Improvement of sticking in tablet compaction for tocopherol acetate

References

• Takeuchi H, Sasaki H, Niwa T, Hino T, Kawashima Y, Uesugi K et al. (1991). Redispersible dry emulsion system as novel oral dosage form of oily drugs: in vivo studies in beagle dogs. Chem Pharm Bull, 39:3362–3364.
   PubMed Web of Science ®Google Scholar
• Kimura T, Fukui E, Kageyu A, Kurohara H, Kurosaki Y, Nakayama T et al. (1989). Enhancement of oral bioavailability of d-alpha-tocopherol acetate by lecithin-dispersed aqueous preparation containing medium-chain triglycerides in rats. Chem Pharm Bull, 37:439–441.
   PubMed Web of Science ®Google Scholar
• Takeuchi H, Sasaki H, Niwa T, Hino T, Kawashima Y, Uesugi K et al. (1992). Design of redispersible dry emulsion as an advanced dosage form of oily drug (vitamin E nicotinate) by spray-drying technique. Drug Dev Ind Pharm, 18:919–937.
   Web of Science ®Google Scholar
• James S, James CB. (2002). Encyclopedia of Pharmaceutical Technology, 2nd ed. Marcel Dekker, New York, p. 2669.
   Google Scholar
• Schmidt Von PC, Stefens KJ, Kneble G. (1983). Vereinfachung der registrierung physikalischer parameter bei der tabletterrung. Pharm Ind, 45:800–805.
   Google Scholar
• Naito SI, Nakamichi K. (1969). Studies on techniques of manufacturing pharmacy. I. Prediction of tableting troubles such as capping and sticking. 1. Chem Pharm Bull, 17:2507–2514.
   PubMed Web of Science ®Google Scholar
• Naito S, Shimizu I, Iwaki S. (1971). Techniques for manufacturing pharmacy. II. Prediction of tableting troubles such as capping and sticking. 2. Chem Pharm Bull, 19:1949–1956.
   PubMed Web of Science ®Google Scholar
• Naito SI, Masui K, Shiraki T. (1977). Prediction of tableting problems such as capping and sticking: theoretical calculations. j Pharm Sci, 66:254–259.
   PubMed Web of Science ®Google Scholar
• Toyoshima K, Yasumura M, Onishi N, Ueda Y. (1988). Quantitative evaluation of tablet sticking by surface roughness measurement. Int J Pharm, 46:211–215.
   Web of Science ®Google Scholar
• Danjo K, Kojima S, Chen CY, Sunada H, Otsuka A. (1997). Effect of water content on sticking during compression. Chem Pharm Bull 45:706–709.
   Web of Science ®Google Scholar
• Kinoshita M, Baba K, Nagayasu A, Yamabe K, Shimooka T, Takeichi Y et al. (2002). Improvement of solubility and oral bioavailability of a poorly water-soluble drug, TAS-301, by its melt-adsorption on a porous calcium silicate. J Pharm Sci, 91:362–370.
   PubMed Web of Science ®Google Scholar
• Oguchi T, Tozuka Y, Okunogi S, Yonemochi E, Yamamoto K. (1997). Improved dissolution of naproxen from Sohd dispersions with porous additives. J Pharm Sci Technol Jpn, 57:168–173.
   Google Scholar
• Takeuchi H, Nagira S, Yamamoto H, Kawashima Y. (2004). Solid dispersion particles of tolbutamide prepared with fine silica particles by the spray-drying method. Powder Tech, 141:187–195.
   Web of Science ®Google Scholar
• Takeuchi H, Nagira S, Yamamoto H, Kawashima Y. (2005). Solid dispersion particles of amorphous indomethacin with fine porous silica particles by using spray-drying method. Int J Pharm, 288:177–183.
   Google Scholar
• Gupta MK, Vanwert A, Bogner RH. (2003). Formation of physically stable amorphous drugs by milling with Neusilin. J Pharm Sci, 92:536–551.
   PubMed Web of Science ®Google Scholar
• Byrne RS, Deasy PB. (2002). Use of commercial porous ceramic particles for sustained drug delivery. Int J Pharm, 246:61–73.
   PubMed Web of Science ®Google Scholar
• Ito Y, Arai H, Uchino K, Iwasaki K, Shibata N, Takada K. (2005). Effect of adsorbents on the absorption of lansoprazole with surfactant. Int J Pharm, 289:69–77.
   PubMed Web of Science ®Google Scholar
• Jain SK, Agrawal GP, Jain NK. (2007). Porous carrier based floating granular delivery system of repaglinide. Drug Dev Ind Pharm, 37:381–391.
