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Formation of acylated growth hormone-releasing peptide-6 by poly(lactide-co-glycolide) and its biological activity

机译:聚(丙交酯-共-乙交酯)酰化生长激素释放肽-6的形成及其生物学活性

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摘要

The purpose of this study was to investigate the formation of acylated impurity resulting from a chemical reaction between the growth hormone-releasing peptide-6 (GHRP-6) and poly(lactide-co-glycolide) (PLGA) and the effect of peptide acylation on the in vivo biological activity of GHRP-6. The peptide acylation pattern of GHRP-6 by hydrophilic PLGA polymers with different molecular weights was characterized by reversed-phase high-performance liquid chromatography and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Higher levels of acylated GHRP-6 were produced with the higher molecular weight PLGA, which might be due to the slower degradation rate of the polymer. The evaluation of the biological activity in rats showed that the acylated GHRP-6 had a much lower activity than the intact GHRP-6. This finding suggests that the acylation reaction would decrease the effectiveness of the GHRP-6 formulation such as PLGA microspheres. There-fore, a strategy for stabilizing the GHRP-6 will be necessary for the development of a successful formulation of PLGA microspheres.
机译:这项研究的目的是研究由生长激素释放肽6(GHRP-6)和聚丙交酯-乙交酯(PLGA)之间的化学反应引起的酰化杂质的形成以及肽酰化的影响对GHRP-6的体内生物活性的影响。通过反相高效液相色谱和基质辅助激光解吸/电离飞行时间质谱分析了不同分子量的亲水性PLGA聚合物对GHRP-6的肽酰化作用。用较高分子量的PLGA产生较高水平的酰化的GHRP-6,这可能是由于聚合物的降解速率较慢。对大鼠生物活性的评估表明,酰化的GHRP-6的活性远低于完整的GHRP-6。该发现表明酰化反应将降低GHRP-6制剂例如PLGA微球的有效性。因此,对于成功开发PLGA微球制剂而言,稳定GHRP-6的策略将是必要的。

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