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评估伊立替康经口腔给药的潜力:通过猪口腔黏膜的物理化学特征和体外渗透评估。

Evaluating the Potential for Delivery of Irinotecan via the Buccal Route: Physicochemical Characterization and In Vitro Permeation Assessment Across Porcine Buccal Mucosa.

机构信息

Division of Pharmaceutical Sciences, Long Island University, Brooklyn, New York, 11201, USA.

Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University/OHSU, Portland, Oregon, 97201, USA.

出版信息

AAPS PharmSciTech. 2017 Apr;18(3):867-874. doi: 10.1208/s12249-016-0578-z. Epub 2016 Jun 30.

Abstract

Irinotecan (CPT-11) is used to treat advanced colorectal cancer as an intravenous therapy. Depending on pH, CPT-11 exists in either a lactone (active) or carboxylate (inactive) form, or both. In this investigation, the feasibility for systemic delivery of CPT-11 through the buccal route was evaluated. Permeation of CPT-11 across porcine buccal mucosa was studied in vitro using side-by-side flow through diffusion cells at 37°C. Experiments were performed over a pH range from 4 to 9, and the permeability of both the lactone and carboxylate forms of CPT-11 was measured. CPT-11 steady state flux was determined over a range of donor concentrations at pH 4 (0.5, 1, 5, 10, 15, 20 mg/ml) and pH 6.8 (0.5, 5, 10 mg/ml). Steady state flux increased linearly with increasing donor concentration of CPT-11 at pH 4 (r  = 0.9935) and at pH 6.8 (r  = 0.9886). CPT-11 permeability was independent of pH, although the distribution coefficient increased with increasing pH. Estimates of permeability for the lactone and carboxylate forms were 4.16 × 10 cm/s and 2.6 × 10 cm/s, respectively. These calculated permeability values were in agreement with the in vitro experimental data. Overall, CPT-11 was found to permeate through porcine buccal mucosa via passive diffusion. CPT-11 permeability was independent of pH, suggesting that the compound was transported mainly via a paracellular route. Overall, the results of this research suggest that the buccal route is a potential extravascular mode of delivery for CPT-11.

摘要

伊立替康(CPT-11)作为静脉内治疗用于治疗晚期结直肠癌。根据 pH 值,CPT-11 以内酯(活性)或羧酸酯(非活性)形式存在,或者两者兼而有之。在本研究中,评估了通过颊途径全身递送 CPT-11 的可行性。在 37°C 下,使用侧流扩散细胞体外研究 CPT-11 穿过猪颊黏膜的渗透情况。实验在 pH 值为 4 至 9 的范围内进行,并测量了 CPT-11 的内酯和羧酸酯两种形式的渗透性。在 pH 值为 4(0.5、1、5、10、15、20 mg/ml)和 pH 值为 6.8(0.5、5、10 mg/ml)时,在一系列供体浓度下确定 CPT-11 的稳态通量。CPT-11 的稳态通量随供体 CPT-11 浓度的增加而呈线性增加,在 pH 值为 4(r = 0.9935)和 pH 值为 6.8(r = 0.9886)时。CPT-11 的渗透性与 pH 值无关,尽管分配系数随 pH 值的增加而增加。内酯和羧酸酯形式的渗透性估计值分别为 4.16×10-6 cm/s 和 2.6×10-6 cm/s。这些计算的渗透性值与体外实验数据一致。总的来说,CPT-11 被发现通过猪颊黏膜通过被动扩散渗透。CPT-11 的渗透性与 pH 值无关,表明该化合物主要通过细胞旁途径运输。总的来说,这项研究的结果表明,颊途径是 CPT-11 的一种潜在的血管外给药途径。

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