameters of dissolution of nifedipine crystals, J. Therm. Anal. Calorim., 111, 2117-2123 (2013).; R.C. Silva, F.S. Semaan, C. Novák, E.T.G. Cavalheiro, Thermal behavior of furosemide, J. Therm. Anal. Calorim., 111, 1933-1937 (2013).; M.A. Oliveira, M.I. Yoshida, E.C.L. Gomes, Thermal analysis applied to pharmaceuticals and pharmaceutical formulations in the pharmaceutical industry, Quím. Nova, 34, 1224-1230 (2011).; D. Grooff, M.M. De Villiers, W. Liebenberg, Thermal methods for evaluating polymorphic transitions in nifedipine, Thermochim. Acta, 454, 33-42 (2007).; I. Jendrzejewska, P. Zajdel, E. Pietrasik, Z. Barsova, T. Goryczka, Application of X-ray powder diffraction and differential scanning calorimetry for identification of counterfeit drugs, Monatsh. Chem., 149, 977-985 (2018).; S.C. Jagdale, V.N. Jadhav, A.R. Chabukswar, B.S. Kuchekar, Solubility enhancement, physicochemical characterization and formulation of fast-dissolving tablet of nifedipine-betacyclodextrin complexes, Braz. J. Pharm. Sci., 48, 131-145 (2012).; M. Gallignani, R.A. Rondón, J.F. Ovalles, M.R. Brunetto, Transmission FTIR derivative spectroscopy for estimation of furosemide in raw material and tablet dosage form, Acta Pharm. Sin. B, 4, 376-383 (2014).; C. Sharma, P.N. Badyal, R.K. Rawal, Simultaneous estimation of hydrochlorothiazide, hydralazine hydrochloride, and reserpine using PCA, NAS, and NAS-PCA, Sci. Pharm., 83, 599-610 (2015).; S.K. Dinakaran, B. Alluria, K.R. Annareddy, V.S. Ayyagari, H. Avasarala, R. Kakaraparthy, P.K. Chintamaneni, R. Gadi, Spectrophotometric method development and validation for atorvastatin calcium and nifedipine HCl in bulk and tablet dosage form using absorption ratio method assay of atorvastatin and nifedipine, J. Pharm. Res., 7, 666-669 (2013).; E. Vaculikova, A. Cernikova, D. Placha, M. Pisarcik, P. Peikertova, K. Dedkova, F. Devinsky, J. Jampilek, Preparation of hydrochlorothiazide nanoparticles for solubility enhancement, Molecules, 21, 1005 (2016).; M.H. Shariare, M.A. Altamimi, A.L. Marzan, R. Tabassum, B. Jahan, H.M. Reza, M. Rahman, G.U. Ahsan, M. Kazi, In vitro dissolution and bioavailability study of furosemide nanosuspension prepared using design of experiment (DoE), Saudi Pharm. J., 27, 96-105 (2019).; Y. Tsume, D.M. Mudie, P. Langguth, G.E. Amidon, G.L. Amidon, The biopharmaceutics classification system: subclasses for in vivo predictive dissolution (IPD) methodology and IVIVC, Eur. J. Pharm. Sci., 57, 152-163 (2014).; G.L. Amidon, H. Lennernas, V.P. Shah, J.R. Crison, A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability, Pharm. Res., 12, 413-420 (1995).; R. Ghadi, N. Dand, BCS class IV drugs: highly notorious candidates for formulation development, ‎J. Control. Release, 248, 71-95 (2017).; C.C. Chung, Biopharmaceutical innovation system and the influence of policies: the case of Taiwan (2000-2008), Int. J. Health Policy Manag., 1, 125-130 (2013).; J. Cook, W. Addicks, Y.H. Wu, Application of the biopharmaceutical classification system in clinical drug development—an industrial view, AAPS J., 10, 306-310 (2008).; National List of Essential Medicines (RENAME) 2020, Ministry of Health