共溶剂对兔肠中富马酸酮替芬吸收清除的影响

S. El-Gizawy, M. Osman, S. Ibrahim
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引用次数: 2

摘要

目的:探讨乙醇、聚乙二醇400、丙二醇、甘油和山梨醇对富马酸酮替芬家兔吸收清除率的影响。方法:采用原位肠灌流技术,采用透、透法测定富马酸酮替芬在家兔十二指肠、空肠、回肠和升结肠的膜转运参数。这些参数包括单位长度吸收清除率PeA/L (ml/min.cm),单位长度吸收百分比(% Fa/cm)和特定节段完全吸收所需的解剖长度(L95%)。结果:吸收顺序为升结肠>十二指肠>空肠>回肠;其中肠段吸收清除率与肠段长度PeA/L (ml/min.cm)归一化分别为0.0071±0.0003、0.0058±0.0001、0.0051±0.0001和0.0047±0.0001。助溶剂在空肠中的作用依次为;乙醇15% >甘油30% >丙二醇(PG40%) >聚乙二醇400 (PEG-400 40%) >山梨醇40%,各共溶剂吸收清除率归一化为肠段长度PeA/L (ml/min.cm),平均±SE分别为:0.0142±0.0011、0.0086±0.0002、0.0075±0.0003、0.0022±0.0001、0.0014±0.0001。在升结肠中也得到了相同的顺序。结论:乙醇、丙二醇和甘油的增强作用可能是由于细胞膜的流化,从而增加了跨细胞吸收,而聚乙二醇和山梨醇的抑制作用可能是由于水的分泌、氢键的形成和药物分子热力学活性的降低。
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INFLUENCE OF COSOLVENTS ON THE ABSORPTIVE CLEARANCE OF KETOTIFEN FUMARATE FROM RABBIT INTESTINE, IN-SITU
Objective: Investigate the effect of ethanol, polyethylene glycol 400, propylene glycol, glycerol and sorbitol on the absorptive clearance of ketotifen fumarate   in the rabbit. Methods: In-situ intestinal perfusion technique, through and through was used for estimation of membrane transport parameters of ketotifen fumarate from duodenum, jejunum, ileum and ascending colon in the rabbit. These parameters include absorptive clearance per unit length PeA/L (ml/min.cm), percentage fraction absorbed per unit length (% Fa/cm) and anatomical length that required for complete absorption in specific segment (L95%). Results: The absorption was in the order ascending colon> duodenum > jejunum> ileum; where the absorptive clearance normalized to intestinal segment length PeA/L (ml/min.cm) was 0.0071 ± 0.0003, 0.0058 ± 0.0001, 0.0051 ± 0.0001, and 0.0047 ± 0.0001 in each segment respectively. The effect of cosolvents in jejunum was in the order; ethanol 15% >glycerol 30% > propylene glycol (PG40%) > polyethylene glycol400 (PEG-400 40%) >sorbitol 40%, Where the absorptive clearance normalized to intestinal segment length PeA/L (ml/min.cm), mean ± SE was: 0.0142 ±0.0011, 0.0086 ± 0.0002, 0.0075 ± 0.0003, 0.0022 ± 0.0001, and 0.0014 ± 0.0001 for each cosolvents respectively. The same order was obtained in the ascending colon. Conclusion: The enhancing action of the ethanol, propylene glycol and glycerol may be due fluidization of the cell membrane with a subsequent increase in transcellular absorption, while the inhibitory effect of polyethylene glycol and sorbitol could attributed to water secretion, H-bonding formation and reduced thermodynamic activity of drug molecules.
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