新型大豆异黄酮磺酸酯的临床前药物动力学

为寻找新的大豆异黄酮前药,采用建立的生物样品中药物浓度测定的液相色谱法对新型大豆异黄酮染料木素磺酸酯(GBS)进行前药判定以及大鼠体内药物动力学研究,以考察前药中染料木素(GE)的口服相对生物利用度是否改善。在大鼠体内药物代谢实验中,灌胃给予的大鼠血浆中能检测到GE的存在。在临床前药物动力学实验中,该前体药以40mg/kg GE在大鼠体内的动力学过程符合一室模型。GBS中GE的相对口服生物利用度为原药的198.6%。结果表明:相对于原药GE,前药中GE的相对口服生物利用度得到极大地改善。该前药有进一步研究的意义。     

新型染料木素磺酸酯的前药判定与大鼠体内生物利用度

为寻找染料木素(GE)新的前药,采用建立的生物样品中药物浓度测定的液相色谱法对新型大豆异黄酮染料木素磺酸酯(GB)进行前药判定以及大鼠体内药物动力学研究,以考察前药中染料木素的口服生物利用度是否改善.在大鼠体内药物代谢实验中,灌胃给予GB的大鼠血浆中能检测到明显的GE.在临床前药物动力学实验中,该前体静注给药和以40 mg/kg灌胃药后,GE在大鼠体内的动力学过程均符合一室模型.GB中GE的相对口服生物利用度为原药的110.9％.研究表明,相对于原药GE,前药中GE的相对口服生物利用度达到预期的改善,该前药有进一步研究意义.     

新型染料木素磺酸酯的合成及对小鼠血吸虫病肝肉芽肿的影响

为寻找抗血吸虫病的新候选化合物,通过正交实验,高选择性、高产率地合成了染料木素的磺酸酯衍生物。结果表明:小鼠感染血吸虫病,经过衍生物治疗后,由血吸虫导致的肉芽肿面积有不同程度的降低,其中低剂量组降低到23.2%,与溶剂组比较,差异显著(P<0.05),优于原药的27.1%及阳性对照组秋水仙碱的27.0%。说明该化合物对血吸虫导致的肉芽肿有一定抑制作用,该化合物有进一步研究价值。     

A novel aldehyde dextran sulfonate matrix for affinity biosensors

Aldehyde dextran sulfonate (ADS), a modified oligosaccharide polymer, was used to prepare a new matrix structure for affinity biosensors. The principal difference between the ADS matrix and similar structures developed previously results from presence of two active functional groups in the matrix, namely, aldehyde and sulfonate. These groups perform two different functions in the matrix. The aldehyde group is responsible for covalent bonding in the biomaterials, and the negatively charged sulfonate group provides electrostatic attraction of the positively charged biomolecules. By varying the ratio between the aldehyde and sulfonate groups in the matrix, one can control contributions from the two binding modes (covalent and electrostatic). A number of oligosaccharides, such as simple dextran, aldehyde dextran (AD), aldehyde dextran sulfonate (ADS) and aldehyde ethylcellulose (AEC), were used for preparation of matrix structures. The properties of the obtained matrices were analysed and compared. Surface plasmon resonance (SPR) was used as the main technique to characterize the matrix structures.     

Anilinonaphthalene sulfonate isomers inactivate phosphoenolpyruvate carboxykinase

Studies with anilinonaphthalene sulfonate and related compounds suggest that the remarkable ability of some of these isomers to inactivate phosphoenolpyruvate carboxykinase depends, in part, on their ability to assume a conformation in which the naphthyl and phenyl rings are coplanar. Comparison with seven anilino, sulfonate isomers gave an order of inactivating effectiveness of (1, 8) > (2, 1) > (2, 5), (2, 6), (2, 7), (2, 8). The (1, 2) isomer, i.e., 1-anilinonaphthalene-2-sulfonate, did not inactivate. 1-Anilinonaphthalene-8-sulfonate is a widely used hydrophobic binding fluorescent probe. The present study contributes information as to the steric and electronic properties of these isomers and their possible importance.     