of Brazil, URL: http://portalarquivos2.saude.gov.br/images/pdf/2019/dezembro/24/Rename-2020-final.pdf, accessed December 2019.; Brazilian Health Surveillance Agency (ANVISA), Concepts and definitions of medicines, Ministry of Health of Brazil, URL: http://portal.anvisa.gov.br/medicamentos/conceitos-e-definicoes, accessed December 2019.; C. Barata-Silva, R.A. Hauser-Davis, A.L.O. Silva, J.C. Moreira, Challenges to drug quality control in Brazil, Cad. Saúde Colet., 25, 362-370 (2017).; Brazilian Pharmacopeia, 6rd ed., Brazilian Health Surveillance Agency (ANVISA), Brasília, Brazil, 2019.; M.S. Ferreira, L.C.M.G. Viana, R.A. Matos, R.R. Sá, F.A.S. Silva, M.D. Mota, E.C.L. Cazedey, H.I.F. Magalhães, A.F. Santos Júnior, Comparative in vitro analysis of dissolution profiles of furosemide tablets marketed in Bahia, Brazil, Lat. Am. J. Pharm., 35, 2064-2070 (2016).; L.C.M.G. Viana, M.S. Ferreira, M.D. Mota, H.I.F. Magalhães, A.F. Santos Júnior, Study of dissolution profiles and disintegration of tablets containing hydrochlorothiazide marketed in Bahia, Brazil, Lat. Am. J. Pharm., 34, 2010-2015 (2015).; The United States Pharmacopeia, 41rd ed. (USP 41), United States Pharmacopeial Convention, Rockville, Maryland, USA, 2018.; K.A. Khan, The concept of dissolution efficiency, J. Pharm. Pharmacol., 27, 48-49 (1975).; Brazilian Health Surveillance Agency (ANVISA), Resolution of the Board of Directors - RDC No. 166., Ministry of Health of Brazil, URL: https://www20.anvisa.gov.br/coifa/pdf/rdc166.pdf, accessed December 2019.; International Conference on Harmonization (ICH), Technical Requirements for Registration of Pharmaceuticals for Human Use - Validation of Analytical Procedures: Text and Methodology Q2(R1), URL: https://database.ich.org/sites/default/files/Q2_R1__Guideline.pdf, accessed January 2020.; R.A. Saber, A.K. Attia, W.M. Salem, Thermal analysis study of antihypertensive drugs telmisartan and cilazapril, Adv. Pharm. Bull., 4, 283-287 (2014).; L.C.S. Cides, A.A.S. Araújo, M. Santos-Filho, J.R. Matos, Thermal behaviour, compatibility study and decomposition kinetics of glimepiride under isothermal and non-isothermal conditions, J. Therm. Anal. Calorim., 84, 441-445 (2006).; C.M.P. Souza, J.A.B. Santos, A.L. Nascimento, J.V. Chaves Júnior, F.J.L. Ramos Júnior, S.A. Lima Neto, F.S. Souza, R.O. Macedo, Thermal analysis study of solid dispersions hydrochlorothiazide, J. Therm. Anal. Calorim., 131, 681-689 (2018).; R.O. Macedo, T.G. Nascimento, J.W.E. Veras, Comparison of generic hydrochlorothiazide formulations by means of TG and DSC coupled to a photovisual system, J. Therm. Anal. Calorim., 64, 757-763 (2001).; R.O.C. Filho, P.I.B.M. Franco, E.C. Conceição, M.I.G. Leles, Stability studies on nifedipine tablets using thermogravimetry and differential scanning calorimetry, J. Therm. Anal. Calorim., 97, 343-347 (2009).; K. Egusa, F. Okazaki, J. Schiewe, U. Werthmann, M. Wolkenhauer, Identification of polymorphic forms of active pharmaceutical ingredient in low-concentration dry powder formulations by synchrotron X-Ray powder diffraction, Drugs R D., 17, 413-418 (2017).; S. Shin, J. Kim, Physicochemical characterization