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Despite recent advances in the formulation of orally disintegrating tablets (ODTs), the efforts to enhance the swallowing of the drug after disintegration have been limited. In this study, the feasibility of the combined use of cyclodextrins (CyDs) and a functional drug carrier, hydroxypropylmethylcellulose stearoxy ether (Sangelose) was investigated to improve usability of ODTs. Glimepiride, a potent third generation hypoglycemic agent for type 2 diabetes was used as a model drug, because it is poorly water-soluble and elimination half life is fairly short. The direct compression method was employed for the preparation of glimepiride tablets, containing CyDs and Sangelose, and various characteristics of the tablets were examined. In the cases of α-CyD and β-CyD, a short disintegration time with an appropriate hardness was obtained, complying with ODT criteria. On the other hand, γ-CyD, HP-β-CyD and HB-β-CyD increased in the hardness and disintegration time of the tablets. The rheological evaluation revealed that CyDs, except γ-CyD, significantly reduced the viscosity of the fluids after disintegration of the tablets, suggesting an ease of swallowing. This was ascribable to the complexation of the hydrophobic stearoyl moiety of Sangelose with CyDs after dissolution, leading to the inhibition of the polymer-polymer interaction of Sangelose and to the decrease in viscosity of the solution. The interaction of glimepiride with α- and β-CyDs was studied by the solubility method, demonstrating that glimepiride formed water-soluble complexes with these CyDs. Results obtained here suggested that α-CyD and β-CyD can be particularly useful for the Sangelose-based ODT formulation, compared to γ-CyD, HP-β-CyD and HB-β-CyD, because of the short disintegration time of the tablets containing α-CyD and β-CyD, their shear-thinning effect on Sangelose solutions and their solubility enhancing effect on the drug. [ABSTRACT FROM AUTHOR]

In a series of studies to develop an effective high speed plankton sampler, hydrodynamic research was carried out on a modified model of the Clarke Jet Net. A theoretical analysis of the motion of the sampler was made using an IBM 7040 computer, and test tows were made in an experimental ship tank and at sea. To maintain the roll angle of the sampler at approximately zero, a v-shape bridle was applied. A pair of towing holes should be selected for the particular range of towing velocity. The calculated longitudinal stability seemed good in all the cases examined. Towing tests in the ship tank at 2 to 3 m/sec revealed sufficient stability. The motion of the sampler at speeds higher than 3 m/sec can be assumed from hydrodynamic coefficients derived from the ship tank experiment. Towing-cable characteristics, assumed by computation, indicated that about 500 m at 6 kt and 1,000 m at 12 kt should be paid out to lower the sampler down to 100 m. The effect of the sampler on the cable is found only adjacent to it and is almost negligible beyond 50 m from it in depth. Results of sea tests at 6 and 9 kt confirmed the stability of the sampler. Examination of the catch suggested that the present model can be used, with some modifications, for the quantitative and qualitative sampling of large zooplankton. [ABSTRACT FROM AUTHOR]

A hydrodynamic study of a modified model of the Clarke Jet Net, a high speed plankton sampler, was made using a wind tunnel and an IBM 7040. Modifications allowed a somewhat larger amount of water filtered than in the original model. By adjusting the size of the net chamber exhaust (water control aperture), an average net chamber velocity of about 100 cm/sec could be obtained at any cruising speed. The curvature of the towing cable of the deep tow of a high speed sampler seemed to be determined mainly by the cable characteristics. The stability, vertical and horizontal, of the modified model was satisfactory. [ABSTRACT FROM AUTHOR]