Input rate-dependent stereoselective pharmacokinetics: Effect of pulsatile oral input

Computer simulation was used to test the effects of pulsatile oral input on the stereoselectivity in the area under the blood concentration–time curves (AUCs) of the enantiomers of racemic drugs. The effects of input rate determinants, namely, dose, dosage interval, and formulation on the stereoselectivity were investigated under both steady-state and nonsteady-state conditions. Simulations were carried out for drugs undergoing Michaelis–Menten hepatic metabolism with different enantiomeric maximum velocity (V_max) or constant (K_m) values. With pulsatile input, the enantiomeric AUC ratios of both types of drugs were dependent on all the determinants of input rate. However, in most cases, the direction of input rate-dependent changes in the enantiomeric AUC ratios for drugs with different enantiomeric V_max was opposite of that for drugs with different enantiomeric K_m. The direction and magnitude of changes in the enantiomeric AUC ratios were also dependent on the selected dose, dosage interval, and formulation. Further, different conclusions could be reached based on the nonsteady-state and steady-state data. Additional simulations were then performed to test the effects of input rate-dependent stereoselective pharmacokinetics on the bioequivalence of chiral drugs with nonlinear metabolism. These simulations suggested that bioequivalence studies based on the racemic drug measurement may result in erroneous conclusions for the individual enantiomers. The results of this study may be used as a tool for the design of experiments to test the input rate dependence of stereoselective pharmacokinetics and bioequivalence of racemic drugs in animals and humans. © 1994 Wiley-Liss, Inc.     

新型大豆苷元磺酸酯抑制血管平滑肌细胞增殖活性

为寻找对血管平滑肌细胞异常增殖有较强抑制作用的化合物,用MMT法考察新型大豆苷元磺酸酯体外抑制血管平滑肌细胞增殖活性.结果表明:该大豆苷元磺酸酯对血管平滑肌细胞增殖在10-6 mol/L时有抑制作用(P＜0.05),该浓度下的抑制率为64.62％,与先导化合物大豆苷元相比活性提高约100倍.构效关系研究表明,大豆苷元经...     

槲皮素化学修饰与体内转运过程研究进展

本文综述了槲皮素的化学修饰和药代动力学等方面的研究进展,为槲皮素的前药分子设计、寻找活性化合物提供科学依据。文献合成的目标产物主要包括槲皮素糖苷等水溶性产物和槲皮素磺酸酯等脂溶性产物,迄今仍未找到药理作用明显,能临床运用的槲皮素修饰物。文献表明槲皮素生物活性低是由于其低的生物利用度,溶解性差与首过效应是影响其生物利用度的主要因素。     

全氟辛烷磺酸生物降解研究进展

全氟化合物(perfluorinated compounds,PFCs)是碳氢类化合物及其衍生物中氢原子全部被氟原子取代后形成的一类化合物。全氟辛烷磺酸(perfluorooctane sulfonate,PFOS)是一种典型的全氟化合物,对于生物具有多方面的毒性。研究发现,PFOS广泛存在于环境中,造成了一定的污染,PFOS的降解成为亟待解决的问题。但是由于PFOS稳定性高,降解较为困难,尤其是在生物降解方面的研究较少。本文主要介绍了PFOS降解技术的发展现状以及存在的问题,并提出PFOS生物降解的可能途径。     

一株十二烷基苯磺酸钠降解菌的分离鉴定及降解特性研究

从受污染河水中筛选分离得到一株能以十二烷基苯磺酸钠(Sodiumdodecylbenzenesulfonate,SDBS)为唯一碳源和能源生长的菌株WZR-A。经对其形态特征、生理生化、以及16SrDNA序列分析,将WZR-A初步鉴定为人苍白杆菌(Ochrobactrumanthropi)。研究表明该菌株利用SDBS生长的最适温度为30℃,最适pH为7·0。SDBS浓度低于400mg/L时菌株对SDBS的降解率可在80%以上。菌株细胞蛋白SDS-PAGE结果显示,菌株在SDBS诱导前后的细胞蛋白组成有明显差异。酶的定域试验表明,该菌株的相关降解酶为胞内酶。相关降解酶活性及降解底物测试结果表明,该菌株可能通过邻位途径裂解芳环并具有对多种芳香族化合物降解的能力。此外,利用质粒检测和消除试验发现菌株WZR-A中含有大质粒且该菌株的相关降解基因初步定位于该质粒。     

Minipig as a potential translatable model for monoclonal antibody pharmacokinetics after intravenous and subcutaneous administration

Subcutaneous (SC) delivery is a common route of administration for therapeutic monoclonal antibodies (mAbs) with pharmacokinetic (PK)/pharmacodynamic (PD) properties requiring long-term or frequent drug administration. An ideal in vivo preclinical model for predicting human PK following SC administration may be one in which the skin and overall physiological characteristics are similar to that of humans. In this study, the PK properties of a series of therapeutic mAbs following intravenous (IV) and SC administration in Göttingen minipigs were compared with data obtained previously from humans. The present studies demonstrated: (1) minipig is predictive of human linear clearance; (2) the SC bioavailabilities in minipigs are weakly correlated with those in human; (3) minipig mAb SC absorption rates are generally higher than those in human and (4) the SC bioavailability appears to correlate with systemic clearance in minipigs. Given the important role of the neonatal Fc-receptor (FcRn) in the PK of mAbs, the in vitro binding affinities of these IgGs against porcine, human and cynomolgus monkey FcRn were tested. The result showed comparable FcRn binding affinities across species. Further, mAbs with higher isoelectric point tended to have faster systemic clearance and lower SC bioavailability in both minipig and human. Taken together, these data lend increased support for the use of the minipig as an alternative predictive model for human IV and SC PK of mAbs.     