of solid dispersion of furosemide with TPGS, Int. J. Pharm., 251, 79-84 (2003).; C. Garnero, A.K. Chattah, M. Longhi, Stability of furosemide polymorphs and the effects of complex formation with β-cyclodextrin and maltodextrin, Carbohyd. Polym., 152, 598-604 (2016).; C. Garnero, A.K. Chattah, M. Longhi, Supramolecular complexes of maltodextrin and furosemide polymorphs: a new approach for delivery systems, Carbohyd. Polym., 94, 292-300 (2013).; M.M. Villiers, J.G. Watt, A.P. Lötter, Kinetic study of the solid-state photolytic degradation of two polymorphic forms of Furosemide, Int. J. Pharm., 88, 275-283 (1992).; Y. Matsuda, E. Tatsumi, Physicochemical characterization of furosemide modifications, Int. J. Pharm., 60, 11-26 (1990).; S.A. El-Gizawy, M.A. Osman, M.F. Arafa, G.M. El Maghraby, Aerosil as a novel co-crystal co-former for improving the dissolution rate of Hydrochlorothiazide, Int. J. Pharm., 478, 773-778 (2015).; J.M. Aceves-Hernández, E. Agacino-Valdés, M. Paz, J. Hinojosa-Torres, Experimental and theoretical study of the conformational analysis of Hydrochlorothiazide, J. Mol. Struct., 786, 1-8 (2006).; N.T. Chinh, N.T.T. Trang, N.V. Giang, D.T.M. Thanh, T.T.X. Hang, N.Q. Tung, C.Q. Truyen, P.M. Quan, P.Q. Long, T. Hoang, In vitro nifedipine release from poly(lactic acid)/chitosan nanoparticles loaded with nifedipine, J. Appl. Polym. Sci., 133, 43330 (2016).; M.E. Brown, B.D. Glass, M.S. Worthington, Binary systems of nifedipine and various cyclodextrins in the solid state. Thermal, FTIR, XRD studies, J. Therm. Anal. Calorim., 68, 631-646 (2002).; A.A. Bunaciu, H.Y. Aboul-Enein, S. Fleschin, Application of Fourier transform infrared spectrophotometry in pharmaceutical drugs analysis, Appl. Spectrosc. Rev., 45, 206-219 (2010).; C. Doherty, P. York, Fresemide crystal forms; solid state and physicochemical analyses, Int. J. Pharm., 47, 141-155 (1988).; R.N. Sonpal, P.K. Shelat, A.N. Lalwani, Solubility enhancement of hydrochlorothiazide using a novel drug-drug solid dispersion technology, Int. J. Pharm. Sci. Nanotech., 8, 2924-2936 (2015).; R. Razzaq, N.M. Ranjha, Z. Rashid, B. Nasir, Preparation, and evaluation of novel pH-sensitive poly(butyl acrylate-co-itaconic acid) hydrogel microspheres for controlled drug delivery, Adv. Polym. Tech., 37, 21663 (2018).; R.G. Ricarte, T.P. Lodge, M.A. Hillmyer, Detection of pharmaceutical drug crystallites in solid dispersions by transmission electron microscopy, Mol. Pharmaceutics, 12, 983-990 (2015).; A. Mantas, A.T. Mihranyan, Immediate-release nifedipine binary dry powder mixtures with nanocellulose featuring enhanced solubility and dissolution rate, Pharmaceutics, 11, E37 (2019).; M.H. Sadr, H. Nabipour, Preparation and identification of furosemide nanoparticles, J. Basic Appl. Sci. Res., 3, 666-670 (2013).; F. Osei-Yeboah, C.C. Sun, Validation and applications of an expedited tablet friability method, Int. J. Pharm., 484, 146-155 (2015).; S. Paul, C.C. Sun, The suitability of common compressibility equations for characterizing plasticity of diverse powders, Int. J. Pharm., 532, 124-130 (2017).; A. Pignato, C.R. Birnie, Analysis of compounded pharmaceutical