烷基和全氟烷基端粒表面活性剂的生物相容性。

L Zarif, J G Riess, B Pucci, A A Pavia
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引用次数: 15

摘要

报道了两个新的非离子型端粒表面活性剂家族的初步比较生物学评价,这些表面活性剂是从Tris(羟甲基)丙烯酰胺甲烷(THAM)中提取的。这些三丙烯酸酯缀合物(TAC)的设计目的是提高用于可注射氧输送系统的氟碳乳液的稳定性和生物相容性。它们的两亲性是由于在同一分子中同时存在几个亲水的THAM残基和一个由碳氢化合物(H-TAC家族)或碳氟化合物(F-TAC家族)链组成的疏水尾部。静脉注射后小鼠的急性毒性较低(H-TAC的LD50在625至1250 mg/kg体重范围内,而F-TAC的LD50在630至4500 mg/kg体重范围内),并且随着疏水链的长度而增加。当浓度达到200 g/l时,F-TAC没有检测到溶血活性,而H-TAC在浓度为5 g/l或更低时则有溶血活性,并且随着烷基链长度的增加而增加。新的表面活性剂对Namalva细胞培养物的生长和活力的影响也随着疏水链的长度而增加,对F-TAC的耐受性也更好。总的来说,氟化两亲体表现出比它们的碳氢化合物类似物更好的耐受性,尽管它们的表面活性显著增加。这两个化合物家族似乎都有潜力作为生物医学应用的强亲水性表面活性剂。
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Biocompatibility of alkyl and perfluoroalkyl telomeric surfactants derived from THAM.

A preliminary, comparative biological evaluation of two new families of non-ionic telomeric surfactants derived from Tris(hydroxymethyl)acrylaminomethane (THAM) is reported. These trisacryl conjugates, or TAC, were designed with the purpose of improving the stability and biocompatibility of fluorocarbon emulsions to be used in injectable oxygen-delivering systems. Their amphiphilic character arises from the simultaneous presence in the same molecule of several hydrophilic THAM residues and of a hydrophobic tail consisting in either a hydrocarbon (H-TAC family) or a fluorocarbon (F-TAC family) chain. The acute toxicity in mice after intravenous injection is low (LD50 in the 625 to 1250 mg/kg body weight range for the H-TAC compared to 630 to 4500 mg/kg body weight range for F-TAC) and increases with the length of the hydrophobic chain. No hemolytic activity was detected for the F-TAC at concentrations up to 200 g/l, while hemolysis is found for the H-TAC at a concentration of 5 g/l or less and increases with the alkyl chain length. The impact of the new surfactants on the growth and viability of Namalva cell cultures also increases with the length of the hydrophobic chain, with again a better tolerance for the F-TAC. Altogether the fluorinated amphiphiles display better tolerance than their hydrocarbon analogs in spite of their significantly increased surface activity. Both families of compounds appear to have potential as strongly hydrophilic surfactants for biomedical applications.

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