Therapeutics & Biotechnology Division, Korea Research Institute of Chemical Technology, 141 Gajeong-ro, Yuseong-gu, Daejeon, 34114, South Korea.
General Technical Institute, Kolmar Korea, 61 (Naegok-dong) 8-gil, Heolleung-ro, Seocho-gu, Seoul, 06800, South Korea.
AAPS PharmSciTech. 2022 Sep 19;23(7):258. doi: 10.1208/s12249-022-02359-w.
In vitro-in vivo correlation (IVIVC) analysis reveals a relationship between in vitro release and in vivo pharmacokinetic response of the drug of interest. Sandostatin LAR Depot (SLD) for endocrine tumors and acromegaly is a sustained-release formulation of octreotide, a cyclic oligomer of 8 amino acids, which prolongs therapeutic efficacy and enhances medication compliance of octreotide. Since the efficacy of SLD is dependent on the pharmacokinetic characteristics of octreotide released from a biodegradable matrix polymer, poly(lactide-co-glycolide)-glucose, of SLD, the IVIVC of SLD is critical for predicting an in vivo behavior of the octreotide. In this study, in vitro release of octreotide from SLD was investigated using the release test media each containing 0.02% or 0.5% surfactant and having different pH values of 7.4 and 5.5. In vivo pharmacokinetic profiles of SLD were determined by LC-MS/MS analysis of the systemic blood concentration of octreotide after the SLD injection to rodents. In IVIVC analysis, the Weibull model was adopted as a drug release model for biodegradable microsphere formulation. The IVIVC analyses revealed the in vitro release test condition of SLD with the highest IVIV correlation coefficient. By applying the in vitro release data to the model derived from the IVIVC analysis, pharmacokinetic parameters of SLD could be predicted with the prediction error of ± 10 ~ 15%. IVIVC analysis and pharmacokinetic prediction model of SLD in our study can be an efficient tool for the development of long-acting pharmaceutical dosage forms.
体外-体内相关性 (IVIVC) 分析揭示了药物在体外释放与体内药代动力学反应之间的关系。用于内分泌肿瘤和肢端肥大症的 Sandostatin LAR Depot (SLD) 是奥曲肽的缓释制剂,奥曲肽是一种由 8 个氨基酸组成的环状寡聚物,可延长奥曲肽的治疗效果并提高其用药依从性。由于 SLD 的疗效取决于从 SLD 的可生物降解基质聚合物聚(乳酸-共-乙醇酸)-葡萄糖中释放的奥曲肽的药代动力学特征,因此 SLD 的 IVIVC 对于预测奥曲肽的体内行为至关重要。在这项研究中,使用含有 0.02%或 0.5%表面活性剂且 pH 值分别为 7.4 和 5.5 的释放测试介质研究了 SLD 中奥曲肽的体外释放。通过 LC-MS/MS 分析 SLD 注射后啮齿动物系统血液中奥曲肽的浓度来确定 SLD 的体内药代动力学特征。在 IVIVC 分析中,Weibull 模型被用作可生物降解微球制剂的药物释放模型。IVIVC 分析显示了与最高 IVIV 相关系数相关的 SLD 体外释放测试条件。通过将体外释放数据应用于 IVIVC 分析得出的模型,可以以预测误差为±10~15%预测 SLD 的药代动力学参数。我们研究中的 SLD 的 IVIVC 分析和药代动力学预测模型可以成为长效药物剂型开发的有效工具。