   Google Scholar
• Streubel A, Siepmann J, Bodmeier R. (2002). Floating microparticles based on low density foam powder. Int J Pharm, 241:279–292.
   PubMed Web of Science ®Google Scholar
• Streubel A, Siepmann J, Bodmeier R. (2003). Floating matrix tablets based on low density foam powder: effects of formulation and processing parameters on drug release. Eur J Pharm Sci, 18:37–45.
   PubMed Web of Science ®Google Scholar
• Yuasa H, Takashima Y, Kanaya Y. (1996). Studies on the development of intragastric floating and sustained release preparation. I. Application of calcium silicate as a floating carrier. Chem Pharm Bull, 44:1361–1366.
   Web of Science ®Google Scholar
• Yuasa H, Akutagawa M, Hashizume T, Kanaya Y. (1996). Studies on internal structure of tablets. VI. Stress dispersion in tablets by excipients. Chem Pharm Bull, 44:378–382.
   PubMed Web of Science ®Google Scholar
• Yuasa H, Asahi D, Takashima Y, Kanaya Y, Shinozawa K. (1994). Application of calcium silicate for medicinal preparation. I. Solid preparation adsorbing an oily medicine to calcium silicate. Chem Pharm Bull, 42:2327–2331.
   PubMed Web of Science ®Google Scholar
• Ali AS, Yamamoto K, El-sayed AM, Habib FS, Nakai Y. (1992). Molecular behavior of flufenamic acid in physical and ground mixtures with florite. Chem Pharm Bull, 40:1289–1294.
   Web of Science ®Google Scholar
• Ekgasit S, Pattayakorn N, Tongsakul D, Thammacharoen C, Kongyou T. (2007). A novel ATR FT-IR microspectroscopy technique for surface contamination analysis without interference of the substrate. Anal Sci, 23:863–868.
   PubMed Web of Science ®Google Scholar
• Planinsek O, Planinsek D, Zega A, Breznik M, Srcic S. (2006). Surface analysis of powder binary mixtures with ATR FTIR spectroscopy. Int J Pharm, 319:13–19.
   PubMedGoogle Scholar
• Tocopherol acetate monograph in JP XV, p. C-2705-9.
   Google Scholar
• Madsen AØ, Sørensen HO, Flensburg C, Stewart RF, Larsen S. (2004). Modeling of the nuclear parameters for H atoms in X-ray charge–density studies. Acta Crystallogr, A, Found Crystallogr, 60:550–561.
   PubMed Web of Science ®Google Scholar
• Xylitol monograph in JP XV, p. C-1040-5.
   Google Scholar
• Kim KH, Frank MJ, Henderson NL. (1985). Application of differential scanning calorimetry to the study of solid drug dispersions. J Pharm Sci, 74:283–289.
   PubMed Web of Science ®Google Scholar
• Konno T, Kinuno K, Kataoka K. (1986). Physical and chemical changes of medicinals in mixtures with adsorbents in the solid state. I. Effect of vapor pressure of the medicinals on changes in crystalline properties. Chem Pharm Bull, 34:301–307.
   PubMed Web of Science ®Google Scholar
• Konno T, Kinuno K. (1989). Physical and chemical changes of medicinals in mixtures with adsorbents in the solid state. II. Application of reduced pressure treatment for the improvement of dissolution of flufenamic acid. Chem Pharm Bull, 37:2481–2484.
   PubMed Web of Science ®Google Scholar
• Nakai Y, Yamamoto K, Terada K, Oguchi T, Yamamoto M. (1987). [Study of the interaction between light anhydrous silicic acid and drugs]. Yakugaku Zasshi, 107:294–300.
   PubMed Web of Science ®Google Scholar
• Ali AS, Yamamoto K, El-sayed AM, Habib FS, Nakai Y. (1992). Molecular interaction between benzoic acid and florite and complex formation. Chem Pharm Bull, 40:467–471.
   Web of Science ®Google Scholar
• Nakai Y, Yamamoto K, Terada K, Ichikawa J. (1984). Interaction of medicinals and porous powder. I. Anomalous thermal behavior of porous glass mixtures. Chem Pharm Bull, 32:4566–4571.
   PubMed Web of Science ®Google Scholar
• Nakai Y, Yamamoto K, Terada K, Oguchi T, Izumikawa S. (1986). Interactions between crystalline medicinals and porous clay. Chem Pharm Bull, 34:4760–4766.
   PubMed Web of Science ®Google Scholar