In vitro confirmation of the quantitative differentiation of liposomal encapsulated and non-encapsulated prednisolone (phosphate) tissue concentrations by murine phosphatases

The quantitative differentiation of liposomal encapsulated and non-encapsulated drug tissue concentrations is desirable, since the efficacy and toxicity are only related to the level of non-encapsulated drug. However, such separate concentration profiles in tissues have still not been reported due to lacking analytical methodology. The encapsulation of prodrugs like prednisolone phosphate (PP) in liposomes offers new, analytical opportunities. Instantaneous dephosphorylation of PP into prednisolone (P) by phosphatases after its release from the liposome in vivo makes it possible to differentiate between the encapsulated and the non-encapsulated drug for such preparations of liposomal PP: PP represents the encapsulated drug, while P represents the non-encapsulated drug. In the here described study, the instantaneous dephosphorylation of PP by murine liver and kidney phosphatases has been verified by incubation of PP in liver and kidney homogenates followed by estimation of the dephosphorylation rate constants k and the dephosphorylation time of the expected maximal in vivo non-encapsulated drug concentrations. In vitro PP has been rapidly converted into P in the presence of homogenate from the excretory organs. The calculated values for k have shown that the liver contains more active sites per gram of tissue than the kidneys. However, the dephosphorylation of PP by these active sites is slower compared with the kidneys. Compared with other pharmacokinetic processes of P, the estimated dephosphorylation times of the expected maximal in vivo non-encapsulated drug concentrations in the liver and the kidneys are considered to be instantaneous. This enables the separate determination of the encapsulated and non-encapsulated drug concentrations in the excretory organs after administration of liposomal PP in mice generating the first pharmacokinetic profile of a liposomal preparation, in which the in vivo encapsulated and free drug tissues concentrations are measured separately. This can also gain important insights into the pharmacokinetics of liposomal formulations in general.     

PFOS对蚯蚓急性毒性和回避行为的影响

全氟辛烷磺酰基化合物(PFOS)作为一种新型持久性有机污染物,已经成为环境科学和毒理学的研究热点,其对生态环境的影响值得深入研究.本文采用OECD标准滤纸接触法、人工土壤法及自然土壤法研究了PFOS对蚯蚓急性致死作用及回避行为的影响.结果表明： PFOS对蚯蚓的急性毒性作用与染毒时间和染毒浓度相关,试验求得滤纸法48 h、人工土壤法14 d和自然土壤法14 d的LC₅₀值分别为13.64 μg·cm^-2、955.28 mg·kg^-1和542.08 mg·kg^-1;人工土壤和自然土壤中蚯蚓在PFOS的最大试验浓度组160 mg·kg^-1中均表现出显著的回避行为,表明蚯蚓可以明显感知较高浓度PFOS污染土壤并作出回避反应.与急性毒性试验的测试终点LC₅₀相比,蚯蚓行为测试终点对PFOS的反应更为敏感.自然土壤中PFOS对蚯蚓的急性毒性大于人工土壤,相同浓度PFOS作用下,蚯蚓于自然土壤中的回避行为较人工土壤明显.     

Renal transport and disposition of Na-2-mercaptoethane sulfonate disulfide (Dimesna) in the rat

The transport and reduction of dimesna (NA-2-mercaptoethane sulfonate disulfide) was studied in vitro using isolated, perfused rat kidney, and isolated renal epithelial cells. Cellular uptake of dimesna was found to be dependent on an active transport mechanism working across the luminal brush border, with an app. K_m of 22 μM and V_max 1.4 nmol. 10⁶ cells⁻¹.min⁻¹. Among other low molecular thiols or disulfides reduced glutathione was the only one to exert competitive inhibition. γ-GT-activity or cellular GSH status had no influence on renal uptake of dimesna, but the intracellular reduction rate was dependent on access to reduced glutathione as a cofactor.     

