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在富含腐殖质的水胶体存在下,选定药物在天然膜和合成膜上的超滤行为。

Ultrafiltration behavior of selected pharmaceuticals on natural and synthetic membranes in the presence of humic-rich hydrocolloids.

作者信息

Burba Peter, Geltenpoth Helma, Nolte Jürgen

机构信息

ISAS, Institute for Analytical Sciences, Bunsen-Kirchhoff-Str. 11, 44139 Dortmund, Germany.

出版信息

Anal Bioanal Chem. 2005 Aug;382(8):1934-41. doi: 10.1007/s00216-005-3296-z. Epub 2005 Jul 15.

Abstract

The separation behavior of the frequently administered pharmaceuticals sulfamethoxazol (Sulfa), carbamazepine (Carba), diclofenac (Diclo), and ibuprofen (Ibu) on different natural and synthetic ultrafiltration membranes was studied. Commercially available cattle intestine natural membranes (NM), polyethersulfone (PES), and regenerated cellulose-based (RC) flat membranes (nominal cut-off 1 kDa) have been investigated as ultrafiltration membranes in a small tangential-flow ultrafiltration unit (TF-UF). First, the nominal cut-off of the NM membranes under study was assessed at approximately 5 kDa, by using polystyrenesulfonate standards for pore-size classification at low TF-UF pressure (0.25 x 10(5) Pa). Working pressures of >1.5 x 10(5) Pa strongly increased the cut-off of NM, in contrast with that of PES and RC membranes. Sulfa, Carba, Diclo and Ibu (1 mg L(-1) each) in colloid-free aqueous solutions (400 mg L(-1) NaCl) completely permeated through NM membranes, but less through PES and RC, which had particular sorption capability towards Diclo. The drugs were routinely determined by using high-performance liquid chromatography (HPLC). Detailed TF-UF investigation of drug retention on NM in the presence of humic hydrocolloids revealed strong interactions between aquatic humic substances (HS) and Diclo and Ibu (but not with Sulfa and Carba) causing retention of up to 80% of Diclo and Ibu, probably because of their binding to macromolecular HS. The standard deviation (SD) of both drug and HS permeation through a single NM was between 2.5 (Sulfa) and 4.0% (Diclo), in contrast with the SD of permeation through separate membranes taken from different lots [SD up to 14.0% (Diclo)], presumably caused by natural variation of the studied NM. Accordingly, membrane filtration of drug-containing water samples on cattle intestines enables both analyte/matrix separations for Carba and Sulfa in the presence of humic colloids and analytical discrimination between free and colloid-bound Diclo and Ibu fractions.

摘要

研究了常用药物磺胺甲恶唑(Sulfa)、卡马西平(Carba)、双氯芬酸(Diclo)和布洛芬(Ibu)在不同天然和合成超滤膜上的分离行为。市售牛肠天然膜(NM)、聚醚砜(PES)和再生纤维素基(RC)平板膜(标称截留分子量1 kDa)已作为超滤膜在小型错流超滤装置(TF-UF)中进行了研究。首先,在低TF-UF压力(0.25×10⁵ Pa)下,使用聚苯乙烯磺酸盐标准进行孔径分类,评估所研究的NM膜的标称截留分子量约为5 kDa。与PES和RC膜相比,>1.5×10⁵ Pa的工作压力会显著增加NM的截留分子量。在无胶体水溶液(400 mg L⁻¹ NaCl)中,Sulfa、Carba、Diclo和Ibu(各1 mg L⁻¹)完全透过NM膜,但透过PES和RC膜的较少,而PES和RC膜对Diclo具有特殊的吸附能力。这些药物通常采用高效液相色谱法(HPLC)进行测定。在腐殖质水胶体存在下,对药物在NM上的截留进行的详细TF-UF研究表明,水生腐殖质(HS)与Diclo和Ibu(但不与Sulfa和Carba)之间存在强烈相互作用,导致Diclo和Ibu的截留率高达80%,这可能是因为它们与大分子HS结合。药物和HS透过单个NM的标准偏差(SD)在2.5%(Sulfa)至4.0%(Diclo)之间,而透过不同批次的单独膜的SD高达14.0%(Diclo),这可能是由于所研究的NM的自然差异所致。因此,在牛肠上对含药水样进行膜过滤,既能在腐殖质胶体存在下实现Carba和Sulfa的分析物/基质分离,又能对游离和胶体结合的Diclo和Ibu组分进行分析鉴别。

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