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Synthesis of highly water-soluble fibrate derivatives via BGLation

机译:通过BGLation合成高水溶性贝特酸酯衍生物

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摘要

Three water-soluble fibrates (fenofibrate, bezafibrate and chlofibrate) conjugated with a symmetrically branched glyceryl trimer (BGL003) were synthesized, and an evaluation of the fenofibrate-BGL003 conjugate as a candidate for anti-hyperlipemia drug was carried out using rats. The water-solubility of the fenofibrate-BGL003 conjugate was several thousand times greater than that of the original fenofibrate. The lipid-lowering effects of the fenofibrate-BGL003 conjugate were as strong as those of the same grams of fenofibrate. The actual active species of fenofibrate, fenofibric acid, was detected in rats' blood, but neither the fenofibrate-BGL003 conjugate nor fenofibrate was detected, probably due to enzymatic hydrolysis of the ester bond. The plasma concentration of fenofibric acid derived from the fenofibrate-BGL003 conjugate was five times higher than that derived from fenofibrate 4 h after administration.
机译:合成了与对称分支的甘油三聚体(BGL003)缀合的三种水溶性贝特类药物(非诺贝特,苯扎贝特和氯贝特),并使用大鼠对非诺贝特-BGL003缀合物作为抗高脂血症药物的候选药物进行了评估。非诺贝特-BGL003缀合物的水溶性比原始非诺贝特大数千倍。非诺贝特-BGL003偶联物的降脂作用与相同克非诺贝特的作用一样强。在大鼠血液中检测到非诺贝特的实际活性物质非诺贝特酸,但未检测到非诺贝特-BGL003共轭物和非诺贝特,可能是由于酯键的酶促水解。给药后4小时,源自非诺贝特-BGL003缀合物的非诺贝特酸的血浆浓度比源自非诺贝特的血浆浓度高五倍。

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