Formulation-dependent differences in paclitaxel distribution to anatomical sites relevant to chemotherapy-induced peripheral neuropathy.

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY Frontiers in Pharmacology Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1486686
Milda Girdenytė, Yang Hu, Aghavni Ginosyan, Margareta Hammarlund-Udenaes, Irena Loryan
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Abstract

Introduction: Chemotherapy-induced peripheral neuropathy (CIPN) is a dose-limiting adverse event observed in patients receiving paclitaxel, associated with initial pathological changes in the peripheral nervous system, i.e., distal nerves and dorsal root ganglia (DRG). The prevalence of CIPN in patients receiving paclitaxel formulated i) in polyethylated castor oil with ethanol (CreEL-PTX), ii) as albumin-bound (nab-PTX), and iii) in XR17 micelles (micellar-PTX), is unexpectedly varying. We hypothesize that the discrepancy in CIPN prevalence could be governed by differences in the extent of paclitaxel distribution across blood-to-tissue barriers at the CIPN-sites, caused by the specific formulation.

Methods: The recently developed Combinatory Mapping Approach for CIPN was used to determine the unbound tissue-to-plasma concentration ratio Kp,uu,tissue, after a 4-h infusion of 4 mg/kg CreEL-PTX, 4 mg/kg nab-PTX or 1 mg/kg micellar-PTX in male and female Sprague Dawley rats. Kp,uu,tissue was determined in conventional (DRG, sciatic nerve) and non-conventional (brain, spinal cord, skeletal muscle) CIPN-sites.

Results: Based on our data, the Cremophor-free paclitaxel formulations were associated with a higher distribution of paclitaxel to CIPN-sites than CreEL-PTX, e.g., Kp,uu,DRG of 0.70 and 0.60 for nab-PTX and micellar-PTX, respectively, in comparison to 0.27 for CreEL-PTX (p < 0.01). In addition, the fraction of unbound paclitaxel in plasma was on average 1.6-fold higher in nab- and micellar PTX arms and equal to 0.061 and 0.065, respectively, compared to 0.039 for the CreEL-PTX treatment arm (p < 0.0001).

Discussion: In the case of similar unbound paclitaxel concentration in the plasma of patients and assumed species-independent extent of paclitaxel transport across the barriers, nab- and micellar-PTX formulations can lead to higher paclitaxel exposure at CIPN-sites in comparison to CreEL-PTX.

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紫杉醇在化疗引起的周围神经病变相关解剖部位的分布因配方而异。
简介化疗诱导的周围神经病变(CIPN)是紫杉醇治疗患者的一种剂量限制性不良反应,与周围神经系统(即远端神经和背根神经节(DRG))的最初病理变化有关。在接受紫杉醇治疗的患者中,CIPN 的发生率出乎意料地各不相同:① 以乙醇聚乙基蓖麻油(CreEL-PTX)的形式;② 以白蛋白结合(nab-PTX)的形式;③ 以 XR17 胶束(micellar-PTX)的形式。我们推测,CIPN发生率的差异可能是由特定制剂导致的紫杉醇在CIPN位点穿过血液-组织屏障的分布程度不同造成的:方法:在雄性和雌性 Sprague Dawley 大鼠体内输注 4 毫克/千克 CreEL-PTX、4 毫克/千克 nab-PTX 或 1 毫克/千克胶束-PTX 4 小时后,采用最近开发的 CIPN 组合映射法测定未结合的组织与血浆浓度比 Kp,uu,组织。测定了常规(DRG、坐骨神经)和非常规(脑、脊髓、骨骼肌)CIPN-位点的 Kp、uu、组织:根据我们的数据,与 CreEL-PTX 相比,不含 Cremophor 的紫杉醇制剂在 CIPN 位点的紫杉醇分布更高,例如,nab-PTX 和胶束-PTX 在 DRG 中的 Kp,uu,DRG 分别为 0.70 和 0.60,而 CreEL-PTX 为 0.27(p < 0.01)。此外,血浆中未结合紫杉醇的比例在nab-PTX和胶束-PTX治疗组平均高出1.6倍,分别为0.061和0.065,而CreEL-PTX治疗组为0.039(p < 0.0001):讨论:在患者血浆中未结合紫杉醇浓度相似且紫杉醇跨屏障转运程度与物种无关的假设情况下,与CreEL-PTX相比,nab和胶束-PTX制剂可导致紫杉醇在CIPN位点的暴露更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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