References
- Abdalla AA, Ahmed UM, Ahmed R, et al. (2009). Physicochemical characterization of traditionally extracted Pearl Millet Starch (Jir). J Appl Sci Res 5:2016–27
- Abu-lazza KA, Vincent LH, Jee LL, et al. (2004). Fast dissolving tablet. US Patent, 6733781
- Adebayo AS, Itiola OA. (1998a). Evaluation of breadfruit and cocoyam starches as exodisintegrants in a paracetamol tablet formulation. Pharm Pharmacol Commun 4:385–9
- Adebayo AS, Itiola OA. (1998b). Properties of starches obtained from Colocasia esculenta and Artocarpus communis. Nig J Nat Prod Med 2:29–33
- Alais C, Linden G. (1999). Food Biochemistry. Frederick (MD): Aspen Publishers, 38–51
- Anonymous (2009). Starch 1500, partially pregelatinized maize starch. Colorcon technical literature. Available from: http://www.colorcon.com/literature/marketing/ex/Starch%201500/ads_starch_1500_used_bind_dis_v3_06_2009.pdf [last accessed 15 May 2013].
- Beleia A, Varriano-marston E, Hoseney RC. (1980). Characterization of starches from pearl millets. Cereal Chem 57:300–3
- Block LH, Moreton RC, Apte SP, et al. (2009). Co-processed excipients. In: Pharmacopeial Forum, vol. 35. Maryland, USA: United States Pharmacopeia Convention Inc, 1026–8
- Bos CE, Bolhuis GK, Van Doorne H, Lerk CF. (1987). Native starch in tablet formulations: Properties on compaction. Pharm Week Sci 9:274–82
- Caramella C, Colombo P, Conte U, et al. (1984). The role of swelling in the disintegration process. Int J Pham Tech Prod Mfr 5:1–5
- Dalziel JM. (1948). The Useful Plants of West Tropical Africa. London: Crown Agents for Overseas Governments and Administrations
- Deshpande AV, Panya LV. (1987). Evaluation of sorghum starch as a tablet disintegrant and binder. J Pharm Pharmacol 39:495–6
- Garr JS, Bangudu AB. (1991). Evaluation of sorghum starch as a tablet excipient. Drug Dev Ind Pharm 17:1–6
- Guyot-Hermann AM. (1992). Table disintegrant and disintegrating agents. STP Pharm Sci 2:445–62
- Hussain MSH, York P, Timmins P, Humphrey P. (1990). Secondary ion mass spectrometry (SIMS) evaluation of magnesium stearate distribution and its effects on the physico-technical properties of sodium chloride tablets. Powder Technol 60:39–45
- Jarosz PJ, Parrot EL. (1984). Effect of lubricants on tensile strength of tablets. Drug Dev Ind Pharm 10:259–73
- Jian-Xin LI, Brian C, Thomas R. (2008). Co-processed microcrystalline cellulose and sugar alcohol as an excipient for tablet formulations. Applicant: FMC Corp. (US), European Patent Office, Patent No. US20080131505
- Jivraj M, Martini LG, Thomson MC. (2000). An overview of the different excipients useful for the direct compression of tablets. Pharm Sci Technol Today 3:58–63
- Kottke MK, Rhodes CT. (1991). Limitations of presently available in vitro release data for the prediction of in vivo performance. Drug Dev Ind Pharm 17:1157–76
- Moore JW, Flanner HH. (1996). Mathematical comparison of dissolution profile. Pharm Tech 20:64–74
- Olayemi OJ, Oyi AR, Allagh TS. (2008). Comparative evaluation of maize, rice and wheat starch powders as pharmaceutical excipients. Nig J Pharm Sci 7:154–61
- Quadir A, Kolter K. (2006). A comparative study of current superdisintegrants. Pharm Tech 30:PS38–42
- Rees JE, Tsardaka KD. (1994). Some effects of moisture on the viscoelastic behaviour of modified starch during powder compaction. Eur J Pharm Biopharm 40:193–7
- Rowe RC. (1989). Surface free energy and polarity effects in the granulation of a model system. Int J Pharm 53:75–8
- Schwartz JB, Martin ET, Deliner EJ. (1975). Intragranular starch: Comparison of starch U.S.P and modified corn starch. J Pharm Sci 64:328–32
- Shangraw RF. (1992). International Harmonization of Compendia Standards for pharmaceutical excipients. In: Crommelin DJA, Midha K, eds. Topics in Pharmaceutical Science. Germany, Stuttgart: Medpharm Scientific Publishers, 205–23
- Sherwood BE, Hunter EA, Staniforth JH. (1996). Pharmaceutical excipient having improved compressibility. Applicant: Edward H Mendell Co. Inc. (US), United States Patent Office, Patent No. 5,585,115
- Stanley-Wood NG, Shubair MS. (1979). The influence of binder concentration on the bond formation of pharmaceutical granules. J Pharm Pharmacol 31:429–33
- Tester RF, Karkalas J, Qi X. (2004). Starch composition, fine structure and architecture (review). J Cereal Sci 39:151–65
- USP 36-NF 31. 2013. The United States Pharmacopoeia – The National Formulary. Rockville (MD): The United States Pharmacopoeial Convention, Inc
- Uhumwangho MU, Okor RS, Eichie FE, Abbah CM. (2006). Influence of some starch binders on the brittle fracture tendency of paracetamol tablets. Afr J Biotech 5:1950–3
- Westerhuis JA, De Haan P, Zwinkels J, et al. (1996). Optimisation of the composition and production of mannitol/microcrystalline cellulose tablets. Int J Pharm 143:151–62
- Yamini K, Chalapathi V, Reddy NL, et al. (2011). Formulation of diclofenac sodium tablets using tapioca starch powder – A promising binder. J Appl Pharm Sci 1:125–7
- Zhao N, Augsburger LL. (2005). The influence of swelling capacity of superdisintegrants in different pH media on the dissolution of hydrochlorothiazide form directly compressed tablets. AAPS Pharm Sci Tech 6:E120–6