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1.
Acta Pharmaceutica Sinica ; (12): 1069-1075, 2014.
Article in Chinese | WPRIM | ID: wpr-299165

ABSTRACT

The purpose of this study is to investigate the preparation of hydroxycamptothecine (HCPT)-loaded cubic crystal liquid embolic precursor solution, and evaluate its in vitro embolic efficiency. Phytantriol was used as cubic crystal liquid embolic material, and the optimal formulation was selected according to ternary phase diagram. Polarized light microscopy, differential scanning calorimetry, and small angle X-ray scattering (SAXS) were used to characterize the cubic crystal structure. High performance liquid chromatography and X-ray diffraction analysis were used to investigate the lactone ring of HCPT. In vitro dissolution was preliminary evaluated, and the simulation embolic model was constructed to evaluate the embolic efficiency of precursor solution. Meanwhile, the gelation time and adhesion force were investigated. The results showed that HCPT-loaded precursor solution for embolization had been successfully prepared with low viscosity which was injectable. The precursor solution could transform into Pn3m structure liquid crystal phase gel rapidly when contracting with excess water. The formed HPCT gel remained its lactone form as the same in precursor solution, and expressed the good ability to block the saline flow, and HCPT could keep sustained releasing drug over 30 days. The prepared drug-loaded embolic precursor solution showed a promising potential for vascular embolization and application in clinical treatment of tumor.


Subject(s)
Antineoplastic Agents, Phytogenic , Chemistry , Calorimetry, Differential Scanning , Camptothecin , Chemistry , Delayed-Action Preparations , Chemistry , Fatty Alcohols , Chemistry , Liquid Crystals , Scattering, Small Angle , Water , X-Ray Diffraction
2.
China Journal of Chinese Materia Medica ; (24): 644-647, 2014.
Article in Chinese | WPRIM | ID: wpr-300176

ABSTRACT

This study was to investigate the permeability and absorbability of capsaicin cubosome across abdominal skin of the SD rats in vitro. Diffusion of capsaicin cubosome and cream was performed with the modified Franz diffusion cell technique. The capsaicin cubosome showed no enhancement of skin permeation within 24 hours. However, the deposition amounts of capsaicin in the rat skin in the cubosome group was markedly higher than those in the commercial cream group (P < 0.01). Cubosome showed excellent characetristic of skin-targed which could be a good carrier for the local transdermal drug delivery system.


Subject(s)
Animals , Male , Rats , Administration, Cutaneous , Capsaicin , Chemistry , Kinetics , Particle Size , Permeability , Rats, Sprague-Dawley , Skin , Metabolism , Skin Absorption
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