Preparation of fast-dissolving tablets based on mannose

Recent developments in fast dissolving (or fast disintegrating) tablets have brought convenience in dosing to elderly and children, who have trouble swallowing tablets. Fast-dissolving tablets dissolve or disintegrate in the mouth without any extra fluid, and so they are highly useful for those who need to take medicine in the absence of water. The key properties of fast-dissolving tablets are fast absorption of water into the core of tablets and disintegration of associated particles into individual components for fast dissolution. The strategy of making fast-dissolving tablets presented in this study is based on using carbohydrates that have extremely high water solubility. D-Mannose is a naturally occurring sugar with aqueous solubility of 2.5 mg/ml that can be compressed at a low pressure. Therefore, mannose was chosen as the main excipient. Tablets with high porosity were made in a 3-step process. First, mannose powder was compressed into a tablet with reasonable strength. Second, this compact was exposed to relative humidity higher than the critical relative humidity of mannose to absorb water. Third, tablets were dried to gain mechanical strength. The disintegration mechanism was studied.

[1]  W. Habib,et al.  Fast-dissolve drug delivery systems. , 2000, Critical reviews in therapeutic drug carrier systems.

[2]  Clive G. Wilson,et al.  A gamma scintigraphic study of gastric coating by Expidet, tablet and liquid formulations , 1989 .

[3]  Z. Chowhan,et al.  The Effect of Low- and High-Humidity Aging on the Hardness, Disintegration Time and Dissolution Rate of Tribasic Calcium Phosphate-Based Tablets , 1979 .

[4]  Kinam Park,et al.  Application of poly(acrylic acid) superporous hydrogel microparticles as a super‐disintegrant in fast‐disintegrating tablets , 2004, The Journal of pharmacy and pharmacology.

[5]  Z T Chowhan,et al.  The effect of low‐ and high‐humidity ageing on the hardness, disintegration time and dissolution rate of dibasic calcium phosphate‐based tablets , 1980, The Journal of pharmacy and pharmacology.

[6]  R.-K. Chang,et al.  Fast-dissolving tablets , 2000 .

[7]  M. Fujii,et al.  Pharmacokinetics of acetaminophen from rapidly disintegrating compressed tablet prepared using microcrystalline cellulose (PH-M-06) and spherical sugar granules. , 2001, Chemical & pharmaceutical bulletin.

[8]  L. Dobetti,et al.  Fast-Melting Tablets: Developments and Technologies , 2001 .

[9]  H. SEAGER,et al.  Drug‐delivery Products and the Zydis Fast‐dissolving Dosage Form * , 1998, The Journal of pharmacy and pharmacology.

[10]  Z. T. Chowhan,et al.  MOISTURE, HARDNESS, DISINTEGRATION AND DISSOLUTION INTERRELATIONSHIPS IN COMPRESSED TABLETS PREPARED BY THE WET GRANULATION PROCESS , 1979 .

[11]  Z. Chowhan Role of binders in moisture-induced hardness increase in compressed tablets and its effect on in vitro disintegration and dissolution. , 1980, Journal of pharmaceutical sciences.

[12]  Clive G. Wilson,et al.  A gamma scintigraphic study to compare oesophageal clearance of “Expidet” formulations, tablets and capsules in supine volunteers , 1988 .

[13]  Sastry,et al.  Recent technological advances in oral drug delivery - a review. , 2000, Pharmaceutical science & technology today.

[14]  Clive G. Wilson,et al.  The behaviour of a fast-dissolving dosage form (Expidet) followed by γ-scintigraphy , 1987 .

[15]  Z. Chowhan,et al.  Hardness increase induced by partial moisture loss in compressed tablets and its effect on in vitro dissolution. , 1978, Journal of pharmaceutical sciences.