Nicklasson M, Ellström K, Sjöqvist R, Sjövall J
J Pharmacokinet Biopharm. 1984 Oct;12(5):467-78. doi: 10.1007/BF01060126.
Linear systems analysis, i.e., numerical convolution/deconvolution, and moment analysis have been performed on data obtained from microcapsules containing the ampicillin prodrug bacampicillin hydrochloride. Three batches with different in vitro dissolution rates were scrutinized. From the results, it is concluded that numerical convolution/deconvolution is a valuable tool for predicting bacampicillin bioavailability. However, it must be emphasized that the selection of an appropriate time module is important for predicting an in vivo response that reflects the actual situation. This was verified by comparing the predicted plasma response values with the values obtained in a bioavailability study in healthy volunteers. A correlation between mean residence time in vivo and mean dissolution time in vitro was also found which thus demonstrates the usefulness of moment analysis for obtaining an in vivo-in vitro relationship. This relationship was compared to a correlation found between the mean dissolution time in vitro and the empirical maximum plasma concentration of bacampicillin.
已对从含有氨苄西林前药盐酸巴氨西林的微胶囊获得的数据进行了线性系统分析,即数值卷积/反卷积和矩分析。对具有不同体外溶解速率的三批产品进行了仔细研究。从结果可以得出结论,数值卷积/反卷积是预测巴氨西林生物利用度的一种有价值的工具。然而,必须强调的是,选择合适的时间模块对于预测反映实际情况的体内反应很重要。通过将预测的血浆反应值与在健康志愿者的生物利用度研究中获得的值进行比较,这一点得到了验证。还发现了体内平均驻留时间与体外平均溶解时间之间的相关性,从而证明了矩分析对于获得体内-体外关系的有用性。将这种关系与体外平均溶解时间与巴氨西林的经验最大血浆浓度之间的相关性进行了比较。