Characterization of Amorphous and Co-Amorphous Simvastatin Formulations Prepared by Spray Drying

In this study, spray drying from aqueous solutions, using the surface-active agent sodium lauryl sulfate (SLS) as a solubilizer, was explored as a production method for co-amorphous simvastatin–lysine (SVS-LYS) at 1:1 molar mixtures, which previously have been observed to form a co-amorphous mixture upon ball milling. In addition, a spray-dried formulation of SVS without LYS was prepared. Energy-dispersive X-ray spectroscopy (EDS) revealed that SLS coated the SVS and SVS-LYS particles upon spray drying. X-ray powder diffraction (XRPD) and differential scanning calorimetry (DSC) showed that in the spray-dried formulations the remaining crystallinity originated from SLS only. The best dissolution properties and a “spring and parachute” effect were found for SVS spray-dried from a 5% SLS solution without LYS. Despite the presence of at least partially crystalline SLS in the mixtures, all the studied formulations were able to significantly extend the stability of amorphous SVS compared to previous co-amorphous formulations of SVS. The best stability (at least 12 months in dry conditions) was observed when SLS was spray-dried with SVS (and LYS). In conclusion, spray drying of SVS and LYS from aqueous surfactant solutions was able to produce formulations with improved physical stability for amorphous SVS.

[1]  P. Kleinebudde,et al.  Preparation and characterization of spray‐dried co‐amorphous drug–amino acid salts , 2016, The Journal of pharmacy and pharmacology.

[2]  Xing Tang,et al.  Extruded Soluplus/SIM as an oral delivery system: characterization, interactions, in vitro and in vivo evaluations , 2014, Drug delivery.

[3]  T. Rades,et al.  Dissolution properties of co-amorphous drug-amino acid formulations in buffer and biorelevant media. , 2015, Die Pharmazie.

[4]  G. Marosi,et al.  Downstream processing of polymer-based amorphous solid dispersions to generate tablet formulations. , 2015, International journal of pharmaceutics.

[5]  L. S. Taylor,et al.  Impact of surfactants on the crystallization of aqueous suspensions of celecoxib amorphous solid dispersion spray dried particles. , 2015, Molecular pharmaceutics.

[6]  M. Videa,et al.  Stabilization of amorphous paracetamol based systems using traditional and novel strategies. , 2014, International journal of pharmaceutics.

[7]  Syed sajjad Hussen,et al.  Preparation and characterization of co-amorphous Ritonavir-Indomethacin systems by solvent evaporation technique: improved dissolution behavior and physical stability without evidence of intermolecular interactions. , 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[8]  C. Strachan,et al.  Amino acids as co-amorphous excipients for simvastatin and glibenclamide: physical properties and stability. , 2014, Molecular pharmaceutics.

[9]  Lynne S Taylor,et al.  Impact of surfactants on the crystal growth of amorphous celecoxib. , 2014, International journal of pharmaceutics.

[10]  Yun Hu,et al.  Mechanochemical Reaction of Sulfathiazole with Carboxylic Acids: Formation of a Cocrystal, a Salt, and Coamorphous Solids , 2014 .

[11]  C. Strachan,et al.  Inhibition of surface crystallisation of amorphous indomethacin particles in physical drug-polymer mixtures. , 2013, International journal of pharmaceutics.

[12]  C. Strachan,et al.  Amino acids as co-amorphous stabilizers for poorly water soluble drugs--Part 1: preparation, stability and dissolution enhancement. , 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[13]  Beom-Jin Lee,et al.  Current trends and future perspectives of solid dispersions containing poorly water-soluble drugs. , 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[14]  A. Jouyban,et al.  Drug–Drug Coamorphous Systems: Characterization and Physicochemical Properties of Coamorphous Atorvastatin with Carvedilol and Glibenclamide , 2013, Journal of Pharmaceutical Innovation.

[15]  R. O. Williams,et al.  Amorphous solid dispersions and nano-crystal technologies for poorly water-soluble drug delivery. , 2013, International journal of pharmaceutics.

[16]  Thomas Rades,et al.  Emerging trends in the stabilization of amorphous drugs. , 2013, International journal of pharmaceutics.

[17]  Jianjun Zhang,et al.  Coamorphous repaglinide-saccharin with enhanced dissolution. , 2013, International journal of pharmaceutics.

[18]  M. Tarnacka,et al.  A new way of stabilization of furosemide upon cryogenic grinding by using acylated saccharides matrices. The role of hydrogen bonds in decomposition mechanism. , 2013, Molecular pharmaceutics.

[19]  Hywel D Williams,et al.  Strategies to Address Low Drug Solubility in Discovery and Development , 2013, Pharmacological Reviews.

