Durrer C, Irache J M, Puisieux F, Duchêne D, Ponchel G
Centre d'Etudes Pharmaceutique, URA CNRS 1218, Université Paris-Sud, Châtenay-Malabry, France.
Pharm Res. 1994 May;11(5):674-9. doi: 10.1023/a:1018968011169.
A Fourier transform infrared spectroscopy/attenuated total reflection technique for direct quantification of adsorbed poly(styrene) latexes on rat intestinal mucosa was developed for deposited latex amounts up to 1.5 g/m2. The method agreed well with another dosage assay of adsorbed particles by turbidimetry after denaturation of the mucus. Adsorption kinetics were made under static conditions at latex concentrations of 4 g/L in physiological saline. Ninety percent of equilibrium was reached after 10 min for a particle size of 230 nm, 20 min for a size of 320 nm, and 30 min for a size of 670 nm. The plateaus were between 0.6 and 0.9 g/m2 (adsorbed mass per apparent surface of mucosa). The first phase of the kinetics was theoretically approached by a diffusion model in the suspension medium. Mucosa from rat jejunum and ileum could be considered as a homogeneous biological model for latex adsorption.
开发了一种傅里叶变换红外光谱/衰减全反射技术,用于直接定量大鼠肠黏膜上吸附的聚苯乙烯乳胶,可测定高达1.5 g/m² 的沉积乳胶量。该方法与另一种在黏液变性后通过比浊法测定吸附颗粒剂量的方法结果吻合良好。吸附动力学是在生理盐水中乳胶浓度为4 g/L的静态条件下进行的。对于粒径为230 nm的颗粒,10分钟后达到平衡的90%;对于粒径为320 nm的颗粒,20分钟后达到;对于粒径为670 nm的颗粒,30分钟后达到。吸附量平台在0.6至0.9 g/m²之间(每黏膜表观表面积的吸附质量)。动力学的第一阶段理论上可通过悬浮介质中的扩散模型来描述。大鼠空肠和回肠的黏膜可被视为乳胶吸附的均匀生物模型。