1,8-Anilinonaphthalene sulfonate binds to central cavity of human hemoglobin

Binding of 1,8-anilinonaphthalene sulfonate (1,8-ANS) to main (HbA(1)) and glycosylated (HbA(1C)) forms of human oxyhemoglobin in the presence/absence of inositolhexaphosphate (IHP) in 50 mM potassium phosphate buffer, pH 7.4, was studied by time-correlated single photon counter with subnanosecond time resolution. The redistribution of contributions of the most long-lived and the most short-lived fluorescent decay components in the presence of IHP provides an evidence of the probe binding within oxyhemoglobin central cavity, namely DPG-binding site. Finally, it was shown that the fluorescent probe is extremely sensitive for hemoglobin central cavity modification, provided by the carbohydrate moiety in case of 1,8-ANS interactions with HbA(1C).     

Specific labelling of the active site of the phosphate translocator in spinach chloroplasts by 2,4,6-trinitrobenzene sulfonate

Phosphate transport across the chloroplast envelope is rapidly inactivated by the amino-group reagent 2,4,6-trinitrobenzene sulfonate. Subsequent exposure to [³H]NaBH₄ leads to an incorporation of the trinitrophenyl moiety into envelope membrane preparations. From the membrane proteins only a polypeptide with 29000 dalton molecular weight is labelled. The inactivation of phosphate transport and the incorporation of radioactivity are both specifically reduced by the presence of substrates.The results lead to the conclusion that a polypeptide with a molecular weight of 29000 dalton and containing a lysyl residue at the substrate binding site is involved in the phosphate translocator function.     

大豆甙元磺酸钠对应激性胃粘膜损伤的影响及其机制探讨

目的：观察大豆甙元磺酸钠对力竭应激性渍疡的影响,探讨其可能的作用途径。方法：采用小鼠力竭性游泳,计数胃部溃疡点数建立应激溃疡模型,腹腔注射不同剂量的大豆甙元磺酸钠及一氧化氮合酶（NOS）抑制剂（L-NAME）并通过NADPH-黄递酶组织化学法检测胃壁NOS阳性神经元的变化。结果：大豆甙元磺酸钠具有保护胃粘膜的作用,且呈剂量效应;L-NAME可防止应激引起的胃粘膜损伤,L-NAME与有效剂量的大豆甙元磺酸钠联合使用后,大豆甙元磺酸钠对胃粘膜的保护作用明显增强;正常及应激小鼠胃壁NOS神经节数目基本不变,大豆甙元磺酸钠对正常小鼠胃壁NOS神经元影响不明显,而对应激小鼠胃壁单位面积及单个神经节内NOS阳性神经元数目均有显著降低作用。结论：应激时NO升高可导致溃疡,大豆甙元磺酸钠能够保护胃粘膜,其作用是通过抑制应激状态下NOS的升高,限制应激状态下NO过度升高,起到保护胃粘膜的作用。     

Investigation on the interaction of catalase with sodium lauryl sulfonate and the underlying mechanisms

As a classic type of anionic surfactants, sodium lauryl sulfonate (SLS) might change the structure and function of antioxidant enzyme catalase (CAT) through their direct interactions. However, the underlying molecular mechanism is still unknown. This study investigated the direct interaction of SLS with CAT molecule and the underlying mechanisms using multi‐spectroscopic methods, isothermal titration calorimetry, and molecular docking studies. No obvious effects were observed on CAT structure and activity under low SLS concentration exposure. The particle size of CAT molecule decreased and CAT activity was slightly inhibited under high SLS concentration exposure. SLS prefers to bind to the interface of CAT mainly via van der Waals’ forces and hydrogen bonds. Subsequently, SLS interacts with the amino acid residues around the heme groups of CAT via hydrophobic interactions and might inhibit CAT activity.     

对萘磺酸钠修饰的石墨烯基纳米银复合抗菌材料的制备及性能评价

制备采用1-萘磺酸钠修饰的石墨烯基纳米银复合材料,并对其性能进行评价。首先制备了石墨烯基纳米银复合材料,采用1-萘磺酸钠修饰,记为AgNP/rGO-NA,然后通过与聚乙烯吡咯烷酮做保护剂的纳米银（PVP/AgNP）的比较,分析其稳定性,抗菌活性,细胞毒性。研究发现,纳米银AgNP在制备的复合材料表面的分布相对均匀,AgNP的质量分数为4.3%,粒径为5~15nm,Zeta电位为-42.5 mV;在无光或光照强度为3000 Lx（勒克斯）的低温光照仪环境下储存10 d,PVP/AgNP聚集作用较为明显,而AgNP/rGO-NA则分散性良好,聚集作用不明显;AgNP/rGO-NA具有更加良好的抗菌活性,生物相容性和相对较低的生物毒性。试验表明经过1-萘磺酸钠修饰的石墨烯基纳米银复合材料质量可靠,性能良好,具有广阔的应用前景。