School of Pharmacy, University of Otago, Dunedin 9054, New Zealand.
J Control Release. 2011 Feb 10;149(3):307-13. doi: 10.1016/j.jconrel.2010.10.029. Epub 2010 Oct 31.
Poly(ethylcyanoacrylate) (PECA) nanoparticles containing the chemical sterilitant D-Lys⁶-GnRH were prepared by an in situ interfacial polymerization technique. Their potential as a peroral delivery system for biocontrol of the brushtail possum, a major pest species in New Zealand, was evaluated. Peptide release from resulting particles was studied in vitro in artificial gastric juice (AGJ), simulated intestinal fluids (SIF) and brushtail possum plasma. The nanoparticles released a small fraction of bioactive over 6h in AGJ and SIF (<5%), while staying intact and retaining fractions of intact D-Lys⁶-GnRH. In contrast, 60% of D-Lys⁶-GnRH was released after 1h in possum plasma. The nanoparticles were also administered in vivo into the caecum of brushtail possums. A significant biological response, measured as an increase in plasma luteinizing hormone (LH), was evident 10 min after administration. This demonstrates not only that PECA nanoparticles were able to facilitate the uptake of D-Lys⁶-GnRH from the caecum into systemic circulation but also that sufficient bioactive peptide reached the pituitary to exert a significant LH response following GnRH receptor mediated endocytosis. Hence, it can be concluded that PECA nanoparticles comprise a promising formulation strategy for the peroral delivery of the chemical sterilitant D-Lys⁶-GnRH to the brushtail possum in New Zealand.
聚(乙基氰基丙烯酸酯)(PECA)纳米粒子含有化学灭菌剂 D-Lys⁶-GnRH,通过原位界面聚合技术制备。评估了它们作为经口递送系统用于生物控制帚尾袋貂的潜力,帚尾袋貂是新西兰的主要害虫物种。研究了在人工胃液(AGJ)、模拟肠液(SIF)和帚尾袋貂血浆中,所得粒子中肽的体外释放情况。纳米粒子在 AGJ 和 SIF 中在 6 小时内释放出一小部分生物活性物质(<5%),而保持完整并保留部分完整的 D-Lys⁶-GnRH。相比之下,在袋貂血浆中 1 小时后释放了 60%的 D-Lys⁶-GnRH。还将纳米粒子体内给药到帚尾袋貂的盲肠中。给药 10 分钟后,可明显观察到血浆促黄体生成素(LH)增加的生物反应。这不仅表明 PECA 纳米粒子能够促进 D-Lys⁶-GnRH 从盲肠吸收到全身循环,而且还表明足够的生物活性肽到达垂体,在 GnRH 受体介导的内吞作用后发挥显著的 LH 反应。因此,可以得出结论,PECA 纳米粒子是一种有前途的制剂策略,用于经口向新西兰帚尾袋貂递送化学灭菌剂 D-Lys⁶-GnRH。