Optimization of valsartan encapsulation in biodegradables polyesters using Box-Behnken design.
暂无分享,去创建一个
[1] Pınar Terzioğlu,et al. Application of Box-Behnken design for modeling of lead adsorption onto unmodified and NaCl-modified zeolite NaA obtained from biosilica. , 2017, Water science and technology : a journal of the International Association on Water Pollution Research.
[2] F. Dahmoune,et al. Full factorial design optimization of anti-inflammatory drug release by PCL-PEG-PCL microspheres. , 2016, Materials science & engineering. C, Materials for biological applications.
[3] Han‐Gon Choi,et al. Effects of Formulation Variables on the Particle Size and Drug Encapsulation of Imatinib-Loaded Solid Lipid Nanoparticles , 2016, AAPS PharmSciTech.
[4] Rameshwar K. Deshmukh,et al. The impact of preparation parameters on sustained release aceclofenac microspheres: A design of experiments , 2015 .
[5] A. Mokhtari,et al. Optimization of heavy metal removal from aqueous solutions by maghemite (γ-Fe2O3) nanoparticles using response surface methodology , 2014 .
[6] S. Honary,et al. Optimization of particle size and encapsulation efficiency of vancomycin nanoparticles by response surface methodology , 2014, Pharmaceutical development and technology.
[7] Khodir Madani,et al. Pistacia lentiscus leaves as a source of phenolic compounds: Microwave-assisted extraction optimized and compared with ultrasound-assisted and conventional solvent extraction , 2014 .
[8] Satyendra Mishra,et al. FORMULATION AND EVALUATION OF GLIPIZIDE LOADED NANOPARTICLES , 2013 .
[9] V. Rives,et al. Drug release from layered double hydroxides and from their polylactic acid (PLA) nanocomposites , 2013 .
[10] S. Etcheverry,et al. Computational study and spectroscopic investigations of antihypertensive drugs , 2012 .
[11] S. Etcheverry,et al. Dinuclear copper(II) complexes with valsartan. Synthesis, characterization and cytotoxicity. , 2012, Journal of inorganic biochemistry.
[12] Han‐Gon Choi,et al. Novel valsartan-loaded solid dispersion with enhanced bioavailability and no crystalline changes. , 2012, International journal of pharmaceutics.
[13] M.Bharathi,et al. Preparation and in vitro and in vivo characterization of valsartan loaded eudragit nanoparticles , 2012 .
[14] R. Manavalan,et al. Preparation and evaluation of sustained release loxoprofen loaded microspheres , 2011, Journal of basic and clinical pharmacy.
[15] D. N. Kumar,et al. Formulation and characterisation of valsartan proniosomes , 2011 .
[16] Patil Sv,et al. FORMULATION AND CHARACTERISTICS OF 5FLUROURACIL MICROSPHERES BY SOLVENT EVAPORATION METHOD , 2011 .
[17] S. Mandal,et al. Valsartan Loaded Solid Lipid Nanoparticles: Development, Characterization, and In vitro and Ex vivo Evaluation , 2011 .
[18] A. Husain,et al. Pharmacological and Pharmaceutical Profile of Valsartan: A Review , 2011 .
[19] D. Sakarkar,et al. Spherically agglomerated solid dispersions of valsartan to improve solubility, dissolution rate and micromeritic properties , 2010 .
[20] Hyo-Kyung Han,et al. Improved pH-independent dissolution and oral absorption of valsartan via the preparation of solid dispersion , 2010, Archives of pharmacal research.
[21] Han‐Gon Choi,et al. Development of valsartan-loaded gelatin microcapsule without crystal change using hydroxypropylmethylcellulose as a stabilizer , 2010, Drug delivery.
[22] R. Sinisterra,et al. Pharmaceutical Composition of Valsartan: β-Cyclodextrin: Physico–Chemical and Characterization Anti-Hypertensive Evaluation , 2010, Molecules.
[23] Kaan Yetilmezsoy,et al. Response surface modeling of Pb(II) removal from aqueous solution by Pistacia vera L.: Box-Behnken experimental design. , 2009, Journal of hazardous materials.
[24] S. Maiti,et al. Investigation on Processing Variables for the Preparation of Fluconazole-Loaded Ethyl Cellulose Microspheres by Modified Multiple Emulsion Technique , 2009, AAPS PharmSciTech.
[25] Kadam Vilasrao,et al. Solid state characterization of the inclusion complex of valsartan with methyl β-cyclodextrin , 2009 .
[26] J. Nedelec,et al. Effects of process parameters on the properties of biocompatible ibuprofen-loaded microcapsules. , 2009, International journal of pharmaceutics.
[27] P. Verma,et al. Preparation and in vitro characterization of Valsartan solid dispersions using skimmed milk powder as carrier. , 2009 .
[28] S. Lakshmanaprabu,et al. Formulation and evaluation of sustained release microspheres of rosin containing aceclofenac , 2009 .
[29] B. Ursekar,et al. Design, optimization, preparation and evaluation of dispersion granules of valsartan and formulation into tablets. , 2009, Current drug delivery.
[30] Hermínio C. de Sousa,et al. Preparation and characterization of flurbiprofen-loaded poly(3-hydroxybutyrate-co-3-hydroxyvalerate) microspheres , 2008, Journal of microencapsulation.
[31] A. Gupta,et al. New emerging trends in synthetic biodegradable polymers – Polylactide: A critique , 2007 .
[32] M. Paquot,et al. Les polymères issus du végétal : matériaux à propriétés spécifiques pour des applications ciblées en industrie plastique , 2006 .
[33] Hoo-Kyun Choi,et al. The effects of surfactants on the dissolution profiles of poorly water-soluble acidic drugs. , 2006, International journal of pharmaceutics.
[34] Yusuf Kaya,et al. Response surface optimization of the removal of nickel from aqueous solution by cone biomass of Pinus sylvestris. , 2006, Bioresource technology.
[35] A. Miro,et al. Improvement of Solubility and Stability of Valsartan by Hydroxypropyl-\boldbeta-Cyclodextrin , 2006 .
[36] Ranjana Gupta,et al. PLGA Nanoparticles of Anti Tubercular Drug: Drug Loading and Release Studies of a Water In-Soluble Drug , 2003 .
[37] D. Voinovich,et al. Gemfibrozil encapsulation and release from microspheres and macromolecular conjugates. , 2002, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[38] A. Lamprecht,et al. The preparation and evaluation of poly(ϵ-caprolactone) microparticles containing both a lipophilic and a hydrophilic drug , 2000 .
[39] J Gillard,et al. Preparation and characterization of protein-loaded poly(epsilon-caprolactone) microparticles for oral vaccine delivery. , 1999, International journal of pharmaceutics.
[40] C. Bastioli. Biodegradable materials — Present situation and future perspectives , 1998 .
[41] A. Coombes,et al. Protein-loaded poly(dl-lactide-co-glycolide) microparticles for oral administration: formulation, structural and release characteristics , 1997 .
[42] P. Sansdrap,et al. Influence of manufacturing parameters on the size characteristics and the release profiles of nifedipine from poly(DL-lactide-co-glycolide) microspheres , 1993 .
[43] 김성종,et al. Microencapsulation , 1974, Springer US.
[44] S. Takka,et al. BIOAVAILABILITY FILE: VALSARTAN , 2022 .