products to teach the importance of quality in an applied pharmaceutics laboratory course, Am. J. Pharm. Educ., 78, 61 (2014).; A.D. Rajkumar, G.K. Reynolds, D. Wilson, S. Wren, M.J. Hounslow, A.D. Salman, Investigating the effect of processing parameters on pharmaceutical tablet disintegration using a real-time particle imaging approach, Eur. J. Pharm. Biopharm., 106, 88-96 (2016).; L.A.L. Soares, P.C. Schmidt, G.G. Ortega, P.R. Petrovick, Effect of compression strength and speed on the properties of tablets containing high concentration of dry plant extract, Acta Farm. Bonaerense, 22, 147-154 (2003).; A.C. Lima, D.C. Michelin, M.R.C. Santos, M.O. Paganelli, R.F. Ignácio, M.V. Chaud, Compression force and humidity on hydrochlorothiazide dissolution profile, Acta Farm. Bonaerense, 25, 104-107 (2006).; O. Anand, L.X. Yu, D.P. Conner, B.M. Davit, Dissolution testing for generic drugs: an FDA perspective, AAPS J., 13, 328-335 (2011).; D. Rumel, S.A. Nishioka, A.A.M. Santos, Drug interchangeability: clinical approach and consumer's point of view, Rev. Saude Publica, 40, 921-927 (2006).; J. Menegola, M. Steppe, E.E.S. Schapoval, Dissolution test for citalopram in tablets and comparison of in vitro dissolution profiles, Eur. J. Pharm. Biopharm., 67, 524-530 (2007).; Brazilian Health Surveillance Agency (ANVISA), Resolution of the Board of Directors (RDC) N.° 31, Ministry of Health of Brazil, URL: http://portal.anvisa.gov.br/documents/33880/2568070/res0031_11_08_2010.pdf/5e157d15-d3d5-4bb9-98db-5667e4d9e0c8, accessed December 2019.; K.J. Souza, P.V. Aléssio, A.J.P.S. Gomes, Specific excipient development for prepared nifedipine capsules masterfully: part I, Rev. Cienc. Farm. Básica Apl., 30, 257-261 (2009).; E.K. De Maria, A.J.P.S. Gomes, Nifedipine manipulated or pharmaceutical specialty? In vitro study, Rev. Eletronica Farm., 5, 31-36 (2008).; G.S. Silveira, L.D. Silva, V.C.F. Mosqueira, J. Souza, Biopharmaceutical evaluation of reference, generic, similar and magisterial medicines containing furosemide, one lower solubility and lower permeability drug, Rev. Bras. Farm., 92, 306-313 (2011).; M.A. Lamolha, A.C.P. Rodrigues, B.C. Silva, F.C. Granata, G.S. Podavin, J.C.O. Lima, Evaluation of pharmaceutical equivalence of furosemide 40mg tablets, Rev. Bras. Farm., 93, 17-21 (2012).; F. Mahle, F. Goelzer, J. Adriano, M. Felippe, N. Vier, R.B.G. Carli, T. Rosa, A.G. Couto, R.M. Lucinda-Silva, Evaluation of the tablet dissolution profile of hydrochlorothiazide marketed in Brazil, Rev. Cienc. Farm. Basica Apl., 28, 265-271 (2007).; M.S. Lee, C.L. Huang, S.H. Huang, Y.P. Chen, C.J. Chen, K.C. Wen, A comparative study on the dissolution profiles of commercial hydrochlorothiazide tablets, J. Food Drug. Anal., 10, 18-24 (2002).; https://revistas.unal.edu.co/index.php/rccquifa/article/view/89486

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    المساهمون: Conselho Nacional de Desenvolvimento Científico e Tecnológico, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

    المصدر: Analytical Methods ; volume 12, issue 13, page 1711-1719 ; ISSN 1759-9660 1759-9679

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