[20]  C. R. Rodrigues,et al.  Efavirenz Dissolution Enhancement I: Co-Micronization , 2012, Pharmaceutics.

[21]  Edward J. Donahue,et al.  To evaluate the effect of addition of an anionic surfactant on solid dispersion using model drug indomethacin , 2012, Drug development and industrial pharmacy.

[22]  R. Viana,et al.  Infrared Spectroscopy of Anionic, Cationic, and Zwitterionic Surfactants , 2012 .

[23]  C. Strachan,et al.  Co-amorphous simvastatin and glipizide combinations show improved physical stability without evidence of intermolecular interactions. , 2012, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[24]  K. Grzybowska,et al.  Enhancement of amorphous celecoxib stability by mixing it with octaacetylmaltose: the molecular dynamics study. , 2012, Molecular pharmaceutics.

[25]  Akash Jain,et al.  Selection of oral bioavailability enhancing formulations during drug discovery , 2012, Drug development and industrial pharmacy.

[26]  M. Brewster,et al.  Supersaturating drug delivery systems: fast is not necessarily good enough. , 2012, Journal of pharmaceutical sciences.

[27]  W. Qian,et al.  Solid dispersions in the form of electrospun core-sheath nanofibers , 2011, International journal of nanomedicine.

[28]  Wouter L J Hinrichs,et al.  Improved dissolution behavior of lipophilic drugs by solid dispersions: the production process as starting point for formulation considerations , 2011, Expert opinion on drug delivery.

[29]  T. Ehtezazi,et al.  The effect of spray drying on the compaction properties of hypromellose acetate succinate , 2011, Drug development and industrial pharmacy.

[30]  M. Khan,et al.  Influence of Formulation and Processing Factors on Stability of Levothyroxine Sodium Pentahydrate , 2010, AAPS PharmSciTech.

[31]  O. Abdel-Kareem,et al.  Morphological, Rheological and Ultrasonic Characterizations of ECO- Friendly Microemulsion Lattices Based on Acrylate Monomers. , 2010 .

[32]  G. Van den Mooter,et al.  Review: physical chemistry of solid dispersions. , 2009, The Journal of pharmacy and pharmacology.

[33]  S. Bhise,et al.  Formulation and Evaluation of Novel FDCs of Antitubercular Drugs , 2009 .

[34]  G. Gupta,et al.  A Discriminatory and Biorelevant Dissolution Test Method for Simvastatin Drug Products , 2009 .

[35]  Patrick J. Marsac,et al.  Estimation of Drug–Polymer Miscibility and Solubility in Amorphous Solid Dispersions Using Experimentally Determined Interaction Parameters , 2008, Pharmaceutical Research.

[36]  Patrick J. Marsac,et al.  A Comparison of the Physical Stability of Amorphous Felodipine and Nifedipine Systems , 2006, Pharmaceutical Research.

[37]  P. Sinko Martin's Physical Pharmacy and Pharmaceutical Sciences , 2005 .

[38]  K. Mahadik,et al.  Spray-Dried Amorphous Solid Dispersions of Simvastatin, a Low Tg Drug: In Vitro and in Vivo Evaluations , 2005, Pharmaceutical Research.

[39]  Y. Kawashima,et al.  Solid dispersion particles of tolbutamide prepared with fine silica particles by the spray-drying method , 2004 .

[40]  F. Sadeghi,et al.  Increasing the Aqueous Solubility of Acetaminophen in the Presence of Polyvinylpyrrolidone and Investigation of the Mechanisms Involved , 2003, Drug development and industrial pharmacy.

[41]  E. Franses,et al.  Infrared reflection absorption spectroscopy (IRRAS) of aqueous nonsurfactant salts, ionic surfactants, and mixed ionic surfactants , 2002 .

[42]  D. Shah,et al.  On the measurement of critical micelle concentrations of pure and technical-grade nonionic surfactants , 2000 .

[43]  M. Malmsten,et al.  Spray-drying of trypsin - surface characterisation and activity preservation. , 1999, International journal of pharmaceutics.

[44]  G. Winter,et al.  Formulation of proteins in vacuum-dried glasses. II. Process and storage stability in sugar-free amino acid systems. , 1999, Pharmaceutical development and technology.

[45]  T. Kawai,et al.  Fourier Transform Infrared Study on the Phase Transitions of a Sodium Dodecyl Sulfate-Water System , 1983 .

[46]  D. E. Cadwallader,et al.  Effect of macromolecules on aqueous solubility of cholesterol and hormone drugs. , 1981, Journal of pharmaceutical sciences.