The aim of this study was to investigate the feasibility of preparing flunarizine-loaded lipid microspheres. Lipid microspheres (LMs) are excellent drug carriers for drug delivery systems (DDS) and are relatively stable and easily mass-produced. They have no particular adverse effects. LMs have been widely studied as drug carriers for water-soluble drugs, lipid-soluble drugs and inadequately soluble (in water or in lipid) drugs, in that they have a lipid layer, a water layer and an emulsifier layer. Flunarizine (FZ), a poorly water-soluble drug, was incorporated in lipid microspheres to reduce side effects by avoiding the use of supplementary agents, compared with solution injection. After investigation, the final formulation was as follows: 10% oil phase (long-chain triglyceride (LCT); medium-chain fatty acid (MCT) = 50:50); 1.2% egg lecithin; 0.2% Tween-80; 2.5% glycerin; 0.3% dl-alpha-tocopherol; 0.02% EDTA; 0.03% sodium oleate; 0.1% FZ and double-distilled water to give a total volume of 100 mL. Homogenization was the main method of preparation and the best conditions were a temperature of 40 degrees C, a pressure of 700-800 bar and a suitable cycle frequency of about 10. The particle size distribution, zeta-potential and entrapment efficacy were found to be 198.7+/-54.0 nm, -26.4 mV and 96.2%, respectively. Its concentration in the preparation was 1.0 mg mL(-1). The lipid microspheres were stable during storage at 4 degrees C, 25 degrees C and 37 degrees C for 3 months. Pharmacokinetic studies were performed in rats using a dose of 1.0 mg kg(-1). The pharmacokinetic parameters were as follows: AUC(0-t) 6.13 mug.h mL(-1), t(1/2) 5.32 h and Ke 0.16 L h(-1). The preparation data fitted a two-compartment model estimated by using 3p87 analysis software. From the observed data, FZ encapsulated in LMs did not significantly alter the pharmacokinetic characteristic compared with the FZ solution injection and did not produce a delayed release effect, when it was released in-vivo in rats. However, the availability of the drug was increased. These results suggested that this LM system is a promising option for the preparation of the liquid form of FZ for intravenous administration.

A new accurate calibrating technique for intrinsic parameters and extrinsic parameters of CCD camera is described. The camera model is derived by the pinhole projection theory. Then other parameters of the model are resolved under the radial alignment constraints and orthogonal constraints. In order to get a fine initial guess for the nonlinear searching solution, the least square method is introduced, and finally uses radial alignment constraint method to get the results. The experimental results show that the mean absolute differences in x direction and y direction are 0.0070 and 0.1430 separately while the standard deviation are 0.5006 and 1.2046 separately.

Two different dendritic 8-hydroxyquinoline ligands were synthesized through convergent approach, and the products were characterized by nuclear magnetic resonance (NMR) and infrared spectrometry (IR); the fluorescence properties of the dendritic 8-hydroxyquinoline ligands and the corresponding metallic complexes with Zn (II) were also studied by fluorescent spectrometry. The results show that the dendritic modifications of 8-hydroxyquinoline nucleus enhanced the intensity of luminescence, and the peripheral functional groups in the dendritic structure may affect the property of luminescence; the obvious red shift observed in the fluorescence profile of dendritic 8-hydroxyquinoline zinc provides it prospect of extensive application in the discipline of organic electroluminescent materials.