利用组织隔离肿瘤灌注系统对多柔比星包裹聚合物胶束进行肿瘤药代动力学-药效学模拟

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Molecular Pharmaceutics Pub Date : 2024-11-04 Epub Date: 2024-10-07 DOI:10.1021/acs.molpharmaceut.4c00729
Shugo Yamashita, Shunsuke Kimura, Akiko Kiriyama
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引用次数: 0

摘要

阐明输送抗癌药物的聚合物胶束的药代动力学(PK)对于精确的抗肿瘤 PK-药效学(PK-PD)模拟至关重要。特别是,建立一种方法来量化包裹在聚合物胶束中的抗癌药物的肿瘤流入和流出是一项重大挑战。一般肿瘤生物分布实验的缺点是,流入的药物容易量化,但流出的药物却很难量化。针对这一问题,我们提出了一种将组织隔离肿瘤灌注系统与微透析相结合的定量方法。这种方法的目的是分别通过肿瘤包埋的微透析探针和灌注液来量化聚合胶束释放的药物,从而确定肿瘤药物的流入和流出。此外,我们还在组织隔离的肿瘤灌注系统中灌注了对pH值敏感的聚乙二醇-聚(天冬氨酸-腙-多柔比星/苯丙氨酸)n(PPDF-Hyd-DOX),并量化了肿瘤流入和流出的DOX释放量,从而评估了该方法的可行性。根据定量结果,我们结合伽马分布延迟函数进行了分区分析,并计算了 PK 速率常数。我们将这些参数输入到肿瘤大鼠分区模型中,对大鼠血浆中 PPDF-Hyd-DOX 的浓度和模拟瘤内释放的 DOX 浓度进行体内外推断 (EVIVE)。模拟曲线与之前报道的 Walker 256 瘤内释放的 DOX 浓度曲线非常吻合。该 EVIVE-PK 模型与阈值自然生长肿瘤 PD 模型相结合,并进行了 PK-PD 分析。与之前报道的PK-PD模型相比,该模型能更好地拟合用PPDF-Hyd-DOX治疗的Walker 256大鼠的肿瘤重量曲线。因此,基于微透析的组织隔离肿瘤灌注系统的EVIVE是一种很有前途的聚合物胶束抗癌治疗PK-PD模拟方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumoral Pharmacokinetic-Pharmacodynamic Simulation of Doxorubicin-Encapsulated Polymeric Micelles Using a Tissue-Isolated Tumor Perfusion System.

Pharmacokinetic (PK) elucidation of polymeric micelles delivering anticancer drugs is crucial for accurate antitumor PK-pharmacodynamic (PK-PD) simulations. Particularly, establishing a methodology to quantify the tumor inflow and outflow of anticancer drugs encapsulated in polymeric micelles is an essential challenge. General tumor biodistribution experiments are disadvantageous in that inflow quantification is easy, but outflow quantification is challenging. We addressed this issue by proposing a quantification method that combines a tissue-isolated tumor perfusion system with microdialysis. This method aims to determine tumoral drug inflow and outflow by quantifying the drugs released from the polymeric micelles via a tumor-embedded microdialysis probe and perfusate, respectively. Furthermore, we evaluated the feasibility of this method by perfusing pH-sensitive polyethylene glycol-poly(aspartate-hydrazone-doxorubicin/phenylalanine)n (PPDF-Hyd-DOX) in a tissue-isolated tumor perfusion system, and we quantified tumor inflow and outflow released DOX. Based on the quantitative results, we performed compartmental analyses by incorporating the gamma-distributed delay function and calculated the PK rate constants. These parameters were input into a tumor-bearing rat compartment model for ex vivo-in vivo extrapolation (EVIVE) of the rat plasma PPDF-Hyd-DOX concentrations and simulated intratumorally released DOX concentrations. The simulation profiles demonstrated a good fit with the Walker 256 intratumoral released DOX concentration profiles previously reported. This EVIVE-PK model was coupled with the threshold natural-growth tumor PD model, and PK-PD analysis was performed. This model exhibited a better fit to the tumor weight profile of Walker 256-bearing rats treated with PPDF-Hyd-DOX than that of our previously reported PK-PD model. Thus, EVIVE, based on a tissue-isolated tumor perfusion system with microdialysis, is a promising approach for the PK-PD simulation of polymeric micelle anticancer therapy.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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